How many more breast cancer predisposition genes are there?
Author:
Publisher
Springer Science and Business Media LLC
Link
http://link.springer.com/content/pdf/10.1186/bcr6.pdf
Reference31 articles.
1. Hall JM, Lee MK, Morrow J, et al: Linkage analysis of early onset familial breast cancer to chromosome 17q21. Science . 1990, 250: 1684-1689.
2. Malkin D, Li FP, Strong LC, et al: Germline p53 mutations in a familial syndrome of breast cancer, sarcomas and other neoplasms. Science. 1990, 250: 1233-1238.
3. Wooster R, Neuhausen S, Mangion J, et al: Localization of a breast cancer susceptibility gene to chromosome 13q12-q13. Science. 1994, 265: 2088-2090.
4. Ford D, Easton DF, Stratton M, et al: Genetic heterogeneity and Penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. Am J Hum Genet. 1998, 62: 334-345. 10.1086/301749.
5. Peto J, Collins N, Barfoot R, et al: The prevalence of BRCA1 and BRCA2 mutations amongst early onset breast cancer cases in the UK. J Natl Cancer Inst. 1999, 91: 943-949. 10.1093/jnci/91.11.943.
Cited by 252 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Discovering predisposing genes for hereditary breast cancer using deep learning;Briefings in Bioinformatics;2024-05-23
2. In Silico-Based Structural Evaluation to Categorize the Pathogenicity of Mutations Identified in the RAD Class of Proteins;ACS Omega;2023-03-08
3. Efficacy of PARP Inhibitor, Platinum, and Immunotherapy in BRCA-Mutated HER2-Negative Breast Cancer Patients: A Systematic Review and Network Meta-Analysis;Journal of Clinical Medicine;2023-02-17
4. Occurrence of variants of unknown clinical significance in genetic testing for hereditary breast and ovarian cancer syndrome and Lynch syndrome: a literature review and analytical observational retrospective cohort study;BMC Medical Genomics;2023-01-16
5. Occurrence of variants of unknown clinical significance in genetic testing for hereditary breast and ovarian cancer syndrome and Lynch syndrome - A Literature review and analytical observational retrospective cohort study;2022-09-27
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3