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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 36-43 |
| Number of pages | 8 |
| Journal | American journal of medical genetics |
| Volume | 54 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1994 |
| Externally published | Yes |
Keywords
- genetic linkage analysis
- heterogeneity
- human chromosome 22
- random search
- schizophrenia
ASJC Scopus subject areas
- Genetics(clinical)