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dc.contributor.authorGudmundsson, Ólafur Ó.en_US
dc.contributor.authorWalters, Gudmundur Bragien_US
dc.contributor.authorIngason, Andrésen_US
dc.contributor.authorJohansson, Stefanen_US
dc.contributor.authorZayats, Tetyanaen_US
dc.contributor.authorAthanasiu, Laviniaen_US
dc.contributor.authorSønderby, Ida Elkenen_US
dc.contributor.authorGustafsson, Omaren_US
dc.contributor.authorNawaz, Muhammad Sulamanen_US
dc.contributor.authorJónsson, Gudbjörn F.en_US
dc.contributor.authorJónsson, Linaen_US
dc.contributor.authorKnappskog, Peren_US
dc.contributor.authorIngvarsdóttir, Esteren_US
dc.contributor.authorDavidsdóttir, Katrinen_US
dc.contributor.authorDjurovic, Srdjanen_US
dc.contributor.authorKnudsen, Gun Peggy Strømstaden_US
dc.contributor.authorAskeland, Ragna Buggeen_US
dc.contributor.authorHaraldsdóttir, Gyda S.en_US
dc.contributor.authorBaldursson, Gíslien_US
dc.contributor.authorMagnússon, Pállen_US
dc.contributor.authorSigurdsson, Engilberten_US
dc.contributor.authorGudbjartsson, Daníel Fannaren_US
dc.contributor.authorStéfansson, Hreinnen_US
dc.contributor.authorAndreassen, Ole Andreasen_US
dc.contributor.authorHaavik, Janen_US
dc.contributor.authorReichborn-Kjennerud, Teden_US
dc.contributor.authorStefánsson, Kárien_US
dc.date.accessioned2020-06-24T12:20:32Z
dc.date.available2020-06-24T12:20:32Z
dc.date.issued2019-10-17
dc.PublishedGudmundsson, Walters, Ingason A, Johansson S, Zayats T, Athanasiu L, Sønderby IE, Gustafsson O, Nawaz, Jónsson, Jónsson, Knappskog PM, Ingvarsdóttir, Davidsdóttir, Djurovic S, Knudsen GPS, Askeland RB, Haraldsdóttir, Baldursson, Magnússon P, Sigurdsson E, Gudbjartsson DF, Stéfansson, Andreassen OA, Haavik J, Reichborn-Kjennerud T, Stefánsson K. Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder. Translational psychiatry. 2019;9:258eng
dc.identifier.issn2158-3188
dc.identifier.urihttps://hdl.handle.net/1956/22933
dc.description.abstractAttention-deficit/hyperactivity disorder (ADHD) is a highly heritable common childhood-onset neurodevelopmental disorder. Some rare copy number variations (CNVs) affect multiple neurodevelopmental disorders such as intellectual disability, autism spectrum disorders (ASD), schizophrenia and ADHD. The aim of this study is to determine to what extent ADHD shares high risk CNV alleles with schizophrenia and ASD. We compiled 19 neuropsychiatric CNVs and test 14, with sufficient power, for association with ADHD in Icelandic and Norwegian samples. Eight associate with ADHD; deletions at 2p16.3 (NRXN1), 15q11.2, 15q13.3 (BP4 & BP4.5–BP5) and 22q11.21, and duplications at 1q21.1 distal, 16p11.2 proximal, 16p13.11 and 22q11.21. Six of the CNVs have not been associated with ADHD before. As a group, the 19 CNVs associate with ADHD (OR = 2.43, P = 1.6 × 10−21), even when comorbid ASD and schizophrenia are excluded from the sample. These results highlight the pleiotropic effect of the neuropsychiatric CNVs and add evidence for ADHD, ASD and schizophrenia being related neurodevelopmental disorders rather than distinct entities.en_US
dc.language.isoengeng
dc.publisherNatureeng
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/4.0eng
dc.titleAttention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorderen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2019-12-20T11:19:42Z
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2019 The Author(s)
dc.identifier.doihttps://doi.org/10.1038/s41398-019-0599-y
dc.identifier.cristin1750441
dc.source.journalTranslational psychiatry


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