(Q34248551)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22262880%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions (English)

1 reference

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20 January 2020

9

1 reference

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20 January 2020

1

Philippe Pinel

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22262880%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

8

Jean-Baptiste Poline

1 reference

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20 January 2020

10

Stanislas Dehaene

1 reference

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20 January 2020

5

Mark Lathrop

1 reference

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20 January 2020

author name string

Fabien Fauchereau

2

1 reference

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20 January 2020

Antonio Moreno

3

1 reference

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20 January 2020

Alexis Barbot

4

1 reference

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20 January 2020

Diana Zelenika

6

1 reference

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20 January 2020

Denis Le Bihan

7

1 reference

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20 January 2020

language of work or name

English

0 references

publication date

1 January 2012

1 reference

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20 January 2020

number of pages

9

0 references

published in

Journal of Neuroscience

1 reference

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20 January 2020

volume

32

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20 January 2020

page(s)

817-825

1 reference

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20 January 2020

issue

3

1 reference

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Language dominance determined by whole brain functional MRI in patients with brain lesions.

20 January 2020

cites work

1 reference

12 December 2020

On the "specifics" of specific reading disability and specific language impairment

1 reference

12 December 2020

Anatomical risk factors for phonological dyslexia

1 reference

12 December 2020

Dyslexia: cultural diversity and biological unity

1 reference

12 December 2020

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

1 reference

12 December 2020

MRI analysis of an inherited speech and language disorder: structural brain abnormalities

1 reference

12 December 2020

A major susceptibility locus for specific language impairment is located on 13q21.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Anatomical risk factors that distinguish dyslexia from SLI predict reading skill in normal children.

1 reference

12 December 2020

Functional neuroimaging of speech perception in infants.

1 reference

12 December 2020

An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets

1 reference

12 December 2020

Language fMRI abnormalities associated with FOXP2 gene mutation

1 reference

12 December 2020

FoxP2 expression in avian vocal learners and non-learners

1 reference

12 December 2020

Highly significant linkage to the SLI1 locus in an expanded sample of individuals affected by specific language impairment

1 reference

12 December 2020

Language-association cortex asymmetry in autism and specific language impairment.

1 reference

12 December 2020

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States

1 reference

12 December 2020

Developmental dyslexia and specific language impairment: same or different?

1 reference

12 December 2020

FOXP2 and the neuroanatomy of speech and language

1 reference

12 December 2020

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia

1 reference

12 December 2020

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

1 reference

12 December 2020

Brain abnormalities underlying altered activation in dyslexia: a voxel based morphometry study

1 reference

12 December 2020

Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene

1 reference

12 December 2020

Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations.

1 reference

12 December 2020

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration

1 reference

12 December 2020

From genes to behavior in developmental dyslexia

1 reference

12 December 2020

Individual differences in anatomy predict reading and oral language impairments in children.

1 reference

12 December 2020

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia.

1 reference

12 December 2020

Evidence That Dyslexia May Represent the Lower Tail of a Normal Distribution of Reading Ability

1 reference

12 December 2020

A review of association and linkage studies for genetical analyses of learning disorders

1 reference

12 December 2020

A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability

1 reference

12 December 2020

Fast reproducible identification and large-scale databasing of individual functional cognitive networks

1 reference

12 December 2020

Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain

1 reference

12 December 2020

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders

1 reference

12 December 2020

A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms

1 reference

12 December 2020

Multiple transcription start sites for FOXP2 with varying cellular specificities

1 reference

12 December 2020

Electrical brain responses in language-impaired children reveal grammar-specific deficits

1 reference

12 December 2020

Children with specific language impairment also show impairment of music-syntactic processing.

1 reference

12 December 2020

Evidence for major gene transmission of developmental dyslexia

1 reference

12 December 2020

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.

1 reference

12 December 2020

A functional genetic link between distinct developmental language disorders

1 reference

12 December 2020

A meta-analysis of functional neuroimaging studies of dyslexia.

1 reference

12 December 2020

The somatotopy of speech: phonation and articulation in the human motor cortex

1 reference

12 December 2020

Beyond hemispheric dominance: brain regions underlying the joint lateralization of language and arithmetic to the left hemisphere.

1 reference

12 December 2020

Reduced neural integration of letters and speech sounds links phonological and reading deficits in adult dyslexia

1 reference

12 December 2020

FOXP2 as a molecular window into speech and language

1 reference

12 December 2020

A common variant associated with dyslexia reduces expression of the KIAA0319 gene

1 reference

12 December 2020

Avoiding the high Bonferroni penalty in genome-wide association studies

1 reference

12 December 2020

Human-specific transcriptional regulation of CNS development genes by FOXP2

1 reference

12 December 2020

Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment

1 reference

12 December 2020

Two-year-olds compute syntactic structure on-line

1 reference

12 December 2020

LocusZoom: regional visualization of genome-wide association scan results

1 reference

12 December 2020

FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies

1 reference

12 December 2020

The speech and language FOXP2 gene modulates the phenotype of frontotemporal lobar degeneration.

1 reference

12 December 2020

Association between FOXP2 gene and speech sound disorder in Chinese population

1 reference

12 December 2020

A map of human genome variation from population-scale sequencing

1 reference

12 December 2020

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

1 reference

12 December 2020

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.

1 reference

12 December 2020

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

12 December 2020

Spatio-temporal transcriptome of the human brain

1 reference

12 December 2020

Developmental dyslexia: four consecutive patients with cortical anomalies

1 reference

12 December 2020

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

1 reference

12 December 2020

Brain morphology in children with specific language impairment

1 reference

12 December 2020

Neural basis of an inherited speech and language disorder.

1 reference

12 December 2020

10.1523/JNEUROSCI.5996-10.2012

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22262880%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference

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20 January 2020

1 reference

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