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Now showing items 1-16 of 16
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.
Analyses of germline variants associated with ovarian cancer survival identify functional candidates at the 1q22 and 19p12 outcome loci
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
Association of p16 expression with prognosis varies across ovarian carcinoma histotypes: an Ovarian Tumor Tissue Analysis consortium study
Combined associations of a polygenic risk score and classical risk factors with breast cancer risk
Common breast cancer susceptibility variants in LSP1 and RAD51L1 are associated with mammographic density measures that predict breast cancer risk
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
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk
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
rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk
Shared heritability and functional enrichment across six solid cancers
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer