ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

作者: Robert C Green , Jonathan S Berg , Wayne W Grody , Sarah S Kalia , Bruce R Korf

DOI: 10.1038/GIM.2013.73

关键词:

摘要: … solicited feedback at an open forum at the ACMG Annual Meeting in March 2012. These … on feedback from ACMG members and were provisionally reviewed by the ACMG Board in May …

参考文章(35)
Robert C. Green, Heidi L. Rehm, Isaac S. Kohane, Clinical Genome Sequencing Genomic and Personalized Medicine (Second Edition)#R##N#V1-2. pp. 102- 122 ,(2013) , 10.1016/B978-0-12-382227-7.00009-4
Geoffrey S. Ginsburg, Huntington F. Willard, Genomic and personalized medicine Elsevier/Academic Press. ,(2009)
Christian M. Simon, Janet K. Williams, Laura Shinkunas, Debra Brandt, Sandra Daack-Hirsch, Martha Driessnack, Informed consent and genomic incidental findings: IRB chair perspectives. Journal of Empirical Research on Human Research Ethics. ,vol. 6, pp. 53- 67 ,(2011) , 10.1525/JER.2011.6.4.53
J I Westbrook, J Braithwaite, J H McIntosh, The outcomes for patients with incidental lesions: serendipitous or iatrogenic? American Journal of Roentgenology. ,vol. 171, pp. 1193- 1196 ,(1998) , 10.2214/AJR.171.5.9798845
Stephanie M. Fullerton, Wendy A. Wolf, Kyle B. Brothers, Ellen Wright Clayton, Dana C. Crawford, Joshua C. Denny, Philip Greenland, Barbara A. Koenig, Kathleen A. Leppig, Noralane M. Lindor, Catherine A. McCarty, Amy L. McGuire, Eugenia R. McPeek Hinz, Daniel B. Mirel, Erin M. Ramos, Marylyn D. Ritchie, Maureen E. Smith, Carol J. Waudby, Wylie Burke, Gail P. Jarvik, Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network. Genetics in Medicine. ,vol. 14, pp. 424- 431 ,(2012) , 10.1038/GIM.2012.15
Teri A. Manolio, Rex L. Chisholm, Brad Ozenberger, Dan M. Roden, Marc S. Williams, Richard Wilson, David Bick, Erwin P. Bottinger, Murray H. Brilliant, Charis Eng, Kelly A. Frazer, Bruce Korf, David H. Ledbetter, James R. Lupski, Clay Marsh, David Mrazek, Michael F. Murray, Peter H. O’Donnell, Daniel J. Rader, Mary V. Relling, Alan R. Shuldiner, David Valle, Richard Weinshilboum, Eric D. Green, Geoffrey S. Ginsburg, Implementing genomic medicine in the clinic: the future is here. Genetics in Medicine. ,vol. 15, pp. 258- 267 ,(2013) , 10.1038/GIM.2012.157
C Sue Richards, Sherri Bale, Daniel B Bellissimo, Soma Das, Wayne W Grody, Madhuri R Hegde, Elaine Lyon, Brian E Ward, None, ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007 Genetics in Medicine. ,vol. 10, pp. 294- 300 ,(2008) , 10.1097/GIM.0B013E31816B5CAE
Adam Fritz, Philip Farrell, Estimating the annual number of false negative cystic fibrosis newborn screening tests Pediatric Pulmonology. ,vol. 47, pp. 207- 208 ,(2012) , 10.1002/PPUL.21561
Muin J Khoury, Public health genomics: The end of the beginning Genetics in Medicine. ,vol. 13, pp. 206- 209 ,(2011) , 10.1097/GIM.0B013E31821024CA