To further understanding of the genetic basis of type 2 diabetes (T2D) susceptibility, we aggregated published meta-analyses of genome-wide association studies (GWAS), including 26,488 cases and 83,964 controls of European, east Asian, south Asian and Mexican and Mexican American ancestry. We observed a significant excess in the directional consistency of T2D risk alleles across ancestry groups, even at SNPs demonstrating only weak evidence of association. By following up the strongest signals of association from the trans-ethnic meta-analysis in an additional 21,491 cases and 55,647 controls of European ancestry, we identified seven new T2D susceptibility loci. Furthermore, we observed considerable improvements in the fine-mapping resoluti...
Elevated blood pressure is a common, heritable cause of cardiovascular disease worldwide. To date, i...
Increased blood lipid levels are heritable risk factors of cardiovascular disease with varied preval...
Christopher Newton-Cheh and colleagues report a genome-wide association study for blood pressure tra...
To further understanding of the genetic basis of type 2 diabetes (T2D) susceptibility, we aggregated...
To identify common alleles associated with different histotypes of epithelial ovarian cancer (EOC), ...
Most common breast cancer susceptibility variants have been identified through genome-wide associati...
Bipolar disorder is a highly heritable psychiatric disorder. We performed a genome-wide association ...
Bone mineral density (BMD) is the most important predictor of fracture risk. We performed the larges...
Risk for late-onset Alzheimer's disease (LOAD), the most prevalent dementia, is partially driven by ...
Genome-wide association studies (GWAS) of psychiatric disorders have identified multiple genetic ass...
Genome-wide association studies (GWAS) of psychiatric disorders have identified multiple genetic ass...
Using the ImmunoChip custom genotyping array, we analysed 14,498 multiple sclerosis subjects and 24,...
To evaluate the shared genetic etiology of type 2 diabetes (T2D) and coronary heart disease (CHD), w...
The cerebral cortex underlies our complex cognitive capabilities, yet little is known about the spec...
Glucose levels 2 h after an oral glucose challenge are a clinical measure of glucose tolerance used ...
Elevated blood pressure is a common, heritable cause of cardiovascular disease worldwide. To date, i...
Increased blood lipid levels are heritable risk factors of cardiovascular disease with varied preval...
Christopher Newton-Cheh and colleagues report a genome-wide association study for blood pressure tra...
To further understanding of the genetic basis of type 2 diabetes (T2D) susceptibility, we aggregated...
To identify common alleles associated with different histotypes of epithelial ovarian cancer (EOC), ...
Most common breast cancer susceptibility variants have been identified through genome-wide associati...
Bipolar disorder is a highly heritable psychiatric disorder. We performed a genome-wide association ...
Bone mineral density (BMD) is the most important predictor of fracture risk. We performed the larges...
Risk for late-onset Alzheimer's disease (LOAD), the most prevalent dementia, is partially driven by ...
Genome-wide association studies (GWAS) of psychiatric disorders have identified multiple genetic ass...
Genome-wide association studies (GWAS) of psychiatric disorders have identified multiple genetic ass...
Using the ImmunoChip custom genotyping array, we analysed 14,498 multiple sclerosis subjects and 24,...
To evaluate the shared genetic etiology of type 2 diabetes (T2D) and coronary heart disease (CHD), w...
The cerebral cortex underlies our complex cognitive capabilities, yet little is known about the spec...
Glucose levels 2 h after an oral glucose challenge are a clinical measure of glucose tolerance used ...
Elevated blood pressure is a common, heritable cause of cardiovascular disease worldwide. To date, i...
Increased blood lipid levels are heritable risk factors of cardiovascular disease with varied preval...
Christopher Newton-Cheh and colleagues report a genome-wide association study for blood pressure tra...