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Detailed investigation of the role of common and low frequency WFS1 variants in type 2 diabetes risk
Re-sequencing and analysis of variation in the TCF7L2 gene in African Americans suggests the SNP rs7903146 is the causal diabetes susceptibility variant
Association of genetic variants in the adiponectin gene with adiponectin level and hypertension in Hong Kong Chinese
WNT receptors, bone mass and fractures: gene-wide association analysis of LRP5 and LRP6 polymorphisms with replication
Association of a melatonin receptor 1B (MTNR1B) gene variant with fasting glucose and HOMA-B in children and adolescents of high BMI-SDS groups
Association of variants in the glucose dependent insulinotropic peptide receptor gene (GIPR) with impaired glucose homeostasis in obese children and adolescents from Berlin
The role of ghrelin and ghrelin-receptor gene variants and promoter activity in type 2 diabetes
Family-based association analysis of 42 hereditary prostate cancer families identifies the Apolipoprotein L3 region on chromosome 22q12 as a risk locus
Validation of Genome-Wide Prostate Cancer Associations in Men of African Descent
Fine mapping of the insulin-induced gene 2 identifies a variant associated with LDL cholesterol and total apolipoprotein B levels