(Q34206301)

31 July 2017

title

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

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obsessive-compulsive disorder

31 July 2017

1 reference

1 reference

5

Peter Heutink

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31 July 2017

2

Carol A Mathews

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31 July 2017

6

Ben A Oostra

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31 July 2017

author name string

Annemieke J M H Verkerk

1

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31 July 2017

Marijke Joosse

3

1 reference

31 July 2017

Bert H J Eussen

4

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31 July 2017

Tourette Syndrome Association International Consortium for Genetics

7

1 reference

31 July 2017

language of work or name

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1 July 2003

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31 July 2017

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31 July 2017

volume

82

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31 July 2017

issue

1

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31 July 2017

page(s)

1-9

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https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

31 July 2017

1 reference

7 January 2021

Course of tic severity in Tourette syndrome: the first two decades

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Gilles de la Tourette's syndrome and obsessive-compulsive disorder. Evidence supporting a genetic relationship

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

The familial phenotype of obsessive-compulsive disorder in relation to tic disorders: the Hopkins OCD family study

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Gilles de la Tourette's syndrome with and without obsessive-compulsive disorder compared with obsessive-compulsive disorder without tics: which symptoms discriminate?

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Evidence for autosomal dominant transmission in Tourette's syndrome. United Kingdom cohort study

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Genome scan for linkage to Gilles de la Tourette syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

A complete genome screen in sib pairs affected by Gilles de la Tourette syndrome. The Tourette Syndrome Association International Consortium for Genetics

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Significant linkage for Tourette syndrome in a large French Canadian family

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosomes 7 and 18

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

9p monosomy in a patient with Gilles de la Tourette's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Candidate region for Gilles de la Tourette syndrome at 7q31

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

The human contactin-associated protein-like 2 gene (CNTNAP2) spans over 2 Mb of DNA at chromosome 7q35

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Ion channel sequestration in central nervous system axons.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Molecular cytogenetic studies in three patients with partial trisomy 2p, including CGH from paraffin-embedded tissue

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Expression pattern of mitochondrial capsule selenoprotein mRNA in the hamster testis

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

A nuclear transcription factor related to plastid ribosome biogenesis is synthesised early during germination and priming.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Identification of a novel contactin-associated transmembrane receptor with multiple domains implicated in protein-protein interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Neurexin IV, caspr and paranodin--novel members of the neurexin family: encounters of axons and glia

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Contactin-associated protein (Caspr) and contactin form a complex that is targeted to the paranodal junctions during myelination.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Organizing principles of the axoglial apparatus

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Discs Lost, a novel multi-PDZ domain protein, establishes and maintains epithelial polarity.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Basal ganglia dysfunction in Tourette's syndrome: a new hypothesis

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

A novel leg-shaking Drosophila mutant defective in a voltage-gated K(+)current and hypersensitive to reactive oxygen species.

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Deletion of the K(V)1.1 potassium channel causes epilepsy in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Temperature-sensitive neuromuscular transmission in Kv1.1 null mice: role of potassium channels under the myelin sheath in young nerves

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS0888-7543%2803%2900097-1

7 January 2021

10.1016/S0888-7543(03)00097-1

Identifiers

DOI

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31 July 2017

1 reference