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From patients to partners : participant-centric initiatives in biomedical research.

Kaye, Jane (author)
Curren, Liam (author)
Anderson, Nick (author)
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Edwards, Kelly (author)
Fullerton, Stephanie M (author)
Kanellopoulou, Nadja (author)
Lund, David (author)
MacArthur, Daniel G (author)
Mascalzoni, Deborah (author)
Uppsala universitet,Centrum för forsknings- och bioetik
Shepherd, James (author)
Taylor, Patrick L (author)
Terry, Sharon F (author)
Winter, Stefan F (author)
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 (creator_code:org_t)
2012-04-03
2012
English.
In: Nature reviews genetics. - : Springer Science and Business Media LLC. - 1471-0056 .- 1471-0064. ; 13:5, s. 371-6
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Advances in computing technology and bioinformatics mean that medical research is increasingly characterized by large international consortia of researchers that are reliant on large data sets and biobanks. These trends raise a number of challenges for obtaining consent, protecting participant privacy concerns and maintaining public trust. Participant-centred initiatives (PCIs) use social media technologies to address these immediate concerns, but they also provide the basis for long-term interactive partnerships. Here, we give an overview of this rapidly moving field by providing an analysis of the different PCI approaches, as well as the benefits and challenges of implementing PCIs.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Medicinsk etik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Medical Ethics (hsv//eng)

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