(Q48851799)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21987501%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

title

Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals (English)

1 reference

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14 February 2020

1 reference

9

1 reference

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14 February 2020

Heather C Whalley

1

1 reference

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14 February 2020

Andrew C Stanfield

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21987501%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Marianna Hayiou-Thomas

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21987501%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Stephen M Lawrie

8

1 reference

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14 February 2020

Jeremy Hall

10

1 reference

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14 February 2020

7

Eve C Johnstone

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21987501%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

author name string

Garret O'Connell

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21987501%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Jessika E Sussmann

3

1 reference

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14 February 2020

Anna Peel

4

1 reference

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14 February 2020

publication date

10 October 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21987501%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

14 February 2020

published in

1 reference

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14 February 2020

volume

156B

1 reference

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14 February 2020

issue

8

1 reference

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14 February 2020

page(s)

941-948

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21987501%20AND%20SRC:MED&resulttype=core&format=json

Advances in autism genetics: on the threshold of a new neurobiology

14 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Genome-wide analyses of human perisylvian cerebral cortical patterning.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Impaired recognition of negative basic emotions in autism: a test of the amygdala theory.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Superior temporal gyrus, language function, and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Completion norms for 329 sentence contexts.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Perception of complex sounds: abnormal pattern of cortical activation in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

FOXP2 and the mirror system.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

FOXP2 as a molecular window into speech and language

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Microstructural connectivity of the arcuate fasciculus in adolescents with high-functioning autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Genetics of austim: complex aetiology for a heterogeneous disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Rightward hemispheric asymmetries in auditory language cortex in children with autistic disorder: an MRI investigation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Abnormal asymmetry in language association cortex in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Atypical functional lateralization of language in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Lateralization in individuals with high-functioning autism and Asperger's disorder: a frontostriatal model

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

A 12Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Handedness, language lateralisation and anatomical asymmetry in schizophrenia: meta-analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

A common genetic variant in the neurexin superfamily member CNTNAP2 is associated with increased risk for selective mutism and social anxiety-related traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Abnormal regional CBF response in left hemisphere of dysphasic children during a language task.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

A functional genetic link between distinct developmental language disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Neural correlates of enhanced genetic risk for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Changes in prefrontal axons may disrupt the network in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31241

21 January 2018

Identifiers

DOI

10.1002/AJMG.B.31241

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21987501%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

1 reference