Informed consent for whole genome sequencing: A qualitative analysis of participant expectations and perceptions of risks, benefits, and harms-Reference-Cited by-同舟云学术

Informed consent for whole genome sequencing: A qualitative analysis of participant expectations and perceptions of risks, benefits, and harms

Published:2012-04-24 Issue:6 Volume:158A Page:1310-1319
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Tabor Holly K.,Stock Jacquie,Brazg Tracy,McMillin Margaret J.,Dent Karin M.,Yu Joon-Ho,Shendure Jay,Bamshad Michael J.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference19 articles.

1. Clinical assessment incorporating a personal genome;Ashley;Lancet,2010

2. Research ethics recommendations for whole-genome research: Consensus statement;Caulfield;PLOS Biol,2008

3. Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays;Homer;PLoS Genet,2008

4. Three approaches to qualitative content analysis;Hseih;Qual Health Res,2005

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