Practical guidance on informed consent for pediatric participants in a biorepository - Wikidata - wikimedia - TriplyDB

Practical guidance on informed consent for pediatric participants in a biorepository

Practical guidance on informed consent for pediatric participants in a biorepository

http://www.wikidata.org/entity/Q28650458

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Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.Considerations for Returning Research Results to Culturally Diverse Participants and Families of Decedents.When Participants in Genomic Research Grow Up: Contact and Consent at the Age of Majority Raising Genomic Citizens: Adolescents and the Return of Secondary Genomic Findings.Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience.

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P2860

Practical guidance on informed consent for pediatric participants in a biorepository

http://www.wikidata.org/entity/Q28650458

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2014 nî lūn-bûn

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2014 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Practical guidance on informed consent for pediatric participants in a biorepository

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Practical guidance on informed consent for pediatric participants in a biorepository

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Practical guidance on informed consent for pediatric participants in a biorepository

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Practical guidance on informed consent for pediatric participants in a biorepository

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Practical guidance on informed consent for pediatric participants in a biorepository

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Practical guidance on informed consent for pediatric participants in a biorepository

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Practical guidance on informed consent for pediatric participants in a biorepository

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Practical guidance on informed consent for pediatric participants in a biorepository

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Practical guidance on informed consent for pediatric participants in a biorepository

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J.MAYOCP.2014.07.006

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Mayo Clinic Proceedings

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Practical guidance on informed consent for pediatric participants in a biorepository

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Armand H M Antommaria

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Ellen W Clayton

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Janet L Williams

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Jennifer B McCormick

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John A Lynch

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John J Connolly

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Kyle B Brothers

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Saskia C Sanderson

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Sharon A Aufox

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Wendy A Wolf

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P2860

Ethical and practical challenges of sharing data from genome-wide association studies: the eMERGE Consortium experience

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

Managing incidental findings and research results in genomic research involving biobanks and archived data sets.

Biological sample collections from minors for genetic research: a systematic review of guidelines and position papers.

Ethical and policy issues in genetic testing and screening of children.

Technical report: Ethical and policy issues in genetic testing and screening of children.

Mandatory extended searches in all genome sequencing: "incidental findings," patient autonomy, and shared decision making.

Addressing the ethical challenges in genetic testing and sequencing of children.

Informed consent in pediatric research.

Practical implementation issues and challenges for biobanks in the return of individual research results.

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1471-80

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scholarly article

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10.1016/J.MAYOCP.2014.07.006

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11

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89

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Ellen Wright Clayton

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2014-11-01T00:00:00Z

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25264176

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informed consent

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4254313

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