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Germ-line variation at a functional p53 binding site increases susceptibility to breast cancer development
IRF4 variants have age-specific effects on nevus count and predispose to melanoma
Polymorphisms in the selenoprotein S and 15-kDa selenoprotein genes are associated with altered susceptibility to colorectal cancer
Missense variants in ATM in 26,101 breast cancer cases and 29,842 controls
Common variants at 19p13 are associated with susceptibility to ovarian cancer
A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk
Germline mutations in breast and ovarian cancer pedigrees established RAD51C as a human cancer susceptibility gene