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Cancer Research|July 9, 2009
Modification of ovarian cancer risk by BRCA1/2-interacting genes in a multicenter cohort of BRCA1/2 mutation carriersTimothy R Rebbeck, Nandita Mitra, Susan M Domchek, et al.
NPJ Breast Cancer|September 30, 2025
Polygenic risk score for breast cancer risk prediction in Asian BRCA1 and BRCA2 pathogenic variants carriersMei-Chee Tai, Joe Dennis, Sue K Park, et al.
Genome Biology|January 9, 2020
Non-coding RNAs underlie genetic predisposition to breast cancerMahdi Moradi Marjaneh, Jonathan Beesley, Tracy A O'Mara, et al.
Cancer Science|December 17, 2017
Ovarian cancer risk, ALDH2 polymorphism and alcohol drinking: Asian data from the Ovarian Cancer Association ConsortiumTomotaka Ugai, Linda E Kelemen, Mika Mizuno, et al.
NPJ Breast Cancer|May 2, 2022
Epigenome erosion and SOX10 drive neural crest phenotypic mimicry in triple-negative breast cancerJodi M Saunus, Xavier M De Luca, Korinne Northwood, et al.
Journal of the National Cancer Institute|May 31, 2019
Genetically Predicted Levels of DNA Methylation Biomarkers and Breast Cancer Risk: Data From 228 951 Women of European DescentYaohua Yang, Lang Wu, Xiao-Ou Shu, et al.
Cancer Research|November 30, 2018
Functional Analysis and Fine Mapping of the 9p22.2 Ovarian Cancer Susceptibility LocusMelissa A Buckley, Nicholas T Woods, Jonathan P Tyrer, et al.
Human Mutation|June 19, 2019
The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countriesYael Laitman, Tara M Friebel, Drakoulis Yannoukakos, et al.
International Journal of Cancer|July 16, 2016
A splicing variant of TERT identified by GWAS interacts with menopausal estrogen therapy in risk of ovarian cancerAlice W Lee, Ashley Bomkamp, Elisa V Bandera, et al.
European Journal of Human Genetics : EJHG|February 2, 2017
Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriersLogan C Walker, Louise Marquart, John F Pearson, et al.
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