Germline Variation in Cancer-Susceptibility Genes in a Healthy, Ancestrally Diverse Cohort: Implications for Individual Genome Sequencing-Reference-Cited by-同舟云学术

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Germline Variation in Cancer-Susceptibility Genes in a Healthy, Ancestrally Diverse Cohort: Implications for Individual Genome Sequencing

Published:2014-04-11 Issue:4 Volume:9 Page:e94554
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Bodian Dale L.,McCutcheon Justine N.,Kothiyal Prachi,Huddleston Kathi C.,Iyer Ramaswamy K.,Vockley Joseph G.,Niederhuber John E.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference84 articles.

1. BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast-ovarian cancer;MJ Hall;Cancer,2009

2. SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes;BR Packer;Nucleic Acids Res,2006

3. Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes;JJ Johnston;Am J Hum Genet,2012

4. Ethnic differences in cancer risk resulting from genetic variation;SL Neuhausen;Cancer,1999

5. Rare genetic variants and the risk of cancer;W Bodmer;Curr Opin Genet Dev,2010

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