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dc.contributor.authorNethander, Maria
dc.contributor.authorMovérare-Skrtic, Sofia
dc.contributor.authorKämpe, Anders
dc.contributor.authorCoward, Eivind
dc.contributor.authorReimann, Ene
dc.contributor.authorGrahnemo, Louise
dc.contributor.authorBorbély, Éva
dc.contributor.authorHelyes, Zsuzsanna
dc.contributor.authorFunck-Brentano, Thomas
dc.contributor.authorCohen-Solal, Martine
dc.contributor.authorTuukkanen, Juha
dc.contributor.authorKoskela, Antti
dc.contributor.authorWu, Jianyao
dc.contributor.authorLi, Lei
dc.contributor.authorLu, Tianyuan
dc.contributor.authorGabrielsen, Maiken Elvestad
dc.contributor.authorMägi, Reedik
dc.contributor.authorHoff, Mari
dc.contributor.authorLerner, Ulf H.
dc.contributor.authorHenning, Petra
dc.contributor.authorUllum, Henrik
dc.contributor.authorErikstrup, Christian
dc.contributor.authorBrunak, Søren
dc.contributor.authorOstrowski, Sisse Rye
dc.contributor.authorLanghammer, Arnulf
dc.contributor.authorTuomi, Tiinamaija
dc.contributor.authorOddsson, Asmundur
dc.contributor.authorStefansson, Kari
dc.contributor.authorPettersson-Kymmer, Ulrika
dc.contributor.authorPedersen, Ole Birger Vesterager
dc.contributor.authorStyrkarsdottir, Unnur
dc.contributor.authorMäkitie, Outi
dc.contributor.authorHveem, Kristian
dc.contributor.authorRichards, J. Brent
dc.contributor.authorOhlsson, Claes
dc.date.accessioned2024-06-14T06:41:21Z
dc.date.available2024-06-14T06:41:21Z
dc.date.created2023-11-28T12:32:33Z
dc.date.issued2023
dc.identifier.citationNature Genetics. 2023, 55 (11), 1820-1830.en_US
dc.identifier.issn1061-4036
dc.identifier.urihttps://hdl.handle.net/11250/3133984
dc.description.abstractOsteoporotic fracture is among the most common and costly of diseases. While reasonably heritable, its genetic determinants have remained elusive. Forearm fractures are the most common clinically recognized osteoporotic fractures with a relatively high heritability. To establish an atlas of the genetic determinants of forearm fractures, we performed genome-wide association analyses including 100,026 forearm fracture cases. We identified 43 loci, including 26 new fracture loci. Although most fracture loci associated with bone mineral density, we also identified loci that primarily regulate bone quality parameters. Functional studies of one such locus, at TAC4, revealed that Tac4–/– mice have reduced mechanical bone strength. The strongest forearm fracture signal, at WNT16, displayed remarkable bone-site-specificity with no association with hip fractures. Tall stature and low body mass index were identified as new causal risk factors for fractures. The insights from this atlas may improve fracture prediction and enable therapeutic development to prevent fractures.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleAn atlas of genetic determinants of forearm fractureen_US
dc.title.alternativeAn atlas of genetic determinants of forearm fractureen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1820-1830en_US
dc.source.volume55en_US
dc.source.journalNature Geneticsen_US
dc.source.issue11en_US
dc.identifier.doi10.1038/s41588-023-01527-3
dc.identifier.cristin2203733
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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