Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS031564-03
Application #
2269499
Study Section
Epidemiology and Disease Control Subcommittee 2 (EDC)
Project Start
1994-05-01
Project End
1999-01-31
Budget Start
1996-02-01
Budget End
1997-01-31
Support Year
3
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Virginia Commonwealth University
Department
Genetics
Type
Schools of Medicine
DUNS #
City
Richmond
State
VA
Country
United States
Zip Code
23298
Seinfeld, Syndi A; Pellock, John M; Kjeldsen, Marianne J et al. (2016) Epilepsy After Febrile Seizures: Twins Suggest Genetic Influence. Pediatr Neurol 55:14-6
Corey, Linda A; Pellock, John M; Kjeldsen, Marianne J et al. (2011) Importance of genetic factors in the occurrence of epilepsy syndrome type: a twin study. Epilepsy Res 97:103-11
Corey, Linda A; Kjeldsen, Marianne J; Solaas, Marit H et al. (2009) The accuracy of self-reported history of seizures in Danish, Norwegian and U.S. twins. Epilepsy Res 84:1-5
Nakken, K O; Solaas, M H; Kjeldsen, M J et al. (2009) The occurrence and characteristics of auras in a large epilepsy cohort. Acta Neurol Scand 119:88-93
Chioza, Barry A; Aicardi, Jean; Aschauer, Harald et al. (2009) Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14. Epilepsy Res 87:247-55
Selmer, K K; Egeland, T; Solaas, M H et al. (2008) Genetic screening of Scandinavian families with febrile seizures and epilepsy or GEFS+. Acta Neurol Scand 117:289-92
Froyen, Guy; Corbett, Mark; Vandewalle, Joke et al. (2008) Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation. Am J Hum Genet 82:432-43
Gilfillan, Gregor D; Selmer, Kaja K; Roxrud, Ingrid et al. (2008) SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome. Am J Hum Genet 82:1003-10
Everett, Kate V; Chioza, Barry; Aicardi, Jean et al. (2007) Linkage and association analysis of CACNG3 in childhood absence epilepsy. Eur J Hum Genet 15:463-72
Vadlamudi, Lata; Kjeldsen, Marianne J; Corey, Linda A et al. (2006) Analyzing the etiology of benign rolandic epilepsy: a multicenter twin collaboration. Epilepsia 47:550-5

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