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A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study
Shared heritability and functional enrichment across six solid cancers