Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders (Q24305646)

limbic system development

GOA release 2020-03-11

1 reference

Contactin associated protein-like 2

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Daniel Geschwind

15

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Brian J O'Roak

object named as

Brian J O'Roak

2

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Ami Klin

8

object named as

Ami Klin

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Katarzyna Chawarska

7

object named as

Katarzyna Chawarska

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author name string

Betul Bakkaloglu

1

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Angeliki Louvi

3

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Abha R Gupta

4

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Jesse F Abelson

5

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Thomas M Morgan

6

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A Gulhan Ercan-Sencicek

9

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Althea A Stillman

10

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Gamze Tanriover

11

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Brett S Abrahams

12

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Jackie A Duvall

13

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Elissa M Robbins

14

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Thomas Biederer

16

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Murat Gunel

17

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Richard P Lifton

18

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Matthew W State

American Journal of Human Genetics

19

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language of work or name

English

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publication date

January 2008

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published in

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volume

82

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issue

1

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page(s)

165-73

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cites work

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

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

19 March 2017

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Strong association of de novo copy number mutations with autism

19 March 2017

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Neurexin-neuroligin signaling in synapse development

19 March 2017

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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

19 March 2017

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Global variation in copy number in the human genome

19 March 2017

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Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome

19 March 2017

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X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

19 March 2017

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Association of TAG-1 with Caspr2 is essential for the molecular organization of juxtaparanodal regions of myelinated fibers

19 March 2017

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

19 March 2017

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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

19 March 2017

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Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

19 March 2017

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

19 March 2017

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Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection

19 March 2017

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Sequence variants in SLITRK1 are associated with Tourette's syndrome

19 March 2017

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NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population

19 March 2017

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Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253974

SynCAM, a synaptic adhesion molecule that drives synapse assembly

19 March 2017

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The hem of the embryonic cerebral cortex is defined by the expression of multiple Wnt genes and is compromised in Gli3-deficient mice

19 March 2017

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

19 March 2017

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Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

7 April 2017

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

7 April 2017

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Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation.

27 September 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253974

Recent advances in the genetics of autism

27 September 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253974

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253974

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253974

Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253974

Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?

27 September 2017

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Isolation of synaptic plasma membrane from brain by combined flotation-sedimentation density gradient centrifugation.

30 May 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253974

Analysis of four neuroligin genes as candidates for autism.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2253974

Guilt beyond a reasonable doubt

29 November 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/18179895