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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
Genomic inflation factors under polygenic inheritance
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes
HUMAN LONGEVITY IS INFLUENCED BY MANY GENETIC VARIANTS: EVIDENCE FROM 75,000 UK BIOBANK PARTICIPANTS
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
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
Mosaic Turner syndrome shows reduced phenotypic penetrance in an adult population study compared to clinically ascertained cases
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
