Ratings
0
Nobody has rated this yet. Be the first!
Works
11
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
Type 2 diabetes TCF7L2 risk genotypes alter birth weight: a study of 24,053 individuals
Association Analysis of 6,736 U.K. Subjects Provides Replication and ConfirmsTCF7L2as a Type 2 Diabetes Susceptibility Gene With a Substantial Effect on Individual Risk
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes
The fat mass- and obesity-associated locus and dietary intake in children
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
Phosphodiesterase 8B Gene Polymorphism Is Associated with Subclinical Hypothyroidism in Pregnancy
Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes
