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(1 - 9 of 9)
Association of genomic domains in BRCA1 and BRCA2 with prostate cancer risk and aggressiveness
Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3
Candidate Genetic Modifiers for Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers
Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers
Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation Carriers