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dc.date.accessioned2024-03-10T18:23:59Z
dc.date.available2024-03-10T18:23:59Z
dc.date.created2024-01-30T15:25:10Z
dc.date.issued2023
dc.identifier.citationVerhoef, Ellen Allegrini, Andrea G. Jansen, Philip R. Lange, Katherine Wang, Carol A. Morgan, Angela Ahluwalia, Tarunveer S. Symeonides, Christos Eising, Else Franken, Marie-Christine Hypponen, Elina Mansell, Toby Olislagers, Mitchell Omerovic, Emina Rimfeld, Kaili Schlag, Fenja Selzam, Saskia Shapland, Chin Yang Tiemeier, Henning Whitehouse, Andrew J.O. Saffery, Richard Bønnelykke, Klaus Reilly, Sheena Pennell, Craig E. Wake, Melissa Cecil, Charlotte A. M. Plomin, Robert Fisher, Simon E. St Pourcain, Beate Andreassen, Ole Bartels, Meike Boomsma, Dorret Dale, Philip S. Ehli, Erik Fernandez-Orth, Dietmar Guxens, Mònica Hakulinen, Christian Harris, Kathleen Mullan Haworth, Simon de Hoyos, Lucía Jaddoe, Vincent Keltikangas-Järvinen, Liisa Lehtimäki, Terho Middeldorp, Christel Min, Josine L. Mishra, Pashupati P. Njølstad, Pål Rasmus Sunyer, Jordi Tate, Ashley E. Timpson, Nicholas van der Laan, Camiel Vrijheid, Martine Vuoksimaa, Eero Whipp, Alyce M. Ystrøm, Eivind . Genome-wide analyses of vocabulary size in infancy and toddlerhood: associations with ADHD, literacy and cognition-related traits. Biological Psychiatry. 2023
dc.identifier.urihttp://hdl.handle.net/10852/109414
dc.description.abstractBackground The number of words children produce (expressive vocabulary) and understand (receptive vocabulary) changes rapidly during early development, partially due to genetic factors. Here, we performed a meta–genome-wide association study of vocabulary acquisition and investigated polygenic overlap with literacy, cognition, developmental phenotypes, and neurodevelopmental conditions, including attention-deficit/hyperactivity disorder (ADHD). Methods We studied 37,913 parent-reported vocabulary size measures (English, Dutch, Danish) for 17,298 children of European descent. Meta-analyses were performed for early-phase expressive (infancy, 15–18 months), late-phase expressive (toddlerhood, 24–38 months), and late-phase receptive (toddlerhood, 24–38 months) vocabulary. Subsequently, we estimated single nucleotide polymorphism–based heritability (SNP-h2) and genetic correlations (rg) and modeled underlying factor structures with multivariate models. Results Early-life vocabulary size was modestly heritable (SNP-h2 = 0.08–0.24). Genetic overlap between infant expressive and toddler receptive vocabulary was negligible (rg = 0.07), although each measure was moderately related to toddler expressive vocabulary (rg = 0.69 and rg = 0.67, respectively), suggesting a multifactorial genetic architecture. Both infant and toddler expressive vocabulary were genetically linked to literacy (e.g., spelling: rg = 0.58 and rg = 0.79, respectively), underlining genetic similarity. However, a genetic association of early-life vocabulary with educational attainment and intelligence emerged only during toddlerhood (e.g., receptive vocabulary and intelligence: rg = 0.36). Increased ADHD risk was genetically associated with larger infant expressive vocabulary (rg = 0.23). Multivariate genetic models in the ALSPAC (Avon Longitudinal Study of Parents and Children) cohort confirmed this finding for ADHD symptoms (e.g., at age 13; rg = 0.54) but showed that the association effect reversed for toddler receptive vocabulary (rg = −0.74), highlighting developmental heterogeneity. Conclusions The genetic architecture of early-life vocabulary changes during development, shaping polygenic association patterns with later-life ADHD, literacy, and cognition-related traits.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleGenome-wide analyses of vocabulary size in infancy and toddlerhood: associations with ADHD, literacy and cognition-related traits
dc.title.alternativeENEngelskEnglishGenome-wide analyses of vocabulary size in infancy and toddlerhood: associations with ADHD, literacy and cognition-related traits
dc.typeJournal article
dc.creator.authorVerhoef, Ellen
dc.creator.authorAllegrini, Andrea G.
dc.creator.authorJansen, Philip R.
dc.creator.authorLange, Katherine
dc.creator.authorWang, Carol A.
dc.creator.authorMorgan, Angela
dc.creator.authorAhluwalia, Tarunveer S.
dc.creator.authorSymeonides, Christos
dc.creator.authorEising, Else
dc.creator.authorFranken, Marie-Christine
dc.creator.authorHypponen, Elina
dc.creator.authorMansell, Toby
dc.creator.authorOlislagers, Mitchell
dc.creator.authorOmerovic, Emina
dc.creator.authorRimfeld, Kaili
dc.creator.authorSchlag, Fenja
dc.creator.authorSelzam, Saskia
dc.creator.authorShapland, Chin Yang
dc.creator.authorTiemeier, Henning
dc.creator.authorWhitehouse, Andrew J.O.
dc.creator.authorSaffery, Richard
dc.creator.authorBønnelykke, Klaus
dc.creator.authorReilly, Sheena
dc.creator.authorPennell, Craig E.
dc.creator.authorWake, Melissa
dc.creator.authorCecil, Charlotte A. M.
dc.creator.authorPlomin, Robert
dc.creator.authorFisher, Simon E.
dc.creator.authorSt Pourcain, Beate
dc.creator.authorAndreassen, Ole
dc.creator.authorBartels, Meike
dc.creator.authorBoomsma, Dorret
dc.creator.authorDale, Philip S.
dc.creator.authorEhli, Erik
dc.creator.authorFernandez-Orth, Dietmar
dc.creator.authorGuxens, Mònica
dc.creator.authorHakulinen, Christian
dc.creator.authorHarris, Kathleen Mullan
dc.creator.authorHaworth, Simon
dc.creator.authorde Hoyos, Lucía
dc.creator.authorJaddoe, Vincent
dc.creator.authorKeltikangas-Järvinen, Liisa
dc.creator.authorLehtimäki, Terho
dc.creator.authorMiddeldorp, Christel
dc.creator.authorMin, Josine L.
dc.creator.authorMishra, Pashupati P.
dc.creator.authorNjølstad, Pål Rasmus
dc.creator.authorSunyer, Jordi
dc.creator.authorTate, Ashley E.
dc.creator.authorTimpson, Nicholas
dc.creator.authorvan der Laan, Camiel
dc.creator.authorVrijheid, Martine
dc.creator.authorVuoksimaa, Eero
dc.creator.authorWhipp, Alyce M.
dc.creator.authorYstrøm, Eivind
cristin.unitcode185,53,46,3
cristin.unitnameK.G. Jebsen senter for utviklingsforstyrrelser
cristin.ispublishedfalse
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin2238554
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Biological Psychiatry&rft.volume=&rft.spage=&rft.date=2023
dc.identifier.jtitleBiological Psychiatry
dc.identifier.doihttps://doi.org/10.1016/j.biopsych.2023.11.025
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn0006-3223
dc.type.versionPublishedVersion
dc.relation.projectNFR/262177
dc.relation.projectNFR/273291
dc.relation.projectHV/Personalized Medicine for Children and Adults
dc.relation.projectNFR/240413
dc.relation.projectNOVO/54741
dc.relation.projectNFR/324252
dc.relation.projectEC/H2020/848158
dc.relation.projectERC/293574
dc.relation.projectNOVO/NNF18OC0052457
dc.relation.projectNFR/288083
dc.relation.projectNFR/223273
dc.relation.projectBFS/Utilizing the Mother and Child Cohort and the Medical Birth
dc.relation.projectOTHER/CPII18/00018
dc.relation.projectOTHER/CEX2018-000806-S
dc.relation.projectOTHER/MC_UU_00032/02


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