Use of deep whole-genome sequencing data to identify structure risk variants in breast cancer susceptibility genes-Reference-Cited by-同舟云学术

Use of deep whole-genome sequencing data to identify structure risk variants in breast cancer susceptibility genes

Published:2018-01-08 Issue:5 Volume:27 Page:853-859
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Guo Xingyi¹^ORCID,Shi Jiajun¹,Cai Qiuyin¹,Shu Xiao-Ou¹,He Jing¹,Wen Wanqing¹,Allen Jamie²³,Pharoah Paul²³,Dunning Alison²³,Hunter David J⁴⁵,Kraft Peter⁴⁵,Easton Douglas F²³,Zheng Wei¹,Long Jirong¹

Affiliation:

1. Division of Epidemiology, Department of Medicine, Vanderbilt Epidemiology Center, and Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, TN 37203, USA

2. Department of Public Health and Primary Care, University of Cambridge, Cambridge CB1 8RN, UK

3. Department of Oncology, Centre for Cancer Genetic Epidemiology, University of Cambridge, Cambridge CB1 8RN, UK

4. Program in Genetic Epidemiology and Statistical Genetics, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA

5. Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA

Funder

Cancer Research UK

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/27/5/853/24044413/ddy005.pdf

Reference41 articles.

1. Hereditary breast cancer: the era of new susceptibility genes;Apostolou;Biomed. Res. Int,2013

2. Lifetime cancer risks in individuals with germline PTEN mutations;Tan;Clin. Cancer. Res,2012

3. Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene;Meindl;Nat. Genet,2010

4. Beyond Li Fraumeni Syndrome: clinical characteristics of families with p53 germline mutations;Gonzalez;J. Clin. Oncol,2009

5. The emerging landscape of breast cancer susceptibility;Stratton;Nat. Genet,2008

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