Experiences with obtaining informed consent for genomic sequencing-Reference-Cited by-同舟云学术

Experiences with obtaining informed consent for genomic sequencing

Published:2015-07-21 Issue:11 Volume:167 Page:2635-2646
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Bernhardt Barbara A.¹,Roche Myra I.²³,Perry Denise L.⁴,Scollon Sarah R.⁵,Tomlinson Ashley N.¹,Skinner Debra⁶

Affiliation:

1. Division of Translational Medicine and Human Genetics; Perelman School of Medicine, University of Pennsylvania; Philadelphia Pennsylvania

2. Department of Pediatrics; University of North Carolina; Chapel Hill North Carolina

3. Department of Genetics; University of North Carolina; Chapel Hill North Carolina

4. Brigham and Women's Hospital; Boston; Massachusetts

5. Department of Pediatrics; Baylor College of Medicine; Houston Texas

6. FPG Child Development Institute; University of North Carolina; Chapel Hill North Carolina

Funder

National Human Genome Research Institute

CSER Coordinating Center

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37256/fullpdf

Reference51 articles.

1. Points to consider for informed consent for genome/exome sequencing;Genet Med,2013

2. ACMG policy statement: Updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing;Genet Med,2014

3. Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process;Ayuso;Eur J Hum Genet,2013

4. Simplifying informed consent for biorepositories: Stakeholder perspectives;Beskow;Genet Med,2010

5. Informed consent for biobanking: Consensus-based guidelines for adequate comprehension;Beskow;Genet Med,2014

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