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Overlap of high-risk individuals across family history, genetic & non-genetic breast cancer risk models: Analysis of 180,398 women from European & Asian ancestries.
Not available
S-EPMC11908272
|
biostudies-literature
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No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.
Not available
S-EPMC4630206
|
biostudies-literature
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Threshold-Based Overlap of Breast Cancer High-Risk Classification Using Family History, Polygenic Risk Scores, and Traditional Risk Models in 180,398 Women.
Not available
S-EPMC12610763
|
biostudies-literature
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Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer.
Not available
S-EPMC6465407
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biostudies-literature
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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.
Not available
S-EPMC6974400
|
biostudies-literature
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Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset.
Not available
S-EPMC11393698
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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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Transcriptome-wide association study of breast cancer risk by estrogen-receptor status.
Not available
S-EPMC7987299
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biostudies-literature
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Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus.
Not available
S-EPMC4962376
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biostudies-literature
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Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers.
Not available
S-EPMC3617380
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biostudies-literature
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