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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
Mammographic density and ageing: A collaborative pooled analysis of cross-sectional data from 22 countries worldwide
rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer