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Ethical concerns on sharing genomic data including patients' family members.
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Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?
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Balancing the risks and benefits of genomic data sharing: genome research participants' perspectives.
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Research participants' attitudes towards the confidentiality of genomic sequence information.
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Attitudes of research participants and the general public towards genomic data sharing: a systematic literature review.
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Participants' recall and understanding of genomic research and large-scale data sharing.
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Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.
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Australian Attitudes Towards Waivers of Consent Within the Context of Genomic Data Sharing.
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Consent as a compositional act - a framework that provides clarity for the retention and use of data.
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Research biobank participants attitudes towards genetic exceptionalism and health record confidentiality.
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A systematic literature review of the 'commercialisation effect' on public attitudes towards biobank and genomic data repositories.
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Ethical and social reflections on the proposed European Health Data Space.
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"My Blood, You Know, My Biology Being out There…": Consent and Participant Control of Biological Samples.
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Studying the impact of translational genomic research: Lessons from eMERGE.
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Australian public perspectives on genomic data governance: responsibility, regulation, and logistical considerations.
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Genetic and Genomic Researchers' Perspectives on Biological Sample Sharing in Collaborative Research in Uganda: A Qualitative Study.
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本文引用的文献

1
Public and biobank participant attitudes toward genetic research participation and data sharing.
Public Health Genomics. 2010;13(6):368-77. doi: 10.1159/000276767. Epub 2010 Jan 15.
2
Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.
PLoS Genet. 2009 Nov;5(11):e1000730. doi: 10.1371/journal.pgen.1000730. Epub 2009 Nov 20.
3
Public opinion about the importance of privacy in biobank research.
Am J Hum Genet. 2009 Nov;85(5):643-54. doi: 10.1016/j.ajhg.2009.10.002. Epub 2009 Oct 29.
4
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.
Nat Genet. 2009 Nov;41(11):1191-8. doi: 10.1038/ng.466. Epub 2009 Oct 11.
5
Public access to genome-wide data: five views on balancing research with privacy and protection.
PLoS Genet. 2009 Oct;5(10):e1000665. doi: 10.1371/journal.pgen.1000665. Epub 2009 Oct 2.
6
The ethical use of existing samples for genome research.
Genet Med. 2009 Oct;11(10):712-5. doi: 10.1097/GIM.0b013e3181b2e168.
7
Trust in health research relationships: accounts of human subjects.
J Empir Res Hum Res Ethics. 2008 Dec;3(4):35-47. doi: 10.1525/jer.2008.3.4.35.
9
Data sharing in genomics--re-shaping scientific practice.
Nat Rev Genet. 2009 May;10(5):331-5. doi: 10.1038/nrg2573.
10
Different patterns of cerebral injury in dementia with or without diabetes.
Arch Neurol. 2009 Mar;66(3):315-22. doi: 10.1001/archneurol.2008.579. Epub 2009 Jan 12.

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