(Q37658896)

21 August 2017

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title

The role of copy number variation in schizophrenia (English)

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21 August 2017

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George Kirov

1

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21 August 2017

publication date

1 January 2010

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Expert Review of Neurotherapeutics: a key contribution to decision making in the treatment of neurologic and neuropsychiatric disorders

21 August 2017

published in

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21 August 2017

volume

10

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21 August 2017

issue

1

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21 August 2017

page(s)

25-32

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High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

21 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Integrated detection and population-genetic analysis of SNPs and copy number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Copy number variants, diseases and gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Strong association of de novo copy number mutations with sporadic schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Large recurrent microdeletions associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

A genome-wide investigation of SNPs and CNVs in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Neurexin 1 (NRXN1) deletions in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Neuroligins and neurexins link synaptic function to cognitive disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Structural variation of chromosomes in autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbances.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

A 15q13.3 microdeletion segregating with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Microduplications of 16p11.2 are associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion).

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Disruption of two novel genes by a translocation co-segregating with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Population analysis of large copy number variants and hotspots of human genetic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Reversing neurodevelopmental disorders in adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2FERN.09.133

21 January 2018

Identifiers

DOI

10.1586/ERN.09.133

1 reference

21 August 2017

1 reference