DCDC2 genetic variants and susceptibility to developmental dyslexia - Test2 - elhamkhani - TriplyDB

DCDC2 genetic variants and susceptibility to developmental dyslexia

DCDC2 genetic variants and susceptibility to developmental dyslexia

http://www.wikidata.org/entity/Q24631569

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The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles.Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.Primary Cilia as a Possible Link between Left-Right Asymmetry and Neurodevelopmental Diseases.Knockdown of Dyslexia-Gene Dcdc2 Interferes with Speech Sound Discrimination in Continuous Streams.Mutation of Dcdc2 in mice leads to impairments in auditory processing and memory ability.The genetics of reading disabilities: from phenotypes to candidate genes 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 Distinct Features of Doublecortin as a Marker of Neuronal Migration and Its Implications in Cancer Cell Mobility.The correlation between reading and mathematics ability at age twelve has a substantial genetic component.Genetic insights into the functional elements of language.Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms Position of neocortical neurons transfected at different gestational ages with shRNA targeted against candidate dyslexia susceptibility genes.The DCDC2/intron 2 deletion and white matter disorganization: focus on developmental dyslexia.Strong motion deficits in dyslexia associated with DCDC2 gene alteration.Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment.Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia.DCDC2 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children.Molecular genetics of dyslexia: an overview.The DCDC2 deletion is not a risk factor for dyslexia Multiple Causal Links Between Magnocellular-Dorsal Pathway Deficit and Developmental Dyslexia.Lessons to be learned: how a comprehensive neurobiological framework of atypical reading development can inform educational practice.Neural Noise Hypothesis of Developmental Dyslexia.Approach to epigenetic analysis in language disorders Mutation of the Dyslexia-Associated Gene Dcdc2 Enhances Glutamatergic Synaptic Transmission Between Layer 4 Neurons in Mouse Neocortex.Chlamydomonas DYX1C1/PF23 is essential for axonemal assembly and proper morphology of inner dynein arms.Study of Genetic Association With DCDC2 and Developmental Dyslexia in Hong Kong Chinese Children.Putative risk factors in developmental dyslexia: a case-control study of Italian children.The role of READ1 and KIAA0319 genetic variations in developmental dyslexia: testing main and interactive effects.Visual motion and rapid auditory processing are solid endophenotypes of developmental dyslexia.The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problems.Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samples.An assessment of gene-by-environment interactions in developmental dyslexia-related phenotypes.Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population.Genetic and environmental risk factors for developmental dyslexia in children: systematic review of the last decade.An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia.The DCDC2 intron 2 deletion impairs illusory motion perception unveiling the selective role of magnocellular-dorsal stream in reading (dis)ability.KIAA0319 and ROBO1: evidence on association with reading and pleiotropic effects on language and mathematics abilities in developmental dyslexia.Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population.Stage 1 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: protocol for a test of the double hit hypothesis.

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P2860

DCDC2 genetic variants and susceptibility to developmental dyslexia

http://www.wikidata.org/entity/Q24631569

description

2012 nî lūn-bûn

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2012 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2012 թվականի փետրվարին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

DCDC2 genetic variants and susceptibility to developmental dyslexia

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DCDC2 genetic variants and susceptibility to developmental dyslexia

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DCDC2 genetic variants and susceptibility to developmental dyslexia

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type

label

DCDC2 genetic variants and susceptibility to developmental dyslexia

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DCDC2 genetic variants and susceptibility to developmental dyslexia

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DCDC2 genetic variants and susceptibility to developmental dyslexia

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DCDC2 genetic variants and susceptibility to developmental dyslexia

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DCDC2 genetic variants and susceptibility to developmental dyslexia

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DCDC2 genetic variants and susceptibility to developmental dyslexia

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Psychiatric Genetics

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DCDC2 genetic variants and susceptibility to developmental dyslexia

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P2093

Haiying Meng

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Jeffrey R Gruen

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Marianna Rusconi

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Natalie Cope

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P2860

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

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.

Chromosome 6p influences on different dyslexia-related cognitive processes: further confirmation

Quantitative-trait locus for specific language and reading deficits on chromosome 6p

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

Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15

Quantitative trait locus for reading disability on chromosome 6

Specific reading disability (dyslexia): what have we learned in the past four decades?

Association of short-term memory with a variant within DYX1C1 in developmental dyslexia

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1

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Massimo Molteni

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21881542

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3232293

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