A common variant on chromosome 9p21 affects the risk of myocardial infarction. |
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. |
Chromosome 7p11.2 (EGFR) variation influences glioma risk. |
Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. |
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. |
Genome-wide association meta-analysis identifies new endometriosis risk loci. |
Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians. |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. |
Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21. |
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm. |
Genome-wide association study identifies five new breast cancer susceptibility loci. |
Genome-wide association study identifies five susceptibility loci for glioma. |
Genome-wide association study identifies three loci associated with melanoma risk. |
Genome-wide association study identifies three new melanoma susceptibility loci. |
Genome-wide association study identifies three novel loci for type 2 diabetes. |
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. |
Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction. |
Genome-wide association study of coronary artery disease in the Japanese. |
Genome-wide association study of intracranial aneurysm identifies three new risk loci. |
Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas. |
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. |
Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma. |
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. |
Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations. |
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. |
Large-scale genotyping identifies 41 new loci associated with breast cancer risk. |
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. |
New gene functions in megakaryopoiesis and platelet formation. |
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. |
Susceptibility loci for intracranial aneurysm in European and Japanese populations. |
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. |
Two-marker association tests yield new disease associations for coronary artery disease and hypertension. |
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype. |