Association of a novel BRCA2 mutation with prostate cancer risk further supports germline genetic testing-Reference-Cited by-同舟云学术

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Association of a novel BRCA2 mutation with prostate cancer risk further supports germline genetic testing

Published:2023-02 Issue: Volume:180 Page:155-157
ISSN:0959-8049
Container-title:European Journal of Cancer
language:en
Short-container-title:European Journal of Cancer

Author:

Foley Georgea R.^ORCID,Marthick James R.,Ostrander Elaine A.,Stanford Janet L.,Dickinson Joanne L.,FitzGerald Liesel M.^ORCID

Publisher

Elsevier BV

Subject

Cancer Research,Oncology

Reference8 articles.

1. Massively parallel sequencing in hereditary prostate cancer families reveals a rare risk variant in the DNA repair gene, RAD51C;Marthick;Eur J Cancer,2021

2. PROREPAIR-B: a prospective cohort study of the impact of germline DNA repair mutations on the outcomes of patients with metastatic castration-resistant prostate cancer;Castro;J Clin Oncol,2019

3. Bock C.,et al. Familial clustering of breast and prostate cancer and risk of postmenopausal breast cancer in the women’s health initiative study;Beebe-Dimmer;Cancer,2015

4. Genetic epidemiology in Tasmania;Dwyer;Australas Epidemiol,2000

5. Dense genome-wide SNP linkage scan in 301 hereditary prostate cancer families identifies multiple regions with suggestive evidence for linkage;Stanford;Hum Mol Genet,2009

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