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Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental survey.
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Genomics and policymaking: from static models to complex systems?
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Informed consent in biobank research: a deliberative approach to the debate.
Soc Sci Med. 2009 Feb;68(4):781-9. doi: 10.1016/j.socscimed.2008.11.020. Epub 2008 Dec 16.
5
Genotype-phenotype databases: challenges and solutions for the post-genomic era.
Nat Rev Genet. 2009 Jan;10(1):9-18. doi: 10.1038/nrg2483.
6
Patients' views on identifiability of samples and informed consent for genetic research.
Am J Bioeth. 2008 Oct;8(10):62-70. doi: 10.1080/15265160802478404.
7
Ethical and practical issues associated with aggregating databases.
PLoS Med. 2008 Sep 23;5(9):e190. doi: 10.1371/journal.pmed.0050190.
8
Informed consent in the genomics era.
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Development of a large-scale de-identified DNA biobank to enable personalized medicine.
Clin Pharmacol Ther. 2008 Sep;84(3):362-9. doi: 10.1038/clpt.2008.89. Epub 2008 May 21.

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