American Journal of Public Health · 2009 · 153 citations · 13 references
Public HealthGeneticsHealth PolicyBioethicsMedical EthicsResearch EthicsBiobanking EthicsConsentGenebank ManagementHealth Information EthicsParticipant ConfidentialityParticipant PrivacyBiobanking ConsentInformed Consent
The National Institutes of Health and other federal health agencies are considering establishing a national biobank to study the roles of genes and environment in health. We assessed the public's attitudes toward the proposed biobank, including preferences for providing informed consent. Sixteen focus groups were conducted, and themes arising from the focus groups were tested in a large, representative survey (n=4659) of the general population. Our research demonstrates that when considering participating in a genomic biobank, individuals want ongoing choices and control over access to their samples and information.
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Informed consent: Legal theory and clinical practice
Richard G. Lonsdorf · Journal of Legal Medicine · 1988 · 367 citations
Law, Health Law, Human Rights Law +11
Public Expectations for Return of Results from Large-Cohort Genetic Research
Juli Murphy, Joan Scott, David Kaufman et al. · The American Journal of Bioethics · 2008 · 277 citations · Full text
The case for a US prospective cohort study of genes and environment
Francis S. Collins · Nature · 2004 · 227 citations