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FOXP2
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scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3992897
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24765219%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 March 2020
title
FOXP2
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3992897
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24765219%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 March 2020
author
Dianne F Newbury
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
3992897
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24765219%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 March 2020
Ron Nudel
series ordinal
1
object named as
Ron Nudel
1 reference
stated in
Europe PubMed Central
PMCID
3992897
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24765219%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 March 2020
language of work or name
English
0 references
publication date
13 August 2013
1 reference
stated in
Europe PubMed Central
PMCID
3992897
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24765219%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 March 2020
published in
Wiley Interdisciplinary Reviews: Cognitive Science
1 reference
stated in
Europe PubMed Central
PMCID
3992897
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24765219%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 March 2020
volume
4
1 reference
stated in
Europe PubMed Central
PMCID
3992897
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24765219%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 March 2020
issue
5
1 reference
stated in
Europe PubMed Central
PMCID
3992897
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24765219%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 March 2020
page(s)
547-560
1 reference
stated in
Europe PubMed Central
PMCID
3992897
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24765219%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 March 2020
cites work
The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders
1 reference
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PubMed Central
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24 March 2017
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
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24 March 2017
De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
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24 March 2017
Human-specific transcriptional regulation of CNS development genes by FOXP2
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
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24 March 2017
What Causes Specific Language Impairment in Children?
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
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24 March 2017
A functional genetic link between distinct developmental language disorders
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PubMed Central
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24 March 2017
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
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24 March 2017
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
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24 March 2017
High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Accelerated FoxP2 evolution in echolocating bats
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
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24 March 2017
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
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24 March 2017
FoxP2 regulation during undirected singing in adult songbirds
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
FOXP2 is not a major susceptibility gene for autism or specific language impairment
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
MRI analysis of an inherited speech and language disorder: structural brain abnormalities
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Neural basis of an inherited speech and language disorder.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
The local differentiation of myelinated axons at nodes of Ranvier
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Molecular evolution of FOXP2, a gene involved in speech and language
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
The derived FOXP2 variant of modern humans was shared with Neandertals
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
A forkhead-domain gene is mutated in a severe speech and language disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Localisation of a gene implicated in a severe speech and language disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Genetic basis of grammar defect
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
An extended family with a dominantly inherited speech disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
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24 March 2017
Feature-blind grammar and dysphagia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Foxp2 mutations impair auditory-motor association learning
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
The structure of innate vocalizations in Foxp2-deficient mouse pups
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Striatal FoxP2 is actively regulated during songbird sensorimotor learning
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Birdsong decreases protein levels of FoxP2, a molecule required for human speech
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
24 March 2017
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
7 April 2017
A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
7 April 2017
Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
7 April 2017
FoxP2 expression in avian vocal learners and non-learners
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
7 April 2017
Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
7 April 2017
FoxP2 in song-learning birds and vocal-learning mammals
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
10 May 2017
Convergent repression of Foxp2 3'UTR by miR-9 and miR-132 in embryonic mouse neocortex: implications for radial migration of neurons.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
CNTNAP2 variants affect early language development in the general population
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
CMIP and ATP2C2 modulate phonological short-term memory in language impairment
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
Conservation and diversity of Foxp2 expression in muroid rodents: functional implications
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
Expression of FOXP2 in the developing monkey forebrain: comparison with the expression of the genes FOXP1, PBX3, and MEIS2.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
Genome-wide analyses of human perisylvian cerebral cortical patterning.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
Intracellular distribution of a speech/language disorder associated FOXP2 mutant
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
Functional genetic analysis of mutations implicated in a human speech and language disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
Genetic influences on language impairment and phonological short-term memory.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
Language fMRI abnormalities associated with FOXP2 gene mutation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
Accelerated protein evolution and origins of human-specific features: Foxp2 as an example
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
FOXP2: novel exons, splice variants, and CAG repeat length stability
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
A major susceptibility locus for specific language impairment is located on 13q21.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
A genomewide scan identifies two novel loci involved in specific language impairment
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
Genetics of spoken language disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
Nonword repetition as a behavioural marker for inherited language impairment: evidence from a twin study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
Familial aggregation of a developmental language disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
27 September 2017
A recent evolutionary change affects a regulatory element in the human FOXP2 gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
30 May 2018
Humanized Foxp2 specifically affects cortico-basal ganglia circuits
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
30 May 2018
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3992897
retrieved
30 May 2018
Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWCS.1247
retrieved
21 January 2018
Phenotype of FOXP2 haploinsufficiency in a mother and son.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWCS.1247
retrieved
21 January 2018
FoxP2 regulates neurogenesis during embryonic cortical development.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWCS.1247
retrieved
21 January 2018
Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWCS.1247
retrieved
21 January 2018
The timing of selection at the human FOXP2 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWCS.1247
retrieved
21 January 2018
Molecular cloning and developmental expression of foxP2 in zebrafish
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWCS.1247
retrieved
21 January 2018
Linkage disequilibrium extends across putative selected sites in FOXP2
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24765219
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Genetic variation in FOXP2 alters grey matter concentrations in schizophrenia patients
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24765219
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The speech geneFOXP2is not imprinted
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24765219
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The Heritability of Language: A Review and Metaanalysis of Twin, Adoption, and Linkage Studies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWCS.1247
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/WCS.1247
1 reference
stated in
Europe PubMed Central
PMCID
3992897
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24765219%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 March 2020
PMCID
3992897
1 reference
stated in
Europe PubMed Central
PMCID
3992897
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24765219%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 March 2020
PubMed ID
24765219
1 reference
stated in
Europe PubMed Central
PMCID
3992897
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24765219%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 March 2020
ResearchGate publication ID
261883731
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