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UnknownTargeted Sequencing of the Mitochondrial Genome of Women at High Risk of Breast Cancer without Detectable Mutations in BRCA1/2.
Not available
S-EPMC4583250 | biostudies-literature
UnknownMutation screening of MIR146A/B and BRCA1/2 3'-UTRs in the GENESIS study.
Not available
S-EPMC4989198 | biostudies-literature
UnknownGermline BAP1 mutations predispose to renal cell carcinomas.
Not available
S-EPMC3675229 | biostudies-literature
UnknownCommon genetic variants and modification of penetrance of BRCA2-associated breast cancer.
Not available
S-EPMC2965747 | 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
UnknownNo association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort study.
Not available
S-EPMC2700286 | biostudies-literature
UnknownRAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies.
Not available
S-EPMC2276351 | 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
UnknownCommon breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.
Not available
S-EPMC2427217 | biostudies-literature
UnknownEffects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers.
Not available
S-EPMC3446398 | biostudies-literature
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