(Q34293550)

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

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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)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

0 references

specific language impairment

1 reference

based on heuristic

inferred from title

object named as

Mark W Logue

3

0 references

Veronica J Vieland

5

object named as

Veronica J Vieland

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

author name string

Christopher W Bartlett

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Judy F Flax

2

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Europe PubMed Central

PubMed publication ID

1 August 2017

Brett J Smith

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Paula Tallal

6

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Europe PubMed Central

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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

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

10-20

1 reference

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

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

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

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

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

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

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

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

Faster sequential genetic linkage computations

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

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

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

Family characteristics of autistic children: a further report

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

Spontaneous Narrative-Discourse Performance of Parents of Autistic Individuals

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 tetranucleotide repeat polymorphism in the cystic fibrosis 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

Social language use in parents of autistic individuals

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

Infantile autism: a genetic study of 21 twin pairs

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

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

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

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

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

Evaluating genetic heterogeneity in complex disorders.

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

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

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

Genomic screen and follow-up analysis for autistic disorder

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

An autosomal genomic screen for autism

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

Incorporating language phenotypes strengthens evidence of linkage to autism

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

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

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

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

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

Evidence supporting WNT2 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

28 October 2018

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

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

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

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

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

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

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

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

28 October 2018

Autism: the phenotype in relatives

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

Significance levels in complex inheritance

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

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

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

A family study of autism: cognitive patterns and levels in parents and siblings

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

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

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

Avoiding recomputation in linkage analysis.

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

The consistency of the posterior probability of linkage

1 reference

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

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

inferred from PubMed ID database lookup

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

reason for deprecated rank

incorrect identifier value

0 references

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