A common variant associated with dyslexia reduces expression of the KIAA0319 gene (Q33422937)

26 July 2017

title

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

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26 July 2017

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26 July 2017

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26 July 2017

Ludmila Prokunina-Olsson

object named as

Ludmila Prokunina-Olsson

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Julian C Knight

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Richard Wade-Martins

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Eric D Green

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26 July 2017

Penny Coggill

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26 July 2017

Megan Y Dennis

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26 July 2017

Thomas S Scerri

series ordinal

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26 July 2017

Stephan Beck

series ordinal

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26 July 2017

publication date

27 March 2009

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26 July 2017

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26 July 2017

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26 July 2017

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26 July 2017

page(s)

e1000436

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Creative Commons CC0 License

26 July 2017

start time

27 March 2009

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April 2022 Public Data File from Crossref

copyrighted, dedicated to the public domain by copyright holder

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cites work

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Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat

21 June 2018

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A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability

21 June 2018

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21 June 2018

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A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

21 June 2018

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Disruption of neuronal migration by RNAi of Dyx1c1 results in neocortical and hippocampal malformations

21 June 2018

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From genes to behavior in developmental dyslexia

21 June 2018

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DYX1C1 functions in neuronal migration in developing neocortex

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The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration

21 June 2018

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Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

21 June 2018

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

21 June 2018

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

21 June 2018

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Evaluation of regulatory potential and conservation scores for detecting cis-regulatory modules in aligned mammalian genome sequences

21 June 2018

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21 June 2018

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

21 June 2018

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Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK

21 June 2018

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

21 June 2018

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21 June 2018

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

21 June 2018

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

21 June 2018

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21 June 2018

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Developmental dyslexia: genetic dissection of a complex cognitive trait

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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A soluble transcription factor, Oct-1, is also found in the insoluble nuclear matrix and possesses silencing activity in its alanine-rich domain

21 June 2018

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21 June 2018

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Developmental dyslexia: four consecutive patients with cortical anomalies

21 June 2018

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Evidence for a genetic aetiology in reading disability of twins.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2653637

The ubiquitous octamer-binding protein Oct-1 contains a POU domain with a homeo box subdomain

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2653637

Nuclear factor ETF specifically stimulates transcription from promoters without a TATA box.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2653637

Prevalence of reading disability in boys and girls. Results of the Connecticut Longitudinal Study

21 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2653637

Reading disability, immune disorders and non-right-handedness: twin and family studies of their relations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2653637

Biological significance of unwinding capability of nuclear matrix-associating DNAs

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2653637

The genetics of specific reading disability

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2653637

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia

21 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000436

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000436

The RFX-type transcription factor DAF-19 regulates sensory neuron cilium formation in C. elegans

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000436

Drosophila regulatory factor X is necessary for ciliated sensory neuron differentiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000436

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000436

Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2653637

Familial Nature of Reading Disability

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19325871

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/19325871

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The POU homeobox protein Oct-1 regulates radial glia formation downstream of Notch signaling

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19325871

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1000436

1 reference

26 July 2017

1 reference

26 July 2017

1 reference