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UnknownAssociation between a germline OCA2 polymorphism at chromosome 15q13.1 and estrogen receptor-negative breast cancer survival.
Not available
S-EPMC2864289 | 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
UnknownHeterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics.
Not available
S-EPMC2291027 | 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 breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.
Not available
S-EPMC2427217 | 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
UnknownMissense variants in ATM in 26,101 breast cancer cases and 29,842 controls.
Not available
S-EPMC2938473 | biostudies-literature
UnknownFive polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium.
Not available
S-EPMC2737177 | biostudies-literature
UnknownAssociations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium.
Not available
S-EPMC3209823 | biostudies-literature
UnknownInheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women.
Not available
S-EPMC5106833 | biostudies-literature
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