Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment (Q34293550)

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Language	Label	Description	Also known as
English	Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

1 August 2017

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

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Europe PubMed Central

PubMed publication ID

1 August 2017

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specific language impairment

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based on heuristic

inferred from title

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Mark W Logue

3

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Veronica J Vieland

5

object named as

Veronica J Vieland

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Europe PubMed Central

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1 August 2017

author name string

Christopher W Bartlett

1

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1 August 2017

Judy F Flax

2

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1 August 2017

Brett J Smith

4

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1 August 2017

Paula Tallal

6

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1 August 2017

Linda M Brzustowicz

7

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Europe PubMed Central

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1 August 2017

publication date

1 January 2004

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Europe PubMed Central

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1 August 2017

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Europe PubMed Central

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1 August 2017

57

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Europe PubMed Central

PubMed publication ID

1 August 2017

1

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Europe PubMed Central

PubMed publication ID

1 August 2017

10-20

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Europe PubMed Central

PubMed publication ID

1 August 2017

An Investigation of Language Impairment in Autism: Implications for Genetic Subgroups

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 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=2976973

6 July 2018

Mutation screening of FOXP2 in individuals diagnosed with autistic disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

A longitudinal investigation of reading outcomes in children with language impairments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Evaluation of FOXP2 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=2976973

6 July 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=2976973

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 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=2976973

6 July 2018

Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Genetics of austim: complex aetiology for a heterogeneous disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 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=2976973

6 July 2018

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

A genomewide screen for autism susceptibility loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Brief report: A case of autism with interstitial deletion of chromosome 13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Educational attainments of school leavers with a preschool history of speech-language impairments.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Comparison of 'model-free' and 'model-based' linkage statistics in the presence of locus heterogeneity: single data set and multiple data set applications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Power to detect linkage based on multiple sets of data in the presence of locus heterogeneity: comparative evaluation of model-based linkage methods for affected sib pair data.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Correcting for a potential bias in the pedigree disequilibrium test

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

On the resolution and feasibility of genome scanning approaches

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Genetics of specific language impairment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

A test for linkage and association in general pedigrees: the pedigree disequilibrium test

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Genetic studies of autistic disorder and chromosome 7

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Primer3 on the WWW for general users and for biologist programmers

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6 July 2018

The epidemiology of autism: a review.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

A genomic screen of autism: evidence for a multilocus etiology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

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6 July 2018

Bayesian linkage analysis, or: how I learned to stop worrying and love the posterior probability of linkage

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Comprehensive human genetic maps: individual and sex-specific variation in recombination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Language-impaired preschoolers: a follow-up into adolescence

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Genetics of spoken language disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 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=2976973

6 July 2018

Use of a quantitative trait to map a locus associated with severity of positive symptoms in familial schizophrenia to chromosome 6p.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

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6 July 2018

Faster sequential genetic linkage computations

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6 July 2018

Psychometric assessment of first-degree relatives of 62 autistic probands in Utah

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6 July 2018

Family characteristics of autistic children: a further report

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6 July 2018

Spontaneous Narrative-Discourse Performance of Parents of Autistic Individuals

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6 July 2018

A tetranucleotide repeat polymorphism in the cystic fibrosis gene

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

6 July 2018

Social language use in parents of autistic individuals

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6 July 2018

Infantile autism: a genetic study of 21 twin pairs

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6 July 2018

Bayesian analysis of a previously published genome screen for panic disorder reveals new and compelling evidence for linkage to chromosome 7.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

28 October 2018

Brief report: A case of autism associated with del(2)(q32.1q32.2) or (q32.2q32.3).

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28 October 2018

Evaluating genetic heterogeneity in complex disorders.

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28 October 2018

Language-impaired children: No sign of the FOXP2 mutation.

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Genomic screen and follow-up analysis for autistic disorder

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28 October 2018

An autosomal genomic screen for autism

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28 October 2018

Incorporating language phenotypes strengthens evidence of linkage to autism

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28 October 2018

HLODs remain powerful tools for detection of linkage in the presence of genetic heterogeneity

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28 October 2018

Determining trait locus position from multipoint analysis: accuracy and power of three different statistics.

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28 October 2018

Evidence supporting WNT2 as an autism susceptibility gene.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2976973

28 October 2018

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.

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28 October 2018

The familial aggregation of the lesser variant in biological and nonbiological relatives of PDD probands: a family history study

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28 October 2018

Variable expression of the autism broader phenotype: findings from extended pedigrees

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28 October 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=2976973

28 October 2018

Direct power comparisons between simple LOD scores and NPL scores for linkage analysis in complex diseases

1 reference

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28 October 2018

Autism: the phenotype in relatives

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28 October 2018

Significance levels in complex inheritance

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28 October 2018

Power, mode of inheritance, and type I error in LOD scores and affecteds-only methods: reply to Kruglyak

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28 October 2018

A Family Study of Autism: Cognitive Patterns and Levels in Parents and Siblings

1 reference

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28 October 2018

Lack of cognitive impairment in first-degree relatives of children with pervasive developmental disorders

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28 October 2018

Avoiding recomputation in linkage analysis.

1 reference

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28 October 2018

The consistency of the posterior probability of linkage

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is preschool language impairment a risk factor for dyslexia in adolescence?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15133308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS

1 reference

https://pubmed.ncbi.nlm.nih.gov/15133308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLODs, Trait Models, and Ascertainment: Implications of Admixture for Parameter Estimation and Linkage Detection

1 reference

https://pubmed.ncbi.nlm.nih.gov/15133308

12 December 2020

based on heuristic

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An approximation for the prior probability of autosomal linkage

1 reference

https://pubmed.ncbi.nlm.nih.gov/15133308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1159/000077385

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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incorrect identifier value

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