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dc.contributor.authorChang, A-M
dc.contributor.authorDuffy, JF
dc.contributor.authorBuxton, OM
dc.contributor.authorLane, JM
dc.contributor.authorAeschbach, D
dc.contributor.authorAnderson, C
dc.contributor.authorBjonnes, AC
dc.contributor.authorCain, SW
dc.contributor.authorCohen, DA
dc.contributor.authorFrayling, TM
dc.contributor.authorGooley, JJ
dc.contributor.authorJones, SE
dc.contributor.authorKlerman, EB
dc.contributor.authorLockley, SW
dc.contributor.authorMunch, M
dc.contributor.authorRajaratnam, SMW
dc.contributor.authorRueger, M
dc.contributor.authorRutter, MK
dc.contributor.authorSanthi, N
dc.contributor.authorScheuermaier, K
dc.contributor.authorVan Reen, E
dc.contributor.authorWeedon, MN
dc.contributor.authorCzeisler, CA
dc.contributor.authorScheer, FAJL
dc.contributor.authorSaxena, R
dc.date.accessioned2019-04-02T12:05:07Z
dc.date.issued2019-03-29
dc.description.abstractThe PERIOD2 (PER2) gene is a core molecular component of the circadian clock and plays an important role in the generation and maintenance of daily rhythms. rs35333999, a missense variant of PER2 common in European populations, has been shown to associate with later chronotype. Chronotype relates to the timing of biological and behavioral activities, including when we sleep, eat, and exercise, and later chronotype is associated with longer intrinsic circadian period (cycle length), a fundamental property of the circadian system. Thus, we tested whether this PER2 variant was associated with circadian period and found significant associations with longer intrinsic circadian period as measured under forced desynchrony protocols, the ‘gold standard’ for intrinsic circadian period assessment. Minor allele (T) carriers exhibited significantly longer circadian periods when determinations were based on either core body temperature or plasma melatonin measurements, as compared to non-carriers (by 12 and 11 min, respectively; accounting for ~7% of inter-individual variance). These findings provide a possible underlying biological mechanism for inter-individual differences in chronotype, and support the central role of PER2 in the human circadian timing system.en_GB
dc.description.sponsorshipEuropean Commissionen_GB
dc.description.sponsorshipWellcome Trusten_GB
dc.description.sponsorshipMedical Research Council (MRC)en_GB
dc.identifier.citationVol. 9, article 5350en_GB
dc.identifier.doi10.1038/s41598-019-41712-1
dc.identifier.grantnumberMR/P012167/1en_GB
dc.identifier.urihttp://hdl.handle.net/10871/36704
dc.language.isoenen_GB
dc.publisherNature Researchen_GB
dc.rights© The Author(s) 2019. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.en_GB
dc.subjectCircadian rhythmen_GB
dc.subjectHuman geneticsen_GB
dc.subjectPER2en_GB
dc.subjectSleepen_GB
dc.subjectBody clocken_GB
dc.titleChronotype Genetic Variant in PER2 is Associated with Intrinsic Circadian Period in Humansen_GB
dc.typeArticleen_GB
dc.date.available2019-04-02T12:05:07Z
dc.identifier.issn2045-2322
dc.descriptionThis is the final version. Available on open access from Nature Research via the DOI in this recorden_GB
dc.descriptionData Availability: The data that support the findings of this study from the UK BioBank will be made available at https://sleepgenetics.org and the underlying genotype and phenotype data are available through application to the UK Biobank. Other phenotype data are available on request, due to privacy or other restrictions, through co-corresponding author Dr. Scheer (fscheer@bwh.harvard.edu).en_GB
dc.identifier.journalScientific Reportsen_GB
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2019-03-14
exeter.funder::European Commissionen_GB
exeter.funder::Wellcome Trusten_GB
exeter.funder::Medical Research Council (MRC)en_GB
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2019-03-14
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2019-04-02T08:45:56Z
refterms.versionFCDAM
refterms.dateFOA2019-04-02T12:05:10Z
refterms.panelAen_GB


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© The Author(s) 2019. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International
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Except where otherwise noted, this item's licence is described as © The Author(s) 2019. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.