FOXP2 is not a major susceptibility gene for autism or specific language impairment (Q24563830)

2

0 references

J A Lamb

3

0 references

S E Fisher

4

0 references

C S L Lai

5

0 references

G Baird

6

0 references

L Jannoun

7

0 references

V Slonims

8

0 references

C M Stott

9

0 references

M J Merricks

10

0 references

P F Bolton

11

0 references

A J Bailey

12

0 references

A P Monaco

American Journal of Human Genetics

13

0 references

language of work or name

English

0 references

publication date

May 2002

0 references

published in

0 references

volume

70

0 references

issue

5

0 references

page(s)

1318-27

0 references

cites work

Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

Chromosome 7q: where autism meets language disorder?

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

A genomic screen of autism: evidence for a multilocus etiology

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

Neural basis of an inherited speech and language disorder.

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

An autosomal genomic screen for autism. Collaborative linkage study of autism

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

Genetic studies of autistic disorder and chromosome 7

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

A case-control family history study of autism

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

Autism as a strongly genetic disorder: evidence from a British twin study

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

Infantile autism: a genetic study of 21 twin pairs

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

Current directions in research on autism

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

A general test of association for quantitative traits in nuclear families

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

A system for the diagnosis of specific language impairment in kindergarten children

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

Is specific language impairment a valid diagnostic category? Genetic and psycholinguistic evidence.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

Autism and developmental receptive language disorder--a comparative follow-up in early adult life. I: Cognitive and language outcomes.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

Heritability of poor language achievement among twins.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

Genetic basis of specific language impairment: evidence from a twin study.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

A study of developmental speech and language disorders in twins

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=447606

28 November 2018

1 reference

12 December 2020

Detection of single-nucleotide polymorphisms with the WAVE DNA fragment analysis system

1 reference

PubMed

12 December 2020

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

1 reference

PubMed

12 December 2020

The extent to which psychometric tests differentiate subgroups of children with SLI

1 reference

PubMed

12 December 2020

2-year-old boy who has been diagnosed with autism

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F339931

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1086/339931

1 reference

2384061

2384061

1 reference

1 reference

1 reference