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Common 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
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The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant.
Not available
S-EPMC8460445
|
biostudies-literature
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Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk.
Not available
S-EPMC3609647
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biostudies-literature
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DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers.
Not available
S-EPMC3974638
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biostudies-literature
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Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers.
Not available
S-EPMC3458423
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biostudies-literature
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Common genetic variants and modification of penetrance of BRCA2-associated breast cancer.
Not available
S-EPMC2965747
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biostudies-literature
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Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2.
Not available
S-EPMC3387216
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biostudies-literature
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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
Not available
S-EPMC7890067
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biostudies-literature
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Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.
Not available
S-EPMC3609646
|
biostudies-literature
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Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction.
Not available
S-EPMC2999830
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biostudies-literature
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