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UnknownMotivators of Inappropriate Ovarian Cancer Screening: A Survey of Women and Their Clinicians.
Not available
S-EPMC7853181 | biostudies-literature
UnknownGerm-line variation at a functional p53 binding site increases susceptibility to breast cancer development.
Not available
S-EPMC2882646 | biostudies-literature
UnknownWhole-genome sequencing reveals clinically relevant insights into the aetiology of familial breast cancers.
Not available
S-EPMC6637375 | biostudies-literature
UnknownNo evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.
Not available
S-EPMC4938802 | biostudies-literature
UnknownHeterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics.
Not available
S-EPMC2291027 | biostudies-literature
UnknownCommon variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.
Not available
S-EPMC2893806 | biostudies-literature
UnknownGenome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk.
Not available
S-EPMC3722904 | biostudies-literature
UnknownAssessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study.
Not available
S-EPMC3046455 | biostudies-literature
UnknownEvidence of gene-environment interactions between common breast cancer susceptibility loci and established environmental risk factors.
Not available
S-EPMC3609648 | biostudies-literature
UnknownFANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.
Not available
S-EPMC4550823 | biostudies-literature
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