(Q34583528)

3 August 2017

Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17. (English)

1 reference

3 August 2017

0 references

Timothy C Bates

1

0 references

Anne Castles

Anne Castles

3

0 references

Margaret J. Wright

Margaret J Wright

5

0 references

Max Coltheart

Max Coltheart

4

0 references

Nick Martin

Nicholas G Martin

6

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author name string

Michelle Luciano

2

1 reference

3 August 2017

22 November 2006

1 reference

European Journal of Human Genetics

3 August 2017

1 reference

3 August 2017

15

1 reference

3 August 2017

2

1 reference

3 August 2017

194-203

1 reference

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201739

3 August 2017

0 references

cites work

Reading problems and antisocial behaviour: developmental trends in comorbidity.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Evidence for a genetic aetiology in reading disability of twins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Genetic and environmental influences on individual differences in printed word recognition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Varieties of developmental dyslexia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

The genetics of developmental dyslexia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Genes, cognition and dyslexia: learning to read the genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

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.5201739

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.5201739

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.5201739

A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

A dominant gene for developmental dyslexia on chromosome 3

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Quantitative trait locus for reading disability on chromosome 6

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Continuing the search for dyslexia genes on 6p.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

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.5201739

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.5201739

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.5201739

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.5201739

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.5201739

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.5201739

Evidence for linkage of spelling disability to chromosome 15

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Two translocations of chromosome 15q associated with dyslexia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

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.5201739

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.5201739

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.5201739

A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

A genetic investigation of the covariation among inspection time, choice reaction time, and IQ subtest scores

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Genetic maps of microsatellite and single-nucleotide polymorphism markers: are the distances accurate?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Multivariate multipoint linkage analysis of quantitative trait loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

An improved multipoint sib-pair analysis of quantitative traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Multipoint quantitative-trait linkage analysis in general pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Using sex-averaged genetic maps in multipoint linkage analysis when identity-by-descent status is incompletely known.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Replication of linkage studies of complex traits: an examination of variation in location estimates

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

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.5201739

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.5201739

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.5201739

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Naming-speed processes, timing, and reading: a conceptual review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

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.5201739

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Is there a causal link from phonological awareness to success in learning to read?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

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.5201739

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

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.5201739

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.5201739

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.5201739

Behaviour genetic analyses of reading and spelling: A component processes approach

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Brisbane Adolescent Twin Study: Outline of study methods and research projects

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

A Note on Including Phenotypic Information from Monozygotic Twins in Variance Components Qtl Linkage Analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

Linkage analyses of chromosomal region 18p11-q12 in dyslexia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

John Marshall and the developmental dyslexias

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

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.5201739

Prevalence of Reading Disability in Boys and Girls

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

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.5201739

7 January 2021

Quantitative trait locus for reading disability: correction

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

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.5201739

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.5201739

7 January 2021

Genetic and environmental contributions to size, color, shape, and other characteristics of melanocytic naevi in a sample of adolescent twins

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

7 January 2021

A high-resolution recombination map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

7 January 2021

Comorbidity of reading disability and attention-deficit/hyperactivity disorder: differences by gender and subtype

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201739

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.5201739

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201739

1 reference

3 August 2017

1 reference

PubMed ID

17119535