Genetic Variation in the KIAA0319 5′ Region as a Possible Contributor to Dyslexia (Q33793644)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21207242%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

Genetic variation in the KIAA0319 5' region as a possible contributor to dyslexia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21207242%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Genetic Variation in the KIAA0319 5′ Region as a Possible Contributor to Dyslexia (English)

1 reference

https://api.crossref.org/works/10.1007/S10519-010-9434-1

21 November 2024

0 references

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21207242

21 November 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21207242%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Adrienne Elbert

1 reference

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19 January 2020

Tasha Cate-Carter

1 reference

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19 January 2020

Ashley Pitch

1 reference

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19 January 2020

Maureen W. Lovett

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21207242

21 November 2024

Elizabeth N. Kerr

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21207242

21 November 2024

language of work or name

English

0 references

publication date

5 January 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21207242%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

19 January 2020

https://europepmc.org/articles/pmc5469622?pdf=render

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21207242

https://europepmc.org/articles/PMC5469622

21 November 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21207242

https://europepmc.org/articles/PMC5469622?pdf=render

21 November 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21207242

https://doi.org/10.1007/s10519-010-9434-1

21 November 2024

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21207242

http://link.springer.com/content/pdf/10.1007/s10519-010-9434-1.pdf

21 November 2024

1 reference

https://api.crossref.org/works/10.1007/S10519-010-9434-1

http://link.springer.com/article/10.1007/s10519-010-9434-1/fulltext.html

21 November 2024

1 reference

https://api.crossref.org/works/10.1007/S10519-010-9434-1

http://link.springer.com/content/pdf/10.1007/s10519-010-9434-1

21 November 2024

1 reference

https://api.crossref.org/works/10.1007/S10519-010-9434-1

21 November 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21207242%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

volume

1 reference

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19 January 2020

issue

1 reference

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19 January 2020

page(s)

77-89

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21207242%20AND%20SRC:MED&resulttype=core&format=json

Core promoter structure and genomic context reflect histone 3 lysine 9 acetylation patterns

19 January 2020

cites work

1 reference

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4 July 2018

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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.

4 July 2018

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

4 July 2018

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The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities

4 July 2018

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Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.

4 July 2018

1 reference

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

4 July 2018

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Colorado longitudinal twin study of reading disability

4 July 2018

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

4 July 2018

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The genetic lexicon of dyslexia

4 July 2018

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Neurotrophin/Trk receptor signaling mediates C/EBPalpha, -beta and NeuroD recruitment to immediate-early gene promoters in neuronal cells and requires C/EBPs to induce immediate-early gene transcription.

4 July 2018

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Breakthroughs in the search for dyslexia candidate genes

4 July 2018

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

4 July 2018

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Cooperative activity of BRG1 and Z-DNA formation in chromatin remodeling

4 July 2018

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Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

4 July 2018

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4 July 2018

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

4 July 2018

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Chromosomal protein HMGN1 enhances the acetylation of lysine 14 in histone H3.

4 July 2018

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Transcriptional regulation of the human CD3 gamma gene: the TATA-less CD3 gamma promoter functions via an initiator and contiguous Sp-binding elements

4 July 2018

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Genetic influences on early word recognition abilities and disabilities: a study of 7-year-old twins

4 July 2018

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

4 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5469622

How frequent is altered gene expression among susceptibility genes to human complex disorders?

4 July 2018

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4 July 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

4 July 2018

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Haploview: analysis and visualization of LD and haplotype maps

4 July 2018

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

4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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A polymorphic dinucleotide repeat in the rat nucleolin gene forms Z-DNA and inhibits promoter activity

4 July 2018

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4 July 2018

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

4 July 2018

1 reference

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4 July 2018

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4 July 2018

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4 July 2018

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

4 July 2018

1 reference

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A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia

4 July 2018

1 reference

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

4 July 2018

1 reference

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Evaluation of the revised Ontario Child Health Study scales

4 July 2018

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Quantitative trait locus for reading disability on chromosome 6

4 July 2018

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4 July 2018

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Effect of the B--Z transition in poly(dG-m5dC) . poly(dG-m5dC) on nucleosome formation

4 July 2018

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Enhanced Gene Expression by the Poly(dT-dG) · Poly(dC-dA) Sequence

4 July 2018

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Developmental dyslexia: four consecutive patients with cortical anomalies

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5469622

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

4 July 2018

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Isolation of a recombinant copy of the gene encoding C/EBP

4 July 2018

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4 July 2018

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4 July 2018

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d(TG)n.d(CA)n sequences upstream of the rat prolactin gene form Z-DNA and inhibit gene transcription

4 July 2018

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Competing B-Z and helix-coil conformational transitions in supercoiled plasmid DNA.

4 July 2018

1 reference

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Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analyses.

4 July 2018

1 reference

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Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia

21 January 2018

1 reference

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Genetic influences on reading difficulties in boys and girls: the Colorado twin study

21 January 2018

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Dynamic expression of murine HOXA5 protein in the central nervous system.

21 January 2018

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Evolutionary tuning knobs

21 January 2018

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Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.

21 January 2018

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21 January 2018

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The role of gene DCDC2 in German dyslexics.

21 January 2018

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Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319.

21 January 2018

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30 October 2018

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Differential genetic etiology of reading disability as a function of IQ

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21207242

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Association of the dopamine receptor D1 gene, DRD1, with inattention symptoms in families selected for reading problems

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21207242

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Purification and biochemical characterization of the promoter-specific transcription factor, Sp1

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PubMed

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inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Biological Psychiatry

M Luciano

2007

1 reference

https://api.crossref.org/works/10.1007/S10519-010-9434-1

Annual Review of Genomics and Human Genetics

21 November 2024

S Paracchini

2007

1 reference

https://api.crossref.org/works/10.1007/S10519-010-9434-1

21 November 2024

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21207242%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

19 January 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21207242%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21207242%20AND%20SRC:MED&resulttype=core&format=json