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Now showing items 1-11 of 11
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.
Combined associations of a polygenic risk score and classical risk factors with breast cancer risk
Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome
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
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic 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
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21.