The long-term goal is to provide new and improved analytical methods that will enable researchers to find gene markers genetically linked with the putative gene(s) for schizophrenia. This, in turn, will open the way to identifying the schizophrenia gene(s). Once such genes are found, there is hope that knowledge of their structure will lead to a deeper understanding of the disease etiology and, thus, to the possibility of ameliorating or curing schizophrenia.
The specific aims consist of 1) developing and implementing chromosome-based computer simulation, 2) implementing exclusion mapping of schizophrenia under heterogeneity, 3) studying and implementing methods of allowing for biological variables in linkage analysis of schizophrenia, 4) adapting the LINKAGE programs for their use on parallel computers for more efficient linkage analysis, 5) to study the feasibility and power of nonparametric ad hoc statistics for major genes in schizophrenia families, and 7) to consult with and give advice to researchers collecting schizophrenia families and to apply the methods obtained to schizophrenia families (data collected through projects of other investigators). Computer programs and methods obtained through this work will be made freely available to researchers.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37MH044292-12
Application #
6343707
Study Section
Special Emphasis Panel (NSS)
Program Officer
Moldin, Steven Owen
Project Start
1989-05-01
Project End
2002-12-31
Budget Start
2001-01-01
Budget End
2001-12-31
Support Year
12
Fiscal Year
2001
Total Cost
$262,756
Indirect Cost
Name
Rockefeller University
Department
Biostatistics & Other Math Sci
Type
Other Domestic Higher Education
DUNS #
071037113
City
New York
State
NY
Country
United States
Zip Code
10065
Xu, Haiyan; Cheng, Rong; Juo, Suh-Hang et al. (2011) Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7q. Am J Med Genet B Neuropsychiatr Genet 156:168-76
He, C; Hamon, S; Li, D et al. (2009) MHC fine mapping of human type 1 diabetes using the T1DGC data. Diabetes Obes Metab 11 Suppl 1:53-9
Cheung, Kenneth M C; Karppinen, Jaro; Chan, Danny et al. (2009) Prevalence and pattern of lumbar magnetic resonance imaging changes in a population study of one thousand forty-three individuals. Spine (Phila Pa 1976) 34:934-40
Long, Quan; Zhang, Qingrun; Ott, Jurg (2009) Detecting disease-associated genotype patterns. BMC Bioinformatics 10 Suppl 1:S75
Yuferov, Vadim; Ji, Fei; Nielsen, David A et al. (2009) A functional haplotype implicated in vulnerability to develop cocaine dependence is associated with reduced PDYN expression in human brain. Neuropsychopharmacology 34:1185-97
Andreoli, Michael T; Morrison, Margaux A; Kim, Ben J et al. (2009) Comprehensive analysis of complement factor H and LOC387715/ARMS2/HTRA1 variants with respect to phenotype in advanced age-related macular degeneration. Am J Ophthalmol 148:869-74
Deangelis, Margaret M; Ji, Fei; Adams, Scott et al. (2008) Alleles in the HtrA serine peptidase 1 gene alter the risk of neovascular age-related macular degeneration. Ophthalmology 115:1209-1215.e7
Li, Dawei; He, Lin (2008) Meta-study on association between the monoamine oxidase A gene (MAOA) and schizophrenia. Am J Med Genet B Neuropsychiatr Genet 147B:174-8
Kim, Ivana K; Ji, Fei; Morrison, Margaux A et al. (2008) Comprehensive analysis of CRP, CFH Y402H and environmental risk factors on risk of neovascular age-related macular degeneration. Mol Vis 14:1487-95
Matthews, Abigail G; Finkelstein, Dianne M; Betensky, Rebecca A (2008) Analysis of familial aggregation studies with complex ascertainment schemes. Stat Med 27:5076-92

Showing the most recent 10 out of 40 publications