Neurexin 1 (NRXN1) deletions in schizophrenia (Q24649863)

Europe PubMed Central

title

Neurexin 1 (NRXN1) deletions in schizophrenia (English)

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2

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George Kirov

1

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Michael C O'Donovan

object named as

Michael C O'Donovan

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author name string

Andres Ingason

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David A Collier

4

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Michael J Owen

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

6

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language of work or name

English

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publication date

September 2009

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published in

Schizophrenia Bulletin

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volume

35

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page(s)

851-4

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issue

5

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cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728827

Disruption of the neurexin 1 gene is associated with schizophrenia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728827

Neuroligins and neurexins link synaptic function to cognitive disease

7 April 2017

1 reference

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Rare chromosomal deletions and duplications increase risk of schizophrenia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728827

Analysis of the neuroligin 4Y gene in patients with autism

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728827

Identifying autism loci and genes by tracing recent shared ancestry

7 April 2017

1 reference

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Structural variation of chromosomes in autism spectrum disorder

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728827

Disruption of neurexin 1 associated with autism spectrum disorder

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728827

A patient with vertebral, cognitive and behavioural abnormalities and a de novo deletion of NRXN1alpha

7 April 2017

1 reference

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High frequency of neurexin 1beta signal peptide structural variants in patients with autism

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728827

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728827

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728827

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

7 April 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728827

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

7 April 2017

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Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome

7 April 2017

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Genetics of autism spectrum disorders.

28 September 2017

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Schizophrenia genetics: advancing on two fronts

28 September 2017

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A genome-wide investigation of SNPs and CNVs in schizophrenia

28 September 2017

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Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

28 September 2017

1 reference

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Recurrent CNVs disrupt three candidate genes in schizophrenia patients

28 September 2017

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Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation

28 September 2017

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Phenotypic variations on the theme of CNVs

28 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FSCHBUL%2FSBP079

Cartography of neurexins: more than 1000 isoforms generated by alternative splicing and expressed in distinct subsets of neurons.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2728827

28 November 2018

Identifiers

DOI

10.1093/SCHBUL/SBP079

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3434036

3434036

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1 reference

1 reference