Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions. - Test2 - elhamkhani - TriplyDB

Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions.

Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions.

http://www.wikidata.org/entity/Q34248551

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Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.FOXP2 Cerebral asymmetry and language development: cause, correlate, or consequence?Speech sound processing deficits and training-induced neural plasticity in rats with dyslexia gene knockdown Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children The role of DNA insertions in phenotypic differentiation between humans and other primates The laryngeal motor cortex: its organization and connectivity.Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.Tackling the 'dyslexia paradox': reading brain and behavior for early markers of developmental dyslexiax.Knockdown of Dyslexia-Gene Dcdc2 Interferes with Speech Sound Discrimination in Continuous Streams.The Contribution of the Corpus Callosum to Language Lateralization Enhanced procedural learning of speech sound categories in a genetic variant of FOXP2.Mutation of Dcdc2 in mice leads to impairments in auditory processing and memory ability.Knockdown of the dyslexia-associated gene Kiaa0319 impairs temporal responses to speech stimuli in rat primary auditory cortex FMRI of phonemic perception and its relationship to reading development in elementary- to middle-school-age children The effects of Kiaa0319 knockdown on cortical and subcortical anatomy in male rats Linking neurogenetics and individual differences in language learning: the dopamine hypothesis.The genetics of reading disabilities: from phenotypes to candidate genes On Variability and Genes: Inter-individual Differences in Auditory Brain Function.Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability.Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ Category fluency, latent semantic analysis and schizophrenia: a candidate gene approach The Functional Genetics of Handedness and Language Lateralization: Insights from Gene Ontology, Pathway and Disease Association Analyses.Epigenetic regulation of lateralized fetal spinal gene expression underlies hemispheric asymmetries Novel QTL at chromosome 6p22 for alcohol consumption: Implications for the genetic liability of alcohol use disorders.Are there susceptibility factors for primary progressive aphasia?Genetic insights into the functional elements of language.The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure.Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms Interaction effect between handedness and CNTNAP2 polymorphism (rs7794745 genotype) on voice-specific frontotemporal activity in healthy individuals: an fMRI study Cerebral Lateralization is Protective in the Very Prematurely Born.The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains Gene-environment interaction on neural mechanisms of orthographic processing in Chinese children Linkage analysis in a Dutch population isolate shows no major gene for left-handedness or atypical language lateralization Dyslexia susceptibility genes influence brain atrophy in frontotemporal dementia.Topological properties of large-scale structural brain networks in children with familial risk for reading difficulties.Impaired auditory sampling in dyslexia: further evidence from combined fMRI and EEG.Genome-wide association study of shared components of reading disability and language impairment.Asymmetry and heterogeneity of Alzheimer's and frontotemporal pathology in primary progressive aphasia.Molecular genetics of dyslexia: an overview.

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P2860

Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions.

http://www.wikidata.org/entity/Q34248551

description

2012 nî lūn-bûn

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2012 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2012 թվականի հունվարին հրատարակված գիտական հոդված

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2012年の論文

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Genetic variants of FOXP2 and ...... inct language-related regions.

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Genetic variants of FOXP2 and ...... inct language-related regions.

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Genetic variants of FOXP2 and ...... inct language-related regions.

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Genetic variants of FOXP2 and ...... inct language-related regions.

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Genetic variants of FOXP2 and ...... inct language-related regions.

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Genetic variants of FOXP2 and ...... inct language-related regions.

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Genetic variants of FOXP2 and ...... inct language-related regions.

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Genetic variants of FOXP2 and ...... inct language-related regions.

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JNEUROSCI.5996-10.2012

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Alexis Barbot

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Antonio Moreno

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Denis Le Bihan

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Diana Zelenika

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817-825

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Thomas Bourgeron

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