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Paper Details

Navigating the research-clinical interface in genomic medicine: analysis from the CSER Consortium.
Genet Med
29
2018
Biomedical Research, Disclosure, Electronic Health Records, Genomics, Health Personnel, Humans, Informed Consent, National Institutes of Health (U.S.), Surveys and Questionnaires, Translational Research, Biomedical, United States
Author NameAffiliation
Susan M WolfLaw School Medical School Consortium on Law and Values in Health, University of Minnesota
Laura M AmendolaUniversity of Washington
Jonathan S BergUniversity of North Carolina at Chapel Hill
Wendy K ChungColumbia University
Wendy K ChungColumbia University
E ClaytonCenter for Biomedical Ethics and Society, Vanderbilt University Medical Center
Robert C GreenBrigham and Women's Hospital, Broad Institute and Harvard Medical School
Julie N HarrisInstitute for Health and Aging, University of California-San Francisco Division of Research, Kaiser Permanente Northern California
Gail E HendersonUniversity of North Carolina at Chapel Hill
Gail P JarvikUniversity of Washington
Gail P JarvikUniversity of Washington
Gail P JarvikUniversity of Washington
Gail P JarvikUniversity of Washington
Barbara A KoenigInstitute for Health and Aging, University of California-San Francisco
Lisa Soleymani LehmannVeterans Administration National Center for Ethics in Health Care
Lisa Soleymani LehmannHarvard University
Amy L McGuireCenter for Medical Ethics and Health Policy, Baylor College of Medicine
Pearl O'Rourke
Carol P SomkinKaiser Permanente Northern California
Benjamin S WilfondTreuman Katz Center for Pediatric Bioethics, Seattle Children's Hospital, University of Washington
Wylie BurkeUniversity of Washington
Wylie BurkeUniversity of Washington
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