A combined analysis of D22S278 marker alleles in affected sib-pairs: Support for a susceptibility locus for schizophrenia at chromosome 22q12

Michael Gill, Homero Vallada, David Collier, Pak C. Sham, Peter Holmans(University of Wales), Robin Murray, Peter McGuffin(University of Wales), Shin Nanko(Teikyo University), Mike Owen(University of Wales), Stylianos E. Antonarakis(University of Geneva), David E. Housman(Massachusetts Institute of Technology), Haig H. Kazazian(University of Pennsylvania), Gerald Nestadt(Johns Hopkins University), Ann E. Pulver(Johns Hopkins University), Richard E. Straub(Virginia Commonwealth University Medical Center), Charles J. MacLean(Virginia Commonwealth University Medical Center), Dermot Walsh(St. Patrick's Hospital), Kenneth S. Kendler(Virginia Commonwealth University Medical Center), Lynn E. DeLisi(Stony Brook University), Mihael H. Polymeropoulos(Stony Brook University), Hilary Coon(University of Utah), William Byerley(University of Utah), R. Lofthouse(Stony Brook University), Elliot S. Gershon, Lynn Golden, Timothy J. Crow(MRC Clinical Trials Unit at UCL), William Byerley(University of Utah), Robert Freedman(University of Colorado Health), Claudine Laurent(Centre National de la Recherche Scientifique), Sylvie Bodeau‐Péan(Centre National de la Recherche Scientifique), Thierry d’Amato(Centre National de la Recherche Scientifique), Maurice Jay(Centre National de la Recherche Scientifique), Dominique Campion(Centre National de la Recherche Scientifique), Jacques Mallet(Centre National de la Recherche Scientifique), Dieter B. Wildenauer(Ludwig-Maximilians-Universität München), Bernard Lerer(Herzog Hospital), Margot Albus, Manfred Ackenheil(Ludwig-Maximilians-Universität München), Richard P. Ebstein(Herzog Hospital), Joachim Hallmayer(Ludwig-Maximilians-Universität München), Wolfgang Maier(Johannes Gutenberg University Mainz), Hugh Gurling(University College London), David Curtis(University College London), G. Kalsi(University College London), Jon Brynjolfsson, Thordur Sigmundson, Hannes Pétursson, Douglas Blackwood(Royal Edinburgh Hospital), Walter Muir(Western General Hospital), David St Clair(Royal Edinburgh Hospital), Lin He(Royal Edinburgh Hospital), Susan Maguire(Royal Edinburgh Hospital), Hans W. Moises(Kiel University), Hai‐Gwo Hwu(National Taiwan University Hospital), Yang Liu(Kiel University), Claudia Wiese(Kiel University), Tao Li, Xiehe Liu, Helgi Kristbjarnason(National University Hospital of Iceland), Douglas F. Levinson(Drexel University), Bryan Mowry(University of Queensland), Helen Donis-Keller(Washington University in St. Louis), Nicholas K. Hayward(QIMR Berghofer Medical Research Institute), Raymond R. Crowe(University of Iowa Hospitals and Clinics), Jeremy M. Silverman, Derek J. Nancarrow(University of Queensland), Christina M. Read(Washington University in St. Louis)
American Journal of Medical Genetics
February 16, 1996
Cited by 235

Abstract

Several groups have reported weak evidence for linkage between schizophrenia and genetic markers located on chromosome 22q using the lod score method of analysis. However these findings involved different genetic markers and methods of analysis, and so were not directly comparable. To resolve this issue we have performed a combined analysis of genotypic data from the marker D22S278 in multiply affected schizophrenic families derived from 11 independent research groups worldwide. This marker was chosen because it showed maximum evidence for linkage in three independent datasets (Vallada et al., Am J Med Genet 60:139-146, 1995; Polymeropoulos et al., Neuropsychiatr Genet 54:93-99, 1994; Lasseter et al., Am J Med Genet, 60:172-173, 1995. Using the affected sib-pair method as implemented by the program ESPA, the combined dataset showed 252 alleles shared compared with 188 alleles not share (chi-square 9.31, 1df, P = 0.001) where parental genotype data was completely known. When sib-pairs for whom parental data was assigned according to probability were included the number of alleles shared was 514.1 compared with 437.8 not shared (chi-square 6.12, 1df, P = 0.006). Similar results were obtained when a likelihood ratio method for sib-pair analysis was used. These results indicate that may be a susceptibility locus for schizophrenia at 22q12.


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