| research consortium | Q20747412 |
| Q35630171 | A robust clustering algorithm for identifying problematic samples in genome-wide association studies |
| Q41731666 | Analysis with the exome array identifies multiple new independent variants in lipid loci |
| Q37394589 | Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts |
| Q42131712 | Bayesian hierarchical mixture modeling to assign copy number from a targeted CNV array |
| Q37217525 | Bayesian refinement of association signals for 14 loci in 3 common diseases |
| Q37239881 | Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23. |
| Q34355379 | Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways |
| Q42043764 | Common variants near TERC are associated with mean telomere length |
| Q36375800 | Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis |
| Q34199600 | Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease |
| Q30426720 | Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease |
| Q48504012 | Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls |
| Q37414526 | Evidence that duplications of 22q11.2 protect against schizophrenia |
| Q47137829 | Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease |
| Q37284963 | Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease |
| Q33575138 | Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept |
| Q36866321 | Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis |
| Q37477713 | Genetic variants influencing circulating lipid levels and risk of coronary artery disease |
| Q108120838 | Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. |
| Q34130337 | Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. |
| Q24645076 | Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants |
| Q24628710 | Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls |
| Q34886162 | Genome-wide association study of genetic predictors of anti-tumor necrosis factor treatment efficacy in rheumatoid arthritis identifies associations with polymorphisms at seven loci |
| Q37681915 | Genome-wide association study of receptive language ability of 12-year-olds |
| Q43617306 | Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease |
| Q36317729 | Genome-wide meta-analysis of common variant differences between men and women |
| Q30419111 | High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis |
| Q34372500 | Hypothesis-based analysis of gene-gene interactions and risk of myocardial infarction |
| Q29417010 | Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies |
| Q35861470 | Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia |
| Q33413624 | Interrogating type 2 diabetes genome-wide association data using a biological pathway-based approach |
| Q34899429 | Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship |
| Q34748177 | LDL-cholesterol concentrations: a genome-wide association study |
| Q30499949 | Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies |
| Q36921066 | Large-scale association analysis identifies new risk loci for coronary artery disease |
| Q37245361 | Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A |
| Q29417138 | Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes |
| Q39002120 | MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls |
| Q28388006 | Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer |
| Q37225243 | New susceptibility locus for coronary artery disease on chromosome 3q22.3. |
| Q29417110 | Novel rheumatoid arthritis susceptibility locus at 22q12 identified in an extended UK genome-wide association study |
| Q30426245 | Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry |
| Q35764622 | Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia |
| Q36769297 | Re-evaluation of putative rheumatoid arthritis susceptibility genes in the post-genome wide association study era and hypothesis of a key pathway underlying susceptibility |
| Q37676896 | Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample |
| Q37172071 | Rheumatoid arthritis association at 6q23. |
| Q43154311 | Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13. |
| Q29614872 | Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility |
| Q30424090 | Seven newly identified loci for autoimmune thyroid disease |
| Q34902898 | Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype |
| Q37147142 | Support for the involvement of large copy number variants in the pathogenesis of schizophrenia |
| Q37648324 | Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease |
| Q24619976 | The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia |
| Q52145849 | The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis. |
| Q37297746 | The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals |
| Q37324554 | Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension |
| Q33820794 | Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight |
Search more.