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Investigation of the association of BMP gene variants with nephropathy in Type 1 diabetes mellitus
No evidence for a role of the catechol-O-methyltransferase pain sensitivity haplotypes in chronic widespread pain
Genetic variation in RNASEL associated with prostate cancer risk and prognosis
Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia breast cancer consortium
Insufficient evidence for association of NOD2/CARD15 or other inflammatory bowel disease-associated markers in GVHD incidence or other adverse outcomes in T-replete, unrelated donor transplantation
Genome-wide association study of alcohol dependence implicates a region on chromosome 11
Interaction between early maternal smoking and variants in TNF and GSTP1 in childhood wheezing
New genetic associations detected in a host response study to hepatitis B vaccine
Association analysis of 3p21 with Crohns disease in a New Zealand population
Multiple Sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients