(Q35109411)

6 August 2017

title

Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients (English)

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6 August 2017

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6

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ORCID Public Data File 2021

6 August 2017

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author name string

Jacobine E Buizer-Voskamp

1

1 reference

6 August 2017

Jan-Willem Muntjewerff

2

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6 August 2017

Genetic Risk and Outcome in Psychosis (GROUP) Consortium Members

3

1 reference

6 August 2017

Eric Strengman

4

1 reference

6 August 2017

Chiara Sabatti

5

1 reference

6 August 2017

Jacob A S Vorstman

7

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6 August 2017

Roel A Ophoff

8

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6 August 2017

language of work or name

English

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publication date

13 April 2011

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6 August 2017

published in

Biological Psychiatry

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6 August 2017

volume

70

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6 August 2017

issue

7

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6 August 2017

page(s)

655-662

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The effect of algorithms on copy number variant detection

6 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=3137747

Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease

9 July 2018

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Genome-wide approaches to schizophrenia

9 July 2018

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Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays

9 July 2018

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The impact of human copy number variation on a new era of genetic testing.

9 July 2018

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9 July 2018

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Origins and functional impact of copy number variation in the human genome

9 July 2018

1 reference

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Copy number variations of chromosome 16p13.1 region associated with schizophrenia

9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

9 July 2018

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9 July 2018

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9 July 2018

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A genome-wide investigation of SNPs and CNVs in schizophrenia

9 July 2018

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

9 July 2018

1 reference

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Recurrent CNVs disrupt three candidate genes in schizophrenia patients

9 July 2018

1 reference

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

9 July 2018

1 reference

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Identification of loci associated with schizophrenia by genome-wide association and follow-up

9 July 2018

1 reference

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Large recurrent microdeletions associated with schizophrenia

9 July 2018

1 reference

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Rare chromosomal deletions and duplications increase risk of schizophrenia

9 July 2018

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9 July 2018

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9 July 2018

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Strong association of de novo copy number mutations with sporadic schizophrenia

9 July 2018

1 reference

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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

9 July 2018

1 reference

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Gene expression in the etiology of schizophrenia.

9 July 2018

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

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophrenia

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders

9 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Copy number variation: new insights in genome diversity

9 July 2018

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Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

The genetics of schizophrenia

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Segmental duplications and copy-number variation in the human genome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

The molecular genetics of the 22q11-associated schizophrenia

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Detection of large-scale variation in the human genome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Assessing the performance of the haplotype block model of linkage disequilibrium

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Epidemiology of schizophrenia: the global burden of disease and disability

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Schizophrenia: genes and environment

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Schizophrenia epigenesis: past, present, and future.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Symptoms, signs, and diagnosis of schizophrenia

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Association within a family of a balanced autosomal translocation with major mental illness

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3137747

Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia

27 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21489405

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Chromosomal abnormalities and psychosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21489405

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.BIOPSYCH.2011.02.015

1 reference

6 August 2017

1 reference

6 August 2017

1 reference