Reporting Incidental Findings in Clinical Whole Exome Sequencing: Incorporation of the 2013 ACMG Recommendations into Current Practices of Genetic Counseling-Reference-Cited by-同舟云学术

Reporting Incidental Findings in Clinical Whole Exome Sequencing: Incorporation of the 2013 ACMG Recommendations into Current Practices of Genetic Counseling

Published:2014-11-18 Issue:4 Volume:24 Page:654-662
ISSN:1059-7700
Container-title:Journal of Genetic Counseling
language:en
Short-container-title:J Genet Counsel

Author:

Smith Lacey A.,Douglas Jessica,Braxton Alicia A.,Kramer Kate

Publisher

Wiley

Subject

Genetics (clinical)

Link

http://link.springer.com/content/pdf/10.1007/s10897-014-9794-4

Reference21 articles.

1. American College of Medical Genetics and Genomics. (2013). Incidental findings in clinical genomics: A clarification.

2. American College of Medical Genetics and Genomics. (2014). Member Statement: ACMG updates recommendation on “opt out” for genome sequencing return of results.

3. Ayuso, C., Millan, J. M., Mancheno, M., & Dal-Re, R. (2013). Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential consent and process. European Journal of Human Genetics, 21, 1054–1059.

4. Bollinger, J., Scott, J., Dvoskin, R., & Kaufman, D. (2012). Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study. Genetics in Medicine, 14, 451–457.

5. Burke, W., Antommaria, A. H. M., Bennett, R., Botkin, J., Clayton, E. W., Henderson, G. E., Holm, I. A., et al. (2013). Recommendations for returning genomic incidental findings? We need to talk! Genetics in Medicine. doi: 10.1038/gim.2013.113 .

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