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Human Mutation|May 23, 2020
Mutation prevalence tables for hereditary cancer derived from multigene panel testingSteven N Hart, Eric C Polley, Amal Yussuf, et al.Gynecologic Oncology|April 19, 2021
PP2A and E3 ubiquitin ligase deficiencies: Seminal biological drivers in endometrial cancerJesus Gonzalez-Bosquet, Jamie N Bakkum-Gamez, Amy L Weaver, et al.Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|April 8, 2020
Real-world experiences with acupuncture among breast cancer survivors: a cross-sectional survey studyJacqueline Zayas, Kathryn J Ruddy, Janet E Olson, et al.European Journal of Human Genetics : EJHG|November 22, 2021
Two distinct mechanisms underlie estrogen-receptor-negative breast cancer susceptibility at the 2p23.2 locusGustavo Mendoza-Fandiño, Paulo Cilas M Lyra, Thales C Nepomuceno, et al.Breast Cancer Research : BCR|March 11, 2010
Genetic variation in the estrogen metabolic pathway and mammographic density as an intermediate phenotype of breast cancerJingmei Li, Louise Eriksson, Keith Humphreys, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 14, 2016
Conflicting Interpretation of Genetic Variants and Cancer Risk by Commercial Laboratories as Assessed by the Prospective Registry of Multiplex TestingJudith Balmaña, Laura Digiovanni, Pragna Gaddam, et al.Cancer Research|May 3, 2008
Functional assays for classification of BRCA2 variants of uncertain significanceDaniel J Farrugia, Mukesh K Agarwal, Vernon S Pankratz, et al.Journal of the National Cancer Institute|February 25, 2020
The Contribution of Germline Predisposition Gene Mutations to Clinical Subtypes of Invasive Breast Cancer From a Clinical Genetic Testing CohortChunling Hu, Eric C Polley, Siddhartha Yadav, et al.Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|April 10, 2004
Utilizing Nottingham Prognostic Index in microarray gene expression profiling of breast carcinomasDylan V Miller, Alexey A Leontovich, Wilma L Lingle, et al.American Journal of Human Genetics|October 10, 2007
A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genesDouglas F Easton, Amie M Deffenbaugh, Dmitry Pruss, et al.Pageof 57