Search Result Details

This page shows the details of why an item matched the keywords from your search.
One or more keywords matched the following items that are connected to MCGUIRE, AMY
Item TypeName
Academic Article Research ethics and the challenge of whole-genome sequencing.
Academic Article Currents in contemporary ethics. Direct-to-consumer genetic testing: is it the practice of medicine?
Academic Article Direct-to-consumer genetic testing: perceptions, problems, and policy responses.
Academic Article Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group.
Academic Article Confidentiality, privacy, and security of genetic and genomic test information in electronic health records: points to consider.
Academic Article Identifiability of DNA data: the need for consistent federal policy.
Academic Article An unwelcome side effect of direct-to-consumer personal genome testing: raiding the medical commons.
Academic Article Science and regulation. Regulating direct-to-consumer personal genome testing.
Academic Article Ethical and practical challenges of sharing data from genome-wide association studies: the eMERGE Consortium experience.
Concept Public Policy
Concept Health Policy
Academic Article Policy uncertainty, sequencing, and cell lines.
Academic Article Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate.
Award or Honor Receipt Clinical Integration of Whole Genome Sequencing: A Policy Analysis (PI)
Academic Article Clinical integration of next generation sequencing: a policy analysis.
Academic Article Development of the clinical next-generation sequencing industry in a shifting policy climate.
Academic Article Legal Barriers to Adolescent Participation in Research About HIV and Other Sexually Transmitted Infections.
Academic Article Developing context-specific next-generation sequencing policy.
Academic Article Barriers to clinical adoption of next generation sequencing: Perspectives of a policy Delphi panel.
Academic Article It depends whose data are being shared: considerations for genomic data sharing policies.
Academic Article Consumer Perspectives on Access to Direct-to-Consumer Genetic Testing: Role of Demographic Factors and the Testing Experience.
Academic Article Barriers to clinical adoption of next-generation sequencing: a policy Delphi panel's solutions.
Academic Article Citizen science, public policy.
Grant The ethics of consent for the public release of potentially identifiable DNA data
Grant Neuroethics of aDBS Systems Targeting Neuropsychiatric and Movement Disorders
Grant Evaluating utility and improving implementation of genomic sequencing for pediatric cancer patients in the diverse population and healthcare settings of Texas: The KidsCanSeq Study
Grant Building the Medical Information Commons: Participant Engagement and Policy
Grant Clinical Integration of Whole Genome Sequencing: A Policy Analysis
Concept Policy
Academic Article Donors, authors, and owners: how is genomic citizen science addressing interests in research outputs?
Academic Article Ventilator Triage Policies During the COVID-19 Pandemic at U.S. Hospitals Associated With Members of the Association of Bioethics Program Directors.
Grant After the Golden State Killer: Public Preferences and Policy Implications of Police Use of Genetic Data (The ForenSeq Study)
Academic Article Challenges to Building a Gene Variant Commons to Assess Hereditary Cancer Risk: Results of a Modified Policy Delphi Panel Deliberation.
Academic Article Pressing regulatory challenges for psychedelic medicine.
Academic Article Policy options to facilitate cancer genomic variant data sharing: outcomes of a modified policy Delphi.
Search Criteria
  • Policy