Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions. (Q34248551)

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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)

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20 January 2020

9

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20 January 2020

1

Philippe Pinel

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20 January 2020

8

Jean-Baptiste Poline

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20 January 2020

10

Stanislas Dehaene

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20 January 2020

5

Mark Lathrop

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20 January 2020

author name string

Fabien Fauchereau

2

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20 January 2020

Antonio Moreno

3

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20 January 2020

Alexis Barbot

4

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20 January 2020

Diana Zelenika

6

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20 January 2020

Denis Le Bihan

7

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20 January 2020

language of work or name

English

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publication date

1 January 2012

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20 January 2020

number of pages

9

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published in

Journal of Neuroscience

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20 January 2020

volume

32

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20 January 2020

page(s)

817-825

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20 January 2020

issue

3

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

20 January 2020

cites work

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

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Language fMRI abnormalities associated with FOXP2 gene mutation

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FoxP2 expression in avian vocal learners and non-learners

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

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

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FOXP2 and the neuroanatomy of speech and language

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

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

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

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

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Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations.

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

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From genes to behavior in developmental dyslexia

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

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

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

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

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

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Multiple transcription start sites for FOXP2 with varying cellular specificities

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12 December 2020

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

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12 December 2020

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

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Evidence for major gene transmission of developmental dyslexia

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

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A functional genetic link between distinct developmental language disorders

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A meta-analysis of functional neuroimaging studies of dyslexia.

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

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

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

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FOXP2 as a molecular window into speech and language

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

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Avoiding the high Bonferroni penalty in genome-wide association studies

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Human-specific transcriptional regulation of CNS development genes by FOXP2

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12 December 2020

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

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Two-year-olds compute syntactic structure on-line

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LocusZoom: regional visualization of genome-wide association scan results

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

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

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Association between FOXP2 gene and speech sound disorder in Chinese population

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A map of human genome variation from population-scale sequencing

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

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

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Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample

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Spatio-temporal transcriptome of the human brain

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12 December 2020

Developmental dyslexia: four consecutive patients with cortical anomalies

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

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10.1523/JNEUROSCI.5996-10.2012

Identifiers

DOI

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