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

Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome.

Schizophrenia research - 1 Mar 2014

Monks Stephen, Niarchou Maria, Davies Aimée R, Walters James T R, Williams Nigel, Owen Michael J, van den Bree Marianne B M, Murphy Kieran C

Abstract excerpt

22q11.2 deletion syndrome (22q11.2DS) is associated with high rates of psychotic disorder, particularly schizophrenia. The deletion is considered to be a biological model for understanding this debilitating psychiatric disorder. It is unclear whether the psychotic manifestations in 22q11.2DS are similar to those in schizophrenia patients without the deletion. Catechol-O-methyltransferase (COMT), a positional...

Read the complete abstract on PubMed

Topics

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

Share to Catechol O-Methyltransferase
Share to DiGeorge Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Intelligence

Share to Psychiatric Status Rating Scales

Share to Schizotypal Personality Disorder

Share to Statistics, Nonparametric

Share to Surveys and Questionnaires

Share to United Kingdom

Source

Identifiers

PMID: 24534796
DOI: 10.1016/j.schres.2014.01.020

Genes

COMT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome.PMID 24534796Read ↗

Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome.Semantic proximity Read ↗

Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.Semantic proximity Read ↗

Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome.Semantic proximity Read ↗

Neuroimaging correlates of 22q11.2 deletion syndrome: implications for schizophrenia research.Semantic proximity Read ↗

The schizophrenia phenotype in 22q11 deletion syndrome.Semantic proximity Read ↗

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

Risk Factors for the Emergence of Psychotic Disorders in Adolescents With 22q11.2 Deletion SyndromeSemantic 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 ↗

Risk factors for the emergence of psychotic disorders in adolescents with 22q11.2 deletion syndrome.Semantic proximity Read ↗

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

Dopamine metabolism in adults with 22q11 deletion syndrome, with and without schizophrenia--relationship with COMT Val¹⁰⁸/¹⁵⁸Met polymorphism, gender and symptomatology.Semantic proximity Read ↗

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

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