Public attitudes regarding the use of electronic health information and residual clinical tissues for research - Wikidata - awgldk - TriplyDB

Public attitudes regarding the use of electronic health information and residual clinical tissues for research

Public attitudes regarding the use of electronic health information and residual clinical tissues for research

http://www.wikidata.org/entity/Q33764068

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Broad Consent for Research With Biological Samples: Workshop Conclusions Public trust in health information sharing: implications for biobanking and electronic health record systems A survey of patient perspectives on the research use of health information and biospecimens Deliberative Discussion Focus Groups.Awareness of risks of biobank research may affect public attitudes toward consent.An Assessment of a Shortened Consent Form for the Storage and Research Use of Residual Newborn Screening Blood Spots.Crushing Consent Under the Weight of Expectations.An empirical assessment of the short-term impacts of a reading of Deborah Zoe Laufer's drama Informed Consent on attitudes and intentions to participate in genetic research.

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P2860

Public attitudes regarding the use of electronic health information and residual clinical tissues for research

http://www.wikidata.org/entity/Q33764068

description

2013 nî lūn-bûn

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2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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Journal of Community Genetics

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Public attitudes regarding the ...... clinical tissues for research

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P2093

Erin Rothwell

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Jeffrey R Botkin

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Joyce Mitchell

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Louisa A Stark

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Rebecca Anderson

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P2860

Active choice but not too active: public perspectives on biobank consent models.

Maximizing results with focus groups: moderator and analysis issues.

Principles of human subjects protections applied in an opt-out, de-identified biobank.

A trial of consent procedures for future research with clinically derived biological samples.

Policy issues and stakeholder concerns regarding the storage and use of residual newborn dried blood samples for research.

Preferences for opt-in and opt-out enrollment and consent models in biobank research: a national survey of Veterans Administration patients.

Two large-scale surveys on community attitudes toward an opt-out biobank.

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s12687-013-0175-8

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