Contribution of BRCA1 large genomic rearrangements to early-onset and familial breast/ovarian cancer in Pakistan-Reference-Cited by-同舟云学术

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Contribution of BRCA1 large genomic rearrangements to early-onset and familial breast/ovarian cancer in Pakistan

Published:2016-11-08 Issue:2 Volume:161 Page:191-201
ISSN:0167-6806
Container-title:Breast Cancer Research and Treatment
language:en
Short-container-title:Breast Cancer Res Treat

Author:

Rashid Muhammad U.,Muhammad Noor,Amin Asim,Loya Asif,Hamann Ute

Funder

Shaukat Khanum Memorial Cancer Hospital and Research Centre

Union for International Cancer Control (UICC) Yamagiwa-Yoshida Memorial International Cancer Study Grant

Deutsches Krebsforschungszentrum

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Oncology

Link

http://link.springer.com/content/pdf/10.1007/s10549-016-4044-0.pdf

Reference60 articles.

1. Wooster R, Bignell G, Lancaster J et al (1995) Identification of the breast cancer susceptibility gene BRCA2. Nature 378:789–792

2. Miki Y, Swensen J, Shattuck-Eidens D et al (1994) A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 266:66–71

3. Ford D, Easton DF, Stratton M et al (1998) Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. Am J Hum Genet 62:676–689

4. Robson M, Offit K (2007) Management of an inherited predisposition to breast cancer. N Engl J Med 357:154–162

5. Rashid MU, Zaidi A, Torres D et al (2006) Prevalence of BRCA1 and BRCA2 mutations in Pakistani breast and ovarian cancer patients. Int J Cancer 119:2832–2839

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2. Contribution of constitutional BRCA1 promoter methylation to early-onset and familial breast cancer patients from Pakistan;Breast Cancer Research and Treatment;2023-08-01

3. Screening of BRCA1/2 variants in Mauritanian breast cancer patients;BMC Cancer;2022-07-20

4. Prevalence of FANCM germline variants in BRCA1/2 negative breast and/or ovarian cancer patients from Pakistan;Familial Cancer;2022-07-08

5. Spectrum of germline pathogenic variants using a targeted next generation sequencing panel and genotype-phenotype correlations in patients with suspected hereditary breast cancer at an academic medical centre in Pakistan;Hereditary Cancer in Clinical Practice;2022-06-16

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