The schizophrenia phenotype in 22q11 deletion syndrome

A.S. Bassett; E.W.C. Chow; P. AbdelMalik; Mirona Gheorghiu; J. Husted; R. Weksberg

doi:10.1176/appi.ajp.160.9.1580

The schizophrenia phenotype in 22q11 deletion syndrome

A.S. Bassett, E.W.C. Chow, P. AbdelMalik, Mirona Gheorghiu, J. Husted, R. Weksberg

Research output: Contribution to journal › Article › peer-review

282 Citations (Scopus)

Abstract

Objective: This study investigated the schizophrenia phenotype in 24 subjects with 22q11 deletion syndrome (22qDS) and schizophrenia (22qDS-schizophrenia), a rare but relatively homogenous genetic subtype of schizophrenia associated with a microdeletion on chromosome 22. Individuals with 22qDS are at genetically high risk for schizophrenia.

Original language	English
Pages (from-to)	1580-1586
Number of pages	7
Journal	American Journal of Psychiatry
Volume	160
Issue number	9
DOIs	https://doi.org/10.1176/appi.ajp.160.9.1580
Publication status	Published - Sept 2003

ASJC Scopus subject areas

Psychiatry and Mental health

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1176/appi.ajp.160.9.1580

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276594/

Cite this

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title = "The schizophrenia phenotype in 22q11 deletion syndrome",

abstract = "Objective: This study investigated the schizophrenia phenotype in 24 subjects with 22q11 deletion syndrome (22qDS) and schizophrenia (22qDS-schizophrenia), a rare but relatively homogenous genetic subtype of schizophrenia associated with a microdeletion on chromosome 22. Individuals with 22qDS are at genetically high risk for schizophrenia.",

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AU - Husted, J.

AU - Weksberg, R.

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N2 - Objective: This study investigated the schizophrenia phenotype in 24 subjects with 22q11 deletion syndrome (22qDS) and schizophrenia (22qDS-schizophrenia), a rare but relatively homogenous genetic subtype of schizophrenia associated with a microdeletion on chromosome 22. Individuals with 22qDS are at genetically high risk for schizophrenia.

AB - Objective: This study investigated the schizophrenia phenotype in 24 subjects with 22q11 deletion syndrome (22qDS) and schizophrenia (22qDS-schizophrenia), a rare but relatively homogenous genetic subtype of schizophrenia associated with a microdeletion on chromosome 22. Individuals with 22qDS are at genetically high risk for schizophrenia.

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DO - 10.1176/appi.ajp.160.9.1580

M3 - Article

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EP - 1586

JO - American Journal of Psychiatry

JF - American Journal of Psychiatry

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ER -

The schizophrenia phenotype in 22q11 deletion syndrome

Abstract

ASJC Scopus subject areas

UN SDGs

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