Secondary findings and carrier test frequencies in a large multiethnic sample-Reference-Cited by-同舟云学术

Secondary findings and carrier test frequencies in a large multiethnic sample

Published:2015-06-13 Issue:1 Volume:7 Page:
ISSN:1756-994X
Container-title:Genome Medicine
language:en
Short-container-title:Genome Med

Author:

Gambin Tomasz,Jhangiani Shalini N.,Below Jennifer E.,Campbell Ian M.,Wiszniewski Wojciech,Muzny Donna M.,Staples Jeffrey,Morrison Alanna C.,Bainbridge Matthew N.,Penney Samantha,McGuire Amy L.,Gibbs Richard A.,Lupski James R.,Boerwinkle Eric

Publisher

Springer Science and Business Media LLC

Subject

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

Link

http://link.springer.com/content/pdf/10.1186/s13073-015-0171-1.pdf

Reference46 articles.

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3. O’Daniel JM, Lee K. Whole-genome and whole-exome sequencing in hereditary cancer: impact on genetic testing and counseling. Cancer J Sudbury Mass. 2012;18:287–92.

4. Van Allen EM, Wagle N, Stojanov P, Perrin DL, Cibulskis K, Marlow S, et al. Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine. Nat Med. 2014;20:682–8.

5. Morrison AC, Bare LA, Chambless LE, Ellis SG, Malloy M, Kane JP, et al. Prediction of coronary heart disease risk using a genetic risk score: the atherosclerosis risk in communities study. Am J Epidemiol. 2007;166:28–35.

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