Support for EKN1 as the susceptibility locus for dyslexia on 15q21 - Wikidata - thesis-toulmin - TriplyDB

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

http://www.wikidata.org/entity/Q28271763

about

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia Genetics of dyslexia: the evolving landscape DYX1C1 is required for axonemal dynein assembly and ciliary motility A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.Rapid automatized naming as an index of genetic liability to autism DCDC2, KIAA0319 and CMIP are associated with reading-related traits The human lexinome: genes of language and reading Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1.Genetic factors contributing to human primary ciliary dyskinesia and male infertility Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation Association of short-term memory with a variant within DYX1C1 in developmental dyslexia Deficits in learning and memory in mice with a mutation of the candidate dyslexia susceptibility gene Dyx1c1 Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.Knockdown of the candidate dyslexia susceptibility gene homolog dyx1c1 in rodents: effects on auditory processing, visual attention, and cortical and thalamic anatomy.The genetics of reading disabilities: from phenotypes to candidate genes Persistent spatial working memory deficits in rats following in utero RNAi of Dyx1c1.The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.An informatics approach to integrating genetic and neurological data in speech and language neuroscience.A common variant associated with dyslexia reduces expression of the KIAA0319 gene The rs3743205 SNP is important for the regulation of the dyslexia candidate gene DYX1C1 by estrogen receptor β and DNA methylation.Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci.Genetic variation in the KIAA0319 5' region as a possible contributor to dyslexia A theoretical molecular network for dyslexia: integrating available genetic findings.Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population The genetics of developmental dyslexia.Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms From genes to behavior in developmental dyslexia.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.Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children.Dissection of genetic associations with language-related traits in population-based cohorts.Evidence-Based Reading and Writing Assessment for Dyslexia in Adolescents and Young Adults.Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region.Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity.Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations.Moving closer to a public health model of language and learning disabilities: the role of genetics and the search for etiologies A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.Molecular genetics of dyslexia: an overview.Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.

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P2860

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

http://www.wikidata.org/entity/Q28271763

description

2004 nî lūn-bûn

@nan

2004 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2004 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

@zh-hant

2004年論文

@zh-hk

2004年論文

@zh-mo

2004年論文

@zh-tw

2004年论文

@wuu

name

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

@ast

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

@en

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

@nl

type

label

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

@ast

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

@en

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

@nl

prefLabel

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

@ast

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

@en

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

@nl

P1433

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P2860

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P921

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P356

P1433

Molecular Psychiatry

P1476

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

@en

P2093

B Anderson

http://www.w3.org/2001/XMLSchema#string

C L Barr

http://www.w3.org/2001/XMLSchema#string

J M Couto

http://www.w3.org/2001/XMLSchema#string

K G Wigg

http://www.w3.org/2001/XMLSchema#string

M W Lovett

http://www.w3.org/2001/XMLSchema#string

R Tannock

http://www.w3.org/2001/XMLSchema#string

T D Cate-Carter

http://www.w3.org/2001/XMLSchema#string

T W Humphries

http://www.w3.org/2001/XMLSchema#string

Y Feng

http://www.w3.org/2001/XMLSchema#string

P2860

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

Evidence for linkage of spelling disability to chromosome 15

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain

Statistical significance for genomewide studies

A simple salting out procedure for extracting DNA from human nucleated cells

Quantitative trait locus for reading disability on chromosome 6

A dominant gene for developmental dyslexia on chromosome 3

The tetratricopeptide repeat: a structural motif mediating protein-protein interactions

A prospective study of the relationship between specific language impairment, phonological disorders and reading retardation.

A comparison of linkage disequilibrium measures for fine-scale mapping.

P2888

P304

1111-21

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P31

scholarly article

P356

10.1038/SJ.MP.4001543

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P407

P433

12

http://www.w3.org/2001/XMLSchema#string

P478

9

http://www.w3.org/2001/XMLSchema#string

P50

Fabio Macciardi

P577

2004-12-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

8459252

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P698

15249932

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P921

susceptibility locus