Sequential strategy to identify a susceptibility gene for schizophrenia: Report of potential linkage on chromosome 22q12‐q13.1: Part 1
- 15 March 1994
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 54 (1) , 36-43
- https://doi.org/10.1002/ajmg.1320540108
Abstract
To identify genes responsible for the susceptibility for schizophrenia, and to test the hypothesis that schizophrenia is etiologically heterogeneous, we have studied 39 multiplex families from a systematic sample of schizophrenic patients. Using a complex autosomal dominant model, which considers only those with a diagnosis of schizophrenia or schizoaffective disorder as affected, a random search of the genome for detection of linkage was undertaken. Pairwise linkage analyses suggest a potential linkage (LRH = 34.7 or maximum lod score = 1.54) for one region (22q12‐q13.1). Reanalyses, varying parameters in the dominant model, maximized the LRH at 660.7 (maximum lod score 2.82). This finding is of sufficient interest to warrant further investigation through collaborative studies.Keywords
This publication has 57 references indexed in Scilit:
- Search for a schizophrenia susceptibility locus on human chromosome 22American Journal of Medical Genetics, 1994
- Search for mutations in the β1 GABAA receptor subunit gene in patients with schizophreniaAmerican Journal of Medical Genetics, 1994
- Confirmation that the velo‐cardio‐facial syndrome is associated with haplo‐insufficiency of genes at chromosome 22q11American Journal of Medical Genetics, 1993
- No Evidence for a Pseudoautosomal Locus for SchizophreniaThe British Journal of Psychiatry, 1992
- Evidence for a Pseudoautosomal Locus for SchizophreniaThe British Journal of Psychiatry, 1992
- Evidence for a Pseudoautosomal Locus for SchizophreniaThe British Journal of Psychiatry, 1992
- The GI T-lymphocyte theory of schizophrenia: Some new observationsMedical Hypotheses, 1992
- The human catechol-O-methyltransferase (COMT) gene maps to band q11.2 of chromosome 22 and shows a frequent RFLP with BglICytogenetic and Genome Research, 1992
- Late‐Onset psychosis in the velo‐cardio‐facial syndromeAmerican Journal of Medical Genetics, 1992
- Linkage analysis and family classification under heterogeneityAnnals of Human Genetics, 1983