PubMed Mentions

The links below are to publications on PubMed referring to PLINK. This list is gathered weekly from PubMed automatically.

Publication/References
Application of genome-wide single nucleotide polymorphism typing: simple association and beyond. Description: Gibbs, J Raphael, et al. Application of genome-wide single nucleotide polymorphism typing: simple association and beyond. ''PLoS Genet''. 2006 Oct 6; '''2''' (10):e150
IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease. Description: Tremelling, Mark, et al. IL23R variation determines susceptibility but not disease phenotype in inflammatory bowel disease. ''Gastroenterology''. 2007 May; '''132''' (5):1657-64
Identification of two independent risk factors for lupus within the MHC in United Kingdom families. Description: Fernando, Michelle M A, et al. Identification of two independent risk factors for lupus within the MHC in United Kingdom families. ''PLoS Genet''. 2007 Nov; '''3''' (11):e192
Evaluation of LOXL1 polymorphisms in primary open-angle glaucoma in southern and northern Chinese. Description: Gong, Wei Fen, et al. Evaluation of LOXL1 polymorphisms in primary open-angle glaucoma in southern and northern Chinese. ''Mol Vis''. 2008; '''14''': 2381-9
Lack of association of polymorphisms in homocysteine metabolism genes with pseudoexfoliation syndrome and glaucoma. Description: Fan, Bao Jian, et al. Lack of association of polymorphisms in homocysteine metabolism genes with pseudoexfoliation syndrome and glaucoma. ''Mol Vis''. 2008; '''14''': 2484-91
Contributions of MYOC and CYP1B1 mutations to JOAG. Description: Bayat, Behnaz, et al. Contributions of MYOC and CYP1B1 mutations to JOAG. ''Mol Vis''. 2008 Mar 13; '''14''': 508-17
A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. Description: Liu, Ying, et al. A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. ''PLoS Genet''. 2008 Mar 28; '''4''' (3):e1000041
Analysis of genomic admixture in Uyghur and its implication in mapping strategy. Description: Xu, Shuhua, et al. Analysis of genomic admixture in Uyghur and its implication in mapping strategy. ''Am J Hum Genet''. 2008 Apr; '''82''' (4):883-94
Specificity of the STAT4 genetic association for severe disease manifestations of systemic lupus erythematosus. Description: Taylor, Kimberly E, et al. Specificity of the STAT4 genetic association for severe disease manifestations of systemic lupus erythematosus. ''PLoS Genet''. 2008 May 30; '''4''' (5):e1000084
Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle. Description: Tallila, Jonna, et al. Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle. ''Am J Hum Genet''. 2008 Jun; '''82''' (6):1361-7
Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations. Description: Kristjansdottir, G, et al. Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations. ''J Med Genet''. 2008 Jun; '''45''' (6):362-9
Common variation in the fat mass and obesity-associated (FTO) gene confers risk of obesity and modulates BMI in the Chinese population. Description: Chang, Yi-Cheng, et al. Common variation in the fat mass and obesity-associated (FTO) gene confers risk of obesity and modulates BMI in the Chinese population. ''Diabetes''. 2008 Aug; '''57''' (8):2245-52
Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians. Description: Ng, Maggie C Y, et al. Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians. ''Diabetes''. 2008 Aug; '''57''' (8):2226-33
Polymorphisms within the adenosine receptor 2a gene are associated with adverse events in RA patients treated with MTX. Description: Hider, S L, et al. Polymorphisms within the adenosine receptor 2a gene are associated with adverse events in RA patients treated with MTX. ''Rheumatology (Oxford)''. 2008 Aug; '''47''' (8):1156-9
WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels. Description: Lee, Jenny C, et al. WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels. ''Am J Hum Genet''. 2008 Aug; '''83''' (2):180-92
Evaluating the role of LPIN1 variation in insulin resistance, body weight, and human lipodystrophy in U.K. Populations. Description: Fawcett, Katherine A, et al. Evaluating the role of LPIN1 variation in insulin resistance, body weight, and human lipodystrophy in U.K. Populations. ''Diabetes''. 2008 Sep; '''57''' (9):2527-33
The Population Reference Sample, POPRES: a resource for population, disease, and pharmacological genetics research. Description: Nelson, Matthew R, et al. The Population Reference Sample, POPRES: a resource for population, disease, and pharmacological genetics research. ''Am J Hum Genet''. 2008 Sep; '''83''' (3):347-58
A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. Description: Abraham, Richard, et al. A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. ''BMC Med Genomics''. 2008 Sep 29; '''1''': 44
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series. Description: Webb, T E F, et al. Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series. ''Brain''. 2008 Oct; '''131''' (Pt 10):2632-46
Tissue-specific genetic control of splicing: implications for the study of complex traits. Description: Heinzen, Erin L, et al. Tissue-specific genetic control of splicing: implications for the study of complex traits. ''PLoS Biol''. 2008 Dec 23; '''6''' (12):e1
Association of genetic variants at 3q22 with nephropathy in patients with type 1 diabetes mellitus. Description: He, Bing, et al. Association of genetic variants at 3q22 with nephropathy in patients with type 1 diabetes mellitus. ''Am J Hum Genet''. 2009 Jan; '''84''' (1):5-13
Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry. Description: Grant, Struan Fa, et al. Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry. ''Appl Clin Genet''. 2009; '''2''': 1-5
Fine mapping linkage analysis identifies a novel susceptibility locus for myopia on chromosome 2q37 adjacent to but not overlapping MYP12. Description: Schache, Maria, et al. Fine mapping linkage analysis identifies a novel susceptibility locus for myopia on chromosome 2q37 adjacent to but not overlapping MYP12. ''Mol Vis''. 2009; '''15''': 722-30
Genetic variation and population substructure in outbred CD-1 mice: implications for genome-wide association studies. Description: Aldinger, Kimberly A, et al. Genetic variation and population substructure in outbred CD-1 mice: implications for genome-wide association studies. ''PLoS One''. 2009; '''4''' (3):e4729
Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysis. Description: Hinks, Anne, et al. Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysis. ''Arthritis Rheum''. 2009 Jan; '''60''' (1):258-63
Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia. Description: Liu, Yang, et al. Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia. ''J Biomed Biotechnol''. 2009; '''2009''': 536918
HECTD2 is associated with susceptibility to mouse and human prion disease. Description: Lloyd, Sarah E, et al. HECTD2 is associated with susceptibility to mouse and human prion disease. ''PLoS Genet''. 2009 Feb; '''5''' (2):e1000383
Positive association of common variants in CD36 with neovascular age-related macular degeneration. Description: Kondo, Naoshi, et al. Positive association of common variants in CD36 with neovascular age-related macular degeneration. ''Aging (Albany NY)''. 2009 Feb 12; '''1''' (2):266-74
A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose. Description: Takeuchi, Fumihiko, et al. A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose. ''PLoS Genet''. 2009 Mar; '''5''' (3):e1000433
Genome-wide association analyses identify SPOCK as a key novel gene underlying age at menarche. Description: Liu, Yao-Zhong, et al. Genome-wide association analyses identify SPOCK as a key novel gene underlying age at menarche. ''PLoS Genet''. 2009 Mar; '''5''' (3):e1000420
Multi-criteria decision making approaches for quality control of genome-wide association studies. Description: Malovini, Alberto, et al. Multi-criteria decision making approaches for quality control of genome-wide association studies. ''Summit Transl Bioinform''. 2009 Mar 1; '''2009''': 74-8
Identification of IFRD1 as a modifier gene for cystic fibrosis lung disease. Description: Gu, YuanYuan, et al. Identification of IFRD1 as a modifier gene for cystic fibrosis lung disease. ''Nature''. 2009 Apr 23; '''458''' (7241):1039-42
Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. Description: Himes, Blanca E, et al. Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. ''Am J Hum Genet''. 2009 May; '''84''' (5):581-93
Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder. Description: Schulze, T G, et al. Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder. ''Mol Psychiatry''. 2009 May; '''14''' (5):487-91
ITGAM is associated with disease susceptibility and renal nephritis of systemic lupus erythematosus in Hong Kong Chinese and Thai. Description: Yang, Wanling, et al. ITGAM is associated with disease susceptibility and renal nephritis of systemic lupus erythematosus in Hong Kong Chinese and Thai. ''Hum Mol Genet''. 2009 Jun 1; '''18''' (11):2063-70
Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritis. Description: Zinovieva, Elena, et al. Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritis. ''PLoS Genet''. 2009 Jun; '''5''' (6):e1000528
Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. Description: He, Chunyan, et al. Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. ''Nat Genet''. 2009 Jun; '''41''' (6):724-8
Postural changes in blood pressure associated with interactions between candidate genes for chronic respiratory diseases and exposure to particulate matter. Description: Wilker, Elissa, et al. Postural changes in blood pressure associated with interactions between candidate genes for chronic respiratory diseases and exposure to particulate matter. ''Environ Health Perspect''. 2009 Jun; '''117''' (6):935-40
Reduced-function SLC22A1 polymorphisms encoding organic cation transporter 1 and glycemic response to metformin: a GoDARTS study. Description: Zhou, Kaixin, et al. Reduced-function SLC22A1 polymorphisms encoding organic cation transporter 1 and glycemic response to metformin: a GoDARTS study. ''Diabetes''. 2009 Jun; '''58''' (6):1434-9
Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk. Description: Drenos, Fotios, et al. Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk. ''Hum Mol Genet''. 2009 Jun 15; '''18''' (12):2305-16
Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array. Description: Sober, Siim, et al. Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array. ''PLoS One''. 2009 Jun 29; '''4''' (6):e6034
A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis imperfecta. Description: Drogemuller, Cord, et al. A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis imperfecta. ''PLoS Genet''. 2009 Jul; '''5''' (7):e1000579
Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. Description: Takeuchi, Fumihiko, et al. Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. ''Diabetes''. 2009 Jul; '''58''' (7):1690-9
Current software for genotype imputation. Description: Ellinghaus, David, et al. Current software for genotype imputation. ''Hum Genomics''. 2009 Jul; '''3''' (4):371-80
Elevated MBL concentrations are not an indication of association between the MBL2 gene and type 1 diabetes or diabetic nephropathy. Description: Kaunisto, Mari A, et al. Elevated MBL concentrations are not an indication of association between the MBL2 gene and type 1 diabetes or diabetic nephropathy. ''Diabetes''. 2009 Jul; '''58''' (7):1710-4
Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE. Description: Morris, D L, et al. Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE. ''Genes Immun''. 2009 Jul; '''10''' (5):404-13
Association between a rare SNP in the second intron of human Agouti related protein gene and increased BMI. Description: Kalnina, Ineta, et al. Association between a rare SNP in the second intron of human Agouti related protein gene and increased BMI. ''BMC Med Genet''. 2009 Jul 14; '''10''': 63
A genome-wide in vitro bacterial-infection screen reveals human variation in the host response associated with inflammatory disease. Description: Ko, Dennis C, et al. A genome-wide in vitro bacterial-infection screen reveals human variation in the host response associated with inflammatory disease. ''Am J Hum Genet''. 2009 Aug; '''85''' (2):214-27
CMIP and ATP2C2 modulate phonological short-term memory in language impairment. Description: Newbury, Dianne F, et al. CMIP and ATP2C2 modulate phonological short-term memory in language impairment. ''Am J Hum Genet''. 2009 Aug; '''85''' (2):264-72
Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children. Description: Hancock, Dana B, et al. Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children. ''PLoS Genet''. 2009 Aug; '''5''' (8):e1000623
Identification of the UBP1 locus as a critical blood pressure determinant using a combination of mouse and human genetics. Description: Koutnikova, Hana, et al. Identification of the UBP1 locus as a critical blood pressure determinant using a combination of mouse and human genetics. ''PLoS Genet''. 2009 Aug; '''5''' (8):e1000591
A strong association of axillary osmidrosis with the wet earwax type determined by genotyping of the ABCC11 gene. Description: Nakano, Motoi, et al. A strong association of axillary osmidrosis with the wet earwax type determined by genotyping of the ABCC11 gene. ''BMC Genet''. 2009 Aug 4; '''10''': 42
Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. Description: Potkin, Steven G, et al. Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. ''PLoS One''. 2009 Aug 7; '''4''' (8):e6501
Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions. Description: Casselbrant, Margaretha L, et al. Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions. ''BMC Med Genet''. 2009 Sep 3; '''10''': 85
Genetic variation in the proximal promoter of ABC and SLC superfamilies: liver and kidney specific expression and promoter activity predict variation. Description: Hesselson, Stephanie E, et al. Genetic variation in the proximal promoter of ABC and SLC superfamilies: liver and kidney specific expression and promoter activity predict variation. ''PLoS One''. 2009 Sep 9; '''4''' (9):e6942
HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q. Description: Lloyd, Sarah E, et al. HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q. ''BMC Med Genet''. 2009 Sep 15; '''10''': 90
Association between KCNJ6 (GIRK2) gene polymorphisms and postoperative analgesic requirements after major abdominal surgery. Description: Nishizawa, Daisuke, et al. Association between KCNJ6 (GIRK2) gene polymorphisms and postoperative analgesic requirements after major abdominal surgery. ''PLoS One''. 2009 Sep 16; '''4''' (9):e7060
Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy. Description: Al-Chalabi, Ammar, et al. Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy. ''PLoS One''. 2009 Sep 22; '''4''' (9):e7114
Genomewide association study for onset age in Parkinson disease. Description: Latourelle, Jeanne C, et al. Genomewide association study for onset age in Parkinson disease. ''BMC Med Genet''. 2009 Sep 22; '''10''': 98
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Description: Harold, Denise, et al. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. ''Nat Genet''. 2009 Oct; '''41''' (10):1088-93
Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population. Description: Simon-Sanchez, Javier, et al. Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population. ''PLoS One''. 2009 Oct 22; '''4''' (10):e7494
Evidence for genetic association of RORB with bipolar disorder. Description: McGrath, Casey L, et al. Evidence for genetic association of RORB with bipolar disorder. ''BMC Psychiatry''. 2009 Nov 12; '''9''': 70
Genetic variation and recent positive selection in worldwide human populations: evidence from nearly 1 million SNPs. Description: Lopez Herraez, David, et al. Genetic variation and recent positive selection in worldwide human populations: evidence from nearly 1 million SNPs. ''PLoS One''. 2009 Nov 18; '''4''' (11):e7888
Genomic dissection of population substructure of Han Chinese and its implication in association studies. Description: Xu, Shuhua, et al. Genomic dissection of population substructure of Han Chinese and its implication in association studies. ''Am J Hum Genet''. 2009 Dec; '''85''' (6):762-74
Sequence variations of ABCB1, SLC6A2, SLC6A3, SLC6A4, CREB1, CRHR1 and NTRK2: association with major depression and antidepressant response in Mexican-Americans. Description: Dong, C, et al. Sequence variations of ABCB1, SLC6A2, SLC6A3, SLC6A4, CREB1, CRHR1 and NTRK2: association with major depression and antidepressant response in Mexican-Americans. ''Mol Psychiatry''. 2009 Dec; '''14''' (12):1105-18
The common FTO variant rs9939609 is not associated with BMI in a longitudinal study on a cohort of Swedish men born 1920-1924. Description: Jacobsson, Josefin A, et al. The common FTO variant rs9939609 is not associated with BMI in a longitudinal study on a cohort of Swedish men born 1920-1924. ''BMC Med Genet''. 2009 Dec 9; '''10''': 131
Application of Bayesian classification with singular value decomposition method in genome-wide association studies. Description: Kwon, Soonil, et al. Application of Bayesian classification with singular value decomposition method in genome-wide association studies. ''BMC Proc''. 2009 Dec 15; '''3 Suppl 7''': S9
Classification tree for detection of single-nucleotide polymorphism (SNP)-by-SNP interactions related to heart disease: Framingham Heart Study. Description: Yao, Li, et al. Classification tree for detection of single-nucleotide polymorphism (SNP)-by-SNP interactions related to heart disease: Framingham Heart Study. ''BMC Proc''. 2009 Dec 15; '''3 Suppl 7''': S83
Transferability and fine-mapping of genome-wide associated loci for adult height across human populations. Description: Shriner, Daniel, et al. Transferability and fine-mapping of genome-wide associated loci for adult height across human populations. ''PLoS One''. 2009 Dec 22; '''4''' (12):e8398
Promoter variant of PIK3C3 is associated with autoimmunity against Ro and Sm epitopes in African-American lupus patients. Description: Kariuki, Silvia N, et al. Promoter variant of PIK3C3 is associated with autoimmunity against Ro and Sm epitopes in African-American lupus patients. ''J Biomed Biotechnol''. 2010; '''2010''': 826434
The role of genetic variation near interferon-kappa in systemic lupus erythematosus. Description: Harley, Isaac T W, et al. The role of genetic variation near interferon-kappa in systemic lupus erythematosus. ''J Biomed Biotechnol''. 2010; '''2010''':
A sequence polymorphism in MSTN predicts sprinting ability and racing stamina in thoroughbred horses. Description: Hill, Emmeline W, et al. A sequence polymorphism in MSTN predicts sprinting ability and racing stamina in thoroughbred horses. ''PLoS One''. 2010 Jan 20; '''5''' (1):e8645
CLOCK is suggested to associate with comorbid alcohol use and depressive disorders. Description: Sjoholm, Louise K, et al. CLOCK is suggested to associate with comorbid alcohol use and depressive disorders. ''J Circadian Rhythms''. 2010 Jan 21; '''8''': 1
Gene expression profiling in monocytes and SNP association suggest the importance of the STAT1 gene for osteoporosis in both Chinese and Caucasians. Description: Chen, Xiang-Ding, et al. Gene expression profiling in monocytes and SNP association suggest the importance of the STAT1 gene for osteoporosis in both Chinese and Caucasians. ''J Bone Miner Res''. 2010 Feb; '''25''' (2):339-55
Maternal and fetal genetic associations of PTGER3 and PON1 with preterm birth. Description: Ryckman, Kelli K, et al. Maternal and fetal genetic associations of PTGER3 and PON1 with preterm birth. ''PLoS One''. 2010 Feb 3; '''5''' (2):e9040
Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies. Description: Kung, Annie W C, et al. Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies. ''Am J Hum Genet''. 2010 Feb 12; '''86''' (2):229-39
Functional gene group analysis reveals a role of synaptic heterotrimeric G proteins in cognitive ability. Description: Ruano, Dina, et al. Functional gene group analysis reveals a role of synaptic heterotrimeric G proteins in cognitive ability. ''Am J Hum Genet''. 2010 Feb 12; '''86''' (2):113-25
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene. Description: Jakkula, Eveliina, et al. Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene. ''Am J Hum Genet''. 2010 Feb 12; '''86''' (2):285-91
Systematic analysis of circadian genes in a population-based sample reveals association of TIMELESS with depression and sleep disturbance. Description: Utge, Siddheshwar J, et al. Systematic analysis of circadian genes in a population-based sample reveals association of TIMELESS with depression and sleep disturbance. ''PLoS One''. 2010 Feb 18; '''5''' (2):e9259
Evaluation of DOK5 as a susceptibility gene for type 2 diabetes and obesity in North Indian population. Description: Tabassum, Rubina, et al. Evaluation of DOK5 as a susceptibility gene for type 2 diabetes and obesity in North Indian population. ''BMC Med Genet''. 2010 Feb 27; '''11''': 35
Genetic variation in the hypothalamic-pituitary-adrenal stress axis influences susceptibility to musculoskeletal pain: results from the EPIFUND study. Description: Holliday, Kate L, et al. Genetic variation in the hypothalamic-pituitary-adrenal stress axis influences susceptibility to musculoskeletal pain: results from the EPIFUND study. ''Ann Rheum Dis''. 2010 Mar; '''69''' (3):556-60
Plasmodium falciparum genome-wide scans for positive selection, recombination hot spots and resistance to antimalarial drugs. Description: Mu, Jianbing, et al. Plasmodium falciparum genome-wide scans for positive selection, recombination hot spots and resistance to antimalarial drugs. ''Nat Genet''. 2010 Mar; '''42''' (3):268-71
A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level. Description: Pattaro, Cristian, et al. A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level. ''BMC Med Genet''. 2010 Mar 11; '''11''': 41
Systems genetics analysis of gene-by-environment interactions in human cells. Description: Romanoski, Casey E, et al. Systems genetics analysis of gene-by-environment interactions in human cells. ''Am J Hum Genet''. 2010 Mar 12; '''86''' (3):399-410
ARNTL (BMAL1) and NPAS2 gene variants contribute to fertility and seasonality. Description: Kovanen, Leena, et al. ARNTL (BMAL1) and NPAS2 gene variants contribute to fertility and seasonality. ''PLoS One''. 2010 Apr 2; '''5''' (4):e10007
Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time. Description: Houlihan, Lorna M, et al. Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time. ''Am J Hum Genet''. 2010 Apr 9; '''86''' (4):626-31
Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset. Description: Glas, Jurgen, et al. Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset. ''PLoS One''. 2010 Apr 29; '''5''' (4):e10373
Interpretation of association signals and identification of causal variants from genome-wide association studies. Description: Wang, Kai, et al. Interpretation of association signals and identification of causal variants from genome-wide association studies. ''Am J Hum Genet''. 2010 May 14; '''86''' (5):730-42
Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population. Description: Han, Xueyao, et al. Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population. ''BMC Med Genet''. 2010 May 28; '''11''': 81
Investigation of rheumatoid arthritis susceptibility genes identifies association of AFF3 and CD226 variants with response to anti-tumour necrosis factor treatment. Description: Tan, Rachael J L, et al. Investigation of rheumatoid arthritis susceptibility genes identifies association of AFF3 and CD226 variants with response to anti-tumour necrosis factor treatment. ''Ann Rheum Dis''. 2010 Jun; '''69''' (6):1029-35
Validation of the CD6 and TNFRSF1A loci as risk factors for multiple sclerosis in Spain. Description: Swaminathan, Bhairavi, et al. Validation of the CD6 and TNFRSF1A loci as risk factors for multiple sclerosis in Spain. ''J Neuroimmunol''. 2010 Jun; '''223''' (1-2):100-3
Pooled association tests for rare variants in exon-resequencing studies. Description: Price, Alkes L, et al. Pooled association tests for rare variants in exon-resequencing studies. ''Am J Hum Genet''. 2010 Jun 11; '''86''' (6):832-8
Principal-component analysis for assessment of population stratification in mitochondrial medical genetics. Description: Biffi, Alessandro, et al. Principal-component analysis for assessment of population stratification in mitochondrial medical genetics. ''Am J Hum Genet''. 2010 Jun 11; '''86''' (6):904-17
Transforming growth factor beta 2 and heme oxygenase 1 genes are risk factors for the cerebral malaria syndrome in Angolan children. Description: Sambo, Maria Rosario, et al. Transforming growth factor beta 2 and heme oxygenase 1 genes are risk factors for the cerebral malaria syndrome in Angolan children. ''PLoS One''. 2010 Jun 16; '''5''' (6):e11141
Haplotypes that include the integrin alpha 11 gene are associated with tick burden in cattle. Description: Porto Neto, Laercio R, et al. Haplotypes that include the integrin alpha 11 gene are associated with tick burden in cattle. ''BMC Genet''. 2010 Jun 21; '''11''': 55
Pathway-based genome-wide association analysis identified the importance of regulation-of-autophagy pathway for ultradistal radius BMD. Description: Zhang, Lishu, et al. Pathway-based genome-wide association analysis identified the importance of regulation-of-autophagy pathway for ultradistal radius BMD. ''J Bone Miner Res''. 2010 Jul; '''25''' (7):1572-80
Quantitative trait analysis suggests human DAZL may be involved in regulating sperm counts and motility. Description: Hsu, Chao-Chin, et al. Quantitative trait analysis suggests human DAZL may be involved in regulating sperm counts and motility. ''Reprod Biomed Online''. 2010 Jul; '''21''' (1):77-83
Visualizing chromosome mosaicism and detecting ethnic outliers by the method of "rare" heterozygotes and homozygotes (RHH). Description: McGinnis, Ralph E, et al. Visualizing chromosome mosaicism and detecting ethnic outliers by the method of "rare" heterozygotes and homozygotes (RHH). ''Hum Mol Genet''. 2010 Jul 1; '''19''' (13):2539-53
Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot". Description: Johnatty, Sharon E, et al. Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot". ''PLoS Genet''. 2010 Jul 8; '''6''' (7):e1001016
A versatile gene-based test for genome-wide association studies. Description: Liu, Jimmy Z, et al. A versatile gene-based test for genome-wide association studies. ''Am J Hum Genet''. 2010 Jul 9; '''87''' (1):139-45
Genome-wide association study of pancreatic cancer in Japanese population. Description: Low, Siew-Kee, et al. Genome-wide association study of pancreatic cancer in Japanese population. ''PLoS One''. 2010 Jul 29; '''5''' (7):e11824
Genetic variation and antioxidant response gene expression in the bronchial airway epithelium of smokers at risk for lung cancer. Description: Wang, Xuting, et al. Genetic variation and antioxidant response gene expression in the bronchial airway epithelium of smokers at risk for lung cancer. ''PLoS One''. 2010 Aug 3; '''5''' (8):e11934
The 5p15.33 locus is associated with risk of lung adenocarcinoma in never-smoking females in Asia. Description: Hsiung, Chao Agnes, et al. The 5p15.33 locus is associated with risk of lung adenocarcinoma in never-smoking females in Asia. ''PLoS Genet''. 2010 Aug 5; '''6''' (8):
Elucidating the chromosome 9 association with AS; CARD9 is a candidate gene. Description: Pointon, J J, et al. Elucidating the chromosome 9 association with AS; CARD9 is a candidate gene. ''Genes Immun''. 2010 Sep; '''11''' (6):490-6
Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. Description: Raychaudhuri, Soumya, et al. Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. ''PLoS Genet''. 2010 Sep 9; '''6''' (9):e1001097
A novel statistic for genome-wide interaction analysis. Description: Wu, Xuesen, et al. A novel statistic for genome-wide interaction analysis. ''PLoS Genet''. 2010 Sep 23; '''6''' (9):e1001131
Association of the CCR5 gene with juvenile idiopathic arthritis. Description: Hinks, A, et al. Association of the CCR5 gene with juvenile idiopathic arthritis. ''Genes Immun''. 2010 Oct; '''11''' (7):584-9
High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene. Description: Strom, S P, et al. High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene. ''Mol Psychiatry''. 2010 Oct; '''15''' (10):996-1005
Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population. Description: Zhao, Fuxin, et al. Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population. ''Mol Vis''. 2010 Oct 2; '''16''': 1920-7
Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy. Description: Stark, Klaus, et al. Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy. ''PLoS Genet''. 2010 Oct 21; '''6''' (10):e1001167
Genome-wide effects of long-term divergent selection. Description: Johansson, Anna M, et al. Genome-wide effects of long-term divergent selection. ''PLoS Genet''. 2010 Nov 4; '''6''' (11):e1001188
Tag SNPs detect association of the CYP1B1 gene with primary open angle glaucoma. Description: Burdon, Kathryn P, et al. Tag SNPs detect association of the CYP1B1 gene with primary open angle glaucoma. ''Mol Vis''. 2010 Nov 4; '''16''': 2286-93
Interaction of Crohn's disease susceptibility genes in an Australian paediatric cohort. Description: Wagner, Josef, et al. Interaction of Crohn's disease susceptibility genes in an Australian paediatric cohort. ''PLoS One''. 2010 Nov 8; '''5''' (11):e15376
Unifying candidate gene and GWAS Approaches in Asthma. Description: Michel, Sven, et al. Unifying candidate gene and GWAS Approaches in Asthma. ''PLoS One''. 2010 Nov 12; '''5''' (11):e13894
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Description: Sotoodehnia, Nona, et al. Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. ''Nat Genet''. 2010 Dec; '''42''' (12):1068-76
Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration. Description: Kopplin, L J, et al. Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration. ''Genes Immun''. 2010 Dec; '''11''' (8):609-21
Genome-wide association analyses of genetic, phenotypic, and environmental risks in the age-related eye disease study. Description: Ryu, Euijung, et al. Genome-wide association analyses of genetic, phenotypic, and environmental risks in the age-related eye disease study. ''Mol Vis''. 2010 Dec 17; '''16''': 2811-21
Genes involved in the metabolism of poly-unsaturated fatty-acids (PUFA) and risk for Crohn's disease in children & young adults. Description: Costea, Irina, et al. Genes involved in the metabolism of poly-unsaturated fatty-acids (PUFA) and risk for Crohn's disease in children & young adults. ''PLoS One''. 2010 Dec 20; '''5''' (12):e15672
The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants. Description: Glas, Jurgen, et al. The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants. ''PLoS One''. 2010 Dec 30; '''5''' (12):e14466
A common CNR1 (cannabinoid receptor 1) haplotype attenuates the decrease in HDL cholesterol that typically accompanies weight gain. Description: Feng, Qiping, et al. A common CNR1 (cannabinoid receptor 1) haplotype attenuates the decrease in HDL cholesterol that typically accompanies weight gain. ''PLoS One''. 2010 Dec 31; '''5''' (12):e15779
Accelerating haplotype-based genome-wide association study using perfect phylogeny and phase-known reference data. Description: He, Yungang, et al. Accelerating haplotype-based genome-wide association study using perfect phylogeny and phase-known reference data. ''PLoS One''. 2011; '''6''' (7):e22097
A common complement C3 variant is associated with protection against wet age-related macular degeneration in a Japanese population. Description: Yanagisawa, Suiho, et al. A common complement C3 variant is associated with protection against wet age-related macular degeneration in a Japanese population. ''PLoS One''. 2011; '''6''' (12):e28847
A comparison of approaches to estimate the inbreeding coefficient and pairwise relatedness using genomic and pedigree data in a sheep population. Description: Li, Meng-Hua, et al. A comparison of approaches to estimate the inbreeding coefficient and pairwise relatedness using genomic and pedigree data in a sheep population. ''PLoS One''. 2011; '''6''' (11):e26256
A frameshift mutation in golden retriever dogs with progressive retinal atrophy endorses SLC4A3 as a candidate gene for human retinal degenerations. Description: Downs, Louise M, et al. A frameshift mutation in golden retriever dogs with progressive retinal atrophy endorses SLC4A3 as a candidate gene for human retinal degenerations. ''PLoS One''. 2011; '''6''' (6):e21452
A genome-wide SNP scan reveals novel loci for egg production and quality traits in white leghorn and brown-egg dwarf layers. Description: Liu, Wenbo, et al. A genome-wide SNP scan reveals novel loci for egg production and quality traits in white leghorn and brown-egg dwarf layers. ''PLoS One''. 2011; '''6''' (12):e28600
A latent model for prioritization of SNPs for functional studies. Description: Fridley, Brooke L, et al. A latent model for prioritization of SNPs for functional studies. ''PLoS One''. 2011; '''6''' (6):e20764
Allelic heterogeneity and genetic modifier loci contribute to clinical variation in males with X-linked retinitis pigmentosa due to RPGR mutations. Description: Fahim, Abigail T, et al. Allelic heterogeneity and genetic modifier loci contribute to clinical variation in males with X-linked retinitis pigmentosa due to RPGR mutations. ''PLoS One''. 2011; '''6''' (8):e23021
A methodology for multivariate phenotype-based genome-wide association studies to mine pleiotropic genes. Description: Park, Sung Hee, et al. A methodology for multivariate phenotype-based genome-wide association studies to mine pleiotropic genes. ''BMC Syst Biol''. 2011; '''5 Suppl 2''': S13
A network-based approach to prioritize results from genome-wide association studies. Description: Akula, Nirmala, et al. A network-based approach to prioritize results from genome-wide association studies. ''PLoS One''. 2011; '''6''' (9):e24220
A novel, functional and replicable risk gene region for alcohol dependence identified by genome-wide association study. Description: Zuo, Lingjun, et al. A novel, functional and replicable risk gene region for alcohol dependence identified by genome-wide association study. ''PLoS One''. 2011; '''6''' (11):e26726
An SNP selection strategy identified IL-22 associating with susceptibility to tuberculosis in Chinese. Description: Zhang, Guoliang, et al. An SNP selection strategy identified IL-22 associating with susceptibility to tuberculosis in Chinese. ''Sci Rep''. 2011; '''1''': 20
A pilot study of the association of tumor necrosis factor alpha polymorphisms with psoriatic arthritis in the Romanian population. Description: Popa, Olivia M, et al. A pilot study of the association of tumor necrosis factor alpha polymorphisms with psoriatic arthritis in the Romanian population. ''Int J Mol Sci''. 2011; '''12''' (8):5052-9
Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population. Description: Kiliszek, Marek, et al. Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population. ''PLoS One''. 2011; '''6''' (7):e21790
Association of MDR1 gene SNPs and haplotypes with the tacrolimus dose requirements in Han Chinese liver transplant recipients. Description: Yu, Xiaobo, et al. Association of MDR1 gene SNPs and haplotypes with the tacrolimus dose requirements in Han Chinese liver transplant recipients. ''PLoS One''. 2011; '''6''' (11):e25933
Association of the adiponectin gene variations with risk of ischemic stroke in a Korean population. Description: Cheong, My-Young, et al. Association of the adiponectin gene variations with risk of ischemic stroke in a Korean population. ''Yonsei Med J''. 2011 Jan; '''52''' (1):20-5
Associations of FTO and MC4R Variants with Obesity Traits in Indians and the Role of Rural/Urban Environment as a Possible Effect Modifier. Description: Taylor, A E, et al. Associations of FTO and MC4R Variants with Obesity Traits in Indians and the Role of Rural/Urban Environment as a Possible Effect Modifier. ''J Obes''. 2011; '''2011''': 307542
A systems genetics approach provides a bridge from discovered genetic variants to biological pathways in rheumatoid arthritis. Description: Nakaoka, Hirofumi, et al. A systems genetics approach provides a bridge from discovered genetic variants to biological pathways in rheumatoid arthritis. ''PLoS One''. 2011; '''6''' (9):e25389
A targeted association study of immunity genes and networks suggests novel associations with placental malaria infection. Description: Sikora, Martin, et al. A targeted association study of immunity genes and networks suggests novel associations with placental malaria infection. ''PLoS One''. 2011; '''6''' (9):e24996
BDNF contributes to the genetic variance of milk fat yield in german holstein cattle. Description: Zielke, Lea G, et al. BDNF contributes to the genetic variance of milk fat yield in german holstein cattle. ''Front Genet''. 2011; '''2''': 16
Bivariate genome-wide association analyses of femoral neck bone geometry and appendicular lean mass. Description: Sun, Lu, et al. Bivariate genome-wide association analyses of femoral neck bone geometry and appendicular lean mass. ''PLoS One''. 2011; '''6''' (11):e27325
Common variation in vitamin D pathway genes predicts circulating 25-hydroxyvitamin D Levels among African Americans. Description: Signorello, Lisa B, et al. Common variation in vitamin D pathway genes predicts circulating 25-hydroxyvitamin D Levels among African Americans. ''PLoS One''. 2011; '''6''' (12):e28623
Comparison of strategies to detect epistasis from eQTL data. Description: Kapur, Karen, et al. Comparison of strategies to detect epistasis from eQTL data. ''PLoS One''. 2011; '''6''' (12):e28415
Contributions of dopamine-related genes and environmental factors to highly sensitive personality: a multi-step neuronal system-level approach. Description: Chen, Chunhui, et al. Contributions of dopamine-related genes and environmental factors to highly sensitive personality: a multi-step neuronal system-level approach. ''PLoS One''. 2011; '''6''' (7):e21636
Convergence of miRNA expression profiling, alpha-synuclein interacton and GWAS in Parkinson's disease. Description: Martins, Madalena, et al. Convergence of miRNA expression profiling, alpha-synuclein interacton and GWAS in Parkinson's disease. ''PLoS One''. 2011; '''6''' (10):e25443
Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk. Description: Salyakina, Daria, et al. Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk. ''PLoS One''. 2011; '''6''' (10):e26049
Copy number variation across European populations. Description: Chen, Wanting, et al. Copy number variation across European populations. ''PLoS One''. 2011; '''6''' (8):e23087
Copy number variation in CNP267 region may be associated with hip bone size. Description: Liu, Shan-Lin, et al. Copy number variation in CNP267 region may be associated with hip bone size. ''PLoS One''. 2011; '''6''' (7):e22035
Copy number variation in familial Parkinson disease. Description: Pankratz, Nathan, et al. Copy number variation in familial Parkinson disease. ''PLoS One''. 2011; '''6''' (8):e20988
Cost-effective prediction of gender-labeling errors and estimation of gender-labeling error rates in candidate-gene association studies. Description: Qu, Conghui, et al. Cost-effective prediction of gender-labeling errors and estimation of gender-labeling error rates in candidate-gene association studies. ''Front Genet''. 2011; '''2''': 31
CYBA Gene Polymorphisms and Adverse Outcomes in Acute Kidney Injury: A Prospective Cohort Study. Description: Perianayagam, Mary C, et al. CYBA Gene Polymorphisms and Adverse Outcomes in Acute Kidney Injury: A Prospective Cohort Study. ''Nephron Extra''. 2011 Jan; '''1''' (1):112-23
Detailed analysis of variants in FTO in association with body composition in a cohort of 70-year-olds suggests a weakened effect among elderly. Description: Jacobsson, Josefin A, et al. Detailed analysis of variants in FTO in association with body composition in a cohort of 70-year-olds suggests a weakened effect among elderly. ''PLoS One''. 2011; '''6''' (5):e20158
Determination of the loss of function complement C4 exon 29 CT insertion using a novel paralog-specific assay in healthy UK and Spanish populations. Description: Boteva, Lora, et al. Determination of the loss of function complement C4 exon 29 CT insertion using a novel paralog-specific assay in healthy UK and Spanish populations. ''PLoS One''. 2011; '''6''' (8):e22128
Dissecting cis regulation of gene expression in human metabolic tissues. Description: Dobrin, Radu, et al. Dissecting cis regulation of gene expression in human metabolic tissues. ''PLoS One''. 2011; '''6''' (8):e23480
EphB2 SNPs and sporadic prostate cancer risk in African American men. Description: Robbins, Christiane M, et al. EphB2 SNPs and sporadic prostate cancer risk in African American men. ''PLoS One''. 2011; '''6''' (5):e19494
Fine Mapping of Loci on BTA2 and BTA26 Associated with Bovine Viral Diarrhea Persistent Infection and Linked with Bovine Respiratory Disease in Cattle. Description: Zanella, Ricardo, et al. Fine Mapping of Loci on BTA2 and BTA26 Associated with Bovine Viral Diarrhea Persistent Infection and Linked with Bovine Respiratory Disease in Cattle. ''Front Genet''. 2011; '''2''': 82
From SNPs to genes: disease association at the gene level. Description: Lehne, Benjamin, et al. From SNPs to genes: disease association at the gene level. ''PLoS One''. 2011; '''6''' (6):e20133
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients. Description: Paraboschi, Elvezia Maria, et al. Genetic association and altered gene expression of mir-155 in multiple sclerosis patients. ''Int J Mol Sci''. 2011; '''12''' (12):8695-712
Genetic associations in the vitamin D receptor and colorectal cancer in African Americans and Caucasians. Description: Kupfer, Sonia S, et al. Genetic associations in the vitamin D receptor and colorectal cancer in African Americans and Caucasians. ''PLoS One''. 2011; '''6''' (10):e26123
Genetic association study of common mitochondrial variants on body fat mass. Description: Yang, Tie-Lin, et al. Genetic association study of common mitochondrial variants on body fat mass. ''PLoS One''. 2011; '''6''' (6):e21595
Genetic Modulation of Training and Transfer in Older Adults: BDNF ValMet Polymorphism is Associated with Wider Useful Field of View. Description: Colzato, Lorenza S, et al. Genetic Modulation of Training and Transfer in Older Adults: BDNF ValMet Polymorphism is Associated with Wider Useful Field of View. ''Front Psychol''. 2011; '''2''': 199
Genetics of sputum gene expression in chronic obstructive pulmonary disease. Description: Qiu, Weiliang, et al. Genetics of sputum gene expression in chronic obstructive pulmonary disease. ''PLoS One''. 2011; '''6''' (9):e24395
Genetic variation of VKORC1 and CYP4F2 genes related to warfarin maintenance dose in patients with myocardial infarction. Description: Kringen, Marianne K, et al. Genetic variation of VKORC1 and CYP4F2 genes related to warfarin maintenance dose in patients with myocardial infarction. ''J Biomed Biotechnol''. 2011; '''2011''': 739751
Genome-wide association study for atopy and allergic rhinitis in a Singapore Chinese population. Description: Andiappan, Anand Kumar, et al. Genome-wide association study for atopy and allergic rhinitis in a Singapore Chinese population. ''PLoS One''. 2011; '''6''' (5):e19719
Genome-wide association study of body weight in chicken F2 resource population. Description: Gu, Xiaorong, et al. Genome-wide association study of body weight in chicken F2 resource population. ''PLoS One''. 2011; '''6''' (7):e21872
Genome-wide association study of hepatocellular carcinoma in Southern Chinese patients with chronic hepatitis B virus infection. Description: Chan, Kelvin Yuen-Kwong, et al. Genome-wide association study of hepatocellular carcinoma in Southern Chinese patients with chronic hepatitis B virus infection. ''PLoS One''. 2011; '''6''' (12):e28798
Genome-wide scan identifies loci associated with classical BSE occurrence. Description: Murdoch, Brenda M, et al. Genome-wide scan identifies loci associated with classical BSE occurrence. ''PLoS One''. 2011; '''6''' (11):e26819
Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study. Description: Swaminathan, Shanker, et al. Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study. ''Int J Alzheimers Dis''. 2011; '''2011''': 729478
Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. Description: Johnson, Catherine, et al. Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. ''PLoS One''. 2011; '''6''' (7):e19210
Host genetic risk factors for West Nile virus infection and disease progression. Description: Bigham, Abigail W, et al. Host genetic risk factors for West Nile virus infection and disease progression. ''PLoS One''. 2011; '''6''' (9):e24745
hzAnalyzer: detection, quantification, and visualization of contiguous homozygosity in high-density genotyping datasets. Description: Johnson, Todd A, et al. hzAnalyzer: detection, quantification, and visualization of contiguous homozygosity in high-density genotyping datasets. ''Genome Biol''. 2011; '''12''' (3):R21
Identification of close relatives in the HUGO Pan-Asian SNP database. Description: Yang, Xiong, et al. Identification of close relatives in the HUGO Pan-Asian SNP database. ''PLoS One''. 2011; '''6''' (12):e29502
Identification of KIF3A as a novel candidate gene for childhood asthma using RNA expression and population allelic frequencies differences. Description: Kovacic, Melinda Butsch, et al. Identification of KIF3A as a novel candidate gene for childhood asthma using RNA expression and population allelic frequencies differences. ''PLoS One''. 2011; '''6''' (8):e23714
Identifying host genetic risk factors in the context of public health surveillance for invasive pneumococcal disease. Description: Lingappa, Jairam R, et al. Identifying host genetic risk factors in the context of public health surveillance for invasive pneumococcal disease. ''PLoS One''. 2011; '''6''' (8):e23413
Impact of genetic variation in SORCS1 on memory retention. Description: Reitz, Christiane, et al. Impact of genetic variation in SORCS1 on memory retention. ''PLoS One''. 2011; '''6''' (10):e24588
Investigating the pathogenic role of PADI4 in oesophageal cancer. Description: Chang, Xiaotian, et al. Investigating the pathogenic role of PADI4 in oesophageal cancer. ''Int J Biol Sci''. 2011; '''7''' (6):769-81
Molecular genetic analysis of retinitis pigmentosa in Indonesia using genome-wide homozygosity mapping. Description: Siemiatkowska, Anna M, et al. Molecular genetic analysis of retinitis pigmentosa in Indonesia using genome-wide homozygosity mapping. ''Mol Vis''. 2011; '''17''': 3013-24
Mucin variable number tandem repeat polymorphisms and severity of cystic fibrosis lung disease: significant association with MUC5AC. Description: Guo, Xueliang, et al. Mucin variable number tandem repeat polymorphisms and severity of cystic fibrosis lung disease: significant association with MUC5AC. ''PLoS One''. 2011; '''6''' (10):e25452
Multifactor dimensionality reduction as a filter-based approach for genome wide association studies. Description: Oki, Noffisat O, et al. Multifactor dimensionality reduction as a filter-based approach for genome wide association studies. ''Front Genet''. 2011; '''2''': 80
Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis--a genome-wide study combined with immunological analyses. Description: Terao, Chikashi, et al. Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis--a genome-wide study combined with immunological analyses. ''PLoS One''. 2011; '''6''' (6):e20457
Oncogenic CagA promotes gastric cancer risk via activating ERK signaling pathways: a nested case-control study. Description: Yang, Jae Jeong, et al. Oncogenic CagA promotes gastric cancer risk via activating ERK signaling pathways: a nested case-control study. ''PLoS One''. 2011; '''6''' (6):e21155
Pathway-based analysis of a melanoma genome-wide association study: analysis of genes related to tumour-immunosuppression. Description: Schoof, Nils, et al. Pathway-based analysis of a melanoma genome-wide association study: analysis of genes related to tumour-immunosuppression. ''PLoS One''. 2011; '''6''' (12):e29451
Replication of putative susceptibility loci from genome-wide association studies associated with coronary atherosclerosis in Chinese Han population. Description: Xie, Fang, et al. Replication of putative susceptibility loci from genome-wide association studies associated with coronary atherosclerosis in Chinese Han population. ''PLoS One''. 2011; '''6''' (6):e20833
Runs of homozygosity do not influence survival to old age. Description: Kuningas, Maris, et al. Runs of homozygosity do not influence survival to old age. ''PLoS One''. 2011; '''6''' (7):e22580
Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population. Description: Moens, Lotte N, et al. Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population. ''PLoS One''. 2011; '''6''' (8):e23450
Statistical epistasis and functional brain imaging support a role of voltage-gated potassium channels in human memory. Description: Heck, Angela, et al. Statistical epistasis and functional brain imaging support a role of voltage-gated potassium channels in human memory. ''PLoS One''. 2011; '''6''' (12):e29337
Strategies for selection of subjects for sequencing after detection of a linkage peak. Description: Allen-Brady, Kristina, et al. Strategies for selection of subjects for sequencing after detection of a linkage peak. ''BMC Proc''. 2011; '''5 Suppl 9''': S77
Survey of SSC12 Regions Affecting Fatty Acid Composition of Intramuscular Fat Using High-Density SNP Data. Description: Munoz, Maria, et al. Survey of SSC12 Regions Affecting Fatty Acid Composition of Intramuscular Fat Using High-Density SNP Data. ''Front Genet''. 2011; '''2''': 101
The fat mass and obesity associated gene, FTO, is also associated with osteoporosis phenotypes. Description: Guo, Yan, et al. The fat mass and obesity associated gene, FTO, is also associated with osteoporosis phenotypes. ''PLoS One''. 2011; '''6''' (11):e27312
The genetic structure of the Swedish population. Description: Humphreys, Keith, et al. The genetic structure of the Swedish population. ''PLoS One''. 2011; '''6''' (8):e22547
The role of osteopontin (OPN/SPP1) haplotypes in the susceptibility to Crohn's disease. Description: Glas, Jurgen, et al. The role of osteopontin (OPN/SPP1) haplotypes in the susceptibility to Crohn's disease. ''PLoS One''. 2011; '''6''' (12):e29309
The role of toll-like receptor variants in acute anterior uveitis. Description: Pratap, Divya S, et al. The role of toll-like receptor variants in acute anterior uveitis. ''Mol Vis''. 2011; '''17''': 2970-7
GCTA: a tool for genome-wide complex trait analysis. Description: Yang, Jian, et al. GCTA: a tool for genome-wide complex trait analysis. ''Am J Hum Genet''. 2011 Jan 7; '''88''' (1):76-82
Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. Description: Lanktree, Matthew B, et al. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. ''Am J Hum Genet''. 2011 Jan 7; '''88''' (1):6-18
Characterization of novel and uncharacterized p53 SNPs in the Chinese population--intron 2 SNP co-segregates with the common codon 72 polymorphism. Description: Phang, Beng Hooi, et al. Characterization of novel and uncharacterized p53 SNPs in the Chinese population--intron 2 SNP co-segregates with the common codon 72 polymorphism. ''PLoS One''. 2011 Jan 10; '''6''' (1):e15320
LINGO1 variants in the French-Canadian population. Description: Bourassa, Cynthia V, et al. LINGO1 variants in the French-Canadian population. ''PLoS One''. 2011 Jan 11; '''6''' (1):e16254
Accuracy of CNV Detection from GWAS Data. Description: Zhang, Dandan, et al. Accuracy of CNV Detection from GWAS Data. ''PLoS One''. 2011 Jan 13; '''6''' (1):e14511
Global analysis of the impact of environmental perturbation on cis-regulation of gene expression. Description: Grundberg, Elin, et al. Global analysis of the impact of environmental perturbation on cis-regulation of gene expression. ''PLoS Genet''. 2011 Jan 20; '''7''' (1):e1001279
Identification of genes with allelic imbalance on 6p associated with nasopharyngeal carcinoma in southern Chinese. Description: Li, Yan, et al. Identification of genes with allelic imbalance on 6p associated with nasopharyngeal carcinoma in southern Chinese. ''PLoS One''. 2011 Jan 20; '''6''' (1):e14562
Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: a study of 3,310 subjects from India and the US. Description: Been, Latonya F, et al. Variants in KCNQ1 increase type II diabetes susceptibility in South Asians: a study of 3,310 subjects from India and the US. ''BMC Med Genet''. 2011 Jan 24; '''12''': 18
Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles. Description: Chen, Pei-Lung, et al. Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles. ''PLoS One''. 2011 Jan 28; '''6''' (1):e16635
Variation in LPA is associated with Lp(a) levels in three populations from the Third National Health and Nutrition Examination Survey. Description: Dumitrescu, Logan, et al. Variation in LPA is associated with Lp(a) levels in three populations from the Third National Health and Nutrition Examination Survey. ''PLoS One''. 2011 Jan 28; '''6''' (1):e16604
An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians. Description: Juyal, Garima, et al. An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians. ''PLoS One''. 2011 Jan 31; '''6''' (1):e16565
Epistasis between COMT and MTHFR in maternal-fetal dyads increases risk for preeclampsia. Description: Hill, Lori D, et al. Epistasis between COMT and MTHFR in maternal-fetal dyads increases risk for preeclampsia. ''PLoS One''. 2011 Jan 31; '''6''' (1):e16681
Pharmacogenetics of telatinib, a VEGFR-2 and VEGFR-3 tyrosine kinase inhibitor, used in patients with solid tumors. Description: Steeghs, Neeltje, et al. Pharmacogenetics of telatinib, a VEGFR-2 and VEGFR-3 tyrosine kinase inhibitor, used in patients with solid tumors. ''Invest New Drugs''. 2011 Feb; '''29''' (1):137-43
The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han population. Description: Cheng, Xiang, et al. The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han population. ''Diabetes''. 2011 Feb; '''60''' (2):680-4
Neuronal genes for subcutaneous fat thickness in human and pig are identified by local genomic sequencing and combined SNP association study. Description: Lee, Kyung-Tai, et al. Neuronal genes for subcutaneous fat thickness in human and pig are identified by local genomic sequencing and combined SNP association study. ''PLoS One''. 2011 Feb 2; '''6''' (2):e16356
Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis. Description: Haataja, Ritva, et al. Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis. ''PLoS Genet''. 2011 Feb 3; '''7''' (2):e1001293
A genome-wide association study of serum uric acid in African Americans. Description: Charles, Bashira A, et al. A genome-wide association study of serum uric acid in African Americans. ''BMC Med Genomics''. 2011 Feb 4; '''4''': 17
Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study. Description: Tsai, Fuu-Jen, et al. Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study. ''PLoS One''. 2011 Feb 4; '''6''' (2):e16853
Polymorphisms in the receptor tyrosine kinase MERTK gene are associated with multiple sclerosis susceptibility. Description: Ma, Gerry Z M, et al. Polymorphisms in the receptor tyrosine kinase MERTK gene are associated with multiple sclerosis susceptibility. ''PLoS One''. 2011 Feb 8; '''6''' (2):e16964
Fine mapping of genetic variants in BIN1, CLU, CR1 and PICALM for association with cerebrospinal fluid biomarkers for Alzheimer's disease. Description: Kauwe, John S K, et al. Fine mapping of genetic variants in BIN1, CLU, CR1 and PICALM for association with cerebrospinal fluid biomarkers for Alzheimer's disease. ''PLoS One''. 2011 Feb 9; '''6''' (2):e15918
Swedish population substructure revealed by genome-wide single nucleotide polymorphism data. Description: Salmela, Elina, et al. Swedish population substructure revealed by genome-wide single nucleotide polymorphism data. ''PLoS One''. 2011 Feb 9; '''6''' (2):e16747
Genome-wide association studies of the PR interval in African Americans. Description: Smith, J Gustav, et al. Genome-wide association studies of the PR interval in African Americans. ''PLoS Genet''. 2011 Feb 10; '''7''' (2):e1001304
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. Description: Lettre, Guillaume, et al. Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. ''PLoS Genet''. 2011 Feb 10; '''7''' (2):e1001300
Prostate cancer susceptibility Loci identified on chromosome 12 in African Americans. Description: Bonilla, Carolina, et al. Prostate cancer susceptibility Loci identified on chromosome 12 in African Americans. ''PLoS One''. 2011 Feb 16; '''6''' (2):e16044
Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. Description: Hu, Xiaolan, et al. Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. ''PLoS One''. 2011 Feb 24; '''6''' (2):e16616
On the origin of Tibetans and their genetic basis in adapting high-altitude environments. Description: Wang, Binbin, et al. On the origin of Tibetans and their genetic basis in adapting high-altitude environments. ''PLoS One''. 2011 Feb 28; '''6''' (2):e17002
A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. Description: McKay, James D, et al. A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. ''PLoS Genet''. 2011 Mar; '''7''' (3):e1001333
An autoimmune-associated variant in PTPN2 reveals an impairment of IL-2R signaling in CD4(+) T cells. Description: Long, S A, et al. An autoimmune-associated variant in PTPN2 reveals an impairment of IL-2R signaling in CD4(+) T cells. ''Genes Immun''. 2011 Mar; '''12''' (2):116-25
A novel unstable duplication upstream of HAS2 predisposes to a breed-defining skin phenotype and a periodic fever syndrome in Chinese Shar-Pei dogs. Description: Olsson, Mia, et al. A novel unstable duplication upstream of HAS2 predisposes to a breed-defining skin phenotype and a periodic fever syndrome in Chinese Shar-Pei dogs. ''PLoS Genet''. 2011 Mar; '''7''' (3):e1001332
Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. Description: Chung, Sharon A, et al. Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. ''PLoS Genet''. 2011 Mar; '''7''' (3):e1001323
Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. Description: Speliotes, Elizabeth K, et al. Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. ''PLoS Genet''. 2011 Mar; '''7''' (3):e1001324
Genome-wide association scan of korean autism spectrum disorders with language delay: a preliminary study. Description: Cho, Soo-Churl, et al. Genome-wide association scan of korean autism spectrum disorders with language delay: a preliminary study. ''Psychiatry Investig''. 2011 Mar; '''8''' (1):61-6
Genome-wide association study of genetic predictors of anti-tumor necrosis factor treatment efficacy in rheumatoid arthritis identifies associations with polymorphisms at seven loci. Description: Plant, Darren, et al. Genome-wide association study of genetic predictors of anti-tumor necrosis factor treatment efficacy in rheumatoid arthritis identifies associations with polymorphisms at seven loci. ''Arthritis Rheum''. 2011 Mar; '''63''' (3):645-53
Study of the common genetic background for rheumatoid arthritis and systemic lupus erythematosus. Description: Orozco, Gisela, et al. Study of the common genetic background for rheumatoid arthritis and systemic lupus erythematosus. ''Ann Rheum Dis''. 2011 Mar; '''70''' (3):463-8
The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects. Description: Rizzi, Thais S, et al. The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects. ''Am J Med Genet B Neuropsychiatr Genet''. 2011 Mar; '''156''' (2):145-57
The impact of childhood abuse and recent stress on serum brain-derived neurotrophic factor and the moderating role of BDNF Val66Met. Description: Elzinga, Bernet M, et al. The impact of childhood abuse and recent stress on serum brain-derived neurotrophic factor and the moderating role of BDNF Val66Met. ''Psychopharmacology (Berl)''. 2011 Mar; '''214''' (1):319-28
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort. Description: van der Zee, Julie, et al. TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort. ''Brain''. 2011 Mar; '''134''' (Pt 3):808-15
GATES: a rapid and powerful gene-based association test using extended Simes procedure. Description: Li, Miao-Xin, et al. GATES: a rapid and powerful gene-based association test using extended Simes procedure. ''Am J Hum Genet''. 2011 Mar 11; '''88''' (3):283-93
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. Description: Cichon, Sven, et al. Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. ''Am J Hum Genet''. 2011 Mar 11; '''88''' (3):372-81
Assessing matched normal and tumor pairs in next-generation sequencing studies. Description: Goh, Liang, et al. Assessing matched normal and tumor pairs in next-generation sequencing studies. ''PLoS One''. 2011 Mar 18; '''6''' (3):e17810
Leukocyte DNA methylation signature differentiates pancreatic cancer patients from healthy controls. Description: Pedersen, Katrina S, et al. Leukocyte DNA methylation signature differentiates pancreatic cancer patients from healthy controls. ''PLoS One''. 2011 Mar 24; '''6''' (3):e18223
A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLE. Description: Sandling, Johanna K, et al. A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLE. ''Eur J Hum Genet''. 2011 Apr; '''19''' (4):479-84
An evolutionary genomic approach to identify genes involved in human birth timing. Description: Plunkett, Jevon, et al. An evolutionary genomic approach to identify genes involved in human birth timing. ''PLoS Genet''. 2011 Apr; '''7''' (4):e1001365
Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci. Description: Pare, Guillaume, et al. Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci. ''PLoS Genet''. 2011 Apr; '''7''' (4):e1001374
Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. Description: Duncan, Emma L, et al. Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. ''PLoS Genet''. 2011 Apr; '''7''' (4):e1001372
Identification and functional validation of the novel antimalarial resistance locus PF10_0355 in Plasmodium falciparum. Description: Van Tyne, Daria, et al. Identification and functional validation of the novel antimalarial resistance locus PF10_0355 in Plasmodium falciparum. ''PLoS Genet''. 2011 Apr; '''7''' (4):e1001383
Polygenic dissection of the bipolar phenotype. Description: Hamshere, M L, et al. Polygenic dissection of the bipolar phenotype. ''Br J Psychiatry''. 2011 Apr; '''198''' (4):284-8
NCI60 cancer cell line panel data and RNAi analysis help identify EAF2 as a modulator of simvastatin and lovastatin response in HCT-116 cells. Description: Savas, Sevtap, et al. NCI60 cancer cell line panel data and RNAi analysis help identify EAF2 as a modulator of simvastatin and lovastatin response in HCT-116 cells. ''PLoS One''. 2011 Apr 4; '''6''' (4):e18306
Genetic and metabolic characterization of insomnia. Description: Ban, Hyo-Jeong, et al. Genetic and metabolic characterization of insomnia. ''PLoS One''. 2011 Apr 6; '''6''' (4):e18455
An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle. Description: Drogemuller, Cord, et al. An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle. ''PLoS One''. 2011 Apr 15; '''6''' (4):e18931
SNP-based pathway enrichment analysis for genome-wide association studies. Description: Weng, Lingjie, et al. SNP-based pathway enrichment analysis for genome-wide association studies. ''BMC Bioinformatics''. 2011 Apr 15; '''12''': 99
Complement factor B polymorphism 32W protects against age-related macular degeneration. Description: Hughes, Anne E, et al. Complement factor B polymorphism 32W protects against age-related macular degeneration. ''Mol Vis''. 2011 Apr 20; '''17''': 983-8
Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy. Description: Li, Yi-Ju, et al. Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy. ''PLoS One''. 2011 Apr 20; '''6''' (4):e18044
The distal end of porcine chromosome 6p is involved in the regulation of skatole levels in boars. Description: Ramos, Antonio M, et al. The distal end of porcine chromosome 6p is involved in the regulation of skatole levels in boars. ''BMC Genet''. 2011 Apr 20; '''12''': 35
Novel autism subtype-dependent genetic variants are revealed by quantitative trait and subphenotype association analyses of published GWAS data. Description: Hu, Valerie W, et al. Novel autism subtype-dependent genetic variants are revealed by quantitative trait and subphenotype association analyses of published GWAS data. ''PLoS One''. 2011 Apr 27; '''6''' (4):e19067
Using functional annotation for the empirical determination of Bayes Factors for genome-wide association study analysis. Description: Knight, Jo, et al. Using functional annotation for the empirical determination of Bayes Factors for genome-wide association study analysis. ''PLoS One''. 2011 Apr 27; '''6''' (4):e14808
A genome-wide association study on obesity and obesity-related traits. Description: Wang, Kai, et al. A genome-wide association study on obesity and obesity-related traits. ''PLoS One''. 2011 Apr 28; '''6''' (4):e18939
The genetic association of variants in CD6, TNFRSF1A and IRF8 to multiple sclerosis: a multicenter case-control study. Description: The genetic association of variants in CD6, TNFRSF1A and IRF8 to multiple sclerosis: a multicenter case-control study. ''PLoS One''. 2011 Apr 28; '''6''' (4):e18813
A genetic risk score combining ten psoriasis risk loci improves disease prediction. Description: Chen, Haoyan, et al. A genetic risk score combining ten psoriasis risk loci improves disease prediction. ''PLoS One''. 2011 Apr 29; '''6''' (4):e19454
Analysis of an extended chromosome locus 2p14-21 for replication of the 2p16.3 association with glaucoma susceptibility. Description: Kim, Kyunglan, et al. Analysis of an extended chromosome locus 2p14-21 for replication of the 2p16.3 association with glaucoma susceptibility. ''Mol Vis''. 2011 Apr 29; '''17''': 1136-43
Association analysis of urotensin II gene (UTS2) and flanking regions with biochemical parameters related to insulin resistance. Description: Saez, Maria E, et al. Association analysis of urotensin II gene (UTS2) and flanking regions with biochemical parameters related to insulin resistance. ''PLoS One''. 2011 Apr 29; '''6''' (4):e19327
CEACAM6 gene variants in inflammatory bowel disease. Description: Glas, Jurgen, et al. CEACAM6 gene variants in inflammatory bowel disease. ''PLoS One''. 2011 Apr 29; '''6''' (4):e19319
A -436C>A polymorphism in the human FAS gene promoter associated with severe childhood malaria. Description: Schuldt, Kathrin, et al. A -436C>A polymorphism in the human FAS gene promoter associated with severe childhood malaria. ''PLoS Genet''. 2011 May; '''7''' (5):e1002066
Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility. Description: Zhao, Jian, et al. Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility. ''PLoS Genet''. 2011 May; '''7''' (5):e1002079
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Description: Naj, Adam C, et al. Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. ''Nat Genet''. 2011 May; '''43''' (5):436-41
Fractalkine is a novel human adipochemokine associated with type 2 diabetes. Description: Shah, Rachana, et al. Fractalkine is a novel human adipochemokine associated with type 2 diabetes. ''Diabetes''. 2011 May; '''60''' (5):1512-8
Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue. Description: Innocenti, Federico, et al. Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue. ''PLoS Genet''. 2011 May; '''7''' (5):e1002078
A frameshift mutation within LAMC2 is responsible for Herlitz type junctional epidermolysis bullosa (HJEB) in black headed mutton sheep. Description: Momke, Stefanie, et al. A frameshift mutation within LAMC2 is responsible for Herlitz type junctional epidermolysis bullosa (HJEB) in black headed mutton sheep. ''PLoS One''. 2011 May 4; '''6''' (5):e18943
Genetic background of patients from a university medical center in Manhattan: implications for personalized medicine. Description: Tayo, Bamidele O, et al. Genetic background of patients from a university medical center in Manhattan: implications for personalized medicine. ''PLoS One''. 2011 May 4; '''6''' (5):e19166
Genes involved in vasoconstriction and vasodilation system affect salt-sensitive hypertension. Description: Citterio, Lorena, et al. Genes involved in vasoconstriction and vasodilation system affect salt-sensitive hypertension. ''PLoS One''. 2011 May 9; '''6''' (5):e19620
Genome-wide association study of relative telomere length. Description: Prescott, Jennifer, et al. Genome-wide association study of relative telomere length. ''PLoS One''. 2011 May 10; '''6''' (5):e19635
Fetal ERAP2 variation is associated with preeclampsia in African Americans in a case-control study. Description: Hill, Lori D, et al. Fetal ERAP2 variation is associated with preeclampsia in African Americans in a case-control study. ''BMC Med Genet''. 2011 May 11; '''12''': 64
Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks. Description: Turner, Stephen D, et al. Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks. ''PLoS One''. 2011 May 11; '''6''' (5):e19586
A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort. Description: Yu, Jindan, et al. A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort. ''Behav Brain Funct''. 2011 May 14; '''7''': 13
Rheumatoid arthritis-associated polymorphisms are not protective against Alzheimer's disease. Description: Simmons, Christopher R, et al. Rheumatoid arthritis-associated polymorphisms are not protective against Alzheimer's disease. ''Mol Neurodegener''. 2011 May 19; '''6''': 33
The impact of FADS genetic variants on omega6 polyunsaturated fatty acid metabolism in African Americans. Description: Mathias, Rasika A, et al. The impact of FADS genetic variants on omega6 polyunsaturated fatty acid metabolism in African Americans. ''BMC Genet''. 2011 May 20; '''12''': 50
A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders. Description: Kim, Soo-Jeong, et al. A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders. ''Mol Autism''. 2011 May 24; '''2''' (1):8
GENIE: a software package for gene-gene interaction analysis in genetic association studies using multiple GPU or CPU cores. Description: Chikkagoudar, Satish, et al. GENIE: a software package for gene-gene interaction analysis in genetic association studies using multiple GPU or CPU cores. ''BMC Res Notes''. 2011 May 26; '''4''': 158
A functional variant in microRNA-146a promoter modulates its expression and confers disease risk for systemic lupus erythematosus. Description: Luo, Xiaobing, et al. A functional variant in microRNA-146a promoter modulates its expression and confers disease risk for systemic lupus erythematosus. ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002128
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study. Description: Fox, Ervin R, et al. Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study. ''Hum Mol Genet''. 2011 Jun 1; '''20''' (11):2273-84
A two-stage meta-analysis identifies several new loci for Parkinson's disease. Description: A two-stage meta-analysis identifies several new loci for Parkinson's disease. ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002142
Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population. Description: Cui, R, et al. Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population. ''Gut''. 2011 Jun; '''60''' (6):799-805
Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans. Description: Freedman, Barry I, et al. Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans. ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002150
Fine Mapping of a QTL for Fertility on BTA7 and Its Association With a CNV in the Israeli Holsteins. Description: Glick, Giora, et al. Fine Mapping of a QTL for Fertility on BTA7 and Its Association With a CNV in the Israeli Holsteins. ''G3 (Bethesda)''. 2011 Jun; '''1''' (1):65-74
Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels. Description: Parikh, Hemang, et al. Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels. ''Hum Genet''. 2011 Jun; '''129''' (6):675-85
Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. Description: Wright, Fred A, et al. Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. ''Nat Genet''. 2011 Jun; '''43''' (6):539-46
Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes. Description: Smith, Erin N, et al. Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes. ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002134
Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). Description: Reiner, Alexander P, et al. Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002108
Glutathione pathway gene variation and risk of autism spectrum disorders. Description: Bowers, Katherine, et al. Glutathione pathway gene variation and risk of autism spectrum disorders. ''J Neurodev Disord''. 2011 Jun; '''3''' (2):132-43
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals. Description: Arking, Dan E, et al. Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals. ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002158
Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. Description: Okada, Yukinori, et al. Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002067
Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer. Description: Tomlinson, Ian P M, et al. Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer. ''PLoS Genet''. 2011 Jun; '''7''' (6):e1002105
Sex-specific role for adenylyl cyclase type 7 in alcohol dependence. Description: Desrivieres, Sylvane, et al. Sex-specific role for adenylyl cyclase type 7 in alcohol dependence. ''Biol Psychiatry''. 2011 Jun 1; '''69''' (11):1100-8
A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms. Description: Pereira, Tiago V, et al. A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms. ''BMC Res Notes''. 2011 Jun 6; '''4''': 172
DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation. Description: Gusev, Alexander, et al. DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation. ''Am J Hum Genet''. 2011 Jun 10; '''88''' (6):706-717
Melatonin receptor 1 B polymorphisms associated with the risk of gestational diabetes mellitus. Description: Kim, Jason Y, et al. Melatonin receptor 1 B polymorphisms associated with the risk of gestational diabetes mellitus. ''BMC Med Genet''. 2011 Jun 10; '''12''': 82
Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects. Description: Hibar, Derrek P, et al. Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects. ''Neuroimage''. 2011 Jun 15; '''56''' (4):1875-91
Comparison of buccal and blood-derived canine DNA, either native or whole genome amplified, for array-based genome-wide association studies. Description: Rincon, Gonzalo, et al. Comparison of buccal and blood-derived canine DNA, either native or whole genome amplified, for array-based genome-wide association studies. ''BMC Res Notes''. 2011 Jun 30; '''4''': 226
Genome Wide Association Study to predict severe asthma exacerbations in children using random forests classifiers. Description: Xu, Mousheng, et al. Genome Wide Association Study to predict severe asthma exacerbations in children using random forests classifiers. ''BMC Med Genet''. 2011 Jun 30; '''12''': 90
A selective sweep of >8 Mb on chromosome 26 in the Boxer genome. Description: Quilez, Javier, et al. A selective sweep of >8 Mb on chromosome 26 in the Boxer genome. ''BMC Genomics''. 2011 Jul 1; '''12''': 339
A worldwide analysis of beta-defensin copy number variation suggests recent selection of a high-expressing DEFB103 gene copy in East Asia. Description: Hardwick, Robert J, et al. A worldwide analysis of beta-defensin copy number variation suggests recent selection of a high-expressing DEFB103 gene copy in East Asia. ''Hum Mutat''. 2011 Jul; '''32''' (7):743-50
Gene-based tests of association. Description: Huang, Hailiang, et al. Gene-based tests of association. ''PLoS Genet''. 2011 Jul; '''7''' (7):e1002177
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. Description: Winkelmann, Juliane, et al. Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. ''PLoS Genet''. 2011 Jul; '''7''' (7):e1002171
Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis. Description: Allanore, Yannick, et al. Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis. ''PLoS Genet''. 2011 Jul; '''7''' (7):e1002091
Glucocorticoid receptor (NR3C1) gene polymorphisms and onset of alcohol abuse in adolescents. Description: Desrivieres, Sylvane, et al. Glucocorticoid receptor (NR3C1) gene polymorphisms and onset of alcohol abuse in adolescents. ''Addict Biol''. 2011 Jul; '''16''' (3):510-3
Identification of a mutation associated with fatal Foal Immunodeficiency Syndrome in the Fell and Dales pony. Description: Fox-Clipsham, Laura Y, et al. Identification of a mutation associated with fatal Foal Immunodeficiency Syndrome in the Fell and Dales pony. ''PLoS Genet''. 2011 Jul; '''7''' (7):e1002133
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. Description: Gorlova, Olga, et al. Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. ''PLoS Genet''. 2011 Jul; '''7''' (7):e1002178
Interactions between glucocorticoid treatment and cis-regulatory polymorphisms contribute to cellular response phenotypes. Description: Maranville, Joseph C, et al. Interactions between glucocorticoid treatment and cis-regulatory polymorphisms contribute to cellular response phenotypes. ''PLoS Genet''. 2011 Jul; '''7''' (7):e1002162
LGI2 truncation causes a remitting focal epilepsy in dogs. Description: Seppala, Eija H, et al. LGI2 truncation causes a remitting focal epilepsy in dogs. ''PLoS Genet''. 2011 Jul; '''7''' (7):e1002194
Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in Europeans. Description: Putku, Margus, et al. Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in Europeans. ''Hum Mutat''. 2011 Jul; '''32''' (7):806-14
Reconstruction of genealogical relationships with applications to Phase III of HapMap. Description: Kyriazopoulou-Panagiotopoulou, Sofia, et al. Reconstruction of genealogical relationships with applications to Phase III of HapMap. ''Bioinformatics''. 2011 Jul 1; '''27''' (13):i333-41
SNPsyn: detection and exploration of SNP-SNP interactions. Description: Curk, Tomaz, et al. SNPsyn: detection and exploration of SNP-SNP interactions. ''Nucleic Acids Res''. 2011 Jul; '''39''' (Web Server issue):W444-9
Recent admixture in an Indian population of African ancestry. Description: Narang, Ankita, et al. Recent admixture in an Indian population of African ancestry. ''Am J Hum Genet''. 2011 Jul 15; '''89''' (1):111-20
Association of VSNL1 with schizophrenia, frontal cortical function, and biological significance for its gene product as a modulator of cAMP levels and neuronal morphology. Description: Braunewell, K H, et al. Association of VSNL1 with schizophrenia, frontal cortical function, and biological significance for its gene product as a modulator of cAMP levels and neuronal morphology. ''Transl Psychiatry''. 2011 Jul 19; '''1''': e22
Genetic regulation of Nrxn1 [corrected] expression: an integrative cross-species analysis of schizophrenia candidate genes. Description: Mozhui, K, et al. Genetic regulation of Nrxn1 [corrected] expression: an integrative cross-species analysis of schizophrenia candidate genes. ''Transl Psychiatry''. 2011 Jul 26; '''1''': e25
Population-genetic comparison of the Sorbian isolate population in Germany with the German KORA population using genome-wide SNP arrays. Description: Gross, Arnd, et al. Population-genetic comparison of the Sorbian isolate population in Germany with the German KORA population using genome-wide SNP arrays. ''BMC Genet''. 2011 Jul 28; '''12''': 67
Replication of EPHA1 and CD33 associations with late-onset Alzheimer's disease: a multi-centre case-control study. Description: Carrasquillo, Minerva M, et al. Replication of EPHA1 and CD33 associations with late-onset Alzheimer's disease: a multi-centre case-control study. ''Mol Neurodegener''. 2011 Jul 28; '''6''' (1):54
Association of the 5-aminoimidazole-4-carboxamide ribonucleotide transformylase gene with response to methotrexate in juvenile idiopathic arthritis. Description: Hinks, Anne, et al. Association of the 5-aminoimidazole-4-carboxamide ribonucleotide transformylase gene with response to methotrexate in juvenile idiopathic arthritis. ''Ann Rheum Dis''. 2011 Aug; '''70''' (8):1395-400
Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited. Description: Deelen, Joris, et al. Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited. ''Aging Cell''. 2011 Aug; '''10''' (4):686-98
Novel locus FER is associated with serum HMW adiponectin levels. Description: Qi, Lu, et al. Novel locus FER is associated with serum HMW adiponectin levels. ''Diabetes''. 2011 Aug; '''60''' (8):2197-201
Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels. Description: Antoni, Guillemette, et al. Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels. ''BMC Med Genet''. 2011 Aug 2; '''12''': 102
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population. Description: Liu, Xinmin, et al. Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population. ''BMC Med Genet''. 2011 Aug 3; '''12''': 104
Polymorphisms in melatonin synthesis pathways: possible influences on depression. Description: Kripke, Daniel F, et al. Polymorphisms in melatonin synthesis pathways: possible influences on depression. ''J Circadian Rhythms''. 2011 Aug 9; '''9''': 8
Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosa. Description: Ozgul, Riza Koksal, et al. Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosa. ''Am J Hum Genet''. 2011 Aug 12; '''89''' (2):253-64
GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development. Description: Larsson, Mats, et al. GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development. ''Am J Hum Genet''. 2011 Aug 12; '''89''' (2):334-43
No association of TNFRSF1B variants with type 2 diabetes in Indians of Indo-European origin. Description: Tabassum, Rubina, et al. No association of TNFRSF1B variants with type 2 diabetes in Indians of Indo-European origin. ''BMC Med Genet''. 2011 Aug 17; '''12''': 110
Parkinson's disease induced pluripotent stem cells with triplication of the alpha-synuclein locus. Description: Devine, Michael J, et al. Parkinson's disease induced pluripotent stem cells with triplication of the alpha-synuclein locus. ''Nat Commun''. 2011 Aug 23; '''2''': 440
Evaluation of the global association between cholesterol-associated polymorphisms and Alzheimer's disease suggests a role for rs3846662 and HMGCR splicing in disease risk. Description: Simmons, Christopher R, et al. Evaluation of the global association between cholesterol-associated polymorphisms and Alzheimer's disease suggests a role for rs3846662 and HMGCR splicing in disease risk. ''Mol Neurodegener''. 2011 Aug 25; '''6''': 62
Interaction of early environment, gender and genes of monoamine neurotransmission in the aetiology of depression in a large population-based Finnish birth cohort. Description: Nyman, Emma S, et al. Interaction of early environment, gender and genes of monoamine neurotransmission in the aetiology of depression in a large population-based Finnish birth cohort. ''BMJ Open''. 2011 Aug 27; '''1''' (1):e000087
A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci. Description: Bradfield, Jonathan P, et al. A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci. ''PLoS Genet''. 2011 Sep; '''7''' (9):e1002293
Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search. Description: Stein, J L, et al. Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search. ''Mol Psychiatry''. 2011 Sep; '''16''' (9):927-37, 881
Genetically determined dosage of follicle-stimulating hormone (FSH) affects male reproductive parameters. Description: Grigorova, Marina, et al. Genetically determined dosage of follicle-stimulating hormone (FSH) affects male reproductive parameters. ''J Clin Endocrinol Metab''. 2011 Sep; '''96''' (9):E1534-41
Genetic association for renal traits among participants of African ancestry reveals new loci for renal function. Description: Liu, Ching-Ti, et al. Genetic association for renal traits among participants of African ancestry reveals new loci for renal function. ''PLoS Genet''. 2011 Sep; '''7''' (9):e1002264
Genome-wide association study identifies four loci associated with eruption of permanent teeth. Description: Geller, Frank, et al. Genome-wide association study identifies four loci associated with eruption of permanent teeth. ''PLoS Genet''. 2011 Sep; '''7''' (9):e1002275
Large-scale gene-centric analysis identifies novel variants for coronary artery disease. Description: Large-scale gene-centric analysis identifies novel variants for coronary artery disease. ''PLoS Genet''. 2011 Sep; '''7''' (9):e1002260
Quantification of inbreeding due to distant ancestors and its detection using dense single nucleotide polymorphism data. Description: Keller, Matthew C, et al. Quantification of inbreeding due to distant ancestors and its detection using dense single nucleotide polymorphism data. ''Genetics''. 2011 Sep; '''189''' (1):237-49
Robust association tests under different genetic models, allowing for binary or quantitative traits and covariates. Description: So, Hon-Cheong, et al. Robust association tests under different genetic models, allowing for binary or quantitative traits and covariates. ''Behav Genet''. 2011 Sep; '''41''' (5):768-75
A global view of porcine transcriptome in three tissues from a full-sib pair with extreme phenotypes in growth and fat deposition by paired-end RNA sequencing. Description: Chen, Congying, et al. A global view of porcine transcriptome in three tissues from a full-sib pair with extreme phenotypes in growth and fat deposition by paired-end RNA sequencing. ''BMC Genomics''. 2011 Sep 10; '''12''': 448
Genome-wide association mapping reveals a rich genetic architecture of complex traits in Oryza sativa. Description: Zhao, Keyan, et al. Genome-wide association mapping reveals a rich genetic architecture of complex traits in Oryza sativa. ''Nat Commun''. 2011 Sep 13; '''2''': 467
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. Description: Yu, Yi, et al. Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. ''Hum Mol Genet''. 2011 Sep 15; '''20''' (18):3699-709
Exome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegia. Description: Takata, Atsushi, et al. Exome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegia. ''Genome Biol''. 2011 Sep 28; '''12''' (9):R92
A one base pair deletion in the canine ATP13A2 gene causes exon skipping and late-onset neuronal ceroid lipofuscinosis in the Tibetan terrier. Description: Wohlke, Anne, et al. A one base pair deletion in the canine ATP13A2 gene causes exon skipping and late-onset neuronal ceroid lipofuscinosis in the Tibetan terrier. ''PLoS Genet''. 2011 Oct; '''7''' (10):e1002304
Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with systemic lupus erythematosus. Description: Cunninghame Graham, Deborah S, et al. Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with systemic lupus erythematosus. ''PLoS Genet''. 2011 Oct; '''7''' (10):e1002341
Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping. Description: Vaysse, Amaury, et al. Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping. ''PLoS Genet''. 2011 Oct; '''7''' (10):e1002316
Identification of QTL genes for BMD variation using both linkage and gene-based association approaches. Description: Li, Gloria Hoi-Yee, et al. Identification of QTL genes for BMD variation using both linkage and gene-based association approaches. ''Hum Genet''. 2011 Oct; '''130''' (4):539-46
Influence of pharmacogenetic variability on the pharmacokinetics and toxicity of the aurora kinase inhibitor danusertib. Description: Steeghs, Neeltje, et al. Influence of pharmacogenetic variability on the pharmacokinetics and toxicity of the aurora kinase inhibitor danusertib. ''Invest New Drugs''. 2011 Oct; '''29''' (5):953-62
Population genomics of wild and laboratory zebrafish (Danio rerio). Description: Whiteley, Andrew R, et al. Population genomics of wild and laboratory zebrafish (Danio rerio). ''Mol Ecol''. 2011 Oct; '''20''' (20):4259-76
Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association. Description: Wood, Andrew R, et al. Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association. ''Hum Mol Genet''. 2011 Oct 15; '''20''' (20):4082-92
Genome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1. Description: Khor, Chiea Chuen, et al. Genome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1. ''Nat Genet''. 2011 Oct 16; '''43''' (11):1139-41
Cumulative Effect of Common Genetic Variants Predicts Incident Type 2 Diabetes: A Study of 21,183 Subjects from Three Large Prospective Cohorts. Description: Yang, Jingyun, et al. Cumulative Effect of Common Genetic Variants Predicts Incident Type 2 Diabetes: A Study of 21,183 Subjects from Three Large Prospective Cohorts. ''Epidemiology (Sunnyvale)''. 2011 Nov 1; '''1''' (3):108
Genetic examination of SETD7 and SUV39H1/H2 methyltransferases and the risk of diabetes complications in patients with type 1 diabetes. Description: Syreeni, Anna, et al. Genetic examination of SETD7 and SUV39H1/H2 methyltransferases and the risk of diabetes complications in patients with type 1 diabetes. ''Diabetes''. 2011 Nov; '''60''' (11):3073-80
Genetic variation in APOE cluster region and Alzheimer's disease risk. Description: Cervantes, Sebastian, et al. Genetic variation in APOE cluster region and Alzheimer's disease risk. ''Neurobiol Aging''. 2011 Nov; '''32''' (11):2107.e7-17
Genome-wide association analysis of ischemic stroke in young adults. Description: Cheng, Yu-Ching, et al. Genome-wide association analysis of ischemic stroke in young adults. ''G3 (Bethesda)''. 2011 Nov; '''1''' (6):505-14
Genome-wide association study identifies multiple novel loci associated with disease progression in subjects with mild cognitive impairment. Description: Hu, X, et al. Genome-wide association study identifies multiple novel loci associated with disease progression in subjects with mild cognitive impairment. ''Transl Psychiatry''. 2011 Nov 15; '''1''': e54
A LASSO-based approach to analyzing rare variants in genetic association studies. Description: Brennan, Jennifer S, et al. A LASSO-based approach to analyzing rare variants in genetic association studies. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S100
A pathway-based association analysis model using common and rare variants. Description: Cheng, Lu, et al. A pathway-based association analysis model using common and rare variants. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S85
Application of Bayesian network structure learning to identify causal variant SNPs from resequencing data. Description: Schlosberg, Christopher E, et al. Application of Bayesian network structure learning to identify causal variant SNPs from resequencing data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S109
Application of Bayesian regression with singular value decomposition method in association studies for sequence data. Description: Kwon, Soonil, et al. Application of Bayesian regression with singular value decomposition method in association studies for sequence data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S57
Comparative study of statistical methods for detecting association with rare variants in exome-resequencing data. Description: Saad, Mohamad, et al. Comparative study of statistical methods for detecting association with rare variants in exome-resequencing data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S33
Comparison of collapsing methods for the statistical analysis of rare variants. Description: Dering, Carmen, et al. Comparison of collapsing methods for the statistical analysis of rare variants. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S115
Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression. Description: Sung, Heejong, et al. Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S15
Evaluating aggregate effects of rare and common variants in the 1000 Genomes Project exon sequencing data using latent variable structural equation modeling. Description: Nock, Nl, et al. Evaluating aggregate effects of rare and common variants in the 1000 Genomes Project exon sequencing data using latent variable structural equation modeling. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S47
Genome-wide association analysis of GAW17 data using an empirical Bayes variable selection. Description: Pungpapong, Vitara, et al. Genome-wide association analysis of GAW17 data using an empirical Bayes variable selection. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S5
Genome-wide case-control study in GAW17 using coalesced rare variants. Description: Wang, Libo, et al. Genome-wide case-control study in GAW17 using coalesced rare variants. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S110
Identification of multiple rare variants associated with a disease. Description: Jung, Jeesun, et al. Identification of multiple rare variants associated with a disease. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S103
Identity-by-descent filtering as a tool for the identification of disease alleles in exome sequence data from distant relatives. Description: Akula, Nirmala, et al. Identity-by-descent filtering as a tool for the identification of disease alleles in exome sequence data from distant relatives. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S76
Mutational load analysis of unrelated individuals. Description: Howrigan, Daniel P, et al. Mutational load analysis of unrelated individuals. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S55
Novel tree-based method to generate markers from rare variant data. Description: Jiang, Yuan, et al. Novel tree-based method to generate markers from rare variant data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S102
Pathway analysis following association study. Description: Ngwa, Julius S, et al. Pathway analysis following association study. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S18
Penalized-regression-based multimarker genotype analysis of Genetic Analysis Workshop 17 data. Description: Ayers, Kristin L, et al. Penalized-regression-based multimarker genotype analysis of Genetic Analysis Workshop 17 data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S92
Performance of random forests and logic regression methods using mini-exome sequence data. Description: Kim, Yoonhee, et al. Performance of random forests and logic regression methods using mini-exome sequence data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S104
Principal components ancestry adjustment for Genetic Analysis Workshop 17 data. Description: Jin, Jing, et al. Principal components ancestry adjustment for Genetic Analysis Workshop 17 data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S66
Rare variant collapsing in conjunction with mean log p-value and gradient boosting approaches applied to Genetic Analysis Workshop 17 data. Description: Cherkas, Yauheniya, et al. Rare variant collapsing in conjunction with mean log p-value and gradient boosting approaches applied to Genetic Analysis Workshop 17 data. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S94
Region-based and pathway-based QTL mapping using a p-value combination method. Description: Yang, Hsin-Chou, et al. Region-based and pathway-based QTL mapping using a p-value combination method. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S43
Using LASSO regression to detect predictive aggregate effects in genetic studies. Description: Fontanarosa, Joel B, et al. Using LASSO regression to detect predictive aggregate effects in genetic studies. ''BMC Proc''. 2011 Nov 29; '''5 Suppl 9''': S69
Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study. Description: Kramer, Patricia L, et al. Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study. ''Neurobiol Aging''. 2011 Dec; '''32''' (12):2113-22
Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation. Description: Lefeber, Dirk J, et al. Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation. ''PLoS Genet''. 2011 Dec; '''7''' (12):e1002427
Genetic variation in base excision repair pathway genes, pesticide exposure, and prostate cancer risk. Description: Barry, Kathryn Hughes, et al. Genetic variation in base excision repair pathway genes, pesticide exposure, and prostate cancer risk. ''Environ Health Perspect''. 2011 Dec; '''119''' (12):1726-32
Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism. Description: Fan, Qiao, et al. Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism. ''PLoS Genet''. 2011 Dec; '''7''' (12):e1002402
Influence of polymorphisms in the RANKL/RANK/OPG signaling pathway on volumetric bone mineral density and bone geometry at the forearm in men. Description: Roshandel, Delnaz, et al. Influence of polymorphisms in the RANKL/RANK/OPG signaling pathway on volumetric bone mineral density and bone geometry at the forearm in men. ''Calcif Tissue Int''. 2011 Dec; '''89''' (6):446-55
Rapid testing of gene-gene interactions in genome-wide association studies of binary and quantitative phenotypes. Description: Bhattacharya, Kanishka, et al. Rapid testing of gene-gene interactions in genome-wide association studies of binary and quantitative phenotypes. ''Genet Epidemiol''. 2011 Dec; '''35''' (8):800-8
The relationship between fertility and lifespan in humans. Description: Kuningas, Maris, et al. The relationship between fertility and lifespan in humans. ''Age (Dordr)''. 2011 Dec; '''33''' (4):615-22
An exonic insertion within Tex14 gene causes spermatogenic arrest in pigs. Description: Sironen, Anu, et al. An exonic insertion within Tex14 gene causes spermatogenic arrest in pigs. ''BMC Genomics''. 2011 Dec 2; '''12''': 591
Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions. Description: Dauber, Andrew, et al. Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions. ''Am J Hum Genet''. 2011 Dec 9; '''89''' (6):751-9
Identification of autoimmune gene signatures in autism. Description: Jung, J-Y, et al. Identification of autoimmune gene signatures in autism. ''Transl Psychiatry''. 2011 Dec 13; '''1''': e63
Risk variants in BMP4 promoters for nonsyndromic cleft lip/palate in a Chilean population. Description: Suazo, Jose, et al. Risk variants in BMP4 promoters for nonsyndromic cleft lip/palate in a Chilean population. ''BMC Med Genet''. 2011 Dec 19; '''12''': 163
High frequencies of de novo CNVs in bipolar disorder and schizophrenia. Description: Malhotra, Dheeraj, et al. High frequencies of de novo CNVs in bipolar disorder and schizophrenia. ''Neuron''. 2011 Dec 22; '''72''' (6):951-63
Candidate gene analysis of spontaneous preterm delivery: new insights from re-analysis of a case-control study using case-parent triads and control-mother dyads. Description: Myking, Solveig, et al. Candidate gene analysis of spontaneous preterm delivery: new insights from re-analysis of a case-control study using case-parent triads and control-mother dyads. ''BMC Med Genet''. 2011 Dec 30; '''12''': 174
A canine BCAN microdeletion associated with episodic falling syndrome. Description: Gill, Jennifer L, et al. A canine BCAN microdeletion associated with episodic falling syndrome. ''Neurobiol Dis''. 2012 Jan; '''45''' (1):130-6
A COL7A1 mutation causes dystrophic epidermolysis bullosa in Rotes Hohenvieh cattle. Description: Menoud, Annie, et al. A COL7A1 mutation causes dystrophic epidermolysis bullosa in Rotes Hohenvieh cattle. ''PLoS One''. 2012; '''7''' (6):e38823
A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorder. Description: Verbeek, Eva C, et al. A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorder. ''PLoS One''. 2012; '''7''' (5):e37384
A functional variant in ERAP1 predisposes to multiple sclerosis. Description: Guerini, Franca Rosa, et al. A functional variant in ERAP1 predisposes to multiple sclerosis. ''PLoS One''. 2012; '''7''' (1):e29931
Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages. Description: Chow, Maggie L, et al. Age-dependent brain gene expression and copy number anomalies in autism suggest distinct pathological processes at young versus mature ages. ''PLoS Genet''. 2012; '''8''' (3):e1002592
A gene co-expression network in whole blood of schizophrenia patients is independent of antipsychotic-use and enriched for brain-expressed genes. Description: de Jong, Simone, et al. A gene co-expression network in whole blood of schizophrenia patients is independent of antipsychotic-use and enriched for brain-expressed genes. ''PLoS One''. 2012; '''7''' (6):e39498
A genome-wide association search for type 2 diabetes genes in African Americans. Description: Palmer, Nicholette D, et al. A genome-wide association search for type 2 diabetes genes in African Americans. ''PLoS One''. 2012; '''7''' (1):e29202
A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese. Description: Okada, Yukinori, et al. A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese. ''PLoS Genet''. 2012 Jan; '''8''' (1):e1002455
A genome-wide association study of circulating galectin-3. Description: de Boer, Rudolf A, et al. A genome-wide association study of circulating galectin-3. ''PLoS One''. 2012; '''7''' (10):e47385
A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1. Description: Urabe, Yuji, et al. A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1. ''PLoS Genet''. 2012; '''8''' (3):e1002541
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. Description: Milton, Jacqueline N, et al. A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. ''PLoS One''. 2012; '''7''' (4):e34741
A genome-wide association study reveals loci influencing height and other conformation traits in horses. Description: Signer-Hasler, Heidi, et al. A genome-wide association study reveals loci influencing height and other conformation traits in horses. ''PLoS One''. 2012; '''7''' (5):e37282
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. Description: Kenny, Eimear E, et al. A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. ''PLoS Genet''. 2012; '''8''' (3):e1002559
A high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studies. Description: McCue, Molly E, et al. A high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studies. ''PLoS Genet''. 2012 Jan; '''8''' (1):e1002451
A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans. Description: Qayyum, Rehan, et al. A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans. ''PLoS Genet''. 2012; '''8''' (3):e1002491
Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals. Description: Swaminathan, Shanker, et al. Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals. ''PLoS One''. 2012; '''7''' (12):e50640
Analysis of IL12B gene variants in inflammatory bowel disease. Description: Glas, Jurgen, et al. Analysis of IL12B gene variants in inflammatory bowel disease. ''PLoS One''. 2012; '''7''' (3):e34349
Analysis of IL28B variants in an Egyptian population defines the 20 kilobases minimal region involved in spontaneous clearance of hepatitis C virus. Description: Pedergnana, Vincent, et al. Analysis of IL28B variants in an Egyptian population defines the 20 kilobases minimal region involved in spontaneous clearance of hepatitis C virus. ''PLoS One''. 2012; '''7''' (6):e38578
Analysis of polymorphisms and haplotype structure of the human thymidylate synthase genetic region: a tool for pharmacogenetic studies. Description: Ghosh, Soma, et al. Analysis of polymorphisms and haplotype structure of the human thymidylate synthase genetic region: a tool for pharmacogenetic studies. ''PLoS One''. 2012; '''7''' (4):e34426
An ICA with reference approach in identification of genetic variation and associated brain networks. Description: Liu, Jingyu, et al. An ICA with reference approach in identification of genetic variation and associated brain networks. ''Front Hum Neurosci''. 2012; '''6''': 21
A novel GUSB mutation in Brazilian terriers with severe skeletal abnormalities defines the disease as mucopolysaccharidosis VII. Description: Hytonen, Marjo K, et al. A novel GUSB mutation in Brazilian terriers with severe skeletal abnormalities defines the disease as mucopolysaccharidosis VII. ''PLoS One''. 2012; '''7''' (7):e40281
An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12. Description: Maher, Bridget H, et al. An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12. ''PLoS One''. 2012; '''7''' (5):e37903
A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers. Description: Karjalainen, Minna K, et al. A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers. ''PLoS One''. 2012; '''7''' (12):e51378
A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides. Description: Braun, Timothy R, et al. A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides. ''PLoS One''. 2012; '''7''' (5):e37056
A SEL1L mutation links a canine progressive early-onset cerebellar ataxia to the endoplasmic reticulum-associated protein degradation (ERAD) machinery. Description: Kyostila, Kaisa, et al. A SEL1L mutation links a canine progressive early-onset cerebellar ataxia to the endoplasmic reticulum-associated protein degradation (ERAD) machinery. ''PLoS Genet''. 2012; '''8''' (6):e1002759
Assessment of genotype imputation performance using 1000 Genomes in African American studies. Description: Hancock, Dana B, et al. Assessment of genotype imputation performance using 1000 Genomes in African American studies. ''PLoS One''. 2012; '''7''' (11):e50610
Assessment of the association of matrix metalloproteinases with myopia, refractive error and ocular biometric measures in an Australian cohort. Description: Schache, Maria, et al. Assessment of the association of matrix metalloproteinases with myopia, refractive error and ocular biometric measures in an Australian cohort. ''PLoS One''. 2012; '''7''' (10):e47181
Association analysis of 94 candidate genes and schizophrenia-related endophenotypes. Description: Greenwood, Tiffany A, et al. Association analysis of 94 candidate genes and schizophrenia-related endophenotypes. ''PLoS One''. 2012; '''7''' (1):e29630
Association analysis of single nucleotide polymorphisms at five loci: comparison between atopic dermatitis and asthma in the Chinese Han population. Description: Tang, Hua-Yang, et al. Association analysis of single nucleotide polymorphisms at five loci: comparison between atopic dermatitis and asthma in the Chinese Han population. ''PLoS One''. 2012; '''7''' (4):e35334
Association analysis of the extended MHC region in celiac disease implicates multiple independent susceptibility loci. Description: Ahn, Richard, et al. Association analysis of the extended MHC region in celiac disease implicates multiple independent susceptibility loci. ''PLoS One''. 2012; '''7''' (5):e36926
Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. Description: Osman, Wael, et al. Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. ''PLoS One''. 2012; '''7''' (4):e32683
Association of OX40L polymorphisms with sporadic breast cancer in northeast Chinese Han population. Description: Weiguang, Yuan, et al. Association of OX40L polymorphisms with sporadic breast cancer in northeast Chinese Han population. ''PLoS One''. 2012; '''7''' (8):e41277
Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population. Description: Zhang, Yuping, et al. Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population. ''PLoS One''. 2012; '''7''' (9):e42969
Association of the type 2 diabetes mellitus susceptibility gene, TCF7L2, with schizophrenia in an Arab-Israeli family sample. Description: Alkelai, Anna, et al. Association of the type 2 diabetes mellitus susceptibility gene, TCF7L2, with schizophrenia in an Arab-Israeli family sample. ''PLoS One''. 2012; '''7''' (1):e29228
ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population. Description: Lahut, Suna, et al. ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population. ''PLoS One''. 2012; '''7''' (8):e42956
A variant in the ABO gene explains the variation in soluble E-selectin levels-results from dense genotyping in two independent populations. Description: Karakas, Mahir, et al. A variant in the ABO gene explains the variation in soluble E-selectin levels-results from dense genotyping in two independent populations. ''PLoS One''. 2012; '''7''' (12):e51441
AVPR1A and SLC6A4 polymorphisms in choral singers and non-musicians: a gene association study. Description: Morley, Andrew P, et al. AVPR1A and SLC6A4 polymorphisms in choral singers and non-musicians: a gene association study. ''PLoS One''. 2012; '''7''' (2):e31763
BMP4 was associated with NSCL/P in an Asian population. Description: Chen, Qianqian, et al. BMP4 was associated with NSCL/P in an Asian population. ''PLoS One''. 2012; '''7''' (4):e35347
CD1 gene polymorphisms and phenotypic variability in X-linked adrenoleukodystrophy. Description: Barbier, Mathieu, et al. CD1 gene polymorphisms and phenotypic variability in X-linked adrenoleukodystrophy. ''PLoS One''. 2012; '''7''' (1):e29872
Centronuclear myopathy in Labrador retrievers: a recent founder mutation in the PTPLA gene has rapidly disseminated worldwide. Description: Maurer, Marie, et al. Centronuclear myopathy in Labrador retrievers: a recent founder mutation in the PTPLA gene has rapidly disseminated worldwide. ''PLoS One''. 2012; '''7''' (10):e46408
Chapter 7: Pharmacogenomics. Description: Karczewski, Konrad J, et al. Chapter 7: Pharmacogenomics. ''PLoS Comput Biol''. 2012; '''8''' (12):e1002817
Cholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular risk. Description: Papp, Audrey C, et al. Cholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular risk. ''PLoS One''. 2012; '''7''' (3):e31930
Chromosome 9 ALS and FTD locus is probably derived from a single founder. Description: Mok, Kin, et al. Chromosome 9 ALS and FTD locus is probably derived from a single founder. ''Neurobiol Aging''. 2012 Jan; '''33''' (1):209.e3-8
CNR1 genotype influences HDL-cholesterol response to change in dietary fat intake. Description: Silver, Heidi J, et al. CNR1 genotype influences HDL-cholesterol response to change in dietary fat intake. ''PLoS One''. 2012; '''7''' (5):e36166
Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS. Description: Ermini, Luca, et al. Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS. ''Mol Immunol''. 2012 Jan; '''49''' (4):640-8
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. Description: Wiggs, Janey L, et al. Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. ''PLoS Genet''. 2012; '''8''' (4):e1002654
Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese. Description: Nakano, Masakazu, et al. Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese. ''PLoS One''. 2012; '''7''' (3):e33389
Common variants in MAGI2 gene are associated with increased risk for cognitive impairment in schizophrenic patients. Description: Koide, Takayoshi, et al. Common variants in MAGI2 gene are associated with increased risk for cognitive impairment in schizophrenic patients. ''PLoS One''. 2012; '''7''' (5):e36836
Common variants of FTO are associated with childhood obesity in a cross-sectional study of 3,126 urban Indian children. Description: Dwivedi, Om Prakash, et al. Common variants of FTO are associated with childhood obesity in a cross-sectional study of 3,126 urban Indian children. ''PLoS One''. 2012; '''7''' (10):e47772
Common variants of homocysteine metabolism pathway genes and risk of type 2 diabetes and related traits in Indians. Description: Chauhan, Ganesh, et al. Common variants of homocysteine metabolism pathway genes and risk of type 2 diabetes and related traits in Indians. ''Exp Diabetes Res''. 2012; '''2012''': 960318
Common variants of the liver fatty acid binding protein gene influence the risk of type 2 diabetes and insulin resistance in Spanish population. Description: Mansego, Maria Luisa, et al. Common variants of the liver fatty acid binding protein gene influence the risk of type 2 diabetes and insulin resistance in Spanish population. ''PLoS One''. 2012; '''7''' (3):e31853
Common variants on chromosome 9p21 are associated with normal tension glaucoma. Description: Takamoto, Mitsuko, et al. Common variants on chromosome 9p21 are associated with normal tension glaucoma. ''PLoS One''. 2012; '''7''' (7):e40107
Comparison of pathway analysis approaches using lung cancer GWAS data sets. Description: Fehringer, Gordon, et al. Comparison of pathway analysis approaches using lung cancer GWAS data sets. ''PLoS One''. 2012; '''7''' (2):e31816
Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration. Description: Cantsilieris, Stuart, et al. Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration. ''PLoS One''. 2012; '''7''' (4):e35255
Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease. Description: Simon-Sanchez, Javier, et al. Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease. ''PLoS One''. 2012; '''7''' (3):e28787
CUBN as a novel locus for end-stage renal disease: insights from renal transplantation. Description: Reznichenko, Anna, et al. CUBN as a novel locus for end-stage renal disease: insights from renal transplantation. ''PLoS One''. 2012; '''7''' (5):e36512
Deep Sequence Analysis of Non-Small Cell Lung Cancer: Integrated Analysis of Gene Expression, Alternative Splicing, and Single Nucleotide Variations in Lung Adenocarcinomas with and without Oncogenic KRAS Mutations. Description: Kalari, Krishna R, et al. Deep Sequence Analysis of Non-Small Cell Lung Cancer: Integrated Analysis of Gene Expression, Alternative Splicing, and Single Nucleotide Variations in Lung Adenocarcinomas with and without Oncogenic KRAS Mutations. ''Front Oncol''. 2012; '''2''': 12
Deletion of CDKAL1 affects high-fat diet-induced fat accumulation and glucose-stimulated insulin secretion in mice, indicating relevance to diabetes. Description: Okamura, Tadashi, et al. Deletion of CDKAL1 affects high-fat diet-induced fat accumulation and glucose-stimulated insulin secretion in mice, indicating relevance to diabetes. ''PLoS One''. 2012; '''7''' (11):e49055
delta-Catenin is genetically and biologically associated with cortical cataract and future Alzheimer-related structural and functional brain changes. Description: Jun, Gyungah, et al. delta-Catenin is genetically and biologically associated with cortical cataract and future Alzheimer-related structural and functional brain changes. ''PLoS One''. 2012; '''7''' (9):e43728
Environmental stress affects DNA methylation of a CpG rich promoter region of serotonin transporter gene in a nurse cohort. Description: Alasaari, Jukka S, et al. Environmental stress affects DNA methylation of a CpG rich promoter region of serotonin transporter gene in a nurse cohort. ''PLoS One''. 2012; '''7''' (9):e45813
Estimating the proportion of variation in susceptibility to multiple sclerosis captured by common SNPs. Description: Watson, Corey T, et al. Estimating the proportion of variation in susceptibility to multiple sclerosis captured by common SNPs. ''Sci Rep''. 2012; '''2''': 770
Evaluation of Parkinson disease risk variants as expression-QTLs. Description: Latourelle, Jeanne C, et al. Evaluation of Parkinson disease risk variants as expression-QTLs. ''PLoS One''. 2012; '''7''' (10):e46199
Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study. Description: Buyske, Steven, et al. Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study. ''PLoS One''. 2012; '''7''' (4):e35651
Evidence for two independent associations with type 1 diabetes at the 12q13 locus. Description: Keene, K L, et al. Evidence for two independent associations with type 1 diabetes at the 12q13 locus. ''Genes Immun''. 2012 Jan; '''13''' (1):66-70
Extensive natural variation for cellular hydrogen peroxide release is genetically controlled. Description: Attar, Homa, et al. Extensive natural variation for cellular hydrogen peroxide release is genetically controlled. ''PLoS One''. 2012; '''7''' (8):e43566
Fine-mapping and initial characterization of QT interval loci in African Americans. Description: Avery, Christy L, et al. Fine-mapping and initial characterization of QT interval loci in African Americans. ''PLoS Genet''. 2012; '''8''' (8):e1002870
First WNK4-hypokalemia animal model identified by genome-wide association in Burmese cats. Description: Gandolfi, Barbara, et al. First WNK4-hypokalemia animal model identified by genome-wide association in Burmese cats. ''PLoS One''. 2012; '''7''' (12):e53173
Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients. Description: Spellicy, Catherine J, et al. Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients. ''PLoS One''. 2012; '''7''' (12):e51330
Functional variant in the autophagy-related 5 gene promotor is associated with childhood asthma. Description: Martin, Lisa J, et al. Functional variant in the autophagy-related 5 gene promotor is associated with childhood asthma. ''PLoS One''. 2012; '''7''' (4):e33454
Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders. Description: Ersland, Kari M, et al. Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders. ''PLoS One''. 2012; '''7''' (2):e31687
Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients. Description: van Eerde, Albertien M, et al. Genes in the ureteric budding pathway: association study on vesico-ureteral reflux patients. ''PLoS One''. 2012; '''7''' (4):e31327
Genetic polymorphisms of the human PNPLA3 gene are strongly associated with severity of non-alcoholic fatty liver disease in Japanese. Description: Kawaguchi, Takahisa, et al. Genetic polymorphisms of the human PNPLA3 gene are strongly associated with severity of non-alcoholic fatty liver disease in Japanese. ''PLoS One''. 2012; '''7''' (6):e38322
Genetic susceptibility factors on genes involved in the steroid hormone biosynthesis pathway and progesterone receptor for gastric cancer risk. Description: Cho, Lisa Y, et al. Genetic susceptibility factors on genes involved in the steroid hormone biosynthesis pathway and progesterone receptor for gastric cancer risk. ''PLoS One''. 2012; '''7''' (10):e47603
Genetic susceptibility on CagA-interacting molecules and gene-environment interaction with phytoestrogens: a putative risk factor for gastric cancer. Description: Yang, Jae Jeong, et al. Genetic susceptibility on CagA-interacting molecules and gene-environment interaction with phytoestrogens: a putative risk factor for gastric cancer. ''PLoS One''. 2012; '''7''' (2):e31020
Genetic variant of AMD1 is associated with obesity in urban Indian children. Description: Tabassum, Rubina, et al. Genetic variant of AMD1 is associated with obesity in urban Indian children. ''PLoS One''. 2012; '''7''' (4):e33162
Genetic variants in ER cofactor genes and endometrial cancer risk. Description: Li, Yuqing, et al. Genetic variants in ER cofactor genes and endometrial cancer risk. ''PLoS One''. 2012; '''7''' (8):e42445
Genetic variants in the Fat and Obesity Associated (FTO) gene and risk of Alzheimer's disease. Description: Reitz, Christiane, et al. Genetic variants in the Fat and Obesity Associated (FTO) gene and risk of Alzheimer's disease. ''PLoS One''. 2012; '''7''' (12):e50354
Genetic variants on chromosome 1q41 influence ocular axial length and high myopia. Description: Fan, Qiao, et al. Genetic variants on chromosome 1q41 influence ocular axial length and high myopia. ''PLoS Genet''. 2012; '''8''' (6):e1002753
Genetic variation in Hyperpolarization-activated cyclic nucleotide-gated channels and its relationship with neuroticism, cognition and risk of depression. Description: McIntosh, Andrew M, et al. Genetic variation in Hyperpolarization-activated cyclic nucleotide-gated channels and its relationship with neuroticism, cognition and risk of depression. ''Front Genet''. 2012; '''3''': 116
Genetic variation in the EGFR gene and the risk of glioma in a Chinese Han population. Description: Hou, Wu-Gang, et al. Genetic variation in the EGFR gene and the risk of glioma in a Chinese Han population. ''PLoS One''. 2012; '''7''' (5):e37531
Genetic variation in TLR genes in Ugandan and South African populations and comparison with HapMap data. Description: Baker, Allison R, et al. Genetic variation in TLR genes in Ugandan and South African populations and comparison with HapMap data. ''PLoS One''. 2012; '''7''' (10):e47597
Gene-wide characterization of common quantitative trait loci for ABCB1 mRNA expression in normal liver tissues in the Chinese population. Description: Shou, Weihua, et al. Gene-wide characterization of common quantitative trait loci for ABCB1 mRNA expression in normal liver tissues in the Chinese population. ''PLoS One''. 2012; '''7''' (9):e46295
Genome features of "Dark-fly", a Drosophila line reared long-term in a dark environment. Description: Izutsu, Minako, et al. Genome features of "Dark-fly", a Drosophila line reared long-term in a dark environment. ''PLoS One''. 2012; '''7''' (3):e33288
Genome-wide analysis in Brazilian Xavante Indians reveals low degree of admixture. Description: Kuhn, Patricia C, et al. Genome-wide analysis in Brazilian Xavante Indians reveals low degree of admixture. ''PLoS One''. 2012; '''7''' (8):e42702
Genome wide assessment of young onset Parkinson's disease from Finland. Description: Hernandez, Dena G, et al. Genome wide assessment of young onset Parkinson's disease from Finland. ''PLoS One''. 2012; '''7''' (7):e41859
Genome-wide association and functional follow-up reveals new loci for kidney function. Description: Pattaro, Cristian, et al. Genome-wide association and functional follow-up reveals new loci for kidney function. ''PLoS Genet''. 2012; '''8''' (3):e1002584
Genome-wide association identifies multiple genomic regions associated with susceptibility to and control of ovine lentivirus. Description: White, Stephen N, et al. Genome-wide association identifies multiple genomic regions associated with susceptibility to and control of ovine lentivirus. ''PLoS One''. 2012; '''7''' (10):e47829
Genome-wide association mapping and identification of candidate genes for the rumpless and ear-tufted traits of the Araucana chicken. Description: Noorai, Rooksana E, et al. Genome-wide association mapping and identification of candidate genes for the rumpless and ear-tufted traits of the Araucana chicken. ''PLoS One''. 2012; '''7''' (7):e40974
Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene. Description: Johnson, Matthew P, et al. Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene. ''PLoS One''. 2012; '''7''' (3):e33666
Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations. Description: Candille, Sophie I, et al. Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations. ''PLoS One''. 2012; '''7''' (10):e48294
Genome-wide association study identifies chromosome 10q24.32 variants associated with arsenic metabolism and toxicity phenotypes in Bangladesh. Description: Pierce, Brandon L, et al. Genome-wide association study identifies chromosome 10q24.32 variants associated with arsenic metabolism and toxicity phenotypes in Bangladesh. ''PLoS Genet''. 2012; '''8''' (2):e1002522
Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer. Description: Long, Jirong, et al. Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer. ''PLoS Genet''. 2012; '''8''' (2):e1002532
Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. Description: Adrianto, Indra, et al. Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. ''PLoS One''. 2012; '''7''' (8):e43907
Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts. Description: Boraska, Vesna, et al. Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts. ''PLoS One''. 2012; '''7''' (3):e31369
Genome-wide linkage and association analysis identifies major gene loci for guttural pouch tympany in Arabian and German warmblood horses. Description: Metzger, Julia, et al. Genome-wide linkage and association analysis identifies major gene loci for guttural pouch tympany in Arabian and German warmblood horses. ''PLoS One''. 2012; '''7''' (7):e41640
Genome-wide scan identifies variant in TNFSF13 associated with serum IgM in a healthy Chinese male population. Description: Yang, Ming, et al. Genome-wide scan identifies variant in TNFSF13 associated with serum IgM in a healthy Chinese male population. ''PLoS One''. 2012; '''7''' (10):e47990
Genome-wide study of gene variants associated with differential cardiovascular event reduction by pravastatin therapy. Description: Shiffman, Dov, et al. Genome-wide study of gene variants associated with differential cardiovascular event reduction by pravastatin therapy. ''PLoS One''. 2012; '''7''' (5):e38240
Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics. Description: Ghani, Mahdi, et al. Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics. ''G3 (Bethesda)''. 2012 Jan; '''2''' (1):71-8
Genomic ancestry of North Africans supports back-to-Africa migrations. Description: Henn, Brenna M, et al. Genomic ancestry of North Africans supports back-to-Africa migrations. ''PLoS Genet''. 2012 Jan; '''8''' (1):e1002397
Genotype Imputation for Latinos Using the HapMap and 1000 Genomes Project Reference Panels. Description: Gao, Xiaoyi, et al. Genotype Imputation for Latinos Using the HapMap and 1000 Genomes Project Reference Panels. ''Front Genet''. 2012; '''3''': 117
Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis. Description: Kiryluk, Krzysztof, et al. Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis. ''PLoS Genet''. 2012; '''8''' (6):e1002765
Glucocorticoid receptor 1B and 1C mRNA transcript alterations in schizophrenia and bipolar disorder, and their possible regulation by GR gene variants. Description: Sinclair, Duncan, et al. Glucocorticoid receptor 1B and 1C mRNA transcript alterations in schizophrenia and bipolar disorder, and their possible regulation by GR gene variants. ''PLoS One''. 2012; '''7''' (3):e31720
GWAS identifies novel susceptibility loci on 6p21.32 and 21q21.3 for hepatocellular carcinoma in chronic hepatitis B virus carriers. Description: Li, Shengping, et al. GWAS identifies novel susceptibility loci on 6p21.32 and 21q21.3 for hepatocellular carcinoma in chronic hepatitis B virus carriers. ''PLoS Genet''. 2012; '''8''' (7):e1002791
Heritability and genetic correlations explained by common SNPs for metabolic syndrome traits. Description: Vattikuti, Shashaank, et al. Heritability and genetic correlations explained by common SNPs for metabolic syndrome traits. ''PLoS Genet''. 2012; '''8''' (3):e1002637
Heterogeneity in genetic admixture across different regions of Argentina. Description: Avena, Sergio, et al. Heterogeneity in genetic admixture across different regions of Argentina. ''PLoS One''. 2012; '''7''' (4):e34695
High-density SNP mapping of the HLA region identifies multiple independent susceptibility loci associated with selective IgA deficiency. Description: Ferreira, Ricardo C, et al. High-density SNP mapping of the HLA region identifies multiple independent susceptibility loci associated with selective IgA deficiency. ''PLoS Genet''. 2012 Jan; '''8''' (1):e1002476
HLA associations in classical Hodgkin lymphoma: EBV status matters. Description: Huang, Xin, et al. HLA associations in classical Hodgkin lymphoma: EBV status matters. ''PLoS One''. 2012; '''7''' (7):e39986
Identification of a novel idiopathic epilepsy locus in Belgian Shepherd dogs. Description: Seppala, Eija H, et al. Identification of a novel idiopathic epilepsy locus in Belgian Shepherd dogs. ''PLoS One''. 2012; '''7''' (3):e33549
Identification of a potential susceptibility locus for macular telangiectasia type 2. Description: Parmalee, Nancy L, et al. Identification of a potential susceptibility locus for macular telangiectasia type 2. ''PLoS One''. 2012; '''7''' (8):e24268
Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study. Description: Yang, Hsin-Chou, et al. Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study. ''PLoS One''. 2012; '''7''' (3):e32907
Identification of sialyltransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26. Description: McAuley, Erica Z, et al. Identification of sialyltransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26. ''PLoS One''. 2012; '''7''' (5):e38172
IL12RB2 gene is associated with the age of type 1 diabetes onset in Croatian family Trios. Description: Pehlic, Marina, et al. IL12RB2 gene is associated with the age of type 1 diabetes onset in Croatian family Trios. ''PLoS One''. 2012; '''7''' (11):e49133
IL28B genetic variation is associated with spontaneous clearance of hepatitis C virus, treatment response, serum IL-28B levels in Chinese population. Description: Shi, Xiaodong, et al. IL28B genetic variation is associated with spontaneous clearance of hepatitis C virus, treatment response, serum IL-28B levels in Chinese population. ''PLoS One''. 2012; '''7''' (5):e37054
Incorporating Information of microRNAs into Pathway Analysis in a Genome-Wide Association Study of Bipolar Disorder. Description: Shih, Wei-Liang, et al. Incorporating Information of microRNAs into Pathway Analysis in a Genome-Wide Association Study of Bipolar Disorder. ''Front Genet''. 2012; '''3''': 293
Innate immunity and non-Hodgkin's lymphoma (NHL) related genes in a nested case-control study for gastric cancer risk. Description: Park, Sue K, et al. Innate immunity and non-Hodgkin's lymphoma (NHL) related genes in a nested case-control study for gastric cancer risk. ''PLoS One''. 2012; '''7''' (9):e45274
Interaction analysis between HLA-DRB1 shared epitope alleles and MHC class II transactivator CIITA gene with regard to risk of rheumatoid arthritis. Description: Ronninger, Marcus, et al. Interaction analysis between HLA-DRB1 shared epitope alleles and MHC class II transactivator CIITA gene with regard to risk of rheumatoid arthritis. ''PLoS One''. 2012; '''7''' (3):e32861
Intracranial aneurysm risk locus 5q23.2 is associated with elevated systolic blood pressure. Description: Gaal, Emilia Ilona, et al. Intracranial aneurysm risk locus 5q23.2 is associated with elevated systolic blood pressure. ''PLoS Genet''. 2012; '''8''' (3):e1002563
Investigation of CD28 gene polymorphisms in patients with sporadic breast cancer in a Chinese Han population in Northeast China. Description: Chen, Shuang, et al. Investigation of CD28 gene polymorphisms in patients with sporadic breast cancer in a Chinese Han population in Northeast China. ''PLoS One''. 2012; '''7''' (10):e48031
Investigation of homocysteine-pathway-related variants in essential hypertension. Description: Fowdar, Javed Y, et al. Investigation of homocysteine-pathway-related variants in essential hypertension. ''Int J Hypertens''. 2012; '''2012''': 190923
Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis. Description: Derks, Eske M, et al. Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis. ''PLoS One''. 2012; '''7''' (6):e37852
KDM2B is implicated in bovine lethal multi-organic developmental dysplasia. Description: Testoni, Stefania, et al. KDM2B is implicated in bovine lethal multi-organic developmental dysplasia. ''PLoS One''. 2012; '''7''' (9):e45634
Knowledge-driven analysis identifies a gene-gene interaction affecting high-density lipoprotein cholesterol levels in multi-ethnic populations. Description: Ma, Li, et al. Knowledge-driven analysis identifies a gene-gene interaction affecting high-density lipoprotein cholesterol levels in multi-ethnic populations. ''PLoS Genet''. 2012; '''8''' (5):e1002714
Lactase persistence and lipid pathway selection in the Maasai. Description: Wagh, Kshitij, et al. Lactase persistence and lipid pathway selection in the Maasai. ''PLoS One''. 2012; '''7''' (9):e44751
Large scale association analysis for drug addiction: results from SNP to gene. Description: Guo, Xiaobo, et al. Large scale association analysis for drug addiction: results from SNP to gene. ''ScientificWorldJournal''. 2012; '''2012''': 939584
Limitations of the human reference genome for personalized genomics. Description: Rosenfeld, Jeffrey A, et al. Limitations of the human reference genome for personalized genomics. ''PLoS One''. 2012; '''7''' (7):e40294
Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS. Description: Diekstra, Frank P, et al. Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS. ''PLoS One''. 2012; '''7''' (4):e35333
Mass homozygotes accumulation in the NCI-60 cancer cell lines as compared to HapMap Trios, and relation to fragile site location. Description: Ruan, Xiaoyang, et al. Mass homozygotes accumulation in the NCI-60 cancer cell lines as compared to HapMap Trios, and relation to fragile site location. ''PLoS One''. 2012; '''7''' (2):e31628
MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphisms. Description: Velez Edwards, Digna R, et al. MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphisms. ''PLoS One''. 2012; '''7''' (2):e32275
Mitochondrial mutations and polymorphisms in psychiatric disorders. Description: Sequeira, Adolfo, et al. Mitochondrial mutations and polymorphisms in psychiatric disorders. ''Front Genet''. 2012; '''3''': 103
*Multiple sclerosis risk variant HLA-DRB11501 associates with high expression of DRB1 gene in different human populations.** Description: Alcina, Antonio, et al. Multiple sclerosis risk variant HLA-DRB1*1501 associates with high expression of DRB1 gene in different human populations. ''PLoS One''. 2012; '''7''' (1):e29819
Multi-species data integration and gene ranking enrich significant results in an alcoholism genome-wide association study. Description: Zhao, Zhongming, et al. Multi-species data integration and gene ranking enrich significant results in an alcoholism genome-wide association study. ''BMC Genomics''. 2012; '''13 Suppl 8''': S16
Mutations in MITF and PAX3 cause "splashed white" and other white spotting phenotypes in horses. Description: Hauswirth, Regula, et al. Mutations in MITF and PAX3 cause "splashed white" and other white spotting phenotypes in horses. ''PLoS Genet''. 2012; '''8''' (4):e1002653
NetView: a high-definition network-visualization approach to detect fine-scale population structures from genome-wide patterns of variation. Description: Neuditschko, Markus, et al. NetView: a high-definition network-visualization approach to detect fine-scale population structures from genome-wide patterns of variation. ''PLoS One''. 2012; '''7''' (10):e48375
Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia. Description: Jia, Peilin, et al. Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia. ''PLoS Comput Biol''. 2012; '''8''' (7):e1002587
Networks of neuronal genes affected by common and rare variants in autism spectrum disorders. Description: Ben-David, Eyal, et al. Networks of neuronal genes affected by common and rare variants in autism spectrum disorders. ''PLoS Genet''. 2012; '''8''' (3):e1002556
Neurobeachin, a regulator of synaptic protein targeting, is associated with body fat mass and feeding behavior in mice and body-mass index in humans. Description: Olszewski, Pawel K, et al. Neurobeachin, a regulator of synaptic protein targeting, is associated with body fat mass and feeding behavior in mice and body-mass index in humans. ''PLoS Genet''. 2012; '''8''' (3):e1002568
Nicotine reward and affective nicotine withdrawal signs are attenuated in calcium/calmodulin-dependent protein kinase IV knockout mice. Description: Jackson, Kia J, et al. Nicotine reward and affective nicotine withdrawal signs are attenuated in calcium/calmodulin-dependent protein kinase IV knockout mice. ''PLoS One''. 2012; '''7''' (11):e51154
No association of a set of candidate genes on haloperidol side effects. Description: Drago, Antonio, et al. No association of a set of candidate genes on haloperidol side effects. ''PLoS One''. 2012; '''7''' (10):e44853
Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis. Description: Inouye, Michael, et al. Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis. ''PLoS Genet''. 2012; '''8''' (8):e1002907
Parallel mapping and simultaneous sequencing reveals deletions in BCAN and FAM83H associated with discrete inherited disorders in a domestic dog breed. Description: Forman, Oliver P, et al. Parallel mapping and simultaneous sequencing reveals deletions in BCAN and FAM83H associated with discrete inherited disorders in a domestic dog breed. ''PLoS Genet''. 2012 Jan; '''8''' (1):e1002462
Parameters in dynamic models of complex traits are containers of missing heritability. Description: Wang, Yunpeng, et al. Parameters in dynamic models of complex traits are containers of missing heritability. ''PLoS Comput Biol''. 2012; '''8''' (4):e1002459
Partial deletion of the sulfate transporter SLC13A1 is associated with an osteochondrodysplasia in the Miniature Poodle breed. Description: Neff, Mark W, et al. Partial deletion of the sulfate transporter SLC13A1 is associated with an osteochondrodysplasia in the Miniature Poodle breed. ''PLoS One''. 2012; '''7''' (12):e51917
Patterns of ancestry, signatures of natural selection, and genetic association with stature in Western African pygmies. Description: Jarvis, Joseph P, et al. Patterns of ancestry, signatures of natural selection, and genetic association with stature in Western African pygmies. ''PLoS Genet''. 2012; '''8''' (4):e1002641
PLXNC1 and RDH13 associated with bilateral convergent strabismus with exophthalmus in German Brown cattle. Description: Fink, Steffen, et al. PLXNC1 and RDH13 associated with bilateral convergent strabismus with exophthalmus in German Brown cattle. ''Mol Vis''. 2012; '''18''': 2229-40
Polymorphisms in HSD17B1: Early Onset and Increased Risk of Alzheimer's Disease in Women with Down Syndrome. Description: Lee, Joseph H, et al. Polymorphisms in HSD17B1: Early Onset and Increased Risk of Alzheimer's Disease in Women with Down Syndrome. ''Curr Gerontol Geriatr Res''. 2012; '''2012''': 361218
Pooled sample-based GWAS: a cost-effective alternative for identifying colorectal and prostate cancer risk variants in the Polish population. Description: Gaj, Pawel, et al. Pooled sample-based GWAS: a cost-effective alternative for identifying colorectal and prostate cancer risk variants in the Polish population. ''PLoS One''. 2012; '''7''' (4):e35307
Population genetic structure and origins of Native Hawaiians in the multiethnic cohort study. Description: Kim, Sung K, et al. Population genetic structure and origins of Native Hawaiians in the multiethnic cohort study. ''PLoS One''. 2012; '''7''' (11):e47881
Population structure of Hispanics in the United States: the multi-ethnic study of atherosclerosis. Description: Manichaikul, Ani, et al. Population structure of Hispanics in the United States: the multi-ethnic study of atherosclerosis. ''PLoS Genet''. 2012; '''8''' (4):e1002640
Predicting signatures of "synthetic associations" and "natural associations" from empirical patterns of human genetic variation. Description: Chang, Diana, et al. Predicting signatures of "synthetic associations" and "natural associations" from empirical patterns of human genetic variation. ''PLoS Comput Biol''. 2012; '''8''' (7):e1002600
PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-kappaB and XBP1 binding sites. Description: Glas, Jurgen, et al. PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-kappaB and XBP1 binding sites. ''PLoS One''. 2012; '''7''' (12):e52873
PTPN2 gene variants are associated with susceptibility to both Crohn's disease and ulcerative colitis supporting a common genetic disease background. Description: Glas, Jurgen, et al. PTPN2 gene variants are associated with susceptibility to both Crohn's disease and ulcerative colitis supporting a common genetic disease background. ''PLoS One''. 2012; '''7''' (3):e33682
Rare and low frequency variant stratification in the UK population: description and impact on association tests. Description: Babron, Marie-Claude, et al. Rare and low frequency variant stratification in the UK population: description and impact on association tests. ''PLoS One''. 2012; '''7''' (10):e46519
Recessive mutations in SPTBN2 implicate beta-III spectrin in both cognitive and motor development. Description: Lise, Stefano, et al. Recessive mutations in SPTBN2 implicate beta-III spectrin in both cognitive and motor development. ''PLoS Genet''. 2012; '''8''' (12):e1003074
Reduced lentivirus susceptibility in sheep with TMEM154 mutations. Description: Heaton, Michael P, et al. Reduced lentivirus susceptibility in sheep with TMEM154 mutations. ''PLoS Genet''. 2012 Jan; '''8''' (1):e1002467
Regions of homozygosity in the porcine genome: consequence of demography and the recombination landscape. Description: Bosse, Mirte, et al. Regions of homozygosity in the porcine genome: consequence of demography and the recombination landscape. ''PLoS Genet''. 2012; '''8''' (11):e1003100
Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. Description: Keller, Matthew C, et al. Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. ''PLoS Genet''. 2012; '''8''' (4):e1002656
Segment-wise genome-wide association analysis identifies a candidate region associated with schizophrenia in three independent samples. Description: Gladwin, Thomas E, et al. Segment-wise genome-wide association analysis identifies a candidate region associated with schizophrenia in three independent samples. ''PLoS One''. 2012; '''7''' (6):e38828
Significant association of estrogen receptor binding site variation with bipolar disorder in females. Description: Graae, Lisette, et al. Significant association of estrogen receptor binding site variation with bipolar disorder in females. ''PLoS One''. 2012; '''7''' (2):e32304
SNP rs1533428 at 2p16.3 as a marker for late-onset primary open-angle glaucoma. Description: Chen, Li Jia, et al. SNP rs1533428 at 2p16.3 as a marker for late-onset primary open-angle glaucoma. ''Mol Vis''. 2012; '''18''': 1629-39
The aromatase gene (CYP19A1) variants and circulating hepatocyte growth factor in postmenopausal women. Description: Lin, Jennifer H, et al. The aromatase gene (CYP19A1) variants and circulating hepatocyte growth factor in postmenopausal women. ''PLoS One''. 2012; '''7''' (7):e42079
The diamine oxidase gene is associated with hypersensitivity response to non-steroidal anti-inflammatory drugs. Description: Agundez, Jose A G, et al. The diamine oxidase gene is associated with hypersensitivity response to non-steroidal anti-inflammatory drugs. ''PLoS One''. 2012; '''7''' (11):e47571
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure. Description: Scerri, Thomas S, et al. The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure. ''PLoS One''. 2012; '''7''' (11):e50321
The Interaction between Pesticide Use and Genetic Variants Involved in Lipid Metabolism on Prostate Cancer Risk. Description: Andreotti, Gabriella, et al. The Interaction between Pesticide Use and Genetic Variants Involved in Lipid Metabolism on Prostate Cancer Risk. ''J Cancer Epidemiol''. 2012; '''2012''': 358076
The interactive effect of SIRT1 promoter region polymorphism on type 2 diabetes susceptibility in the North Indian population. Description: Rai, Ekta, et al. The interactive effect of SIRT1 promoter region polymorphism on type 2 diabetes susceptibility in the North Indian population. ''PLoS One''. 2012; '''7''' (11):e48621
The interleukin 3 gene (IL3) contributes to human brain volume variation by regulating proliferation and survival of neural progenitors. Description: Luo, Xiong-jian, et al. The interleukin 3 gene (IL3) contributes to human brain volume variation by regulating proliferation and survival of neural progenitors. ''PLoS One''. 2012; '''7''' (11):e50375
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits. Description: Voight, Benjamin F, et al. The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits. ''PLoS Genet''. 2012; '''8''' (8):e1002793
The principal genetic determinants for nasopharyngeal carcinoma in China involve the HLA class I antigen recognition groove. Description: Tang, Minzhong, et al. The principal genetic determinants for nasopharyngeal carcinoma in China involve the HLA class I antigen recognition groove. ''PLoS Genet''. 2012; '''8''' (11):e1003103
Tracking the emergence of a new breed using 49,034 SNP in sheep. Description: Kijas, James W, et al. Tracking the emergence of a new breed using 49,034 SNP in sheep. ''PLoS One''. 2012; '''7''' (7):e41508
Unexpected relationships and inbreeding in HapMap phase III populations. Description: Stevens, Eric L, et al. Unexpected relationships and inbreeding in HapMap phase III populations. ''PLoS One''. 2012; '''7''' (11):e49575
Unraveling the regulatory mechanisms underlying tissue-dependent genetic variation of gene expression. Description: Fu, Jingyuan, et al. Unraveling the regulatory mechanisms underlying tissue-dependent genetic variation of gene expression. ''PLoS Genet''. 2012 Jan; '''8''' (1):e1002431
Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays. Description: Smith, Andrew J P, et al. Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays. ''PLoS Genet''. 2012; '''8''' (8):e1002908
Variation of BMP3 contributes to dog breed skull diversity. Description: Schoenebeck, Jeffrey J, et al. Variation of BMP3 contributes to dog breed skull diversity. ''PLoS Genet''. 2012; '''8''' (8):e1002849
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. Description: Chahrour, Maria H, et al. Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. ''PLoS Genet''. 2012; '''8''' (4):e1002635
Widespread site-dependent buffering of human regulatory polymorphism. Description: Maurano, Matthew T, et al. Widespread site-dependent buffering of human regulatory polymorphism. ''PLoS Genet''. 2012; '''8''' (3):e1002599
Further evidence for a male-selective genetic association of synapse-associated protein 97 (SAP97) gene with schizophrenia. Description: Uezato, Akihito, et al. Further evidence for a male-selective genetic association of synapse-associated protein 97 (SAP97) gene with schizophrenia. ''Behav Brain Funct''. 2012 Jan 6; '''8''': 2
Genome-wide association scan and phased haplotype construction for quantitative trait loci affecting boar taint in three pig breeds. Description: Gregersen, Vivi R, et al. Genome-wide association scan and phased haplotype construction for quantitative trait loci affecting boar taint in three pig breeds. ''BMC Genomics''. 2012 Jan 13; '''13''': 22
Genetic adaptation to high altitude in the Ethiopian highlands. Description: Scheinfeldt, Laura B, et al. Genetic adaptation to high altitude in the Ethiopian highlands. ''Genome Biol''. 2012 Jan 20; '''13''' (1):R1
TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data. Description: Londono, Douglas, et al. TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data. ''BMC Bioinformatics''. 2012 Jan 20; '''13''': 13
Implications for health and disease in the genetic signature of the Ashkenazi Jewish population. Description: Guha, Saurav, et al. Implications for health and disease in the genetic signature of the Ashkenazi Jewish population. ''Genome Biol''. 2012 Jan 25; '''13''' (1):R2
Combining evidence of selection with association analysis increases power to detect regions influencing complex traits in dairy cattle. Description: Schwarzenbacher, Hermann, et al. Combining evidence of selection with association analysis increases power to detect regions influencing complex traits in dairy cattle. ''BMC Genomics''. 2012 Jan 30; '''13''': 48
BDNF val66met affects hippocampal volume and emotion-related hippocampal memory activity. Description: Molendijk, M L, et al. BDNF val66met affects hippocampal volume and emotion-related hippocampal memory activity. ''Transl Psychiatry''. 2012 Jan 31; '''2''': e74
A genome-wide association study of gestational diabetes mellitus in Korean women. Description: Kwak, Soo Heon, et al. A genome-wide association study of gestational diabetes mellitus in Korean women. ''Diabetes''. 2012 Feb; '''61''' (2):531-41
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. Description: Williams, Nigel M, et al. Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. ''Am J Psychiatry''. 2012 Feb; '''169''' (2):195-204
Genome-wide analysis of the world's sheep breeds reveals high levels of historic mixture and strong recent selection. Description: Kijas, James W, et al. Genome-wide analysis of the world's sheep breeds reveals high levels of historic mixture and strong recent selection. ''PLoS Biol''. 2012 Feb; '''10''' (2):e1001258
Mixed effects modeling of proliferation rates in cell-based models: consequence for pharmacogenomics and cancer. Description: Im, Hae Kyung, et al. Mixed effects modeling of proliferation rates in cell-based models: consequence for pharmacogenomics and cancer. ''PLoS Genet''. 2012 Feb; '''8''' (2):e1002525
Modeling the functional genomics of autism using human neurons. Description: Konopka, G, et al. Modeling the functional genomics of autism using human neurons. ''Mol Psychiatry''. 2012 Feb; '''17''' (2):202-14
Psoriasis patients are enriched for genetic variants that protect against HIV-1 disease. Description: Chen, Haoyan, et al. Psoriasis patients are enriched for genetic variants that protect against HIV-1 disease. ''PLoS Genet''. 2012 Feb; '''8''' (2):e1002514
Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13. Description: Spain, Sarah L, et al. Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13. ''Hum Mol Genet''. 2012 Feb 15; '''21''' (4):934-46
Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes. Description: Lotta, Luca A, et al. Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes. ''BMC Med Genomics''. 2012 Feb 21; '''5''': 7
Characterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphisms. Description: Lu, James T, et al. Characterizing linkage disequilibrium and evaluating imputation power of human genomic insertion-deletion polymorphisms. ''Genome Biol''. 2012 Feb 29; '''13''' (2):R15
Amyloid pathway-based candidate gene analysis of [(11)C]PiB-PET in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort. Description: Swaminathan, Shanker, et al. Amyloid pathway-based candidate gene analysis of [(11)C]PiB-PET in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort. ''Brain Imaging Behav''. 2012 Mar; '''6''' (1):1-15
Common variants of IL6, LEPR, and PBEF1 are associated with obesity in Indian children. Description: Tabassum, Rubina, et al. Common variants of IL6, LEPR, and PBEF1 are associated with obesity in Indian children. ''Diabetes''. 2012 Mar; '''61''' (3):626-31
Genetic variants in interferon regulatory factor 2 (IRF2) are associated with atopic dermatitis and eczema herpeticum. Description: Gao, Pei-Song, et al. Genetic variants in interferon regulatory factor 2 (IRF2) are associated with atopic dermatitis and eczema herpeticum. ''J Invest Dermatol''. 2012 Mar; '''132''' (3 Pt 1):650-7
Replication of association of the PTPRC gene with response to anti-tumor necrosis factor therapy in a large UK cohort. Description: Plant, Darren, et al. Replication of association of the PTPRC gene with response to anti-tumor necrosis factor therapy in a large UK cohort. ''Arthritis Rheum''. 2012 Mar; '''64''' (3):665-70
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population. Description: Trotta, Luca, et al. SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population. ''Parkinsonism Relat Disord''. 2012 Mar; '''18''' (3):257-62
The same ELA class II risk factors confer equine insect bite hypersensitivity in two distinct populations. Description: Andersson, Lisa S, et al. The same ELA class II risk factors confer equine insect bite hypersensitivity in two distinct populations. ''Immunogenetics''. 2012 Mar; '''64''' (3):201-8
Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24. Description: Jones, Angela M, et al. Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24. ''J Med Genet''. 2012 Mar; '''49''' (3):158-63
TNFAIP3 gene polymorphisms are associated with response to TNF blockade in psoriasis. Description: Tejasvi, Trilokraj, et al. TNFAIP3 gene polymorphisms are associated with response to TNF blockade in psoriasis. ''J Invest Dermatol''. 2012 Mar; '''132''' (3 Pt 1):593-600
Polymorphisms in Toll-like receptor genes influence antibody responses to cytomegalovirus glycoprotein B vaccine. Description: Arav-Boger, Ravit, et al. Polymorphisms in Toll-like receptor genes influence antibody responses to cytomegalovirus glycoprotein B vaccine. ''BMC Res Notes''. 2012 Mar 13; '''5''': 140
TRIB1 constitutes a molecular link between regulation of sleep and lipid metabolism in humans. Description: Ollila, H M, et al. TRIB1 constitutes a molecular link between regulation of sleep and lipid metabolism in humans. ''Transl Psychiatry''. 2012 Mar 20; '''2''': e97
IFITM3 restricts the morbidity and mortality associated with influenza. Description: Everitt, Aaron R, et al. IFITM3 restricts the morbidity and mortality associated with influenza. ''Nature''. 2012 Mar 25; '''484''' (7395):519-23
A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases. Description: Li, Miao-Xin, et al. A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases. ''Nucleic Acids Res''. 2012 Apr; '''40''' (7):e53
Amino acid position 11 of HLA-DRbeta1 is a major determinant of chromosome 6p association with ulcerative colitis. Description: Achkar, J-P, et al. Amino acid position 11 of HLA-DRbeta1 is a major determinant of chromosome 6p association with ulcerative colitis. ''Genes Immun''. 2012 Apr; '''13''' (3):245-52
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Description: Casey, Jillian P, et al. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. ''Hum Genet''. 2012 Apr; '''131''' (4):565-79
Distribution of functional polymorphic variants of inflammation-related genes RANTES and CCR5 in long-lived individuals. Description: Laplana, Marina, et al. Distribution of functional polymorphic variants of inflammation-related genes RANTES and CCR5 in long-lived individuals. ''Cytokine''. 2012 Apr; '''58''' (1):10-3
Genome-wide meta-analysis of psoriatic arthritis identifies susceptibility locus at REL. Description: Ellinghaus, Eva, et al. Genome-wide meta-analysis of psoriatic arthritis identifies susceptibility locus at REL. ''J Invest Dermatol''. 2012 Apr; '''132''' (4):1133-40
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls. Description: Soemedi, Rachel, et al. Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls. ''Hum Mol Genet''. 2012 Apr 1; '''21''' (7):1513-20
Tau acts as an independent genetic risk factor in pathologically proven PD. Description: Charlesworth, Gavin, et al. Tau acts as an independent genetic risk factor in pathologically proven PD. ''Neurobiol Aging''. 2012 Apr; '''33''' (4):838.e7-11
UGT1A1 is a major locus influencing bilirubin levels in African Americans. Description: Chen, Guanjie, et al. UGT1A1 is a major locus influencing bilirubin levels in African Americans. ''Eur J Hum Genet''. 2012 Apr; '''20''' (4):463-8
Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci. Description: Ellinghaus, David, et al. Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci. ''Am J Hum Genet''. 2012 Apr 6; '''90''' (4):636-47
Linkage-disequilibrium-based binning affects the interpretation of GWASs. Description: Christoforou, Andrea, et al. Linkage-disequilibrium-based binning affects the interpretation of GWASs. ''Am J Hum Genet''. 2012 Apr 6; '''90''' (4):727-33
Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study. Description: Hammer, C, et al. Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study. ''Transl Psychiatry''. 2012 Apr 17; '''2''': e103
The renal urate transporter SLC17A1 locus: confirmation of association with gout. Description: Hollis-Moffatt, Jade E, et al. The renal urate transporter SLC17A1 locus: confirmation of association with gout. ''Arthritis Res Ther''. 2012 Apr 27; '''14''' (2):R92
A community-based study of nucleotide excision repair polymorphisms in relation to the risk of non-melanoma skin cancer. Description: Wheless, Lee, et al. A community-based study of nucleotide excision repair polymorphisms in relation to the risk of non-melanoma skin cancer. ''J Invest Dermatol''. 2012 May; '''132''' (5):1354-62
Evaluating the evidence for transmission distortion in human pedigrees. Description: Meyer, Wynn K, et al. Evaluating the evidence for transmission distortion in human pedigrees. ''Genetics''. 2012 May; '''191''' (1):215-32
Footprints of genetic susceptibility to pulmonary tuberculosis: cytokine gene variants in north Indians. Description: Bose, Mridula, et al. Footprints of genetic susceptibility to pulmonary tuberculosis: cytokine gene variants in north Indians. ''Indian J Med Res''. 2012 May; '''135''' (5):763-70
Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia. Description: Ellinghaus, E, et al. Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia. ''Leukemia''. 2012 May; '''26''' (5):902-9
Quantitative genetics in the genomics era. Description: Hill, William G. Quantitative genetics in the genomics era. ''Curr Genomics''. 2012 May; '''13''' (3):196-206
Ultrahigh-dimensional variable selection method for whole-genome gene-gene interaction analysis. Description: Ueki, Masao, et al. Ultrahigh-dimensional variable selection method for whole-genome gene-gene interaction analysis. ''BMC Bioinformatics''. 2012 May 3; '''13''': 72
Association between SNPs and gene expression in multiple regions of the human brain. Description: Kim, S, et al. Association between SNPs and gene expression in multiple regions of the human brain. ''Transl Psychiatry''. 2012 May 8; '''2''': e113
Complexity of a complex trait locus: HP, HPR, haemoglobin and cholesterol. Description: Guthrie, Philip A I, et al. Complexity of a complex trait locus: HP, HPR, haemoglobin and cholesterol. ''Gene''. 2012 May 10; '''499''' (1):8-13
SparSNP: fast and memory-efficient analysis of all SNPs for phenotype prediction. Description: Abraham, Gad, et al. SparSNP: fast and memory-efficient analysis of all SNPs for phenotype prediction. ''BMC Bioinformatics''. 2012 May 10; '''13''': 88
Genome-wide association study of Alzheimer's disease. Description: Kamboh, M I, et al. Genome-wide association study of Alzheimer's disease. ''Transl Psychiatry''. 2012 May 15; '''2''': e117
Variation in regulator of G-protein signaling 17 gene (RGS17) is associated with multiple substance dependence diagnoses. Description: Zhang, Huiping, et al. Variation in regulator of G-protein signaling 17 gene (RGS17) is associated with multiple substance dependence diagnoses. ''Behav Brain Funct''. 2012 May 16; '''8''': 23
The MAP2K5-linked SNP rs2241423 is associated with BMI and obesity in two cohorts of Swedish and Greek children. Description: Rask-Andersen, Mathias, et al. The MAP2K5-linked SNP rs2241423 is associated with BMI and obesity in two cohorts of Swedish and Greek children. ''BMC Med Genet''. 2012 May 17; '''13''': 36
Genome-wide linkage analysis of QTL for growth and body composition employing the PorcineSNP60 BeadChip. Description: Fernandez, Ana I, et al. Genome-wide linkage analysis of QTL for growth and body composition employing the PorcineSNP60 BeadChip. ''BMC Genet''. 2012 May 20; '''13''': 41
Discovery of regulatory elements in human ATP-binding cassette transporters through expression quantitative trait mapping. Description: Matsson, P, et al. Discovery of regulatory elements in human ATP-binding cassette transporters through expression quantitative trait mapping. ''Pharmacogenomics J''. 2012 Jun; '''12''' (3):214-26
Effect of genetic predisposition on blood lipid traits using cumulative risk assessment in the korean population. Description: Go, Min Jin, et al. Effect of genetic predisposition on blood lipid traits using cumulative risk assessment in the korean population. ''Genomics Inform''. 2012 Jun; '''10''' (2):99-105
Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation. Description: Dumitriu, Alexandra, et al. Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation. ''PLoS Genet''. 2012 Jun; '''8''' (6):e1002794
Genetic mapping of habitual substance use, obesity-related traits, responses to mental and physical stress, and heart rate and blood pressure measurements reveals shared genes that are overrepresented in the neural synapse. Description: Nikpay, Majid, et al. Genetic mapping of habitual substance use, obesity-related traits, responses to mental and physical stress, and heart rate and blood pressure measurements reveals shared genes that are overrepresented in the neural synapse. ''Hypertens Res''. 2012 Jun; '''35''' (6):585-91
Interaction Effects of Lipoprotein Lipase Polymorphisms with Lifestyle on Lipid Levels in a Korean Population: A Cross-sectional Study. Description: Pyun, Jung-A, et al. Interaction Effects of Lipoprotein Lipase Polymorphisms with Lifestyle on Lipid Levels in a Korean Population: A Cross-sectional Study. ''Genomics Inform''. 2012 Jun; '''10''' (2):88-98
Prediction of susceptibility to major depression by a model of interactions of multiple functional genetic variants and environmental factors. Description: Wong, M-L, et al. Prediction of susceptibility to major depression by a model of interactions of multiple functional genetic variants and environmental factors. ''Mol Psychiatry''. 2012 Jun; '''17''' (6):624-33
P-selectin genotype is associated with the development of cancer cachexia. Description: Tan, Benjamin H L, et al. P-selectin genotype is associated with the development of cancer cachexia. ''EMBO Mol Med''. 2012 Jun; '''4''' (6):462-71
Replication of the Association of the 6q22.31c Locus near GJA1 with Pulse Rate in the Korean Population. Description: Kim, Nam Hee, et al. Replication of the Association of the 6q22.31c Locus near GJA1 with Pulse Rate in the Korean Population. ''Genomics Inform''. 2012 Jun; '''10''' (2):106-9
Scan-statistic approach identifies clusters of rare disease variants in LRP2, a gene linked and associated with autism spectrum disorders, in three datasets. Description: Ionita-Laza, Iuliana, et al. Scan-statistic approach identifies clusters of rare disease variants in LRP2, a gene linked and associated with autism spectrum disorders, in three datasets. ''Am J Hum Genet''. 2012 Jun 8; '''90''' (6):1002-13
A defect in dystrophin causes a novel porcine stress syndrome. Description: Nonneman, Dan J, et al. A defect in dystrophin causes a novel porcine stress syndrome. ''BMC Genomics''. 2012 Jun 12; '''13''': 233
Leveraging input and output structures for joint mapping of epistatic and marginal eQTLs. Description: Lee, Seunghak, et al. Leveraging input and output structures for joint mapping of epistatic and marginal eQTLs. ''Bioinformatics''. 2012 Jun 15; '''28''' (12):i137-46
No association for Chinese HBV-related hepatocellular carcinoma susceptibility SNP in other East Asian populations. Description: Sawai, Hiromi, et al. No association for Chinese HBV-related hepatocellular carcinoma susceptibility SNP in other East Asian populations. ''BMC Med Genet''. 2012 Jun 19; '''13''': 47
Inferring genome-wide patterns of admixture in Qataris using fifty-five ancestral populations. Description: Omberg, Larsson, et al. Inferring genome-wide patterns of admixture in Qataris using fifty-five ancestral populations. ''BMC Genet''. 2012 Jun 26; '''13''': 49
Genetic variation in glutathione S-transferase omega-1, arsenic methyltransferase and methylene-tetrahydrofolate reductase, arsenic exposure and bladder cancer: a case-control study. Description: Beebe-Dimmer, Jennifer L, et al. Genetic variation in glutathione S-transferase omega-1, arsenic methyltransferase and methylene-tetrahydrofolate reductase, arsenic exposure and bladder cancer: a case-control study. ''Environ Health''. 2012 Jun 29; '''11''': 43
Genome-wide association analysis in asthma subjects identifies SPATS2L as a novel bronchodilator response gene. Description: Himes, Blanca E, et al. Genome-wide association analysis in asthma subjects identifies SPATS2L as a novel bronchodilator response gene. ''PLoS Genet''. 2012 Jul; '''8''' (7):e1002824
Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms. Description: Badner, J A, et al. Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms. ''Mol Psychiatry''. 2012 Jul; '''17''' (8):818-26
Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain. Description: Hernandez, Dena G, et al. Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain. ''Neurobiol Dis''. 2012 Jul; '''47''' (1):20-8
Protective effect of human endogenous retrovirus K dUTPase variants on psoriasis susceptibility. Description: Lai, Olivia Y, et al. Protective effect of human endogenous retrovirus K dUTPase variants on psoriasis susceptibility. ''J Invest Dermatol''. 2012 Jul; '''132''' (7):1833-40
Reprioritizing genetic associations in hit regions using LASSO-based resample model averaging. Description: Valdar, William, et al. Reprioritizing genetic associations in hit regions using LASSO-based resample model averaging. ''Genet Epidemiol''. 2012 Jul; '''36''' (5):451-62
*Genome-wide pharmacogenomic study of citalopram-induced side effects in STARD.** Description: Adkins, D E, et al. Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D. ''Transl Psychiatry''. 2012 Jul 3; '''2''': e129
A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval. Description: Kim, Jong Wook, et al. A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval. ''Am J Hum Genet''. 2012 Jul 13; '''91''' (1):180-4
Ethiopian genetic diversity reveals linguistic stratification and complex influences on the Ethiopian gene pool. Description: Pagani, Luca, et al. Ethiopian genetic diversity reveals linguistic stratification and complex influences on the Ethiopian gene pool. ''Am J Hum Genet''. 2012 Jul 13; '''91''' (1):83-96
Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease. Description: Tang, Weihong, et al. Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease. ''Am J Hum Genet''. 2012 Jul 13; '''91''' (1):152-62
Multifaceted genomic risk for brain function in schizophrenia. Description: Chen, Jiayu, et al. Multifaceted genomic risk for brain function in schizophrenia. ''Neuroimage''. 2012 Jul 16; '''61''' (4):866-75
Glucocorticoid receptor mRNA and protein isoform alterations in the orbitofrontal cortex in schizophrenia and bipolar disorder. Description: Sinclair, Duncan, et al. Glucocorticoid receptor mRNA and protein isoform alterations in the orbitofrontal cortex in schizophrenia and bipolar disorder. ''BMC Psychiatry''. 2012 Jul 20; '''12''': 84
Association study of genes associated to asthma in a specific environment, in an asthma familial collection located in a rural area influenced by different industries. Description: Morin, Andreanne, et al. Association study of genes associated to asthma in a specific environment, in an asthma familial collection located in a rural area influenced by different industries. ''Int J Environ Res Public Health''. 2012 Aug; '''9''' (8):2620-35
Association testing of previously reported variants in a large case-control meta-analysis of diabetic nephropathy. Description: Williams, Winfred W, et al. Association testing of previously reported variants in a large case-control meta-analysis of diabetic nephropathy. ''Diabetes''. 2012 Aug; '''61''' (8):2187-94
Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus. Description: Hamilton, Gillian, et al. Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus. ''Neurobiol Aging''. 2012 Aug; '''33''' (8):1848.e1-13
High-throughput analysis of epistasis in genome-wide association studies with BiForce. Description: Gyenesei, Attila, et al. High-throughput analysis of epistasis in genome-wide association studies with BiForce. ''Bioinformatics''. 2012 Aug 1; '''28''' (15):1957-64
Runs of homozygosity and population history in cattle. Description: Purfield, Deirdre C, et al. Runs of homozygosity and population history in cattle. ''BMC Genet''. 2012 Aug 14; '''13''': 70
Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction. Description: Ayalew, M, et al. Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction. ''Mol Psychiatry''. 2012 Sep; '''17''' (9):887-905
Functional variants in NFKBIE and RTKN2 involved in activation of the NF-kappaB pathway are associated with rheumatoid arthritis in Japanese. Description: Myouzen, Keiko, et al. Functional variants in NFKBIE and RTKN2 involved in activation of the NF-kappaB pathway are associated with rheumatoid arthritis in Japanese. ''PLoS Genet''. 2012 Sep; '''8''' (9):e1002949
Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. Description: Yang, Xiaobo, et al. Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. ''PLoS Genet''. 2012 Sep; '''8''' (9):e1002916
New susceptibility loci associated with kidney disease in type 1 diabetes. Description: Sandholm, Niina, et al. New susceptibility loci associated with kidney disease in type 1 diabetes. ''PLoS Genet''. 2012 Sep; '''8''' (9):e1002921
Polymorphisms in AKR1C4 and HSD3B2 and differences in serum DHEAS and progesterone are associated with paranoid ideation during mania or hypomania in bipolar disorder. Description: Johansson, Anette G M, et al. Polymorphisms in AKR1C4 and HSD3B2 and differences in serum DHEAS and progesterone are associated with paranoid ideation during mania or hypomania in bipolar disorder. ''Eur Neuropsychopharmacol''. 2012 Sep; '''22''' (9):632-40
Prediction of Colorectal Cancer Risk Using a Genetic Risk Score: The Korean Cancer Prevention Study-II (KCPS-II). Description: Jo, Jaeseong, et al. Prediction of Colorectal Cancer Risk Using a Genetic Risk Score: The Korean Cancer Prevention Study-II (KCPS-II). ''Genomics Inform''. 2012 Sep; '''10''' (3):175-83
Rare copy number variants contribute to congenital left-sided heart disease. Description: Hitz, Marc-Phillip, et al. Rare copy number variants contribute to congenital left-sided heart disease. ''PLoS Genet''. 2012 Sep; '''8''' (9):e1002903
Variation in genes related to cochlear biology is strongly associated with adult-onset deafness in border collies. Description: Yokoyama, Jennifer S, et al. Variation in genes related to cochlear biology is strongly associated with adult-onset deafness in border collies. ''PLoS Genet''. 2012 Sep; '''8''' (9):e1002898
Replication and meta-analysis of TMEM132D gene variants in panic disorder. Description: Erhardt, A, et al. Replication and meta-analysis of TMEM132D gene variants in panic disorder. ''Transl Psychiatry''. 2012 Sep 4; '''2''': e156
UMOD as a susceptibility gene for end-stage renal disease. Description: Reznichenko, Anna, et al. UMOD as a susceptibility gene for end-stage renal disease. ''BMC Med Genet''. 2012 Sep 5; '''13''': 78
Association between the ABO locus and hematological traits in Korean. Description: Hong, Kyung-Won, et al. Association between the ABO locus and hematological traits in Korean. ''BMC Genet''. 2012 Sep 10; '''13''': 78
Custom genotyping for substance addiction susceptibility genes in Jordanians of Arab descent. Description: Al-Eitan, Laith N, et al. Custom genotyping for substance addiction susceptibility genes in Jordanians of Arab descent. ''BMC Res Notes''. 2012 Sep 10; '''5''': 497
The non-synonymous SNP, R1150W, in SCN9A is not associated with chronic widespread pain susceptibility. Description: Holliday, Kate L, et al. The non-synonymous SNP, R1150W, in SCN9A is not associated with chronic widespread pain susceptibility. ''Mol Pain''. 2012 Sep 24; '''8''': 72
Fine-mapping in African-American women confirms the importance of the 10p12 locus to sarcoidosis. Description: Cozier, Y C, et al. Fine-mapping in African-American women confirms the importance of the 10p12 locus to sarcoidosis. ''Genes Immun''. 2012 Oct; '''13''' (7):573-8
Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia. Description: Lips, E S, et al. Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia. ''Mol Psychiatry''. 2012 Oct; '''17''' (10):996-1006
Polymorphisms in the myeloperoxidase gene locus are associated with acute kidney injury-related outcomes. Description: Perianayagam, Mary C, et al. Polymorphisms in the myeloperoxidase gene locus are associated with acute kidney injury-related outcomes. ''Kidney Int''. 2012 Oct; '''82''' (8):909-19
A genome-wide association study using international breeding-evaluation data identifies major loci affecting production traits and stature in the Brown Swiss cattle breed. Description: Guo, Jiazhong, et al. A genome-wide association study using international breeding-evaluation data identifies major loci affecting production traits and stature in the Brown Swiss cattle breed. ''BMC Genet''. 2012 Oct 2; '''13''': 82
Genetic association of cyclic AMP signaling genes with bipolar disorder. Description: McDonald, M L, et al. Genetic association of cyclic AMP signaling genes with bipolar disorder. ''Transl Psychiatry''. 2012 Oct 2; '''2''': e169
Lack of association between four SNPs in the SLC22A3-LPAL2-LPA gene cluster and coronary artery disease in a Chinese Han population: a case control study. Description: Lv, Xiaofei, et al. Lack of association between four SNPs in the SLC22A3-LPAL2-LPA gene cluster and coronary artery disease in a Chinese Han population: a case control study. ''Lipids Health Dis''. 2012 Oct 4; '''11''': 128
Fine mapping of complex traits in non-model species: using next generation sequencing and advanced intercross lines in Japanese quail. Description: Fresard, Laure, et al. Fine mapping of complex traits in non-model species: using next generation sequencing and advanced intercross lines in Japanese quail. ''BMC Genomics''. 2012 Oct 15; '''13''': 551
Convergent animal and human evidence suggests the activin/inhibin pathway to be involved in antidepressant response. Description: Ganea, K, et al. Convergent animal and human evidence suggests the activin/inhibin pathway to be involved in antidepressant response. ''Transl Psychiatry''. 2012 Oct 23; '''2''': e177
Genome-wide association of mood-incongruent psychotic bipolar disorder. Description: Goes, F S, et al. Genome-wide association of mood-incongruent psychotic bipolar disorder. ''Transl Psychiatry''. 2012 Oct 23; '''2''': e180
Association study of nicotinic acetylcholine receptor genes identifies a novel lung cancer susceptibility locus near CHRNA1 in African-Americans. Description: Walsh, Kyle M, et al. Association study of nicotinic acetylcholine receptor genes identifies a novel lung cancer susceptibility locus near CHRNA1 in African-Americans. ''Oncotarget''. 2012 Nov; '''3''' (11):1428-38
Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM. Description: Amin, N, et al. Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM. ''Mol Psychiatry''. 2012 Nov; '''17''' (11):1116-29
Genome-wide meta-analysis of common variant differences between men and women. Description: Boraska, Vesna, et al. Genome-wide meta-analysis of common variant differences between men and women. ''Hum Mol Genet''. 2012 Nov 1; '''21''' (21):4805-15
Individual common variants exert weak effects on the risk for autism spectrum disorders. Description: Anney, Richard, et al. Individual common variants exert weak effects on the risk for autism spectrum disorders. ''Hum Mol Genet''. 2012 Nov 1; '''21''' (21):4781-92
A novel analytical method, Birth Date Selection Mapping, detects response of the Angus (Bos taurus) genome to selection on complex traits. Description: Decker, Jared E, et al. A novel analytical method, Birth Date Selection Mapping, detects response of the Angus (Bos taurus) genome to selection on complex traits. ''BMC Genomics''. 2012 Nov 9; '''13''': 606
From expression pattern to genetic association in asthma and asthma-related phenotypes. Description: Vaillancourt, Vanessa T, et al. From expression pattern to genetic association in asthma and asthma-related phenotypes. ''BMC Res Notes''. 2012 Nov 13; '''5''': 630
Meta-analysis of genome-wide association studies for panic disorder in the Japanese population. Description: Otowa, T, et al. Meta-analysis of genome-wide association studies for panic disorder in the Japanese population. ''Transl Psychiatry''. 2012 Nov 13; '''2''': e186
Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls. Description: Timofeeva, Maria N, et al. Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls. ''Hum Mol Genet''. 2012 Nov 15; '''21''' (22):4980-95
Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects. Description: van Eijk, Kristel R, et al. Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects. ''BMC Genomics''. 2012 Nov 17; '''13''': 636
Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans. Description: Brambilla, Paola, et al. Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans. ''Neurosci Lett''. 2012 Nov 21; '''530''' (2):155-60
A discovery resource of rare copy number variations in individuals with autism spectrum disorder. Description: Prasad, Aparna, et al. A discovery resource of rare copy number variations in individuals with autism spectrum disorder. ''G3 (Bethesda)''. 2012 Dec; '''2''' (12):1665-85
Association analysis of reactive oxygen species-hypertension genes discovered by literature mining. Description: Lim, Ji Eun, et al. Association analysis of reactive oxygen species-hypertension genes discovered by literature mining. ''Genomics Inform''. 2012 Dec; '''10''' (4):244-8
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Description: Eyre, Steve, et al. High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. ''Nat Genet''. 2012 Dec; '''44''' (12):1336-40
Network graph analysis of gene-gene interactions in genome-wide association study data. Description: Lee, Sungyoung, et al. Network graph analysis of gene-gene interactions in genome-wide association study data. ''Genomics Inform''. 2012 Dec; '''10''' (4):256-62
No evidence for genetic association with the let-7 microRNA-binding site or other common KRAS variants in risk of endometriosis. Description: Luong, Hien T T, et al. No evidence for genetic association with the let-7 microRNA-binding site or other common KRAS variants in risk of endometriosis. ''Hum Reprod''. 2012 Dec; '''27''' (12):3616-21
Population stratification may bias analysis of PGC-1alpha as a modifier of age at Huntington disease motor onset. Description: Ramos, Eliana Marisa, et al. Population stratification may bias analysis of PGC-1alpha as a modifier of age at Huntington disease motor onset. ''Hum Genet''. 2012 Dec; '''131''' (12):1833-40
Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans. Description: Mangino, Massimo, et al. Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans. ''Hum Mol Genet''. 2012 Dec 15; '''21''' (24):5385-94
Genome-wide association scan of dental caries in the permanent dentition. Description: Wang, Xiaojing, et al. Genome-wide association scan of dental caries in the permanent dentition. ''BMC Oral Health''. 2012 Dec 21; '''12''': 57
Four new loci associations discovered by pathway-based and network analyses of the genome-wide variability profile of Hirschsprung's disease. Description: Fernandez, Raquel Ma, et al. Four new loci associations discovered by pathway-based and network analyses of the genome-wide variability profile of Hirschsprung's disease. ''Orphanet J Rare Dis''. 2012 Dec 28; '''7''': 103
1,25-dihydroxyvitamin D and the vitamin D receptor gene polymorphism Apa1 influence bone mineral density in primary hyperparathyroidism. Description: Christensen, Monika H E, et al. 1,25-dihydroxyvitamin D and the vitamin D receptor gene polymorphism Apa1 influence bone mineral density in primary hyperparathyroidism. ''PLoS One''. 2013; '''8''' (2):e56019
Accumulating mutations in series of haplotypes at the KIT and MITF loci are major determinants of white markings in Franches-Montagnes horses. Description: Haase, Bianca, et al. Accumulating mutations in series of haplotypes at the KIT and MITF loci are major determinants of white markings in Franches-Montagnes horses. ''PLoS One''. 2013; '''8''' (9):e75071
A CNGB1 frameshift mutation in Papillon and Phalene dogs with progressive retinal atrophy. Description: Ahonen, Saija J, et al. A CNGB1 frameshift mutation in Papillon and Phalene dogs with progressive retinal atrophy. ''PLoS One''. 2013; '''8''' (8):e72122
A COL11A2 mutation in Labrador retrievers with mild disproportionate dwarfism. Description: Frischknecht, Mirjam, et al. A COL11A2 mutation in Labrador retrievers with mild disproportionate dwarfism. ''PLoS One''. 2013; '''8''' (3):e60149
A common functional promoter variant links CNR1 gene expression to HDL cholesterol level. Description: Feng, Q, et al. A common functional promoter variant links CNR1 gene expression to HDL cholesterol level. ''Nat Commun''. 2013; '''4''': 1973
Adaptation of maize to temperate climates: mid-density genome-wide association genetics and diversity patterns reveal key genomic regions, with a major contribution of the Vgt2 (ZCN8) locus. Description: Bouchet, Sophie, et al. Adaptation of maize to temperate climates: mid-density genome-wide association genetics and diversity patterns reveal key genomic regions, with a major contribution of the Vgt2 (ZCN8) locus. ''PLoS One''. 2013; '''8''' (8):e71377
A discovery study of daunorubicin induced cardiotoxicity in a sample of acute myeloid leukemia patients prioritizes P450 oxidoreductase polymorphisms as a potential risk factor. Description: Lubieniecka, Joanna M, et al. A discovery study of daunorubicin induced cardiotoxicity in a sample of acute myeloid leukemia patients prioritizes P450 oxidoreductase polymorphisms as a potential risk factor. ''Front Genet''. 2013; '''4''': 231
Admixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody production. Description: Molineros, Julio E, et al. Admixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody production. ''PLoS Genet''. 2013; '''9''' (2):e1003222
A frameshift mutation in the cubilin gene (CUBN) in Border Collies with Imerslund-Grasbeck syndrome (selective cobalamin malabsorption). Description: Owczarek-Lipska, Marta, et al. A frameshift mutation in the cubilin gene (CUBN) in Border Collies with Imerslund-Grasbeck syndrome (selective cobalamin malabsorption). ''PLoS One''. 2013; '''8''' (4):e61144
A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder. Description: Fernandes, Carla P D, et al. A genetic deconstruction of neurocognitive traits in schizophrenia and bipolar disorder. ''PLoS One''. 2013; '''8''' (12):e81052
A genome-wide analysis of populations from European Russia reveals a new pole of genetic diversity in northern Europe. Description: Khrunin, Andrey V, et al. A genome-wide analysis of populations from European Russia reveals a new pole of genetic diversity in northern Europe. ''PLoS One''. 2013; '''8''' (3):e58552
A genome-wide association study for somatic cell score using the Illumina high-density bovine beadchip identifies several novel QTL potentially related to mastitis susceptibility. Description: Meredith, Brian K, et al. A genome-wide association study for somatic cell score using the Illumina high-density bovine beadchip identifies several novel QTL potentially related to mastitis susceptibility. ''Front Genet''. 2013; '''4''': 229
A genome wide association study identifies common variants associated with lipid levels in the Chinese population. Description: Zhou, Li, et al. A genome wide association study identifies common variants associated with lipid levels in the Chinese population. ''PLoS One''. 2013; '''8''' (12):e82420
A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans. Description: Li, Huaixing, et al. A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans. ''Diabetes''. 2013 Jan; '''62''' (1):291-8
A genome-wide association study identifies risk loci to equine recurrent uveitis in German warmblood horses. Description: Kulbrock, Maike, et al. A genome-wide association study identifies risk loci to equine recurrent uveitis in German warmblood horses. ''PLoS One''. 2013; '''8''' (8):e71619
A genome-wide association study points out the causal implication of SOX9 in the sex-reversal phenotype in XX pigs. Description: Rousseau, Sarah, et al. A genome-wide association study points out the causal implication of SOX9 in the sex-reversal phenotype in XX pigs. ''PLoS One''. 2013; '''8''' (11):e79882
A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype. Description: Hass, Johanna, et al. A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype. ''PLoS One''. 2013; '''8''' (6):e64872
A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation. Description: Bendjilali, Nasrine, et al. A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation. ''PLoS One''. 2013; '''8''' (10):e71434
A genome-wide survey of transgenerational genetic effects in autism. Description: Tsang, Kathryn M, et al. A genome-wide survey of transgenerational genetic effects in autism. ''PLoS One''. 2013; '''8''' (10):e76978
Alzheimer's disease: analyzing the missing heritability. Description: Ridge, Perry G, et al. Alzheimer's disease: analyzing the missing heritability. ''PLoS One''. 2013; '''8''' (11):e79771
AMD-associated genes encoding stress-activated MAPK pathway constituents are identified by interval-based enrichment analysis. Description: SanGiovanni, John Paul, et al. AMD-associated genes encoding stress-activated MAPK pathway constituents are identified by interval-based enrichment analysis. ''PLoS One''. 2013; '''8''' (8):e71239
A mutation in the SUV39H2 gene in Labrador Retrievers with hereditary nasal parakeratosis (HNPK) provides insights into the epigenetics of keratinocyte differentiation. Description: Jagannathan, Vidhya, et al. A mutation in the SUV39H2 gene in Labrador Retrievers with hereditary nasal parakeratosis (HNPK) provides insights into the epigenetics of keratinocyte differentiation. ''PLoS Genet''. 2013; '''9''' (10):e1003848
An empirical workflow for genome-wide single nucleotide polymorphism-based predictive modeling. Description: Floudas, Charalampos S, et al. An empirical workflow for genome-wide single nucleotide polymorphism-based predictive modeling. ''AMIA Jt Summits Transl Sci Proc''. 2013; '''2013''': 53-7
A next-generation sequencing method for genotyping-by-sequencing of highly heterozygous autotetraploid potato. Description: Uitdewilligen, Jan G A M L, et al. A next-generation sequencing method for genotyping-by-sequencing of highly heterozygous autotetraploid potato. ''PLoS One''. 2013; '''8''' (5):e62355
An in-depth characterization of the major psoriasis susceptibility locus identifies candidate susceptibility alleles within an HLA-C enhancer element. Description: Clop, Alex, et al. An in-depth characterization of the major psoriasis susceptibility locus identifies candidate susceptibility alleles within an HLA-C enhancer element. ''PLoS One''. 2013; '''8''' (8):e71690
A panel of ancestry informative markers for the complex five-way admixed South African coloured population. Description: Daya, Michelle, et al. A panel of ancestry informative markers for the complex five-way admixed South African coloured population. ''PLoS One''. 2013; '''8''' (12):e82224
A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease. Description: Ostensson, Malin, et al. A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease. ''PLoS One''. 2013; '''8''' (8):e70174
Apparent variation in Neanderthal admixture among African populations is consistent with gene flow from Non-African populations. Description: Wang, Shuoguo, et al. Apparent variation in Neanderthal admixture among African populations is consistent with gene flow from Non-African populations. ''Genome Biol Evol''. 2013; '''5''' (11):2075-81
A refined study of FCRL genes from a genome-wide association study for Graves' disease. Description: Zhao, Shuang-Xia, et al. A refined study of FCRL genes from a genome-wide association study for Graves' disease. ''PLoS One''. 2013; '''8''' (3):e57758
ARLTS1 and prostate cancer risk--analysis of expression and regulation. Description: Siltanen, Sanna, et al. ARLTS1 and prostate cancer risk--analysis of expression and regulation. ''PLoS One''. 2013; '''8''' (8):e72040
A SNP profiling panel for sample tracking in whole-exome sequencing studies. Description: Pengelly, Reuben J, et al. A SNP profiling panel for sample tracking in whole-exome sequencing studies. ''Genome Med''. 2013; '''5''' (9):89
A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats. Description: Gandolfi, Barbara, et al. A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats. ''Sci Rep''. 2013; '''3''': 2000
Association analysis of genetic variants in the myosin IXB gene in acute pancreatitis. Description: Nijmeijer, Rian M, et al. Association analysis of genetic variants in the myosin IXB gene in acute pancreatitis. ''PLoS One''. 2013; '''8''' (12):e85870
Association analysis of the SLC22A11 (organic anion transporter 4) and SLC22A12 (urate transporter 1) urate transporter locus with gout in New Zealand case-control sample sets reveals multiple ancestral-specific effects. Description: Flynn, Tanya J, et al. Association analysis of the SLC22A11 (organic anion transporter 4) and SLC22A12 (urate transporter 1) urate transporter locus with gout in New Zealand case-control sample sets reveals multiple ancestral-specific effects. ''Arthritis Res Ther''. 2013; '''15''' (6):R220
Association between a multi-locus genetic risk score and inflammatory bowel disease. Description: Hu, Pingzhao, et al. Association between a multi-locus genetic risk score and inflammatory bowel disease. ''Bioinform Biol Insights''. 2013; '''7''': 143-52
Association between IL28B polymorphisms and spontaneous clearance of hepatitis B virus infection. Description: Kim, Seung Up, et al. Association between IL28B polymorphisms and spontaneous clearance of hepatitis B virus infection. ''PLoS One''. 2013; '''8''' (7):e69166
Association between the SPRY1 gene polymorphism and obesity-related traits and osteoporosis in Korean women. Description: Jin, Hyun-Seok, et al. Association between the SPRY1 gene polymorphism and obesity-related traits and osteoporosis in Korean women. ''Mol Genet Metab''. 2013 Jan; '''108''' (1):95-101
Association of a common variant at 10q26 and benign prostatic hyperplasia aggressiveness in han chinese descent. Description: Gu, Xin, et al. Association of a common variant at 10q26 and benign prostatic hyperplasia aggressiveness in han chinese descent. ''Biochem Res Int''. 2013; '''2013''': 820849
Association of CD247 polymorphisms with rheumatoid arthritis: a replication study and a meta-analysis. Description: Teruel, Maria, et al. Association of CD247 polymorphisms with rheumatoid arthritis: a replication study and a meta-analysis. ''PLoS One''. 2013; '''8''' (7):e68295
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients. Description: Leone, Maurizio A, et al. Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients. ''PLoS One''. 2013; '''8''' (6):e64408
Association of STAT4 polymorphism with severe renal insufficiency in lupus nephritis. Description: Bolin, Karin, et al. Association of STAT4 polymorphism with severe renal insufficiency in lupus nephritis. ''PLoS One''. 2013; '''8''' (12):e84450
Association of the del443ins54 at the ARMS2 locus in Indian and Australian cohorts with age-related macular degeneration. Description: Kaur, Inderjeet, et al. Association of the del443ins54 at the ARMS2 locus in Indian and Australian cohorts with age-related macular degeneration. ''Mol Vis''. 2013; '''19''': 822-8
Association of two variants in SMAD7 with the risk of congenital heart disease in the Han Chinese population. Description: Wang, Erli, et al. Association of two variants in SMAD7 with the risk of congenital heart disease in the Han Chinese population. ''PLoS One''. 2013; '''8''' (9):e72423
Association signals unveiled by a comprehensive gene set enrichment analysis of dental caries genome-wide association studies. Description: Wang, Quan, et al. Association signals unveiled by a comprehensive gene set enrichment analysis of dental caries genome-wide association studies. ''PLoS One''. 2013; '''8''' (8):e72653
Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language. Description: Eicher, John D, et al. Associations of prenatal nicotine exposure and the dopamine related genes ANKK1 and DRD2 to verbal language. ''PLoS One''. 2013; '''8''' (5):e63762
Association study confirmed susceptibility loci with keloid in the Chinese Han population. Description: Zhu, Fei, et al. Association study confirmed susceptibility loci with keloid in the Chinese Han population. ''PLoS One''. 2013; '''8''' (5):e62377
Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis. Description: Zhao, Zhongming, et al. Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis. ''PLoS One''. 2013; '''8''' (7):e67776
Association study of 25 type 2 diabetes related Loci with measures of obesity in Indian sib pairs. Description: Gupta, Vipin, et al. Association study of 25 type 2 diabetes related Loci with measures of obesity in Indian sib pairs. ''PLoS One''. 2013; '''8''' (1):e53944
Association study of common genetic variants and HIV-1 acquisition in 6,300 infected cases and 7,200 controls. Description: McLaren, Paul J, et al. Association study of common genetic variants and HIV-1 acquisition in 6,300 infected cases and 7,200 controls. ''PLoS Pathog''. 2013; '''9''' (7):e1003515
Association study of fibroblast growth factor 10 (FGF10) polymorphisms with susceptibility to extreme myopia in a Japanese population. Description: Yoshida, Masao, et al. Association study of fibroblast growth factor 10 (FGF10) polymorphisms with susceptibility to extreme myopia in a Japanese population. ''Mol Vis''. 2013; '''19''': 2321-9
A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study. Description: Peters, Ulrike, et al. A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study. ''PLoS Genet''. 2013; '''9''' (1):e1003171
Atenolol induced HDL-C change in the pharmacogenomic evaluation of antihypertensive responses (PEAR) study. Description: McDonough, Caitrin W, et al. Atenolol induced HDL-C change in the pharmacogenomic evaluation of antihypertensive responses (PEAR) study. ''PLoS One''. 2013; '''8''' (10):e76984
Autozygome sequencing expands the horizon of human knockout research and provides novel insights into human phenotypic variation. Description: Alsalem, Ahmed B, et al. Autozygome sequencing expands the horizon of human knockout research and provides novel insights into human phenotypic variation. ''PLoS Genet''. 2013; '''9''' (12):e1004030
Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium. Description: Grove, Megan L, et al. Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium. ''PLoS One''. 2013; '''8''' (7):e68095
Bivariate genome-wide association analyses identified genes with pleiotropic effects for femoral neck bone geometry and age at menarche. Description: Ran, Shu, et al. Bivariate genome-wide association analyses identified genes with pleiotropic effects for femoral neck bone geometry and age at menarche. ''PLoS One''. 2013; '''8''' (4):e60362
Bivariate genome-wide association analysis of the growth and intake components of feed efficiency. Description: Serao, Nick V L, et al. Bivariate genome-wide association analysis of the growth and intake components of feed efficiency. ''PLoS One''. 2013; '''8''' (10):e78530
CACNA1C risk variant and amygdala activity in bipolar disorder, schizophrenia and healthy controls. Description: Tesli, Martin, et al. CACNA1C risk variant and amygdala activity in bipolar disorder, schizophrenia and healthy controls. ''PLoS One''. 2013; '''8''' (2):e56970
Canine chondrodysplasia caused by a truncating mutation in collagen-binding integrin alpha subunit 10. Description: Kyostila, Kaisa, et al. Canine chondrodysplasia caused by a truncating mutation in collagen-binding integrin alpha subunit 10. ''PLoS One''. 2013; '''8''' (9):e75621
cgaTOH: extended approach for identifying tracts of homozygosity. Description: Zhang, Li, et al. cgaTOH: extended approach for identifying tracts of homozygosity. ''PLoS One''. 2013; '''8''' (3):e57772
Cis-regulatory variants affect CHRNA5 mRNA expression in populations of African and European ancestry. Description: Wang, Jen-Chyong, et al. Cis-regulatory variants affect CHRNA5 mRNA expression in populations of African and European ancestry. ''PLoS One''. 2013; '''8''' (11):e80204
Cognitive manic symptoms in bipolar disorder associated with polymorphisms in the DAOA and COMT genes. Description: Hukic, Dzana Sudic, et al. Cognitive manic symptoms in bipolar disorder associated with polymorphisms in the DAOA and COMT genes. ''PLoS One''. 2013; '''8''' (7):e67450
Common variant rs9939609 in gene FTO confers risk to polycystic ovary syndrome. Description: Li, Tao, et al. Common variant rs9939609 in gene FTO confers risk to polycystic ovary syndrome. ''PLoS One''. 2013; '''8''' (7):e66250
Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese samples. Description: Jiang, Lei, et al. Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese samples. ''G3 (Bethesda)''. 2013 Jan; '''3''' (1):23-9
Complex variation in measures of general intelligence and cognitive change. Description: Rowe, Suzanne J, et al. Complex variation in measures of general intelligence and cognitive change. ''PLoS One''. 2013; '''8''' (12):e81189
Comprehensive SNP scan of DNA repair and DNA damage response genes reveal multiple susceptibility loci conferring risk to tobacco associated leukoplakia and oral cancer. Description: Mondal, Pinaki, et al. Comprehensive SNP scan of DNA repair and DNA damage response genes reveal multiple susceptibility loci conferring risk to tobacco associated leukoplakia and oral cancer. ''PLoS One''. 2013; '''8''' (2):e56952
Contribution of 32 GWAS-identified common variants to severe obesity in European adults referred for bariatric surgery. Description: Magi, Reedik, et al. Contribution of 32 GWAS-identified common variants to severe obesity in European adults referred for bariatric surgery. ''PLoS One''. 2013; '''8''' (8):e70735
Contribution of common PCSK1 genetic variants to obesity in 8,359 subjects from multi-ethnic American population. Description: Choquet, Helene, et al. Contribution of common PCSK1 genetic variants to obesity in 8,359 subjects from multi-ethnic American population. ''PLoS One''. 2013; '''8''' (2):e57857
Copy number variants in German patients with schizophrenia. Description: Priebe, Lutz, et al. Copy number variants in German patients with schizophrenia. ''PLoS One''. 2013; '''8''' (7):e64035
Copy number variations in alternative splicing gene networks impact lifespan. Description: Glessner, Joseph T, et al. Copy number variations in alternative splicing gene networks impact lifespan. ''PLoS One''. 2013; '''8''' (1):e53846
CpG methylation changes within the IL2RA promoter in type 1 diabetes of childhood onset. Description: Belot, Marie-Pierre, et al. CpG methylation changes within the IL2RA promoter in type 1 diabetes of childhood onset. ''PLoS One''. 2013; '''8''' (7):e68093
CRY2 genetic variants associate with dysthymia. Description: Kovanen, Leena, et al. CRY2 genetic variants associate with dysthymia. ''PLoS One''. 2013; '''8''' (8):e71450
Defining the contribution of CNTNAP2 to autism susceptibility. Description: Sampath, Srirangan, et al. Defining the contribution of CNTNAP2 to autism susceptibility. ''PLoS One''. 2013; '''8''' (10):e77906
Determining ancestry proportions in complex admixture scenarios in South Africa using a novel proxy ancestry selection method. Description: Chimusa, Emile R, et al. Determining ancestry proportions in complex admixture scenarios in South Africa using a novel proxy ancestry selection method. ''PLoS One''. 2013; '''8''' (9):e73971
Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia. Description: Agim, Zeynep Sena, et al. Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia. ''PLoS One''. 2013; '''8''' (1):e53042
Disease-related growth factor and embryonic signaling pathways modulate an enhancer of TCF21 expression at the 6q23.2 coronary heart disease locus. Description: Miller, Clint L, et al. Disease-related growth factor and embryonic signaling pathways modulate an enhancer of TCF21 expression at the 6q23.2 coronary heart disease locus. ''PLoS Genet''. 2013; '''9''' (7):e1003652
DNA sequence variants in PPARGC1A, a gene encoding a coactivator of the omega-3 LCPUFA sensing PPAR-RXR transcription complex, are associated with NV AMD and AMD-associated loci in genes of complement and VEGF signaling pathways. Description: SanGiovanni, John Paul, et al. DNA sequence variants in PPARGC1A, a gene encoding a coactivator of the omega-3 LCPUFA sensing PPAR-RXR transcription complex, are associated with NV AMD and AMD-associated loci in genes of complement and VEGF signaling pathways. ''PLoS One''. 2013; '''8''' (1):e53155
Dogs and humans share a common susceptibility gene SRBD1 for glaucoma risk. Description: Kanemaki, Nobuyuki, et al. Dogs and humans share a common susceptibility gene SRBD1 for glaucoma risk. ''PLoS One''. 2013; '''8''' (9):e74372
Effects of fertility on gene expression and function of the bovine endometrium. Description: Minten, Megan A, et al. Effects of fertility on gene expression and function of the bovine endometrium. ''PLoS One''. 2013; '''8''' (8):e69444
EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children. Description: Namjou, Bahram, et al. EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children. ''Front Genet''. 2013; '''4''': 268
Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records. Description: McDavid, Andrew, et al. Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records. ''PLoS One''. 2013; '''8''' (6):e63481
Epistatic genetic effects among Alzheimer's candidate genes. Description: Hohman, Timothy J, et al. Epistatic genetic effects among Alzheimer's candidate genes. ''PLoS One''. 2013; '''8''' (11):e80839
Evaluation of five candidate genes from GWAS for association with oligozoospermia in a Han Chinese population. Description: Xu, Miaofei, et al. Evaluation of five candidate genes from GWAS for association with oligozoospermia in a Han Chinese population. ''PLoS One''. 2013; '''8''' (11):e80374
Evidence of new risk genetic factor to systemic lupus erythematosus: the UBASH3A gene. Description: Diaz-Gallo, Lina-Marcela, et al. Evidence of new risk genetic factor to systemic lupus erythematosus: the UBASH3A gene. ''PLoS One''. 2013; '''8''' (4):e60646
Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes. Description: Pasquale, Louis R, et al. Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes. ''Front Genet''. 2013; '''4''': 7
Expression levels of LCORL are associated with body size in horses. Description: Metzger, Julia, et al. Expression levels of LCORL are associated with body size in horses. ''PLoS One''. 2013; '''8''' (2):e56497
Finding type 2 diabetes causal single nucleotide polymorphism combinations and functional modules from genome-wide association data. Description: Kang, Chiyong, et al. Finding type 2 diabetes causal single nucleotide polymorphism combinations and functional modules from genome-wide association data. ''BMC Med Inform Decis Mak''. 2013; '''13 Suppl 1''': S3
Fine mapping and functional analysis of the multiple sclerosis risk gene CD6. Description: Swaminathan, Bhairavi, et al. Fine mapping and functional analysis of the multiple sclerosis risk gene CD6. ''PLoS One''. 2013; '''8''' (4):e62376
Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus. Description: Trabzuni, Daniah, et al. Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus. ''PLoS One''. 2013; '''8''' (8):e70724
Functional coding variants in SLC6A15, a possible risk gene for major depression. Description: Quast, Carina, et al. Functional coding variants in SLC6A15, a possible risk gene for major depression. ''PLoS One''. 2013; '''8''' (7):e68645
Functional genomics identifies type I interferon pathway as central for host defense against Candida albicans. Description: Smeekens, Sanne P, et al. Functional genomics identifies type I interferon pathway as central for host defense against Candida albicans. ''Nat Commun''. 2013; '''4''': 1342
Functional properties of rare missense variants of human CDH13 found in adult attention deficit/hyperactivity disorder (ADHD) patients. Description: Mavroconstanti, Thegna, et al. Functional properties of rare missense variants of human CDH13 found in adult attention deficit/hyperactivity disorder (ADHD) patients. ''PLoS One''. 2013; '''8''' (8):e71445
Gene-based testing of interactions in association studies of quantitative traits. Description: Ma, Li, et al. Gene-based testing of interactions in association studies of quantitative traits. ''PLoS Genet''. 2013; '''9''' (2):e1003321
Gene network analysis in a pediatric cohort identifies novel lung function genes. Description: Ong, Bruce A, et al. Gene network analysis in a pediatric cohort identifies novel lung function genes. ''PLoS One''. 2013; '''8''' (9):e72899
Gene polymorphisms in African buffalo associated with susceptibility to bovine tuberculosis infection. Description: le Roex, Nikki, et al. Gene polymorphisms in African buffalo associated with susceptibility to bovine tuberculosis infection. ''PLoS One''. 2013; '''8''' (5):e64494
Gene set of nuclear-encoded mitochondrial regulators is enriched for common inherited variation in obesity. Description: Knoll, Nadja, et al. Gene set of nuclear-encoded mitochondrial regulators is enriched for common inherited variation in obesity. ''PLoS One''. 2013; '''8''' (2):e55884
Genetic analysis of a rat model of aerobic capacity and metabolic fitness. Description: Ren, Yu-Yu, et al. Genetic analysis of a rat model of aerobic capacity and metabolic fitness. ''PLoS One''. 2013; '''8''' (10):e77588
Genetic Association of Peptidoglycan Recognition Protein Variants with Inflammatory Bowel Disease. Description: Zulfiqar, Fareeha, et al. Genetic Association of Peptidoglycan Recognition Protein Variants with Inflammatory Bowel Disease. ''PLoS One''. 2013; '''8''' (6):e67393
Genetic associations of type 2 diabetes with islet amyloid polypeptide processing and degrading pathways in asian populations. Description: Lam, Vincent Kwok Lim, et al. Genetic associations of type 2 diabetes with islet amyloid polypeptide processing and degrading pathways in asian populations. ''PLoS One''. 2013; '''8''' (6):e62378
Genetic diversity in the modern horse illustrated from genome-wide SNP data. Description: Petersen, Jessica L, et al. Genetic diversity in the modern horse illustrated from genome-wide SNP data. ''PLoS One''. 2013; '''8''' (1):e54997
Genetic diversity, linkage disequilibrium and selection signatures in chinese and Western pigs revealed by genome-wide SNP markers. Description: Ai, Huashui, et al. Genetic diversity, linkage disequilibrium and selection signatures in chinese and Western pigs revealed by genome-wide SNP markers. ''PLoS One''. 2013; '''8''' (2):e56001
Genetic heterogeneity of susceptibility gene in different ethnic populations: refining association study of PTPN22 for Graves' disease in a Chinese Han population. Description: Xue, Liqiong, et al. Genetic heterogeneity of susceptibility gene in different ethnic populations: refining association study of PTPN22 for Graves' disease in a Chinese Han population. ''PLoS One''. 2013; '''8''' (12):e84514
Genetic modification of the association between peripubertal dioxin exposure and pubertal onset in a cohort of Russian boys. Description: Humblet, Olivier, et al. Genetic modification of the association between peripubertal dioxin exposure and pubertal onset in a cohort of Russian boys. ''Environ Health Perspect''. 2013 Jan; '''121''' (1):111-7
Genetic structure of Tibeto-Burman populations of Bangladesh: evaluating the gene flow along the sides of Bay-of-Bengal. Description: Gazi, Nurun Nahar, et al. Genetic structure of Tibeto-Burman populations of Bangladesh: evaluating the gene flow along the sides of Bay-of-Bengal. ''PLoS One''. 2013; '''8''' (10):e75064
Genetic substructure of Kuwaiti population reveals migration history. Description: Alsmadi, Osama, et al. Genetic substructure of Kuwaiti population reveals migration history. ''PLoS One''. 2013; '''8''' (9):e74913
Genetic susceptibility to refractive error: association of vasoactive intestinal peptide receptor 2 (VIPR2) with high myopia in Chinese. Description: Yiu, Wai Chi, et al. Genetic susceptibility to refractive error: association of vasoactive intestinal peptide receptor 2 (VIPR2) with high myopia in Chinese. ''PLoS One''. 2013; '''8''' (4):e61805
Genetic variation of ITGB3 is associated with asthma in Chinese Han children. Description: Zhang, Yan, et al. Genetic variation of ITGB3 is associated with asthma in Chinese Han children. ''PLoS One''. 2013; '''8''' (2):e56914
Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes. Description: Behr, Elijah R, et al. Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes. ''PLoS One''. 2013; '''8''' (11):e78511
Genome-wide analysis reveals selection for important traits in domestic horse breeds. Description: Petersen, Jessica L, et al. Genome-wide analysis reveals selection for important traits in domestic horse breeds. ''PLoS Genet''. 2013; '''9''' (1):e1003211
Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathy. Description: Vernau, Karen M, et al. Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathy. ''PLoS One''. 2013; '''8''' (3):e57195
Genome-wide association analysis with gray matter volume as a quantitative phenotype in first-episode treatment-naive patients with schizophrenia. Description: Wang, Qiang, et al. Genome-wide association analysis with gray matter volume as a quantitative phenotype in first-episode treatment-naive patients with schizophrenia. ''PLoS One''. 2013; '''8''' (9):e75083
Genome wide association and linkage analyses identified three loci-4q25, 17q23.2, and 10q11.21-associated with variation in leukocyte telomere length: the Long Life Family Study. Description: Lee, Joseph H, et al. Genome wide association and linkage analyses identified three loci-4q25, 17q23.2, and 10q11.21-associated with variation in leukocyte telomere length: the Long Life Family Study. ''Front Genet''. 2013; '''4''': 310
Genome-wide association mapping in dogs enables identification of the homeobox gene, NKX2-8, as a genetic component of neural tube defects in humans. Description: Safra, Noa, et al. Genome-wide association mapping in dogs enables identification of the homeobox gene, NKX2-8, as a genetic component of neural tube defects in humans. ''PLoS Genet''. 2013; '''9''' (7):e1003646
Genome-wide association studies for growth and meat production traits in sheep. Description: Zhang, Li, et al. Genome-wide association studies for growth and meat production traits in sheep. ''PLoS One''. 2013; '''8''' (6):e66569
Genome-wide association study for levels of total serum IgE identifies HLA-C in a Japanese population. Description: Yatagai, Yohei, et al. Genome-wide association study for levels of total serum IgE identifies HLA-C in a Japanese population. ''PLoS One''. 2013; '''8''' (12):e80941
Genome-wide association study identifies a novel canine glaucoma locus. Description: Ahonen, Saija J, et al. Genome-wide association study identifies a novel canine glaucoma locus. ''PLoS One''. 2013; '''8''' (8):e70903
Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese. Description: Dong, Jing, et al. Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese. ''PLoS Genet''. 2013; '''9''' (1):e1003190
Genome-wide association study identifies Loci and candidate genes for body composition and meat quality traits in Beijing-You chickens. Description: Liu, Ranran, et al. Genome-wide association study identifies Loci and candidate genes for body composition and meat quality traits in Beijing-You chickens. ''PLoS One''. 2013; '''8''' (4):e61172
Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder. Description: Lencz, Todd, et al. Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder. ''Nat Commun''. 2013; '''4''': 2739
Genome-wide association study link novel loci to endometriosis. Description: Albertsen, Hans M, et al. Genome-wide association study link novel loci to endometriosis. ''PLoS One''. 2013; '''8''' (3):e58257
Genome wide association study of age at menarche in the Japanese population. Description: Tanikawa, Chizu, et al. Genome wide association study of age at menarche in the Japanese population. ''PLoS One''. 2013; '''8''' (5):e63821
Genome-wide association study of antiphospholipid antibodies. Description: Kamboh, M Ilyas, et al. Genome-wide association study of antiphospholipid antibodies. ''Autoimmune Dis''. 2013; '''2013''': 761046
Genome-wide association study of breast cancer in the Japanese population. Description: Low, Siew-Kee, et al. Genome-wide association study of breast cancer in the Japanese population. ''PLoS One''. 2013; '''8''' (10):e76463
*Genome-wide association study of HLA-DQB106:02 negative essential hypersomnia.** Description: Khor, Seik-Soon, et al. Genome-wide association study of HLA-DQB1*06:02 negative essential hypersomnia. ''PeerJ''. 2013; '''1''': e66
Genome-wide association study of irritable vs. elated mania suggests genetic differences between clinical subtypes of bipolar disorder. Description: Greenwood, Tiffany A, et al. Genome-wide association study of irritable vs. elated mania suggests genetic differences between clinical subtypes of bipolar disorder. ''PLoS One''. 2013; '''8''' (1):e53804
Genome-wide association study of meat quality traits in a White DurocxErhualian F2 intercross and Chinese Sutai pigs. Description: Ma, Junwu, et al. Genome-wide association study of meat quality traits in a White DurocxErhualian F2 intercross and Chinese Sutai pigs. ''PLoS One''. 2013; '''8''' (5):e64047
Genome-wide association study on the development of cross-reactive neutralizing antibodies in HIV-1 infected individuals. Description: Euler, Zelda, et al. Genome-wide association study on the development of cross-reactive neutralizing antibodies in HIV-1 infected individuals. ''PLoS One''. 2013; '''8''' (1):e54684
Genome-wide association study reveals genetic architecture of eating behavior in pigs and its implications for humans obesity by comparative mapping. Description: Do, Duy Ngoc, et al. Genome-wide association study reveals genetic architecture of eating behavior in pigs and its implications for humans obesity by comparative mapping. ''PLoS One''. 2013; '''8''' (8):e71509
Genome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music. Description: Ukkola-Vuoti, Liisa, et al. Genome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music. ''PLoS One''. 2013; '''8''' (2):e56356
Genome-wide diversity in the levant reveals recent structuring by culture. Description: Haber, Marc, et al. Genome-wide diversity in the levant reveals recent structuring by culture. ''PLoS Genet''. 2013; '''9''' (2):e1003316
Genome-wide genetic diversity and differentially selected regions among Suffolk, Rambouillet, Columbia, Polypay, and Targhee sheep. Description: Zhang, Lifan, et al. Genome-wide genetic diversity and differentially selected regions among Suffolk, Rambouillet, Columbia, Polypay, and Targhee sheep. ''PLoS One''. 2013; '''8''' (6):e65942
Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family. Description: Nolan, Daniel, et al. Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family. ''PLoS One''. 2013; '''8''' (8):e71779
Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease. Description: Bhatnagar, Pallav, et al. Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease. ''PLoS One''. 2013; '''8''' (9):e74193
Genome-wide survey of interindividual differences of RNA stability in human lymphoblastoid cell lines. Description: Duan, Jubao, et al. Genome-wide survey of interindividual differences of RNA stability in human lymphoblastoid cell lines. ''Sci Rep''. 2013; '''3''': 1318
Genomic analysis of natural selection and phenotypic variation in high-altitude mongolians. Description: Xing, Jinchuan, et al. Genomic analysis of natural selection and phenotypic variation in high-altitude mongolians. ''PLoS Genet''. 2013; '''9''' (7):e1003634
Genomic risk models improve prediction of longitudinal lipid levels in children and young adults. Description: Wineinger, Nathan E, et al. Genomic risk models improve prediction of longitudinal lipid levels in children and young adults. ''Front Genet''. 2013; '''4''': 86
Genomics assisted ancestry deconvolution in grape. Description: Sawler, Jason, et al. Genomics assisted ancestry deconvolution in grape. ''PLoS One''. 2013; '''8''' (11):e80791
Global patterns of diversity and selection in human tyrosinase gene. Description: Hudjashov, Georgi, et al. Global patterns of diversity and selection in human tyrosinase gene. ''PLoS One''. 2013; '''8''' (9):e74307
Heritable influence of DBH on adrenergic and renal function: twin and disease studies. Description: Pasha, Dalal N, et al. Heritable influence of DBH on adrenergic and renal function: twin and disease studies. ''PLoS One''. 2013; '''8''' (12):e82956
*HLA-DQB103 confers susceptibility to chronic hepatitis C in Japanese: a genome-wide association study.** Description: Miki, Daiki, et al. HLA-DQB1*03 confers susceptibility to chronic hepatitis C in Japanese: a genome-wide association study. ''PLoS One''. 2013; '''8''' (12):e84226
How genome-wide SNP-SNP interactions relate to nasopharyngeal carcinoma susceptibility. Description: Su, Wen-Hui, et al. How genome-wide SNP-SNP interactions relate to nasopharyngeal carcinoma susceptibility. ''PLoS One''. 2013; '''8''' (12):e83034
HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG). Description: Xu, Jianfeng, et al. HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG). ''Hum Genet''. 2013 Jan; '''132''' (1):5-14
Identification and functional study of a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11). Description: Sang, Qing, et al. Identification and functional study of a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11). ''PLoS One''. 2013; '''8''' (1):e55178
Identification and MS-assisted interpretation of genetically influenced NMR signals in human plasma. Description: Raffler, Johannes, et al. Identification and MS-assisted interpretation of genetically influenced NMR signals in human plasma. ''Genome Med''. 2013; '''5''' (2):13
Identification of a 31-bp deletion in the RELN gene causing lissencephaly with cerebellar hypoplasia in sheep. Description: Suarez-Vega, Aroa, et al. Identification of a 31-bp deletion in the RELN gene causing lissencephaly with cerebellar hypoplasia in sheep. ''PLoS One''. 2013; '''8''' (11):e81072
Identification of a breast cancer susceptibility locus at 4q31.22 using a genome-wide association study paradigm. Description: Sapkota, Yadav, et al. Identification of a breast cancer susceptibility locus at 4q31.22 using a genome-wide association study paradigm. ''PLoS One''. 2013; '''8''' (5):e62550
Identification of a KEAP1 germline mutation in a family with multinodular goitre. Description: Teshiba, Risa, et al. Identification of a KEAP1 germline mutation in a family with multinodular goitre. ''PLoS One''. 2013; '''8''' (5):e65141
Identification of single nucleotide polymorphisms regulating peripheral blood mRNA expression with genome-wide significance: an eQTL study in the Japanese population. Description: Sasayama, Daimei, et al. Identification of single nucleotide polymorphisms regulating peripheral blood mRNA expression with genome-wide significance: an eQTL study in the Japanese population. ''PLoS One''. 2013; '''8''' (1):e54967
Identification of two maternal transmission ratio distortion loci in pedigrees of the Framingham heart study. Description: Liu, Yang, et al. Identification of two maternal transmission ratio distortion loci in pedigrees of the Framingham heart study. ''Sci Rep''. 2013; '''3''': 2147
Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis. Description: Lin, Rui, et al. Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis. ''PLoS One''. 2013; '''8''' (3):e56379
ImmunoChip study implicates antigen presentation to T cells in narcolepsy. Description: Faraco, Juliette, et al. ImmunoChip study implicates antigen presentation to T cells in narcolepsy. ''PLoS Genet''. 2013; '''9''' (2):e1003270
Impact of PSCA variation on gastric ulcer susceptibility. Description: Tanikawa, Chizu, et al. Impact of PSCA variation on gastric ulcer susceptibility. ''PLoS One''. 2013; '''8''' (5):e63698
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Description: Wood, Andrew R, et al. Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. ''PLoS One''. 2013; '''8''' (5):e64343
Indian signatures in the westernmost edge of the European Romani diaspora: new insight from mitogenomes. Description: Gomez-Carballa, Alberto, et al. Indian signatures in the westernmost edge of the European Romani diaspora: new insight from mitogenomes. ''PLoS One''. 2013; '''8''' (10):e75397
Influence of genetic variation on plasma protein levels in older adults using a multi-analyte panel. Description: Kim, Sungeun, et al. Influence of genetic variation on plasma protein levels in older adults using a multi-analyte panel. ''PLoS One''. 2013; '''8''' (7):e70269
Insight into the peopling of Mainland Southeast Asia from Thai population genetic structure. Description: Wangkumhang, Pongsakorn, et al. Insight into the peopling of Mainland Southeast Asia from Thai population genetic structure. ''PLoS One''. 2013; '''8''' (11):e79522
Insulin-like growth factor 1 is not associated with high myopia in a large Japanese cohort. Description: Miyake, Masahiro, et al. Insulin-like growth factor 1 is not associated with high myopia in a large Japanese cohort. ''Mol Vis''. 2013; '''19''': 1074-81
Integrative analysis of mRNA expression and half-life data reveals trans-acting genetic variants associated with increased expression of stable transcripts. Description: Nguyen, Thong T, et al. Integrative analysis of mRNA expression and half-life data reveals trans-acting genetic variants associated with increased expression of stable transcripts. ''PLoS One''. 2013; '''8''' (11):e79627
Interactions between genetic variants in AMH and AMHR2 may modify age at natural menopause. Description: Braem, Marieke G M, et al. Interactions between genetic variants in AMH and AMHR2 may modify age at natural menopause. ''PLoS One''. 2013; '''8''' (3):e59819
Intestinal DMBT1 expression is modulated by Crohn's disease-associated IL23R variants and by a DMBT1 variant which influences binding of the transcription factors CREB1 and ATF-2. Description: Diegelmann, Julia, et al. Intestinal DMBT1 expression is modulated by Crohn's disease-associated IL23R variants and by a DMBT1 variant which influences binding of the transcription factors CREB1 and ATF-2. ''PLoS One''. 2013; '''8''' (11):e77773
Involvement of the neutral amino acid transporter SLC6A15 and leucine in obesity-related phenotypes. Description: Drgonova, Jana, et al. Involvement of the neutral amino acid transporter SLC6A15 and leucine in obesity-related phenotypes. ''PLoS One''. 2013; '''8''' (9):e68245
IRGM variants and susceptibility to inflammatory bowel disease in the German population. Description: Glas, Jurgen, et al. IRGM variants and susceptibility to inflammatory bowel disease in the German population. ''PLoS One''. 2013; '''8''' (1):e54338
Linking protective GAB2 variants, increased cortical GAB2 expression and decreased Alzheimer's disease pathology. Description: Zou, Fanggeng, et al. Linking protective GAB2 variants, increased cortical GAB2 expression and decreased Alzheimer's disease pathology. ''PLoS One''. 2013; '''8''' (5):e64802
Low frequency variants, collapsed based on biological knowledge, uncover complexity of population stratification in 1000 genomes project data. Description: Moore, Carrie B, et al. Low frequency variants, collapsed based on biological knowledge, uncover complexity of population stratification in 1000 genomes project data. ''PLoS Genet''. 2013; '''9''' (12):e1003959
Mapping of PARK2 and PACRG overlapping regulatory region reveals LD structure and functional variants in association with leprosy in unrelated indian population groups. Description: Chopra, Rupali, et al. Mapping of PARK2 and PACRG overlapping regulatory region reveals LD structure and functional variants in association with leprosy in unrelated indian population groups. ''PLoS Genet''. 2013; '''9''' (7):e1003578
Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data. Description: Mosley, Jonathan D, et al. Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data. ''PLoS One''. 2013; '''8''' (12):e81503
MicroRNA-3148 modulates allelic expression of toll-like receptor 7 variant associated with systemic lupus erythematosus. Description: Deng, Yun, et al. MicroRNA-3148 modulates allelic expression of toll-like receptor 7 variant associated with systemic lupus erythematosus. ''PLoS Genet''. 2013; '''9''' (2):e1003336
Missense mutation in CAPN1 is associated with spinocerebellar ataxia in the Parson Russell Terrier dog breed. Description: Forman, Oliver P, et al. Missense mutation in CAPN1 is associated with spinocerebellar ataxia in the Parson Russell Terrier dog breed. ''PLoS One''. 2013; '''8''' (5):e64627
Multiple autoimmune-associated variants confer decreased IL-2R signaling in CD4+ CD25(hi) T cells of type 1 diabetic and multiple sclerosis patients. Description: Cerosaletti, Karen, et al. Multiple autoimmune-associated variants confer decreased IL-2R signaling in CD4+ CD25(hi) T cells of type 1 diabetic and multiple sclerosis patients. ''PLoS One''. 2013; '''8''' (12):e83811
Multi-population classical HLA type imputation. Description: Dilthey, Alexander, et al. Multi-population classical HLA type imputation. ''PLoS Comput Biol''. 2013; '''9''' (2):e1002877
Native American admixture in the Quebec founder population. Description: Moreau, Claudia, et al. Native American admixture in the Quebec founder population. ''PLoS One''. 2013; '''8''' (6):e65507
New insights into the genetic mechanism of IQ in autism spectrum disorders. Description: Wang, Harold Z, et al. New insights into the genetic mechanism of IQ in autism spectrum disorders. ''Front Genet''. 2013; '''4''': 195
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. Description: Horikoshi, Momoko, et al. New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. ''Nat Genet''. 2013 Jan; '''45''' (1):76-82
No effect of genome-wide copy number variation on measures of intelligence in a New Zealand birth cohort. Description: Bagshaw, Andrew T M, et al. No effect of genome-wide copy number variation on measures of intelligence in a New Zealand birth cohort. ''PLoS One''. 2013; '''8''' (1):e55208
No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controls. Description: Hudson, Gavin, et al. No evidence of an association between mitochondrial DNA variants and osteoarthritis in 7393 cases and 5122 controls. ''Ann Rheum Dis''. 2013 Jan; '''72''' (1):136-9
No evidence of association between common autoimmunity STAT4 and IL23R risk polymorphisms and non-anterior uveitis. Description: Cenit, Maria Carmen, et al. No evidence of association between common autoimmunity STAT4 and IL23R risk polymorphisms and non-anterior uveitis. ''PLoS One''. 2013; '''8''' (11):e72892
North-South differentiation and a region of high diversity in European wolves (Canis lupus). Description: Stronen, Astrid V, et al. North-South differentiation and a region of high diversity in European wolves (Canis lupus). ''PLoS One''. 2013; '''8''' (10):e76454
Novel SACS mutations identified by whole exome sequencing in a norwegian family with autosomal recessive spastic ataxia of Charlevoix-Saguenay. Description: Tzoulis, Charalampos, et al. Novel SACS mutations identified by whole exome sequencing in a norwegian family with autosomal recessive spastic ataxia of Charlevoix-Saguenay. ''PLoS One''. 2013; '''8''' (6):e66145
Novel single nucleotide polymorphisms in interleukin 6 affect tacrolimus metabolism in liver transplant patients. Description: Chen, Dawei, et al. Novel single nucleotide polymorphisms in interleukin 6 affect tacrolimus metabolism in liver transplant patients. ''PLoS One''. 2013; '''8''' (8):e73405
Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. Description: Mero, Inger-Lise, et al. Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. ''PLoS One''. 2013; '''8''' (3):e58352
Ovine HSP90AA1 expression rate is affected by several SNPs at the promoter under both basal and heat stress conditions. Description: Salces-Ortiz, Judit, et al. Ovine HSP90AA1 expression rate is affected by several SNPs at the promoter under both basal and heat stress conditions. ''PLoS One''. 2013; '''8''' (6):e66641
PADI2 is significantly associated with rheumatoid arthritis. Description: Chang, Xiaotian, et al. PADI2 is significantly associated with rheumatoid arthritis. ''PLoS One''. 2013; '''8''' (12):e81259
Pathway analysis using information from allele-specific gene methylation in genome-wide association studies for bipolar disorder. Description: Chuang, Li-Chung, et al. Pathway analysis using information from allele-specific gene methylation in genome-wide association studies for bipolar disorder. ''PLoS One''. 2013; '''8''' (1):e53092
Pharmacometabolomics reveals racial differences in response to atenolol treatment. Description: Wikoff, William R, et al. Pharmacometabolomics reveals racial differences in response to atenolol treatment. ''PLoS One''. 2013; '''8''' (3):e57639
Plasma level of adrenomedullin is influenced by a single nucleotide polymorphism in the adiponectin gene. Description: Wong, Hoi Kin, et al. Plasma level of adrenomedullin is influenced by a single nucleotide polymorphism in the adiponectin gene. ''PLoS One''. 2013; '''8''' (8):e70335
Polymorphism in serotonin receptor 3B is associated with pain catastrophizing. Description: Horjales-Araujo, Emilia, et al. Polymorphism in serotonin receptor 3B is associated with pain catastrophizing. ''PLoS One''. 2013; '''8''' (11):e78889
Population genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) Consortium. Description: Shah, Tina, et al. Population genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) Consortium. ''PLoS One''. 2013; '''8''' (8):e71345
Power analysis of C-TDT for small sample size genome-wide association studies by the joint use of case-parent trios and pairs. Description: Rajabli, Farid, et al. Power analysis of C-TDT for small sample size genome-wide association studies by the joint use of case-parent trios and pairs. ''Comput Math Methods Med''. 2013; '''2013''': 235825
Preferential binding to Elk-1 by SLE-associated IL10 risk allele upregulates IL10 expression. Description: Sakurai, Daisuke, et al. Preferential binding to Elk-1 by SLE-associated IL10 risk allele upregulates IL10 expression. ''PLoS Genet''. 2013; '''9''' (10):e1003870
PTPN22 association in systemic lupus erythematosus (SLE) with respect to individual ancestry and clinical sub-phenotypes. Description: Namjou, Bahram, et al. PTPN22 association in systemic lupus erythematosus (SLE) with respect to individual ancestry and clinical sub-phenotypes. ''PLoS One''. 2013; '''8''' (8):e69404
PUMA: a unified framework for penalized multiple regression analysis of GWAS data. Description: Hoffman, Gabriel E, et al. PUMA: a unified framework for penalized multiple regression analysis of GWAS data. ''PLoS Comput Biol''. 2013; '''9''' (6):e1003101
Rare copy number variants are a common cause of short stature. Description: Zahnleiter, Diana, et al. Rare copy number variants are a common cause of short stature. ''PLoS Genet''. 2013; '''9''' (3):e1003365
Rare Genomic Variants Link Bipolar Disorder with Anxiety Disorders to CREB-Regulated Intracellular Signaling Pathways. Description: Kerner, Berit, et al. Rare Genomic Variants Link Bipolar Disorder with Anxiety Disorders to CREB-Regulated Intracellular Signaling Pathways. ''Front Psychiatry''. 2013; '''4''': 154
Rare variants in PLXNA4 and Parkinson's disease. Description: Schulte, Eva C, et al. Rare variants in PLXNA4 and Parkinson's disease. ''PLoS One''. 2013; '''8''' (11):e79145
Reconstructing Roma history from genome-wide data. Description: Moorjani, Priya, et al. Reconstructing Roma history from genome-wide data. ''PLoS One''. 2013; '''8''' (3):e58633
Refining susceptibility loci of chronic obstructive pulmonary disease with lung eqtls. Description: Lamontagne, Maxime, et al. Refining susceptibility loci of chronic obstructive pulmonary disease with lung eqtls. ''PLoS One''. 2013; '''8''' (7):e70220
Replication and meta-analysis of GWAS identified susceptibility loci in Kawasaki disease confirm the importance of B lymphoid tyrosine kinase (BLK) in disease susceptibility. Description: Chang, Chia-Jung, et al. Replication and meta-analysis of GWAS identified susceptibility loci in Kawasaki disease confirm the importance of B lymphoid tyrosine kinase (BLK) in disease susceptibility. ''PLoS One''. 2013; '''8''' (8):e72037
Replication of association between schizophrenia and chromosome 6p21-6p22.1 polymorphisms in Chinese Han population. Description: Zhang, Yang, et al. Replication of association between schizophrenia and chromosome 6p21-6p22.1 polymorphisms in Chinese Han population. ''PLoS One''. 2013; '''8''' (2):e56732
Replication of genome wide association studies of alcohol dependence: support for association with variation in ADH1C. Description: Biernacka, Joanna M, et al. Replication of genome wide association studies of alcohol dependence: support for association with variation in ADH1C. ''PLoS One''. 2013; '''8''' (3):e58798
Replication of type 2 diabetes candidate genes variations in three geographically unrelated Indian population groups. Description: Ali, Shafat, et al. Replication of type 2 diabetes candidate genes variations in three geographically unrelated Indian population groups. ''PLoS One''. 2013; '''8''' (3):e58881
Replication study confirms link between TSPAN18 mutation and schizophrenia in Han Chinese. Description: Yuan, Jianmin, et al. Replication study confirms link between TSPAN18 mutation and schizophrenia in Han Chinese. ''PLoS One''. 2013; '''8''' (3):e58785
Resequencing three candidate genes for major depressive disorder in a Dutch cohort. Description: Verbeek, Eva C, et al. Resequencing three candidate genes for major depressive disorder in a Dutch cohort. ''PLoS One''. 2013; '''8''' (11):e79921
Role of HLA-DP polymorphisms on chronicity and disease activity of hepatitis B infection in Southern Chinese. Description: Wong, Danny Ka-Ho, et al. Role of HLA-DP polymorphisms on chronicity and disease activity of hepatitis B infection in Southern Chinese. ''PLoS One''. 2013; '''8''' (6):e66920
RPS19 and TYMS SNPs and Prevalent High Risk Human Papilloma Virus Infection in Nigerian Women. Description: Famooto, Ayo, et al. RPS19 and TYMS SNPs and Prevalent High Risk Human Papilloma Virus Infection in Nigerian Women. ''PLoS One''. 2013; '''8''' (6):e66930
Rs4074134 near BDNF gene is associated with type 2 diabetes mellitus in Chinese Han population independently of body mass index. Description: Han, Xueyao, et al. Rs4074134 near BDNF gene is associated with type 2 diabetes mellitus in Chinese Han population independently of body mass index. ''PLoS One''. 2013; '''8''' (2):e56898
RTK/ERK pathway under natural selection associated with prostate cancer. Description: Chen, Yang, et al. RTK/ERK pathway under natural selection associated with prostate cancer. ''PLoS One''. 2013; '''8''' (11):e78254
SNP association mapping across the extended major histocompatibility complex and risk of B-cell precursor acute lymphoblastic leukemia in children. Description: Urayama, Kevin Y, et al. SNP association mapping across the extended major histocompatibility complex and risk of B-cell precursor acute lymphoblastic leukemia in children. ''PLoS One''. 2013; '''8''' (8):e72557
SNPflow: a lightweight application for the processing, storing and automatic quality checking of genotyping assays. Description: Weissensteiner, Hansi, et al. SNPflow: a lightweight application for the processing, storing and automatic quality checking of genotyping assays. ''PLoS One''. 2013; '''8''' (3):e59508
Soluble guanylate cyclase alpha1-deficient mice: a novel murine model for primary open angle glaucoma. Description: Buys, Emmanuel S, et al. Soluble guanylate cyclase alpha1-deficient mice: a novel murine model for primary open angle glaucoma. ''PLoS One''. 2013; '''8''' (3):e60156
SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians. Description: Miyashita, Akinori, et al. SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians. ''PLoS One''. 2013; '''8''' (4):e58618
Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates. Description: Markunas, Christina A, et al. Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates. ''PLoS One''. 2013; '''8''' (4):e61521
Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies. Description: Vijai, Joseph, et al. Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies. ''PLoS Genet''. 2013; '''9''' (1):e1003220
TATES: efficient multivariate genotype-phenotype analysis for genome-wide association studies. Description: van der Sluis, Sophie, et al. TATES: efficient multivariate genotype-phenotype analysis for genome-wide association studies. ''PLoS Genet''. 2013; '''9''' (1):e1003235
The association of common SNPs and haplotypes in CETP gene with HDL cholesterol levels in Latvian population. Description: Radovica, Ilze, et al. The association of common SNPs and haplotypes in CETP gene with HDL cholesterol levels in Latvian population. ''PLoS One''. 2013; '''8''' (5):e64191
The Association Study between Twenty One Polymorphisms in Seven Candidate Genes and Coronary Heart Diseases in Chinese Han Population. Description: Alobeidy, Barrak F, et al. The Association Study between Twenty One Polymorphisms in Seven Candidate Genes and Coronary Heart Diseases in Chinese Han Population. ''PLoS One''. 2013; '''8''' (6):e66976
The geography of recent genetic ancestry across Europe. Description: Ralph, Peter, et al. The geography of recent genetic ancestry across Europe. ''PLoS Biol''. 2013; '''11''' (5):e1001555
The impact of genome-wide supported schizophrenia risk variants in the neurogranin gene on brain structure and function. Description: Walton, Esther, et al. The impact of genome-wide supported schizophrenia risk variants in the neurogranin gene on brain structure and function. ''PLoS One''. 2013; '''8''' (10):e76815
The impact of phenotypic and genetic heterogeneity on results of genome wide association studies of complex diseases. Description: Manchia, Mirko, et al. The impact of phenotypic and genetic heterogeneity on results of genome wide association studies of complex diseases. ''PLoS One''. 2013; '''8''' (10):e76295
The missing link of Jewish European ancestry: contrasting the Rhineland and the Khazarian hypotheses. Description: Elhaik, Eran. The missing link of Jewish European ancestry: contrasting the Rhineland and the Khazarian hypotheses. ''Genome Biol Evol''. 2013; '''5''' (1):61-74
The molecular genetic architecture of self-employment. Description: van der Loos, Matthijs J H M, et al. The molecular genetic architecture of self-employment. ''PLoS One''. 2013; '''8''' (4):e60542
The power of regional heritability analysis for rare and common variant detection: simulations and application to eye biometrical traits. Description: Uemoto, Yoshinobu, et al. The power of regional heritability analysis for rare and common variant detection: simulations and application to eye biometrical traits. ''Front Genet''. 2013; '''4''': 232
The presence of methylation quantitative trait loci indicates a direct genetic influence on the level of DNA methylation in adipose tissue. Description: Drong, Alexander W, et al. The presence of methylation quantitative trait loci indicates a direct genetic influence on the level of DNA methylation in adipose tissue. ''PLoS One''. 2013; '''8''' (2):e55923
The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-epsilon4 carriers. Description: Benitez, Bruno A, et al. The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-epsilon4 carriers. ''PLoS Genet''. 2013; '''9''' (8):e1003685
The role of SNP-loop diuretic interactions in hypertension across ethnic groups in HyperGEN. Description: de Las Fuentes, Lisa, et al. The role of SNP-loop diuretic interactions in hypertension across ethnic groups in HyperGEN. ''Front Genet''. 2013; '''4''': 304
The rs1142345 in TPMT Affects the Therapeutic Effect of Traditional Hypoglycemic Herbs in Prediabetes. Description: Li, Xi, et al. The rs1142345 in TPMT Affects the Therapeutic Effect of Traditional Hypoglycemic Herbs in Prediabetes. ''Evid Based Complement Alternat Med''. 2013; '''2013''': 327629
The STK33-linked SNP rs4929949 is associated with obesity and BMI in two independent cohorts of Swedish and Greek children. Description: Rask-Andersen, Mathias, et al. The STK33-linked SNP rs4929949 is associated with obesity and BMI in two independent cohorts of Swedish and Greek children. ''PLoS One''. 2013; '''8''' (8):e71353
The systemic lupus erythematosus IRF5 risk haplotype is associated with systemic sclerosis. Description: Carmona, F David, et al. The systemic lupus erythematosus IRF5 risk haplotype is associated with systemic sclerosis. ''PLoS One''. 2013; '''8''' (1):e54419
Thorough investigation of a canine autoinflammatory disease (AID) confirms one main risk locus and suggests a modifier locus for amyloidosis. Description: Olsson, Mia, et al. Thorough investigation of a canine autoinflammatory disease (AID) confirms one main risk locus and suggests a modifier locus for amyloidosis. ''PLoS One''. 2013; '''8''' (10):e75242
To the Root of the Curl: A Signature of a Recent Selective Sweep Identifies a Mutation That Defines the Cornish Rex Cat Breed. Description: Gandolfi, Barbara, et al. To the Root of the Curl: A Signature of a Recent Selective Sweep Identifies a Mutation That Defines the Cornish Rex Cat Breed. ''PLoS One''. 2013; '''8''' (6):e67105
Trans-ancestral studies fine map the SLE-susceptibility locus TNFSF4. Description: Manku, Harinder, et al. Trans-ancestral studies fine map the SLE-susceptibility locus TNFSF4. ''PLoS Genet''. 2013; '''9''' (7):e1003554
Two functional variants of IRF5 influence the development of macular edema in patients with non-anterior uveitis. Description: Marquez, Ana, et al. Two functional variants of IRF5 influence the development of macular edema in patients with non-anterior uveitis. ''PLoS One''. 2013; '''8''' (10):e76777
Ubiquitous polygenicity of human complex traits: genome-wide analysis of 49 traits in Koreans. Description: Yang, Jian, et al. Ubiquitous polygenicity of human complex traits: genome-wide analysis of 49 traits in Koreans. ''PLoS Genet''. 2013; '''9''' (3):e1003355
Use of net reclassification improvement (NRI) method confirms the utility of combined genetic risk score to predict type 2 diabetes. Description: Tam, Claudia H T, et al. Use of net reclassification improvement (NRI) method confirms the utility of combined genetic risk score to predict type 2 diabetes. ''PLoS One''. 2013; '''8''' (12):e83093
Using eQTL weights to improve power for genome-wide association studies: a genetic study of childhood asthma. Description: Li, Lin, et al. Using eQTL weights to improve power for genome-wide association studies: a genetic study of childhood asthma. ''Front Genet''. 2013; '''4''': 103
Utilizing twins as controls for non-twin case-materials in genome wide association studies. Description: Ganna, Andrea, et al. Utilizing twins as controls for non-twin case-materials in genome wide association studies. ''PLoS One''. 2013; '''8''' (12):e83101
Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. Description: Frampton, Matthew, et al. Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. ''Nat Commun''. 2013; '''4''': 2549
Vitis phylogenomics: hybridization intensities from a SNP array outperform genotype calls. Description: Miller, Allison J, et al. Vitis phylogenomics: hybridization intensities from a SNP array outperform genotype calls. ''PLoS One''. 2013; '''8''' (11):e78680
Weighted SNP set analysis in genome-wide association study. Description: Dai, Hui, et al. Weighted SNP set analysis in genome-wide association study. ''PLoS One''. 2013; '''8''' (9):e75897
Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles. Description: Gracia-Aznarez, Francisco Javier, et al. Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles. ''PLoS One''. 2013; '''8''' (2):e55681
Whole Genome Association Studies of Residual Feed Intake and Related Traits in the Pig. Description: Onteru, Suneel K, et al. Whole Genome Association Studies of Residual Feed Intake and Related Traits in the Pig. ''PLoS One''. 2013; '''8''' (6):e61756
Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism. Description: Proverbio, Maria Carla, et al. Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism. ''PLoS One''. 2013; '''8''' (7):e68740
Softwares and methods for estimating genetic ancestry in human populations. Description: Liu, Yushi, et al. Softwares and methods for estimating genetic ancestry in human populations. ''Hum Genomics''. 2013 Jan 5; '''7''': 1
From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software. Description: Forster, Michael, et al. From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software. ''Nucleic Acids Res''. 2013 Jan 7; '''41''' (1):e16
A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12. Description: Fernandez-Rozadilla, Ceres, et al. A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12. ''BMC Genomics''. 2013 Jan 26; '''14''': 55
Association between paraoxonase gene and stroke in the Han Chinese population. Description: Zhang, Guojun, et al. Association between paraoxonase gene and stroke in the Han Chinese population. ''BMC Med Genet''. 2013 Jan 28; '''14''': 16
A gene-centric study of common carotid artery remodelling. Description: Harrison, Seamus C, et al. A gene-centric study of common carotid artery remodelling. ''Atherosclerosis''. 2013 Feb; '''226''' (2):440-6
CYP4A11 variant is associated with high-density lipoprotein cholesterol in women. Description: White, C C, et al. CYP4A11 variant is associated with high-density lipoprotein cholesterol in women. ''Pharmacogenomics J''. 2013 Feb; '''13''' (1):44-51
Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis. Description: Liu, Yun, et al. Epigenome-wide association data implicate DNA methylation as an intermediary of genetic risk in rheumatoid arthritis. ''Nat Biotechnol''. 2013 Feb; '''31''' (2):142-7
Gene set analysis of GWAS data for human longevity highlights the relevance of the insulin/IGF-1 signaling and telomere maintenance pathways. Description: Deelen, Joris, et al. Gene set analysis of GWAS data for human longevity highlights the relevance of the insulin/IGF-1 signaling and telomere maintenance pathways. ''Age (Dordr)''. 2013 Feb; '''35''' (1):235-49
*Genetic association with ERAP1 in psoriasis is confined to disease onset after puberty and not dependent on HLA-C06.** Description: Lysell, Josefin, et al. Genetic association with ERAP1 in psoriasis is confined to disease onset after puberty and not dependent on HLA-C*06. ''J Invest Dermatol''. 2013 Feb; '''133''' (2):411-7
Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer. Description: Jia, Wei-Hua, et al. Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer. ''Nat Genet''. 2013 Feb; '''45''' (2):191-6
Genome-wide association analysis of copy number variation in recurrent depressive disorder. Description: Rucker, J J H, et al. Genome-wide association analysis of copy number variation in recurrent depressive disorder. ''Mol Psychiatry''. 2013 Feb; '''18''' (2):183-9
Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations. Description: Wheeler, H E, et al. Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations. ''Pharmacogenomics J''. 2013 Feb; '''13''' (1):35-43
The catechol-O-methyltransferase gene (COMT) and cognitive function from childhood through adolescence. Description: Gaysina, Darya, et al. The catechol-O-methyltransferase gene (COMT) and cognitive function from childhood through adolescence. ''Biol Psychol''. 2013 Feb; '''92''' (2):359-64
CrypticIBDcheck: an R package for checking cryptic relatedness in nominally unrelated individuals. Description: Nembot-Simo, Annick, et al. CrypticIBDcheck: an R package for checking cryptic relatedness in nominally unrelated individuals. ''Source Code Biol Med''. 2013 Feb 6; '''8''' (1):5
A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. Description: Chapman, Jade, et al. A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. ''Hum Mol Genet''. 2013 Feb 15; '''22''' (4):816-24
High-density SNP-based genetic map development and linkage disequilibrium assessment in Brassica napus L. Description: Delourme, Regine, et al. High-density SNP-based genetic map development and linkage disequilibrium assessment in Brassica napus L. ''BMC Genomics''. 2013 Feb 22; '''14''': 120
A copy number variant at the KITLG locus likely confers risk for canine squamous cell carcinoma of the digit. Description: Karyadi, Danielle M, et al. A copy number variant at the KITLG locus likely confers risk for canine squamous cell carcinoma of the digit. ''PLoS Genet''. 2013 Mar; '''9''' (3):e1003409
Association between Interferon-Inducible Protein 6 (IFI6) Polymorphisms and Hepatitis B Virus Clearance. Description: Park, Geun-Hee, et al. Association between Interferon-Inducible Protein 6 (IFI6) Polymorphisms and Hepatitis B Virus Clearance. ''Genomics Inform''. 2013 Mar; '''11''' (1):15-23
Combined genome-wide linkage and association analyses of fasting glucose level in healthy twins and families of Korea. Description: Suh, Young Ju, et al. Combined genome-wide linkage and association analyses of fasting glucose level in healthy twins and families of Korea. ''J Korean Med Sci''. 2013 Mar; '''28''' (3):415-23
Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants. Description: Gamazon, E R, et al. Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants. ''Mol Psychiatry''. 2013 Mar; '''18''' (3):340-6
Genetic architecture of skin and eye color in an African-European admixed population. Description: Beleza, Sandra, et al. Genetic architecture of skin and eye color in an African-European admixed population. ''PLoS Genet''. 2013 Mar; '''9''' (3):e1003372
Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis. Description: Cui, Jing, et al. Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis. ''PLoS Genet''. 2013 Mar; '''9''' (3):e1003394
Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21. Description: Tabassum, Rubina, et al. Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21. ''Diabetes''. 2013 Mar; '''62''' (3):977-86
Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region. Description: Peters, Marjolein J, et al. Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region. ''Ann Rheum Dis''. 2013 Mar; '''72''' (3):427-36
Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1. Description: Lopes, Alexandra M, et al. Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1. ''PLoS Genet''. 2013 Mar; '''9''' (3):e1003349
Maize chromosomal knobs are located in gene-dense areas and suppress local recombination. Description: Ghaffari, Rashin, et al. Maize chromosomal knobs are located in gene-dense areas and suppress local recombination. ''Chromosoma''. 2013 Mar; '''122''' (1-2):67-75
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing. Description: Kirby, Andrew, et al. Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing. ''Nat Genet''. 2013 Mar; '''45''' (3):299-303
Study in 1790 Baltic men: FSHR Asn680Ser polymorphism affects total testes volume. Description: Grigorova, M, et al. Study in 1790 Baltic men: FSHR Asn680Ser polymorphism affects total testes volume. ''Andrology''. 2013 Mar; '''1''' (2):293-300
Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained. Description: Wu, Ying, et al. Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained. ''PLoS Genet''. 2013 Mar; '''9''' (3):e1003379
Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study. Description: Ng, Maggie C Y, et al. Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study. ''Diabetes''. 2013 Mar; '''62''' (3):965-76
A candidate gene based approach validates Md-PG1 as the main responsible for a QTL impacting fruit texture in apple (Malus x domestica Borkh). Description: Longhi, Sara, et al. A candidate gene based approach validates Md-PG1 as the main responsible for a QTL impacting fruit texture in apple (Malus x domestica Borkh). ''BMC Plant Biol''. 2013 Mar 4; '''13''': 37
Multigenic nature of the mouse pulmonary adenoma progression 1 locus. Description: Dassano, Alice, et al. Multigenic nature of the mouse pulmonary adenoma progression 1 locus. ''BMC Genomics''. 2013 Mar 6; '''14''': 152
Schizophrenia susceptibility and NMDA-receptor mediated signalling: an association study involving 32 tagSNPs of DAO, DAOA, PPP3CC, and DTNBP1 genes. Description: Sacchetti, Emilio, et al. Schizophrenia susceptibility and NMDA-receptor mediated signalling: an association study involving 32 tagSNPs of DAO, DAOA, PPP3CC, and DTNBP1 genes. ''BMC Med Genet''. 2013 Mar 9; '''14''': 33
Patterns of population epigenomic diversity. Description: Schmitz, Robert J, et al. Patterns of population epigenomic diversity. ''Nature''. 2013 Mar 14; '''495''' (7440):193-8
A genome-wide association study of early menopause and the combined impact of identified variants. Description: Perry, John R B, et al. A genome-wide association study of early menopause and the combined impact of identified variants. ''Hum Mol Genet''. 2013 Apr 1; '''22''' (7):1465-72
All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. Description: Schork, Andrew J, et al. All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. ''PLoS Genet''. 2013 Apr; '''9''' (4):e1003449
A polymorphism in the thyroid hormone receptor gene is associated with bronchodilator response in asthmatics. Description: Duan, Q L, et al. A polymorphism in the thyroid hormone receptor gene is associated with bronchodilator response in asthmatics. ''Pharmacogenomics J''. 2013 Apr; '''13''' (2):130-6
Genetic associations with neonatal thyroid-stimulating hormone levels. Description: Alul, Farah Y, et al. Genetic associations with neonatal thyroid-stimulating hormone levels. ''Pediatr Res''. 2013 Apr; '''73''' (4 Pt 1):484-91
Genetic diversity and phylogenetic analysis of native mountain ponies of Britain and Ireland reveals a novel rare population. Description: Winton, Clare L, et al. Genetic diversity and phylogenetic analysis of native mountain ponies of Britain and Ireland reveals a novel rare population. ''Ecol Evol''. 2013 Apr; '''3''' (4):934-47
Genome-wide association studies identify two novel BMP15 mutations responsible for an atypical hyperprolificacy phenotype in sheep. Description: Demars, Julie, et al. Genome-wide association studies identify two novel BMP15 mutations responsible for an atypical hyperprolificacy phenotype in sheep. ''PLoS Genet''. 2013 Apr; '''9''' (4):e1003482
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot. Description: Cordell, Heather J, et al. Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot. ''Hum Mol Genet''. 2013 Apr 1; '''22''' (7):1473-81
LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis. Description: Garcia-Martin, Elena, et al. LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis. ''BMC Neurol''. 2013 Apr 10; '''13''': 34
The ESR1 gene is associated with risk for canine mammary tumours. Description: Borge, Kaja Sverdrup, et al. The ESR1 gene is associated with risk for canine mammary tumours. ''BMC Vet Res''. 2013 Apr 10; '''9''': 69
LILRA3 is associated with benign prostatic hyperplasia risk in a Chinese Population. Description: Jiao, Yang, et al. LILRA3 is associated with benign prostatic hyperplasia risk in a Chinese Population. ''Int J Mol Sci''. 2013 Apr 24; '''14''' (5):8832-40
Centenarians as super-controls to assess the biological relevance of genetic risk factors for common age-related diseases: a proof of principle on type 2 diabetes. Description: Garagnani, Paolo, et al. Centenarians as super-controls to assess the biological relevance of genetic risk factors for common age-related diseases: a proof of principle on type 2 diabetes. ''Aging (Albany NY)''. 2013 May; '''5''' (5):373-85
Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data. Description: Powell, Joseph E, et al. Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data. ''PLoS Genet''. 2013 May; '''9''' (5):e1003502
Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement. Description: Schmidts, Miriam, et al. Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement. ''J Med Genet''. 2013 May; '''50''' (5):309-23
Genes encoding heterotrimeric G-proteins are associated with gray matter volume variations in the medial frontal cortex. Description: Chavarria-Siles, Ivan, et al. Genes encoding heterotrimeric G-proteins are associated with gray matter volume variations in the medial frontal cortex. ''Cereb Cortex''. 2013 May; '''23''' (5):1025-30
Genome-wide analysis in German shepherd dogs reveals association of a locus on CFA 27 with atopic dermatitis. Description: Tengvall, Katarina, et al. Genome-wide analysis in German shepherd dogs reveals association of a locus on CFA 27 with atopic dermatitis. ''PLoS Genet''. 2013 May; '''9''' (5):e1003475
Genome-wide analysis of runs of homozygosity identifies new susceptibility regions of lung cancer in Han Chinese. Description: Wang, Cheng, et al. Genome-wide analysis of runs of homozygosity identifies new susceptibility regions of lung cancer in Han Chinese. ''J Biomed Res''. 2013 May; '''27''' (3):208-14
Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. Description: Saxena, Richa, et al. Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. ''Diabetes''. 2013 May; '''62''' (5):1746-55
Human genetics in rheumatoid arthritis guides a high-throughput drug screen of the CD40 signaling pathway. Description: Li, Gang, et al. Human genetics in rheumatoid arthritis guides a high-throughput drug screen of the CD40 signaling pathway. ''PLoS Genet''. 2013 May; '''9''' (5):e1003487
Replication of established common genetic variants for adult BMI and childhood obesity in Greek adolescents: the TEENAGE study. Description: Ntalla, Ioanna, et al. Replication of established common genetic variants for adult BMI and childhood obesity in Greek adolescents: the TEENAGE study. ''Ann Hum Genet''. 2013 May; '''77''' (3):268-74
The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. Description: Weinhold, Niels, et al. The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. ''Nat Genet''. 2013 May; '''45''' (5):522-525
The confounding effect of cryptic relatedness for environmental risks of systolic blood pressure on cohort studies. Description: Shibata, Kyoko, et al. The confounding effect of cryptic relatedness for environmental risks of systolic blood pressure on cohort studies. ''Mol Genet Genomic Med''. 2013 May; '''1''' (1):45-53
The impact of polymorphisms in STAT6 on treatment outcome in HCV infected Taiwanese Chinese. Description: Lim, Yun-Ping, et al. The impact of polymorphisms in STAT6 on treatment outcome in HCV infected Taiwanese Chinese. ''BMC Immunol''. 2013 May 8; '''14''': 21
Genome-wide association study of antibody response to Newcastle disease virus in chicken. Description: Luo, Chenglong, et al. Genome-wide association study of antibody response to Newcastle disease virus in chicken. ''BMC Genet''. 2013 May 10; '''14''': 42
Variants in the 3' UTR of general Transcription factor IIF, polypeptide 2 affect female calving efficiency in Japanese Black cattle. Description: Sasaki, Shinji, et al. Variants in the 3' UTR of general Transcription factor IIF, polypeptide 2 affect female calving efficiency in Japanese Black cattle. ''BMC Genet''. 2013 May 10; '''14''': 41
Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP). Description: Reitz, C, et al. Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP). ''Transl Psychiatry''. 2013 May 14; '''3''': e256
Evaluation of the IL2/IL21, IL2RA and IL2RB genetic variants influence on the endogenous non-anterior uveitis genetic predisposition. Description: Cenit, Maria Carmen, et al. Evaluation of the IL2/IL21, IL2RA and IL2RB genetic variants influence on the endogenous non-anterior uveitis genetic predisposition. ''BMC Med Genet''. 2013 May 15; '''14''': 52
RTEL1 tagging SNPs and haplotypes were associated with glioma development. Description: Li, Gang, et al. RTEL1 tagging SNPs and haplotypes were associated with glioma development. ''Diagn Pathol''. 2013 May 17; '''8''': 83
Alzheimer's disease risk gene CD33 inhibits microglial uptake of amyloid beta. Description: Griciuc, Ana, et al. Alzheimer's disease risk gene CD33 inhibits microglial uptake of amyloid beta. ''Neuron''. 2013 May 22; '''78''' (4):631-43
A modest but significant effect of CGB5 gene promoter polymorphisms in modulating the risk of recurrent miscarriage. Description: Rull, Kristiina, et al. A modest but significant effect of CGB5 gene promoter polymorphisms in modulating the risk of recurrent miscarriage. ''Fertil Steril''. 2013 Jun; '''99''' (7):1930-6.e6
Association of chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression. Description: Duarte, J D, et al. Association of chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression. ''Pharmacogenomics J''. 2013 Jun; '''13''' (3):257-63
Common genetic variants associated with disease from genome-wide association studies are mutually exclusive in prostate cancer and rheumatoid arthritis. Description: Orozco, Gisela, et al. Common genetic variants associated with disease from genome-wide association studies are mutually exclusive in prostate cancer and rheumatoid arthritis. ''BJU Int''. 2013 Jun; '''111''' (7):1148-55
Definition of high-risk type 1 diabetes HLA-DR and HLA-DQ types using only three single nucleotide polymorphisms. Description: Nguyen, Cao, et al. Definition of high-risk type 1 diabetes HLA-DR and HLA-DQ types using only three single nucleotide polymorphisms. ''Diabetes''. 2013 Jun; '''62''' (6):2135-40
Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. Description: Hinks, Anne, et al. Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. ''Nat Genet''. 2013 Jun; '''45''' (6):664-9
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Description: Liu, Jimmy Z, et al. Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. ''Nat Genet''. 2013 Jun; '''45''' (6):670-5
Exploring the genetic basis of chronic periodontitis: a genome-wide association study. Description: Divaris, Kimon, et al. Exploring the genetic basis of chronic periodontitis: a genome-wide association study. ''Hum Mol Genet''. 2013 Jun 1; '''22''' (11):2312-24
Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets. Description: Grarup, Niels, et al. Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets. ''PLoS Genet''. 2013 Jun; '''9''' (6):e1003530
Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity. Description: Esko, Tonu, et al. Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity. ''Eur J Hum Genet''. 2013 Jun; '''21''' (6):659-65
Genetic polymorphisms in key methotrexate pathway genes are associated with response to treatment in rheumatoid arthritis patients. Description: Owen, S A, et al. Genetic polymorphisms in key methotrexate pathway genes are associated with response to treatment in rheumatoid arthritis patients. ''Pharmacogenomics J''. 2013 Jun; '''13''' (3):227-34
Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4. Description: Ma, R C W, et al. Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4. ''Diabetologia''. 2013 Jun; '''56''' (6):1291-305
Genome-wide association study of lung cancer in Korean non-smoking women. Description: Kim, Jin Hee, et al. Genome-wide association study of lung cancer in Korean non-smoking women. ''J Korean Med Sci''. 2013 Jun; '''28''' (6):840-7
Genome-wide association study of Tourette's syndrome. Description: Scharf, J M, et al. Genome-wide association study of Tourette's syndrome. ''Mol Psychiatry''. 2013 Jun; '''18''' (6):721-8
Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14. Description: Ruark, Elise, et al. Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14. ''Nat Genet''. 2013 Jun; '''45''' (6):686-9
Link between GIP and osteopontin in adipose tissue and insulin resistance. Description: Ahlqvist, Emma, et al. Link between GIP and osteopontin in adipose tissue and insulin resistance. ''Diabetes''. 2013 Jun; '''62''' (6):2088-94
Multiple populations of artemisinin-resistant Plasmodium falciparum in Cambodia. Description: Miotto, Olivo, et al. Multiple populations of artemisinin-resistant Plasmodium falciparum in Cambodia. ''Nat Genet''. 2013 Jun; '''45''' (6):648-55
Peeling back the evolutionary layers of molecular mechanisms responsive to exercise-stress in the skeletal muscle of the racing horse. Description: Kim, Hyeongmin, et al. Peeling back the evolutionary layers of molecular mechanisms responsive to exercise-stress in the skeletal muscle of the racing horse. ''DNA Res''. 2013 Jun; '''20''' (3):287-98
Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. Description: Randall, Joshua C, et al. Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. ''PLoS Genet''. 2013 Jun; '''9''' (6):e1003500
Association study of NRXN3 polymorphisms with schizophrenia and risperidone-induced bodyweight gain in Chinese Han population. Description: Hu, Xiaofeng, et al. Association study of NRXN3 polymorphisms with schizophrenia and risperidone-induced bodyweight gain in Chinese Han population. ''Prog Neuropsychopharmacol Biol Psychiatry''. 2013 Jun 3; '''43''': 197-202
Passive and active DNA methylation and the interplay with genetic variation in gene regulation. Description: Gutierrez-Arcelus, Maria, et al. Passive and active DNA methylation and the interplay with genetic variation in gene regulation. ''Elife''. 2013 Jun 4; '''2''': e00523
Comprehensive genotyping of the USA national maize inbred seed bank. Description: Romay, Maria C, et al. Comprehensive genotyping of the USA national maize inbred seed bank. ''Genome Biol''. 2013 Jun 11; '''14''' (6):R55
Novel genomic approaches unravel genetic architecture of complex traits in apple. Description: Kumar, Satish, et al. Novel genomic approaches unravel genetic architecture of complex traits in apple. ''BMC Genomics''. 2013 Jun 12; '''14''': 393
Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression. Description: Kote-Jarai, Zsofia, et al. Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression. ''Hum Mol Genet''. 2013 Jun 15; '''22''' (12):2520-8
Autosomal and uniparental portraits of the native populations of Sakha (Yakutia): implications for the peopling of Northeast Eurasia. Description: Fedorova, Sardana A, et al. Autosomal and uniparental portraits of the native populations of Sakha (Yakutia): implications for the peopling of Northeast Eurasia. ''BMC Evol Biol''. 2013 Jun 19; '''13''': 127
A DPYD variant (Y186C) in individuals of african ancestry is associated with reduced DPD enzyme activity. Description: Offer, S M, et al. A DPYD variant (Y186C) in individuals of african ancestry is associated with reduced DPD enzyme activity. ''Clin Pharmacol Ther''. 2013 Jul; '''94''' (1):158-66
A Novel ERAP2 Haplotype Structure in a Chilean Population: Implications for ERAP2 Protein Expression and Preeclampsia Risk. Description: Vanhille, Derek L, et al. A Novel ERAP2 Haplotype Structure in a Chilean Population: Implications for ERAP2 Protein Expression and Preeclampsia Risk. ''Mol Genet Genomic Med''. 2013 Jul 1; '''1''' (2):98-107
An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease. Description: Chu, Xun, et al. An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease. ''J Med Genet''. 2013 Jul; '''50''' (7):479-85
CD33 Alzheimer's disease locus: altered monocyte function and amyloid biology. Description: Bradshaw, Elizabeth M, et al. CD33 Alzheimer's disease locus: altered monocyte function and amyloid biology. ''Nat Neurosci''. 2013 Jul; '''16''' (7):848-50
Further evidence for association of polymorphisms in the CNR1 gene with cocaine addiction: confirmation in an independent sample and meta-analysis. Description: Clarke, Toni-Kim, et al. Further evidence for association of polymorphisms in the CNR1 gene with cocaine addiction: confirmation in an independent sample and meta-analysis. ''Addict Biol''. 2013 Jul; '''18''' (4):702-8
Identification of the NF-kappaB activating protein-like locus as a risk locus for rheumatoid arthritis. Description: Xie, Gang, et al. Identification of the NF-kappaB activating protein-like locus as a risk locus for rheumatoid arthritis. ''Ann Rheum Dis''. 2013 Jul; '''72''' (7):1249-54
Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panel. Description: Nievergelt, Caroline M, et al. Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panel. ''Investig Genet''. 2013 Jul 1; '''4''' (1):13
Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects. Description: Williams, Frances M K, et al. Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects. ''Ann Rheum Dis''. 2013 Jul; '''72''' (7):1141-8
Resistance to antidepressant treatment is associated with polymorphisms in the leptin gene, decreased leptin mRNA expression, and decreased leptin serum levels. Description: Kloiber, Stefan, et al. Resistance to antidepressant treatment is associated with polymorphisms in the leptin gene, decreased leptin mRNA expression, and decreased leptin serum levels. ''Eur Neuropsychopharmacol''. 2013 Jul; '''23''' (7):653-62
Variation in tau isoform expression in different brain regions and disease states. Description: Majounie, Elisa, et al. Variation in tau isoform expression in different brain regions and disease states. ''Neurobiol Aging''. 2013 Jul; '''34''' (7):1922.e7-1922.e12
Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study. Description: Ding, Keyue, et al. Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study. ''G3 (Bethesda)''. 2013 Jul 8; '''3''' (7):1061-8
The identification of 14 new genes for meat quality traits in chicken using a genome-wide association study. Description: Sun, Yanfa, et al. The identification of 14 new genes for meat quality traits in chicken using a genome-wide association study. ''BMC Genomics''. 2013 Jul 8; '''14''': 458
Using genome-wide association analysis to characterize environmental sensitivity of milk traits in dairy cattle. Description: Streit, Melanie, et al. Using genome-wide association analysis to characterize environmental sensitivity of milk traits in dairy cattle. ''G3 (Bethesda)''. 2013 Jul 8; '''3''' (7):1085-93
SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling. Description: Chudasama, Kishan Kumar, et al. SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling. ''Am J Hum Genet''. 2013 Jul 11; '''93''' (1):150-7
Integrative genomic analysis of the human immune response to influenza vaccination. Description: Franco, Luis M, et al. Integrative genomic analysis of the human immune response to influenza vaccination. ''Elife''. 2013 Jul 16; '''2''': e00299
Analysis of copy number variants by three detection algorithms and their association with body size in horses. Description: Metzger, Julia, et al. Analysis of copy number variants by three detection algorithms and their association with body size in horses. ''BMC Genomics''. 2013 Jul 18; '''14''': 487
Genetic variants predicting left ventricular hypertrophy in a diabetic population: a Go-DARTS study including meta-analysis. Description: Parry, Helen M, et al. Genetic variants predicting left ventricular hypertrophy in a diabetic population: a Go-DARTS study including meta-analysis. ''Cardiovasc Diabetol''. 2013 Jul 23; '''12''': 109
Possible association between common variants of the phenylalanine hydroxylase (PAH) gene and memory performance in healthy adults. Description: Teraishi, Toshiya, et al. Possible association between common variants of the phenylalanine hydroxylase (PAH) gene and memory performance in healthy adults. ''Behav Brain Funct''. 2013 Jul 30; '''9''': 30
A genome-wide association study of post-traumatic stress disorder identifies the retinoid-related orphan receptor alpha (RORA) gene as a significant risk locus. Description: Logue, M W, et al. A genome-wide association study of post-traumatic stress disorder identifies the retinoid-related orphan receptor alpha (RORA) gene as a significant risk locus. ''Mol Psychiatry''. 2013 Aug; '''18''' (8):937-42
Effects of common genetic variants associated with type 2 diabetes and glycemic traits on alpha- and beta-cell function and insulin action in humans. Description: Jonsson, Anna, et al. Effects of common genetic variants associated with type 2 diabetes and glycemic traits on alpha- and beta-cell function and insulin action in humans. ''Diabetes''. 2013 Aug; '''62''' (8):2978-83
EvoSNP-DB: A database of genetic diversity in East Asian populations. Description: Kim, Young Uk, et al. EvoSNP-DB: A database of genetic diversity in East Asian populations. ''BMB Rep''. 2013 Aug; '''46''' (8):416-21
Polygenic risk and white matter integrity in individuals at high risk of mood disorder. Description: Whalley, Heather C, et al. Polygenic risk and white matter integrity in individuals at high risk of mood disorder. ''Biol Psychiatry''. 2013 Aug 15; '''74''' (4):280-6
QTL mapping of egg albumen quality in egg layers. Description: Honkatukia, Mervi, et al. QTL mapping of egg albumen quality in egg layers. ''Genet Sel Evol''. 2013 Aug 16; '''45''': 31
Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome. Description: Campbell, Nicholas G, et al. Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome. ''Mol Autism''. 2013 Aug 16; '''4''' (1):28
Generalization of adiposity genetic loci to US Hispanic women. Description: Graff, M, et al. Generalization of adiposity genetic loci to US Hispanic women. ''Nutr Diabetes''. 2013 Aug 26; '''3''': e85
Molecular footprints of domestication and improvement in soybean revealed by whole genome re-sequencing. Description: Li, Ying-hui, et al. Molecular footprints of domestication and improvement in soybean revealed by whole genome re-sequencing. ''BMC Genomics''. 2013 Aug 28; '''14''': 579
A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome. Description: Clayton, P, et al. A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome. ''Eur J Endocrinol''. 2013 Sep; '''169''' (3):277-89
Association of matrix metalloproteinase 8 genetic polymorphisms with bronchial asthma in a Japanese population. Description: Shimoda, Terufumi, et al. Association of matrix metalloproteinase 8 genetic polymorphisms with bronchial asthma in a Japanese population. ''Allergy Rhinol (Providence)''. 2013 Fall; '''4''' (3):e132-9
Gene set analyses of genome-wide association studies on 49 quantitative traits measured in a single genetic epidemiology dataset. Description: Kim, Jihye, et al. Gene set analyses of genome-wide association studies on 49 quantitative traits measured in a single genetic epidemiology dataset. ''Genomics Inform''. 2013 Sep; '''11''' (3):135-41
Genome-wide association study of liver enzymes in korean children. Description: Park, Tae-Joon, et al. Genome-wide association study of liver enzymes in korean children. ''Genomics Inform''. 2013 Sep; '''11''' (3):149-54
Genome-wide association study of orthostatic hypotension and supine-standing blood pressure changes in two korean populations. Description: Hong, Kyung-Won, et al. Genome-wide association study of orthostatic hypotension and supine-standing blood pressure changes in two korean populations. ''Genomics Inform''. 2013 Sep; '''11''' (3):129-34
Identification of grouped rare and common variants via penalized logistic regression. Description: Ayers, Kristin L, et al. Identification of grouped rare and common variants via penalized logistic regression. ''Genet Epidemiol''. 2013 Sep; '''37''' (6):592-602
Increased Rate of Sporadic and Recurrent Rare Genic Copy Number Variants in Parkinson's Disease Among Ashkenazi Jews. Description: Liu, X, et al. Increased Rate of Sporadic and Recurrent Rare Genic Copy Number Variants in Parkinson's Disease Among Ashkenazi Jews. ''Mol Genet Genomic Med''. 2013 Sep; '''1''' (3):142-154
mu-Opioid receptor gene (OPRM1) polymorphism A118G: lack of association in Finnish populations with alcohol dependence or alcohol consumption. Description: Rouvinen-Lagerstrom, Noora, et al. mu-Opioid receptor gene (OPRM1) polymorphism A118G: lack of association in Finnish populations with alcohol dependence or alcohol consumption. ''Alcohol Alcohol''. 2013 Sep-Oct; '''48''' (5):519-25
Replication study of RAD54B and GREB1 polymorphisms and risk of PCOS in Han Chinese. Description: Wang, Zhenyan, et al. Replication study of RAD54B and GREB1 polymorphisms and risk of PCOS in Han Chinese. ''Reprod Biomed Online''. 2013 Sep; '''27''' (3):316-21
Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. Description: Jones, Ashley R, et al. Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. ''Neurobiol Aging''. 2013 Sep; '''34''' (9):2234.e1-7
A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation. Description: Martin, P-M, et al. A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation. ''Transl Psychiatry''. 2013 Sep 3; '''3''': e301
Signatures of selection identify loci associated with milk yield in sheep. Description: Moioli, Bianca, et al. Signatures of selection identify loci associated with milk yield in sheep. ''BMC Genet''. 2013 Sep 3; '''14''': 76
Association between rs10118757(A/G) in methylthioadenosine phosphorylase gene and coronary artery disease in Chinese Hans. Description: Lv, Xiaofei, et al. Association between rs10118757(A/G) in methylthioadenosine phosphorylase gene and coronary artery disease in Chinese Hans. ''Gene''. 2013 Sep 10; '''526''' (2):344-6
Genome-wide association analyses for carcass quality in crossbred beef cattle. Description: Lu, Duc, et al. Genome-wide association analyses for carcass quality in crossbred beef cattle. ''BMC Genet''. 2013 Sep 11; '''14''': 80
Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob disease. Description: Bishop, Matthew T, et al. Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob disease. ''BMC Med Genet''. 2013 Sep 12; '''14''': 91
Genetic diversity in black South Africans from Soweto. Description: May, Andrew, et al. Genetic diversity in black South Africans from Soweto. ''BMC Genomics''. 2013 Sep 23; '''14''': 644
Genetic analysis of the FBXO42 gene in Chinese Han patients with Parkinson's disease. Description: Gao, Kai, et al. Genetic analysis of the FBXO42 gene in Chinese Han patients with Parkinson's disease. ''BMC Neurol''. 2013 Sep 25; '''13''': 125
Improved estimation of inbreeding and kinship in pigs using optimized SNP panels. Description: Lopes, Marcos S, et al. Improved estimation of inbreeding and kinship in pigs using optimized SNP panels. ''BMC Genet''. 2013 Sep 25; '''14''': 92
Single nucleotide polymorphisms and haplotypes associated with feed efficiency in beef cattle. Description: Serao, Nick Vl, et al. Single nucleotide polymorphisms and haplotypes associated with feed efficiency in beef cattle. ''BMC Genet''. 2013 Sep 25; '''14''': 94
Human SNP links differential outcomes in inflammatory and infectious disease to a FOXO3-regulated pathway. Description: Lee, James C, et al. Human SNP links differential outcomes in inflammatory and infectious disease to a FOXO3-regulated pathway. ''Cell''. 2013 Sep 26; '''155''' (1):57-69
Associations between single-nucleotide polymorphism in the FNDC3A and autism spectrum disorder in a Korean population. Description: Ro, Myungja, et al. Associations between single-nucleotide polymorphism in the FNDC3A and autism spectrum disorder in a Korean population. ''Psychiatry Res''. 2013 Sep 30; '''209''' (2):246-8
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. Description: Chubb, Daniel, et al. Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. ''Nat Genet''. 2013 Oct; '''45''' (10):1221-1225
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. Description: Kasperaviciute, Dalia, et al. Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. ''Brain''. 2013 Oct; '''136''' (Pt 10):3140-50
Evidence that PICALM affects age at onset of Alzheimer's dementia in Down syndrome. Description: Jones, Emma L, et al. Evidence that PICALM affects age at onset of Alzheimer's dementia in Down syndrome. ''Neurobiol Aging''. 2013 Oct; '''34''' (10):2441.e1-5
Genetic modifiers of cystic fibrosis-related diabetes. Description: Blackman, Scott M, et al. Genetic modifiers of cystic fibrosis-related diabetes. ''Diabetes''. 2013 Oct; '''62''' (10):3627-35
Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic. Description: Han, Fang, et al. Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic. ''PLoS Genet''. 2013 Oct; '''9''' (10):e1003880
Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Description: Ripke, Stephan, et al. Genome-wide association analysis identifies 13 new risk loci for schizophrenia. ''Nat Genet''. 2013 Oct; '''45''' (10):1150-9
Mining the human phenome using allelic scores that index biological intermediates. Description: Evans, David M, et al. Mining the human phenome using allelic scores that index biological intermediates. ''PLoS Genet''. 2013 Oct; '''9''' (10):e1003919
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. Description: Davis, Lea K, et al. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. ''PLoS Genet''. 2013 Oct; '''9''' (10):e1003864
Genome-wide association study on serum alkaline phosphatase levels in a Chinese population. Description: Li, Jun, et al. Genome-wide association study on serum alkaline phosphatase levels in a Chinese population. ''BMC Genomics''. 2013 Oct 5; '''14''': 684
A genome-to-genome analysis of associations between human genetic variation, HIV-1 sequence diversity, and viral control. Description: Bartha, Istvan, et al. A genome-to-genome analysis of associations between human genetic variation, HIV-1 sequence diversity, and viral control. ''Elife''. 2013 Oct 29; '''2''': e01123
Aromatase inhibitor-induced modulation of breast density: clinical and genetic effects. Description: Henry, N L, et al. Aromatase inhibitor-induced modulation of breast density: clinical and genetic effects. ''Br J Cancer''. 2013 Oct 29; '''109''' (9):2331-9
An association study of TOLL and CARD with leprosy susceptibility in Chinese population. Description: Liu, Hong, et al. An association study of TOLL and CARD with leprosy susceptibility in Chinese population. ''Hum Mol Genet''. 2013 Nov 1; '''22''' (21):4430-7
Autosomal dominant diabetes arising from a Wolfram syndrome 1 mutation. Description: Bonnycastle, Lori L, et al. Autosomal dominant diabetes arising from a Wolfram syndrome 1 mutation. ''Diabetes''. 2013 Nov; '''62''' (11):3943-50
Developmental programming of growth: genetic variant in GH2 gene encoding placental growth hormone contributes to adult height determination. Description: Timasheva, Y, et al. Developmental programming of growth: genetic variant in GH2 gene encoding placental growth hormone contributes to adult height determination. ''Placenta''. 2013 Nov; '''34''' (11):995-1001
Discovery and refinement of loci associated with lipid levels. Description: Willer, Cristen J, et al. Discovery and refinement of loci associated with lipid levels. ''Nat Genet''. 2013 Nov; '''45''' (11):1274-1283
Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects. Description: Patsopoulos, Nikolaos A, et al. Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects. ''PLoS Genet''. 2013 Nov; '''9''' (11):e1003926
Genetic susceptibility to obesity and diet intakes: association and interaction analyses in the Malmo Diet and Cancer Study. Description: Rukh, Gull, et al. Genetic susceptibility to obesity and diet intakes: association and interaction analyses in the Malmo Diet and Cancer Study. ''Genes Nutr''. 2013 Nov; '''8''' (6):535-47
Genome-wide Association Study of Chicken Plumage Pigmentation. Description: Park, Mi Na, et al. Genome-wide Association Study of Chicken Plumage Pigmentation. ''Asian-Australas J Anim Sci''. 2013 Nov; '''26''' (11):1523-8
Reconstructing the population genetic history of the Caribbean. Description: Moreno-Estrada, Andres, et al. Reconstructing the population genetic history of the Caribbean. ''PLoS Genet''. 2013 Nov; '''9''' (11):e1003925
Ridge regression in prediction problems: automatic choice of the ridge parameter. Description: Cule, Erika, et al. Ridge regression in prediction problems: automatic choice of the ridge parameter. ''Genet Epidemiol''. 2013 Nov; '''37''' (7):704-14
Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjogren's syndrome. Description: Lessard, Christopher J, et al. Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjogren's syndrome. ''Nat Genet''. 2013 Nov; '''45''' (11):1284-92
Variation in psychosis gene ZNF804A is associated with a refined schizotypy phenotype but not neurocognitive performance in a large young male population. Description: Stefanis, Nicholas C, et al. Variation in psychosis gene ZNF804A is associated with a refined schizotypy phenotype but not neurocognitive performance in a large young male population. ''Schizophr Bull''. 2013 Nov; '''39''' (6):1252-60
Association of Parkinson disease with structural and regulatory variants in the HLA region. Description: Wissemann, William T, et al. Association of Parkinson disease with structural and regulatory variants in the HLA region. ''Am J Hum Genet''. 2013 Nov 7; '''93''' (5):984-93
The roles of FMRP-regulated genes in autism spectrum disorder: single- and multiple-hit genetic etiologies. Description: Steinberg, Julia, et al. The roles of FMRP-regulated genes in autism spectrum disorder: single- and multiple-hit genetic etiologies. ''Am J Hum Genet''. 2013 Nov 7; '''93''' (5):825-39
Body mass index, but not FTO genotype or major depressive disorder, influences brain structure. Description: Cole, J H, et al. Body mass index, but not FTO genotype or major depressive disorder, influences brain structure. ''Neuroscience''. 2013 Nov 12; '''252''': 109-17
Emerging paradigms in genomics-based crop improvement. Description: Bohra, Abhishek. Emerging paradigms in genomics-based crop improvement. ''ScientificWorldJournal''. 2013 Nov 17; '''2013''': 585467
A genetic basis for the variable effect of smoking/nicotine on Parkinson's disease. Description: Hill-Burns, E M, et al. A genetic basis for the variable effect of smoking/nicotine on Parkinson's disease. ''Pharmacogenomics J''. 2013 Dec; '''13''' (6):530-7
A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis. Description: Weidinger, Stephan, et al. A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis. ''Hum Mol Genet''. 2013 Dec 1; '''22''' (23):4841-56
Gene-environment interaction effects on lung function- a genome-wide association study within the Framingham heart study. Description: Liao, Shu-Yi, et al. Gene-environment interaction effects on lung function- a genome-wide association study within the Framingham heart study. ''Environ Health''. 2013 Dec 1; '''12''': 101
Guided exploration of genomic risk for gray matter abnormalities in schizophrenia using parallel independent component analysis with reference. Description: Chen, Jiayu, et al. Guided exploration of genomic risk for gray matter abnormalities in schizophrenia using parallel independent component analysis with reference. ''Neuroimage''. 2013 Dec; '''83''': 384-96
RTN4 and FBXL17 Genes are Associated with Coronary Heart Disease in Genome-Wide Association Analysis of Lithuanian Families. Description: Domarkiene, I, et al. RTN4 and FBXL17 Genes are Associated with Coronary Heart Disease in Genome-Wide Association Analysis of Lithuanian Families. ''Balkan J Med Genet''. 2013 Dec; '''16''' (2):17-22
Pathways systematically associated to Hirschsprung's disease. Description: Fernandez, Raquel M, et al. Pathways systematically associated to Hirschsprung's disease. ''Orphanet J Rare Dis''. 2013 Dec 2; '''8''': 187
Discovering epistasis in large scale genetic association studies by exploiting graphics cards. Description: Chen, Gary K, et al. Discovering epistasis in large scale genetic association studies by exploiting graphics cards. ''Front Genet''. 2013 Dec 3; '''4''': 266
Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism. Description: Warrier, Varun, et al. Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism. ''Mol Autism''. 2013 Dec 9; '''4''' (1):48
Genome-wide analyses implicate 33 loci in heritable dog osteosarcoma, including regulatory variants near CDKN2A/B. Description: Karlsson, Elinor K, et al. Genome-wide analyses implicate 33 loci in heritable dog osteosarcoma, including regulatory variants near CDKN2A/B. ''Genome Biol''. 2013 Dec 12; '''14''' (12):R132
Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease). Description: Xie, Zhihui, et al. Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease). ''Rare Dis''. 2013 Dec 12; '''1''' (1):
Genomic divergence of zebu and taurine cattle identified through high-density SNP genotyping. Description: Porto-Neto, Laercio R, et al. Genomic divergence of zebu and taurine cattle identified through high-density SNP genotyping. ''BMC Genomics''. 2013 Dec 13; '''14''': 876
A genome wide study of genetic adaptation to high altitude in feral Andean Horses of the paramo. Description: Hendrickson, Sher L. A genome wide study of genetic adaptation to high altitude in feral Andean Horses of the paramo. ''BMC Evol Biol''. 2013 Dec 17; '''13''': 273
RNA-Seq optimization with eQTL gold standards. Description: Ellis, Shannon E, et al. RNA-Seq optimization with eQTL gold standards. ''BMC Genomics''. 2013 Dec 17; '''14''': 892
Dysregulation of glucocorticoid receptor co-factors FKBP5, BAG1 and PTGES3 in prefrontal cortex in psychotic illness. Description: Sinclair, Duncan, et al. Dysregulation of glucocorticoid receptor co-factors FKBP5, BAG1 and PTGES3 in prefrontal cortex in psychotic illness. ''Sci Rep''. 2013 Dec 18; '''3''': 3539
Genome wide association studies in presence of misclassified binary responses. Description: Smith, Shannon, et al. Genome wide association studies in presence of misclassified binary responses. ''BMC Genet''. 2013 Dec 26; '''14''': 124
A 3'UTR polymorphism of IL-6R is associated with Chinese pediatric tuberculosis. Description: Shen, Chen, et al. A 3'UTR polymorphism of IL-6R is associated with Chinese pediatric tuberculosis. ''Biomed Res Int''. 2014; '''2014''': 483759
A candidate gene approach identifies an IL33 genetic variant as a novel genetic risk factor for GCA. Description: Marquez, Ana, et al. A candidate gene approach identifies an IL33 genetic variant as a novel genetic risk factor for GCA. ''PLoS One''. 2014; '''9''' (11):e113476
A CARD9 polymorphism is associated with decreased likelihood of persistent conjugated hyperbilirubinemia in intestinal failure. Description: Burghardt, Karolina Maria, et al. A CARD9 polymorphism is associated with decreased likelihood of persistent conjugated hyperbilirubinemia in intestinal failure. ''PLoS One''. 2014; '''9''' (1):e85915
Accounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases. Description: Chang, Diana, et al. Accounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases. ''PLoS One''. 2014; '''9''' (12):e113684
Accounting for relatedness in family-based association studies: application to Genetic Analysis Workshop 18 data. Description: Eu-Ahsunthornwattana, Jakris, et al. Accounting for relatedness in family-based association studies: application to Genetic Analysis Workshop 18 data. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S79
Accurate and robust prediction of genetic relationship from whole-genome sequences. Description: Li, Hong, et al. Accurate and robust prediction of genetic relationship from whole-genome sequences. ''PLoS One''. 2014; '''9''' (2):e85437
A chromosomal region on ECA13 is associated with maxillary prognathism in horses. Description: Signer-Hasler, Heidi, et al. A chromosomal region on ECA13 is associated with maxillary prognathism in horses. ''PLoS One''. 2014; '''9''' (1):e86607
A co-association network analysis of the genetic determination of pig conformation, growth and fatness. Description: Puig-Oliveras, Anna, et al. A co-association network analysis of the genetic determination of pig conformation, growth and fatness. ''PLoS One''. 2014; '''9''' (12):e114862
A colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis. Description: Real, Luis M, et al. A colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis. ''PLoS One''. 2014; '''9''' (6):e101178
A COLQ missense mutation in Labrador Retrievers having congenital myasthenic syndrome. Description: Rinz, Caitlin J, et al. A COLQ missense mutation in Labrador Retrievers having congenital myasthenic syndrome. ''PLoS One''. 2014; '''9''' (8):e106425
A comparison of multivariate genome-wide association methods. Description: Galesloot, Tessel E, et al. A comparison of multivariate genome-wide association methods. ''PLoS One''. 2014; '''9''' (4):e95923
A comparison of whole genome sequencing with exome sequencing for family-based association studies. Description: Lacey, Sean, et al. A comparison of whole genome sequencing with exome sequencing for family-based association studies. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S38
Admixture mapping and subsequent fine-mapping suggests a biologically relevant and novel association on chromosome 11 for type 2 diabetes in African Americans. Description: Jeff, Janina M, et al. Admixture mapping and subsequent fine-mapping suggests a biologically relevant and novel association on chromosome 11 for type 2 diabetes in African Americans. ''PLoS One''. 2014; '''9''' (3):e86931
A genetic variant in 12q13, a possible risk factor for bipolar disorder, is associated with depressive state, accounting for stressful life events. Description: Shimasaki, Ayu, et al. A genetic variant in 12q13, a possible risk factor for bipolar disorder, is associated with depressive state, accounting for stressful life events. ''PLoS One''. 2014; '''9''' (12):e115135
A genome-wide association study for diabetic retinopathy in a Japanese population: potential association with a long intergenic non-coding RNA. Description: Awata, Takuya, et al. A genome-wide association study for diabetic retinopathy in a Japanese population: potential association with a long intergenic non-coding RNA. ''PLoS One''. 2014; '''9''' (11):e111715
A genome-wide association study identifies a locus on TERT for mean telomere length in Han Chinese. Description: Liu, Yun, et al. A genome-wide association study identifies a locus on TERT for mean telomere length in Han Chinese. ''PLoS One''. 2014; '''9''' (1):e85043
A genome wide association study of mathematical ability reveals an association at chromosome 3q29, a locus associated with autism and learning difficulties: a preliminary study. Description: Baron-Cohen, Simon, et al. A genome wide association study of mathematical ability reveals an association at chromosome 3q29, a locus associated with autism and learning difficulties: a preliminary study. ''PLoS One''. 2014; '''9''' (5):e96374
A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese. Description: Chang, Su-Wei, et al. A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese. ''PLoS One''. 2014; '''9''' (6):e99724
A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis. Description: Rafiq, Sajjad, et al. A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis. ''PLoS One''. 2014; '''9''' (12):e101488
A genome-wide "pleiotropy scan" does not identify new susceptibility loci for estrogen receptor negative breast cancer. Description: Campa, Daniele, et al. A genome-wide "pleiotropy scan" does not identify new susceptibility loci for estrogen receptor negative breast cancer. ''PLoS One''. 2014; '''9''' (2):e85955
Allele-specific methylation occurs at genetic variants associated with complex disease. Description: Hutchinson, John N, et al. Allele-specific methylation occurs at genetic variants associated with complex disease. ''PLoS One''. 2014; '''9''' (6):e98464
Allelic variant in the anti-Mullerian hormone gene leads to autosomal and temperature-dependent sex reversal in a selected Nile tilapia line. Description: Wessels, Stephan, et al. Allelic variant in the anti-Mullerian hormone gene leads to autosomal and temperature-dependent sex reversal in a selected Nile tilapia line. ''PLoS One''. 2014; '''9''' (8):e104795
A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH). Description: Drogemuller, Michaela, et al. A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH). ''PLoS Genet''. 2014; '''10''' (5):e1004370
An adaptive permutation approach for genome-wide association study: evaluation and recommendations for use. Description: Che, Ronglin, et al. An adaptive permutation approach for genome-wide association study: evaluation and recommendations for use. ''BioData Min''. 2014; '''7''': 9
Analysis of ancestral and functionally relevant CD5 variants in systemic lupus erythematosus patients. Description: Cenit, Maria Carmen, et al. Analysis of ancestral and functionally relevant CD5 variants in systemic lupus erythematosus patients. ''PLoS One''. 2014; '''9''' (11):e113090
Analysis of multiple association studies provides evidence of an expression QTL hub in gene-gene interaction network affecting HDL cholesterol levels. Description: Ma, Li, et al. Analysis of multiple association studies provides evidence of an expression QTL hub in gene-gene interaction network affecting HDL cholesterol levels. ''PLoS One''. 2014; '''9''' (3):e92469
Analysis of nuclear export sequence regions of FUS-Related RNA-binding proteins in essential tremor. Description: Lorenzo-Betancor, Oswaldo, et al. Analysis of nuclear export sequence regions of FUS-Related RNA-binding proteins in essential tremor. ''PLoS One''. 2014; '''9''' (11):e111989
A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development. Description: Darlow, J M, et al. A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development. ''Mol Genet Genomic Med''. 2014 Jan; '''2''' (1):7-29
An Intronic SINE insertion in FAM161A that causes exon-skipping is associated with progressive retinal atrophy in Tibetan Spaniels and Tibetan Terriers. Description: Downs, Louise M, et al. An Intronic SINE insertion in FAM161A that causes exon-skipping is associated with progressive retinal atrophy in Tibetan Spaniels and Tibetan Terriers. ''PLoS One''. 2014; '''9''' (4):e93990
A novel missense mutation in ADAMTS10 in Norwegian Elkhound primary glaucoma. Description: Ahonen, Saija J, et al. A novel missense mutation in ADAMTS10 in Norwegian Elkhound primary glaucoma. ''PLoS One''. 2014; '''9''' (11):e111941
A novel mutation in TTC8 is associated with progressive retinal atrophy in the golden retriever. Description: Downs, Louise M, et al. A novel mutation in TTC8 is associated with progressive retinal atrophy in the golden retriever. ''Canine Genet Epidemiol''. 2014; '''1''': 4
A novel splice-site mutation in ALS2 establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias. Description: Siddiqi, Saima, et al. A novel splice-site mutation in ALS2 establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias. ''PLoS One''. 2014; '''9''' (12):e113258
Applying compressed sensing to genome-wide association studies. Description: Vattikuti, Shashaank, et al. Applying compressed sensing to genome-wide association studies. ''Gigascience''. 2014; '''3''': 10
Are genetic risk factors for psychosis also associated with dimension-specific psychotic experiences in adolescence? Description: Sieradzka, Dominika, et al. Are genetic risk factors for psychosis also associated with dimension-specific psychotic experiences in adolescence? ''PLoS One''. 2014; '''9''' (4):e94398
A regulatory polymorphism in HAVCR2 modulates susceptibility to HIV-1 infection. Description: Sironi, Manuela, et al. A regulatory polymorphism in HAVCR2 modulates susceptibility to HIV-1 infection. ''PLoS One''. 2014; '''9''' (9):e106442
A review of multivariate analyses in imaging genetics. Description: Liu, Jingyu, et al. A review of multivariate analyses in imaging genetics. ''Front Neuroinform''. 2014; '''8''': 29
Assessing SNP-SNP interactions among DNA repair, modification and metabolism related pathway genes in breast cancer susceptibility. Description: Sapkota, Yadav, et al. Assessing SNP-SNP interactions among DNA repair, modification and metabolism related pathway genes in breast cancer susceptibility. ''PLoS One''. 2014; '''8''' (6):e64896
Assessing the effects of common variation in the FOXP2 gene on human brain structure. Description: Hoogman, Martine, et al. Assessing the effects of common variation in the FOXP2 gene on human brain structure. ''Front Hum Neurosci''. 2014; '''8''': 473
Association between Expression Quantitative Trait Loci and Metabolic Traits in Two Korean Populations. Description: Hong, Kyung-Won, et al. Association between Expression Quantitative Trait Loci and Metabolic Traits in Two Korean Populations. ''PLoS One''. 2014; '''9''' (12):e114128
Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhauser syndrome and central corneal thickness. Description: Davidson, Alice E, et al. Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhauser syndrome and central corneal thickness. ''PLoS One''. 2014; '''9''' (8):e104163
Association of COMT and COMT-DRD2 interaction with creative potential. Description: Zhang, Shun, et al. Association of COMT and COMT-DRD2 interaction with creative potential. ''Front Hum Neurosci''. 2014; '''8''': 216
Association of genetic ancestry with breast cancer in ethnically diverse women from Chicago. Description: Al-Alem, Umaima, et al. Association of genetic ancestry with breast cancer in ethnically diverse women from Chicago. ''PLoS One''. 2014; '''9''' (11):e112916
Association of IRGM gene mutations with inflammatory bowel disease in the Indian population. Description: Baskaran, Kirankumar, et al. Association of IRGM gene mutations with inflammatory bowel disease in the Indian population. ''PLoS One''. 2014; '''9''' (9):e106863
Association of NOD2 and IL23R with inflammatory bowel disease in Puerto Rico. Description: Ballester, Veroushka, et al. Association of NOD2 and IL23R with inflammatory bowel disease in Puerto Rico. ''PLoS One''. 2014; '''9''' (9):e108204
Association of the hepatocyte growth factor gene with keratoconus in an Australian population. Description: Sahebjada, Srujana, et al. Association of the hepatocyte growth factor gene with keratoconus in an Australian population. ''PLoS One''. 2014; '''9''' (1):e84067
Association of variants at BCL11A and HBS1L-MYB with hemoglobin F and hospitalization rates among sickle cell patients in Cameroon. Description: Wonkam, Ambroise, et al. Association of variants at BCL11A and HBS1L-MYB with hemoglobin F and hospitalization rates among sickle cell patients in Cameroon. ''PLoS One''. 2014; '''9''' (3):e92506
ATP-Binding Cassette Genes Genotype and Expression: A Potential Association with Pancreatic Cancer Development and Chemoresistance? Description: Pang, Li, et al. ATP-Binding Cassette Genes Genotype and Expression: A Potential Association with Pancreatic Cancer Development and Chemoresistance? ''Gastroenterol Res Pract''. 2014; '''2014''': 414931
A two-stage association study suggests BRAP as a susceptibility gene for schizophrenia. Description: Zhang, Fuquan, et al. A two-stage association study suggests BRAP as a susceptibility gene for schizophrenia. ''PLoS One''. 2014; '''9''' (1):e86037
A variant of IL6R is associated with the recurrence of atrial fibrillation after catheter ablation in a Chinese Han population. Description: Wu, Gang, et al. A variant of IL6R is associated with the recurrence of atrial fibrillation after catheter ablation in a Chinese Han population. ''PLoS One''. 2014; '''9''' (6):e99623
A web-portal for interactive data exploration, visualization, and hypothesis testing. Description: Bartsch, Hauke, et al. A web-portal for interactive data exploration, visualization, and hypothesis testing. ''Front Neuroinform''. 2014; '''8''': 25
BAIAP2 is related to emotional modulation of human memory strength. Description: Luksys, Gediminas, et al. BAIAP2 is related to emotional modulation of human memory strength. ''PLoS One''. 2014; '''9''' (1):e83707
Bivariate linear mixed model analysis to test joint associations of genetic variants on systolic and diastolic blood pressure. Description: Neupane, Binod, et al. Bivariate linear mixed model analysis to test joint associations of genetic variants on systolic and diastolic blood pressure. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S75
Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome. Description: Schulte, Eva C, et al. Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome. ''PLoS One''. 2014; '''9''' (5):e98092
CARAT-GxG: CUDA-Accelerated Regression Analysis Toolkit for Large-Scale Gene-Gene Interaction with GPU Computing System. Description: Lee, Sungyoung, et al. CARAT-GxG: CUDA-Accelerated Regression Analysis Toolkit for Large-Scale Gene-Gene Interaction with GPU Computing System. ''Cancer Inform''. 2014; '''13''' (Suppl 7):27-33
Catechol-O-methyltransferase Val158Met polymorphism is associated with somatosensory amplification and nocebo responses. Description: Wendt, Laura, et al. Catechol-O-methyltransferase Val158Met polymorphism is associated with somatosensory amplification and nocebo responses. ''PLoS One''. 2014; '''9''' (9):e107665
CDKAL1-related single nucleotide polymorphisms are associated with insulin resistance in a cross-sectional cohort of Greek children. Description: Rask-Andersen, Mathias, et al. CDKAL1-related single nucleotide polymorphisms are associated with insulin resistance in a cross-sectional cohort of Greek children. ''PLoS One''. 2014; '''9''' (4):e93193
Characterisation of genetic variation in ST8SIA2 and its interaction region in NCAM1 in patients with bipolar disorder. Description: Shaw, Alex D, et al. Characterisation of genetic variation in ST8SIA2 and its interaction region in NCAM1 in patients with bipolar disorder. ''PLoS One''. 2014; '''9''' (3):e92556
Characterization of genome-methylome interactions in 22 nuclear pedigrees. Description: Plongthongkum, Nongluk, et al. Characterization of genome-methylome interactions in 22 nuclear pedigrees. ''PLoS One''. 2014; '''9''' (7):e99313
Combined analysis with copy number variation identifies risk loci in lung cancer. Description: Li, Xinlei, et al. Combined analysis with copy number variation identifies risk loci in lung cancer. ''Biomed Res Int''. 2014; '''2014''': 469103
Combined linkage and association studies show that HLA class II variants control levels of antibodies against Epstein-Barr virus antigens. Description: Pedergnana, Vincent, et al. Combined linkage and association studies show that HLA class II variants control levels of antibodies against Epstein-Barr virus antigens. ''PLoS One''. 2014; '''9''' (7):e102501
Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery disease. Description: Sabater-Lleal, Maria, et al. Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery disease. ''PLoS One''. 2014; '''9''' (8):e104082
Comparison of two methods for analysis of gene-environment interactions in longitudinal family data: the Framingham heart study. Description: Sung, Yun Ju, et al. Comparison of two methods for analysis of gene-environment interactions in longitudinal family data: the Framingham heart study. ''Front Genet''. 2014; '''5''': 9
Comprehensive analysis of the association of EGFR, CALM3 and SMARCD1 gene polymorphisms with BMD in Caucasian women. Description: Zhou, Qiu-Hong, et al. Comprehensive analysis of the association of EGFR, CALM3 and SMARCD1 gene polymorphisms with BMD in Caucasian women. ''PLoS One''. 2014; '''9''' (11):e112358
Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures. Description: Evans, Tiffany-Jane, et al. Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures. ''PLoS One''. 2014; '''9''' (10):e110255
Congenital cataracts: de novo gene conversion event in CRYBB2. Description: Garnai, Sarah J, et al. Congenital cataracts: de novo gene conversion event in CRYBB2. ''Mol Vis''. 2014; '''20''': 1579-93
Congenital hepatic fibrosis in the Franches-Montagnes horse is associated with the polycystic kidney and hepatic disease 1 (PKHD1) gene. Description: Drogemuller, Michaela, et al. Congenital hepatic fibrosis in the Franches-Montagnes horse is associated with the polycystic kidney and hepatic disease 1 (PKHD1) gene. ''PLoS One''. 2014; '''9''' (10):e110125
Copy number variation in Thai population. Description: Suktitipat, Bhoom, et al. Copy number variation in Thai population. ''PLoS One''. 2014; '''9''' (8):e104355
Creation and Validation of an EMR-based Algorithm for Identifying Major Adverse Cardiac Events while on Statins. Description: Wei, Wei-Qi, et al. Creation and Validation of an EMR-based Algorithm for Identifying Major Adverse Cardiac Events while on Statins. ''AMIA Jt Summits Transl Sci Proc''. 2014; '''2014''': 112-9
Deletion in the EVC2 gene causes chondrodysplastic dwarfism in Tyrolean Grey cattle. Description: Murgiano, Leonardo, et al. Deletion in the EVC2 gene causes chondrodysplastic dwarfism in Tyrolean Grey cattle. ''PLoS One''. 2014; '''9''' (4):e94861
Dense genotyping of immune-related loci identifies variants associated with clearance of HPV among HIV-positive women in the HIV epidemiology research study (HERS). Description: Sudenga, Staci L, et al. Dense genotyping of immune-related loci identifies variants associated with clearance of HPV among HIV-positive women in the HIV epidemiology research study (HERS). ''PLoS One''. 2014; '''9''' (6):e99109
Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma. Description: Carnes, Megan Ulmer, et al. Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma. ''PLoS Genet''. 2014; '''10''' (5):e1004372
DNA methylation changes in the postmortem dorsolateral prefrontal cortex of patients with schizophrenia. Description: Numata, Shusuke, et al. DNA methylation changes in the postmortem dorsolateral prefrontal cortex of patients with schizophrenia. ''Front Genet''. 2014; '''5''': 280
Endometriosis is associated with rare copy number variants. Description: Chettier, Rakesh, et al. Endometriosis is associated with rare copy number variants. ''PLoS One''. 2014; '''9''' (8):e103968
Endothelial protein C receptor gene variants not associated with severe malaria in ghanaian children. Description: Schuldt, Kathrin, et al. Endothelial protein C receptor gene variants not associated with severe malaria in ghanaian children. ''PLoS One''. 2014; '''9''' (12):e115770
Environmental and genetic contributors to salivary testosterone levels in infants. Description: Xia, Kai, et al. Environmental and genetic contributors to salivary testosterone levels in infants. ''Front Endocrinol (Lausanne)''. 2014; '''5''': 187
Estimating and adjusting for ancestry admixture in statistical methods for relatedness inference, heritability estimation, and association testing. Description: Thornton, Timothy, et al. Estimating and adjusting for ancestry admixture in statistical methods for relatedness inference, heritability estimation, and association testing. ''BMC Proc''. 2014; '''8''' (Suppl 1):S5
Evaluating the coverage and potential of imputing the exome microarray with next-generation imputation using the 1000 Genomes Project. Description: Tantoso, Erwin, et al. Evaluating the coverage and potential of imputing the exome microarray with next-generation imputation using the 1000 Genomes Project. ''PLoS One''. 2014; '''9''' (9):e106681
Evaluation of SLE Susceptibility Genes in Malaysians. Description: Molineros, Julio E, et al. Evaluation of SLE Susceptibility Genes in Malaysians. ''Autoimmune Dis''. 2014; '''2014''': 305436
False-positive rates in two-point parametric linkage analysis. Description: Szymczak, Silke, et al. False-positive rates in two-point parametric linkage analysis. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S110
Familial young-onset diabetes, pre-diabetes and cardiovascular disease are associated with genetic variants of DACH1 in Chinese. Description: Ma, Ronald Ching Wan, et al. Familial young-onset diabetes, pre-diabetes and cardiovascular disease are associated with genetic variants of DACH1 in Chinese. ''PLoS One''. 2014; '''9''' (1):e84770
Fast principal component analysis of large-scale genome-wide data. Description: Abraham, Gad, et al. Fast principal component analysis of large-scale genome-wide data. ''PLoS One''. 2014; '''9''' (4):e93766
First regional evaluation of nuclear genetic diversity and population structure in northeastern coyotes ( Canis latrans). Description: Monzon, Javier. First regional evaluation of nuclear genetic diversity and population structure in northeastern coyotes ( Canis latrans). ''F1000Res''. 2014; '''3''': 66
Footprints of directional selection in wild Atlantic salmon populations: evidence for parasite-driven evolution? Description: Zueva, Ksenia J, et al. Footprints of directional selection in wild Atlantic salmon populations: evidence for parasite-driven evolution? ''PLoS One''. 2014; '''9''' (3):e91672
Functional annotation of putative regulatory elements at cancer susceptibility Loci. Description: Rosse, Stephanie A, et al. Functional annotation of putative regulatory elements at cancer susceptibility Loci. ''Cancer Inform''. 2014; '''13''' (Suppl 2):5-17
Gender specific association of RAS gene polymorphism with essential hypertension: a case-control study. Description: Dhanachandra Singh, Kh, et al. Gender specific association of RAS gene polymorphism with essential hypertension: a case-control study. ''Biomed Res Int''. 2014; '''2014''': 538053
Gene polymorphisms of micrornas in Helicobacter pylori-induced high risk atrophic gastritis and gastric cancer. Description: Kupcinskas, Juozas, et al. Gene polymorphisms of micrornas in Helicobacter pylori-induced high risk atrophic gastritis and gastric cancer. ''PLoS One''. 2014; '''9''' (1):e87467
Genetic association analysis for common variants in the Genetic Analysis Workshop 18 data: a Dirichlet regression approach. Description: Espin-Garcia, Osvaldo, et al. Genetic association analysis for common variants in the Genetic Analysis Workshop 18 data: a Dirichlet regression approach. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S70
Genetic association analysis of paratuberculosis forms in holstein-friesian cattle. Description: Vazquez, Patricia, et al. Genetic association analysis of paratuberculosis forms in holstein-friesian cattle. ''Vet Med Int''. 2014; '''2014''': 321327
Genetic association analysis using weighted false discovery rate approach on Genetic Analysis Workshop 18 data. Description: Qiu, Xin, et al. Genetic association analysis using weighted false discovery rate approach on Genetic Analysis Workshop 18 data. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S76
Genetic basis of delay discounting in frequent gamblers: examination of a priori candidates and exploration of a panel of dopamine-related loci. Description: Gray, Joshua C, et al. Genetic basis of delay discounting in frequent gamblers: examination of a priori candidates and exploration of a panel of dopamine-related loci. ''Brain Behav''. 2014; '''4''' (6):812-21
Genetic determinants of chronic obstructive pulmonary disease in South Indian male smokers. Description: Arja, Cholendra, et al. Genetic determinants of chronic obstructive pulmonary disease in South Indian male smokers. ''PLoS One''. 2014; '''9''' (2):e89957
Genetic diversity and population structure among six cattle breeds in South Africa using a whole genome SNP panel. Description: Makina, Sithembile O, et al. Genetic diversity and population structure among six cattle breeds in South Africa using a whole genome SNP panel. ''Front Genet''. 2014; '''5''': 333
Genetic factors regulating lung vasculature and immune cell functions associate with resistance to pneumococcal infection. Description: Jonczyk, Magda S, et al. Genetic factors regulating lung vasculature and immune cell functions associate with resistance to pneumococcal infection. ''PLoS One''. 2014; '''9''' (3):e89831
Genetic risk score of NOS gene variants associated with myocardial infarction correlates with coronary incidence across Europe. Description: Carreras-Torres, Robert, et al. Genetic risk score of NOS gene variants associated with myocardial infarction correlates with coronary incidence across Europe. ''PLoS One''. 2014; '''9''' (5):e96504
Genetic variability of the grey wolf Canis lupus in the Caucasus in comparison with Europe and the Middle East: distinct or intermediary population? Description: Pilot, Malgorzata, et al. Genetic variability of the grey wolf Canis lupus in the Caucasus in comparison with Europe and the Middle East: distinct or intermediary population? ''PLoS One''. 2014; '''9''' (4):e93828
Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network. Description: Malinowski, Jennifer R, et al. Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network. ''PLoS One''. 2014; '''9''' (12):e111301
Genetic variation in DNA repair pathways and risk of non-Hodgkin's lymphoma. Description: Rendleman, Justin, et al. Genetic variation in DNA repair pathways and risk of non-Hodgkin's lymphoma. ''PLoS One''. 2014; '''9''' (7):e101685
Genetic variation modifies risk for neurodegeneration based on biomarker status. Description: Hohman, Timothy J, et al. Genetic variation modifies risk for neurodegeneration based on biomarker status. ''Front Aging Neurosci''. 2014; '''6''': 183
Genetic variations of PIP4K2A confer vulnerability to poor antipsychotic response in severely ill schizophrenia patients. Description: Kaur, Harpreet, et al. Genetic variations of PIP4K2A confer vulnerability to poor antipsychotic response in severely ill schizophrenia patients. ''PLoS One''. 2014; '''9''' (7):e102556
Genome wide analysis indicates genes for basement membrane and cartilage matrix proteins as candidates for hip dysplasia in Labrador Retrievers. Description: Lavrijsen, Ineke C M, et al. Genome wide analysis indicates genes for basement membrane and cartilage matrix proteins as candidates for hip dysplasia in Labrador Retrievers. ''PLoS One''. 2014; '''9''' (1):e87735
Genome-wide analysis of cold adaptation in indigenous Siberian populations. Description: Cardona, Alexia, et al. Genome-wide analysis of cold adaptation in indigenous Siberian populations. ''PLoS One''. 2014; '''9''' (5):e98076
Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. Description: Jarick, I, et al. Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. ''Mol Psychiatry''. 2014 Jan; '''19''' (1):115-21
Genome-wide analysis of the role of copy-number variation in pancreatic cancer risk. Description: Willis, Jason A, et al. Genome-wide analysis of the role of copy-number variation in pancreatic cancer risk. ''Front Genet''. 2014; '''5''': 29
Genome-wide association scan for variants associated with early-onset prostate cancer. Description: Lange, Ethan M, et al. Genome-wide association scan for variants associated with early-onset prostate cancer. ''PLoS One''. 2014; '''9''' (4):e93436
Genome-wide association studies using haplotypes and individual SNPs in Simmental cattle. Description: Wu, Yang, et al. Genome-wide association studies using haplotypes and individual SNPs in Simmental cattle. ''PLoS One''. 2014; '''9''' (10):e109330
Genome-wide association study and ancestral origins of the slick-hair coat in tropically adapted cattle. Description: Huson, Heather J, et al. Genome-wide association study and ancestral origins of the slick-hair coat in tropically adapted cattle. ''Front Genet''. 2014; '''5''': 101
Genome wide association study identifies 20 novel promising genes associated with milk fatty acid traits in Chinese Holstein. Description: Li, Cong, et al. Genome wide association study identifies 20 novel promising genes associated with milk fatty acid traits in Chinese Holstein. ''PLoS One''. 2014; '''9''' (5):e96186
Genome-wide association study identifies a potent locus associated with human opioid sensitivity. Description: Nishizawa, D, et al. Genome-wide association study identifies a potent locus associated with human opioid sensitivity. ''Mol Psychiatry''. 2014 Jan; '''19''' (1):55-62
Genome-wide association study identifies phospholipase C zeta 1 (PLCz1) as a stallion fertility locus in Hanoverian warmblood horses. Description: Schrimpf, Rahel, et al. Genome-wide association study identifies phospholipase C zeta 1 (PLCz1) as a stallion fertility locus in Hanoverian warmblood horses. ''PLoS One''. 2014; '''9''' (10):e109675
Genome-wide association study identifies variants in PMS1 associated with serum ferritin in a Chinese population. Description: Liao, Ming, et al. Genome-wide association study identifies variants in PMS1 associated with serum ferritin in a Chinese population. ''PLoS One''. 2014; '''9''' (8):e105844
Genome-wide association study of maternal and inherited loci for conotruncal heart defects. Description: Agopian, A J, et al. Genome-wide association study of maternal and inherited loci for conotruncal heart defects. ''PLoS One''. 2014; '''9''' (5):e96057
Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections. Description: Ye, Zhan, et al. Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections. ''Front Genet''. 2014; '''5''': 125
Genome-wide association study of susceptibility to infection by Mycobacterium avium subspecies paratuberculosis in Holstein cattle. Description: Alpay, Fazli, et al. Genome-wide association study of susceptibility to infection by Mycobacterium avium subspecies paratuberculosis in Holstein cattle. ''PLoS One''. 2014; '''9''' (12):e111704
Genome-wide association study reveals a polymorphism in the podocyte receptor RANK for the decline of renal function in coronary patients. Description: Leiherer, Andreas, et al. Genome-wide association study reveals a polymorphism in the podocyte receptor RANK for the decline of renal function in coronary patients. ''PLoS One''. 2014; '''9''' (12):e114240
Genome-wide linkage study suggests a susceptibility locus for isolated bilateral microtia on 4p15.32-4p16.2. Description: Li, Xin, et al. Genome-wide linkage study suggests a susceptibility locus for isolated bilateral microtia on 4p15.32-4p16.2. ''PLoS One''. 2014; '''9''' (7):e101152
Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. Description: Simpson, Claire L, et al. Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. ''PLoS One''. 2014; '''9''' (9):e107110
Genome wide screening of candidate genes for improving piglet birth weight using high and low estimated breeding value populations. Description: Zhang, Lifan, et al. Genome wide screening of candidate genes for improving piglet birth weight using high and low estimated breeding value populations. ''Int J Biol Sci''. 2014; '''10''' (3):236-44
Genomic and metabolomic profile associated to microalbuminuria. Description: Marrachelli, Vannina G, et al. Genomic and metabolomic profile associated to microalbuminuria. ''PLoS One''. 2014; '''9''' (2):e98227
Genomic architecture of sickle cell disease in West African children. Description: Quinlan, Jacklyn, et al. Genomic architecture of sickle cell disease in West African children. ''Front Genet''. 2014; '''5''': 26
Genomic assortative mating in marriages in the United States. Description: Guo, Guang, et al. Genomic assortative mating in marriages in the United States. ''PLoS One''. 2014; '''9''' (11):e112322
Genomic scan reveals loci under altitude adaptation in Tibetan and Dahe pigs. Description: Dong, Kunzhe, et al. Genomic scan reveals loci under altitude adaptation in Tibetan and Dahe pigs. ''PLoS One''. 2014; '''9''' (10):e110520
Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing. Description: Bodian, Dale L, et al. Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing. ''PLoS One''. 2014; '''9''' (4):e94554
Haplotype approach for association analysis on hypertension. Description: Shen, Xiaowei, et al. Haplotype approach for association analysis on hypertension. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S57
Host genetic variants and gene expression patterns associated with Epstein-Barr virus copy number in lymphoblastoid cell lines. Description: Houldcroft, Charlotte J, et al. Host genetic variants and gene expression patterns associated with Epstein-Barr virus copy number in lymphoblastoid cell lines. ''PLoS One''. 2014; '''9''' (10):e108384
Hybrid origin of European commercial pigs examined by an in-depth haplotype analysis on chromosome 1. Description: Bosse, Mirte, et al. Hybrid origin of European commercial pigs examined by an in-depth haplotype analysis on chromosome 1. ''Front Genet''. 2014; '''5''': 442
Identification of genetic loci associated with primary angle-closure glaucoma in the basset hound. Description: Ahram, Dina F, et al. Identification of genetic loci associated with primary angle-closure glaucoma in the basset hound. ''Mol Vis''. 2014; '''20''': 497-510
Identification of genomic loci associated with Rhodococcus equi susceptibility in foals. Description: McQueen, Cole M, et al. Identification of genomic loci associated with Rhodococcus equi susceptibility in foals. ''PLoS One''. 2014; '''9''' (6):e98710
Identification of novel genetic risk loci in Maltese dogs with necrotizing meningoencephalitis and evidence of a shared genetic risk across toy dog breeds. Description: Schrauwen, Isabelle, et al. Identification of novel genetic risk loci in Maltese dogs with necrotizing meningoencephalitis and evidence of a shared genetic risk across toy dog breeds. ''PLoS One''. 2014; '''9''' (11):e112755
Identification of rare variants for hypertension with incorporation of linkage information. Description: Chiu, Yen-Feng, et al. Identification of rare variants for hypertension with incorporation of linkage information. ''BMC Proc''. 2014; '''8''' (Suppl 1):S109
Identifying genetic interactions associated with late-onset Alzheimer's disease. Description: Floudas, Charalampos S, et al. Identifying genetic interactions associated with late-onset Alzheimer's disease. ''BioData Min''. 2014; '''7''' (1):35
Identifying rare variants associated with hypertension using the C-alpha test. Description: Faino, Anna, et al. Identifying rare variants associated with hypertension using the C-alpha test. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S56
Immunization associated with erectile dysfunction based on cross-sectional and genetic analyses. Description: Chen, Yang, et al. Immunization associated with erectile dysfunction based on cross-sectional and genetic analyses. ''PLoS One''. 2014; '''9''' (10):e111269
Impact of measurement error on testing genetic association with quantitative traits. Description: Liao, Jiemin, et al. Impact of measurement error on testing genetic association with quantitative traits. ''PLoS One''. 2014; '''9''' (1):e87044
Imputation of TPMT defective alleles for the identification of patients with high-risk phenotypes. Description: Almoguera, Berta, et al. Imputation of TPMT defective alleles for the identification of patients with high-risk phenotypes. ''Front Genet''. 2014; '''5''': 96
Increased expression of MERTK is associated with a unique form of canine retinopathy. Description: Ahonen, Saija J, et al. Increased expression of MERTK is associated with a unique form of canine retinopathy. ''PLoS One''. 2014; '''9''' (12):e114552
Influence of genetic variants in TPMT and COMT associated with cisplatin induced hearing loss in patients with cancer: two new cohorts and a meta-analysis reveal significant heterogeneity between cohorts. Description: Hagleitner, Melanie M, et al. Influence of genetic variants in TPMT and COMT associated with cisplatin induced hearing loss in patients with cancer: two new cohorts and a meta-analysis reveal significant heterogeneity between cohorts. ''PLoS One''. 2014; '''9''' (12):e115869
Integrated analysis of germline and somatic variants in ovarian cancer. Description: Kanchi, Krishna L, et al. Integrated analysis of germline and somatic variants in ovarian cancer. ''Nat Commun''. 2014; '''5''': 3156
Integrating EMR-linked and in vivo functional genetic data to identify new genotype-phenotype associations. Description: Mosley, Jonathan D, et al. Integrating EMR-linked and in vivo functional genetic data to identify new genotype-phenotype associations. ''PLoS One''. 2014; '''9''' (6):e100322
Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene. Description: Okada, Yukinori, et al. Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene. ''PLoS One''. 2014; '''9''' (2):e87645
Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease. Description: Cabrera, Sonia, et al. Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease. ''PLoS One''. 2014; '''9''' (11):e112171
Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies. Description: Mitchell, Sabrina L, et al. Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies. ''BioData Min''. 2014; '''7''': 6
Investigating the Role of Gene-Gene Interactions in TB Susceptibility. Description: Daya, Michelle, et al. Investigating the Role of Gene-Gene Interactions in TB Susceptibility. ''PLoS One''. 2014; '''10''' (4):e0123970
Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy. Description: Moreira, Danielle P, et al. Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy. ''PLoS One''. 2014; '''9''' (9):e107705
Lack of association of the caspase-12 long allele with community-acquired pneumonia in people of African descent. Description: Chen, Jiwang, et al. Lack of association of the caspase-12 long allele with community-acquired pneumonia in people of African descent. ''PLoS One''. 2014; '''9''' (2):e89194
Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants. Description: Narahara, Maiko, et al. Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants. ''PLoS One''. 2014; '''9''' (6):e100924
Linkage disequilibrium and haplotype block structure in a composite beef cattle breed. Description: Mokry, Fabiana Barichello, et al. Linkage disequilibrium and haplotype block structure in a composite beef cattle breed. ''BMC Genomics''. 2014; '''15 Suppl 7''': S6
Looking the cow in the eye: deletion in the NID1 gene is associated with recessive inherited cataract in Romagnola cattle. Description: Murgiano, Leonardo, et al. Looking the cow in the eye: deletion in the NID1 gene is associated with recessive inherited cataract in Romagnola cattle. ''PLoS One''. 2014; '''9''' (10):e110628
Lupus risk variants in the PXK locus alter B-cell receptor internalization. Description: Vaughn, Samuel E, et al. Lupus risk variants in the PXK locus alter B-cell receptor internalization. ''Front Genet''. 2014; '''5''': 450
MAPKAP1 rs10118570 polymorphism is associated with anti-infection and anti-hepatic fibrogenesis in schistosomiasis japonica. Description: Zhu, Xiao, et al. MAPKAP1 rs10118570 polymorphism is associated with anti-infection and anti-hepatic fibrogenesis in schistosomiasis japonica. ''PLoS One''. 2014; '''9''' (8):e105995
Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities. Description: Musolf, Anthony, et al. Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S81
Mapping the genetic architecture of gene regulation in whole blood. Description: Schramm, Katharina, et al. Mapping the genetic architecture of gene regulation in whole blood. ''PLoS One''. 2014; '''9''' (4):e93844
Matrix metalloproteinase-1 (MMP-1) Promoter polymorphisms are well linked with lower stomach tumor formation in eastern Indian population. Description: Dey, Sanjib, et al. Matrix metalloproteinase-1 (MMP-1) Promoter polymorphisms are well linked with lower stomach tumor formation in eastern Indian population. ''PLoS One''. 2014; '''9''' (2):e88040
Multivariate dimensionality reduction approaches to identify gene-gene and gene-environment interactions underlying multiple complex traits. Description: Xu, Hai-Ming, et al. Multivariate dimensionality reduction approaches to identify gene-gene and gene-environment interactions underlying multiple complex traits. ''PLoS One''. 2014; '''9''' (9):e108103
NAT2 genetic variations among South Indian populations. Description: Lakkakula, Saikrishna, et al. NAT2 genetic variations among South Indian populations. ''Hum Genome Var''. 2014; '''1''': 14014
New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis. Description: Vinayagamoorthy, Nadimuthu, et al. New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis. ''PLoS One''. 2014; '''9''' (4):e95866
Novel host genetic variations associated with spontaneous clearance of a single-source outbreak of HCV1b infections. Description: You, Hong, et al. Novel host genetic variations associated with spontaneous clearance of a single-source outbreak of HCV1b infections. ''BMJ Open Gastroenterol''. 2014; '''1''' (1):e000010
Novel insights into the regulatory architecture of CD4+ T cells in rheumatoid arthritis. Description: Aterido, Adria, et al. Novel insights into the regulatory architecture of CD4+ T cells in rheumatoid arthritis. ''PLoS One''. 2014; '''9''' (6):e100690
OTX2 duplication is implicated in hemifacial microsomia. Description: Zielinski, Dina, et al. OTX2 duplication is implicated in hemifacial microsomia. ''PLoS One''. 2014; '''9''' (5):e96788
Overrepresentation of glutamate signaling in Alzheimer's disease: network-based pathway enrichment using meta-analysis of genome-wide association studies. Description: Perez-Palma, Eduardo, et al. Overrepresentation of glutamate signaling in Alzheimer's disease: network-based pathway enrichment using meta-analysis of genome-wide association studies. ''PLoS One''. 2014; '''9''' (4):e95413
Pharmacogenetic associations with long-term response to anti-vascular endothelial growth factor treatment in neovascular AMD patients. Description: Park, Un Chul, et al. Pharmacogenetic associations with long-term response to anti-vascular endothelial growth factor treatment in neovascular AMD patients. ''Mol Vis''. 2014; '''20''': 1680-94
Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index. Description: Cronin, Robert M, et al. Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index. ''Front Genet''. 2014; '''5''': 250
Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis. Description: Namjou, Bahram, et al. Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis. ''Front Genet''. 2014; '''5''': 401
Phenotype refinement strengthens the association of AHR and CYP1A1 genotype with caffeine consumption. Description: McMahon, George, et al. Phenotype refinement strengthens the association of AHR and CYP1A1 genotype with caffeine consumption. ''PLoS One''. 2014; '''9''' (7):e103448
Placental genome and maternal-placental genetic interactions: a genome-wide and candidate gene association study of placental abruption. Description: Denis, Marie, et al. Placental genome and maternal-placental genetic interactions: a genome-wide and candidate gene association study of placental abruption. ''PLoS One''. 2014; '''9''' (12):e116346
Pleiotropic effect of common variants at ABO Glycosyltranferase locus in 9q32 on plasma levels of pancreatic lipase and angiotensin converting enzyme. Description: Pleiotropic effect of common variants at ABO Glycosyltranferase locus in 9q32 on plasma levels of pancreatic lipase and angiotensin converting enzyme. ''PLoS One''. 2014; '''9''' (2):e55903
Population genomic analyses based on 1 million SNPs in commercial egg layers. Description: Gholami, Mahmood, et al. Population genomic analyses based on 1 million SNPs in commercial egg layers. ''PLoS One''. 2014; '''9''' (4):e94509
Potentially functional SNPs (pfSNPs) as novel genomic predictors of 5-FU response in metastatic colorectal cancer patients. Description: Wang, Jingbo, et al. Potentially functional SNPs (pfSNPs) as novel genomic predictors of 5-FU response in metastatic colorectal cancer patients. ''PLoS One''. 2014; '''9''' (11):e111694
Practical issues in screening and variable selection in genome-wide association analysis. Description: Hong, Sungyeon, et al. Practical issues in screening and variable selection in genome-wide association analysis. ''Cancer Inform''. 2014; '''13''' (Suppl 7):55-65
Prediction of genetic contributions to complex traits using whole genome sequencing data. Description: Yao, Chen, et al. Prediction of genetic contributions to complex traits using whole genome sequencing data. ''BMC Proc''. 2014; '''8''' (Suppl 1):S68
PREST-plus identifies pedigree errors and cryptic relatedness in the GAW18 sample using genome-wide SNP data. Description: Sun, Lei, et al. PREST-plus identifies pedigree errors and cryptic relatedness in the GAW18 sample using genome-wide SNP data. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S23
Protective association of tumor necrosis factor superfamily 15 (TNFSF15) polymorphic haplotype with Ulcerative Colitis and Crohn's disease in an Indian population. Description: Baskaran, Kirankumar, et al. Protective association of tumor necrosis factor superfamily 15 (TNFSF15) polymorphic haplotype with Ulcerative Colitis and Crohn's disease in an Indian population. ''PLoS One''. 2014; '''9''' (12):e114665
Quantitative trait loci (QTL) study identifies novel genomic regions associated to Chiari-like malformation in Griffon Bruxellois dogs. Description: Lemay, Philippe, et al. Quantitative trait loci (QTL) study identifies novel genomic regions associated to Chiari-like malformation in Griffon Bruxellois dogs. ''PLoS One''. 2014; '''9''' (4):e89816
Rare variant analysis of blood pressure phenotypes in the Genetic Analysis Workshop 18 whole genome sequencing data using sequence kernel association test. Description: Mallaney, Cates, et al. Rare variant analysis of blood pressure phenotypes in the Genetic Analysis Workshop 18 whole genome sequencing data using sequence kernel association test. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S10
Refined candidate region for F4ab/ac enterotoxigenic Escherichia coli susceptibility situated proximal to MUC13 in pigs. Description: Goetstouwers, Tiphanie, et al. Refined candidate region for F4ab/ac enterotoxigenic Escherichia coli susceptibility situated proximal to MUC13 in pigs. ''PLoS One''. 2014; '''9''' (8):e105013
Refinement of the MHC risk map in a scandinavian primary sclerosing cholangitis population. Description: Naess, Sigrid, et al. Refinement of the MHC risk map in a scandinavian primary sclerosing cholangitis population. ''PLoS One''. 2014; '''9''' (12):e114486
Replication of 6 obesity genes in a meta-analysis of genome-wide association studies from diverse ancestries. Description: Tan, Li-Jun, et al. Replication of 6 obesity genes in a meta-analysis of genome-wide association studies from diverse ancestries. ''PLoS One''. 2014; '''9''' (5):e96149
Replication of the 4p16 susceptibility locus in congenital heart disease in Han Chinese populations. Description: Zhao, Bijun, et al. Replication of the 4p16 susceptibility locus in congenital heart disease in Han Chinese populations. ''PLoS One''. 2014; '''9''' (9):e107411
Reproductive physiology in young men is cumulatively affected by FSH-action modulating genetic variants: FSHR -29G/A and c.2039 A/G, FSHB -211G/T. Description: Grigorova, Marina, et al. Reproductive physiology in young men is cumulatively affected by FSH-action modulating genetic variants: FSHR -29G/A and c.2039 A/G, FSHB -211G/T. ''PLoS One''. 2014; '''9''' (4):e94244
Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci. Description: Service, Susan K, et al. Re-sequencing expands our understanding of the phenotypic impact of variants at GWAS loci. ''PLoS Genet''. 2014 Jan; '''10''' (1):e1004147
RNA-Seq transcriptome profiling identifies CRISPLD2 as a glucocorticoid responsive gene that modulates cytokine function in airway smooth muscle cells. Description: Himes, Blanca E, et al. RNA-Seq transcriptome profiling identifies CRISPLD2 as a glucocorticoid responsive gene that modulates cytokine function in airway smooth muscle cells. ''PLoS One''. 2014; '''9''' (6):e99625
Role of nicotine dependence in the association between the dopamine receptor gene DRD3 and major depressive disorder. Description: Korhonen, Tellervo, et al. Role of nicotine dependence in the association between the dopamine receptor gene DRD3 and major depressive disorder. ''PLoS One''. 2014; '''9''' (6):e98199
Rs7206790 and rs11644943 in FTO gene are associated with risk of obesity in Chinese school-age population. Description: Xu, Yuyang, et al. Rs7206790 and rs11644943 in FTO gene are associated with risk of obesity in Chinese school-age population. ''PLoS One''. 2014; '''9''' (9):e108050
Sardinians genetic background explained by runs of homozygosity and genomic regions under positive selection. Description: Di Gaetano, Cornelia, et al. Sardinians genetic background explained by runs of homozygosity and genomic regions under positive selection. ''PLoS One''. 2014; '''9''' (3):e91237
Searching for "monogenic diabetes" in dogs using a candidate gene approach. Description: Short, Andrea D, et al. Searching for "monogenic diabetes" in dogs using a candidate gene approach. ''Canine Genet Epidemiol''. 2014; '''1''': 8
Shared and unique signals of high-altitude adaptation in geographically distinct Tibetan populations. Description: Wuren, Tana, et al. Shared and unique signals of high-altitude adaptation in geographically distinct Tibetan populations. ''PLoS One''. 2014; '''9''' (3):e88252
Single-marker and multi-marker mixed models for polygenic score analysis in family-based data. Description: Bohossian, Nora, et al. Single-marker and multi-marker mixed models for polygenic score analysis in family-based data. ''BMC Proc''. 2014; '''8''' (Suppl 1):S63
Smoking quit success genotype score predicts quit success and distinct patterns of developmental involvement with common addictive substances. Description: Uhl, G R, et al. Smoking quit success genotype score predicts quit success and distinct patterns of developmental involvement with common addictive substances. ''Mol Psychiatry''. 2014 Jan; '''19''' (1):50-4
SNP identification by transcriptome sequencing and candidate gene-based association analysis for heat tolerance in the bay scallop Argopecten irradians. Description: Du, Xuedi, et al. SNP identification by transcriptome sequencing and candidate gene-based association analysis for heat tolerance in the bay scallop Argopecten irradians. ''PLoS One''. 2014; '''9''' (8):e104960
Standing at the gateway to Europe--the genetic structure of Western balkan populations based on autosomal and haploid markers. Description: Kovacevic, Lejla, et al. Standing at the gateway to Europe--the genetic structure of Western balkan populations based on autosomal and haploid markers. ''PLoS One''. 2014; '''9''' (8):e105090
Study of a Functional Polymorphism in the PER3 Gene and Diurnal Preference in a Colombian Sample. Description: Perea, Claudia S, et al. Study of a Functional Polymorphism in the PER3 Gene and Diurnal Preference in a Colombian Sample. ''Open Neurol J''. 2014; '''8''': 7-10
Systematic fine-mapping of association with BMI and type 2 diabetes at the FTO locus by integrating results from multiple ethnic groups. Description: Akiyama, Koichi, et al. Systematic fine-mapping of association with BMI and type 2 diabetes at the FTO locus by integrating results from multiple ethnic groups. ''PLoS One''. 2014; '''9''' (6):e101329
Systematic pathway enrichment analysis of a genome-wide association study on breast cancer survival reveals an influence of genes involved in cell adhesion and calcium signaling on the patients' clinical outcome. Description: Woltmann, Andrea, et al. Systematic pathway enrichment analysis of a genome-wide association study on breast cancer survival reveals an influence of genes involved in cell adhesion and calcium signaling on the patients' clinical outcome. ''PLoS One''. 2014; '''9''' (6):e98229
Testing for associations between systolic blood pressure and single-nucleotide polymorphism profiles obtained from sparse principal component analysis. Description: Bonner, Ashley, et al. Testing for associations between systolic blood pressure and single-nucleotide polymorphism profiles obtained from sparse principal component analysis. ''BMC Proc''. 2014; '''8''' (Suppl 1):S95
Testing optimally weighted combination of variants for hypertension. Description: Zhao, Xingwang, et al. Testing optimally weighted combination of variants for hypertension. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S59
The Andean adaptive toolkit to counteract high altitude maladaptation: genome-wide and phenotypic analysis of the Collas. Description: Eichstaedt, Christina A, et al. The Andean adaptive toolkit to counteract high altitude maladaptation: genome-wide and phenotypic analysis of the Collas. ''PLoS One''. 2014; '''9''' (3):e93314
The association of genotype-based inbreeding coefficient with a range of physical and psychological human traits. Description: Verweij, Karin J H, et al. The association of genotype-based inbreeding coefficient with a range of physical and psychological human traits. ''PLoS One''. 2014; '''9''' (7):e103102
The association of transporter genes polymorphisms and lung cancer chemotherapy response. Description: Wang, Ying, et al. The association of transporter genes polymorphisms and lung cancer chemotherapy response. ''PLoS One''. 2014; '''9''' (3):e91967
The associations between immunity-related genes and breast cancer prognosis in Korean women. Description: Choi, Jaesung, et al. The associations between immunity-related genes and breast cancer prognosis in Korean women. ''PLoS One''. 2014; '''9''' (7):e103593
The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study. Description: Kullo, Iftikhar J, et al. The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study. ''Front Genet''. 2014; '''5''': 166
The effect of inversion at 8p23 on BLK association with lupus in Caucasian population. Description: Namjou, Bahram, et al. The effect of inversion at 8p23 on BLK association with lupus in Caucasian population. ''PLoS One''. 2014; '''9''' (12):e115614
The effects of socioeconomic status, clinical factors, and genetic ancestry on pulmonary tuberculosis disease in northeastern Mexico. Description: Young, Bonnie N, et al. The effects of socioeconomic status, clinical factors, and genetic ancestry on pulmonary tuberculosis disease in northeastern Mexico. ''PLoS One''. 2014; '''9''' (4):e94303
The episode of genetic drift defining the migration of humans out of Africa is derived from a large east African population size. Description: Elhassan, Nuha, et al. The episode of genetic drift defining the migration of humans out of Africa is derived from a large east African population size. ''PLoS One''. 2014; '''9''' (5):e97674
The gene-gene interaction of INSIG-SCAP-SREBP pathway on the risk of obesity in Chinese children. Description: Liu, Fang-Hong, et al. The gene-gene interaction of INSIG-SCAP-SREBP pathway on the risk of obesity in Chinese children. ''Biomed Res Int''. 2014; '''2014''': 538564
The genetic architecture of climatic adaptation of tropical cattle. Description: Porto-Neto, Laercio R, et al. The genetic architecture of climatic adaptation of tropical cattle. ''PLoS One''. 2014; '''9''' (11):e113284
The interplay between natural selection and susceptibility to melanoma on allele 374F of SLC45A2 gene in a South European population. Description: Lopez, Saioa, et al. The interplay between natural selection and susceptibility to melanoma on allele 374F of SLC45A2 gene in a South European population. ''PLoS One''. 2014; '''9''' (8):e104367
The MLH1 c.1852_1853delinsGC (p.K618A) variant in colorectal cancer: genetic association study in 18,723 individuals. Description: Abuli, Anna, et al. The MLH1 c.1852_1853delinsGC (p.K618A) variant in colorectal cancer: genetic association study in 18,723 individuals. ''PLoS One''. 2014; '''9''' (4):e95022
The NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067. Description: Schnitzler, Fabian, et al. The NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067. ''PLoS One''. 2014; '''9''' (11):e108503
The peculiar epidemiology of dracunculiasis in Chad. Description: Eberhard, Mark L, et al. The peculiar epidemiology of dracunculiasis in Chad. ''Am J Trop Med Hyg''. 2014 Jan; '''90''' (1):61-70
The SNP rs3128965 of HLA-DPB1 as a genetic marker of the AERD phenotype. Description: Kim, Seung-Hyun, et al. The SNP rs3128965 of HLA-DPB1 as a genetic marker of the AERD phenotype. ''PLoS One''. 2014; '''9''' (12):e111220
Transcriptome profiling of human ulcerative colitis mucosa reveals altered expression of pathways enriched in genetic susceptibility loci. Description: Cardinale, Christopher J, et al. Transcriptome profiling of human ulcerative colitis mucosa reveals altered expression of pathways enriched in genetic susceptibility loci. ''PLoS One''. 2014; '''9''' (5):e96153
tranSMART: An Open Source Knowledge Management and High Content Data Analytics Platform. Description: Scheufele, Elisabeth, et al. tranSMART: An Open Source Knowledge Management and High Content Data Analytics Platform. ''AMIA Jt Summits Transl Sci Proc''. 2014; '''2014''': 96-101
Trps1 differentially modulates the bone mineral density between male and female mice and its polymorphism associates with BMD differently between women and men. Description: Wang, Lishi, et al. Trps1 differentially modulates the bone mineral density between male and female mice and its polymorphism associates with BMD differently between women and men. ''PLoS One''. 2014; '''9''' (1):e84485
Using Mendelian inheritance errors as quality control criteria in whole genome sequencing data set. Description: Pilipenko, Valentina V, et al. Using Mendelian inheritance errors as quality control criteria in whole genome sequencing data set. ''BMC Proc''. 2014; '''8''' (Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S21
Variation in genes involved in epigenetic processes offers insights into tropically adapted cattle diversity. Description: Porto-Neto, Laercio R, et al. Variation in genes involved in epigenetic processes offers insights into tropically adapted cattle diversity. ''Front Genet''. 2014; '''5''': 89
ViVar: a comprehensive platform for the analysis and visualization of structural genomic variation. Description: Sante, Tom, et al. ViVar: a comprehensive platform for the analysis and visualization of structural genomic variation. ''PLoS One''. 2014; '''9''' (12):e113800
Whole brain expression of bipolar disorder associated genes: structural and genetic analyses. Description: McCarthy, Michael J, et al. Whole brain expression of bipolar disorder associated genes: structural and genetic analyses. ''PLoS One''. 2014; '''9''' (6):e100204
Whole-exome sequencing for the identification of susceptibility genes of Kashin-Beck disease. Description: Yang, Zhenxing, et al. Whole-exome sequencing for the identification of susceptibility genes of Kashin-Beck disease. ''PLoS One''. 2014; '''9''' (4):e92298
Whole genome sequence and analysis of the Marwari horse breed and its genetic origin. Description: Jun, JeHoon, et al. Whole genome sequence and analysis of the Marwari horse breed and its genetic origin. ''BMC Genomics''. 2014; '''15 Suppl 9''': S4
Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis. Description: Mayes, Maureen D, et al. Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis. ''Am J Hum Genet''. 2014 Jan 2; '''94''' (1):47-61
Genome-wide eQTLs and heritability for gene expression traits in unrelated individuals. Description: Yang, Shengjie, et al. Genome-wide eQTLs and heritability for gene expression traits in unrelated individuals. ''BMC Genomics''. 2014 Jan 9; '''15''': 13
Association between JY-1 gene polymorphisms and reproductive traits in beef cattle. Description: de Camargo, Gregorio Miguel Ferreira, et al. Association between JY-1 gene polymorphisms and reproductive traits in beef cattle. ''Gene''. 2014 Jan 10; '''533''' (2):477-80
Diversity, differentiation, and linkage disequilibrium: prospects for association mapping in the malaria vector Anopheles arabiensis. Description: Marsden, Clare Diana, et al. Diversity, differentiation, and linkage disequilibrium: prospects for association mapping in the malaria vector Anopheles arabiensis. ''G3 (Bethesda)''. 2014 Jan 10; '''4''' (1):121-31
Analysis of schizophrenia-related genes and electrophysiological measures reveals ZNF804A association with amplitude of P300b elicited by novel sounds. Description: Del Re, E C, et al. Analysis of schizophrenia-related genes and electrophysiological measures reveals ZNF804A association with amplitude of P300b elicited by novel sounds. ''Transl Psychiatry''. 2014 Jan 14; '''4''': e346
Association of the RYR3 gene polymorphisms with atherosclerosis in elderly Japanese population. Description: Zhao, Chenxi, et al. Association of the RYR3 gene polymorphisms with atherosclerosis in elderly Japanese population. ''BMC Cardiovasc Disord''. 2014 Jan 14; '''14''': 6
A genome-wide scan for signatures of selection in Chinese indigenous and commercial pig breeds. Description: Yang, Songbai, et al. A genome-wide scan for signatures of selection in Chinese indigenous and commercial pig breeds. ''BMC Genet''. 2014 Jan 15; '''15''': 7
Identification of a major locus interacting with MC1R and modifying black coat color in an F(2) Nellore-Angus population. Description: Hanna, Lauren L Hulsman, et al. Identification of a major locus interacting with MC1R and modifying black coat color in an F(2) Nellore-Angus population. ''Genet Sel Evol''. 2014 Jan 24; '''46''': 4
The PARK2 gene is involved in the maintenance of pancreatic beta-cell functions related to insulin production and secretion. Description: Jin, Hyun-Seok, et al. The PARK2 gene is involved in the maintenance of pancreatic beta-cell functions related to insulin production and secretion. ''Mol Cell Endocrinol''. 2014 Jan 25; '''382''' (1):178-189
Critical role for mast cell Stat5 activity in skin inflammation. Description: Ando, Tomoaki, et al. Critical role for mast cell Stat5 activity in skin inflammation. ''Cell Rep''. 2014 Jan 30; '''6''' (2):366-76
Analysis of copy number variations at 15 schizophrenia-associated loci. Description: Rees, Elliott, et al. Analysis of copy number variations at 15 schizophrenia-associated loci. ''Br J Psychiatry''. 2014 Feb; '''204''' (2):108-14
Association of four insulin resistance genes with type 2 diabetes mellitus and hypertension in the Chinese Han population. Description: Jiang, Bo, et al. Association of four insulin resistance genes with type 2 diabetes mellitus and hypertension in the Chinese Han population. ''Mol Biol Rep''. 2014 Feb; '''41''' (2):925-33
Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24. Description: Agler, Caryline, et al. Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24. ''PLoS Genet''. 2014 Feb; '''10''' (2):e1003991
Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval. Description: Avery, C L, et al. Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval. ''Pharmacogenomics J''. 2014 Feb; '''14''' (1):6-13
Effect of genetic variation in a Drosophila model of diabetes-associated misfolded human proinsulin. Description: He, Bin Z, et al. Effect of genetic variation in a Drosophila model of diabetes-associated misfolded human proinsulin. ''Genetics''. 2014 Feb; '''196''' (2):557-67
Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer. Description: Saunders, Edward J, et al. Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer. ''PLoS Genet''. 2014 Feb; '''10''' (2):e1004129
Genetic variants associated with methotrexate efficacy and toxicity in early rheumatoid arthritis: results from the treatment of early aggressive rheumatoid arthritis trial. Description: Aslibekyan, S, et al. Genetic variants associated with methotrexate efficacy and toxicity in early rheumatoid arthritis: results from the treatment of early aggressive rheumatoid arthritis trial. ''Pharmacogenomics J''. 2014 Feb; '''14''' (1):48-53
Genome-wide association study of endometrial cancer in E2C2. Description: De Vivo, Immaculata, et al. Genome-wide association study of endometrial cancer in E2C2. ''Hum Genet''. 2014 Feb; '''133''' (2):211-24
Genome-wide association study of metabolic traits reveals novel gene-metabolite-disease links. Description: Rueedi, Rico, et al. Genome-wide association study of metabolic traits reveals novel gene-metabolite-disease links. ''PLoS Genet''. 2014 Feb; '''10''' (2):e1004132
Genome-wide protein QTL mapping identifies human plasma kallikrein as a post-translational regulator of serum uPAR levels. Description: Portelli, Michael A, et al. Genome-wide protein QTL mapping identifies human plasma kallikrein as a post-translational regulator of serum uPAR levels. ''FASEB J''. 2014 Feb; '''28''' (2):923-34
Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene. Description: Ruiz, A, et al. Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene. ''Transl Psychiatry''. 2014 Feb 4; '''4''': e358
The utility of low-density genotyping for imputation in the Thoroughbred horse. Description: Corbin, Laura J, et al. The utility of low-density genotyping for imputation in the Thoroughbred horse. ''Genet Sel Evol''. 2014 Feb 4; '''46''': 9
A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population. Description: Yang, Binyao, et al. A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population. ''BMC Med Genomics''. 2014 Feb 11; '''7''': 10
A genome-wide association study of variants associated with acquisition of Staphylococcus aureus bacteremia in a healthcare setting. Description: Nelson, Charlotte L, et al. A genome-wide association study of variants associated with acquisition of Staphylococcus aureus bacteremia in a healthcare setting. ''BMC Infect Dis''. 2014 Feb 13; '''14''': 83
Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder. Description: Werling, Donna M, et al. Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder. ''Mol Autism''. 2014 Feb 17; '''5''' (1):13
STX1A and Asperger syndrome: a replication study. Description: Durdiakova, Jaroslava, et al. STX1A and Asperger syndrome: a replication study. ''Mol Autism''. 2014 Feb 18; '''5''' (1):14
Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years. Description: Shaffer, John R, et al. Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years. ''G3 (Bethesda)''. 2014 Feb 19; '''4''' (2):307-14
Whole genome sequencing of Ethiopian highlanders reveals conserved hypoxia tolerance genes. Description: Udpa, Nitin, et al. Whole genome sequencing of Ethiopian highlanders reveals conserved hypoxia tolerance genes. ''Genome Biol''. 2014 Feb 20; '''15''' (2):R36
Methylation quantitative trait loci (meQTLs) are consistently detected across ancestry, developmental stage, and tissue type. Description: Smith, Alicia K, et al. Methylation quantitative trait loci (meQTLs) are consistently detected across ancestry, developmental stage, and tissue type. ''BMC Genomics''. 2014 Feb 21; '''15''': 145
Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue. Description: Shi, Jianxin, et al. Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue. ''Nat Commun''. 2014 Feb 27; '''5''': 3365
Linkage maps of the Atlantic salmon (Salmo salar) genome derived from RAD sequencing. Description: Gonen, Serap, et al. Linkage maps of the Atlantic salmon (Salmo salar) genome derived from RAD sequencing. ''BMC Genomics''. 2014 Feb 27; '''15''': 166
Analysis of PRICKLE1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations. Description: Yang, Tian, et al. Analysis of PRICKLE1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations. ''Mol Genet Genomic Med''. 2014 Mar; '''2''' (2):138-51
An evolutionary analysis of antigen processing and presentation across different timescales reveals pervasive selection. Description: Forni, Diego, et al. An evolutionary analysis of antigen processing and presentation across different timescales reveals pervasive selection. ''PLoS Genet''. 2014 Mar; '''10''' (3):e1004189
APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study. Description: Ramanan, V K, et al. APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study. ''Mol Psychiatry''. 2014 Mar; '''19''' (3):351-7
Gene-based sequencing identifies lipid-influencing variants with ethnicity-specific effects in African Americans. Description: Bentley, Amy R, et al. Gene-based sequencing identifies lipid-influencing variants with ethnicity-specific effects in African Americans. ''PLoS Genet''. 2014 Mar; '''10''' (3):e1004190
Genome-wide association studies and prediction of 17 traits related to phenology, biomass and cell wall composition in the energy grass Miscanthus sinensis. Description: Slavov, Gancho T, et al. Genome-wide association studies and prediction of 17 traits related to phenology, biomass and cell wall composition in the energy grass Miscanthus sinensis. ''New Phytol''. 2014 Mar; '''201''' (4):1227-39
Genome-Wide Association Study of Human Immunodeficiency Virus (HIV)-1 Coreceptor Usage in Treatment-Naive Patients from An AIDS Clinical Trials Group Study. Description: Henrich, Timothy J, et al. Genome-Wide Association Study of Human Immunodeficiency Virus (HIV)-1 Coreceptor Usage in Treatment-Naive Patients from An AIDS Clinical Trials Group Study. ''Open Forum Infect Dis''. 2014 Mar; '''1''' (1):ofu018
Genome-wide Association Study of Integrated Meat Quality-related Traits of the Duroc Pig Breed. Description: Lee, Taeheon, et al. Genome-wide Association Study of Integrated Meat Quality-related Traits of the Duroc Pig Breed. ''Asian-Australas J Anim Sci''. 2014 Mar; '''27''' (3):303-9
Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke. Description: Williams, Stephen R, et al. Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke. ''PLoS Genet''. 2014 Mar; '''10''' (3):e1004214
Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci. Description: Borglum, A D, et al. Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci. ''Mol Psychiatry''. 2014 Mar; '''19''' (3):325-33
Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate. Description: Georgi, Benjamin, et al. Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate. ''PLoS Genet''. 2014 Mar; '''10''' (3):e1004229
Global footprints of purifying selection on Toll-like receptor genes primarily associated with response to bacterial infections in humans. Description: Mukherjee, Souvik, et al. Global footprints of purifying selection on Toll-like receptor genes primarily associated with response to bacterial infections in humans. ''Genome Biol Evol''. 2014 Mar; '''6''' (3):551-8
Identification of genes promoting skin youthfulness by genome-wide association study. Description: Chang, Anne L S, et al. Identification of genes promoting skin youthfulness by genome-wide association study. ''J Invest Dermatol''. 2014 Mar; '''134''' (3):651-657
Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants. Description: Romanos, Jihane, et al. Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants. ''Gut''. 2014 Mar; '''63''' (3):415-22
Rare variants in LRRK1 and Parkinson's disease. Description: Schulte, Eva C, et al. Rare variants in LRRK1 and Parkinson's disease. ''Neurogenetics''. 2014 Mar; '''15''' (1):49-57
The rate of nonallelic homologous recombination in males is highly variable, correlated between monozygotic twins and independent of age. Description: MacArthur, Jacqueline A L, et al. The rate of nonallelic homologous recombination in males is highly variable, correlated between monozygotic twins and independent of age. ''PLoS Genet''. 2014 Mar; '''10''' (3):e1004195
Worldwide patterns of ancestry, divergence, and admixture in domesticated cattle. Description: Decker, Jared E, et al. Worldwide patterns of ancestry, divergence, and admixture in domesticated cattle. ''PLoS Genet''. 2014 Mar; '''10''' (3):e1004254
ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer's disease. Description: Medway, Christopher W, et al. ApoE variant p.V236E is associated with markedly reduced risk of Alzheimer's disease. ''Mol Neurodegener''. 2014 Mar 10; '''9''': 11
Candidate genes and functional noncoding variants identified in a canine model of obsessive-compulsive disorder. Description: Tang, Ruqi, et al. Candidate genes and functional noncoding variants identified in a canine model of obsessive-compulsive disorder. ''Genome Biol''. 2014 Mar 14; '''15''' (3):R25
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. Description: Rees, Elliott, et al. CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. ''Hum Mol Genet''. 2014 Mar 15; '''23''' (6):1669-76
Composite selection signals can localize the trait specific genomic regions in multi-breed populations of cattle and sheep. Description: Randhawa, Imtiaz Ahmed Sajid, et al. Composite selection signals can localize the trait specific genomic regions in multi-breed populations of cattle and sheep. ''BMC Genet''. 2014 Mar 17; '''15''': 34
The extent of linkage disequilibrium in beef cattle breeds using high-density SNP genotypes. Description: Porto-Neto, Laercio R, et al. The extent of linkage disequilibrium in beef cattle breeds using high-density SNP genotypes. ''Genet Sel Evol''. 2014 Mar 24; '''46''': 22
Genome-wide association studies for hematological traits in Chinese Sutai pigs. Description: Zhang, Feng, et al. Genome-wide association studies for hematological traits in Chinese Sutai pigs. ''BMC Genet''. 2014 Mar 27; '''15''': 41
Variants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy. Description: Sadler, Brooke, et al. Variants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy. ''Sci Rep''. 2014 Mar 28; '''4''': 4497
Single nucleotide polymorphism rs6716901 in SLC25A12 gene is associated with Asperger syndrome. Description: Durdiakova, Jaroslava, et al. Single nucleotide polymorphism rs6716901 in SLC25A12 gene is associated with Asperger syndrome. ''Mol Autism''. 2014 Mar 31; '''5''' (1):25
A central role for GRB10 in regulation of islet function in man. Description: Prokopenko, Inga, et al. A central role for GRB10 in regulation of islet function in man. ''PLoS Genet''. 2014 Apr; '''10''' (4):e1004235
A high-definition view of functional genetic variation from natural yeast genomes. Description: Bergstrom, Anders, et al. A high-definition view of functional genetic variation from natural yeast genomes. ''Mol Biol Evol''. 2014 Apr; '''31''' (4):872-88
A LINE-1 insertion in DLX6 is responsible for cleft palate and mandibular abnormalities in a canine model of Pierre Robin sequence. Description: Wolf, Zena T, et al. A LINE-1 insertion in DLX6 is responsible for cleft palate and mandibular abnormalities in a canine model of Pierre Robin sequence. ''PLoS Genet''. 2014 Apr; '''10''' (4):e1004257
Association of the CHRNA4 neuronal nicotinic receptor subunit gene with frequency of binge drinking in young adults. Description: Coon, Hilary, et al. Association of the CHRNA4 neuronal nicotinic receptor subunit gene with frequency of binge drinking in young adults. ''Alcohol Clin Exp Res''. 2014 Apr; '''38''' (4):930-7
Epigenomic and transcriptomic signatures of a Klinefelter syndrome (47,XXY) karyotype in the brain. Description: Viana, Joana, et al. Epigenomic and transcriptomic signatures of a Klinefelter syndrome (47,XXY) karyotype in the brain. ''Epigenetics''. 2014 Apr; '''9''' (4):587-99
Genetic predisposition to in situ and invasive lobular carcinoma of the breast. Description: Sawyer, Elinor, et al. Genetic predisposition to in situ and invasive lobular carcinoma of the breast. ''PLoS Genet''. 2014 Apr; '''10''' (4):e1004285
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. Description: Nudel, R, et al. Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. ''Genes Brain Behav''. 2014 Apr; '''13''' (4):418-29
Imputation without doing imputation: a new method for the detection of non-genotyped causal variants. Description: Howey, Richard, et al. Imputation without doing imputation: a new method for the detection of non-genotyped causal variants. ''Genet Epidemiol''. 2014 Apr; '''38''' (3):173-90
One in four individuals of African-American ancestry harbors a 5.5kb deletion at chromosome 11q13.1. Description: Zainabadi, Kayvan, et al. One in four individuals of African-American ancestry harbors a 5.5kb deletion at chromosome 11q13.1. ''Genomics''. 2014 Apr; '''103''' (4):276-87
The 8p23 inversion polymorphism determines local recombination heterogeneity across human populations. Description: Alves, Joao M, et al. The 8p23 inversion polymorphism determines local recombination heterogeneity across human populations. ''Genome Biol Evol''. 2014 Apr; '''6''' (4):921-30
Genomic analysis establishes correlation between growth and laryngeal neuropathy in Thoroughbreds. Description: Boyko, Adam R, et al. Genomic analysis establishes correlation between growth and laryngeal neuropathy in Thoroughbreds. ''BMC Genomics''. 2014 Apr 3; '''15''': 259
mtDNA haplogroup and single nucleotide polymorphisms structure human microbiome communities. Description: Ma, Jun, et al. mtDNA haplogroup and single nucleotide polymorphisms structure human microbiome communities. ''BMC Genomics''. 2014 Apr 3; '''15''': 257
Analysis of common and coding variants with cardiovascular disease in the Diabetes Heart Study. Description: Adams, Jeremy N, et al. Analysis of common and coding variants with cardiovascular disease in the Diabetes Heart Study. ''Cardiovasc Diabetol''. 2014 Apr 12; '''13''': 77
Genome-wide linkage analysis and association study identifies loci for polydactyly in chickens. Description: Sun, Yanfa, et al. Genome-wide linkage analysis and association study identifies loci for polydactyly in chickens. ''G3 (Bethesda)''. 2014 Apr 21; '''4''' (6):1167-72
The total burden of rare, non-synonymous exome genetic variants is not associated with childhood or late-life cognitive ability. Description: Marioni, Riccardo E, et al. The total burden of rare, non-synonymous exome genetic variants is not associated with childhood or late-life cognitive ability. ''Proc Biol Sci''. 2014 Apr 22; '''281''' (1781):20140117
New insight into the SSC8 genetic determination of fatty acid composition in pigs. Description: Revilla, Manuel, et al. New insight into the SSC8 genetic determination of fatty acid composition in pigs. ''Genet Sel Evol''. 2014 Apr 23; '''46''': 28
Development and evaluation of the first high-throughput SNP array for common carp (Cyprinus carpio). Description: Xu, Jian, et al. Development and evaluation of the first high-throughput SNP array for common carp (Cyprinus carpio). ''BMC Genomics''. 2014 Apr 24; '''15''': 307
Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome). Description: Glover, Mark, et al. Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome). ''Clin Sci (Lond)''. 2014 May; '''126''' (10):721-6
Dose-dependent incidence of hepatic tumors in adult mice following perinatal exposure to bisphenol A. Description: Weinhouse, Caren, et al. Dose-dependent incidence of hepatic tumors in adult mice following perinatal exposure to bisphenol A. ''Environ Health Perspect''. 2014 May; '''122''' (5):485-91
Fine mapping of the celiac disease-associated LPP locus reveals a potential functional variant. Description: Almeida, Rodrigo, et al. Fine mapping of the celiac disease-associated LPP locus reveals a potential functional variant. ''Hum Mol Genet''. 2014 May 1; '''23''' (9):2481-9
Genetic variation in vitamin D-related genes and risk of colorectal cancer in African Americans. Description: Pibiri, Fabio, et al. Genetic variation in vitamin D-related genes and risk of colorectal cancer in African Americans. ''Cancer Causes Control''. 2014 May; '''25''' (5):561-70
Genome-wide association study identifies novel loci associated with resistance to bovine tuberculosis. Description: Bermingham, M L, et al. Genome-wide association study identifies novel loci associated with resistance to bovine tuberculosis. ''Heredity (Edinb)''. 2014 May; '''112''' (5):543-51
Mild expression differences of MECP2 influencing aggressive social behavior. Description: Tantra, Martesa, et al. Mild expression differences of MECP2 influencing aggressive social behavior. ''EMBO Mol Med''. 2014 May; '''6''' (5):662-84
On detecting incomplete soft or hard selective sweeps using haplotype structure. Description: Ferrer-Admetlla, Anna, et al. On detecting incomplete soft or hard selective sweeps using haplotype structure. ''Mol Biol Evol''. 2014 May; '''31''' (5):1275-91
POT1 loss-of-function variants predispose to familial melanoma. Description: Robles-Espinoza, Carla Daniela, et al. POT1 loss-of-function variants predispose to familial melanoma. ''Nat Genet''. 2014 May; '''46''' (5):478-481
Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma. Description: Shi, Jianxin, et al. Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma. ''Nat Genet''. 2014 May; '''46''' (5):482-6
Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases. Description: Hudson, Gavin, et al. Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases. ''PLoS Genet''. 2014 May; '''10''' (5):e1004369
Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland. Description: Wang, Sophie R, et al. Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland. ''Am J Hum Genet''. 2014 May 1; '''94''' (5):710-20
The impairment of MAGMAS function in human is responsible for a severe skeletal dysplasia. Description: Mehawej, Cybel, et al. The impairment of MAGMAS function in human is responsible for a severe skeletal dysplasia. ''PLoS Genet''. 2014 May; '''10''' (5):e1004311
TLR4 single nucleotide polymorphisms (SNPs) associated with Salmonella shedding in pigs. Description: Kich, Jalusa Deon, et al. TLR4 single nucleotide polymorphisms (SNPs) associated with Salmonella shedding in pigs. ''J Appl Genet''. 2014 May; '''55''' (2):267-71
Association of serine racemase gene variants with type 2 diabetes in the Chinese Han population. Description: Zhang, Simin, et al. Association of serine racemase gene variants with type 2 diabetes in the Chinese Han population. ''J Diabetes Investig''. 2014 May 4; '''5''' (3):286-9
Epidermal growth factor receptor (EGFR) pathway genes and interstitial lung disease: an association study. Description: Li, Chong, et al. Epidermal growth factor receptor (EGFR) pathway genes and interstitial lung disease: an association study. ''Sci Rep''. 2014 May 13; '''4''': 4893
Deciphering the genetic blueprint behind Holstein milk proteins and production. Description: Lee, Hyun-Jeong, et al. Deciphering the genetic blueprint behind Holstein milk proteins and production. ''Genome Biol Evol''. 2014 May 14; '''6''' (6):1366-74
Association between risk of oral precancer and genetic variations in microRNA and related processing genes. Description: Roy, Roshni, et al. Association between risk of oral precancer and genetic variations in microRNA and related processing genes. ''J Biomed Sci''. 2014 May 17; '''21''': 48
Genome-wide survey indicates involvement of loci on canine chromosomes 7 and 31 in patellar luxation in Flat-Coated Retrievers. Description: Lavrijsen, Ineke C M, et al. Genome-wide survey indicates involvement of loci on canine chromosomes 7 and 31 in patellar luxation in Flat-Coated Retrievers. ''BMC Genet''. 2014 May 28; '''15''': 64
Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian population. Description: Vishal, Mansi, et al. Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian population. ''Sci Rep''. 2014 May 30; '''4''': 5115
Allelic association, DNA resequencing and copy number variation at the metabotropic glutamate receptor GRM7 gene locus in bipolar disorder. Description: Kandaswamy, Radhika, et al. Allelic association, DNA resequencing and copy number variation at the metabotropic glutamate receptor GRM7 gene locus in bipolar disorder. ''Am J Med Genet B Neuropsychiatr Genet''. 2014 Jun; '''165B''' (4):365-72
ATP5H/KCTD2 locus is associated with Alzheimer's disease risk. Description: Boada, M, et al. ATP5H/KCTD2 locus is associated with Alzheimer's disease risk. ''Mol Psychiatry''. 2014 Jun; '''19''' (6):682-7
Early back-to-Africa migration into the Horn of Africa. Description: Hodgson, Jason A, et al. Early back-to-Africa migration into the Horn of Africa. ''PLoS Genet''. 2014 Jun; '''10''' (6):e1004393
Gene-set based genome-wide association analysis for the speed of sound in two skeletal sites of Korean women. Description: Kwon, Ji-Sun, et al. Gene-set based genome-wide association analysis for the speed of sound in two skeletal sites of Korean women. ''BMB Rep''. 2014 Jun; '''47''' (6):348-53
Genetic determinants of long-term changes in blood lipid concentrations: 10-year follow-up of the GLACIER study. Description: Varga, Tibor V, et al. Genetic determinants of long-term changes in blood lipid concentrations: 10-year follow-up of the GLACIER study. ''PLoS Genet''. 2014 Jun; '''10''' (6):e1004388
Genetic variation in OPRD1 and the response to treatment for opioid dependence with buprenorphine in European-American females. Description: Clarke, T-K, et al. Genetic variation in OPRD1 and the response to treatment for opioid dependence with buprenorphine in European-American females. ''Pharmacogenomics J''. 2014 Jun; '''14''' (3):303-8
Germline genetic variants in ABCB1, ABCC1 and ALDH1A1, and risk of hematological and gastrointestinal toxicities in a SWOG Phase III trial S0221 for breast cancer. Description: Yao, S, et al. Germline genetic variants in ABCB1, ABCC1 and ALDH1A1, and risk of hematological and gastrointestinal toxicities in a SWOG Phase III trial S0221 for breast cancer. ''Pharmacogenomics J''. 2014 Jun; '''14''' (3):241-7
Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia. Description: Juraeva, Dilafruz, et al. Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia. ''PLoS Genet''. 2014 Jun; '''10''' (6):e1004345
Introgression from domestic goat generated variation at the major histocompatibility complex of Alpine ibex. Description: Grossen, Christine, et al. Introgression from domestic goat generated variation at the major histocompatibility complex of Alpine ibex. ''PLoS Genet''. 2014 Jun; '''10''' (6):e1004438
Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. Description: Zhang, Ben, et al. Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. ''Nat Genet''. 2014 Jun; '''46''' (6):533-42
Missense variant in TREML2 protects against Alzheimer's disease. Description: Benitez, Bruno A, et al. Missense variant in TREML2 protects against Alzheimer's disease. ''Neurobiol Aging''. 2014 Jun; '''35''' (6):1510.e19-26
Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome. Description: Mok, Kin Y, et al. Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome. ''Neurobiol Aging''. 2014 Jun; '''35''' (6):1513.e1-5
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits. Description: Auer, Paul L, et al. Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits. ''Nat Genet''. 2014 Jun; '''46''' (6):629-34
Variants in host viral replication cycle genes are associated with heterosexual HIV-1 acquisition in Africans. Description: Bigham, Abigail W, et al. Variants in host viral replication cycle genes are associated with heterosexual HIV-1 acquisition in Africans. ''J Acquir Immune Defic Syndr''. 2014 Jun 1; '''66''' (2):127-34
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos. Description: Ko, Arthur, et al. Amerindian-specific regions under positive selection harbour new lipid variants in Latinos. ''Nat Commun''. 2014 Jun 2; '''5''': 3983
Functional analysis of the TRIB1 associated locus linked to plasma triglycerides and coronary artery disease. Description: Douvris, Adrianna, et al. Functional analysis of the TRIB1 associated locus linked to plasma triglycerides and coronary artery disease. ''J Am Heart Assoc''. 2014 Jun 3; '''3''' (3):e000884
Genetic architecture of rind penetrometer resistance in two maize recombinant inbred line populations. Description: Li, Kun, et al. Genetic architecture of rind penetrometer resistance in two maize recombinant inbred line populations. ''BMC Plant Biol''. 2014 Jun 3; '''14''': 152
Single nucleotide polymorphism and haplotype effects associated with somatic cell score in German Holstein cattle. Description: Abdel-Shafy, Hamdy, et al. Single nucleotide polymorphism and haplotype effects associated with somatic cell score in German Holstein cattle. ''Genet Sel Evol''. 2014 Jun 4; '''46''': 35
Association mapping of germination traits in Arabidopsis thaliana under light and nutrient treatments: searching for GxE effects. Description: Morrison, Ginnie D, et al. Association mapping of germination traits in Arabidopsis thaliana under light and nutrient treatments: searching for GxE effects. ''G3 (Bethesda)''. 2014 Jun 5; '''4''' (8):1465-78
Population-specific common SNPs reflect demographic histories and highlight regions of genomic plasticity with functional relevance. Description: Choudhury, Ananyo, et al. Population-specific common SNPs reflect demographic histories and highlight regions of genomic plasticity with functional relevance. ''BMC Genomics''. 2014 Jun 6; '''15''': 437
Regulatory and coding genome regions are enriched for trait associated variants in dairy and beef cattle. Description: Koufariotis, Lambros, et al. Regulatory and coding genome regions are enriched for trait associated variants in dairy and beef cattle. ''BMC Genomics''. 2014 Jun 6; '''15''': 436
The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism. Description: Hadley, Dexter, et al. The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism. ''Nat Commun''. 2014 Jun 13; '''5''': 4074
Weighted risk score-based multifactor dimensionality reduction to detect gene-gene interactions in nasopharyngeal carcinoma. Description: Li, Chao-Feng, et al. Weighted risk score-based multifactor dimensionality reduction to detect gene-gene interactions in nasopharyngeal carcinoma. ''Int J Mol Sci''. 2014 Jun 13; '''15''' (6):10724-37
Performance of HLA allele prediction methods in African Americans for class II genes HLA-DRB1, -DQB1, and -DPB1. Description: Levin, Albert M, et al. Performance of HLA allele prediction methods in African Americans for class II genes HLA-DRB1, -DQB1, and -DPB1. ''BMC Genet''. 2014 Jun 16; '''15''': 72
Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population. Description: Nakano, Masakazu, et al. Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population. ''Sci Rep''. 2014 Jun 18; '''4''': 5340
Homoeologous duplicated regions are involved in quantitative resistance of Brassica napus to stem canker. Description: Fopa Fomeju, Berline, et al. Homoeologous duplicated regions are involved in quantitative resistance of Brassica napus to stem canker. ''BMC Genomics''. 2014 Jun 19; '''15''': 498
The role of FKBP5 genotype in moderating long-term effectiveness of exposure-based psychotherapy for posttraumatic stress disorder. Description: Wilker, S, et al. The role of FKBP5 genotype in moderating long-term effectiveness of exposure-based psychotherapy for posttraumatic stress disorder. ''Transl Psychiatry''. 2014 Jun 24; '''4''': e403
A linkage map of transcribed single nucleotide polymorphisms in rohu (Labeo rohita) and QTL associated with resistance to Aeromonas hydrophila. Description: Robinson, Nicholas, et al. A linkage map of transcribed single nucleotide polymorphisms in rohu (Labeo rohita) and QTL associated with resistance to Aeromonas hydrophila. ''BMC Genomics''. 2014 Jun 30; '''15''': 541
Evaluating the accuracy of AIM panels at quantifying genome ancestry. Description: Pardo-Seco, Jacobo, et al. Evaluating the accuracy of AIM panels at quantifying genome ancestry. ''BMC Genomics''. 2014 Jun 30; '''15''': 543
TM6SF2 rs58542926 influences hepatic fibrosis progression in patients with non-alcoholic fatty liver disease. Description: Liu, Yang-Lin, et al. TM6SF2 rs58542926 influences hepatic fibrosis progression in patients with non-alcoholic fatty liver disease. ''Nat Commun''. 2014 Jun 30; '''5''': 4309
A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach. Description: Traylor, Matthew, et al. A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach. ''PLoS Genet''. 2014 Jul; '''10''' (7):e1004469
Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ. Description: Eicher, John D, et al. Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ. ''Hum Genet''. 2014 Jul; '''133''' (7):869-81
CYP1A1 Ile462Val polymorphism and colorectal cancer risk in Polish patients. Description: Gil, Justyna, et al. CYP1A1 Ile462Val polymorphism and colorectal cancer risk in Polish patients. ''Med Oncol''. 2014 Jul; '''31''' (7):72
Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study. Description: Mullins, Niamh, et al. Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study. ''Am J Med Genet B Neuropsychiatr Genet''. 2014 Jul; '''165B''' (5):428-37
Microsatellite interruptions stabilize primate genomes and exist as population-specific single nucleotide polymorphisms within individual human genomes. Description: Ananda, Guruprasad, et al. Microsatellite interruptions stabilize primate genomes and exist as population-specific single nucleotide polymorphisms within individual human genomes. ''PLoS Genet''. 2014 Jul; '''10''' (7):e1004498
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer. Description: Wang, Yufei, et al. Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer. ''Nat Genet''. 2014 Jul; '''46''' (7):736-41
Sorafenib dose escalation is not uniformly associated with blood pressure elevations in normotensive patients with advanced malignancies. Description: Karovic, S, et al. Sorafenib dose escalation is not uniformly associated with blood pressure elevations in normotensive patients with advanced malignancies. ''Clin Pharmacol Ther''. 2014 Jul; '''96''' (1):27-35
Whole genome and exome sequencing of monozygotic twins discordant for Crohn's disease. Description: Petersen, Britt-Sabina, et al. Whole genome and exome sequencing of monozygotic twins discordant for Crohn's disease. ''BMC Genomics''. 2014 Jul 5; '''15''': 564
Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission. Description: Karayannis, T, et al. Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission. ''Nature''. 2014 Jul 10; '''511''' (7508):236-40
Joint identification of genetic variants for physical activity in Korean population. Description: Kim, Jayoun, et al. Joint identification of genetic variants for physical activity in Korean population. ''Int J Mol Sci''. 2014 Jul 14; '''15''' (7):12407-21
Insight into genetic determinants of resting heart rate. Description: Mezzavilla, Massimo, et al. Insight into genetic determinants of resting heart rate. ''Gene''. 2014 Jul 15; '''545''' (1):170-4
Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay. Description: Weber, Megan L, et al. Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay. ''BMC Med Genet''. 2014 Jul 15; '''15''': 81
Fast and cost-effective genetic mapping in apple using next-generation sequencing. Description: Gardner, Kyle M, et al. Fast and cost-effective genetic mapping in apple using next-generation sequencing. ''G3 (Bethesda)''. 2014 Jul 16; '''4''' (9):1681-7
Whole-genome sequence analysis reveals differences in population management and selection of European low-input pig breeds. Description: Herrero-Medrano, Juan Manuel, et al. Whole-genome sequence analysis reveals differences in population management and selection of European low-input pig breeds. ''BMC Genomics''. 2014 Jul 16; '''15''': 601
Systematic permutation testing in GWAS pathway analyses: identification of genetic networks in dilated cardiomyopathy and ulcerative colitis. Description: Backes, Christina, et al. Systematic permutation testing in GWAS pathway analyses: identification of genetic networks in dilated cardiomyopathy and ulcerative colitis. ''BMC Genomics''. 2014 Jul 22; '''15''': 622
Validation and assessment of variant calling pipelines for next-generation sequencing. Description: Pirooznia, Mehdi, et al. Validation and assessment of variant calling pipelines for next-generation sequencing. ''Hum Genomics''. 2014 Jul 30; '''8''': 14
A rare mutation of CACNA1C in a patient with bipolar disorder, and decreased gene expression associated with a bipolar-associated common SNP of CACNA1C in brain. Description: Gershon, E S, et al. A rare mutation of CACNA1C in a patient with bipolar disorder, and decreased gene expression associated with a bipolar-associated common SNP of CACNA1C in brain. ''Mol Psychiatry''. 2014 Aug; '''19''' (8):890-4
Comprehensive identification of single nucleotide polymorphisms associated with beta-lactam resistance within pneumococcal mosaic genes. Description: Chewapreecha, Claire, et al. Comprehensive identification of single nucleotide polymorphisms associated with beta-lactam resistance within pneumococcal mosaic genes. ''PLoS Genet''. 2014 Aug; '''10''' (8):e1004547
Genetic variation of oxidative phosphorylation genes in stroke and Alzheimer's disease. Description: Biffi, Alessandro, et al. Genetic variation of oxidative phosphorylation genes in stroke and Alzheimer's disease. ''Neurobiol Aging''. 2014 Aug; '''35''' (8):1956.e1-8
Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1. Description: Cai, Qiuyin, et al. Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1. ''Nat Genet''. 2014 Aug; '''46''' (8):886-90
Genome-wide association and linkage analyses localize a progressive retinal atrophy locus in Persian cats. Description: Alhaddad, Hasan, et al. Genome-wide association and linkage analyses localize a progressive retinal atrophy locus in Persian cats. ''Mamm Genome''. 2014 Aug; '''25''' (7-8):354-62
Genome-wide data reveal novel genes for methotrexate response in a large cohort of juvenile idiopathic arthritis cases. Description: Cobb, J, et al. Genome-wide data reveal novel genes for methotrexate response in a large cohort of juvenile idiopathic arthritis cases. ''Pharmacogenomics J''. 2014 Aug; '''14''' (4):356-64
Global genetic variations predict brain response to faces. Description: Dickie, Erin W, et al. Global genetic variations predict brain response to faces. ''PLoS Genet''. 2014 Aug; '''10''' (8):e1004523
Heritability and genetic association analysis of cognition in the Diabetes Heart Study. Description: Cox, Amanda J, et al. Heritability and genetic association analysis of cognition in the Diabetes Heart Study. ''Neurobiol Aging''. 2014 Aug; '''35''' (8):1958.e3-1958.e12
MODMatcher: multi-omics data matcher for integrative genomic analysis. Description: Yoo, Seungyeul, et al. MODMatcher: multi-omics data matcher for integrative genomic analysis. ''PLoS Comput Biol''. 2014 Aug; '''10''' (8):e1003790
Patterns of admixture and population structure in native populations of Northwest North America. Description: Verdu, Paul, et al. Patterns of admixture and population structure in native populations of Northwest North America. ''PLoS Genet''. 2014 Aug; '''10''' (8):e1004530
Genetic evidence of African slavery at the beginning of the trans-Atlantic slave trade. Description: Martiniano, Rui, et al. Genetic evidence of African slavery at the beginning of the trans-Atlantic slave trade. ''Sci Rep''. 2014 Aug 8; '''4''': 5994
Lack of association between miR-27a, miR-146a, miR-196a-2, miR-492 and miR-608 gene polymorphisms and colorectal cancer. Description: Kupcinskas, Juozas, et al. Lack of association between miR-27a, miR-146a, miR-196a-2, miR-492 and miR-608 gene polymorphisms and colorectal cancer. ''Sci Rep''. 2014 Aug 8; '''4''': 5993
Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A. Description: Wang, Hansong, et al. Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A. ''Nat Commun''. 2014 Aug 8; '''5''': 4613
Validation of multiple single nucleotide variation calls by additional exome analysis with a semiconductor sequencer to supplement data of whole-genome sequencing of a human population. Description: Motoike, Ikuko N, et al. Validation of multiple single nucleotide variation calls by additional exome analysis with a semiconductor sequencer to supplement data of whole-genome sequencing of a human population. ''BMC Genomics''. 2014 Aug 10; '''15''': 673
Impact of pre-imputation SNP-filtering on genotype imputation results. Description: Roshyara, Nab Raj, et al. Impact of pre-imputation SNP-filtering on genotype imputation results. ''BMC Genet''. 2014 Aug 12; '''15''': 88
Association study of genes controlling IL-12-dependent IFN-gamma immunity: STAT4 alleles increase risk of pulmonary tuberculosis in Morocco. Description: Sabri, Ayoub, et al. Association study of genes controlling IL-12-dependent IFN-gamma immunity: STAT4 alleles increase risk of pulmonary tuberculosis in Morocco. ''J Infect Dis''. 2014 Aug 15; '''210''' (4):611-8
Impact of a functional polymorphism in the PAR-1 gene promoter in COPD and COPD exacerbations. Description: Plate, Manuela, et al. Impact of a functional polymorphism in the PAR-1 gene promoter in COPD and COPD exacerbations. ''Am J Physiol Lung Cell Mol Physiol''. 2014 Aug 15; '''307''' (4):L311-6
Top associated SNPs in prostate cancer are significantly enriched in cis-expression quantitative trait loci and at transcription factor binding sites. Description: Jiang, Junfeng, et al. Top associated SNPs in prostate cancer are significantly enriched in cis-expression quantitative trait loci and at transcription factor binding sites. ''Oncotarget''. 2014 Aug 15; '''5''' (15):6168-77
Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. Description: Enroth, Stefan, et al. Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. ''Nat Commun''. 2014 Aug 22; '''5''': 4684
MORC1 exhibits cross-species differential methylation in association with early life stress as well as genome-wide association with MDD. Description: Nieratschker, V, et al. MORC1 exhibits cross-species differential methylation in association with early life stress as well as genome-wide association with MDD. ''Transl Psychiatry''. 2014 Aug 26; '''4''': e429
QTL for white spot syndrome virus resistance and the sex-determining locus in the Indian black tiger shrimp (Penaeus monodon). Description: Robinson, Nicholas A, et al. QTL for white spot syndrome virus resistance and the sex-determining locus in the Indian black tiger shrimp (Penaeus monodon). ''BMC Genomics''. 2014 Aug 28; '''15''': 731
An intronic PICALM polymorphism, rs588076, is associated with allelic expression of a PICALM isoform. Description: Parikh, Ishita, et al. An intronic PICALM polymorphism, rs588076, is associated with allelic expression of a PICALM isoform. ''Mol Neurodegener''. 2014 Aug 29; '''9''': 32
A Follow-up Association Study of Genetic Variants for Bone Mineral Density in a Korean Population. Description: Ham, Seokjin, et al. A Follow-up Association Study of Genetic Variants for Bone Mineral Density in a Korean Population. ''Genomics Inform''. 2014 Sep; '''12''' (3):114-20
A single codon insertion in PICALM is associated with development of familial subvalvular aortic stenosis in Newfoundland dogs. Description: Stern, Joshua A, et al. A single codon insertion in PICALM is associated with development of familial subvalvular aortic stenosis in Newfoundland dogs. ''Hum Genet''. 2014 Sep; '''133''' (9):1139-48
A whole genome association study on meat palatability in hanwoo. Description: Hyeong, K-E, et al. A whole genome association study on meat palatability in hanwoo. ''Asian-Australas J Anim Sci''. 2014 Sep; '''27''' (9):1219-27
Co-regulated transcripts associated to cooperating eSNPs define Bi-fan motifs in human gene networks. Description: Kreimer, Anat, et al. Co-regulated transcripts associated to cooperating eSNPs define Bi-fan motifs in human gene networks. ''PLoS Genet''. 2014 Sep; '''10''' (9):e1004587
Epidemiological and genome-wide association study of gastritis or gastric ulcer in korean populations. Description: Oh, Sumin, et al. Epidemiological and genome-wide association study of gastritis or gastric ulcer in korean populations. ''Genomics Inform''. 2014 Sep; '''12''' (3):127-33
Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. Description: Beecham, Gary W, et al. Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. ''PLoS Genet''. 2014 Sep; '''10''' (9):e1004606
Genome-wide association study of medication adherence in chronic diseases in the korean population. Description: Seo, Incheol, et al. Genome-wide association study of medication adherence in chronic diseases in the korean population. ''Genomics Inform''. 2014 Sep; '''12''' (3):121-6
Genome-wide screening for DNA variants associated with reading and language traits. Description: Gialluisi, A, et al. Genome-wide screening for DNA variants associated with reading and language traits. ''Genes Brain Behav''. 2014 Sep; '''13''' (7):686-701
GWAS-based pathway analysis differentiates between fluid and crystallized intelligence. Description: Christoforou, A, et al. GWAS-based pathway analysis differentiates between fluid and crystallized intelligence. ''Genes Brain Behav''. 2014 Sep; '''13''' (7):663-74
Inferring population structure and relationship using minimal independent evolutionary markers in Y-chromosome: a hybrid approach of recursive feature selection for hierarchical clustering. Description: Srivastava, Amit Kumar, et al. Inferring population structure and relationship using minimal independent evolutionary markers in Y-chromosome: a hybrid approach of recursive feature selection for hierarchical clustering. ''Nucleic Acids Res''. 2014 Sep; '''42''' (15):e122
Principal component analysis characterizes shared pathogenetics from genome-wide association studies. Description: Chang, Diana, et al. Principal component analysis characterizes shared pathogenetics from genome-wide association studies. ''PLoS Comput Biol''. 2014 Sep; '''10''' (9):e1003820
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles. Description: Goldstein, Jacqueline I, et al. Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles. ''Nat Commun''. 2014 Sep 4; '''5''': 4757
EYA4 is inactivated biallelically at a high frequency in sporadic lung cancer and is associated with familial lung cancer risk. Description: Wilson, I M, et al. EYA4 is inactivated biallelically at a high frequency in sporadic lung cancer and is associated with familial lung cancer risk. ''Oncogene''. 2014 Sep 4; '''33''' (36):4464-73
Genetic polymorphisms and asthma: findings from a case-control study in the Madeira island population. Description: Berenguer, Anabela Goncalves, et al. Genetic polymorphisms and asthma: findings from a case-control study in the Madeira island population. ''Biol Res''. 2014 Sep 4; '''47''': 40
Genetic variation in taste receptor pseudogenes provides evidence for a dynamic role in human evolution. Description: Risso, Davide, et al. Genetic variation in taste receptor pseudogenes provides evidence for a dynamic role in human evolution. ''BMC Evol Biol''. 2014 Sep 13; '''14''': 198
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans. Description: Timpson, Nicholas J, et al. A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans. ''Nat Commun''. 2014 Sep 16; '''5''': 4871
Common variation near ROBO2 is associated with expressive vocabulary in infancy. Description: St Pourcain, Beate, et al. Common variation near ROBO2 is associated with expressive vocabulary in infancy. ''Nat Commun''. 2014 Sep 16; '''5''': 4831
Ancient human genomes suggest three ancestral populations for present-day Europeans. Description: Lazaridis, Iosif, et al. Ancient human genomes suggest three ancestral populations for present-day Europeans. ''Nature''. 2014 Sep 18; '''513''' (7518):409-13
A powerful tool for genome analysis in maize: development and evaluation of the high density 600 k SNP genotyping array. Description: Unterseer, Sandra, et al. A powerful tool for genome analysis in maize: development and evaluation of the high density 600 k SNP genotyping array. ''BMC Genomics''. 2014 Sep 29; '''15''': 823
Genetic association of impulsivity in young adults: a multivariate study. Description: Khadka, S, et al. Genetic association of impulsivity in young adults: a multivariate study. ''Transl Psychiatry''. 2014 Sep 30; '''4''': e451
Genomic evidence for a globally distributed, bimodal population in the ovine footrot pathogen Dichelobacter nodosus. Description: Kennan, Ruth M, et al. Genomic evidence for a globally distributed, bimodal population in the ovine footrot pathogen Dichelobacter nodosus. ''MBio''. 2014 Sep 30; '''5''' (5):e01821-14
A Genome Wide Association Study on Age at First Calving Using High Density Single Nucleotide Polymorphism Chips in Hanwoo (Bos taurus coreanae). Description: Hyeong, K-E, et al. A Genome Wide Association Study on Age at First Calving Using High Density Single Nucleotide Polymorphism Chips in Hanwoo (Bos taurus coreanae). ''Asian-Australas J Anim Sci''. 2014 Oct; '''27''' (10):1406-10
An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs. Description: Ekenstedt, Kari J, et al. An ARHGEF10 deletion is highly associated with a juvenile-onset inherited polyneuropathy in Leonberger and Saint Bernard dogs. ''PLoS Genet''. 2014 Oct; '''10''' (10):e1004635
A splice mutation in the PHKG1 gene causes high glycogen content and low meat quality in pig skeletal muscle. Description: Ma, Junwu, et al. A splice mutation in the PHKG1 gene causes high glycogen content and low meat quality in pig skeletal muscle. ''PLoS Genet''. 2014 Oct; '''10''' (10):e1004710
Circadian polymorphisms in night owls, in bipolars, and in non-24-hour sleep cycles. Description: Kripke, Daniel F, et al. Circadian polymorphisms in night owls, in bipolars, and in non-24-hour sleep cycles. ''Psychiatry Investig''. 2014 Oct; '''11''' (4):345-62
Genome-wide association study of CSF levels of 59 alzheimer's disease candidate proteins: significant associations with proteins involved in amyloid processing and inflammation. Description: Kauwe, John S K, et al. Genome-wide association study of CSF levels of 59 alzheimer's disease candidate proteins: significant associations with proteins involved in amyloid processing and inflammation. ''PLoS Genet''. 2014 Oct; '''10''' (10):e1004758
Genome-wide discovery of drug-dependent human liver regulatory elements. Description: Smith, Robin P, et al. Genome-wide discovery of drug-dependent human liver regulatory elements. ''PLoS Genet''. 2014 Oct; '''10''' (10):e1004648
Genomic prediction based on data from three layer lines: a comparison between linear methods. Description: Calus, Mario Pl, et al. Genomic prediction based on data from three layer lines: a comparison between linear methods. ''Genet Sel Evol''. 2014 Oct 1; '''46''': 57
Germline mutations in MAP3K6 are associated with familial gastric cancer. Description: Gaston, Daniel, et al. Germline mutations in MAP3K6 are associated with familial gastric cancer. ''PLoS Genet''. 2014 Oct; '''10''' (10):e1004669
Imputation of sequence level genotypes in the Franches-Montagnes horse breed. Description: Frischknecht, Mirjam, et al. Imputation of sequence level genotypes in the Franches-Montagnes horse breed. ''Genet Sel Evol''. 2014 Oct 1; '''46''': 63
Pathway-based analysis tools for complex diseases: a review. Description: Jin, Lv, et al. Pathway-based analysis tools for complex diseases: a review. ''Genomics Proteomics Bioinformatics''. 2014 Oct; '''12''' (5):210-20
Population history and genomic signatures for high-altitude adaptation in Tibetan pigs. Description: Ai, Huashui, et al. Population history and genomic signatures for high-altitude adaptation in Tibetan pigs. ''BMC Genomics''. 2014 Oct 1; '''15''': 834
Quantitative trait loci mapping for canine hip dysplasia and its related traits in UK Labrador Retrievers. Description: Sanchez-Molano, Enrique, et al. Quantitative trait loci mapping for canine hip dysplasia and its related traits in UK Labrador Retrievers. ''BMC Genomics''. 2014 Oct 1; '''15''': 833
Study of five novel non-synonymous polymorphisms in human brain-expressed genes in a Colombian sample. Description: Ojeda, Diego A, et al. Study of five novel non-synonymous polymorphisms in human brain-expressed genes in a Colombian sample. ''Ann Neurosci''. 2014 Oct; '''21''' (4):138-43
Using ancestry-informative markers to identify fine structure across 15 populations of European origin. Description: Huckins, Laura M, et al. Using ancestry-informative markers to identify fine structure across 15 populations of European origin. ''Eur J Hum Genet''. 2014 Oct; '''22''' (10):1190-200
Comparative genomics reveals multiple genetic backgrounds of human pathogenicity in the Trypanosoma brucei complex. Description: Sistrom, Mark, et al. Comparative genomics reveals multiple genetic backgrounds of human pathogenicity in the Trypanosoma brucei complex. ''Genome Biol Evol''. 2014 Oct 5; '''6''' (10):2811-9
alphaCaMKII controls the establishment of cocaine's reinforcing effects in mice and humans. Description: Easton, A C, et al. alphaCaMKII controls the establishment of cocaine's reinforcing effects in mice and humans. ''Transl Psychiatry''. 2014 Oct 7; '''4''': e457
A meta-analysis of gene expression quantitative trait loci in brain. Description: Kim, Y, et al. A meta-analysis of gene expression quantitative trait loci in brain. ''Transl Psychiatry''. 2014 Oct 7; '''4''': e459
A comprehensive evaluation of the role of genetic variation in follicular lymphoma survival. Description: Baecklund, Fredrik, et al. A comprehensive evaluation of the role of genetic variation in follicular lymphoma survival. ''BMC Med Genet''. 2014 Oct 8; '''15''': 113
Genome wide linkage disequilibrium and genetic structure in Sicilian dairy sheep breeds. Description: Mastrangelo, Salvatore, et al. Genome wide linkage disequilibrium and genetic structure in Sicilian dairy sheep breeds. ''BMC Genet''. 2014 Oct 10; '''15''': 108
The genetics of monarch butterfly migration and warning colouration. Description: Zhan, Shuai, et al. The genetics of monarch butterfly migration and warning colouration. ''Nature''. 2014 Oct 16; '''514''' (7522):317-21
Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25. Description: Fejerman, Laura, et al. Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25. ''Nat Commun''. 2014 Oct 20; '''5''': 5260
An Immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3. Description: Zochling, Jane, et al. An Immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3. ''Arthritis Res Ther''. 2014 Oct 21; '''16''' (5):438
Common variants at 1p36 are associated with superior frontal gyrus volume. Description: Hashimoto, R, et al. Common variants at 1p36 are associated with superior frontal gyrus volume. ''Transl Psychiatry''. 2014 Oct 21; '''4''': e472
Genome flux and stasis in a five millennium transect of European prehistory. Description: Gamba, Cristina, et al. Genome flux and stasis in a five millennium transect of European prehistory. ''Nat Commun''. 2014 Oct 21; '''5''': 5257
Identifying rare variants for genetic risk through a combined pedigree and phenotype approach: application to suicide and asthma. Description: Darlington, T M, et al. Identifying rare variants for genetic risk through a combined pedigree and phenotype approach: application to suicide and asthma. ''Transl Psychiatry''. 2014 Oct 21; '''4''': e471
Identified single-nucleotide polymorphisms and haplotypes at 16q22.1 increase diabetic nephropathy risk in Han Chinese population. Description: Liao, Li-Na, et al. Identified single-nucleotide polymorphisms and haplotypes at 16q22.1 increase diabetic nephropathy risk in Han Chinese population. ''BMC Genet''. 2014 Oct 31; '''15''': 113
Adiposity significantly modifies genetic risk for dyslipidemia. Description: Cole, Christopher B, et al. Adiposity significantly modifies genetic risk for dyslipidemia. ''J Lipid Res''. 2014 Nov; '''55''' (11):2416-22
Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2). Description: Karaderi, T, et al. Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2). ''Ann Rheum Dis''. 2014 Nov; '''73''' (11):2054-8
A population-based study of genetic variation and psychotic experiences in adolescents. Description: Zammit, Stanley, et al. A population-based study of genetic variation and psychotic experiences in adolescents. ''Schizophr Bull''. 2014 Nov; '''40''' (6):1254-62
A study of genes encoding cytokines (IL6, IL10, TNF), cytokine receptors (IL6R, IL6ST), and glucocorticoid receptor (NR3C1) and susceptibility to bronchopulmonary dysplasia. Description: Huusko, Johanna M, et al. A study of genes encoding cytokines (IL6, IL10, TNF), cytokine receptors (IL6R, IL6ST), and glucocorticoid receptor (NR3C1) and susceptibility to bronchopulmonary dysplasia. ''BMC Med Genet''. 2014 Nov 1; '''15''': 120
BAT2 and BAT3 polymorphisms as novel genetic risk factors for rejection after HLA-related SCT. Description: Piras, Ignazio Stefano, et al. BAT2 and BAT3 polymorphisms as novel genetic risk factors for rejection after HLA-related SCT. ''Bone Marrow Transplant''. 2014 Nov; '''49''' (11):1400-1404
Common vitamin D pathway gene variants reveal contrasting effects on serum vitamin D levels in African Americans and European Americans. Description: Batai, Ken, et al. Common vitamin D pathway gene variants reveal contrasting effects on serum vitamin D levels in African Americans and European Americans. ''Hum Genet''. 2014 Nov; '''133''' (11):1395-405
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens. Description: Kiryluk, Krzysztof, et al. Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens. ''Nat Genet''. 2014 Nov; '''46''' (11):1187-96
Evaluation of genome based estimated breeding values for meat quality in a berkshire population using high density single nucleotide polymorphism chips. Description: Baby, S, et al. Evaluation of genome based estimated breeding values for meat quality in a berkshire population using high density single nucleotide polymorphism chips. ''Asian-Australas J Anim Sci''. 2014 Nov; '''27''' (11):1540-7
Evaluation of variant identification methods for whole genome sequencing data in dairy cattle. Description: Baes, Christine F, et al. Evaluation of variant identification methods for whole genome sequencing data in dairy cattle. ''BMC Genomics''. 2014 Nov 1; '''15''': 948
Genetic determinants in the development of sensitization to environmental allergens in early childhood. Description: Tripathi, Priya, et al. Genetic determinants in the development of sensitization to environmental allergens in early childhood. ''Immun Inflamm Dis''. 2014 Nov; '''2''' (3):193-204
Genetic variations in protocadherin 15 and their interactions with noise exposure associated with noise-induced hearing loss in Chinese population. Description: Zhang, Xuhui, et al. Genetic variations in protocadherin 15 and their interactions with noise exposure associated with noise-induced hearing loss in Chinese population. ''Environ Res''. 2014 Nov; '''135''': 247-52
Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'. Description: Deelen, Patrick, et al. Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'. ''Eur J Hum Genet''. 2014 Nov; '''22''' (11):1321-6
No effect of schizophrenia risk genes MIR137, TCF4, and ZNF804A on macroscopic brain structure. Description: Cousijn, Helena, et al. No effect of schizophrenia risk genes MIR137, TCF4, and ZNF804A on macroscopic brain structure. ''Schizophr Res''. 2014 Nov; '''159''' (2-3):329-32
Unusual Stuve-Wiedemann syndrome with complete maternal chromosome 5 isodisomy. Description: Melone, Mariarosa A B, et al. Unusual Stuve-Wiedemann syndrome with complete maternal chromosome 5 isodisomy. ''Ann Clin Transl Neurol''. 2014 Nov; '''1''' (11):926-32
Genetic variants in ADAM33 are associated with airway inflammation and lung function in COPD. Description: Wang, Xinyan, et al. Genetic variants in ADAM33 are associated with airway inflammation and lung function in COPD. ''BMC Pulm Med''. 2014 Nov 4; '''14''': 173
The genome of a Mongolian individual reveals the genetic imprints of Mongolians on modern human populations. Description: Bai, Haihua, et al. The genome of a Mongolian individual reveals the genetic imprints of Mongolians on modern human populations. ''Genome Biol Evol''. 2014 Nov 5; '''6''' (12):3122-36
Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants. Description: Panoutsopoulou, Kalliope, et al. Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants. ''Nat Commun''. 2014 Nov 6; '''5''': 5345
Sexually dimorphic genetic architecture of complex traits in a large-scale F2 cross in pigs. Description: Cui, Leilei, et al. Sexually dimorphic genetic architecture of complex traits in a large-scale F2 cross in pigs. ''Genet Sel Evol''. 2014 Nov 6; '''46''': 76
Whole genome sequencing of Turkish genomes reveals functional private alleles and impact of genetic interactions with Europe, Asia and Africa. Description: Alkan, Can, et al. Whole genome sequencing of Turkish genomes reveals functional private alleles and impact of genetic interactions with Europe, Asia and Africa. ''BMC Genomics''. 2014 Nov 7; '''15''': 963
Large-scale gene-centric analysis identifies polymorphisms for resistant hypertension. Description: Fontana, Vanessa, et al. Large-scale gene-centric analysis identifies polymorphisms for resistant hypertension. ''J Am Heart Assoc''. 2014 Nov 10; '''3''' (6):e001398
Gender specific association of a complement component 3 polymorphism with polypoidal choroidal vasculopathy. Description: Liu, Ke, et al. Gender specific association of a complement component 3 polymorphism with polypoidal choroidal vasculopathy. ''Sci Rep''. 2014 Nov 12; '''4''': 7018
WISP1 polymorphisms contribute to platinum-based chemotherapy toxicity in lung cancer patients. Description: Chen, Juan, et al. WISP1 polymorphisms contribute to platinum-based chemotherapy toxicity in lung cancer patients. ''Int J Mol Sci''. 2014 Nov 14; '''15''' (11):21011-27
Sparse representation based biomarker selection for schizophrenia with integrated analysis of fMRI and SNPs. Description: Cao, Hongbao, et al. Sparse representation based biomarker selection for schizophrenia with integrated analysis of fMRI and SNPs. ''Neuroimage''. 2014 Nov 15; '''102 Pt 1''': 220-8
Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity. Description: Willmann, Katharina L, et al. Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity. ''Nat Commun''. 2014 Nov 19; '''5''': 5360
Association of rs6982567 near GDF6 with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy in a Han Chinese cohort. Description: Ji, Yuying, et al. Association of rs6982567 near GDF6 with neovascular age-related macular degeneration and polypoidal choroidal vasculopathy in a Han Chinese cohort. ''BMC Ophthalmol''. 2014 Nov 22; '''14''': 140
Effect of diversity and missing data on genetic assignment with RAD-Seq markers. Description: Chattopadhyay, Balaji, et al. Effect of diversity and missing data on genetic assignment with RAD-Seq markers. ''BMC Res Notes''. 2014 Nov 25; '''7''': 841
Using multi-way admixture mapping to elucidate TB susceptibility in the South African Coloured population. Description: Daya, Michelle, et al. Using multi-way admixture mapping to elucidate TB susceptibility in the South African Coloured population. ''BMC Genomics''. 2014 Nov 25; '''15''': 1021
Endophenotypes for Age-Related Macular Degeneration: Extending Our Reach into the Preclinical Stages of Disease. Description: Gorin, Michael B, et al. Endophenotypes for Age-Related Macular Degeneration: Extending Our Reach into the Preclinical Stages of Disease. ''J Clin Med''. 2014 Nov 28; '''3''' (4):1335-56
Adaptations to climate-mediated selective pressures in sheep. Description: Lv, Feng-Hua, et al. Adaptations to climate-mediated selective pressures in sheep. ''Mol Biol Evol''. 2014 Dec; '''31''' (12):3324-43
A genome-wide association study identifies a LEPR gene as a novel predisposing factor for childhood fasting plasma glucose. Description: Go, Min Jin, et al. A genome-wide association study identifies a LEPR gene as a novel predisposing factor for childhood fasting plasma glucose. ''Genomics''. 2014 Dec; '''104''' (6 Pt B):594-8
Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder. Description: Witt, Stephanie H, et al. Analysis of genome-wide significant bipolar disorder genes in borderline personality disorder. ''Psychiatr Genet''. 2014 Dec; '''24''' (6):262-5
Association between CETP, MLXIPL, and TOMM40 polymorphisms and serum lipid levels in a Latvian population. Description: Radovica, I, et al. Association between CETP, MLXIPL, and TOMM40 polymorphisms and serum lipid levels in a Latvian population. ''Meta Gene''. 2014 Dec; '''2''': 565-78
Association of Toll-like receptor polymorphisms with HIV status in North Americans. Description: Willie, B, et al. Association of Toll-like receptor polymorphisms with HIV status in North Americans. ''Genes Immun''. 2014 Dec; '''15''' (8):569-77
Drosophila suzukii: the genetic footprint of a recent, worldwide invasion. Description: Adrion, Jeffrey R, et al. Drosophila suzukii: the genetic footprint of a recent, worldwide invasion. ''Mol Biol Evol''. 2014 Dec; '''31''' (12):3148-63
Establishment of CYP2D6 reference samples by multiple validated genotyping platforms. Description: Fang, H, et al. Establishment of CYP2D6 reference samples by multiple validated genotyping platforms. ''Pharmacogenomics J''. 2014 Dec; '''14''' (6):564-72
Fine mapping and functional studies of risk variants for type 1 diabetes at chromosome 16p13.13. Description: Tomlinson, M Joseph 4th, et al. Fine mapping and functional studies of risk variants for type 1 diabetes at chromosome 16p13.13. ''Diabetes''. 2014 Dec; '''63''' (12):4360-8
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies. Description: Bras, Jose, et al. Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies. ''Hum Mol Genet''. 2014 Dec 1; '''23''' (23):6139-46
Genetic analysis of axial length genes in high grade myopia from Indian population. Description: Sharmila, Ferdinamarie, et al. Genetic analysis of axial length genes in high grade myopia from Indian population. ''Meta Gene''. 2014 Dec; '''2''': 164-75
Genome-wide association study identifies candidate Loci associated with platelet count in koreans. Description: Oh, Ji Hee, et al. Genome-wide association study identifies candidate Loci associated with platelet count in koreans. ''Genomics Inform''. 2014 Dec; '''12''' (4):225-30
Genome-wide association study of hepatitis in korean populations. Description: Hong, Youngbok, et al. Genome-wide association study of hepatitis in korean populations. ''Genomics Inform''. 2014 Dec; '''12''' (4):203-7
Genome-wide association study of metabolic syndrome in koreans. Description: Jeong, Seok Won, et al. Genome-wide association study of metabolic syndrome in koreans. ''Genomics Inform''. 2014 Dec; '''12''' (4):187-94
High-density genotyping of immune loci in Kawasaki disease and IVIG treatment response in European-American case-parent trio study. Description: Shendre, A, et al. High-density genotyping of immune loci in Kawasaki disease and IVIG treatment response in European-American case-parent trio study. ''Genes Immun''. 2014 Dec; '''15''' (8):534-42
Joint GWAS Analysis: Comparing similar GWAS at different genomic resolutions identifies novel pathway associations with six complex diseases. Description: McGeachie, Michael J, et al. Joint GWAS Analysis: Comparing similar GWAS at different genomic resolutions identifies novel pathway associations with six complex diseases. ''Genom Data''. 2014 Dec 1; '''2''': 202-211
Large-scale metabolomic profiling identifies novel biomarkers for incident coronary heart disease. Description: Ganna, Andrea, et al. Large-scale metabolomic profiling identifies novel biomarkers for incident coronary heart disease. ''PLoS Genet''. 2014 Dec; '''10''' (12):e1004801
Pathway Analysis of Metabolic Syndrome Using a Genome-Wide Association Study of Korea Associated Resource (KARE) Cohorts. Description: Shim, Unjin, et al. Pathway Analysis of Metabolic Syndrome Using a Genome-Wide Association Study of Korea Associated Resource (KARE) Cohorts. ''Genomics Inform''. 2014 Dec; '''12''' (4):195-202
Profile of differential promoter activity by nucleotide substitution at GWAS signals for multiple sclerosis. Description: Ryu, Jihye, et al. Profile of differential promoter activity by nucleotide substitution at GWAS signals for multiple sclerosis. ''Medicine (Baltimore)''. 2014 Dec; '''93''' (28):e281
Relevance Epistasis Network of Gastritis for Intra-chromosomes in the Korea Associated Resource (KARE) Cohort Study. Description: Jeong, Hyun-Hwan, et al. Relevance Epistasis Network of Gastritis for Intra-chromosomes in the Korea Associated Resource (KARE) Cohort Study. ''Genomics Inform''. 2014 Dec; '''12''' (4):216-24
Replication of Interactions between Genome-Wide Genetic Variants and Body Mass Index in Fasting Glucose and Insulin Levels. Description: Hong, Kyung-Won, et al. Replication of Interactions between Genome-Wide Genetic Variants and Body Mass Index in Fasting Glucose and Insulin Levels. ''Genomics Inform''. 2014 Dec; '''12''' (4):236-9
Short reads phasing to construct haplotypes in genomic regions that are associated with body mass index in korean individuals. Description: Lee, Kichan, et al. Short reads phasing to construct haplotypes in genomic regions that are associated with body mass index in korean individuals. ''Genomics Inform''. 2014 Dec; '''12''' (4):165-70
The ABCG2 Polymorphism rs2725220 Is Associated with Hyperuricemia in the Korean Population. Description: Sull, Jae Woong, et al. The ABCG2 Polymorphism rs2725220 Is Associated with Hyperuricemia in the Korean Population. ''Genomics Inform''. 2014 Dec; '''12''' (4):231-5
The Usage of an SNP-SNP Relationship Matrix for Best Linear Unbiased Prediction (BLUP) Analysis Using a Community-Based Cohort Study. Description: Lee, Young-Sup, et al. The Usage of an SNP-SNP Relationship Matrix for Best Linear Unbiased Prediction (BLUP) Analysis Using a Community-Based Cohort Study. ''Genomics Inform''. 2014 Dec; '''12''' (4):254-60
Characterization of the porcine nutrient and taste receptor gene repertoire in domestic and wild populations across the globe. Description: da Silva, Elizabete C, et al. Characterization of the porcine nutrient and taste receptor gene repertoire in domestic and wild populations across the globe. ''BMC Genomics''. 2014 Dec 3; '''15''': 1057
Khoisan hunter-gatherers have been the largest population throughout most of modern-human demographic history. Description: Kim, Hie Lim, et al. Khoisan hunter-gatherers have been the largest population throughout most of modern-human demographic history. ''Nat Commun''. 2014 Dec 4; '''5''': 5692
Genetic landscape of populations along the Silk Road: admixture and migration patterns. Description: Mezzavilla, Massimo, et al. Genetic landscape of populations along the Silk Road: admixture and migration patterns. ''BMC Genet''. 2014 Dec 5; '''15''': 131
Genome-wide mapping in a house mouse hybrid zone reveals hybrid sterility loci and Dobzhansky-Muller interactions. Description: Turner, Leslie M, et al. Genome-wide mapping in a house mouse hybrid zone reveals hybrid sterility loci and Dobzhansky-Muller interactions. ''Elife''. 2014 Dec 9; '''3''':
A hereditary disposition for bovine peripheral nerve sheath tumors in Danish Holstein cattle. Description: Grossi, Anette B, et al. A hereditary disposition for bovine peripheral nerve sheath tumors in Danish Holstein cattle. ''Acta Vet Scand''. 2014 Dec 10; '''56''': 85
An integrated epigenomic analysis for type 2 diabetes susceptibility loci in monozygotic twins. Description: Yuan, Wei, et al. An integrated epigenomic analysis for type 2 diabetes susceptibility loci in monozygotic twins. ''Nat Commun''. 2014 Dec 12; '''5''': 5719
Identification of single nucleotide polymorphisms in Toll-like receptor candidate genes associated with tuberculosis infection in water buffalo (Bubalus bubalis). Description: Alfano, Flora, et al. Identification of single nucleotide polymorphisms in Toll-like receptor candidate genes associated with tuberculosis infection in water buffalo (Bubalus bubalis). ''BMC Genet''. 2014 Dec 14; '''15''': 139
De novo CNVs in bipolar affective disorder and schizophrenia. Description: Georgieva, Lyudmila, et al. De novo CNVs in bipolar affective disorder and schizophrenia. ''Hum Mol Genet''. 2014 Dec 15; '''23''' (24):6677-83
Functionally reciprocal mutations of the prolactin signalling pathway define hairy and slick cattle. Description: Littlejohn, Mathew D, et al. Functionally reciprocal mutations of the prolactin signalling pathway define hairy and slick cattle. ''Nat Commun''. 2014 Dec 18; '''5''': 5861
ESR1 and ESR2 gene polymorphisms are associated with human reproduction outcomes in Brazilian women. Description: de Mattos, Clarissa Santiago, et al. ESR1 and ESR2 gene polymorphisms are associated with human reproduction outcomes in Brazilian women. ''J Ovarian Res''. 2014 Dec 20; '''7''': 114
Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss. Description: Haraksingh, Rajini R, et al. Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss. ''BMC Genomics''. 2014 Dec 20; '''15''': 1155
Genetic association between germline JAK2 polymorphisms and myeloproliferative neoplasms in Hong Kong Chinese population: a case-control study. Description: Koh, Su Pin, et al. Genetic association between germline JAK2 polymorphisms and myeloproliferative neoplasms in Hong Kong Chinese population: a case-control study. ''BMC Genet''. 2014 Dec 20; '''15''': 147
Protective variant associated with alcohol dependence in a Mexican American cohort. Description: Norden-Krichmar, Trina M, et al. Protective variant associated with alcohol dependence in a Mexican American cohort. ''BMC Med Genet''. 2014 Dec 21; '''15''': 136
A candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMS. Description: Rosmarin, Dan, et al. A candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMS. ''Gut''. 2015 Jan; '''64''' (1):111-20
Accounting for genetic architecture improves sequence based genomic prediction for a Drosophila fitness trait. Description: Ober, Ulrike, et al. Accounting for genetic architecture improves sequence based genomic prediction for a Drosophila fitness trait. ''PLoS One''. 2015; '''10''' (5):e0126880
A Common Variant of NGEF Is Associated with Abdominal Visceral Fat in Korean Men. Description: Kim, Hyun-Jin, et al. A Common Variant of NGEF Is Associated with Abdominal Visceral Fat in Korean Men. ''PLoS One''. 2015; '''10''' (9):e0137564
A deletion in the VLDLR gene in Eurasier dogs with cerebellar hypoplasia resembling a Dandy-Walker-like malformation (DWLM). Description: Gerber, Martina, et al. A deletion in the VLDLR gene in Eurasier dogs with cerebellar hypoplasia resembling a Dandy-Walker-like malformation (DWLM). ''PLoS One''. 2015; '''10''' (2):e0108917
Affected kindred analysis of human X chromosome exomes to identify novel X-linked intellectual disability genes. Description: Niranjan, Tejasvi S, et al. Affected kindred analysis of human X chromosome exomes to identify novel X-linked intellectual disability genes. ''PLoS One''. 2015; '''10''' (2):e0116454
A genetic predictive model for canine hip dysplasia: integration of Genome Wide Association Study (GWAS) and candidate gene approaches. Description: Bartolome, Nerea, et al. A genetic predictive model for canine hip dysplasia: integration of Genome Wide Association Study (GWAS) and candidate gene approaches. ''PLoS One''. 2015; '''10''' (4):e0122558
A Genome-Wide Association Analysis Reveals Epistatic Cancellation of Additive Genetic Variance for Root Length in Arabidopsis thaliana. Description: Lachowiec, Jennifer, et al. A Genome-Wide Association Analysis Reveals Epistatic Cancellation of Additive Genetic Variance for Root Length in Arabidopsis thaliana. ''PLoS Genet''. 2015; '''11''' (9):e1005541
A genome wide association study on Newfoundland colorectal cancer patients' survival outcomes. Description: Xu, Wei, et al. A genome wide association study on Newfoundland colorectal cancer patients' survival outcomes. ''Biomark Res''. 2015; '''3''': 6
A Genome-Wide Association Study Uncovers a Genetic Locus Associated with Thoracic-to-Hip Ratio in Koreans. Description: Cha, Seongwon, et al. A Genome-Wide Association Study Uncovers a Genetic Locus Associated with Thoracic-to-Hip Ratio in Koreans. ''PLoS One''. 2015; '''10''' (12):e0145220
A Genome-wide Combinatorial Strategy Dissects Complex Genetic Architecture of Seed Coat Color in Chickpea. Description: Bajaj, Deepak, et al. A Genome-wide Combinatorial Strategy Dissects Complex Genetic Architecture of Seed Coat Color in Chickpea. ''Front Plant Sci''. 2015; '''6''': 979
A genome-wide copy number variant study of suicidal behavior. Description: Gross, Jeffrey A, et al. A genome-wide copy number variant study of suicidal behavior. ''PLoS One''. 2015; '''10''' (5):e0128369
A GWAS Study on Liver Function Test Using eMERGE Network Participants. Description: Namjou, Bahram, et al. A GWAS Study on Liver Function Test Using eMERGE Network Participants. ''PLoS One''. 2015; '''10''' (9):e0138677
Altered Brain Activation during Emotional Face Processing in Relation to Both Diagnosis and Polygenic Risk of Bipolar Disorder. Description: Tesli, Martin, et al. Altered Brain Activation during Emotional Face Processing in Relation to Both Diagnosis and Polygenic Risk of Bipolar Disorder. ''PLoS One''. 2015; '''10''' (7):e0134202
Altered CSMD1 Expression Alters Cocaine-Conditioned Place Preference: Mutual Support for a Complex Locus from Human and Mouse Models. Description: Drgonova, Jana, et al. Altered CSMD1 Expression Alters Cocaine-Conditioned Place Preference: Mutual Support for a Complex Locus from Human and Mouse Models. ''PLoS One''. 2015; '''10''' (7):e0120908
A Multi-Marker Genetic Association Test Based on the Rasch Model Applied to Alzheimer's Disease. Description: Wang, Wenjia, et al. A Multi-Marker Genetic Association Test Based on the Rasch Model Applied to Alzheimer's Disease. ''PLoS One''. 2015; '''10''' (9):e0138223
Analysis of gene-gene interactions among common variants in candidate cardiovascular genes in coronary artery disease. Description: Musameh, Muntaser D, et al. Analysis of gene-gene interactions among common variants in candidate cardiovascular genes in coronary artery disease. ''PLoS One''. 2015; '''10''' (2):e0117684
Analysis of Genetic and Environmental Risk Factors and Their Interactions in Korean Patients with Age-Related Macular Degeneration. Description: Woo, Se Joon, et al. Analysis of Genetic and Environmental Risk Factors and Their Interactions in Korean Patients with Age-Related Macular Degeneration. ''PLoS One''. 2015; '''10''' (7):e0132771
Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world. Description: Morrison, Margaux A, et al. Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world. ''Front Genet''. 2015; '''6''': 238
An exploratory study of the association between SORL1 polymorphisms and sporadic Alzheimer's disease in the Han Chinese population. Description: Zhang, Feng, et al. An exploratory study of the association between SORL1 polymorphisms and sporadic Alzheimer's disease in the Han Chinese population. ''Neuropsychiatr Dis Treat''. 2015; '''11''': 1443-8
An IL-13 promoter polymorphism associated with liver fibrosis in patients with Schistosoma japonicum. Description: Long, Xin, et al. An IL-13 promoter polymorphism associated with liver fibrosis in patients with Schistosoma japonicum. ''PLoS One''. 2015; '''10''' (8):e0135360
A Novel Genome-Wide Association Study Approach Using Genotyping by Exome Sequencing Leads to the Identification of a Primary Open Angle Glaucoma Associated Inversion Disrupting ADAMTS17. Description: Forman, Oliver P, et al. A Novel Genome-Wide Association Study Approach Using Genotyping by Exome Sequencing Leads to the Identification of a Primary Open Angle Glaucoma Associated Inversion Disrupting ADAMTS17. ''PLoS One''. 2015; '''10''' (12):e0143546
A Pooled Genome-Wide Association Study of Asperger Syndrome. Description: Warrier, Varun, et al. A Pooled Genome-Wide Association Study of Asperger Syndrome. ''PLoS One''. 2015; '''10''' (7):e0131202
Application of LogitBoost Classifier for Traceability Using SNP Chip Data. Description: Kim, Kwondo, et al. Application of LogitBoost Classifier for Traceability Using SNP Chip Data. ''PLoS One''. 2015; '''10''' (10):e0139685
Aquaporin 5 Interacts with Fluoride and Possibly Protects against Caries. Description: Anjomshoaa, Ida, et al. Aquaporin 5 Interacts with Fluoride and Possibly Protects against Caries. ''PLoS One''. 2015; '''10''' (12):e0143068
A rare co-segregation-mutation in the insulin receptor substrate 1 gene in one Chinese family with ankylosing spondylitis. Description: Rong, Ju, et al. A rare co-segregation-mutation in the insulin receptor substrate 1 gene in one Chinese family with ankylosing spondylitis. ''PLoS One''. 2015; '''10''' (5):e0126348
A re-formulation of generalized linear mixed models to fit family data in genetic association studies. Description: Wang, Tao, et al. A re-formulation of generalized linear mixed models to fit family data in genetic association studies. ''Front Genet''. 2015; '''6''': 120
A significant risk locus on 19q13 for bipolar disorder identified using a combined genome-wide linkage and copy number variation analysis. Description: Lekman, Magnus, et al. A significant risk locus on 19q13 for bipolar disorder identified using a combined genome-wide linkage and copy number variation analysis. ''BioData Min''. 2015; '''8''': 42
Association between Genetic Variation in the Oxytocin Receptor Gene and Emotional Withdrawal, but not between Oxytocin Pathway Genes and Diagnosis in Psychotic Disorders. Description: Haram, Marit, et al. Association between Genetic Variation in the Oxytocin Receptor Gene and Emotional Withdrawal, but not between Oxytocin Pathway Genes and Diagnosis in Psychotic Disorders. ''Front Hum Neurosci''. 2015; '''9''': 9
Association between the European GWAS-identified susceptibility locus at chromosome 4p16 and the risk of atrial septal defect: a case-control study in Southwest China and a meta-analysis. Description: Zhao, Li, et al. Association between the European GWAS-identified susceptibility locus at chromosome 4p16 and the risk of atrial septal defect: a case-control study in Southwest China and a meta-analysis. ''PLoS One''. 2015; '''10''' (4):e0123959
Association between the Interaction of Key Genes Involved in Effector T-Cell Pathways and Susceptibility to Develop allergic Rhinitis: A Population-Based Case-Control Association Study. Description: Zhang, Yuan, et al. Association between the Interaction of Key Genes Involved in Effector T-Cell Pathways and Susceptibility to Develop allergic Rhinitis: A Population-Based Case-Control Association Study. ''PLoS One''. 2015; '''10''' (7):e0131248
Association between Variants in Atopy-Related Immunologic Candidate Genes and Pancreatic Cancer Risk. Description: Cotterchio, Michelle, et al. Association between Variants in Atopy-Related Immunologic Candidate Genes and Pancreatic Cancer Risk. ''PLoS One''. 2015; '''10''' (5):e0125273
Association Mapping of Total Carotenoids in Diverse Soybean Genotypes Based on Leaf Extracts and High-Throughput Canopy Spectral Reflectance Measurements. Description: Dhanapal, Arun Prabhu, et al. Association Mapping of Total Carotenoids in Diverse Soybean Genotypes Based on Leaf Extracts and High-Throughput Canopy Spectral Reflectance Measurements. ''PLoS One''. 2015; '''10''' (9):e0137213
Association of Genes, Pathways, and Haplogroups of the Mitochondrial Genome with the Risk of Colorectal Cancer: The Multiethnic Cohort. Description: Li, Yuqing, et al. Association of Genes, Pathways, and Haplogroups of the Mitochondrial Genome with the Risk of Colorectal Cancer: The Multiethnic Cohort. ''PLoS One''. 2015; '''10''' (9):e0136796
Association of HMOX1 and NQO1 Polymorphisms with Metabolic Syndrome Components. Description: Martinez-Hernandez, Angelica, et al. Association of HMOX1 and NQO1 Polymorphisms with Metabolic Syndrome Components. ''PLoS One''. 2015; '''10''' (5):e0123313
Association of interleukin 7 receptor (rs1494555 and rs6897932) gene polymorphisms with asthma in a north Indian population. Description: Sinha, Shweta, et al. Association of interleukin 7 receptor (rs1494555 and rs6897932) gene polymorphisms with asthma in a north Indian population. ''Allergy Rhinol (Providence)''. 2015 Jan; '''6''' (3):168-76
Association of SNP Rs9943582 in APLNR with Left Ventricle Systolic Dysfunction in Patients with Coronary Artery Disease in a Chinese Han GeneID Population. Description: Wang, Pengyun, et al. Association of SNP Rs9943582 in APLNR with Left Ventricle Systolic Dysfunction in Patients with Coronary Artery Disease in a Chinese Han GeneID Population. ''PLoS One''. 2015; '''10''' (5):e0125926
Association of SNPs in EGR3 and ARC with Schizophrenia Supports a Biological Pathway for Schizophrenia Risk. Description: Huentelman, Matthew J, et al. Association of SNPs in EGR3 and ARC with Schizophrenia Supports a Biological Pathway for Schizophrenia Risk. ''PLoS One''. 2015; '''10''' (10):e0135076
Association of the I264T variant in the sulfide quinone reductase-like (SQRDL) gene with osteoporosis in Korean postmenopausal women. Description: Jin, Hyun-Seok, et al. Association of the I264T variant in the sulfide quinone reductase-like (SQRDL) gene with osteoporosis in Korean postmenopausal women. ''PLoS One''. 2015; '''10''' (8):e0135285
Association of the NOTCH4 Gene Polymorphism rs204993 with Schizophrenia in the Chinese Han Population. Description: Zhang, Bao, et al. Association of the NOTCH4 Gene Polymorphism rs204993 with Schizophrenia in the Chinese Han Population. ''Biomed Res Int''. 2015; '''2015''': 408096
Assumption-free estimation of the genetic contribution to refractive error across childhood. Description: Guggenheim, Jeremy A, et al. Assumption-free estimation of the genetic contribution to refractive error across childhood. ''Mol Vis''. 2015; '''21''': 621-32
A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer. Description: Savas, Sevtap, et al. A Survival Association Study of 102 Polymorphisms Previously Associated with Survival Outcomes in Colorectal Cancer. ''Biomed Res Int''. 2015; '''2015''': 968743
Attenuated monocyte apoptosis, a new mechanism for osteoporosis suggested by a transcriptome-wide expression study of monocytes. Description: Liu, Yao-Zhong, et al. Attenuated monocyte apoptosis, a new mechanism for osteoporosis suggested by a transcriptome-wide expression study of monocytes. ''PLoS One''. 2015; '''10''' (2):e0116792
Breast cancer risk and genetic ancestry: a case-control study in Uruguay. Description: Bonilla, Carolina, et al. Breast cancer risk and genetic ancestry: a case-control study in Uruguay. ''BMC Womens Health''. 2015; '''15''': 11
Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levels. Description: Deelen, Patrick, et al. Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levels. ''Genome Med''. 2015; '''7''' (1):30
Candidate gene analysis supports a role for polymorphisms at TCF7L2 as risk factors for type 2 diabetes in Sudan. Description: Ibrahim, Amir T, et al. Candidate gene analysis supports a role for polymorphisms at TCF7L2 as risk factors for type 2 diabetes in Sudan. ''J Diabetes Metab Disord''. 2015; '''15''': 4
Candidate Gene Association Analysis of Neuroblastoma in Chinese Children Strengthens the Role of LMO1. Description: Lu, Jie, et al. Candidate Gene Association Analysis of Neuroblastoma in Chinese Children Strengthens the Role of LMO1. ''PLoS One''. 2015; '''10''' (6):e0127856
Canine disorder mirrors human disease: exonic deletion in HES7 causes autosomal recessive spondylocostal dysostosis in miniature Schnauzer dogs. Description: Willet, Cali E, et al. Canine disorder mirrors human disease: exonic deletion in HES7 causes autosomal recessive spondylocostal dysostosis in miniature Schnauzer dogs. ''PLoS One''. 2015; '''10''' (2):e0117055
Case-control study of ADARB1 and ADARB2 gene variants in migraine. Description: Gasparini, Claudia F, et al. Case-control study of ADARB1 and ADARB2 gene variants in migraine. ''J Headache Pain''. 2015; '''16''': 511
Characterization of genetic diversity and gene mapping in two Swedish local chicken breeds. Description: Johansson, Anna M, et al. Characterization of genetic diversity and gene mapping in two Swedish local chicken breeds. ''Front Genet''. 2015; '''6''': 44
Characterizing neutral genomic diversity and selection signatures in indigenous populations of Moroccan goats (Capra hircus) using WGS data. Description: Benjelloun, Badr, et al. Characterizing neutral genomic diversity and selection signatures in indigenous populations of Moroccan goats (Capra hircus) using WGS data. ''Front Genet''. 2015; '''6''': 107
Combining GWAS and RNA-Seq Approaches for Detection of the Causal Mutation for Hereditary Junctional Epidermolysis Bullosa in Sheep. Description: Suarez-Vega, Aroa, et al. Combining GWAS and RNA-Seq Approaches for Detection of the Causal Mutation for Hereditary Junctional Epidermolysis Bullosa in Sheep. ''PLoS One''. 2015; '''10''' (5):e0126416
Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk. Description: Chornokur, Ganna, et al. Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk. ''PLoS One''. 2015; '''10''' (6):e0128106
Common variants related to serum uric acid concentrations are associated with glucose metabolism and insulin secretion in a Chinese population. Description: Sun, Xue, et al. Common variants related to serum uric acid concentrations are associated with glucose metabolism and insulin secretion in a Chinese population. ''PLoS One''. 2015; '''10''' (1):e0116714
Comparison of DNA methylation profiles in human fetal and adult red blood cell progenitors. Description: Lessard, Samuel, et al. Comparison of DNA methylation profiles in human fetal and adult red blood cell progenitors. ''Genome Med''. 2015; '''7''' (1):1
Comparison of linkage disequilibrium levels in Iranian indigenous cattle using whole genome SNPs data. Description: Karimi, Karim, et al. Comparison of linkage disequilibrium levels in Iranian indigenous cattle using whole genome SNPs data. ''J Anim Sci Technol''. 2015; '''57''': 47
Comprehensive assessment of genetic sequence variants in the antioxidant 'master regulator' NRF2 in idiopathic Parkinson's disease. Description: Todorovic, Michael, et al. Comprehensive assessment of genetic sequence variants in the antioxidant 'master regulator' NRF2 in idiopathic Parkinson's disease. ''PLoS One''. 2015; '''10''' (5):e0128030
COMT and MAO-A polymorphisms and obsessive-compulsive disorder: a family-based association study. Description: Sampaio, Aline Santos, et al. COMT and MAO-A polymorphisms and obsessive-compulsive disorder: a family-based association study. ''PLoS One''. 2015; '''10''' (3):e0119592
Cryptic relatedness in epidemiologic collections accessed for genetic association studies: experiences from the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) study and the National Health and Nutrition Examination Surveys (NHANES). Description: Malinowski, Jennifer, et al. Cryptic relatedness in epidemiologic collections accessed for genetic association studies: experiences from the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) study and the National Health and Nutrition Examination Surveys (NHANES). ''Front Genet''. 2015; '''6''': 317
Cumulative effect and predictive value of genetic variants associated with type 2 diabetes in Han Chinese: a case-control study. Description: Qian, Yun, et al. Cumulative effect and predictive value of genetic variants associated with type 2 diabetes in Han Chinese: a case-control study. ''PLoS One''. 2015; '''10''' (1):e0116537
dcVar: a method for identifying common variants that modulate differential correlation structures in gene expression data. Description: Lareau, Caleb A, et al. dcVar: a method for identifying common variants that modulate differential correlation structures in gene expression data. ''Front Genet''. 2015; '''6''': 312
Detection and analysis of disease-associated single nucleotide polymorphism influencing post-translational modification. Description: Kim, Yul, et al. Detection and analysis of disease-associated single nucleotide polymorphism influencing post-translational modification. ''BMC Med Genomics''. 2015; '''8 Suppl 2''': S7
Detection of convergent genome-wide signals of adaptation to tropical forests in humans. Description: Amorim, Carlos Eduardo G, et al. Detection of convergent genome-wide signals of adaptation to tropical forests in humans. ''PLoS One''. 2015; '''10''' (4):e0121557
Differences in the ovine HSP90AA1 gene expression rates caused by two linked polymorphisms at its promoter affect rams sperm DNA fragmentation under environmental heat stress conditions. Description: Salces-Ortiz, Judit, et al. Differences in the ovine HSP90AA1 gene expression rates caused by two linked polymorphisms at its promoter affect rams sperm DNA fragmentation under environmental heat stress conditions. ''PLoS One''. 2015; '''10''' (2):e0116360
Differential Evolution approach to detect recent admixture. Description: Kozlov, Konstantin, et al. Differential Evolution approach to detect recent admixture. ''BMC Genomics''. 2015; '''16 Suppl 8''': S9
Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC). Description: Salfati, Elias, et al. Direct Estimates of the Genomic Contributions to Blood Pressure Heritability within a Population-Based Cohort (ARIC). ''PLoS One''. 2015; '''10''' (7):e0133031
Discovering Alzheimer Genetic Biomarkers Using Bayesian Networks. Description: Sherif, Fayroz F, et al. Discovering Alzheimer Genetic Biomarkers Using Bayesian Networks. ''Adv Bioinformatics''. 2015; '''2015''': 639367
Dissecting Allele Architecture of Early Onset IBD Using High-Density Genotyping. Description: Cutler, David J, et al. Dissecting Allele Architecture of Early Onset IBD Using High-Density Genotyping. ''PLoS One''. 2015; '''10''' (6):e0128074
Do variants associated with susceptibility to pancreatic cancer and type 2 diabetes reciprocally affect risk? Description: Wu, Lang, et al. Do variants associated with susceptibility to pancreatic cancer and type 2 diabetes reciprocally affect risk? ''PLoS One''. 2015; '''10''' (2):e0117230
Early modern human dispersal from Africa: genomic evidence for multiple waves of migration. Description: Tassi, Francesca, et al. Early modern human dispersal from Africa: genomic evidence for multiple waves of migration. ''Investig Genet''. 2015; '''6''': 13
Educational attainment influences levels of homozygosity through migration and assortative mating. Description: Abdellaoui, Abdel, et al. Educational attainment influences levels of homozygosity through migration and assortative mating. ''PLoS One''. 2015; '''10''' (3):e0118935
Effective population size, extended linkage disequilibrium and signatures of selection in the rare dog breed lundehund. Description: Pfahler, Sophia, et al. Effective population size, extended linkage disequilibrium and signatures of selection in the rare dog breed lundehund. ''PLoS One''. 2015; '''10''' (4):e0122680
Employing genome-wide SNP discovery and genotyping strategy to extrapolate the natural allelic diversity and domestication patterns in chickpea. Description: Kujur, Alice, et al. Employing genome-wide SNP discovery and genotyping strategy to extrapolate the natural allelic diversity and domestication patterns in chickpea. ''Front Plant Sci''. 2015; '''6''': 162
Enrichment of Minor Alleles of Common SNPs and Improved Risk Prediction for Parkinson's Disease. Description: Zhu, Zuobin, et al. Enrichment of Minor Alleles of Common SNPs and Improved Risk Prediction for Parkinson's Disease. ''PLoS One''. 2015; '''10''' (7):e0133421
Epidemiological support for genetic variability at hypothalamic-pituitary-adrenal axis and serotonergic system as risk factors for major depression. Description: Ching-Lopez, Ana, et al. Epidemiological support for genetic variability at hypothalamic-pituitary-adrenal axis and serotonergic system as risk factors for major depression. ''Neuropsychiatr Dis Treat''. 2015; '''11''': 2743-54
Evidence for Association of Cell Adhesion Molecules Pathway and NLGN1 Polymorphisms with Schizophrenia in Chinese Han Population. Description: Zhang, Zhengrong, et al. Evidence for Association of Cell Adhesion Molecules Pathway and NLGN1 Polymorphisms with Schizophrenia in Chinese Han Population. ''PLoS One''. 2015; '''10''' (12):e0144719
Evolutionary Trade-Offs Underlie the Multi-faceted Virulence of Staphylococcus aureus. Description: Laabei, Maisem, et al. Evolutionary Trade-Offs Underlie the Multi-faceted Virulence of Staphylococcus aureus. ''PLoS Biol''. 2015; '''13''' (9):e1002229
Examination of candidate exonic variants for association to Alzheimer disease in the Amish. Description: D'Aoust, Laura N, et al. Examination of candidate exonic variants for association to Alzheimer disease in the Amish. ''PLoS One''. 2015; '''10''' (2):e0118043
Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes. Description: Shigemizu, Daichi, et al. Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes. ''PLoS One''. 2015; '''10''' (7):e0130329
Exome sequencing of 75 individuals from multiply affected coeliac families and large scale resequencing follow up. Description: Mistry, Vanisha, et al. Exome sequencing of 75 individuals from multiply affected coeliac families and large scale resequencing follow up. ''PLoS One''. 2015; '''10''' (1):e0116845
Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus. Description: Labbe, Catherine, et al. Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus. ''PLoS One''. 2015; '''10''' (6):e0128586
Exploring the genetic signature of body size in Yucatan miniature pig. Description: Kim, Hyeongmin, et al. Exploring the genetic signature of body size in Yucatan miniature pig. ''PLoS One''. 2015; '''10''' (4):e0121732
Expression-associated polymorphisms of CAV1-CAV2 affect intraocular pressure and high-tension glaucoma risk. Description: Kim, Sewon, et al. Expression-associated polymorphisms of CAV1-CAV2 affect intraocular pressure and high-tension glaucoma risk. ''Mol Vis''. 2015; '''21''': 548-54
Expression Quantitative Trait Loci Information Improves Predictive Modeling of Disease Relevance of Non-Coding Genetic Variation. Description: Croteau-Chonka, Damien C, et al. Expression Quantitative Trait Loci Information Improves Predictive Modeling of Disease Relevance of Non-Coding Genetic Variation. ''PLoS One''. 2015; '''10''' (10):e0140758
Extent of Linkage Disequilibrium and Effective Population Size in Four South African Sanga Cattle Breeds. Description: Makina, Sithembile O, et al. Extent of Linkage Disequilibrium and Effective Population Size in Four South African Sanga Cattle Breeds. ''Front Genet''. 2015; '''6''': 337
Fine Mapping of a GWAS-Derived Obesity Candidate Region on Chromosome 16p11.2. Description: Volckmar, Anna-Lena, et al. Fine Mapping of a GWAS-Derived Obesity Candidate Region on Chromosome 16p11.2. ''PLoS One''. 2015; '''10''' (5):e0125660
Gene interactions and structural brain change in early-onset Alzheimer's disease subjects using the pipeline environment. Description: Moon, Seok Woo, et al. Gene interactions and structural brain change in early-onset Alzheimer's disease subjects using the pipeline environment. ''Psychiatry Investig''. 2015 Jan; '''12''' (1):125-35
Genes Regulated by Vitamin D in Bone Cells Are Positively Selected in East Asians. Description: Arciero, Elena, et al. Genes Regulated by Vitamin D in Bone Cells Are Positively Selected in East Asians. ''PLoS One''. 2015; '''10''' (12):e0146072
Genetic Affinity of the Bhil, Kol and Gond Mentioned in Epic Ramayana. Description: Chaubey, Gyaneshwer, et al. Genetic Affinity of the Bhil, Kol and Gond Mentioned in Epic Ramayana. ''PLoS One''. 2015; '''10''' (6):e0127655
Genetic analysis identifies DDR2 as a novel gene affecting bone mineral density and osteoporotic fractures in Chinese population. Description: Guo, Yan, et al. Genetic analysis identifies DDR2 as a novel gene affecting bone mineral density and osteoporotic fractures in Chinese population. ''PLoS One''. 2015; '''10''' (2):e0117102
Genetic analysis of membrane cofactor protein (CD46) of the complement system in women with and without preeclamptic pregnancies. Description: Lokki, A Inkeri, et al. Genetic analysis of membrane cofactor protein (CD46) of the complement system in women with and without preeclamptic pregnancies. ''PLoS One''. 2015; '''10''' (2):e0117840
Genetic analysis of Thai cattle reveals a Southeast Asian indicine ancestry. Description: Wangkumhang, Pongsakorn, et al. Genetic analysis of Thai cattle reveals a Southeast Asian indicine ancestry. ''PeerJ''. 2015; '''3''': e1318
Genetic determinants for gestational diabetes mellitus and related metabolic traits in Mexican women. Description: Huerta-Chagoya, Alicia, et al. Genetic determinants for gestational diabetes mellitus and related metabolic traits in Mexican women. ''PLoS One''. 2015; '''10''' (5):e0126408
Genetic Determinants of Metabolism and Benign Prostate Enlargement: Associations with Prostate Volume. Description: Giri, Ayush, et al. Genetic Determinants of Metabolism and Benign Prostate Enlargement: Associations with Prostate Volume. ''PLoS One''. 2015; '''10''' (7):e0132028
Genetic Determinants of Pelvic Organ Prolapse among African American and Hispanic Women in the Women's Health Initiative. Description: Giri, Ayush, et al. Genetic Determinants of Pelvic Organ Prolapse among African American and Hispanic Women in the Women's Health Initiative. ''PLoS One''. 2015; '''10''' (11):e0141647
Genetic Effects on Longitudinal Changes from Healthy to Adverse Weight and Metabolic Status - The HUNT Study. Description: Kvaloy, Kirsti, et al. Genetic Effects on Longitudinal Changes from Healthy to Adverse Weight and Metabolic Status - The HUNT Study. ''PLoS One''. 2015; '''10''' (10):e0139632
Genetic Geostatistical Framework for Spatial Analysis of Fine-Scale Genetic Heterogeneity in Modern Populations: Results from the KORA Study. Description: Diaz-Lacava, A N, et al. Genetic Geostatistical Framework for Spatial Analysis of Fine-Scale Genetic Heterogeneity in Modern Populations: Results from the KORA Study. ''Int J Genomics''. 2015; '''2015''': 693193
Genetic Heterogeneity in Algerian Human Populations. Description: Bekada, Asmahan, et al. Genetic Heterogeneity in Algerian Human Populations. ''PLoS One''. 2015; '''10''' (9):e0138453
Genetic Interactions Explain Variance in Cingulate Amyloid Burden: An AV-45 PET Genome-Wide Association and Interaction Study in the ADNI Cohort. Description: Li, Jin, et al. Genetic Interactions Explain Variance in Cingulate Amyloid Burden: An AV-45 PET Genome-Wide Association and Interaction Study in the ADNI Cohort. ''Biomed Res Int''. 2015; '''2015''': 647389
Genetic Loci Associated with Allergic Sensitization in Lithuanians. Description: Sauliene, Ingrida, et al. Genetic Loci Associated with Allergic Sensitization in Lithuanians. ''PLoS One''. 2015; '''10''' (7):e0134188
Genetic markers of white matter integrity in schizophrenia revealed by parallel ICA. Description: Gupta, Cota Navin, et al. Genetic markers of white matter integrity in schizophrenia revealed by parallel ICA. ''Front Hum Neurosci''. 2015; '''9''': 100
Genetic Polymorphisms Associated with Hearing Threshold Shift in Subjects during First Encounter with Occupational Impulse Noise. Description: Grondin, Yohann, et al. Genetic Polymorphisms Associated with Hearing Threshold Shift in Subjects during First Encounter with Occupational Impulse Noise. ''PLoS One''. 2015; '''10''' (6):e0130827
Genetic stratigraphy of key demographic events in Arabia. Description: Fernandes, Veronica, et al. Genetic stratigraphy of key demographic events in Arabia. ''PLoS One''. 2015; '''10''' (3):e0118625
Genetic variant rs17225178 in the ARNT2 gene is associated with Asperger Syndrome. Description: Di Napoli, Agnese, et al. Genetic variant rs17225178 in the ARNT2 gene is associated with Asperger Syndrome. ''Mol Autism''. 2015; '''6''': 9
Genetic Variants Associated with Lipid Profiles in Chinese Patients with Type 2 Diabetes. Description: Kong, Xiaomu, et al. Genetic Variants Associated with Lipid Profiles in Chinese Patients with Type 2 Diabetes. ''PLoS One''. 2015; '''10''' (8):e0135145
Genetic variants modulating CRIPTO serum levels identified by genome-wide association study in Cilento isolates. Description: Ruggiero, Daniela, et al. Genetic variants modulating CRIPTO serum levels identified by genome-wide association study in Cilento isolates. ''PLoS Genet''. 2015 Jan; '''11''' (1):e1004976
Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population. Description: Salo, Perttu P, et al. Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population. ''PLoS One''. 2015; '''10''' (10):e0140576
Genetic variation at the human connexin 43 locus but not at the connexin 40 locus is associated with left bundle branch block. Description: Ladenvall, Per, et al. Genetic variation at the human connexin 43 locus but not at the connexin 40 locus is associated with left bundle branch block. ''Open Heart''. 2015; '''2''' (1):e000187
Genetic variations in the serotonergic system contribute to amygdala volume in humans. Description: Li, Jin, et al. Genetic variations in the serotonergic system contribute to amygdala volume in humans. ''Front Neuroanat''. 2015; '''9''': 129
Gene-wise association of variants in four lysosomal storage disorder genes in neuropathologically confirmed Lewy body disease. Description: Clark, Lorraine N, et al. Gene-wise association of variants in four lysosomal storage disorder genes in neuropathologically confirmed Lewy body disease. ''PLoS One''. 2015; '''10''' (5):e0125204
Genome Scan for Selection in Structured Layer Chicken Populations Exploiting Linkage Disequilibrium Information. Description: Gholami, Mahmood, et al. Genome Scan for Selection in Structured Layer Chicken Populations Exploiting Linkage Disequilibrium Information. ''PLoS One''. 2015; '''10''' (7):e0130497
Genome-wide analysis of attention deficit hyperactivity disorder in Norway. Description: Zayats, Tetyana, et al. Genome-wide analysis of attention deficit hyperactivity disorder in Norway. ''PLoS One''. 2015; '''10''' (4):e0122501
Genome-Wide Assessment of Differential DNA Methylation Associated with Autoantibody Production in Systemic Lupus Erythematosus. Description: Chung, Sharon A, et al. Genome-Wide Assessment of Differential DNA Methylation Associated with Autoantibody Production in Systemic Lupus Erythematosus. ''PLoS One''. 2015; '''10''' (7):e0129813
Genome-Wide Association Analysis for Blood Lipid Traits Measured in Three Pig Populations Reveals a Substantial Level of Genetic Heterogeneity. Description: Yang, Hui, et al. Genome-Wide Association Analysis for Blood Lipid Traits Measured in Three Pig Populations Reveals a Substantial Level of Genetic Heterogeneity. ''PLoS One''. 2015; '''10''' (6):e0131667
Genome Wide Association Analysis Reveals New Production Trait Genes in a Male Duroc Population. Description: Wang, Kejun, et al. Genome Wide Association Analysis Reveals New Production Trait Genes in a Male Duroc Population. ''PLoS One''. 2015; '''10''' (9):e0139207
Genome-Wide Association Identifies SLC2A9 and NLN Gene Regions as Associated with Entropion in Domestic Sheep. Description: Mousel, Michelle R, et al. Genome-Wide Association Identifies SLC2A9 and NLN Gene Regions as Associated with Entropion in Domestic Sheep. ''PLoS One''. 2015; '''10''' (6):e0128909
Genome-wide association mapping for yield and other agronomic traits in an elite breeding population of tropical rice (Oryza sativa). Description: Begum, Hasina, et al. Genome-wide association mapping for yield and other agronomic traits in an elite breeding population of tropical rice (Oryza sativa). ''PLoS One''. 2015; '''10''' (3):e0119873
Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians. Description: Hwang, Joo-Yeon, et al. Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians. ''Diabetes''. 2015 Jan; '''64''' (1):291-8
Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population. Description: Kuo, Po-Hsiu, et al. Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population. ''PLoS One''. 2015; '''10''' (9):e0138695
Genome-Wide Association Study Identifies Novel Pharmacogenomic Loci For Therapeutic Response to Montelukast in Asthma. Description: Dahlin, Amber, et al. Genome-Wide Association Study Identifies Novel Pharmacogenomic Loci For Therapeutic Response to Montelukast in Asthma. ''PLoS One''. 2015; '''10''' (6):e0129385
Genome-wide association study in an admixed case series reveals IL12A as a new candidate in Behcet disease. Description: Kappen, Jasper H, et al. Genome-wide association study in an admixed case series reveals IL12A as a new candidate in Behcet disease. ''PLoS One''. 2015; '''10''' (3):e0119085
Genome-wide association study of parity in Bangladeshi women. Description: Aschebrook-Kilfoy, Briseis, et al. Genome-wide association study of parity in Bangladeshi women. ''PLoS One''. 2015; '''10''' (3):e0118488
Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population. Description: Matsukura, Mitsuru, et al. Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population. ''PLoS One''. 2015; '''10''' (10):e0139262
Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy. Description: Van Driest, Sara L, et al. Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy. ''PLoS One''. 2015; '''10''' (6):e0127791
Genome-wide association study of serum minerals levels in children of different ethnic background. Description: Chang, Xiao, et al. Genome-wide association study of serum minerals levels in children of different ethnic background. ''PLoS One''. 2015; '''10''' (4):e0123499
Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas. Description: Brown, Eric L, et al. Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas. ''PLoS One''. 2015; '''10''' (11):e0142130
Genome-Wide Gene by Environment Interaction Analysis Identifies Common SNPs at 17q21.2 that Are Associated with Increased Body Mass Index Only among Asthmatics. Description: Wang, Leyao, et al. Genome-Wide Gene by Environment Interaction Analysis Identifies Common SNPs at 17q21.2 that Are Associated with Increased Body Mass Index Only among Asthmatics. ''PLoS One''. 2015; '''10''' (12):e0144114
Genomic analysis for managing small and endangered populations: a case study in Tyrol Grey cattle. Description: Meszaros, Gabor, et al. Genomic analysis for managing small and endangered populations: a case study in Tyrol Grey cattle. ''Front Genet''. 2015; '''6''': 173
Genomic data as the "hitchhiker's guide" to cattle adaptation: tracking the milestones of past selection in the bovine genome. Description: Utsunomiya, Yuri T, et al. Genomic data as the "hitchhiker's guide" to cattle adaptation: tracking the milestones of past selection in the bovine genome. ''Front Genet''. 2015; '''6''': 36
Genomic prediction of traits related to canine hip dysplasia. Description: Sanchez-Molano, Enrique, et al. Genomic prediction of traits related to canine hip dysplasia. ''Front Genet''. 2015; '''6''': 97
Genotypic and allelic variability in CYP19A1 among populations of African and European ancestry. Description: Starlard-Davenport, Athena, et al. Genotypic and allelic variability in CYP19A1 among populations of African and European ancestry. ''PLoS One''. 2015; '''10''' (2):e0117347
Haplotype analysis of the Apolipoprotein A5 gene in Moroccan patients with the metabolic syndrome. Description: Ajjemami, Maria, et al. Haplotype analysis of the Apolipoprotein A5 gene in Moroccan patients with the metabolic syndrome. ''J Diabetes Metab Disord''. 2015; '''14''': 29
Haplotypes at LBX1 have distinct inheritance patterns with opposite effects in adolescent idiopathic scoliosis. Description: Chettier, Rakesh, et al. Haplotypes at LBX1 have distinct inheritance patterns with opposite effects in adolescent idiopathic scoliosis. ''PLoS One''. 2015; '''10''' (2):e0117708
Hippocampal transcriptome-guided genetic analysis of correlated episodic memory phenotypes in Alzheimer's disease. Description: Yan, Jingwen, et al. Hippocampal transcriptome-guided genetic analysis of correlated episodic memory phenotypes in Alzheimer's disease. ''Front Genet''. 2015; '''6''': 117
Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogs. Description: Akkad, Denis A, et al. Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogs. ''Canine Genet Epidemiol''. 2015; '''2''': 5
Human Genetic Ancestral Composition Correlates with the Origin of Mycobacterium leprae Strains in a Leprosy Endemic Population. Description: Cardona-Castro, Nora, et al. Human Genetic Ancestral Composition Correlates with the Origin of Mycobacterium leprae Strains in a Leprosy Endemic Population. ''PLoS Negl Trop Dis''. 2015; '''9''' (9):e0004045
Identification of an interaction between VWF rs7965413 and platelet count as a novel risk marker for metabolic syndrome: an extensive search of candidate polymorphisms in a case-control study. Description: Nakatochi, Masahiro, et al. Identification of an interaction between VWF rs7965413 and platelet count as a novel risk marker for metabolic syndrome: an extensive search of candidate polymorphisms in a case-control study. ''PLoS One''. 2015; '''10''' (2):e0117591
Identification of Genetic Variation between Obligate Plant Pathogens Pseudoperonospora cubensis and P. humuli Using RNA Sequencing and Genotyping-By-Sequencing. Description: Summers, Carly F, et al. Identification of Genetic Variation between Obligate Plant Pathogens Pseudoperonospora cubensis and P. humuli Using RNA Sequencing and Genotyping-By-Sequencing. ''PLoS One''. 2015; '''10''' (11):e0143665
Identification of novel loci associated with gastrointestinal parasite resistance in a Red Maasai x Dorper backcross population. Description: Benavides, Magda Vieira, et al. Identification of novel loci associated with gastrointestinal parasite resistance in a Red Maasai x Dorper backcross population. ''PLoS One''. 2015; '''10''' (4):e0122797
Identification of Promising Mutants Associated with Egg Production Traits Revealed by Genome-Wide Association Study. Description: Yuan, Jingwei, et al. Identification of Promising Mutants Associated with Egg Production Traits Revealed by Genome-Wide Association Study. ''PLoS One''. 2015; '''10''' (10):e0140615
Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR). Description: De, Rishika, et al. Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR). ''BioData Min''. 2015; '''8''': 41
IL10 Variant g.5311A Is Associated with Visceral Leishmaniasis in Indian Population. Description: Mishra, Anshuman, et al. IL10 Variant g.5311A Is Associated with Visceral Leishmaniasis in Indian Population. ''PLoS One''. 2015; '''10''' (5):e0124559
Imputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohort. Description: Hoffmann, Thomas J, et al. Imputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohort. ''PLoS Genet''. 2015 Jan; '''11''' (1):e1004930
Increased Insulin following an Oral Glucose Load, Genetic Variation near the Melatonin Receptor MTNR1B, but No Biochemical Evidence of Endothelial Dysfunction in Young Asian Men and Women. Description: Matuszek, Maria A, et al. Increased Insulin following an Oral Glucose Load, Genetic Variation near the Melatonin Receptor MTNR1B, but No Biochemical Evidence of Endothelial Dysfunction in Young Asian Men and Women. ''PLoS One''. 2015; '''10''' (7):e0133611
Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population. Description: Zhou, Sirui, et al. Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population. ''PLoS One''. 2015; '''10''' (5):e0128255
Increase in Dickkopf-1 Serum Level in Recent Spondyloarthritis. Data from the DESIR Cohort. Description: Nocturne, Gaetane, et al. Increase in Dickkopf-1 Serum Level in Recent Spondyloarthritis. Data from the DESIR Cohort. ''PLoS One''. 2015; '''10''' (8):e0134974
Indications for potential parent-of-origin effects within the FTO gene. Description: Liu, Xuanshi, et al. Indications for potential parent-of-origin effects within the FTO gene. ''PLoS One''. 2015; '''10''' (3):e0119206
Infection and inflammation in schizophrenia and bipolar disorder: a genome wide study for interactions with genetic variation. Description: Avramopoulos, Dimitrios, et al. Infection and inflammation in schizophrenia and bipolar disorder: a genome wide study for interactions with genetic variation. ''PLoS One''. 2015; '''10''' (3):e0116696
Influence of Feature Encoding and Choice of Classifier on Disease Risk Prediction in Genome-Wide Association Studies. Description: Mittag, Florian, et al. Influence of Feature Encoding and Choice of Classifier on Disease Risk Prediction in Genome-Wide Association Studies. ''PLoS One''. 2015; '''10''' (8):e0135832
Influence of Genetic Variants in EGF and Other Genes on Hematological Traits in Korean Populations by a Genome-Wide Approach. Description: Kim, Yun Kyoung, et al. Influence of Genetic Variants in EGF and Other Genes on Hematological Traits in Korean Populations by a Genome-Wide Approach. ''Biomed Res Int''. 2015; '''2015''': 914965
Influences of gestational obesity on associations between genotypes and gene expression levels in offspring following maternal gastrointestinal bypass surgery for obesity. Description: Guenard, Frederic, et al. Influences of gestational obesity on associations between genotypes and gene expression levels in offspring following maternal gastrointestinal bypass surgery for obesity. ''PLoS One''. 2015; '''10''' (1):e0117011
In Search for the Genetic Basis of Quality of Life in Healthy Swedish Women--A GWAS Study Using the iCOGS Custom Genotyping Array. Description: Schoormans, Dounya, et al. In Search for the Genetic Basis of Quality of Life in Healthy Swedish Women--A GWAS Study Using the iCOGS Custom Genotyping Array. ''PLoS One''. 2015; '''10''' (10):e0140563
Integrating mRNA and miRNA Weighted Gene Co-Expression Networks with eQTLs in the Nucleus Accumbens of Subjects with Alcohol Dependence. Description: Mamdani, Mohammed, et al. Integrating mRNA and miRNA Weighted Gene Co-Expression Networks with eQTLs in the Nucleus Accumbens of Subjects with Alcohol Dependence. ''PLoS One''. 2015; '''10''' (9):e0137671
Interaction of genetic markers associated with serum alkaline phosphatase levels in the Japanese population. Description: Masuda, Masatoshi, et al. Interaction of genetic markers associated with serum alkaline phosphatase levels in the Japanese population. ''Hum Genome Var''. 2015; '''2''': 15019
Interferon gamma polymorphisms and hepatitis B virus-related liver cirrhosis risk in a Chinese population. Description: Sun, Yifan, et al. Interferon gamma polymorphisms and hepatitis B virus-related liver cirrhosis risk in a Chinese population. ''Cancer Cell Int''. 2015; '''15''': 35
Investigating the genetics of hippocampal volume in older adults without dementia. Description: Mather, Karen A, et al. Investigating the genetics of hippocampal volume in older adults without dementia. ''PLoS One''. 2015; '''10''' (1):e0116920
Investigation of associations between NR1D1, RORA and RORB genes and bipolar disorder. Description: Lai, Yin-Chieh, et al. Investigation of associations between NR1D1, RORA and RORB genes and bipolar disorder. ''PLoS One''. 2015; '''10''' (3):e0121245
Lack of Associations of CHRNA5-A3-B4 Genetic Variants with Smoking Cessation Treatment Outcomes in Caucasian Smokers despite Associations with Baseline Smoking. Description: Tyndale, Rachel F, et al. Lack of Associations of CHRNA5-A3-B4 Genetic Variants with Smoking Cessation Treatment Outcomes in Caucasian Smokers despite Associations with Baseline Smoking. ''PLoS One''. 2015; '''10''' (5):e0128109
Landscape genomics reveal signatures of local adaptation in barley (Hordeum vulgare L.). Description: Abebe, Tiegist D, et al. Landscape genomics reveal signatures of local adaptation in barley (Hordeum vulgare L.). ''Front Plant Sci''. 2015; '''6''': 813
Leveraging an Electronic Health Record-Linked Biorepository to Generate a Metformin Pharmacogenomics Hypothesis. Description: Breitenstein, Matthew K, et al. Leveraging an Electronic Health Record-Linked Biorepository to Generate a Metformin Pharmacogenomics Hypothesis. ''AMIA Jt Summits Transl Sci Proc''. 2015; '''2015''': 26-30
Loss of TLR3 aggravates CHIKV replication and pathology due to an altered virus-specific neutralizing antibody response. Description: Her, Zhisheng, et al. Loss of TLR3 aggravates CHIKV replication and pathology due to an altered virus-specific neutralizing antibody response. ''EMBO Mol Med''. 2015 Jan; '''7''' (1):24-41
Meta gene set enrichment analyses link miR-137-regulated pathways with schizophrenia risk. Description: Wright, Carrie, et al. Meta gene set enrichment analyses link miR-137-regulated pathways with schizophrenia risk. ''Front Genet''. 2015; '''6''': 147
Methodological Considerations in Estimation of Phenotype Heritability Using Genome-Wide SNP Data, Illustrated by an Analysis of the Heritability of Height in a Large Sample of African Ancestry Adults. Description: Chen, Fang, et al. Methodological Considerations in Estimation of Phenotype Heritability Using Genome-Wide SNP Data, Illustrated by an Analysis of the Heritability of Height in a Large Sample of African Ancestry Adults. ''PLoS One''. 2015; '''10''' (6):e0131106
Molecular Effects of Polymorphism in the 3'UTR of Unc-5 homolog C Associated with Conception Rate in Holsteins. Description: Sugimoto, Mayumi, et al. Molecular Effects of Polymorphism in the 3'UTR of Unc-5 homolog C Associated with Conception Rate in Holsteins. ''PLoS One''. 2015; '''10''' (7):e0131283
Multilocus heterozygosity and coronary heart disease: nested case-control studies in men and women. Description: Mukamal, Kenneth J, et al. Multilocus heterozygosity and coronary heart disease: nested case-control studies in men and women. ''PLoS One''. 2015; '''10''' (5):e0124847
'Mutiny on the Bounty': the genetic history of Norfolk Island reveals extreme gender-biased admixture. Description: Benton, Miles C, et al. 'Mutiny on the Bounty': the genetic history of Norfolk Island reveals extreme gender-biased admixture. ''Investig Genet''. 2015; '''6''': 11
Netrin-1 - DCC Signaling Systems and Age-Related Macular Degeneration. Description: SanGiovanni, John Paul, et al. Netrin-1 - DCC Signaling Systems and Age-Related Macular Degeneration. ''PLoS One''. 2015; '''10''' (5):e0125548
Network-Based Analysis of Schizophrenia Genome-Wide Association Data to Detect the Joint Functional Association Signals. Description: Chang, Suhua, et al. Network-Based Analysis of Schizophrenia Genome-Wide Association Data to Detect the Joint Functional Association Signals. ''PLoS One''. 2015; '''10''' (7):e0133404
No Additional Prognostic Value of Genetic Information in the Prediction of Vascular Events after Cerebral Ischemia of Arterial Origin: The PROMISe Study. Description: Achterberg, Sefanja, et al. No Additional Prognostic Value of Genetic Information in the Prediction of Vascular Events after Cerebral Ischemia of Arterial Origin: The PROMISe Study. ''PLoS One''. 2015; '''10''' (4):e0119203
No association between apolipoprotein E or N-acetyltransferase 2 gene polymorphisms and age-related hearing loss. Description: Dawes, Piers, et al. No association between apolipoprotein E or N-acetyltransferase 2 gene polymorphisms and age-related hearing loss. ''Laryngoscope''. 2015 Jan; '''125''' (1):E33-8
No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity. Description: Garcia-Etxebarria, Koldo, et al. No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity. ''PLoS One''. 2015; '''10''' (9):e0135983
Novel loci for non-syndromic coarctation of the aorta in sporadic and familial cases. Description: Moosmann, Julia, et al. Novel loci for non-syndromic coarctation of the aorta in sporadic and familial cases. ''PLoS One''. 2015; '''10''' (5):e0126873
Pathway Analysis Based on a Genome-Wide Association Study of Polycystic Ovary Syndrome. Description: Shim, Unjin, et al. Pathway Analysis Based on a Genome-Wide Association Study of Polycystic Ovary Syndrome. ''PLoS One''. 2015; '''10''' (8):e0136609
Pathway-Based Genome-Wide Association Studies for Plasma Triglycerides in Obese Females and Normal-Weight Controls. Description: Jiao, Hongxiao, et al. Pathway-Based Genome-Wide Association Studies for Plasma Triglycerides in Obese Females and Normal-Weight Controls. ''PLoS One''. 2015; '''10''' (8):e0134923
Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols. Description: Moore, Carrie B, et al. Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols. ''Open Forum Infect Dis''. 2015 Jan; '''2''' (1):ofu113
Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein. Description: Ligthart, Symen, et al. Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein. ''PLoS One''. 2015; '''10''' (3):e0118859
Pooled Sequencing of Candidate Genes Implicates Rare Variants in the Development of Asthma Following Severe RSV Bronchiolitis in Infancy. Description: Torgerson, Dara G, et al. Pooled Sequencing of Candidate Genes Implicates Rare Variants in the Development of Asthma Following Severe RSV Bronchiolitis in Infancy. ''PLoS One''. 2015; '''10''' (11):e0142649
Population genetic structure, linkage disequilibrium and effective population size of conserved and extensively raised village chicken populations of Southern Africa. Description: Khanyile, Khulekani S, et al. Population genetic structure, linkage disequilibrium and effective population size of conserved and extensively raised village chicken populations of Southern Africa. ''Front Genet''. 2015; '''6''': 13
Population genomics reveals chromosome-scale heterogeneous evolution in a protoploid yeast. Description: Friedrich, Anne, et al. Population genomics reveals chromosome-scale heterogeneous evolution in a protoploid yeast. ''Mol Biol Evol''. 2015 Jan; '''32''' (1):184-92
Potential Signals of Natural Selection in the Top Risk Loci for Coronary Artery Disease: 9p21 and 10q11. Description: Zanetti, Daniela, et al. Potential Signals of Natural Selection in the Top Risk Loci for Coronary Artery Disease: 9p21 and 10q11. ''PLoS One''. 2015; '''10''' (8):e0134840
Practical Calling Approach for Exome Array-Based Genome-Wide Association Studies in Korean Population. Description: Park, Tae-Joon, et al. Practical Calling Approach for Exome Array-Based Genome-Wide Association Studies in Korean Population. ''Int J Genomics''. 2015; '''2015''': 421715
Prediction of breast cancer survival using clinical and genetic markers by tumor subtypes. Description: Song, Nan, et al. Prediction of breast cancer survival using clinical and genetic markers by tumor subtypes. ''PLoS One''. 2015; '''10''' (4):e0122413
Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus. Description: Hafren, Lena, et al. Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus. ''PLoS One''. 2015; '''10''' (7):e0132551
Promising Loci and Genes for Yolk and Ovary Weight in Chickens Revealed by a Genome-Wide Association Study. Description: Sun, Congjiao, et al. Promising Loci and Genes for Yolk and Ovary Weight in Chickens Revealed by a Genome-Wide Association Study. ''PLoS One''. 2015; '''10''' (9):e0137145
Psoriasis drug development and GWAS interpretation through in silico analysis of transcription factor binding sites. Description: Swindell, William R, et al. Psoriasis drug development and GWAS interpretation through in silico analysis of transcription factor binding sites. ''Clin Transl Med''. 2015; '''4''': 13
Race Does Not Predict Melanocyte Heterogeneous Responses to Dermal Fibroblast-Derived Mediators. Description: Sirimahachaiyakul, Pornthep, et al. Race Does Not Predict Melanocyte Heterogeneous Responses to Dermal Fibroblast-Derived Mediators. ''PLoS One''. 2015; '''10''' (9):e0139135
Rare Variants in Transcript and Potential Regulatory Regions Explain a Small Percentage of the Missing Heritability of Complex Traits in Cattle. Description: Gonzalez-Recio, Oscar, et al. Rare Variants in Transcript and Potential Regulatory Regions Explain a Small Percentage of the Missing Heritability of Complex Traits in Cattle. ''PLoS One''. 2015; '''10''' (12):e0143945
Reduced SNP panels for genetic identification and introgression analysis in the dark honey bee (Apis mellifera mellifera). Description: Munoz, Irene, et al. Reduced SNP panels for genetic identification and introgression analysis in the dark honey bee (Apis mellifera mellifera). ''PLoS One''. 2015; '''10''' (4):e0124365
Resequencing and Association Analysis of CLN8 with Autism Spectrum Disorder in a Japanese Population. Description: Inoue, Emiko, et al. Resequencing and Association Analysis of CLN8 with Autism Spectrum Disorder in a Japanese Population. ''PLoS One''. 2015; '''10''' (12):e0144624
Revisiting demographic processes in cattle with genome-wide population genetic analysis. Description: Orozco-terWengel, Pablo, et al. Revisiting demographic processes in cattle with genome-wide population genetic analysis. ''Front Genet''. 2015; '''6''': 191
Scanning and Filling: Ultra-Dense SNP Genotyping Combining Genotyping-By-Sequencing, SNP Array and Whole-Genome Resequencing Data. Description: Torkamaneh, Davoud, et al. Scanning and Filling: Ultra-Dense SNP Genotyping Combining Genotyping-By-Sequencing, SNP Array and Whole-Genome Resequencing Data. ''PLoS One''. 2015; '''10''' (7):e0131533
Schizophrenia risk variants modulate white matter volume across the psychosis spectrum: evidence from two independent cohorts. Description: Oertel-Knochel, Viola, et al. Schizophrenia risk variants modulate white matter volume across the psychosis spectrum: evidence from two independent cohorts. ''Neuroimage Clin''. 2015; '''7''': 764-70
SHBG gene polymorphism (rs1799941) associates with metabolic syndrome in children and adolescents. Description: White, Marquitta J, et al. SHBG gene polymorphism (rs1799941) associates with metabolic syndrome in children and adolescents. ''PLoS One''. 2015; '''10''' (2):e0116915
Signatures of natural selection at the FTO (fat mass and obesity associated) locus in human populations. Description: Liu, Xuanshi, et al. Signatures of natural selection at the FTO (fat mass and obesity associated) locus in human populations. ''PLoS One''. 2015; '''10''' (2):e0117093
SIRT1 Polymorphisms Associate with Seasonal Weight Variation, Depressive Disorders, and Diastolic Blood Pressure in the General Population. Description: Kovanen, Leena, et al. SIRT1 Polymorphisms Associate with Seasonal Weight Variation, Depressive Disorders, and Diastolic Blood Pressure in the General Population. ''PLoS One''. 2015; '''10''' (10):e0141001
Strong selection for behavioural resilience in Australian stock working dogs identified by selective sweep analysis. Description: Arnott, Elizabeth R, et al. Strong selection for behavioural resilience in Australian stock working dogs identified by selective sweep analysis. ''Canine Genet Epidemiol''. 2015; '''2''': 6
Susceptibility to invasive meningococcal disease: polymorphism of complement system genes and Neisseria meningitidis factor H binding protein. Description: Bradley, Declan T, et al. Susceptibility to invasive meningococcal disease: polymorphism of complement system genes and Neisseria meningitidis factor H binding protein. ''PLoS One''. 2015; '''10''' (3):e0120757
Systematic Evaluation of Genetic Variants for Polycystic Ovary Syndrome in a Chinese Population. Description: Xu, Yuping, et al. Systematic Evaluation of Genetic Variants for Polycystic Ovary Syndrome in a Chinese Population. ''PLoS One''. 2015; '''10''' (10):e0140695
Targeted resequencing of the pericentromere of chromosome 2 linked to constitutional delay of growth and puberty. Description: Cousminer, Diana L, et al. Targeted resequencing of the pericentromere of chromosome 2 linked to constitutional delay of growth and puberty. ''PLoS One''. 2015; '''10''' (6):e0128524
TECPR2 Associated Neuroaxonal Dystrophy in Spanish Water Dogs. Description: Hahn, Kerstin, et al. TECPR2 Associated Neuroaxonal Dystrophy in Spanish Water Dogs. ''PLoS One''. 2015; '''10''' (11):e0141824
The association between carbohydrate-rich foods and risk of cardiovascular disease is not modified by genetic susceptibility to dyslipidemia as determined by 80 validated variants. Description: Sonestedt, Emily, et al. The association between carbohydrate-rich foods and risk of cardiovascular disease is not modified by genetic susceptibility to dyslipidemia as determined by 80 validated variants. ''PLoS One''. 2015; '''10''' (4):e0126104
The Association of Type 2 Diabetes Loci Identified in Genome-Wide Association Studies with Metabolic Syndrome and Its Components in a Chinese Population with Type 2 Diabetes. Description: Kong, Xiaomu, et al. The Association of Type 2 Diabetes Loci Identified in Genome-Wide Association Studies with Metabolic Syndrome and Its Components in a Chinese Population with Type 2 Diabetes. ''PLoS One''. 2015; '''10''' (11):e0143607
The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey). Description: Helgeland, Oyvind, et al. The Chromosome 9p21 CVD- and T2D-Associated Regions in a Norwegian Population (The HUNT2 Survey). ''Int J Endocrinol''. 2015; '''2015''': 164652
The effects of electronic medical record phenotyping details on genetic association studies: HDL-C as a case study. Description: Dumitrescu, Logan, et al. The effects of electronic medical record phenotyping details on genetic association studies: HDL-C as a case study. ''BioData Min''. 2015; '''8''': 15
The female protective effect in autism spectrum disorder is not mediated by a single genetic locus. Description: Gockley, Jake, et al. The female protective effect in autism spectrum disorder is not mediated by a single genetic locus. ''Mol Autism''. 2015; '''6''': 25
The genetic basis of quality of life in healthy Swedish women: a candidate gene approach. Description: Schoormans, Dounya, et al. The genetic basis of quality of life in healthy Swedish women: a candidate gene approach. ''PLoS One''. 2015; '''10''' (2):e0118292
The Genetic Structure of Marijuana and Hemp. Description: Sawler, Jason, et al. The Genetic Structure of Marijuana and Hemp. ''PLoS One''. 2015; '''10''' (8):e0133292
The Genomic Legacy of the Transatlantic Slave Trade in the Yungas Valley of Bolivia. Description: Heinz, Tanja, et al. The Genomic Legacy of the Transatlantic Slave Trade in the Yungas Valley of Bolivia. ''PLoS One''. 2015; '''10''' (8):e0134129
The identification of loci for immune traits in chickens using a genome-wide association study. Description: Zhang, Lei, et al. The identification of loci for immune traits in chickens using a genome-wide association study. ''PLoS One''. 2015; '''10''' (3):e0117269
The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations. Description: Schnitzler, Fabian, et al. The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations. ''PLoS One''. 2015; '''10''' (7):e0116044
The relationship between dopamine receptor D1 and cognitive performance. Description: Tsang, Jonathan, et al. The relationship between dopamine receptor D1 and cognitive performance. ''NPJ Schizophr''. 2015; '''1''': 14002
The Relationship between Runs of Homozygosity and Inbreeding in Jersey Cattle under Selection. Description: Kim, Eui-Soo, et al. The Relationship between Runs of Homozygosity and Inbreeding in Jersey Cattle under Selection. ''PLoS One''. 2015; '''10''' (7):e0129967
The type 2 diabetes risk allele of TMEM154-rs6813195 associates with decreased beta cell function in a study of 6,486 Danes. Description: Harder, Marie Neergaard, et al. The type 2 diabetes risk allele of TMEM154-rs6813195 associates with decreased beta cell function in a study of 6,486 Danes. ''PLoS One''. 2015; '''10''' (3):e0120890
Toll-Like Receptor Family Polymorphisms Are Associated with Primary Renal Diseases but Not with Renal Outcomes Following Kidney Transplantation. Description: Dessing, Mark C, et al. Toll-Like Receptor Family Polymorphisms Are Associated with Primary Renal Diseases but Not with Renal Outcomes Following Kidney Transplantation. ''PLoS One''. 2015; '''10''' (10):e0139769
Transcriptome Analysis of CD4+ T Cells in Coeliac Disease Reveals Imprint of BACH2 and IFNgamma Regulation. Description: Quinn, Emma M, et al. Transcriptome Analysis of CD4+ T Cells in Coeliac Disease Reveals Imprint of BACH2 and IFNgamma Regulation. ''PLoS One''. 2015; '''10''' (10):e0140049
Triploidy--Observations in 154 Diandric Cases. Description: Scholz, Nanna Brink, et al. Triploidy--Observations in 154 Diandric Cases. ''PLoS One''. 2015; '''10''' (11):e0142545
Trypanosomosis: potential driver of selection in African cattle. Description: Smetko, Anamarija, et al. Trypanosomosis: potential driver of selection in African cattle. ''Front Genet''. 2015; '''6''': 137
Two Independent Mutations in ADAMTS17 Are Associated with Primary Open Angle Glaucoma in the Basset Hound and Basset Fauve de Bretagne Breeds of Dog. Description: Oliver, James A C, et al. Two Independent Mutations in ADAMTS17 Are Associated with Primary Open Angle Glaucoma in the Basset Hound and Basset Fauve de Bretagne Breeds of Dog. ''PLoS One''. 2015; '''10''' (10):e0140436
TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits. Description: Diogo, Dorothee, et al. TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits. ''PLoS One''. 2015; '''10''' (4):e0122271
Variability in the effect of 5-HTTLPR on depression in a large European population: the role of age, symptom profile, type and intensity of life stressors. Description: Juhasz, Gabriella, et al. Variability in the effect of 5-HTTLPR on depression in a large European population: the role of age, symptom profile, type and intensity of life stressors. ''PLoS One''. 2015; '''10''' (3):e0116316
Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Abeta1-42 Level. Description: Li, Qingqin S, et al. Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Abeta1-42 Level. ''PLoS One''. 2015; '''10''' (8):e0134000
Visualization of Genome Diversity in German Shepherd Dogs. Description: Mortlock, Sally-Anne, et al. Visualization of Genome Diversity in German Shepherd Dogs. ''Bioinform Biol Insights''. 2015; '''9''' (Suppl 2):37-42
When Does Choice of Accuracy Measure Alter Imputation Accuracy Assessments? Description: Ramnarine, Shelina, et al. When Does Choice of Accuracy Measure Alter Imputation Accuracy Assessments? ''PLoS One''. 2015; '''10''' (10):e0137601
Whole-Genome Analysis of Diversity and SNP-Major Gene Association in Peach Germplasm. Description: Micheletti, Diego, et al. Whole-Genome Analysis of Diversity and SNP-Major Gene Association in Peach Germplasm. ''PLoS One''. 2015; '''10''' (9):e0136803
Whole genome sequencing of elite rice cultivars as a comprehensive information resource for marker assisted selection. Description: Duitama, Jorge, et al. Whole genome sequencing of elite rice cultivars as a comprehensive information resource for marker assisted selection. ''PLoS One''. 2015; '''10''' (4):e0124617
A genome-wide association study of marginal zone lymphoma shows association to the HLA region. Description: Vijai, Joseph, et al. A genome-wide association study of marginal zone lymphoma shows association to the HLA region. ''Nat Commun''. 2015 Jan 8; '''6''': 5751
A genome-wide association study for nutritional indices in Drosophila. Description: Unckless, Robert L, et al. A genome-wide association study for nutritional indices in Drosophila. ''G3 (Bethesda)''. 2015 Jan 12; '''5''' (3):417-25
Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma. Description: Igartua, Catherine, et al. Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma. ''Nat Commun''. 2015 Jan 16; '''6''': 5965
Fast individual ancestry inference from DNA sequence data leveraging allele frequencies for multiple populations. Description: Bansal, Vikas, et al. Fast individual ancestry inference from DNA sequence data leveraging allele frequencies for multiple populations. ''BMC Bioinformatics''. 2015 Jan 16; '''16''': 4
Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios. Description: Besenbacher, Soren, et al. Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios. ''Nat Commun''. 2015 Jan 19; '''6''': 5969
Paging through history: parchment as a reservoir of ancient DNA for next generation sequencing. Description: Teasdale, M D, et al. Paging through history: parchment as a reservoir of ancient DNA for next generation sequencing. ''Philos Trans R Soc Lond B Biol Sci''. 2015 Jan 19; '''370''' (1660):20130379
Unravelling genes and pathways implicated in working memory of schizophrenia in Han Chinese. Description: Ren, Hongyan, et al. Unravelling genes and pathways implicated in working memory of schizophrenia in Han Chinese. ''Int J Mol Sci''. 2015 Jan 20; '''16''' (1):2145-61
A medium density genetic map and QTL for behavioral and production traits in Japanese quail. Description: Recoquillay, Julien, et al. A medium density genetic map and QTL for behavioral and production traits in Japanese quail. ''BMC Genomics''. 2015 Jan 22; '''16''': 10
Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci. Description: Betz, Regina C, et al. Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci. ''Nat Commun''. 2015 Jan 22; '''6''': 5966
Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation. Description: Lock, Eric F, et al. Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation. ''BMC Genomics''. 2015 Jan 22; '''16''': 11
Pharmacogenomics of hypertension: a genome-wide, placebo-controlled cross-over study, using four classes of antihypertensive drugs. Description: Hiltunen, Timo P, et al. Pharmacogenomics of hypertension: a genome-wide, placebo-controlled cross-over study, using four classes of antihypertensive drugs. ''J Am Heart Assoc''. 2015 Jan 26; '''4''' (1):e001521
New loci and coding variants confer risk for age-related macular degeneration in East Asians. Description: Cheng, Ching-Yu, et al. New loci and coding variants confer risk for age-related macular degeneration in East Asians. ''Nat Commun''. 2015 Jan 28; '''6''': 6063
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Description: Wessel, Jennifer, et al. Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. ''Nat Commun''. 2015 Jan 29; '''6''': 5897
Genome-wide detection and characterization of positive selection in Korean Native Black Pig from Jeju Island. Description: Kim, Jaemin, et al. Genome-wide detection and characterization of positive selection in Korean Native Black Pig from Jeju Island. ''BMC Genet''. 2015 Jan 30; '''16''': 3
Highlighting nonlinear patterns in population genetics datasets. Description: Alanis-Lobato, Gregorio, et al. Highlighting nonlinear patterns in population genetics datasets. ''Sci Rep''. 2015 Jan 30; '''5''': 8140
A clinicogenetic model to predict lymph node invasion by use of genome-based biomarkers from exome arrays in prostate cancer patients. Description: Oh, Jong Jin, et al. A clinicogenetic model to predict lymph node invasion by use of genome-based biomarkers from exome arrays in prostate cancer patients. ''Korean J Urol''. 2015 Feb; '''56''' (2):109-16
A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions. Description: Oikkonen, J, et al. A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions. ''Mol Psychiatry''. 2015 Feb; '''20''' (2):275-82
Bovine Genome-wide Association Study for Genetic Elements to Resist the Infection of Foot-and-mouth Disease in the Field. Description: Lee, Bo-Young, et al. Bovine Genome-wide Association Study for Genetic Elements to Resist the Infection of Foot-and-mouth Disease in the Field. ''Asian-Australas J Anim Sci''. 2015 Feb; '''28''' (2):166-70
Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk. Description: Carvajal-Carmona, Luis G, et al. Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk. ''Hum Genet''. 2015 Feb; '''134''' (2):231-45
Characterization of expression quantitative trait loci in the human colon. Description: Singh, Tarjinder, et al. Characterization of expression quantitative trait loci in the human colon. ''Inflamm Bowel Dis''. 2015 Feb; '''21''' (2):251-6
Genes from a translational analysis support a multifactorial nature of white matter hyperintensities. Description: Lopez, Lorna M, et al. Genes from a translational analysis support a multifactorial nature of white matter hyperintensities. ''Stroke''. 2015 Feb; '''46''' (2):341-7
Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke. Description: Adib-Samii, Poneh, et al. Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke. ''Stroke''. 2015 Feb; '''46''' (2):348-53
Genetic associations with brain cortical thickness in multiple sclerosis. Description: Matsushita, T, et al. Genetic associations with brain cortical thickness in multiple sclerosis. ''Genes Brain Behav''. 2015 Feb; '''14''' (2):217-27
Genetic variants associated with sleep disorders. Description: Kripke, Daniel F, et al. Genetic variants associated with sleep disorders. ''Sleep Med''. 2015 Feb; '''16''' (2):217-24
Genome-wide association study identifies shared risk loci common to two malignancies in golden retrievers. Description: Tonomura, Noriko, et al. Genome-wide association study identifies shared risk loci common to two malignancies in golden retrievers. ''PLoS Genet''. 2015 Feb; '''11''' (2):e1004922
Genomic profiling of thousands of candidate polymorphisms predicts risk of relapse in 778 Danish and German childhood acute lymphoblastic leukemia patients. Description: Wesolowska-Andersen, A, et al. Genomic profiling of thousands of candidate polymorphisms predicts risk of relapse in 778 Danish and German childhood acute lymphoblastic leukemia patients. ''Leukemia''. 2015 Feb; '''29''' (2):297-303
Identification of additive, dominant, and epistatic variation conferred by key genes in cellulose biosynthesis pathway in Populus tomentosadagger. Description: Du, Qingzhang, et al. Identification of additive, dominant, and epistatic variation conferred by key genes in cellulose biosynthesis pathway in Populus tomentosadagger. ''DNA Res''. 2015 Feb; '''22''' (1):53-67
Impact of cross-disorder polygenic risk on frontal brain activation with specific effect of schizophrenia risk. Description: Whalley, Heather C, et al. Impact of cross-disorder polygenic risk on frontal brain activation with specific effect of schizophrenia risk. ''Schizophr Res''. 2015 Feb; '''161''' (2-3):484-9
Pathogenic EFHC1 mutations are tolerated in healthy individuals dependent on reported ancestry. Description: Subaran, Ryan L, et al. Pathogenic EFHC1 mutations are tolerated in healthy individuals dependent on reported ancestry. ''Epilepsia''. 2015 Feb; '''56''' (2):188-94
Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes. Description: Prescott, Natalie J, et al. Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes. ''PLoS Genet''. 2015 Feb; '''11''' (2):e1004955
Single nucleotide polymorphism in the neuroplastin locus associates with cortical thickness and intellectual ability in adolescents. Description: Desrivieres, S, et al. Single nucleotide polymorphism in the neuroplastin locus associates with cortical thickness and intellectual ability in adolescents. ''Mol Psychiatry''. 2015 Feb; '''20''' (2):263-74
The association of previously reported polymorphisms for microvascular complications in a meta-analysis of diabetic retinopathy. Description: Hosseini, S Mohsen, et al. The association of previously reported polymorphisms for microvascular complications in a meta-analysis of diabetic retinopathy. ''Hum Genet''. 2015 Feb; '''134''' (2):247-57
Heritable variation in courtship patterns in Drosophila melanogaster. Description: Gaertner, Bryn E, et al. Heritable variation in courtship patterns in Drosophila melanogaster. ''G3 (Bethesda)''. 2015 Feb 3; '''5''' (4):531-9
LRP5 regulates human body fat distribution by modulating adipose progenitor biology in a dose- and depot-specific fashion. Description: Loh, Nellie Y, et al. LRP5 regulates human body fat distribution by modulating adipose progenitor biology in a dose- and depot-specific fashion. ''Cell Metab''. 2015 Feb 3; '''21''' (2):262-273
Looking for adaptive footprints in the HSP90AA1 ovine gene. Description: Salces-Ortiz, Judit, et al. Looking for adaptive footprints in the HSP90AA1 ovine gene. ''BMC Evol Biol''. 2015 Feb 4; '''15''': 7
Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis. Description: Bowes, John, et al. Dense genotyping of immune-related susceptibility loci reveals new insights into the genetics of psoriatic arthritis. ''Nat Commun''. 2015 Feb 5; '''6''': 6046
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. Description: Do, Ron, et al. Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. ''Nature''. 2015 Feb 5; '''518''' (7537):102-6
Filter-free exhaustive odds ratio-based genome-wide interaction approach pinpoints evidence for interaction in the HLA region in psoriasis. Description: Grange, Laura, et al. Filter-free exhaustive odds ratio-based genome-wide interaction approach pinpoints evidence for interaction in the HLA region in psoriasis. ''BMC Genet''. 2015 Feb 6; '''16''': 11
Epidermolysis bullosa in Danish Hereford calves is caused by a deletion in LAMC2 gene. Description: Murgiano, Leonardo, et al. Epidermolysis bullosa in Danish Hereford calves is caused by a deletion in LAMC2 gene. ''BMC Vet Res''. 2015 Feb 7; '''11''': 23
Apolipoprotein L1, income and early kidney damage. Description: Tamrat, Ruth, et al. Apolipoprotein L1, income and early kidney damage. ''BMC Nephrol''. 2015 Feb 10; '''16''': 14
Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy. Description: Lei, Jieping, et al. Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy. ''Breast Cancer Res''. 2015 Feb 10; '''17''': 18
Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer. Description: Mtatiro, Siana N, et al. Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer. ''BMC Med Genet''. 2015 Feb 10; '''16''': 4
Exome sequencing of a family with lone, autosomal dominant atrial flutter identifies a rare variation in ABCB4 significantly enriched in cases. Description: Maciag, Anna, et al. Exome sequencing of a family with lone, autosomal dominant atrial flutter identifies a rare variation in ABCB4 significantly enriched in cases. ''BMC Genet''. 2015 Feb 11; '''16''': 15
The genetics of POAG in black South Africans: a candidate gene association study. Description: Williams, Susan E I, et al. The genetics of POAG in black South Africans: a candidate gene association study. ''Sci Rep''. 2015 Feb 11; '''5''': 8378
New genetic loci link adipose and insulin biology to body fat distribution. Description: Shungin, Dmitry, et al. New genetic loci link adipose and insulin biology to body fat distribution. ''Nature''. 2015 Feb 12; '''518''' (7538):187-196
Association between genetic polymorphisms and carotid atherosclerosis in patients treated with radiotherapy for nasopharyngeal carcinoma. Description: Yuan, Chuang, et al. Association between genetic polymorphisms and carotid atherosclerosis in patients treated with radiotherapy for nasopharyngeal carcinoma. ''Radiat Oncol''. 2015 Feb 13; '''10''': 39
MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene. Description: Nischwitz, S, et al. MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene. ''J Neuroimmunol''. 2015 Feb 15; '''279''': 46-9
Genetic variants in the inositol phosphate metabolism pathway and risk of different types of cancer. Description: Tan, Juan, et al. Genetic variants in the inositol phosphate metabolism pathway and risk of different types of cancer. ''Sci Rep''. 2015 Feb 16; '''5''': 8473
Saving more teeth-a case for personalized care. Description: Vieira, Alexandre R, et al. Saving more teeth-a case for personalized care. ''J Pers Med''. 2015 Feb 16; '''5''' (1):30-5
Functional variants regulating LGALS1 (Galectin 1) expression affect human susceptibility to influenza A(H7N9). Description: Chen, Yu, et al. Functional variants regulating LGALS1 (Galectin 1) expression affect human susceptibility to influenza A(H7N9). ''Sci Rep''. 2015 Feb 17; '''5''': 8517
c.620C>T mutation in GATA4 is associated with congenital heart disease in South India. Description: Mattapally, Saidulu, et al. c.620C>T mutation in GATA4 is associated with congenital heart disease in South India. ''BMC Med Genet''. 2015 Feb 18; '''16''': 7
Genome-wide epistatic expression quantitative trait loci discovery in four human tissues reveals the importance of local chromosomal interactions governing gene expression. Description: Fitzpatrick, Darren J, et al. Genome-wide epistatic expression quantitative trait loci discovery in four human tissues reveals the importance of local chromosomal interactions governing gene expression. ''BMC Genomics''. 2015 Feb 21; '''16''': 109
A genome-wide scan for signatures of directional selection in domesticated pigs. Description: Moon, Sunjin, et al. A genome-wide scan for signatures of directional selection in domesticated pigs. ''BMC Genomics''. 2015 Feb 25; '''16''': 130
Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci. Description: Lemire, Mathieu, et al. Long-range epigenetic regulation is conferred by genetic variation located at thousands of independent loci. ''Nat Commun''. 2015 Feb 26; '''6''': 6326
Phenotypic population screen identifies a new mutation in bovine DGAT1 responsible for unsaturated milk fat. Description: Lehnert, Klaus, et al. Phenotypic population screen identifies a new mutation in bovine DGAT1 responsible for unsaturated milk fat. ''Sci Rep''. 2015 Feb 26; '''5''': 8484
Non-coding genomic regions possessing enhancer and silencer potential are associated with healthy aging and exceptional survival. Description: Kim, Sangkyu, et al. Non-coding genomic regions possessing enhancer and silencer potential are associated with healthy aging and exceptional survival. ''Oncotarget''. 2015 Feb 28; '''6''' (6):3600-12
Association of symptoms and severity of rift valley fever with genetic polymorphisms in human innate immune pathways. Description: Hise, Amy G, et al. Association of symptoms and severity of rift valley fever with genetic polymorphisms in human innate immune pathways. ''PLoS Negl Trop Dis''. 2015 Mar; '''9''' (3):e0003584
CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs. Description: Putku, Margus, et al. CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs. ''Hum Genet''. 2015 Mar; '''134''' (3):291-303
Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment. Description: Villanueva, Pia, et al. Exome sequencing in an admixed isolated population indicates NFXL1 variants confer a risk for specific language impairment. ''PLoS Genet''. 2015 Mar; '''11''' (3):e1004925
Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate. Description: Wolf, Zena T, et al. Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate. ''PLoS Genet''. 2015 Mar; '''11''' (3):e1005059
Genome-wide association study identifies three novel genetic markers associated with elite endurance performance. Description: Ahmetov, Ii, et al. Genome-wide association study identifies three novel genetic markers associated with elite endurance performance. ''Biol Sport''. 2015 Mar; '''32''' (1):3-9
Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS. Description: Mattheisen, M, et al. Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS. ''Mol Psychiatry''. 2015 Mar; '''20''' (3):337-44
Influence of genetic variants in SORL1 gene on the manifestation of Alzheimer's disease. Description: Louwersheimer, Eva, et al. Influence of genetic variants in SORL1 gene on the manifestation of Alzheimer's disease. ''Neurobiol Aging''. 2015 Mar; '''36''' (3):1605.e13-20
*Insights into the origin of rare haplogroup C3 Y chromosomes in South America from high-density autosomal SNP genotyping.** Description: Mezzavilla, Massimo, et al. Insights into the origin of rare haplogroup C3* Y chromosomes in South America from high-density autosomal SNP genotyping. ''Forensic Sci Int Genet''. 2015 Mar; '''15''': 115-20
Maternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritance. Description: Esparza-Gordillo, Jorge, et al. Maternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritance. ''PLoS Genet''. 2015 Mar; '''11''' (3):e1005076
Meta-analysis of the TNFAIP3 region in psoriasis reveals a risk haplotype that is distinct from other autoimmune diseases. Description: Nititham, J, et al. Meta-analysis of the TNFAIP3 region in psoriasis reveals a risk haplotype that is distinct from other autoimmune diseases. ''Genes Immun''. 2015 Mar; '''16''' (2):120-6
Rare variation facilitates inferences of fine-scale population structure in humans. Description: O'Connor, Timothy D, et al. Rare variation facilitates inferences of fine-scale population structure in humans. ''Mol Biol Evol''. 2015 Mar; '''32''' (3):653-60
Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes. Description: Wood, Andrew R, et al. Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes. ''Hum Mol Genet''. 2015 Mar 1; '''24''' (5):1504-12
Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problems. Description: Iqbal, Zafar, et al. Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problems. ''Am J Hum Genet''. 2015 Mar 5; '''96''' (3):386-96
Whole-genome sequence-based analysis of thyroid function. Description: Taylor, Peter N, et al. Whole-genome sequence-based analysis of thyroid function. ''Nat Commun''. 2015 Mar 6; '''6''': 5681
Comparing variant calling algorithms for target-exon sequencing in a large sample. Description: Lo, Yancy, et al. Comparing variant calling algorithms for target-exon sequencing in a large sample. ''BMC Bioinformatics''. 2015 Mar 7; '''16''': 75
Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels. Description: van Leeuwen, Elisabeth M, et al. Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels. ''Nat Commun''. 2015 Mar 9; '''6''': 6065
A polymorphism at the translation start site of the vitamin D receptor gene is associated with the response to anti-osteoporotic therapy in postmenopausal women from southern Italy. Description: Conti, Valeria, et al. A polymorphism at the translation start site of the vitamin D receptor gene is associated with the response to anti-osteoporotic therapy in postmenopausal women from southern Italy. ''Int J Mol Sci''. 2015 Mar 10; '''16''' (3):5452-66
Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies. Description: Levine, Adam P, et al. Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies. ''BMC Genomics''. 2015 Mar 10; '''16''': 163
CYB5A polymorphism increases androgens and reduces risk of rheumatoid arthritis in women. Description: Stark, Klaus, et al. CYB5A polymorphism increases androgens and reduces risk of rheumatoid arthritis in women. ''Arthritis Res Ther''. 2015 Mar 11; '''17''': 56
Whole genome sequencing of an ethnic Pathan (Pakhtun) from the north-west of Pakistan. Description: Ilyas, Muhammad, et al. Whole genome sequencing of an ethnic Pathan (Pakhtun) from the north-west of Pakistan. ''BMC Genomics''. 2015 Mar 12; '''16''': 172
Association of FPGS genetic polymorphisms with primary retroperitoneal liposarcoma. Description: Miao, Chengli, et al. Association of FPGS genetic polymorphisms with primary retroperitoneal liposarcoma. ''Sci Rep''. 2015 Mar 13; '''5''': 9079
Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder. Description: Kember, Rachel L, et al. Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder. ''BMC Genet''. 2015 Mar 15; '''16''': 27
Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes. Description: Cooper, Nicholas J, et al. Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes. ''Hum Mol Genet''. 2015 Mar 15; '''24''' (6):1774-90
Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions. Description: Barrett, Jennifer H, et al. Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions. ''Int J Cancer''. 2015 Mar 15; '''136''' (6):1351-60
Validation study of candidate single nucleotide polymorphisms associated with left ventricular hypertrophy in the Korean population. Description: Park, Jin-Kyu, et al. Validation study of candidate single nucleotide polymorphisms associated with left ventricular hypertrophy in the Korean population. ''BMC Med Genet''. 2015 Mar 15; '''16''': 13
Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS. Description: Steinberg, Karyn Meltz, et al. Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS. ''Sci Rep''. 2015 Mar 16; '''5''': 9124
Genome-wide analysis reveals population structure and selection in Chinese indigenous sheep breeds. Description: Wei, Caihong, et al. Genome-wide analysis reveals population structure and selection in Chinese indigenous sheep breeds. ''BMC Genomics''. 2015 Mar 17; '''16''': 194
A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females. Description: Sharma, Swarkar, et al. A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females. ''Nat Commun''. 2015 Mar 18; '''6''': 6452
Meta-analysis of two Chinese populations identifies an autoimmune disease risk allele in 22q11.21 as associated with systemic lupus erythematosus. Description: Zhang, Yan, et al. Meta-analysis of two Chinese populations identifies an autoimmune disease risk allele in 22q11.21 as associated with systemic lupus erythematosus. ''Arthritis Res Ther''. 2015 Mar 20; '''17''': 67
Identification of NF-kappaB and PLCL2 as new susceptibility genes and highlights on a potential role of IRF8 through interferon signature modulation in systemic sclerosis. Description: Arismendi, Maria, et al. Identification of NF-kappaB and PLCL2 as new susceptibility genes and highlights on a potential role of IRF8 through interferon signature modulation in systemic sclerosis. ''Arthritis Res Ther''. 2015 Mar 21; '''17''': 71
Ethnic differences in the association of SERPING1 with age-related macular degeneration and polypoidal choroidal vasculopathy. Description: Liu, Ke, et al. Ethnic differences in the association of SERPING1 with age-related macular degeneration and polypoidal choroidal vasculopathy. ''Sci Rep''. 2015 Mar 24; '''5''': 9424
Unravelling the hidden ancestry of American admixed populations. Description: Montinaro, Francesco, et al. Unravelling the hidden ancestry of American admixed populations. ''Nat Commun''. 2015 Mar 24; '''6''': 6596
X-inactivation informs variance-based testing for X-linked association of a quantitative trait. Description: Ma, Li, et al. X-inactivation informs variance-based testing for X-linked association of a quantitative trait. ''BMC Genomics''. 2015 Mar 25; '''16''': 241
Association analyses confirm five susceptibility loci for systemic lupus erythematosus in the Han Chinese population. Description: Sheng, Yu-jun, et al. Association analyses confirm five susceptibility loci for systemic lupus erythematosus in the Han Chinese population. ''Arthritis Res Ther''. 2015 Mar 28; '''17''': 85
Decision tree analysis of genetic risk for clinically heterogeneous Alzheimer's disease. Description: Yokoyama, Jennifer S, et al. Decision tree analysis of genetic risk for clinically heterogeneous Alzheimer's disease. ''BMC Neurol''. 2015 Mar 28; '''15''': 47
Genomic signatures of human and animal disease in the zoonotic pathogen Streptococcus suis. Description: Weinert, Lucy A, et al. Genomic signatures of human and animal disease in the zoonotic pathogen Streptococcus suis. ''Nat Commun''. 2015 Mar 31; '''6''': 6740
RNA expression profiling in depressed patients suggests retinoid-related orphan receptor alpha as a biomarker for antidepressant response. Description: Hennings, J M, et al. RNA expression profiling in depressed patients suggests retinoid-related orphan receptor alpha as a biomarker for antidepressant response. ''Transl Psychiatry''. 2015 Mar 31; '''5''': e538
A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease. Description: Kyostila, Kaisa, et al. A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease. ''PLoS Genet''. 2015 Apr; '''11''' (4):e1005169
Associations of epithelial sodium channel genes with blood pressure: the GenSalt study. Description: Liu, F, et al. Associations of epithelial sodium channel genes with blood pressure: the GenSalt study. ''J Hum Hypertens''. 2015 Apr; '''29''' (4):224-8
Challenges in conducting genome-wide association studies in highly admixed multi-ethnic populations: the Generation R Study. Description: Medina-Gomez, Carolina, et al. Challenges in conducting genome-wide association studies in highly admixed multi-ethnic populations: the Generation R Study. ''Eur J Epidemiol''. 2015 Apr; '''30''' (4):317-30
Contribution of large region joint associations to complex traits genetics. Description: Pare, Guillaume, et al. Contribution of large region joint associations to complex traits genetics. ''PLoS Genet''. 2015 Apr; '''11''' (4):e1005103
Genetic modifiers of ambulation in the Cooperative International Neuromuscular Research Group Duchenne Natural History Study. Description: Bello, Luca, et al. Genetic modifiers of ambulation in the Cooperative International Neuromuscular Research Group Duchenne Natural History Study. ''Ann Neurol''. 2015 Apr; '''77''' (4):684-96
Immunogenetic influences on acquisition of HIV-1 infection: consensus findings from two African cohorts point to an enhancer element in IL19 (1q32.2). Description: Li, X, et al. Immunogenetic influences on acquisition of HIV-1 infection: consensus findings from two African cohorts point to an enhancer element in IL19 (1q32.2). ''Genes Immun''. 2015 Apr-May; '''16''' (3):213-20
MAGMA: generalized gene-set analysis of GWAS data. Description: de Leeuw, Christiaan A, et al. MAGMA: generalized gene-set analysis of GWAS data. ''PLoS Comput Biol''. 2015 Apr; '''11''' (4):e1004219
MGAS: a powerful tool for multivariate gene-based genome-wide association analysis. Description: Van der Sluis, Sophie, et al. MGAS: a powerful tool for multivariate gene-based genome-wide association analysis. ''Bioinformatics''. 2015 Apr 1; '''31''' (7):1007-15
Polygenic risk of Parkinson disease is correlated with disease age at onset. Description: Escott-Price, Valentina, et al. Polygenic risk of Parkinson disease is correlated with disease age at onset. ''Ann Neurol''. 2015 Apr; '''77''' (4):582-91
SERPINB11 frameshift variant associated with novel hoof specific phenotype in Connemara ponies. Description: Finno, Carrie J, et al. SERPINB11 frameshift variant associated with novel hoof specific phenotype in Connemara ponies. ''PLoS Genet''. 2015 Apr; '''11''' (4):e1005122
Shared genetic influences between attention-deficit/hyperactivity disorder (ADHD) traits in children and clinical ADHD. Description: Stergiakouli, Evie, et al. Shared genetic influences between attention-deficit/hyperactivity disorder (ADHD) traits in children and clinical ADHD. ''J Am Acad Child Adolesc Psychiatry''. 2015 Apr; '''54''' (4):322-7
Simultaneous discovery, estimation and prediction analysis of complex traits using a bayesian mixture model. Description: Moser, Gerhard, et al. Simultaneous discovery, estimation and prediction analysis of complex traits using a bayesian mixture model. ''PLoS Genet''. 2015 Apr; '''11''' (4):e1004969
The cumulative effects of known susceptibility variants to predict primary biliary cirrhosis risk. Description: Tang, R, et al. The cumulative effects of known susceptibility variants to predict primary biliary cirrhosis risk. ''Genes Immun''. 2015 Apr-May; '''16''' (3):193-8
The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains. Description: Eicher, J D, et al. The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains. ''Genes Brain Behav''. 2015 Apr; '''14''' (4):377-85
The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort. Description: Robinson, E B, et al. The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort. ''Mol Psychiatry''. 2015 Apr; '''20''' (4):454-8
Relative extended haplotype homozygosity signals across breeds reveal dairy and beef specific signatures of selection. Description: Bomba, Lorenzo, et al. Relative extended haplotype homozygosity signals across breeds reveal dairy and beef specific signatures of selection. ''Genet Sel Evol''. 2015 Apr 2; '''47''': 25
Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms. Description: Tapper, William, et al. Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms. ''Nat Commun''. 2015 Apr 7; '''6''': 6691
Genome-wide association studies (GWAS) identify a QTL close to PRKAG3 affecting meat pH and colour in crossbred commercial pigs. Description: Zhang, Chunyan, et al. Genome-wide association studies (GWAS) identify a QTL close to PRKAG3 affecting meat pH and colour in crossbred commercial pigs. ''BMC Genet''. 2015 Apr 7; '''16''': 33
Relative performance of gene- and pathway-level methods as secondary analyses for genome-wide association studies. Description: Wojcik, Genevieve L, et al. Relative performance of gene- and pathway-level methods as secondary analyses for genome-wide association studies. ''BMC Genet''. 2015 Apr 8; '''16''': 34
Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis. Description: Zuo, Xianbo, et al. Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis. ''Nat Commun''. 2015 Apr 9; '''6''': 6793
*Association of HLA-B41:02 with Henoch-Schonlein Purpura (IgA Vasculitis) in Spanish individuals irrespective of the HLA-DRB1 status.** Description: Lopez-Mejias, Raquel, et al. Association of HLA-B*41:02 with Henoch-Schonlein Purpura (IgA Vasculitis) in Spanish individuals irrespective of the HLA-DRB1 status. ''Arthritis Res Ther''. 2015 Apr 14; '''17''': 102
Unravelling the genetic history of Negritos and indigenous populations of Southeast Asia. Description: Aghakhanian, Farhang, et al. Unravelling the genetic history of Negritos and indigenous populations of Southeast Asia. ''Genome Biol Evol''. 2015 Apr 14; '''7''' (5):1206-15
The obesity-risk variant of FTO is inversely related with the So-Eum constitutional type: genome-wide association and replication analyses. Description: Cha, Seongwon, et al. The obesity-risk variant of FTO is inversely related with the So-Eum constitutional type: genome-wide association and replication analyses. ''BMC Complement Altern Med''. 2015 Apr 15; '''15''': 120
Genome-Wide Association Study on Resistance to Stalk Rot Diseases in Grain Sorghum. Description: Adeyanju, Adedayo, et al. Genome-Wide Association Study on Resistance to Stalk Rot Diseases in Grain Sorghum. ''G3 (Bethesda)''. 2015 Apr 16; '''5''' (6):1165-75
Low levels of taurine introgression in the current Brazilian Nelore and Gir indicine cattle populations. Description: O'Brien, Ana M Perez, et al. Low levels of taurine introgression in the current Brazilian Nelore and Gir indicine cattle populations. ''Genet Sel Evol''. 2015 Apr 17; '''47''': 31
ReMo-SNPs: a new software tool for identification of polymorphisms in regions and motifs genome-wide. Description: Graae, Lisette, et al. ReMo-SNPs: a new software tool for identification of polymorphisms in regions and motifs genome-wide. ''Genet Res (Camb)''. 2015 Apr 17; '''97''': e8
Anti-citrullinated peptide/protein antibody (ACPA)-negative RA shares a large proportion of susceptibility loci with ACPA-positive RA: a meta-analysis of genome-wide association study in a Japanese population. Description: Terao, Chikashi, et al. Anti-citrullinated peptide/protein antibody (ACPA)-negative RA shares a large proportion of susceptibility loci with ACPA-positive RA: a meta-analysis of genome-wide association study in a Japanese population. ''Arthritis Res Ther''. 2015 Apr 18; '''17''': 104
Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells. Description: Li, Jin, et al. Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells. ''Nat Commun''. 2015 Apr 20; '''6''': 6804
Genome-wide association study of behavioural and psychiatric features in human prion disease. Description: Thompson, A G B, et al. Genome-wide association study of behavioural and psychiatric features in human prion disease. ''Transl Psychiatry''. 2015 Apr 21; '''5''': e552
Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility. Description: Yin, Xianyong, et al. Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility. ''Nat Commun''. 2015 Apr 23; '''6''': 6916
Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism. Description: Scholl, Ute I, et al. Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism. ''Elife''. 2015 Apr 24; '''4''': e06315
Genome-wide association data suggest ABCB1 and immune-related gene sets may be involved in adult antisocial behavior. Description: Salvatore, J E, et al. Genome-wide association data suggest ABCB1 and immune-related gene sets may be involved in adult antisocial behavior. ''Transl Psychiatry''. 2015 Apr 28; '''5''': e558
Composite Selection Signals for Complex Traits Exemplified Through Bovine Stature Using Multibreed Cohorts of European and African Bos taurus. Description: Randhawa, Imtiaz A S, et al. Composite Selection Signals for Complex Traits Exemplified Through Bovine Stature Using Multibreed Cohorts of European and African Bos taurus. ''G3 (Bethesda)''. 2015 Apr 30; '''5''' (7):1391-401
Associations of EDNRA and EDN1 polymorphisms with carotid intima media thickness through interactions with gender, regular exercise, and obesity in subjects in Taiwan: Taichung Community Health Study (TCHS). Description: Li, Tsai-Chung, et al. Associations of EDNRA and EDN1 polymorphisms with carotid intima media thickness through interactions with gender, regular exercise, and obesity in subjects in Taiwan: Taichung Community Health Study (TCHS). ''Biomedicine (Taipei)''. 2015 May; '''5''' (2):8
'Carriers of variant luteinizing hormone (V-LH) among 1593 Baltic men have significantly higher serum LH'. Description: Punab, A M, et al. 'Carriers of variant luteinizing hormone (V-LH) among 1593 Baltic men have significantly higher serum LH'. ''Andrology''. 2015 May; '''3''' (3):512-9
Genetic and phenotypic differentiation of an Andean intermediate altitude population. Description: Eichstaedt, Christina A, et al. Genetic and phenotypic differentiation of an Andean intermediate altitude population. ''Physiol Rep''. 2015 May; '''3''' (5):
Identity-by-descent mapping in a Scandinavian multiple sclerosis cohort. Description: Westerlind, Helga, et al. Identity-by-descent mapping in a Scandinavian multiple sclerosis cohort. ''Eur J Hum Genet''. 2015 May; '''23''' (5):688-92
IL28B is associated with outcomes of chronic HBV infection. Description: Shi, Xiaodong, et al. IL28B is associated with outcomes of chronic HBV infection. ''Yonsei Med J''. 2015 May; '''56''' (3):625-33
Investigation of association between hip osteoarthritis susceptibility loci and radiographic proximal femur shape. Description: Lindner, Claudia, et al. Investigation of association between hip osteoarthritis susceptibility loci and radiographic proximal femur shape. ''Arthritis Rheumatol''. 2015 May; '''67''' (8):2076-84
Psoriasis and cardiometabolic traits: modest association but distinct genetic architectures. Description: Koch, Manja, et al. Psoriasis and cardiometabolic traits: modest association but distinct genetic architectures. ''J Invest Dermatol''. 2015 May; '''135''' (5):1283-1293
Quantifying the cumulative effect of low-penetrance genetic variants on breast cancer risk. Description: Smyth, Conor, et al. Quantifying the cumulative effect of low-penetrance genetic variants on breast cancer risk. ''Mol Genet Genomic Med''. 2015 May; '''3''' (3):182-8
Rare structural genetic variation in human prion diseases. Description: Lukic, Ana, et al. Rare structural genetic variation in human prion diseases. ''Neurobiol Aging''. 2015 May; '''36''' (5):2004.e1-8
Role of Type 1 Diabetes-Associated SNPs on Risk of Autoantibody Positivity in the TEDDY Study. Description: Torn, Carina, et al. Role of Type 1 Diabetes-Associated SNPs on Risk of Autoantibody Positivity in the TEDDY Study. ''Diabetes''. 2015 May; '''64''' (5):1818-29
The cerebellum ages slowly according to the epigenetic clock. Description: Horvath, Steve, et al. The cerebellum ages slowly according to the epigenetic clock. ''Aging (Albany NY)''. 2015 May; '''7''' (5):294-306
Genome-wide association study of perioperative myocardial infarction after coronary artery bypass surgery. Description: Kertai, Miklos D, et al. Genome-wide association study of perioperative myocardial infarction after coronary artery bypass surgery. ''BMJ Open''. 2015 May 6; '''5''' (5):e006920
Genome-wide association mapping in a wild avian population identifies a link between genetic and phenotypic variation in a life-history trait. Description: Husby, Arild, et al. Genome-wide association mapping in a wild avian population identifies a link between genetic and phenotypic variation in a life-history trait. ''Proc Biol Sci''. 2015 May 7; '''282''' (1806):20150156
Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population. Description: Chen, Shanshan, et al. Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population. ''J Am Heart Assoc''. 2015 May 7; '''4''' (5):
Performance of a blockwise approach in variable selection using linkage disequilibrium information. Description: Dehman, Alia, et al. Performance of a blockwise approach in variable selection using linkage disequilibrium information. ''BMC Bioinformatics''. 2015 May 8; '''16''': 148
Insm1 cooperates with Neurod1 and Foxa2 to maintain mature pancreatic beta-cell function. Description: Jia, Shiqi, et al. Insm1 cooperates with Neurod1 and Foxa2 to maintain mature pancreatic beta-cell function. ''EMBO J''. 2015 May 12; '''34''' (10):1417-33
Genome-wide association analysis identifies three new risk loci for gout arthritis in Han Chinese. Description: Li, Changgui, et al. Genome-wide association analysis identifies three new risk loci for gout arthritis in Han Chinese. ''Nat Commun''. 2015 May 13; '''6''': 7041
A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families. Description: Wang, Yi-Ting, et al. A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families. ''BMC Genomics''. 2015 May 15; '''16''': 381
Mosaic structural variation in children with developmental disorders. Description: King, Daniel A, et al. Mosaic structural variation in children with developmental disorders. ''Hum Mol Genet''. 2015 May 15; '''24''' (10):2733-45
Application of high-dimensional feature selection: evaluation for genomic prediction in man. Description: Bermingham, M L, et al. Application of high-dimensional feature selection: evaluation for genomic prediction in man. ''Sci Rep''. 2015 May 19; '''5''': 10312
Genetic association study of circadian genes with seasonal pattern in bipolar disorders. Description: Geoffroy, Pierre Alexis, et al. Genetic association study of circadian genes with seasonal pattern in bipolar disorders. ''Sci Rep''. 2015 May 19; '''5''': 10232
Adaptation to Low Salinity Promotes Genomic Divergence in Atlantic Cod (Gadus morhua L.). Description: Berg, Paul R, et al. Adaptation to Low Salinity Promotes Genomic Divergence in Atlantic Cod (Gadus morhua L.). ''Genome Biol Evol''. 2015 May 20; '''7''' (6):1644-63
affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling. Description: Hernandez-Ferrer, Carles, et al. affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling. ''BMC Bioinformatics''. 2015 May 20; '''16''': 167
A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer. Description: Al-Tassan, Nada A, et al. A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer. ''Sci Rep''. 2015 May 20; '''5''': 10442
Lack of Association between the TSPAN18 Gene and Schizophrenia Based on New Data from Han Chinese and a Meta-Analysis. Description: Zhang, Bao, et al. Lack of Association between the TSPAN18 Gene and Schizophrenia Based on New Data from Han Chinese and a Meta-Analysis. ''Int J Mol Sci''. 2015 May 26; '''16''' (6):11864-72
Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. Description: Swaminathan, Bhairavi, et al. Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. ''Nat Commun''. 2015 May 26; '''6''': 7213
Exploring the relationship between lifestyles, diets and genetic adaptations in humans. Description: Valente, Cristina, et al. Exploring the relationship between lifestyles, diets and genetic adaptations in humans. ''BMC Genet''. 2015 May 28; '''16''': 55
A variant of PSMD6 is associated with the therapeutic efficacy of oral antidiabetic drugs in Chinese type 2 diabetes patients. Description: Chen, Miao, et al. A variant of PSMD6 is associated with the therapeutic efficacy of oral antidiabetic drugs in Chinese type 2 diabetes patients. ''Sci Rep''. 2015 May 29; '''5''': 10701
Genetic loci for serum magnesium among African-Americans and gene-environment interaction at MUC1 and TRPM6 in European-Americans: the Atherosclerosis Risk in Communities (ARIC) study. Description: Tin, Adrienne, et al. Genetic loci for serum magnesium among African-Americans and gene-environment interaction at MUC1 and TRPM6 in European-Americans: the Atherosclerosis Risk in Communities (ARIC) study. ''BMC Genet''. 2015 May 29; '''16''': 56
Adaptive divergence in the monkey flower Mimulus guttatus is maintained by a chromosomal inversion. Description: Twyford, Alex D, et al. Adaptive divergence in the monkey flower Mimulus guttatus is maintained by a chromosomal inversion. ''Evolution''. 2015 Jun; '''69''' (6):1476-1486
A genome-wide sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13. Description: Evans, P D, et al. A genome-wide sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13. ''Genes Brain Behav''. 2015 Jun; '''14''' (5):387-97
Common NOTCH3 Variants and Cerebral Small-Vessel Disease. Description: Rutten-Jacobs, Loes C A, et al. Common NOTCH3 Variants and Cerebral Small-Vessel Disease. ''Stroke''. 2015 Jun; '''46''' (6):1482-7
Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor. Description: Ayuso, Pedro, et al. Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor. ''Medicine (Baltimore)''. 2015 Jun; '''94''' (24):e968
Identification of new susceptibility loci for IgA nephropathy in Han Chinese. Description: Li, Ming, et al. Identification of new susceptibility loci for IgA nephropathy in Han Chinese. ''Nat Commun''. 2015 Jun 1; '''6''': 7270
Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease. Description: Wilbe, Maria, et al. Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease. ''PLoS Genet''. 2015 Jun; '''11''' (6):e1005248
Multiple Genes Related to Muscle Identified through a Joint Analysis of a Two-stage Genome-wide Association Study for Racing Performance of 1,156 Thoroughbreds. Description: Shin, Dong-Hyun, et al. Multiple Genes Related to Muscle Identified through a Joint Analysis of a Two-stage Genome-wide Association Study for Racing Performance of 1,156 Thoroughbreds. ''Asian-Australas J Anim Sci''. 2015 Jun; '''28''' (6):771-81
Reconstructing Past Admixture Processes from Local Genomic Ancestry Using Wavelet Transformation. Description: Sanderson, Jean, et al. Reconstructing Past Admixture Processes from Local Genomic Ancestry Using Wavelet Transformation. ''Genetics''. 2015 Jun; '''200''' (2):469-81
Single nucleotide polymorphisms in the FAM167A-BLK gene are associated with polymyositis/dermatomyositis in the Han Chinese population. Description: Chen, Si, et al. Single nucleotide polymorphisms in the FAM167A-BLK gene are associated with polymyositis/dermatomyositis in the Han Chinese population. ''Immunol Res''. 2015 Jun; '''62''' (2):153-62
Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone. Description: Vallet, Maheva, et al. Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone. ''Hum Mol Genet''. 2015 Jun 1; '''24''' (11):3286-95
Understanding the molecular mechanisms of human microtia via a pig model of HOXA1 syndrome. Description: Qiao, Ruimin, et al. Understanding the molecular mechanisms of human microtia via a pig model of HOXA1 syndrome. ''Dis Model Mech''. 2015 Jun; '''8''' (6):611-22
Interaction between common variants of FTO and MC4R is associated with risk of PCOS. Description: Yuan, Huiqin, et al. Interaction between common variants of FTO and MC4R is associated with risk of PCOS. ''Reprod Biol Endocrinol''. 2015 Jun 2; '''13''': 55
Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders. Description: Arloth, Janine, et al. Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders. ''Neuron''. 2015 Jun 3; '''86''' (5):1189-202
Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations. Description: Wei, Zejun, et al. Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations. ''Sci Rep''. 2015 Jun 3; '''5''': 10879
Identification of two novel mammographic density loci at 6Q25.1. Description: Brand, Judith S, et al. Identification of two novel mammographic density loci at 6Q25.1. ''Breast Cancer Res''. 2015 Jun 3; '''17''': 75
Recent genomic heritage in Scotland. Description: Amador, Carmen, et al. Recent genomic heritage in Scotland. ''BMC Genomics''. 2015 Jun 6; '''16''': 437
Do nuclear-encoded core subunits of mitochondrial complex I confer genetic susceptibility to schizophrenia in Han Chinese populations? Description: Li, Xiao, et al. Do nuclear-encoded core subunits of mitochondrial complex I confer genetic susceptibility to schizophrenia in Han Chinese populations? ''Sci Rep''. 2015 Jun 8; '''5''': 11076
In silico phenotyping via co-training for improved phenotype prediction from genotype. Description: Roqueiro, Damian, et al. In silico phenotyping via co-training for improved phenotype prediction from genotype. ''Bioinformatics''. 2015 Jun 15; '''31''' (12):i303-10
Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy. Description: Kouri, Naomi, et al. Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy. ''Nat Commun''. 2015 Jun 16; '''6''': 7247
Polymerase Theta is a key driver of genome evolution and of CRISPR/Cas9-mediated mutagenesis. Description: van Schendel, Robin, et al. Polymerase Theta is a key driver of genome evolution and of CRISPR/Cas9-mediated mutagenesis. ''Nat Commun''. 2015 Jun 16; '''6''': 7394
The glucagon-like peptide-1 receptor as a potential treatment target in alcohol use disorder: evidence from human genetic association studies and a mouse model of alcohol dependence. Description: Suchankova, P, et al. The glucagon-like peptide-1 receptor as a potential treatment target in alcohol use disorder: evidence from human genetic association studies and a mouse model of alcohol dependence. ''Transl Psychiatry''. 2015 Jun 16; '''5''': e583
Population structure and history of the Welsh sheep breeds determined by whole genome genotyping. Description: Beynon, Sarah E, et al. Population structure and history of the Welsh sheep breeds determined by whole genome genotyping. ''BMC Genet''. 2015 Jun 20; '''16''': 65
Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits. Description: Huang, Yu S, et al. Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits. ''BMC Biol''. 2015 Jun 20; '''13''': 41
Frequency of alcohol consumption in humans; the role of metabotropic glutamate receptors and downstream signaling pathways. Description: Meyers, J L, et al. Frequency of alcohol consumption in humans; the role of metabotropic glutamate receptors and downstream signaling pathways. ''Transl Psychiatry''. 2015 Jun 23; '''5''': e586
Genome-wide Association Study on Platinum-induced Hepatotoxicity in Non-Small Cell Lung Cancer Patients. Description: Cao, Songyu, et al. Genome-wide Association Study on Platinum-induced Hepatotoxicity in Non-Small Cell Lung Cancer Patients. ''Sci Rep''. 2015 Jun 23; '''5''': 11556
Study of genetic variability in Vitis vinifera L. germplasm by high-throughput Vitis18kSNP array: the case of Georgian genetic resources. Description: De Lorenzis, Gabriella, et al. Study of genetic variability in Vitis vinifera L. germplasm by high-throughput Vitis18kSNP array: the case of Georgian genetic resources. ''BMC Plant Biol''. 2015 Jun 23; '''15''': 154
A genome-wide association study identifies multiple loci for variation in human ear morphology. Description: Adhikari, Kaustubh, et al. A genome-wide association study identifies multiple loci for variation in human ear morphology. ''Nat Commun''. 2015 Jun 24; '''6''': 7500
Allelic variation at the rpv1 locus controls partial resistance to Plum pox virus infection in Arabidopsis thaliana. Description: Poque, S, et al. Allelic variation at the rpv1 locus controls partial resistance to Plum pox virus infection in Arabidopsis thaliana. ''BMC Plant Biol''. 2015 Jun 25; '''15''': 159
Demographic, psychosocial, and genetic risk associated with smokeless tobacco use among Mexican heritage youth. Description: Wilkinson, Anna V, et al. Demographic, psychosocial, and genetic risk associated with smokeless tobacco use among Mexican heritage youth. ''BMC Med Genet''. 2015 Jun 26; '''16''': 43
Single-copy gene based 50 K SNP chip for genetic studies and molecular breeding in rice. Description: Singh, Nisha, et al. Single-copy gene based 50 K SNP chip for genetic studies and molecular breeding in rice. ''Sci Rep''. 2015 Jun 26; '''5''': 11600
An analysis of the association between prostate cancer risk loci, PSA levels, disease aggressiveness and disease-specific mortality. Description: Sullivan, J, et al. An analysis of the association between prostate cancer risk loci, PSA levels, disease aggressiveness and disease-specific mortality. ''Br J Cancer''. 2015 Jun 30; '''113''' (1):166-72
Association between IL7R polymorphisms and severe liver disease in HIV/HCV coinfected patients: a cross-sectional study. Description: Guzman-Fulgencio, Maria, et al. Association between IL7R polymorphisms and severe liver disease in HIV/HCV coinfected patients: a cross-sectional study. ''J Transl Med''. 2015 Jun 30; '''13''': 206
A common variant near TGFBR3 is associated with primary open angle glaucoma. Description: Li, Zheng, et al. A common variant near TGFBR3 is associated with primary open angle glaucoma. ''Hum Mol Genet''. 2015 Jul 1; '''24''' (13):3880-92
A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment. Description: Nyegaard, Mette, et al. A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment. ''PLoS Genet''. 2015 Jul; '''11''' (7):e1005386
Association of polymorphisms in the beta-2 adrenergic receptor gene with fracture risk and bone mineral density. Description: Veldhuis-Vlug, A G, et al. Association of polymorphisms in the beta-2 adrenergic receptor gene with fracture risk and bone mineral density. ''Osteoporos Int''. 2015 Jul; '''26''' (7):2019-27
Association of serotonin transporter (SLC6A4) and receptor (5HTR1A, 5HTR2A) polymorphisms with response to treatment with escitalopram in patients with major depressive disorder: A preliminary study. Description: Basu, Aniruddha, et al. Association of serotonin transporter (SLC6A4) and receptor (5HTR1A, 5HTR2A) polymorphisms with response to treatment with escitalopram in patients with major depressive disorder: A preliminary study. ''Indian J Med Res''. 2015 Jul; '''142''' (1):40-5
Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network. Description: Hall, Molly A, et al. Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network. ''Genet Epidemiol''. 2015 Jul; '''39''' (5):376-84
CDH13 and HCRTR2 May Be Associated with Hypersomnia Symptom of Bipolar Depression: A Genome-Wide Functional Enrichment Pathway Analysis. Description: Cho, Chul-Hyun, et al. CDH13 and HCRTR2 May Be Associated with Hypersomnia Symptom of Bipolar Depression: A Genome-Wide Functional Enrichment Pathway Analysis. ''Psychiatry Investig''. 2015 Jul; '''12''' (3):402-7
Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood. Description: Hatzimanolis, Alex, et al. Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood. ''Am J Med Genet B Neuropsychiatr Genet''. 2015 Jul; '''168B''' (5):392-401
Familiality and SNP heritability of age at onset and episodicity in major depressive disorder. Description: Ferentinos, P, et al. Familiality and SNP heritability of age at onset and episodicity in major depressive disorder. ''Psychol Med''. 2015 Jul; '''45''' (10):2215-25
Glutamate Networks Implicate Cognitive Impairments in Schizophrenia: Genome-Wide Association Studies of 52 Cognitive Phenotypes. Description: Ohi, Kazutaka, et al. Glutamate Networks Implicate Cognitive Impairments in Schizophrenia: Genome-Wide Association Studies of 52 Cognitive Phenotypes. ''Schizophr Bull''. 2015 Jul; '''41''' (4):909-18
Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation. Description: Murgiano, Leonardo, et al. Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation. ''PLoS Genet''. 2015 Jul; '''11''' (7):e1005427
Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levels. Description: Kavanagh, David, et al. Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levels. ''Hum Mol Genet''. 2015 Jul 1; '''24''' (13):3861-70
TOX and CDKN2A/B Gene Polymorphisms Are Associated with Type 2 Diabetes in Han Chinese. Description: Wei, Fengjiang, et al. TOX and CDKN2A/B Gene Polymorphisms Are Associated with Type 2 Diabetes in Han Chinese. ''Sci Rep''. 2015 Jul 3; '''5''': 11900
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study. Description: Chen, Pei-Lung, et al. Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study. ''Nat Commun''. 2015 Jul 7; '''6''': 7633
Response and inbreeding from a genomic selection experiment in layer chickens. Description: Wolc, Anna, et al. Response and inbreeding from a genomic selection experiment in layer chickens. ''Genet Sel Evol''. 2015 Jul 7; '''47''': 59
Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse. Description: Perrocheau, Maelle, et al. Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse. ''J Cardiovasc Dev Dis''. 2015 Jul 10; '''2''' (3):176-189
Iron and hepcidin as risk factors in atherosclerosis: what do the genes say? Description: Galesloot, Tessel E, et al. Iron and hepcidin as risk factors in atherosclerosis: what do the genes say? ''BMC Genet''. 2015 Jul 11; '''16''': 79
Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample. Description: Lin, Bochao Danae, et al. Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample. ''Genes (Basel)''. 2015 Jul 13; '''6''' (3):559-76
Susceptible gene of stasis-stagnation constitution from genome-wide association study related to cardiovascular disturbance and possible regulated traditional Chinese medicine. Description: Huang, Kuo-Chin, et al. Susceptible gene of stasis-stagnation constitution from genome-wide association study related to cardiovascular disturbance and possible regulated traditional Chinese medicine. ''BMC Complement Altern Med''. 2015 Jul 14; '''15''': 229
Three missense variants of metabolic syndrome-related genes are associated with alpha-1 antitrypsin levels. Description: Setoh, Kazuya, et al. Three missense variants of metabolic syndrome-related genes are associated with alpha-1 antitrypsin levels. ''Nat Commun''. 2015 Jul 15; '''6''': 7754
Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome. Description: Kelmemi, W, et al. Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome. ''BMC Med Genet''. 2015 Jul 20; '''16''': 50
Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. Description: Ramachandran, Dhanya, et al. Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. ''G3 (Bethesda)''. 2015 Jul 20; '''5''' (10):1961-71
Large-scale genomics unveil polygenic architecture of human cortical surface area. Description: Chen, Chi-Hua, et al. Large-scale genomics unveil polygenic architecture of human cortical surface area. ''Nat Commun''. 2015 Jul 20; '''6''': 7549
Performance of genetic risk factors in prediction of trichloroethylene induced hypersensitivity syndrome. Description: Dai, Yufei, et al. Performance of genetic risk factors in prediction of trichloroethylene induced hypersensitivity syndrome. ''Sci Rep''. 2015 Jul 20; '''5''': 12169
Ancestry, admixture and fitness in Colombian genomes. Description: Rishishwar, Lavanya, et al. Ancestry, admixture and fitness in Colombian genomes. ''Sci Rep''. 2015 Jul 21; '''5''': 12376
Estimation of inbreeding using pedigree, 50k SNP chip genotypes and full sequence data in three cattle breeds. Description: Zhang, Qianqian, et al. Estimation of inbreeding using pedigree, 50k SNP chip genotypes and full sequence data in three cattle breeds. ''BMC Genet''. 2015 Jul 22; '''16''': 88
Fine-scale population structure of Malays in Peninsular Malaysia and Singapore and implications for association studies. Description: Hoh, Boon-Peng, et al. Fine-scale population structure of Malays in Peninsular Malaysia and Singapore and implications for association studies. ''Hum Genomics''. 2015 Jul 22; '''9''': 16
Genetic variation in insulin-induced kinase signaling. Description: Wang, Isabel Xiaorong, et al. Genetic variation in insulin-induced kinase signaling. ''Mol Syst Biol''. 2015 Jul 22; '''11''' (7):820
Impact of genetic similarity on imputation accuracy. Description: Roshyara, Nab Raj, et al. Impact of genetic similarity on imputation accuracy. ''BMC Genet''. 2015 Jul 22; '''16''': 90
Genome-wide high-throughput SNP discovery and genotyping for understanding natural (functional) allelic diversity and domestication patterns in wild chickpea. Description: Bajaj, Deepak, et al. Genome-wide high-throughput SNP discovery and genotyping for understanding natural (functional) allelic diversity and domestication patterns in wild chickpea. ''Sci Rep''. 2015 Jul 24; '''5''': 12468
Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy. Description: Ruggieri, Alessandra, et al. Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy. ''Acta Neuropathol Commun''. 2015 Jul 25; '''3''': 44
Genetic, molecular and physiological basis of variation in Drosophila gut immunocompetence. Description: Bou Sleiman, Maroun S, et al. Genetic, molecular and physiological basis of variation in Drosophila gut immunocompetence. ''Nat Commun''. 2015 Jul 27; '''6''': 7829
A double amino-acid change in the HLA-A peptide-binding groove is associated with response to psychotropic treatment in patients with schizophrenia. Description: Le Clerc, S, et al. A double amino-acid change in the HLA-A peptide-binding groove is associated with response to psychotropic treatment in patients with schizophrenia. ''Transl Psychiatry''. 2015 Jul 28; '''5''': e608
Fingerprinting Soybean Germplasm and Its Utility in Genomic Research. Description: Song, Qijian, et al. Fingerprinting Soybean Germplasm and Its Utility in Genomic Research. ''G3 (Bethesda)''. 2015 Jul 28; '''5''' (10):1999-2006
Genetic contribution to multiple sclerosis risk among Ashkenazi Jews. Description: Khankhanian, Pouya, et al. Genetic contribution to multiple sclerosis risk among Ashkenazi Jews. ''BMC Med Genet''. 2015 Jul 28; '''16''': 55
Genome-wide association study revealed a promising region and candidate genes for eggshell quality in an F2 resource population. Description: Sun, Congjiao, et al. Genome-wide association study revealed a promising region and candidate genes for eggshell quality in an F2 resource population. ''BMC Genomics''. 2015 Jul 31; '''16''': 565
Genetic risk factors affecting mitochondrial function are associated with kidney disease in people with Type 1 diabetes. Description: Swan, E J, et al. Genetic risk factors affecting mitochondrial function are associated with kidney disease in people with Type 1 diabetes. ''Diabet Med''. 2015 Aug; '''32''' (8):1104-9
Across language families: Genome diversity mirrors linguistic variation within Europe. Description: Longobardi, Giuseppe, et al. Across language families: Genome diversity mirrors linguistic variation within Europe. ''Am J Phys Anthropol''. 2015 Aug; '''157''' (4):630-40
Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer. Description: Childs, Erica J, et al. Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer. ''Nat Genet''. 2015 Aug; '''47''' (8):911-6
CREB-BDNF pathway influences alcohol cue-elicited activation in drinkers. Description: Chen, Jiayu, et al. CREB-BDNF pathway influences alcohol cue-elicited activation in drinkers. ''Hum Brain Mapp''. 2015 Aug; '''36''' (8):3007-19
Dimethylglycine Deficiency and the Development of Diabetes. Description: Magnusson, Martin, et al. Dimethylglycine Deficiency and the Development of Diabetes. ''Diabetes''. 2015 Aug; '''64''' (8):3010-6
Evidence for a Common Origin of Blacksmiths and Cultivators in the Ethiopian Ari within the Last 4500 Years: Lessons for Clustering-Based Inference. Description: van Dorp, Lucy, et al. Evidence for a Common Origin of Blacksmiths and Cultivators in the Ethiopian Ari within the Last 4500 Years: Lessons for Clustering-Based Inference. ''PLoS Genet''. 2015 Aug; '''11''' (8):e1005397
F-box/LRR-repeat protein 7 is genetically associated with Alzheimer's disease. Description: Tosto, Giuseppe, et al. F-box/LRR-repeat protein 7 is genetically associated with Alzheimer's disease. ''Ann Clin Transl Neurol''. 2015 Aug; '''2''' (8):810-20
Genome-Wide Association Study of HIV-Related Lipoatrophy in Thai Patients: Association of a DLGAP1 Polymorphism with Fat Loss. Description: Uttayamakul, Sumonmal, et al. Genome-Wide Association Study of HIV-Related Lipoatrophy in Thai Patients: Association of a DLGAP1 Polymorphism with Fat Loss. ''AIDS Res Hum Retroviruses''. 2015 Aug; '''31''' (8):792-6
Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome. Description: Garcia-Martin, Elena, et al. Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome. ''Medicine (Baltimore)''. 2015 Aug; '''94''' (34):e1448
Making a chocolate chip: development and evaluation of a 6K SNP array for Theobroma cacao. Description: Livingstone, Donald, et al. Making a chocolate chip: development and evaluation of a 6K SNP array for Theobroma cacao. ''DNA Res''. 2015 Aug; '''22''' (4):279-91
Novel Association Between Immune-Mediated Susceptibility Loci and Persistent Autoantibody Positivity in Type 1 Diabetes. Description: Brorsson, Caroline A, et al. Novel Association Between Immune-Mediated Susceptibility Loci and Persistent Autoantibody Positivity in Type 1 Diabetes. ''Diabetes''. 2015 Aug; '''64''' (8):3017-27
Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity. Description: Usher, Christina L, et al. Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity. ''Nat Genet''. 2015 Aug; '''47''' (8):921-5
Clinically relevant copy number variations detected in cerebral palsy. Description: Oskoui, Maryam, et al. Clinically relevant copy number variations detected in cerebral palsy. ''Nat Commun''. 2015 Aug 3; '''6''': 7949
Genetic diversity of Italian goat breeds assessed with a medium-density SNP chip. Description: Nicoloso, Letizia, et al. Genetic diversity of Italian goat breeds assessed with a medium-density SNP chip. ''Genet Sel Evol''. 2015 Aug 4; '''47''': 62
Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia. Description: Ma, Yuanlin, et al. Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia. ''Sci Rep''. 2015 Aug 5; '''5''': 10299
A Validated Phenotyping Algorithm for Genetic Association Studies in Age-related Macular Degeneration. Description: Simonett, Joseph M, et al. A Validated Phenotyping Algorithm for Genetic Association Studies in Age-related Macular Degeneration. ''Sci Rep''. 2015 Aug 10; '''5''': 12875
Two novel genetic variants in the mineralocorticoid receptor gene associated with spontaneous preterm birth. Description: Christiaens, Inge, et al. Two novel genetic variants in the mineralocorticoid receptor gene associated with spontaneous preterm birth. ''BMC Med Genet''. 2015 Aug 11; '''16''': 59
Pathway analysis of body mass index genome-wide association study highlights risk pathways in cardiovascular disease. Description: Zhao, Xin, et al. Pathway analysis of body mass index genome-wide association study highlights risk pathways in cardiovascular disease. ''Sci Rep''. 2015 Aug 12; '''5''': 13025
Merino and Merino-derived sheep breeds: a genome-wide intercontinental study. Description: Ciani, Elena, et al. Merino and Merino-derived sheep breeds: a genome-wide intercontinental study. ''Genet Sel Evol''. 2015 Aug 14; '''47''': 64
Sex-Specific Effects of Adiponectin on Carotid Intima-Media Thickness and Incident Cardiovascular Disease. Description: Persson, Jonas, et al. Sex-Specific Effects of Adiponectin on Carotid Intima-Media Thickness and Incident Cardiovascular Disease. ''J Am Heart Assoc''. 2015 Aug 14; '''4''' (8):e001853
Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding locidagger. Description: Kirsten, Holger, et al. Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding locidagger. ''Hum Mol Genet''. 2015 Aug 15; '''24''' (16):4746-63
Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations. Description: Hayes, M Geoffrey, et al. Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations. ''Nat Commun''. 2015 Aug 18; '''6''': 7502
Associations between the orexin (hypocretin) receptor 2 gene polymorphism Val308Ile and nicotine dependence in genome-wide and subsequent association studies. Description: Nishizawa, Daisuke, et al. Associations between the orexin (hypocretin) receptor 2 gene polymorphism Val308Ile and nicotine dependence in genome-wide and subsequent association studies. ''Mol Brain''. 2015 Aug 20; '''8''': 50
Exploring evidence of positive selection reveals genetic basis of meat quality traits in Berkshire pigs through whole genome sequencing. Description: Jeong, Hyeonsoo, et al. Exploring evidence of positive selection reveals genetic basis of meat quality traits in Berkshire pigs through whole genome sequencing. ''BMC Genet''. 2015 Aug 20; '''16''': 104
Gender-specific associations between ADIPOQ gene polymorphisms and adiponectin levels and obesity in the Jackson Heart Study cohort. Description: Riestra, Pia, et al. Gender-specific associations between ADIPOQ gene polymorphisms and adiponectin levels and obesity in the Jackson Heart Study cohort. ''BMC Med Genet''. 2015 Aug 20; '''16''': 65
Barley landraces are characterized by geographically heterogeneous genomic origins. Description: Poets, Ana M, et al. Barley landraces are characterized by geographically heterogeneous genomic origins. ''Genome Biol''. 2015 Aug 21; '''16''': 173
CNV Analysis Associates AKNAD1 with Type-2 Diabetes in Jordan Subpopulations. Description: Dajani, Rana, et al. CNV Analysis Associates AKNAD1 with Type-2 Diabetes in Jordan Subpopulations. ''Sci Rep''. 2015 Aug 21; '''5''': 13391
Pathway-Based Genome-wide Association Studies Reveal That the Rac1 Pathway Is Associated with Plasma Adiponectin Levels. Description: Li, Wei-Dong, et al. Pathway-Based Genome-wide Association Studies Reveal That the Rac1 Pathway Is Associated with Plasma Adiponectin Levels. ''Sci Rep''. 2015 Aug 24; '''5''': 13422
Polymorphisms of PRLHR and HSPA12A and risk of gastric and colorectal cancer in the Chinese Han population. Description: Su, Qinghua, et al. Polymorphisms of PRLHR and HSPA12A and risk of gastric and colorectal cancer in the Chinese Han population. ''BMC Gastroenterol''. 2015 Aug 25; '''15''': 107
Detection of Selection Signatures on the X Chromosome in Three Sheep Breeds. Description: Zhu, Caiye, et al. Detection of Selection Signatures on the X Chromosome in Three Sheep Breeds. ''Int J Mol Sci''. 2015 Aug 28; '''16''' (9):20360-74
LOXL1 gene variants and their association with pseudoexfoliation glaucoma (XFG) in Spanish patients. Description: Alvarez, Lydia, et al. LOXL1 gene variants and their association with pseudoexfoliation glaucoma (XFG) in Spanish patients. ''BMC Med Genet''. 2015 Aug 31; '''16''': 72
A common oxytocin receptor gene (OXTR) polymorphism modulates intranasal oxytocin effects on the neural response to social cooperation in humans. Description: Feng, C, et al. A common oxytocin receptor gene (OXTR) polymorphism modulates intranasal oxytocin effects on the neural response to social cooperation in humans. ''Genes Brain Behav''. 2015 Sep; '''14''' (7):516-25
Association of rare variation in the glutamate receptor gene SLC1A2 with susceptibility to bipolar disorder and schizophrenia. Description: Fiorentino, Alessia, et al. Association of rare variation in the glutamate receptor gene SLC1A2 with susceptibility to bipolar disorder and schizophrenia. ''Eur J Hum Genet''. 2015 Sep; '''23''' (9):1200-6
Data in support of association study of the brain-derived neurotrophic factor gene SNPs and completed suicide in the Slovenian sample. Description: Ropret, Sandra, et al. Data in support of association study of the brain-derived neurotrophic factor gene SNPs and completed suicide in the Slovenian sample. ''Data Brief''. 2015 Sep; '''4''': 529-33
Epistatic and gene wide effects in YWHA and aromatic amino hydroxylase genes across ADHD and other common neuropsychiatric disorders: Association with YWHAE. Description: Jacobsen, Kaya K, et al. Epistatic and gene wide effects in YWHA and aromatic amino hydroxylase genes across ADHD and other common neuropsychiatric disorders: Association with YWHAE. ''Am J Med Genet B Neuropsychiatr Genet''. 2015 Sep; '''168''' (6):423-432
Estimation of Genetic Relationships Between Individuals Across Cohorts and Platforms: Application to Childhood Height. Description: Fedko, Iryna O, et al. Estimation of Genetic Relationships Between Individuals Across Cohorts and Platforms: Application to Childhood Height. ''Behav Genet''. 2015 Sep; '''45''' (5):514-28
Exome sequencing followed by genotyping suggests SYPL2 as a susceptibility gene for morbid obesity. Description: Jiao, Hong, et al. Exome sequencing followed by genotyping suggests SYPL2 as a susceptibility gene for morbid obesity. ''Eur J Hum Genet''. 2015 Sep; '''23''' (9):1216-22
Gene-gene and gene-environment interactions in the etiology of type 2 diabetes mellitus in the population of Hyderabad, India. Description: Uma Jyothi, Kommoju, et al. Gene-gene and gene-environment interactions in the etiology of type 2 diabetes mellitus in the population of Hyderabad, India. ''Meta Gene''. 2015 Sep; '''5''': 9-20
Genome-wide association study of neocortical Lewy-related pathology. Description: Peuralinna, Terhi, et al. Genome-wide association study of neocortical Lewy-related pathology. ''Ann Clin Transl Neurol''. 2015 Sep; '''2''' (9):920-31
Genome-wide association study of rice (Oryza sativa L.) leaf traits with a high-throughput leaf scorer. Description: Yang, Wanneng, et al. Genome-wide association study of rice (Oryza sativa L.) leaf traits with a high-throughput leaf scorer. ''J Exp Bot''. 2015 Sep; '''66''' (18):5605-15
Genome-Wide Association Study with Targeted and Non-targeted NMR Metabolomics Identifies 15 Novel Loci of Urinary Human Metabolic Individuality. Description: Raffler, Johannes, et al. Genome-Wide Association Study with Targeted and Non-targeted NMR Metabolomics Identifies 15 Novel Loci of Urinary Human Metabolic Individuality. ''PLoS Genet''. 2015 Sep; '''11''' (9):e1005487
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Description: Law, Matthew H, et al. Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. ''Nat Genet''. 2015 Sep; '''47''' (9):987-995
Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy. Description: Leu, Costin, et al. Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy. ''EBioMedicine''. 2015 Sep; '''2''' (9):1063-70
Heritability of Individual Psychotic Experiences Captured by