Managing clinically significant findings in research: The UK10K example

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dc.identifier.uri http://dx.doi.org/10.15488/1073
dc.identifier.uri http://www.repo.uni-hannover.de/handle/123456789/1097
dc.contributor.author Kaye, Jane
dc.contributor.author Hurles, Matthew
dc.contributor.author Griffin, Heather
dc.contributor.author Grewal, Jasjote
dc.contributor.author Bobrow, Martin
dc.contributor.author Timpson, Nic
dc.contributor.author Smee, Carol
dc.contributor.author Bolton, Patrick
dc.contributor.author Durbin, Richard
dc.contributor.author Dyke, Stephanie
dc.contributor.author Fitzpatrick, David
dc.contributor.author Kennedy, Karen
dc.contributor.author Kent, Alastair
dc.contributor.author Muddyman, Dawn
dc.contributor.author Muntoni, Francesco
dc.contributor.author Raymond, Lucy F.
dc.contributor.author Semple, Robert
dc.contributor.author Spector, Tim
dc.date.accessioned 2017-01-27T08:36:56Z
dc.date.available 2017-01-27T08:36:56Z
dc.date.issued 2014
dc.identifier.citation Kaye, J.; Hurles, M.; Griffin, H.; Grewal, Jasote; Bobrow, M. et al.: Managing clinically significant findings in research: The UK10K example. In: European Journal of Human Genetics 22 (2014), Nr. 9, S. 1100-1104. DOI: https://doi.org/10.1038/ejhg.2013.290
dc.description.abstract Recent advances in sequencing technology allow data on the human genome to be generated more quickly and in greater detail than ever before. Such detail includes findings that may be of significance to the health of the research participant involved. Although research studies generally do not feed back information on clinically significant findings (CSFs) to participants, this stance is increasingly being questioned. There may be difficulties and risks in feeding clinically significant information back to research participants, however, the UK10K consortium sought to address these by creating a detailed management pathway. This was not intended to create any obligation upon the researchers to feed back any CSFs they discovered. Instead, it provides a mechanism to ensure that any such findings can be passed on to the participant where appropriate. This paper describes this mechanism and the specific criteria, which must be fulfilled in order for a finding and participant to qualify for feedback. This mechanism could be used by future research consortia, and may also assist in the development of sound principles for dealing with CSFs. © 2014 Macmillan Publishers Limited All rights reserved. eng
dc.description.sponsorship Wellcome Trust/WT091310
dc.description.sponsorship Wellcome Trust/WT096599/2/11/Z
dc.language.iso eng
dc.publisher London : Nature Publishing Group
dc.relation.ispartofseries European Journal of Human Genetics 22 (2014), Nr. 9
dc.rights CC BY 3.0 Unported
dc.rights.uri https://creativecommons.org/licenses/by/3.0/
dc.subject consortia eng
dc.subject ethics eng
dc.subject incidental findings eng
dc.subject management pathway eng
dc.subject research eng
dc.subject sequencing eng
dc.subject article eng
dc.subject clinical genetics eng
dc.subject clinical research eng
dc.subject clinically significant finding eng
dc.subject feedback system eng
dc.subject gene sequence eng
dc.subject genetic counseling eng
dc.subject genetic variability eng
dc.subject human eng
dc.subject human genome eng
dc.subject incidental finding eng
dc.subject informed consent eng
dc.subject interpersonal communication eng
dc.subject lifespan eng
dc.subject.ddc 500 | Naturwissenschaften ger
dc.subject.ddc 570 | Biowissenschaften, Biologie ger
dc.title Managing clinically significant findings in research: The UK10K example
dc.type Article
dc.type Text
dc.relation.issn 1018-4813
dc.relation.doi https://doi.org/10.1038/ejhg.2013.290
dc.bibliographicCitation.issue 9
dc.bibliographicCitation.volume 22
dc.bibliographicCitation.firstPage 1100
dc.bibliographicCitation.lastPage 1104
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


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