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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Haploinsufficiency for BRCA1 leads to cell-type-specific genomic instability and premature senescence
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