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Genome-wide association studies of brain imaging phenotypes in UK Biobank.
Elliott, Lloyd T; Sharp, Kevin; Alfaro-Almagro, Fidel; Shi, Sinan; Miller, Karla L; Douaud, Gwenaëlle; Marchini, Jonathan; Smith, Stephen M.
Afiliación
  • Elliott LT; Department of Statistics, University of Oxford, Oxford, UK.
  • Sharp K; Department of Statistics, University of Oxford, Oxford, UK.
  • Alfaro-Almagro F; Centre for Functional MRI of the Brain (FMRIB), Wellcome Centre for Integrative Neuroimaging, University of Oxford, Oxford, UK.
  • Shi S; Department of Statistics, University of Oxford, Oxford, UK.
  • Miller KL; Centre for Functional MRI of the Brain (FMRIB), Wellcome Centre for Integrative Neuroimaging, University of Oxford, Oxford, UK.
  • Douaud G; Centre for Functional MRI of the Brain (FMRIB), Wellcome Centre for Integrative Neuroimaging, University of Oxford, Oxford, UK.
  • Marchini J; Department of Statistics, University of Oxford, Oxford, UK. marchini@stats.ox.ac.uk.
  • Smith SM; The Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK. marchini@stats.ox.ac.uk.
Nature ; 562(7726): 210-216, 2018 10.
Article en En | MEDLINE | ID: mdl-30305740
ABSTRACT
The genetic architecture of brain structure and function is largely unknown. To investigate this, we carried out genome-wide association studies of 3,144 functional and structural brain imaging phenotypes from UK Biobank (discovery dataset 8,428 subjects). Here we show that many of these phenotypes are heritable. We identify 148 clusters of associations between single nucleotide polymorphisms and imaging phenotypes that replicate at P < 0.05, when we would expect 21 to replicate by chance. Notable significant, interpretable associations include iron transport and storage genes, related to magnetic susceptibility of subcortical brain tissue; extracellular matrix and epidermal growth factor genes, associated with white matter micro-structure and lesions; genes that regulate mid-line axon development, associated with organization of the pontine crossing tract; and overall 17 genes involved in development, pathway signalling and plasticity. Our results provide insights into the genetic architecture of the brain that are relevant to neurological and psychiatric disorders, brain development and ageing.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenotipo / Encéfalo / Bancos de Muestras Biológicas / Polimorfismo de Nucleótido Simple / Herencia / Estudio de Asociación del Genoma Completo / Neuroimagen Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Nature Año: 2018 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fenotipo / Encéfalo / Bancos de Muestras Biológicas / Polimorfismo de Nucleótido Simple / Herencia / Estudio de Asociación del Genoma Completo / Neuroimagen Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male País/Región como asunto: Europa Idioma: En Revista: Nature Año: 2018 Tipo del documento: Article País de afiliación: Reino Unido