A survey of the 22q11 microdeletion in a large cohort of schizophrenia patients.

Abstract:

:The occurrence of a microdeletion at 22q11 has long been considered to constitute a risk factor for schizophrenia. Higher rates of 22q11 deletions have been reported in cohorts of patients with schizophrenia. In order to estimate the prevalence of the 22q11 deletion in schizophrenia patients more accurately, a screening for 22q11 deletions was conducted on a cohort of 634 schizophrenia patients, the largest sample size screened to date. Seven microsatellites and three SNPs were used to assess the deletion genotype. In cases where all markers were found to be homozygous (hemizygous), the individual was assumed to carry the deletion. The method used here is simple and efficient in comparison with hybridization technologies. Moreover, the rate of false positives is very low (P-value in the range of 10(-4) to 10(-3)). Approximately 1% of the patient cohort was found to carry 22q11 deletions.

journal_name

Schizophr Res

journal_title

Schizophrenia research

authors

Horowitz A,Shifman S,Rivlin N,Pisanté A,Darvasi A

doi

10.1016/j.schres.2004.02.008

subject

Has Abstract

pub_date

2005-03-01 00:00:00

pages

263-7

issue

2-3

eissn

0920-9964

issn

1573-2509

pii

S092099640400060X

journal_volume

73

pub_type

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