Genetic factors constitute the most important known risk factor for schizophrenia. We request in this application three years of continued support for a multi-faceted epidemiologic project, the goal of which is to increase our knowledge of the role of genetic factors in the etiology of schizophrenia. The project has two components: i) a case controlled family study of schizophrenia based on the psychiatric and electoral registries of County Roscommon, Ireland, and ii) a high density study of families with multiple cases of schizophrenia ascertained systematically from the entire island of Ireland (the Republic of Ireland and Northern Ireland). This renewal has three major goals. The first is to complete the ascertainment, study and sampling of families with a high density of schizophrenia from throughout the island of Ireland. Evidence is presented that the sample size required for high power to detect linkage for a disorder like schizophrenia is much larger than that needed for classic mendelian traits. Ireland represents an ideal environment in which to conduct such studies, as is proven by our work accomplished to date. Our second goal is to use the extensive clinical data obtained on affected members of these high-density pedigrees to search for patterns of clinical heterogeneity within schizophrenia that are transmitted within families. Such patterns, if detected, can serve as the basis of a priori tests for heterogeneity in future linkage analyses. Our third goal is to conduct further data analysis of our recently completed case-controlled family study to address such issues as the boundaries of the schizophrenia spectrum, the relationship between major clinical features of schizophrenia such as age at onset and outcome and the familial vulnerability to illness and the association between personality traits such as introversion, social anhedonia and magical thinking and the familial liability to schizophrenia.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH041953-07
Application #
3380929
Study Section
Epidemiologic and Services Research Review Committee (EPS)
Project Start
1986-12-01
Project End
1995-03-31
Budget Start
1993-04-01
Budget End
1994-03-31
Support Year
7
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Virginia Commonwealth University
Department
Type
Schools of Medicine
DUNS #
City
Richmond
State
VA
Country
United States
Zip Code
23298
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Heron, Elizabeth A; Cormican, Paul; Donohoe, Gary et al. (2014) No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset. Schizophr Res 154:79-82
Rees, Elliott; Walters, James T R; Chambert, Kimberly D et al. (2014) CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1. Hum Mol Genet 23:1669-76
Morris, Derek W; Pearson, Richard D; Cormican, Paul et al. (2014) An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis. Hum Mol Genet 23:3316-26

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