Access the full text.
Sign up today, get DeepDyve free for 14 days.
J. Knight, A. Knight, G. Ungvari (1992)
Can Autoimmune Mechanisms Account for the Genetic Predisposition to Schizophrenia?British Journal of Psychiatry, 160
D. Clair, D. Blackwood, Walter Muir, Walter Muir, D. Baillie, A. Hubbard, A. Wright, H. Evans (1989)
No linkage of chromosome 5q11-q13 markers to schizophrenia in Scottish familiesNature, 339
R. Winqvist, K. Lundström, M. Salminen, M. Laatikainen, I. Ulmanen (1992)
The human catechol-O-methyltransferase (COMT) gene maps to band q11.2 of chromosome 22 and shows a frequent RFLP with BglI.Cytogenetics and cell genetics, 59 4
P. Green (1990)
Genetic linkage and complex diseases: A commentGenetic Epidemiology, 7
T. D’amato, D. Campion, P. Gorwood, M. Jay, O. Sabaté, C. Petit, M. Abbar, A. Malafosse, M. Leboyer, D. Hillaire, F. Clerget-Darpoux, J. Feingold, G. Waksman, J. Mallet (1992)
Evidence for a Pseudoautosomal Locus for SchizophreniaBritish Journal of Psychiatry, 161
R. Murray, A. Reveley, P. McGuffin (1986)
Genetic vulnerability to schizophrenia.The Psychiatric clinics of North America, 9 1
R. Sherrington, J. Brynjólfsson, H. Pétursson, M. Potter, K. Dudleston, B. Barraclough, J. Wasmuth, M. Dobbs, H. Gurling (1988)
Localization of a susceptibility locus for schizophrenia on chromosome 5Nature, 336
M. Green, P. Satz, D. Gaier, S. Ganzell, F. Kharabi (1989)
Minor physical anomalies in schizophrenia.Schizophrenia bulletin, 15 1
A. Pulver, Maria Karayiorgou, V. Lasseter, P. Wolyniec, L. Kasch, S. Antonarakis, D. Housman, H. Kazazian, D. Meyers, G. Nestadt, Jurg Ott, Kung-Yee Liang, M. Lamacz, Marion Thomas, B. Childs, Scott Diehl, Shengbiao Wang, B. Murphy, Cui-e Sun, F. O’Neill, Li Nie, Pak Sham, J. Burke, Betty Duke, Fiona Duke, B. Kipps, J. Bray, Wanda Hunt, Rosmarie Shinkwin, Maurin Nuallain, Ying Su, Charles MacLean, D. Walsh, K. Kendler, Michael Gill, H. Vallada, R. Mant, P. Asherson, D. Collier, Elizabeth Parfitt, Enriquetta Roberts, S. Nanko, Cathy Walsh, J. Daniels, Robin Murray, P. McGuffin, M. Owen, Claudine Laurent, J. Dumas, Thierry d'Amato, M. Jay, Maria Martinez, Dominique Campion, Jacques Mallet (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
K. Kendler, Scott Diehl (1993)
The genetics of schizophrenia: a current, genetic-epidemiologic perspective.Schizophrenia bulletin, 19 2
S. Detera-Wadleigh, L. Goldin, R. Sherrington, I. Encío, C. Miguel, W. Berrettini, H. Gurling, E. Gershon (1989)
Exclusion of linkage to 5qll13 in families with schizophrenia and other psychiatric disordersNature, 340
A. Pulver, K. Liang, G. Vogler (1991)
Estimating effects of proband characteristics on familial risk: II. The association between age at onset and familial risk in the Maryland schizophrenia sampleGenetic Epidemiology, 8
N. Risch (1990)
Genetic linkage and complex diseases: A responseGenetic Epidemiology, 7
J. Ott (1983)
Linkage analysis and family classification under heterogeneityAnnals of Human Genetics, 47
M. Owen (1992)
Will schizophrenia become a graveyard for molecular geneticists?Psychological Medicine, 22
S. Hodge, C. Anderson, K. Neiswanger, R. Sparkes, D. Rimoin (1983)
The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneity.American journal of human genetics, 35 6
H. Vallada, D. Collier, E. Dawson, M. Owen, S. Nanko, R. Murray, M. Gill (1992)
Debrisoquine 4-hydroxylase (CYP2D) locus and possible susceptibility to schizophreniaThe Lancet, 340
T d'Amato, D Campion, Ph Gorwood, M Jay, O Sabate, C Petit, M Abbar, A Malafosse, M Leboyer, D Hillaire, F Clerget‐Darpoux, J Feingold, G Waksman, J Mallet (1992)
Evidence for a pseudoautosomal locus for schizophrenia II: Replication of a non‐random segregation of alleles at the DXYS14 locus, 161
Gualtieri Ct, A. Adams, Shen Cd, D. Loiselle (1982)
Minor physical anomalies in alcoholic and schizophrenic adults and hyperactive and autistic children.The American journal of psychiatry, 139 5
J. Guy, Lawrence Majorski, C. Wallace, Margaret Guy (1983)
The incidence of minor physical anomalies in adult male schizophrenics.Schizophrenia bulletin, 9 4
P. Wolyniec, AnnE. Pulver, J. McGrath, Doreen Tam (1992)
Schizophrenia: gender and familial risk.Journal of psychiatric research, 26 1
David Kelly, R. Goldberg, D. Wilson, Elizabeth Lindsay, Alisoun Carey, J. Goodship, J. Burn, I. Cross, R. Shprintzen, P. Scambler (1993)
Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11.American journal of medical genetics, 45 3
M. Baron, L. Asnis, R. Gruen (1981)
The Schedule for Schizotypal Personalities (SSP): A diagnostic interview for schizotypal featuresPsychiatry Research, 4
E. Healy, C. Buckley, C. Ivison, L. Poulter, M. Rustin, K. McKenna, A. Hughes, E. Bingham, N. Nevin, M. Sheehan, G. Gibson, E. McGinnity, J. Walshe, M. Carmody, J. Donohoe, P. McGrath, R. O'Moore, G. Murphy (1993)
Royal academy of medicine in ireland section of dermatologyIrish Journal of Medical Science, 162
J. Goldstein, S. Faraone, Wei Chen, George Tolomiczencko, M. Tsuang (1990)
Sex Differences in the Familial Transmission of SchizophreniaBritish Journal of Psychiatry, 156
D. Black, R. Fisher (1992)
Mortality in DSM-IIIR schizophreniaSchizophrenia Research, 7
Golding-Kushner Kj, G. Weller, R. Shprintzen (1985)
Velo-cardio-facial syndrome: language and psychological profiles.Journal of craniofacial genetics and developmental biology, 5 3
M. Polymeropoulos, H. Coon, W. Byerley, E. Gershon, L. Goldin, T. Crow, J. Rubenstein, M. Hoff, J. Holik, A. Smith (1994)
Search for a schizophrenia susceptibility locus on human chromosome 22.American journal of medical genetics, 54 2
W. Eaton (1991)
Update on the epidemiology of schizophrenia.Epidemiologic reviews, 13
P. McGuffin, M. Sargeant, G. Hetti, Simon Tidmarsh, Sharon Whatley, R. Marchbanks (1990)
Exclusion of a schizophrenia susceptibility gene from the chromosome 5q11-q13 region: new data and a reanalysis of previous reports.American journal of human genetics, 47 3
A. Pulver, S. Bale, D. Rao, G. Vogler (1989)
Availability of schizophrenic patients and their families for genetic linkage studies: Findings from the Maryland epidemiology sampleGenetic Epidemiology, 6
J. Weissenbach, G. Gyapay, C. Dib, A. Vignal, J. Morissette, P. Millasseau, G. Vaysseix, M. Lathrop (1992)
A second-generation linkage map of the human genomeNature, 359
Jurg Ott (1992)
Strategies for characterizing highly polymorphic markers in human gene mapping.American journal of human genetics, 51 2
R. Smith (1991)
Is schizophrenia caused by excessive production of interleukin-2 and interleukin-2 receptors by gastrointestinal lymphocytes?Medical hypotheses, 34 3
R. Shprintzen, R. Goldberg, K. Golding-Kushner, R. Marion (1992)
Late-onset psychosis in the velo-cardio-facial syndrome.American journal of medical genetics, 42 1
H. Aschauer, G. Aschauer-Treiber, K. Isenberg, R. Todd, M. Knesevich, D. Garver, T. Reich, C. Cloninger (1990)
No evidence for linkage between chromosome 5 markers and schizophrenia.Human heredity, 40 2
P Asherson, E Parfitt, M Sargeant, S Tidmarsh, P Buckland, C Taylor, A Clements, M Gill, P McGuffin, M Owen (1992)
No evidence for a pseudoautosomal locus for schizophrenia. Linkage analysis of multiply affected families, 161
P. Asherson, E. Parfitt, M. Sargeant, S. Tidmarsh, P. Buckland, C. Taylor, A. Clements, M. Gill, P. McGuffin, M. Owen (1992)
No Evidence for a Pseudoautosomal Locus for SchizophreniaBritish Journal of Psychiatry, 161
A. Pulver, K. Liang, C. Brown, P. Wolyniec, John McGrath, L. Adler, Doreen Tam, W. Carpenter, B. Childs (1992)
Risk Factors in SchizophreniaBritish Journal of Psychiatry, 160
P. Pearson (1991)
The genome data base (GDB)--a human gene mapping repository.Nucleic acids research, 19 Suppl
R. Smith (1992)
The GI T-lymphocyte theory of schizophrenia: some new observations.Medical hypotheses, 37 1
MA Anderson, JF Gusella (1984)
Use of cyclosporin A in establishing Epstein‐Barr virus transformed human lymphoblastoid cell lines, 20
G. Lathrop, J. Lalouel, C. Julier, J. Ott (1984)
Strategies for multilocus linkage analysis in humans.Proceedings of the National Academy of Sciences of the United States of America, 81 11
M. Rapaport, C. Mcallister, D. Pickar, D. Nelson, S. Paul (1989)
Elevated levels of soluble interleukin 2 receptors in schizophrenia.Archives of general psychiatry, 46 3
N. Dracopoli, B. Alhadeff, A. Houghton, L. Old (1987)
Loss of heterozygosity at autosomal and X-linked loci during tumor progression in a patient with melanoma.Cancer research, 47 15
D. Stangl, B. Pfohl, M. Zimmerman, W. Bowers, C. Corenthal (1985)
A structured interview for the DSM-III personality disorders. A preliminary report.Archives of general psychiatry, 42 6
Hilary Coon, J. Sobell, Leonard Heston, Steve Sommer, Mark Hoff, J. Holik, F. Umar, Margaret Robertson, Fred Reimherr, Paul Wender, Kevin Vest, M. Myles‐Worsley, E. Gershon, Lynn DeLisi, G. Shields, Paul Dale, A. Polloi, Merilyne Waldo, Sherry Leonard, James Sikela, R. Freedman, William Byerley (1994)
Search for mutations in the beta 1 GABAA receptor subunit gene in patients with schizophrenia.American journal of medical genetics, 54 1
A. Feinberg, B. Vogelstein (1983)
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.Analytical biochemistry, 132 1
J. Kennedy, L. Giuffra, H. Moises, L. Cavalli-Sforza, A. Pakstis, J. Kidd, C. Castiglione, Barbro Sjogren, L. Wetterberg, K. Kidd (1988)
Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigreeNature, 336
R. Ganguli, B. Rabin (1989)
Increased serum interleukin 2 receptor concentration in schizophrenic and brain-damaged subjects.Archives of general psychiatry, 46 3
T. Hudson, M. Engelstein, Matthias Lee, Elizabeth Ho, M. Rubenfield, Christopher Adams, D. Housman, N. Dracopoli (1992)
Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms.Genomics, 13 3
J. Wing, T. Babor, T. Brugha, J. Burke, J. Cooper, R. Giel, A. Jablenski, D. Regier, N. Sartorius (1990)
SCAN. Schedules for Clinical Assessment in Neuropsychiatry.Archives of general psychiatry, 47 6
L. Robins, J. Helzer, J. Croughan, K. Ratcliff (1981)
National Institute of Mental Health Diagnostic Interview Schedule. Its history, characteristics, and validity.Archives of general psychiatry, 38 4
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. © 1994 Wiley‐Liss, Inc.
American Journal of Medical Genetics Part A – Wiley
Published: Mar 15, 1995
Keywords: ; ; ; ;
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.