Correlation between the risk of ovarian cancer and BRCA recurrent pathogenic variants in Japan
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://www.nature.com/articles/s10038-021-01002-z.pdf
Reference38 articles.
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2. Wooster R, Bignell G, Lancaster J, Swift S, Seal S, Mangion J, et al. Identification of the breast cancer susceptibility gene BRCA2. Nature. 1995;378:789–92.
3. Sekine M, Nishino K, Enomoto T. BRCA genetic test and risk-reducing salpingo-oophorectomy for hereditary breast and ovarian cancer: state-of-the-art. Cancers. 2021;13:2562.
4. Sekine M, Enomoto T. Precision medicine for hereditary tumors in gynecologic malignancies. J Obstet Gynaecol Res. 2021;47::2597–606.
5. Shanmughapriya S, Nachiappan V, Natarajaseenivasan K. BRCA1 and BRCA2 mutations in the ovarian cancer population across race and ethnicity: special reference to Asia. Oncology. 2013;84:226–32.
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1. The frequency and pathogenicity of BRCA1 and BRCA2 variants in the general Japanese population;Journal of Human Genetics;2024-02-27
2. Registration Data of Japanese Organization of Hereditary Breast and Ovarian Cancer Till 2020;Practical Guide to Hereditary Breast and Ovarian Cancer;2023
3. Genetic medicine in companion diagnostics of germline BRCA testing of Japanese pancreatic cancer patients;Journal of Human Genetics;2022-12-08
4. An in-Depth Analysis of Ovarian Cancer: Pathogenesis and Clinical Manifestation;Drug Research;2022-06-27
5. Prevalence of Pathogenic Germline BRCA1/2 Variants and Their Association with Clinical Characteristics in Patients with Epithelial Ovarian Cancer in a Rural Area of Japan;Genes;2022-06-18
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