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Now showing items 1-7 of 7
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.
E-cadherin breast tumor expression, risk factors and survival: Pooled analysis of 5,933 cases from 12 studies in the Breast Cancer Association Consortium
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
Shared heritability and functional enrichment across six solid cancers
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer