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Shared heritability and functional enrichment across six solid cancers
Shared heritability and functional enrichment across six solid cancers
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers
Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%
Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mapping