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Accès ouvert déclaré 2022 article

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

137Citations signalées, ce qui n’est pas une note de qualité
86Institutions déclarées
16Pays d’affiliation déclarés

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Le résumé fourni par la source

The use of spoken and written language is a fundamental human capacity. Individual differences in reading- and language-related skills are influenced by genetic variation, with twin-based heritability estimates of 30 to 80% depending on the trait. The genetic architecture is complex, heterogeneous, and multifactorial, but investigations of contributions of single-nucleotide polymorphisms (SNPs) were thus far underpowered. We present a multicohort genome-wide association study (GWAS) of five traits assessed individually using psychometric measures (word reading, nonword reading, spelling, phoneme awareness, and nonword repetition) in samples of 13,633 to 33,959 participants aged 5 to 26 y. We identified genome-wide significant association with word reading (rs11208009, P = 1.098 × 10 −8 ) at a locus that has not been associated with intelligence or educational attainment. All five reading-/language-related traits showed robust SNP heritability, accounting for 13 to 26% of trait variability. Genomic structural equation modeling revealed a shared genetic factor explaining most of the variation in word/nonword reading, spelling, and phoneme awareness, which only partially overlapped with genetic variation contributing to nonword repetition, intelligence, and educational attainment. A multivariate GWAS of word/nonword reading, spelling, and phoneme awareness maximized power for follow-up investigation. Genetic correlation analysis with neuroimaging traits identified an association with the surface area of the banks of the left superior temporal sulcus, a brain region linked to the processing of spoken and written language. Heritability was enriched for genomic elements regulating gene expression in the fetal brain and in chromosomal regions that are depleted of Neanderthal variants. Together, these results provide avenues for deciphering the biological underpinnings of uniquely human traits.

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Le contrôle bibliographique ouvert

DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people
Date Crossref
23/08/2022
Éditeur
National Academy of Sciences
Type
journal-article

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.

Les institutions déclarées

Max Planck Institute for PsycholinguisticsHelmholtz MunichVrije Universiteit AmsterdamHunter Medical Research InstituteUniversity of Newcastle AustraliaPediatrics and GeneticsKing's College LondonUniversity of BristolQIMR Berghofer Medical Research InstituteUniversity Health NetworkKrembil Research InstituteUniversity of InsubriaIstituto Neurologico MediterraneoMax Planck Institute of PsychiatryUniversity of St AndrewsRoyal Holloway University of LondonUniversity of TorontoErasmus MCAmsterdam NeuroscienceAmsterdam UMC Location Vrije Universiteit AmsterdamTUM KlinikumTechnical University of MunichUniversity of EdinburghHospital for Sick ChildrenMaastricht UniversityAarhus UniversityLundbeck FoundationCentre National de la Recherche ScientifiqueInstitut PasteurUniversité Paris CitéGènes, synapses et cognitionUniversity of ZurichHeidelberg UniversityUniversity Hospital HeidelbergETH ZurichCentral Institute of Mental HealthSwiss Integrative Center for Human HealthOxford Brookes UniversityUniversity of BolognaUniversity of PannoniaHUN-REN Research Centre for Natural SciencesUniversity of New MexicoUniversity of AmsterdamUniversity of Colorado BoulderUniversity of LausanneUniversity of YorkUniversity of OxfordUniversity of HelsinkiKarolinska InstitutetFolkhälsans ForskningscentrumSickKids FoundationUniversity of IowaUniversity of GrazBioTechMed-GrazMcGill UniversityUniversity of JyväskyläChinese University of Hong KongLudwig-Maximilians-Universität MünchenTufts UniversityRoyal Children's HospitalThe University of MelbourneSpeech Pathology AustraliaMurdoch Children's Research InstituteUniversity Hospital BonnJohn Hunter HospitalUniversity of DenverLaboratoire de Sciences Cognitives et PsycholinguistiqueÉcole des hautes études en sciences socialesUniversité du Québec à ChicoutimiUniversity of Nebraska Medical CenterAston UniversityHarvard UniversityThe University of QueenslandHersenstichtingIkerbasqueUniversity of the Basque CountryBasque Center on Cognition, Brain and LanguageUniversity of LiverpoolCentre Hospitalier Universitaire Sainte-JustineUniversité de MontréalGriffith UniversityThe Kids Research Institute AustraliaThe University of Western AustraliaRadboud University NijmegenUniversity Medical CenterRadboud University Medical Center

Une affiliation ne permet pas de déduire la nationalité d’un auteur.

Les sujets associés

Reading and Literacy DevelopmentGenetics and Neurodevelopmental DisordersGenetic Associations and Epidemiology

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