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Cancer Discovery|September 23, 2016
A Recurrent ERCC3 Truncating Mutation Confers Moderate Risk for Breast CancerJoseph Vijai, Sabine Topka, Danylo Villano, et al.Cancer Discovery|September 1, 2022
Genetic Ancestry Correlates with Somatic Differences in a Real-World Clinical Cancer Sequencing CohortKanika Arora, Thinh N Tran, Yelena Kemel, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 21, 2012
Breast and ovarian cancer risk and risk reduction in Jewish BRCA1/2 mutation carriersBrian S Finkelman, Wendy S Rubinstein, Sue Friedman, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 30, 2026
A Longitudinal Comprehensive Biospecimen and Clinical Data Repository for Cancer Early Detection: The InAdvance StudyTia L Kauffman, Elizabeth K O'Donnell, Catherine R Marinac, et al.Journal of the National Comprehensive Cancer Network : JNCCN|July 8, 2015
Breast Cancer Risk Reduction, Version 2.2015Therese B Bevers, John H Ward, Banu K Arun, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|July 14, 2007
AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a consortium of investigators of modifiers of BRCA1/2 studyFergus J Couch, Olga Sinilnikova, Robert A Vierkant, et al.Cancer|April 23, 2020
11p15.5 epimutations in children with Wilms tumor and hepatoblastoma detected in peripheral bloodElise M Fiala, Michael V Ortiz, Jennifer A Kennedy, et al.Nature Communications|September 10, 2014
Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European originsShai Carmi, Ken Y Hui, Ethan Kochav, et al.JCO Precision Oncology|June 1, 2023
Prevalence and Clinical Implications of Mismatch Repair-Proficient Colorectal Cancer in Patients With Lynch SyndromeMegha Ranganathan, Rosalba E Sacca, Magan Trottier, et al.Cancer|October 27, 2023
Pathogenic germline variants in patients with endometrial cancer of diverse ancestryYing L Liu, Sushmita Gordhandas, Kanika Arora, et al.Pageof 68