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Works
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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
Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers
Protein-altering germline mutations implicate novel genes related to lung cancer development
Risk of Endometrial Carcinoma Associated with BRCA Mutation
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%
BRCA1 and BRCA2 Pathogenic Sequence Variants in Women of African Origin or Ancestry
Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mapping
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