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Human Mutation|May 10, 2024
A likelihood ratio approach for utilizing case-control data in the clinical classification of rare sequence variants: application to BRCA1 and BRCA2Maria Zanti, Denise G O'Mahony, Michael T Parsons, et al.Breast Cancer Research : BCR|August 9, 2023
A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestryPooja Middha, Xiaoliang Wang, Sabine Behrens, et al.International Journal of Cancer|April 19, 2016
Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancerJiajun Shi, Yanfeng Zhang, Wei Zheng, et al.Journal of Medical Genetics|February 28, 2016
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testingDouglas F Easton, Fabienne Lesueur, Brennan Decker, et al.Journal of the National Cancer Institute|May 3, 2020
Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer RiskPooja Middha Kapoor, Nasim Mavaddat, Parichoy Pal Choudhury, et al.Human Molecular Genetics|November 19, 2013
A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortiumRoger L Milne, Jesús Herranz, Kyriaki Michailidou, et al.Plos Genetics|April 19, 2014
Genetic predisposition to in situ and invasive lobular carcinoma of the breastElinor Sawyer, Rebecca Roylance, Christos Petridis, et al.Breast Cancer Research : BCR|April 22, 2015
Common germline polymorphisms associated with breast cancer-specific survivalAilith Pirie, Qi Guo, Peter Kraft, et al.Nature Communications|January 18, 2020
A network analysis to identify mediators of germline-driven differences in breast cancer prognosisMaria Escala-Garcia, Jean Abraham, Irene L Andrulis, et al.American Journal of Human Genetics|October 6, 2020
Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer RiskIris Kramer, Maartje J Hooning, Nasim Mavaddat, et al.Pageof 33