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Research Square|February 6, 2026
Factors associated with and patterns of alcohol intake in late survivorship for breast cancer survivorsSanjna Rajput, Robert A Vierkant, Kayleigh N Olson, et al.
JCO Clinical Cancer Informatics|May 6, 2024
Assessment of <i>BRCA1</i> and <i>BRCA2</i> Germline Variant Data From Patients With Breast Cancer in a Real-World Data RegistryThales C Nepomuceno, Paulo Lyra, Jianbin Zhu, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|August 19, 2008
Association of genetic variation in genes implicated in the beta-catenin destruction complex with risk of breast cancerXianshu Wang, Ellen L Goode, Zachary S Fredericksen, et al.
Cancer Prevention Research (Philadelphia, Pa.)|December 28, 2023
Breast Cancer Polygenic-Risk Score Influence on Risk-Reducing Endocrine Therapy Use: Genetic Risk Estimate (GENRE) Trial 1-Year and 2-Year Follow-UpDaniela L Stan, Julian O Kim, Daniel J Schaid, et al.
Breast Cancer Research and Treatment|April 16, 2026
Factors associated with and patterns of alcohol intake in late survivorship for breast cancer survivorsSanjna Rajput, Robert A Vierkant, Kayleigh N Olson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 20, 2019
Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel testing cohortHongyan Li, Holly LaDuca, Tina Pesaran, et al.
Cancer Medicine|August 30, 2022
Association of raloxifene and tamoxifen therapy with cognitive performance, odds of mild cognitive impairment, and brain MRI markers of neurodegenerationFirat Kara, Christine M Lohse, Anna M Castillo, et al.
JAMA Oncology|May 27, 2021
Comparison of the Prevalence of Pathogenic Variants in Cancer Susceptibility Genes in Black Women and Non-Hispanic White Women With Breast Cancer in the United StatesSusan M Domchek, Song Yao, Fei Chen, et al.
Human Mutation|October 13, 2011
ENIGMA--evidence-based network for the interpretation of germline mutant alleles: an international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genesAmanda B Spurdle, Sue Healey, Andrew Devereau, et al.
Scientific Reports|September 28, 2022
Assessment of small in-frame indels and C-terminal nonsense variants of BRCA1 using a validated functional assayThales C Nepomuceno, Ana P P Dos Santos, Vanessa C Fernandes, et al.
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