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Now showing items 1-8 of 8
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers.
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
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
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 Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases.