(Q35532389)

8 August 2017

title

Contactin 4 as an autism susceptibility locus (English)

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8 August 2017

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1 reference

Kim L McBride

13

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Julie Gastier-Foster

12

object named as

Julie M Gastier-Foster

1 reference

8 August 2017

Catherine E Cottrell

1

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8 August 2017

Natalie Bir

2

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8 August 2017

Elizabeth Varga

3

1 reference

8 August 2017

Carlos E Alvarez

4

1 reference

8 August 2017

Samuel Bouyain

5

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8 August 2017

Randall Zernzach

6

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8 August 2017

Devon L Thrush

7

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8 August 2017

Johnna Evans

8

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8 August 2017

Michael Trimarchi

9

1 reference

8 August 2017

Eric M Butter

10

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8 August 2017

David Cunningham

11

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8 August 2017

Gail E Herman

14

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8 August 2017

publication date

9 February 2011

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8 August 2017

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8 August 2017

volume

4

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8 August 2017

issue

3

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8 August 2017

page(s)

189-199

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A map of human genome variation from population-scale sequencing

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Clinical genetic testing for patients with autism spectrum disorders

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Hotspots of large rare deletions in the human genome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

The protein tyrosine phosphatases PTPRZ and PTPRG bind to distinct members of the contactin family of neural recognition molecules

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Contactins: emerging key roles in the development and function of the nervous system

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

The immunoglobulin superfamily of neuronal cell adhesion molecules: lessons from animal models and correlation with human disease.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Mutations in contactin-1, a neural adhesion and neuromuscular junction protein, cause a familial form of lethal congenital myopathy

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Impairment of learning and memory in TAG-1 deficient mice associated with shorter CNS internodes and disrupted juxtaparanodes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Disruption of contactin 4 in three subjects with autism spectrum disorder

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Structural variation of chromosomes in autism spectrum disorder

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Association between microdeletion and microduplication at 16p11.2 and autism

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Recurrent 16p11.2 microdeletions in autism

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Contribution of SHANK3 mutations to autism spectrum disorder

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Heterozygous deletion of ITPR1, but not SUMF1, in spinocerebellar ataxia type 16

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Clustal W and Clustal X version 2.0

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Strong association of de novo copy number mutations with autism

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

The contactin 4 gene locus at 3p26 is a candidate gene of SCA16.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Detection of large-scale variation in the human genome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Human non-synonymous SNPs: server and survey

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Predicting deleterious amino acid substitutions

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Molecular characterization of de novo secondary trisomy 13.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

The carbonic anhydrase domain of receptor tyrosine phosphatase beta is a functional ligand for the axonal cell recognition molecule contactin

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

Basic local alignment search tool

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3209658

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

27 July 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?

21 January 2018

1 reference

Ataxia and abnormal cerebellar microorganization in mice with ablated contactin gene expression

21 January 2018

1 reference

Contact in the genetics of autism and schizophrenia.

21 January 2018

1 reference

FISH and array-CGH analysis of a complex chromosome 3 aberration suggests that loss of CNTN4 and CRBN contributes to mental retardation in 3pter deletions.

21 January 2018

1 reference

Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.

21 January 2018

1 reference

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

21 January 2018

1 reference

Identifying autism loci and genes by tracing recent shared ancestry

21 January 2018

1 reference

Terminal 3p deletions in two families--correlation between molecular karyotype and phenotype.

21 January 2018

1 reference

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

21 January 2018

1 reference

Microarray based analysis of 3p25-p26 deletions (3p- syndrome).

21 January 2018

1 reference

Impaired motor coordination in mice lacking neural recognition molecule NB-3 of the contactin/F3 subgroup.

21 January 2018

1 reference

Deficiency of neural recognition molecule NB-2 affects the development of glutamatergic auditory pathways from the ventral cochlear nucleus to the superior olivary complex in mouse.

21 January 2018

1 reference

The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly.

21 January 2018

1 reference

Distal 3p deletion syndrome: detailed molecular cytogenetic and clinical characterization of three small distal deletions and review

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21308999

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

BIG-2 mediates olfactory axon convergence to target glomeruli

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21308999

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/AUR.184

1 reference

8 August 2017

1 reference

8 August 2017

1 reference