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Follow-up of a report of a potential linkage for schizophrenia on chromosome 22q12-q13.1: Part 2

Pulver, Ann E., Karayiorgou, Maria, Lasseter, Virginia K., Wolyniec, Paula, Kasch, Laura, Antonarakis, Stylianos, Housman, David, Kazazian, Haig H., Meyers, Deborah, Nestadt, Gerald, Ott, Jurg, Liang, Kung-Yee, Lamacz, Malgorzata, Thomas, Marion, Childs, Barton, Diehl, Scott R., Wang, Shengbiao, Murphy, Bernadette, Sun, Cui-E, O'Neill, F. Anthony, Nie, Li, Sham, Pak, Burke, John, Duke, Betty W., Duke, Fiona, Kipps, Barbara R., Bray, Joseph, Hunt, Wanda, Shinkwin, Rosmarie, Nuallain, Maurin Ni, Su, Ying, Maclean, Charles J., Walsh, Dermot, Kendler, Kenneth S., Gill, Michael, Vallada, Homero, Mant, Rebecca, Asherson, Philip, Collier, David, Parfitt, Elizabeth, Roberts, Enriquetta, Nanko, Shin, Walsh, Cathy, Daniels, Johanna, Murray, Robin, McGuffin, Peter, Owen, Michael John, Laurent, Claudine, Dumas, Jean-Baptiste, d'Amato, Thierry, Jay, Maurice, Martinez, Maria, Campion, Dominique and Mallet, Jacques 1994. Follow-up of a report of a potential linkage for schizophrenia on chromosome 22q12-q13.1: Part 2. American Journal of Medical Genetics 54 (1) , pp. 44-50. 10.1002/ajmg.1320540109

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Abstract

A collaboration involving four groups of investigators (Johns Hopkins University/Massachusetts Institute of Technology; Medical College of Virginia/The Health Research Board, Dublin; Institute of Psychiatry, London/University of Wales, Cardiff; Centre National de la Recherche Scientifique, Paris) was organized to confirm results suggestive of a schizophrenia susceptibility locus on chromosome 22 identified by the JHU/MIT group after a random search of the genome. Diagnostic, laboratory, and analytical reliability exercises were conducted among the groups to ensure uniformity of procedures. Data from genotyping of 3 dinucleotide repeat polymorphisms (at the loci D22S268, IL2RB, 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 heterogeneity for the region 22q12-q13 under this model. We conclude that if this region confers susceptibility to schizophrenia, it must be in only a small proportion of families. Collaborative efforts to obtain large samples must continue to play an important role in the genetic search for clues to complex psychiatric disorders such as schizophrenia

Item Type: Article
Date Type: Publication
Status: Published
Schools: MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG)
Medicine
Neuroscience and Mental Health Research Institute (NMHRI)
Subjects: R Medicine > R Medicine (General)
Publisher: Wiley
ISSN: 0148-7299
Last Modified: 04 Jun 2017 08:35
URI: http://orca.cf.ac.uk/id/eprint/80623

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