Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

Schizophrenia research - 1 Jan 2008

Hoogendoorn Mechteld L C, Vorstman Jacob A S, Jalali Gholam R, Selten Jean-Paul, Sinke Richard J, Emanuel Beverly S, Kahn René S

Abstract excerpt

UNLABELLED: The objectives of this study were 1) to examine whether the prevalence of 22q11.2 deletion syndrome (22q11DS) in schizophrenia patients with the Deficit syndrome is higher than the reported approximately 2% for the population of schizophrenia patients as a whole, and 2) to estimate the overall prevalence of 22q11DS among schizophrenia patients by combining all available studies. Our sample, enriched...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Age of Onset
Share to Chromosomes, Human, Pair 22

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Comorbidity

Share to DiGeorge Syndrome

Share to Netherlands

Share to Psychiatric Status Rating Scales

Share to Schizophrenia

Share to Schizophrenic Psychology

Source

Open in PubMed Open full text

Identifiers

PMID: 17964762
DOI: 10.1016/j.schres.2007.09.025
PMCID: PMC2810966

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophrenia.PMID 17964762Read ↗

[Schizophrenia and the 22q11 deletion syndrome].Semantic proximity Read ↗

Schizophrenia and 22q11.2 deletion syndromeSemantic proximity Read ↗

22q11 deletion syndrome: a genetic subtype of schizophrenia.Semantic proximity Read ↗

[22q11.2DS Syndrome as a Genetic Subtype of Schizophrenia].Semantic proximity Read ↗

22q11 deletion syndrome in childhood onset schizophrenia: an updateSemantic proximity Read ↗

A survey of the 22q11 microdeletion in a large cohort of schizophrenia patients.Semantic proximity Read ↗

Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based Study.Semantic proximity Read ↗

22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basisSemantic proximity Read ↗

Evidence that duplications of 22q11.2 protect against schizophrenia.Semantic proximity Read ↗

Implication of a rare deletion at distal 16p11.2 in schizophrenia.Semantic proximity Read ↗

Schizophrenic Phenotype and Therapeutic Course Associated With Chromosome 22q11.2 Deletion in a Cohort Without Prior Diagnosis of Chromosome 22q11.2 Deletion Syndrome.Semantic proximity Read ↗

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.