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- 2023
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Mark
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk
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- Contribution to journal › Article
- 2022
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Mark
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
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- Contribution to journal › Article
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Mark
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
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- Contribution to journal › Article
- 2021
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Mark
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
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- Contribution to journal › Article
- 2019
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Mark
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
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- Contribution to journal › Article