(Q34529947)

2 August 2017

1 reference

title

The genetics of developmental dyslexia (English)

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2 August 2017

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2

1 reference

2 August 2017

Julie Williams

1

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2 August 2017

publication date

1 June 2006

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European Journal of Human Genetics

2 August 2017

published in

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2 August 2017

volume

14

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2 August 2017

issue

6

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2 August 2017

page(s)

681-689

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201575

2 August 2017

exact match

0 references

cites work

Theories of developmental dyslexia: insights from a multiple case study of dyslexic adults

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Children of West Indian Immigrants--II. Intellectual performance and reading attainment

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

The genetics of specific reading disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Family history as an indicator of risk for reading disability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

21 January 2018

The genetics of dyslexia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Evidence for a genetic aetiology in reading disability of twins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

A twin study of genetic influences on reading and spelling ability and disability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Causal models of reading disability: a twin study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Evidence for major gene transmission of developmental dyslexia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Sex differences in developmental reading disability: new findings from 4 epidemiological studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Evidence for linkage of spelling disability to chromosome 15

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

A whole-genome scan in 164 Dutch sib pairs with attention-deficit/hyperactivity disorder: suggestive evidence for linkage on chromosomes 7p and 15q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Association analysis of two candidate phospholipase genes that map to the chromosome 15q15.1-15.3 region associated with reading disability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

A locus on 15q15-15qter influences dyslexia: further support from a transmission/disequilibrium study in an Italian speaking population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Quantitative trait locus for reading disability on chromosome 6

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Use of multivariate linkage analysis for dissection of a complex cognitive trait

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Absence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Absence of significant linkage between phonological coding dyslexia and chromosome 6p23-21.3, as determined by use of quantitative-trait methods: confirmation of qualitative analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Evidence for linkage and association with reading disability on 6p21.3-22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

A dominant gene for developmental dyslexia on chromosome 3

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Two translocations of chromosome 15q associated with dyslexia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

A dyslexia susceptibility locus (DYX7) linked to dopamine D4 receptor (DRD4) region on chromosome 11p15.5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Suggestive linkage of developmental dyslexia to chromosome 1p34-p36.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Confirmation of a dyslexia susceptibility locus on chromosome 1p34-p36 in a set of 100 Canadian families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

Two Cases of Hereditary Congenital Word-Blindness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

7 January 2021

The structure of genetic influences on general cognitive, language, phonological, and reading abilities

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

7 January 2021

Common and specific gender influences on individual differences in reading performance: a twin study

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

7 January 2021

Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit/hyperactivity disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

7 January 2021

Specific reading disability: identification of an inherited form through linkage analysis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

7 January 2021

Genetic linkage analysis with dyslexia: evidence for linkage of spelling disability to chromosome 15.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

7 January 2021

Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

7 January 2021

Quantitative trait locus for reading disability: correction

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

7 January 2021

Evidence for a susceptibility locus on chromosome 6q influencing phonological coding dyslexia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

7 January 2021

Linkage analyses of chromosomal region 18p11-q12 in dyslexia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

7 January 2021

Cosegregation of balanced translocation (1;2) with retarded speech development and dyslexia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

7 January 2021

Linkage studies suggest a possible locus for developmental dyslexia on chromosome 1p

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201575

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201575

1 reference

2 August 2017

1 reference