Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study-Reference-Cited by-同舟云学术

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Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study

Published:2012-08-15 Issue:3 Volume:21 Page:261-265
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Facio Flavia M,Eidem Haley,Fisher Tyler,Brooks Stephanie,Linn Amy,Kaphingst Kimberly A,Biesecker Leslie G,Biesecker Barbara B

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2012179.pdf

Reference28 articles.

1. Singleton AB : Exome sequencing: a transformative technology. Lancet Neurol 2011; 10: 942–946.

2. Torkamani A, Scott-Van Zeeland AA, Topol EJ, Schork NJ : Annotating individual human genomes. Genomics 2011; 98: 233–241.

3. Wolf SM, Crock BN, Van Ness B et al. Managing incidental findings and research results in genomic research involving biobanks and archived data sets. Genet Med 2012; 14: 361–384.

4. Ferriere M, Van Ness B : Return of individual research results and incidental findings in the clinical trials cooperative group setting. Genet Med 2012; 14: 411–416.

5. Fullerton SM, Wolf WA, Brothers KB et al. Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network. Genet Med 2012; 14: 424–431.

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