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Obtaining valid consent for doing large genetic studies in developing countries

Genetic research has the potential to improve global health by discovering what makes people susceptible or resistant to certain diseases, and what causes the diseases themselves, thereby guiding prevention efforts. Genetic studies, for example, are providing clues for scientists working on vaccines against HIV, malaria, and TB. But it is crucial, say Dave Chokshi (Wellcome Trust Centre for Human Genetics, University of Oxford) and colleagues in a policy paper in PLoS Medicine, to ensure that those who choose to participate in such research have given their fully informed consent.

While there has been much discussion setting out ethical principles for conducting medical research in low-income countries, there has been little discussion of how to apply these principles to large-scale genomic studies. The authors lay out a new set of ethical principles for obtaining ethically valid consent for such studies conducted in the developing world.

Citation: Chokshi DA, Thera MA, Parker M, Diakite M, Makani J, et al. (2007) Valid consent for genomic epidemiology in developing countries. PLoS Med 4(4): e95.

PLEASE ADD THE LINK TO THE PUBLISHED ARTICLE IN ONLINE VERSIONS OF YOUR REPORT: http://medicine.plosjournals.org/perlserv/?request=get-document&doi=10.1371/journal.pmed.0040095

PRESS-ONLY PREVIEW OF THE ARTICLE: http://www.plos.org/press/plme-04-04-chokshi.pdf

CONTACT:

Dave Chokshi
University of Pennsylvania
School of Medicine
3434 Sansom St.
Philadelphia, PA PA 19104
United States of America
+1 225-354-6673
daveash@med.upenn.edu


ALSO FROM THE PLoS MEDICINE MAGAZINE SECTION:

A case of unstable blood pressure


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Contact: Andrew Hyde
press@plos.org
44-122-346-3330
Public Library of Science
23-Apr-2007


Page: 1 2

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