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Now showing items 1-13 of 13
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.
Combined associations of a polygenic risk score and classical risk factors with breast cancer risk
Crowdsourcing the General Public for Large Scale Molecular Pathology Studies in Cancer.
E-cadherin breast tumor expression, risk factors and survival: Pooled analysis of 5,933 cases from 12 studies in the Breast Cancer Association Consortium
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
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
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer