Trust, vulnerable populations, and genetic data sharing
نویسندگان
چکیده
منابع مشابه
Trust, vulnerable populations, and genetic data sharing
Recent policies and proposed regulations, including the Notice of Proposed Rulemaking for the Common Rule and the 2014 NIH Genetic Data Sharing Policy, seek to improve research subject protections. Protections for subjects whose genetic data is shared are critical to reduce risks such as loss of confidentiality, stigma, and discrimination. In the article 'It depends whose data are being shared:...
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[ 411 ] Kennedy Institute of Ethics Journal Vol. 14, No. 4, 411–425 © 2004 by the National Reference Center for Bioethics Literature Produced at the National Reference Center for Bioethics Literature, Kennedy Institute of Ethics, Georgetown University, Box 571212, Washington, DC 20057-1212. The Center operates on a contract with the National Library of Medicine, National Institutes of Health. A...
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This study provided a national profile of health insurance of certain vulnerable populations including children, racial/ethnic minorities, low-income families, non-metropolitan statistical area (MSA) residents, and those with poor health status. The study shows an increase in the proportion of uninsured nonelderly population. While public insurance helped reduce the employment- and health-relat...
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ژورنال
عنوان ژورنال: Journal of Law and the Biosciences
سال: 2015
ISSN: 2053-9711
DOI: 10.1093/jlb/lsv044