Simplifying informed consent for biorepositories: stakeholder perspectives
about
Attitudes of research participants and the general public towards genomic data sharing: a systematic literature reviewThe MICHR Genomic DNA BioLibrary: An Empirical Study of the Ethics of Biorepository DevelopmentInformed Consent in Genome-Scale Research: What Do Prospective Participants Think?Participants' recall and understanding of genomic research and large-scale data sharing.Improving biobank consent comprehension: a national randomized survey to assess the effect of a simplified form and review/retest interventionDeveloping a simplified consent form for biobanking.Bio-collections in autism research.Broad data sharing in genetic research: views of institutional review board professionals.Strategies for enrollment of African Americans into cancer genetic studies.The translational potential of research on the ethical, legal, and social implications of genomicsEthical aspects of human biobanks: a systematic review.Informed consent for biobanking: consensus-based guidelines for adequate comprehension.Demographic differences in willingness to provide broad and narrow consent for biobank research.Informed consent and genomic incidental findings: IRB chair perspectives.Specimen collection for induced pluripotent stem cell research: harmonizing the approach to informed consentLessons from HeLa Cells: The Ethics and Policy of Biospecimens.Factors influencing public participation in biobanking.IRB decision-making with imperfect knowledge: a framework for evidence-based research ethics review.Informed consent for human genetic and genomic studies: a systematic review.Ethical issues of informed consent in malaria research proposals submitted to a research ethics committee in Thailand: a retrospective document review.How do clinical genetics consent forms address the familial approach to confidentiality and incidental findings? A mixed-methods study.Views of Cohort Study Participants about Returning Research Results in the Context of Precision Medicine.An Assessment of a Shortened Consent Form for the Storage and Research Use of Residual Newborn Screening Blood Spots.Risk, reward, and the double-edged sword: perspectives on pharmacogenetic research and clinical testing among Alaska Native people.Experiences with obtaining informed consent for genomic sequencing.
P2860
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P2860
Simplifying informed consent for biorepositories: stakeholder perspectives
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Simplifying informed consent for biorepositories: stakeholder perspectives
@ast
Simplifying informed consent for biorepositories: stakeholder perspectives
@en
type
label
Simplifying informed consent for biorepositories: stakeholder perspectives
@ast
Simplifying informed consent for biorepositories: stakeholder perspectives
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prefLabel
Simplifying informed consent for biorepositories: stakeholder perspectives
@ast
Simplifying informed consent for biorepositories: stakeholder perspectives
@en
P2093
P2860
P1433
P1476
Simplifying informed consent for biorepositories: stakeholder perspectives
@en
P2093
Joëlle Y Friedman
Kevin P Weinfurt
N Chantelle Hardy
P2860
P2888
P304
P356
10.1097/GIM.0B013E3181EAD64D
P407
P577
2010-09-01T00:00:00Z
P6179
1035640678