(Q34932472)

5 August 2017

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title

Developmental dyslexia: genetic dissection of a complex cognitive trait (English)

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5 August 2017

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1

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5 August 2017

John C DeFries

2

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5 August 2017

language of work or name

English

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publication date

1 October 2002

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Nature Reviews Neuroscience

5 August 2017

published in

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5 August 2017

volume

3

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5 August 2017

issue

10

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5 August 2017

page(s)

767-780

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"WORD-BLINDNESS" IN SCHOOL CHILDREN

5 August 2017

cites work

1 reference

From language to reading and dyslexia.

21 January 2018

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Naming-speed processes and developmental reading disabilities: an introduction to the special issue on the double-deficit hypothesis

21 January 2018

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Abnormal processing of visual motion in dyslexia revealed by functional brain imaging.

21 January 2018

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Disruption of the neural response to rapid acoustic stimuli in dyslexia: evidence from functional MRI

21 January 2018

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Developmental dyslexia: the cerebellar deficit hypothesis

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To see but not to read; the magnocellular theory of dyslexia

21 January 2018

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Impaired processing of rapid stimulus sequences in dyslexia

21 January 2018

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The neurological basis of developmental dyslexia: an overview and working hypothesis

21 January 2018

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The genetics of specific reading disability

21 January 2018

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Family history as an indicator of risk for reading disability.

21 January 2018

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Evidence for major gene transmission of developmental dyslexia

21 January 2018

1 reference

Family patterns of developmental dyslexia: clinical findings.

21 January 2018

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

21 January 2018

1 reference

Evidence for a genetic aetiology in reading disability of twins.

21 January 2018

1 reference

Early reading development in children at family risk for dyslexia

21 January 2018

1 reference

Multiple regression analysis of twin data

21 January 2018

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Genetic and environmental influences on orthographic and phonological skills in children with reading disabilities

21 January 2018

1 reference

Different origin of auditory and phonological processing problems in children with language impairment: evidence from a twin study

21 January 2018

1 reference

Quantitative trait locus for reading disability on chromosome 6

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Evidence for linkage of spelling disability to chromosome 15

21 January 2018

1 reference

A dominant gene for developmental dyslexia on chromosome 3

21 January 2018

1 reference

Varieties of developmental dyslexia.

21 January 2018

1 reference

Varieties of developmental reading disorder: genetic and environmental influences.

21 January 2018

1 reference

Genetic dissection of complex traits

21 January 2018

1 reference

Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

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Segregation analysis of phenotypic components of learning disabilities. I. Nonword memory and digit span

21 January 2018

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Familial aggregation of dyslexia phenotypes.

21 January 2018

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A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia).

21 January 2018

1 reference

Localisation of a gene implicated in a severe speech and language disorder

21 January 2018

1 reference

A genomewide scan identifies two novel loci involved in specific language impairment

21 January 2018

1 reference

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

21 January 2018

1 reference

Genomewide scans of complex human diseases: true linkage is hard to find

21 January 2018

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

21 January 2018

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

21 January 2018

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Left-handedness: association with immune disease, migraine, and developmental learning disorder

21 January 2018

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A twin and family study of the association between immune system dysfunction and dyslexia using blood serum immunoassay and survey data

21 January 2018

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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

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

21 January 2018

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Supportive evidence for the DYX3 dyslexia susceptibility gene in Canadian families

21 January 2018

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Two translocations of chromosome 15q associated with dyslexia

21 January 2018

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Association study designs for complex diseases

21 January 2018

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

21 January 2018

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Large upward bias in estimation of locus-specific effects from genomewide scans

21 January 2018

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The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder

21 January 2018

1 reference

A forkhead-domain gene is mutated in a severe speech and language disorder

21 January 2018

1 reference

FOXP2 is not a major susceptibility gene for autism or specific language impairment

21 January 2018

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Genetic effects on human cognition: lessons from the study of mental retardation syndromes

21 January 2018

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Specific reading disability: a multiplanar view

21 January 2018

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New member of the winged-helix protein family disrupted in mouse and rat nude mutations

21 January 2018

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The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

21 January 2018

1 reference

Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome

21 January 2018

1 reference

Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse

21 January 2018

1 reference

The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

21 January 2018

1 reference

Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder

21 January 2018

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21 January 2018

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Putting language genes in perspective

21 January 2018

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A Case of Congenital Word Blindness

21 January 2018

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Genetic models of reading disability

31 March 2020

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Evidence for a genetic etiology in hyperactivity in children

31 March 2020

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

31 March 2020

1 reference

Quantitative trait locus for reading disability: correction

31 March 2020

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Dyslexia and chromosome 15 heteromorphism: negative lod score in a Danish material.

31 March 2020

1 reference

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

31 March 2020

1 reference

The investigation of linkage between a quantitative trait and a marker locus

31 March 2020

1 reference

Etiology of reading difficulties and rapid naming: the Colorado Twin Study of Reading Disability

31 March 2020

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

31 March 2020

1 reference

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

31 March 2020

1 reference

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

31 March 2020

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

31 March 2020

1 reference

The assessment of children with specific reading difficulties (dyslexia) using the British Ability Scales.

31 March 2020

1 reference

The external validity of age- versus IQ-discrepancy definitions of reading disability: lessons from a twin study

31 March 2020

1 reference

Persistence of dyslexia: the Connecticut Longitudinal Study at adolescence

31 March 2020

1 reference

Reading disability in twins

31 March 2020

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NRN936

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Dimensions Publication ID

5 August 2017

1017742510

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