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Dissection of the genetics of Parkinson’s disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21
A comprehensive study of the association between EGFR and ERBB2 genes and glioma risk
Dysbindin gene (DTNBP1) in major depressive disorder (MDD) patients: Lack of association with clinical phenotypes
Obesity susceptibility genetic variants identified from recent genome-wide association studies: Implications in a Chinese population
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
A candidate gene study of folate-associated one carbon metabolism genes and colorectal cancer risk
Polymorphisms at the microseminoprotein-? locus associated with physiologic variation in ?-microseminoprotein and prostate-specific antigen levels