CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy. (Q51901247)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646849%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

title

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy (English)

1 reference

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Erratum: CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy

2 January 2020

main subject

schizophrenia

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corrigendum / erratum

1 reference

12 July 2019

http://api.crossref.org/works?select=update-to&filter=doi:10.1038/MP.2010.20

author

Cisca Wijmenga

15

1 reference

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2 January 2020

Joris A Veltman

17

1 reference

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2 January 2020

author name string

J I Friedman

1

1 reference

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2 January 2020

T Vrijenhoek

2

1 reference

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2 January 2020

S Markx

3

1 reference

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2 January 2020

I M Janssen

4

1 reference

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2 January 2020

W A van der Vliet

5

1 reference

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2 January 2020

B H W Faas

6

1 reference

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2 January 2020

N V Knoers

7

1 reference

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2 January 2020

W Cahn

8

1 reference

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2 January 2020

R S Kahn

9

1 reference

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2 January 2020

L Edelmann

10

1 reference

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2 January 2020

K L Davis

11

1 reference

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2 January 2020

J M Silverman

12

1 reference

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2 January 2020

H G Brunner

13

1 reference

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2 January 2020

A Geurts van Kessel

14

1 reference

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2 January 2020

R A Ophoff

16

1 reference

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2 January 2020

language of work or name

English

0 references

publication date

24 July 2007

1 reference

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2 January 2020

1 reference

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2 January 2020

volume

13

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2 January 2020

issue

3

1 reference

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2 January 2020

page(s)

261-266

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Symptoms, signs, and diagnosis of schizophrenia

2 January 2020

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Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia

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Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

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DNA copy-number analysis in bipolar disorder and schizophrenia reveals aberrations in genes involved in glutamate signaling.

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

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Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels

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CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder

21 January 2018

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Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome.

21 January 2018

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Altered distribution of nicotinamide-adenine dinucleotide phosphate-diaphorase cells in frontal lobe of schizophrenics implies disturbances of cortical development.

21 January 2018

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Some cytoarchitectural abnormalities of the entorhinal cortex in schizophrenia

21 January 2018

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21 January 2018

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Specific interaction between the XNP/ATR-X gene product and the SET domain of the human EZH2 protein

21 January 2018

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21 January 2018

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21 January 2018

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A nonsense mutation in the synaptogyrin 1 gene in a family with schizophrenia

21 January 2018

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21 January 2018

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Dynamic potassium channel distributions during axonal development prevent aberrant firing patterns

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7 January 2021

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Identifiers

DOI

10.1038/SJ.MP.4002049

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17646849%20AND%20SRC:MED&resulttype=core&format=json

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2 January 2020

Fatcat ID

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mapped directly with Wikidata item

24 November 2022

based on heuristic

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