ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
Year: 2013
Type: article
Source: Genetics in Medicine
DOI: 10.1038/gim.2013.73
Institutions: Brigham and Women's Hospital, Harvard University, University of North Carolina at Chapel Hill, University of California, Los Angeles, University of Alabama at Birmingham, Autism & Developmental Medicine Institute, Geisinger Health System, Baylor College of Medicine, University of California, San Francisco, Stanford University, American College of Medical Genetics, National Institutes of Health, National Human Genome Research Institute
Language: English
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Open Access status: bronze
Funders: U.S. Department of Defense, National Institutes of Health, National Institute on Aging, National Human Genome Research Institute, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Environmental Health Sciences, National Center for Research Resources
Awards: G1114824556, Center for Integration of Research on Genetics and Ethics, Impact of Direct to Consumer Genetic Testing, G1695142652, Combined BAC Transgenic and Knock-Out Mouse Model of Lowe Syndrome Nephropathy, G2106123527, G2235079334, G2683385584, Combined BAC Transgenic and Knock-Out Mouse Model of Lowe Syndrome Nephropathy, G3264670853, Center for Genomics and Society, G3731955438, G4056564310, G4119534169, G4203152021, G445807363, Managing Incidental Findings and Research Results in Genomic Biobanks and Archive, Disclosing Genomic Incidental Findings in a Cancer Biobank: An ELSI Experiment, G521457947, UNC Clinical Translation Science Award-K12 Scholars Program (KL2), G530516336, G5492247610, Evaluating utility and improving implementation of genomic sequencing for pediatric cancer patients in the diverse population and healthcare settings of Texas: The KidsCanSeq Study, G5679500696, G5796869029, Returning research results in children: Parental Preferences and Expert Oversight, G6456551059, G6519161563, UNC Clinical and Translational Science Award, North Carolina Clinical Genomic Evaluation by Next-gen Exome Sequencing 2, G6708861783, G6709977666, Characterizing and Communicating Genetic Risk for Alzheimer's Disease, Geisinger eGenonic Medicine (GeM) Program, Returning Research Results of Pediatric Genomic Research to Participants, UNC Clinical Translation Science Award-T32 Program (TL1), G7703604398, GI Endotoxin as an Environmental Trigger in an alpha-Synuclein Transgenic Mouse, G8048365466, Molecular and Genomic Imaging Center, G8667566742, G8872486161, Integration of Whole Genome Sequencing into Clinical Medicine, Training Grant in Genetics
OpenAlex ID: W2145922766