Work

Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium

Year: 2013

Type: article

Source: Genetics in Medicine

DOI: 10.1038/gim.2013.133

Authors: Jonathan S. Berg, Laura M. Amendola, Christine Eng, Eliezer Van Allen, Stacy W. Gray, Nikhil Wagle, Heidi L. Rehm, Elizabeth T. DeChene, Matthew C. Dulik, Fuki M. Hisama, Wylie Burke, Nancy B. Spinner, Levi Garraway, Robert C. Green, Sharon Plon, James P. Evans, Gail P. Jarvik

Institutions: University of North Carolina at Chapel Hill, UNC Lineberger Comprehensive Cancer Center, University of Washington, Baylor College of Medicine, Broad Institute, Dana-Farber Cancer Institute, Brigham and Women's Hospital, Harvard University, Dana-Farber Brigham Cancer Center, Children's Hospital of Philadelphia, University of Pennsylvania

Language: English

Topic: Genomics and Rare Diseases

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: National Institutes of Health, National Human Genome Research Institute, National Cancer Institute

Awards: G1547207268, G1569999668, G1581081233, G2641303909, G2681125283, G2683385584, Impact of return of incidental genetic test results to research participants in t, G3300265552, CSER RoRC Centralized Support Coordinating Center, G4189385495, Applying Genomic Sequencing in Pediatrics, G4748628049, G561653141, G56831423, Returning research results in children: Parental Preferences and Expert Oversight, G7273035524, G8864180235, Integration of Whole Genome Sequencing into Clinical Medicine, Cancer Center Support Grant

OpenAlex ID: W2039298047

FWCI: 9.701

Cites: 9

Cited by: 105

Related to: 10