Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment (Q30492191)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment	scientific article

Statements

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

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

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q30492191&oldid=2194905293"