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Fine scale mapping of the 6p25.3 chronic lymphocytic leukaemia susceptibility locus
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
Association of the SLC22A1, SLC22A2, and SLC22A3 genes encoding organic cation transporters with diabetic nephtopathy and hypertension
Dysbindin gene (DTNBP1) in major depressive disorder (MDD) patients: Lack of association with clinical phenotypes
Detailed investigation of the role of common and low frequency WFS1 variants in type 2 diabetes risk
Fine-mapping quantitative trait loci for twinning rate on BTA14 in North American Holsteins
Re-sequencing and analysis of variation in the TCF7L2 gene in African Americans suggests the SNP rs7903146 is the causal diabetes susceptibility variant
Obesity susceptibility genetic variants identified from recent genome-wide association studies: Implications in a Chinese population
Association of genetic variants in the adiponectin gene with adiponectin level and hypertension in Hong Kong Chinese