Consent for genetic testing and disclosure of results: Shifting the paradigm to non-genetics clinicians

Hara Levy, Amanda Buchanan, Holly L. Peay(RTI International), Melissa Stosic(Columbia University), Louanne Hudgins(Lucile Packard Children's Hospital), W. Andrew Faucett(Geisinger Medical Center), Wendy R. Uhlmann(University of Michigan), Maureen E. Smith(Northwestern University), Eric P. Tricou(Stanford University), Miranda L. G. Hallquist, Karen E. Wain(Geisinger Medical Center), Myra I. Roche(University of North Carolina at Chapel Hill), Laura Hercher(National Society of Genetic Counselors), Curtis R. Coughlin(University of Colorado Denver), Kelly E. Ormond(Stanford University)
Unknown
June 30, 2019
Cited by 0

Related Papers

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future
|Genetics in Medicine|2013|741
Clinical Interpretation and Implications of Whole-Genome Sequencing
|JAMA|2014|458
Further Delineation of Deletion 1p36 Syndrome in 60 Patients: A Recognizable Phenotype and Common Cause of Developmental Delay and Mental Retardation
|PEDIATRICS|2008|310
Recommendations for returning genomic incidental findings? We need to talk!
|Genetics in Medicine|2013|288
Public and Biobank Participant Attitudes toward Genetic Research Participation and Data Sharing
|Public Health Genomics|2010|274