A common variant associated with dyslexia reduces expression of the KIAA0319 gene - Wikidata - wikimedia - TriplyDB

A common variant associated with dyslexia reduces expression of the KIAA0319 gene

A common variant associated with dyslexia reduces expression of the KIAA0319 gene

http://www.wikidata.org/entity/Q33422937

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Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.DCDC2, KIAA0319 and CMIP are associated with reading-related traits The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles.Opposite Associations between Individual KIAA0319 Polymorphisms and Developmental Dyslexia Risk across Populations: A Stratified Meta-Analysis by the Study Population.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 Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice.Knockdown of the dyslexia-associated gene Kiaa0319 impairs temporal responses to speech stimuli in rat primary auditory cortex The genetics of reading disabilities: from phenotypes to candidate genes Progress towards a cellular neurobiology of reading disability.Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ An informatics approach to integrating genetic and neurological data in speech and language neuroscience.Balancing selection maintains a form of ERAP2 that undergoes nonsense-mediated decay and affects antigen presentation.Identification of candidate genes for dyslexia susceptibility on chromosome 18.Genetic variation in the KIAA0319 5' region as a possible contributor to dyslexia Maps of open chromatin guide the functional follow-up of genome-wide association signals: application to hematological traits.A common haplotype of KIAA0319 contributes to the phonological awareness skill in Chinese children A theoretical molecular network for dyslexia: integrating available genetic findings.Monogenic and chromosomal causes of isolated speech and language impairment.Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes.Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.Risk alleles for chronic hepatitis B are associated with decreased mRNA expression of HLA-DPA1 and HLA-DPB1 in normal human liver.Dissection of genetic associations with language-related traits in population-based cohorts.The BDNF Val66Met Polymorphism Influences Reading Ability and Patterns of Neural Activation in Children.Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment.KIAA0319 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children.Ciliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by Regulatory Factor X (RFX) transcription factors through X-box promoter motifs.Genome-wide association study of shared components of reading disability and language impairment.Chromatin and epigenetic features of long-range gene regulation.Molecular genetics of dyslexia: an overview.Insights into the genetic foundations of human communication.The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling.Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.Association analysis of dyslexia candidate genes in a Dutch longitudinal sample.Neural Noise Hypothesis of Developmental Dyslexia.Approach to epigenetic analysis in language disorders The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage.

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A common variant associated with dyslexia reduces expression of the KIAA0319 gene

http://www.wikidata.org/entity/Q33422937

description

2009 nî lūn-bûn

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2009 թուականի Մարտին հրատարակուած գիտական յօդուած

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2009 թվականի մարտին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

A common variant associated with dyslexia reduces expression of the KIAA0319 gene

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A common variant associated with dyslexia reduces expression of the KIAA0319 gene

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type

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A common variant associated with dyslexia reduces expression of the KIAA0319 gene

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A common variant associated with dyslexia reduces expression of the KIAA0319 gene

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prefLabel

A common variant associated with dyslexia reduces expression of the KIAA0319 gene

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A common variant associated with dyslexia reduces expression of the KIAA0319 gene

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A common variant associated with dyslexia reduces expression of the KIAA0319 gene

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Megan Y Dennis

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Stephan Beck

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Thomas S Scerri

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Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia

DCDC2 is associated with reading disability and modulates neuronal development in the brain.

DYX1C1 functions in neuronal migration in developing neocortex

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia.

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.

Neuroimaging studies of word reading.

Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1.

The human genome browser at UCSC

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