Publicaciones (20) Publicaciones de Amaia Carrión Castillo

2024

  1. Genetic variants for head size share genes and pathways with cancer

    Cell Reports Medicine, Vol. 5, Núm. 5

  2. Imaging genetics of language network functional connectivity reveals links with language-related abilities, dyslexia and handedness

    Communications Biology, Vol. 7, Núm. 1

  3. Insights into the genetic architecture of cerebellar lobules derived from the UK Biobank

    Scientific Reports, Vol. 14, Núm. 1

2023

  1. Brain structure, phenotypic and genetic correlates of reading performance

    Nature Human Behaviour, Vol. 7, Núm. 7, pp. 1120-1134

2022

  1. The genetic architecture of language functional connectivity

    NeuroImage, Vol. 249

2021

  1. Global and regional development of the human cerebral cortex: Molecular architecture and occupational aptitudes

    Cerebral Cortex, Vol. 30, Núm. 7, pp. 4121-4139

  2. Handedness and its genetic influences are associated with structural asymmetries of the cerebral cortex in 31,864 individuals

    Proceedings of the National Academy of Sciences of the United States of America, Vol. 118, Núm. 47

  3. Large-Scale Phenomic and Genomic Analysis of Brain Asymmetrical Skew

    Cerebral Cortex, Vol. 31, Núm. 9, pp. 4151-4168

  4. The genetic architecture of structural left–right asymmetry of the human brain

    Nature Human Behaviour, Vol. 5, Núm. 9, pp. 1226-1239

  5. Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family

    Human Genetics, Vol. 140, Núm. 8, pp. 1183-1200

2020

  1. Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment

    Cortex, Vol. 124, pp. 137-153

  2. The genetics of situs inversus without primary ciliary dyskinesia

    Scientific Reports, Vol. 10, Núm. 1

2019

  1. A large-scale population study of early life factors influencing left-handedness

    Scientific Reports, Vol. 9, Núm. 1

  2. A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development

    Molecular Psychiatry, Vol. 24, Núm. 7, pp. 1065-1078

  3. Genome sequencing for rightward hemispheric language dominance

    Genes, Brain and Behavior, Vol. 18, Núm. 5

  4. Zer genek laguntzen digute irakurtzen?

    Elhuyar: zientzia eta teknika, Núm. 333, pp. 64-68

2017

  1. Association analysis of dyslexia candidate genes in a Dutch longitudinal sample

    European Journal of Human Genetics, Vol. 25, Núm. 4, pp. 452-460

2016

  1. Evaluation of results from genome-wide studies of language and reading in a novel independent dataset

    Genes, Brain and Behavior, Vol. 15, Núm. 6, pp. 531-541

2014

  1. Perceptual learning of acoustic noise by individuals with dyslexia

    Journal of Speech, Language, and Hearing Research, Vol. 57, Núm. 3, pp. 1069-1077

2013

  1. Molecular genetics of dyslexia: An overview

    Dyslexia, Vol. 19, Núm. 4, pp. 214-240