Models of consent to return of incidental findings in genomic research
about
Incidental Findings with Genomic Testing: Implications for Genetic Counseling PracticeImproving the informed consent process in international collaborative rare disease research: effective consent for effective research.Rethinking the ethical approach to health information management through narration: pertinence of Ricœur's 'little ethics'Findings made in gene panel to whole genome sequencing: data, knowledge, ethics - and consequences?Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.Researchers' views on informed consent for return of secondary results in genomic research.Genomic analysis in the clinic: benefits and challenges for health care professionals and patients in BrazilIllustrative case studies in the return of exome and genome sequencing results.Becoming partners, retaining autonomy: ethical considerations on the development of precision medicine.Ethical Considerations for the Return of Incidental Findings in Ophthalmic Genomic Research.Raising Genomic Citizens: Adolescents and the Return of Secondary Genomic Findings.Ethical challenges in conducting clinical research in lung cancer.Sharpening the cutting edge: additional considerations for the UK debates on embryonic interventions for mitochondrial diseases.Is "incidental finding" the best term?: a study of patients' preferencesRecommendations for the integration of genomics into clinical practiceSocial and Communicative Functions of Informed Consent Forms in East Asia and Beyond.Whole exome sequencing: a state-of-the-art approach for defining (and exploring!) genetic landscapes in pediatric nephrology.Overcoming challenges to meaningful informed consent for whole genome sequencing in pediatric cancer research."Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.Patient understanding of, satisfaction with, and perceived utility of whole-genome sequencing: findings from the MedSeq Project.The Precision Medicine Nation.Clinical providers' experiences with returning results from genomic sequencing: an interview study.Informed Consent in Translational Genomics: Insufficient Without Trustworthy GovernanceGenomics, Big Data, and Broad Consent: a New Ethics Frontier for Prevention ScienceInformed consent for next-generation nucleotide sequencing studies: Aiding communication between participants and investigatorsImproved ethical guidance for the return of results from psychiatric genomics researchMeeting Patients' Right to the Correct Diagnosis: Ongoing International Initiatives on Undiagnosed Rare Diseases and Ethical and Social Issues
P2860
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P2860
Models of consent to return of incidental findings in genomic research
description
2014 nî lūn-bûn
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2014 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2014年の論文
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2014年論文
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2014年論文
@zh-hant
2014年論文
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2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Models of consent to return of incidental findings in genomic research
@ast
Models of consent to return of incidental findings in genomic research
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type
label
Models of consent to return of incidental findings in genomic research
@ast
Models of consent to return of incidental findings in genomic research
@en
prefLabel
Models of consent to return of incidental findings in genomic research
@ast
Models of consent to return of incidental findings in genomic research
@en
P2093
P2860
P356
P1476
Models of consent to return of incidental findings in genomic research
@en
P2093
Cameron R Waldman
Erik Parens
Josue Martinez
Robert Klitzman
W Nicholson Price
Wendy K Chung
P2860
P356
10.1002/HAST.328
P577
2014-06-11T00:00:00Z