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dc.contributor.authorUrsin, Lars
dc.contributor.authorSteinsbekk, Kristin Solum
dc.date.accessioned2015-01-29T14:51:16Z
dc.date.accessioned2015-08-24T11:02:04Z
dc.date.available2015-01-29T14:51:16Z
dc.date.available2015-08-24T11:02:04Z
dc.date.issued2012
dc.identifier.citationNorsk Epidemiologi 2012, 21(2):269-276nb_NO
dc.identifier.issn0803-2491
dc.identifier.urihttp://hdl.handle.net/11250/297885
dc.description.abstractBiobank research deals with personal information and data from blood and tissue analysis, making the questions of legitimate recruitment of participants and handling of their data to be intimately connected with the issue of privacy. Thus, identification of the privacy interests of biobank participants is vital to the legitimacy of biobank projects. In this article, we ask: How do participants articulate the nature of privacy issues in biobanking? Here we report from a focus group study on biobank participants’ view of privacy and consent in relation to biobank research. Based on our analysis, we found that participants viewed privacy as a concept that describes several dimensions of the fundamental need to be recognized and respected as an individual and as a person. Interestingly, the needs to be recognized and respected were also viewed as the basic purpose of biobank consent.nb_NO
dc.language.isoengnb_NO
dc.publisherNTNUnb_NO
dc.titlePeeking into the black box of privacy - biobank participants on the importance of recognitionnb_NO
dc.typeJournal articlenb_NO
dc.typePeer revieweden_GB
dc.date.updated2015-01-29T14:51:16Z
dc.source.volume21nb_NO
dc.source.journalNorsk Epidemiologinb_NO
dc.source.issue2nb_NO
dc.identifier.cristin946346
dc.description.localcodeThis work is licensed under a Creative Commons Attribution 3.0 License.nb_NO


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