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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.
Combined associations of a polygenic risk score and classical risk factors with breast cancer risk
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer
Polymorphisms within the TNFSF4 and MAPKAPK2 Loci Influence the Risk of Developing Invasive Aspergillosis: A Two-Stage Case Control Study in the Context of the aspBIOmics Consortium.
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.