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

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scientific article published on 24 July 2007

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English	CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.	scientific article published on 24 July 2007

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scholarly article

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2 January 2020

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

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2 January 2020

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corrigendum / erratum

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

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10.1038/MP.2010.20

12 July 2019

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

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2 January 2020

Joris A Veltman

17

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2 January 2020

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J I Friedman

1

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2 January 2020

T Vrijenhoek

2

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S Markx

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2 January 2020

I M Janssen

4

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2 January 2020

W A van der Vliet

5

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2 January 2020

B H W Faas

6

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2 January 2020

N V Knoers

7

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W Cahn

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2 January 2020

R S Kahn

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2 January 2020

L Edelmann

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2 January 2020

K L Davis

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J M Silverman

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2 January 2020

H G Brunner

13

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2 January 2020

A Geurts van Kessel

14

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2 January 2020

R A Ophoff

16

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2 January 2020

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24 July 2007

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2 January 2020

Molecular Psychiatry

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2 January 2020

13

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2 January 2020

3

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261-266

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2 January 2020

Symptoms, signs, and diagnosis of schizophrenia

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002049

21 January 2018

Schizophrenia: genes at last?

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Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia

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Genetic association studies in epilepsy: "the truth is out there".

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Global variation in copy number in the human genome

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A comprehensive analysis of common copy-number variations in the human genome

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

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Identification of disease genes by whole genome CGH arrays

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Structural variants: changing the landscape of chromosomes and design of disease studies

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Diagnostic genome profiling in mental retardation

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The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

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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

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

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White matter changes in schizophrenia: evidence for myelin-related dysfunction

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

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