Stakeholder Perspectives on Returning Nonactionable Apolipoprotein L1 (APOL1) Genetic Results to African American Research Participants
Author:
Affiliation:
1. University of Washington, Seattle, WA, USA
2. Vanderbilt University Medical Center, Nashville, TN, USA
3. Center for Practical Bioethics, Kansas City, MO, USA
4. VA Puget Sound Health Care System, Seattle, WA, USA
Abstract
Funder
National Human Genome Research Institute
National Center for Advancing Translational Sciences
Publisher
SAGE Publications
Subject
Communication,Education,Social Psychology
Link
http://journals.sagepub.com/doi/pdf/10.1177/15562646211063267
Reference52 articles.
1. Opinions of African American adults about the use of apolipoprotein L1 (ApoL1) genetic testing in living kidney donation and transplantation
2. Returning Individual Genetic Research Results to Research Participants: Uptake and Outcomes Among Patients With Breast Cancer
3. Qualitative Data Analysis for Health Services Research: Developing Taxonomy, Themes, and Theory
4. Personal utility in genomic testing: is there such a thing?
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Returning personalized, genetic health test results to individuals of African descent or ancestry in precision medicine research;Health Affairs Scholar;2023-12
2. APOL1 Genetic Testing in Patients With Recent African Ancestry and Hypertension: A Pilot Study of Attitudes and Perceptions;Kidney Medicine;2022-12
3. Race, Ancestry, and Genetic Risk for Kidney Failure;American Journal of Kidney Diseases;2022-12
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