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LINKAGE STUDIES ON CHROMOSOME-22 IN FAMILIAL SCHIZOPHRENIA
Author(s): VALLADA HP, GILL M, SHAM P, LIM LCC, NANKO S, ASHERSON P, MURRAY RM, MCGUFFIN P, OWEN M, COLLIER D
Source: AMERICAN JOURNAL OF MEDICAL GENETICS    Volume: 60    Issue: 2    Pages: 139-146    Published: APR 24 1995  
Times Cited: 79     References: 60     
Abstract: As part of a systematic search for a major genetic locus for schizophrenia we have examined chromosome 22 using 14 highly polymorphic markers in 23 disease pedigrees. The markers were distributed at an average distance of 6.6 cM, covering 70-80% of the chromosome, We analyzed the data by the lod score method using five plausible genetic models ranging from dominant to recessive, after testing the power of our sample under the same genetic parameters. The most positive lod score found was 1.51 under a recessive model for the marker D22S278, which is insufficient to conclude linkage. However, an excess of shared alleles in affected siblings (P <.01) was found for both D22S278 and D22S283, For D22S278, the A statistic was equal to the lod score (1.51) and therefore did not provide additional evidence for linkage allowing for heterogeneity, but the Liang statistic was more significant (P =.002). Our results suggest the possibility that the region around D22S278 and D22S283 contains a gene which contributes to the aetiology of schizophrenia. (C) 1995 Wiley-Liss, Inc.
Document Type: Article
Language: English
Reprint Address: VALLADA, HP (reprint author), INST PSYCHIAT, DEPT PSYCHOL MED, DE CRESPIGNY PK, LONDON SE5 8AF, ENGLAND
Addresses:
1. UNIV WALES COLL CARDIFF, COLL MED, DEPT PSYCHOL MED, CARDIFF, S GLAM WALES
2. TEIKYO UNIV, SCH MED, DEPT PSYCHIAT, TOKYO 173, JAPAN
Publisher: WILEY-LISS, DIV JOHN WILEY & SONS INC 605 THIRD AVE, NEW YORK, NY 10158-0012
Subject Category: Genetics & Heredity
IDS Number: QT745
ISSN: 0148-7299
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