Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia - Wikidata - wikimedia - TriplyDB

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

http://www.wikidata.org/entity/Q28298886

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The effect of variation in expression of the candidate dyslexia susceptibility gene homolog Kiaa0319 on neuronal migration and dendritic morphology in the rat.Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample DCDC2, KIAA0319 and CMIP are associated with reading-related traits DCDC2 genetic variants and susceptibility to developmental dyslexia Opposite Associations between Individual KIAA0319 Polymorphisms and Developmental Dyslexia Risk across Populations: A Stratified Meta-Analysis by the Study Population.Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.IFRD1 is a candidate gene for SMNA on chromosome 7q22-q23.The genetics of reading disabilities: from phenotypes to candidate genes Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.Progress towards a cellular neurobiology of reading disability.Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colors An informatics approach to integrating genetic and neurological data in speech and language neuroscience.Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat Brain classification reveals the right cerebellum as the best biomarker of dyslexia.The rs3743205 SNP is important for the regulation of the dyslexia candidate gene DYX1C1 by estrogen receptor β and DNA methylation.A common haplotype of KIAA0319 contributes to the phonological awareness skill in Chinese children A theoretical molecular network for dyslexia: integrating available genetic findings.Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms A dyslexia-associated variant in DCDC2 changes gene expression.In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes.A multidisciplinary approach to understanding developmental dyslexia within working-memory architecture: genotypes, phenotypes, brain, and instruction.Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children.The DCDC2/intron 2 deletion and white matter disorganization: focus on developmental dyslexia.Dissection of genetic associations with language-related traits in population-based cohorts.Gene-environment interaction on neural mechanisms of orthographic processing in Chinese children Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region.Strong motion deficits in dyslexia associated with DCDC2 gene alteration.Comparative genomics of aldehyde dehydrogenase 5a1 (succinate semialdehyde dehydrogenase) and accumulation of gamma-hydroxybutyrate associated with its deficiency KIAA0319 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children.Genetics of developmental dyslexia.DCDC2 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children.A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.Meta-analysis of the association between DCDC2 polymorphisms and risk of dyslexia.Molecular genetics of dyslexia: an overview.Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.The DCDC2 deletion is not a risk factor for dyslexia Association analysis of dyslexia candidate genes in a Dutch longitudinal sample.

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P2860

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

http://www.wikidata.org/entity/Q28298886

description

2007 nî lūn-bûn

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2007 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2007 թվականի հունիսին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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name

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

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Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

@en

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

@nl

type

label

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

@ast

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

@en

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

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prefLabel

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

@ast

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

@en

Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

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American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

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Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

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P2093

Elizabeth Cochrane

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Kathleen Nielsen

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Lani Chun

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Mark M Matsushita

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Nicola H Chapman

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Virginia W Berninger

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Wendy H Raskind

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Zoran Brkanac

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556-60

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scholarly article

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707408

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10.1002/AJMG.B.30471

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4

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144B

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Ellen M. Wijsman

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2007-06-05T00:00:00Z

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17450541

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