Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits (Q24530823)

Elena Bonora

2

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Simon Fisher

Simon E Fisher

11

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Anthony Monaco

Anthony P Monaco

10

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Faraneh Vargha-Khadem

Faraneh Vargha-Khadem

7

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author name string

Kay D MacDermot

1

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Nuala Sykes

3

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Anne-Marie Coupe

4

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Cecilia S L Lai

5

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Fiona McKenzie

8

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Robert L Smith

American Journal of Human Genetics

9

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language of work or name

English

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publication date

June 2005

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published in

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volume

76

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issue

6

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page(s)

1074-80

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cites work

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

24 March 2017

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Predicting deleterious amino acid substitutions

24 March 2017

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Neural basis of an inherited speech and language disorder.

24 March 2017

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Molecular evolution of FOXP2, a gene involved in speech and language

24 March 2017

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FOXP2 and the neuroanatomy of speech and language

24 March 2017

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FoxP4, a novel forkhead transcription factor

24 March 2017

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Mutation screening of FOXP2 in individuals diagnosed with autistic disorder

24 March 2017

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Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia

24 March 2017

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

24 March 2017

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Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum

24 March 2017

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Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors

24 March 2017

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Human non-synonymous SNPs: server and survey

24 March 2017

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FoxP2 expression in avian vocal learners and non-learners

7 April 2017

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Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction

7 April 2017

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FoxP2 in song-learning birds and vocal-learning mammals

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Language fMRI abnormalities associated with FOXP2 gene mutation

10 May 2017

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

27 September 2017

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

27 September 2017

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Multiple Domains Define the Expression and Regulatory Properties of Foxp1 Forkhead Transcriptional Repressors

27 September 2017

1 reference

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Deciphering the genetic basis of speech and language disorders

27 September 2017

1 reference

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Accelerated protein evolution and origins of human-specific features: Foxp2 as an example

27 September 2017

1 reference

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FOXP2: novel exons, splice variants, and CAG repeat length stability

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196445

Evaluation of FOXP2 as an autism susceptibility gene

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196445

Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196445

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196445

FOXP2 in focus: what can genes tell us about speech and language?

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196445

Family pedigrees of children with suspected childhood apraxia of speech.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196445

The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196445

Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196445

Detecting polymorphisms and mutations in candidate genes

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1196445

29 November 2018

Identifiers

DOI

10.1086/430841

1 reference

1 reference

1 reference

PubMed publication ID

15877281

1 reference