from genotyping of 3 dinucleotide repeat polymorphisms (at the loci D22S268, ILSRB, D22S307) for a combined replication sample of 256 families, each having 2 or more affected individuals with DNA, were analysed using a complex autosomal dominant model. This study provided no evidence for linkage or
Sequential strategy to identify a susceptibility gene for schizophrenia: Report of potential linkage on chromosome 22q12-q13.1: Part 1
โ Scribed by Pulver, Ann E. ;Karayiorgou, Maria ;Wolyniec, Paula S. ;Lasseter, Virginia K. ;Kasch, Laura ;Nestadt, Gerald ;Antonarakis, Stylianos ;Housman, David ;Kazazian, Haig H. ;Meyers, Deborah ;Ott, Jurg ;Lamacz, Malgorzata ;Liang, Kung-Yee ;Hanfelt, John ;Ullrich, Gail ;DeMarchi, Nicola ;Ramu, Elango ;McHugh, Paul R. ;Adler, Lawrence ;Thomas, Marion ;Carpenter, William T. ;Manschreck, Theo ;Gordon, C. T. ;Kimberland, Michelle ;Babb, Robert ;Puck, Jennifer ;Childs, Barton
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 1000 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
โฆ Synopsis
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.
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