(Q30492191)

English

Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment (English)

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

specific language impairment

1 reference

based on heuristic

inferred from title

object named as

Mabel L Rice

1

0 references

author name string

Shelley D Smith

2

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Javier Gayán

3

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

publication date

26 August 2009

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Journal of Neurodevelopmental Disorders

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

1

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

4

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

264-282

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

https://scigraph.springernature.com/pub.10.1007/s11689-009-9031-x

0 references

Judgments of omitted BE and DO in questions as extended finiteness clinical markers of specific language impairment (SLI) to 15 years: a study of growth and asymptote

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

A functional genetic link between distinct developmental language disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Relations among speech, language, and reading disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Language outcomes of 7-year-old children with or without a history of late language emergence at 24 months

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

A second-generation combined linkage physical map of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Heritability of specific language impairment depends on diagnostic criteria.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Genetics of dyslexia: the evolving landscape

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Children's history of speech-language difficulties: genetic influences and associations with reading-related measures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

The dimensionality of language ability in school-age children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

From genes to behavior in developmental dyslexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

DYX1C1 functions in neuronal migration in developing neocortex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Mean length of utterance in children with specific language impairment and in younger control children shows concurrent validity and stable and parallel growth trajectories

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

From single to multiple deficit models of developmental disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Breakthroughs in the search for dyslexia candidate genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

The genetics of developmental dyslexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Language deficits in poor comprehenders: a case for the simple view of reading

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Generalist genes: implications for the cognitive sciences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Genetic influences on language impairment and phonological short-term memory.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Association of specific language impairment (SLI) to the region of 7q31.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

A major susceptibility locus for specific language impairment is located on 13q21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Motor immaturity and specific speech and language impairment: evidence for a common genetic basis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

A dominant gene for developmental dyslexia on chromosome 3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

DeFries-Fulker multiple regression analysis of sibship QTL data: a SAS macro

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Implementing a unified approach to family-based tests of association.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

A general test of association for quantitative traits in nuclear families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Present and future possibilities for defining a phenotype for specific language impairment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

A new gene (DYX3) for dyslexia is located on chromosome 2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Fourteen-year follow-up of children with and without speech/language impairments: speech/language stability and outcomes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Prevalence of specific language impairment in kindergarten children.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Using genetics to dissect cognition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Quantitative trait locus for reading disability on chromosome 6

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Familial concentration of developmental language impairment.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

20 June 2018

Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment.

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

Family histories of children with SLI who show extended optional infinitives.

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

Distinct genetic influences on grammar and phonological short-term memory deficits: evidence from 6-year-old twins.

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

Morphological productivity in children with normal language and SLI: a study of the English past tense.

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

Linkage of speech sound disorder to reading disability loci.

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

Speech sound disorder influenced by a locus in 15q14 region.

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

Further evidence of pleiotropy influencing speech and language: analysis of the DYX8 region.

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

The simple view of reading

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

Segregation analysis of phenotypic components of learning disabilities. II. Phonological decoding.

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

Tense over time: the longitudinal course of tense acquisition in children with specific language impairment.

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

Acquisition of irregular past tense by children with specific language impairment.

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

Multivariate Linkage Analysis of Specific Language Impairment (SLI)

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib-pair collection

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

Grammaticality Judgments of an Extended Optional Infinitive Grammar

1 reference

https://api.crossref.org/works/10.1007%2FS11689-009-9031-X

21 January 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

26 November 2018

Prevalence of speech delay in 6-year-old children and comorbidity with language impairment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2788915

26 November 2018

Psycholinguistic markers for specific language impairment (SLI)

1 reference

https://pubmed.ncbi.nlm.nih.gov/19997522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial aggregation in specific language impairment

1 reference

https://pubmed.ncbi.nlm.nih.gov/19997522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Children's Test of Nonword Repetition: a test of phonological working memory

1 reference

https://pubmed.ncbi.nlm.nih.gov/19997522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of speech and language impairments

1 reference

https://pubmed.ncbi.nlm.nih.gov/19997522

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S11689-009-9031-X

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Dimensions Publication ID

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1007/s11689-009-9031-x

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

ResearchGate publication ID

0 references

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