Eccles, Diana

Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies

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Genome-wide association study identifies novel breast cancer susceptibility loci

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Cancer Risks for BRCA1 and BRCA2 Mutation Carriers: Results From Prospective Analysis of EMBRACE

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Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results

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Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

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Associations of breast cancer risk factors with tumor subtypes: A pooled analysis from the breast cancer association consortium studies

Yang, X. R., Chang-Claude, J., Goode, E. L., Couch, F. J., Nevanlinna, H., Milne, R. L., Gaudet, M., Schmidt, M. K., Broeks, A., Cox, A., et al. (2011) · JNCI: Journal of the National Cancer Institute

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Genome-wide association study identifies five new breast cancer susceptibility loci

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Association of Type and Location of BRCA1 and BRCA2 Mutations With Risk of Breast and Ovarian Cancer

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Identification of six new susceptibility loci for invasive epithelial ovarian cancer

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The landscape of somatic genetic alterations in breast cancers from ATM germline mutation carriers

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A novel HER2-positive breast cancer phenotype arising from germline TP53 mutations: Table 1

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A Dominantly Inherited 5′ UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian Cancer

Evans, D. G. R., van Veen, E. M., Byers, H. J., Wallace, A. J., Ellingford, J. M., Beaman, G., Santoyo-Lopez, J., Aitman, T. J., Eccles, D. M., Lalloo, F. I., et al. (2018) · The American Journal of Human Genetics

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Body mass index and breast cancer survival: a Mendelian randomization analysis

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Familial breast cancer: an investigation into the outcome of treatment for early stage disease

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