Managing incidental findings in human subjects research: analysis and recommendations. - Wikidata - thesis-toulmin - TriplyDB

Managing incidental findings in human subjects research: analysis and recommendations.

Managing incidental findings in human subjects research: analysis and recommendations.

http://www.wikidata.org/entity/Q36954360

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The law of incidental findings in human subjects research: establishing researchers' duties Incidental Findings with Genomic Testing: Implications for Genetic Counseling Practice Genetic studies of quantitative MCI and AD phenotypes in ADNI: Progress, opportunities, and plans Genetic data and electronic health records: a discussion of ethical, logistical and technological considerations Biobanks and personalized medicine The tension between data sharing and the protection of privacy in genomics research Communicating results in post-Belmont era biomonitoring studies: lessons from genetics and neuroimaging research Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics Return of individual research results and incidental findings: facing the challenges of translational science Participant use and communication of findings from exome sequencing: a mixed-methods study.Scientists' perspectives on consent in the context of biobanking research.Spectrum of intracranial incidental findings on pediatric brain magnetic resonance imaging: What clinician should know?Incidental findings on brain magnetic resonance imaging: systematic review and meta-analysis A system for addressing incidental findings in neuroimaging research Incidental findings found in "healthy" volunteers during imaging performed for research: current legal and ethical implications Genomics really gets personal: how exome and whole genome sequencing challenge the ethical framework of human genetics research Ethical considerations of research policy for personal genome analysis: the approach of the Genome Science Project in Japan Evaluating the consent preferences of UK research volunteers for genetic and clinical studies Do researchers have an obligation to actively look for genetic incidental findings?Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research setting Online questionnaire development: using film to engage participants and then gather attitudes towards the sharing of genomic data Biobanking: The Melding of Research with Clinical Care Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network Offering aggregate results to participants in genomic research: opportunities and challenges Biobanking in pediatrics: the human nonsubjects approach Ethical implications of the use of whole genome methods in medical research Handling ethical, legal and social issues in birth cohort studies involving genetic research: responses from studies in six countries Following the giant's paces-governance issues and bioethical reflections in China.Advising patients about obtaining genomic profiles.Short read (next-generation) sequencing: a tutorial with cardiomyopathy diagnostics as an exemplar.Recommendations for ethical approaches to genotype-driven research recruitment.Public preferences regarding the return of individual genetic research results: findings from a qualitative focus group study Incidental findings in youths volunteering for brain MRI research.Disclosing incidental findings in brain research: the rights of minors in decision-making.Precision medicine in the age of big data: The present and future role of large-scale unbiased sequencing in drug discovery and development.Findings made in gene panel to whole genome sequencing: data, knowledge, ethics - and consequences?Structural brain anomalies in healthy adolescents in the NCANDA cohort: relation to neuropsychological test performance, sex, and ethnicity.Whole genome scanning: resolving clinical diagnosis and management amidst complex data.The bioethics of stem cell research and therapy Self-guided management of exome and whole-genome sequencing results: changing the results return model.

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P2860

Managing incidental findings in human subjects research: analysis and recommendations.

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Managing incidental findings in human subjects research: analysis and recommendations.

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Managing incidental findings in human subjects research: analysis and recommendations.

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Managing incidental findings in human subjects research: analysis and recommendations.

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J.1748-720X.2008.00266.X

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Journal of Law, Medicine, and Ethics

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Managing incidental findings in human subjects research: analysis and recommendations.

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Bonnie S Leroy

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Brian Van Ness

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Charles A Nelson

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Dale Hammerschmidt

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Elizabeth G McFarland

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Frances P Lawrenz

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Jeffrey P Kahn

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Joel G Fletcher

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Jordan Paradise

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Judy Illes

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P2860

Research ethics recommendations for whole-genome research: consensus statement

Guidelines for Management of Small Pulmonary Nodules Detected on CT Scans: A Statement from the Fleischner Society 1

Findings on brain MRI from research studies of occupational exposure to known neurotoxicants

The personal genome project

Ethical issues with genetic testing in pediatrics

Incidentalomas. A disease of modern technology

When "minimal risk" research yields clinically-significant data, maybe the risks aren't so minimal.

Incidental extracolonic findings at CT colonography.

What makes clinical research ethical?

Legal and ethical issues in neuroimaging research: human subjects protection, medical privacy, and the public communication of research results.

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219-48, 211

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10.1111/J.1748-720X.2008.00266.X

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2

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Ellen Wright Clayton

Barbara A Koenig

Sharon F. Terry

Benjamin S Wilfond

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2008-01-01T00:00:00Z

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human subject research

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