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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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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.
Not available
S-EPMC6974400
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biostudies-literature
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Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers.
Not available
S-EPMC4382299
|
biostudies-literature
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The <i>FANCM</i>:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer.
Not available
S-EPMC6825205
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biostudies-literature
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Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.
Not available
S-EPMC3326552
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biostudies-literature
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Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.
Not available
S-EPMC5023955
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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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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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Identification of six new susceptibility loci for invasive epithelial ovarian cancer.
Not available
S-EPMC4445140
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biostudies-literature
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