Comorbidities of epilepsy: results from the Epilepsy Comorbidities and Health (EPIC) survey.
Ottman R, Lipton RB, Ettinger AB, Cramer JA, Reed ML, Morrison A, Wan GJ.
Epilepsia 2011;52:308-315.
Accuracy of family history information on epilepsy and other seizure disorders.
Ottman R, Barker-Cummings C, Leibson CL, Vasoli VM, Hauser WA, Buchhalter JR. Neurology 2011;76:390-396.
Genetic testing in the epilepsies--report of the ILAE Genetics Commission. Ottman R, Hirose S, Jain S, Lerche H, Lopes-Cendes I, Noebels JL, Serratosa J, et al.
Epilepsia 2010;51:655-670.
Validation of a brief screening instrument for the ascertainment of epilepsy.
Ottman R, Barker-Cummings C, Leibson CL, Vasoli VM, Hauser WA, Buchhalter JR.
Epilepsia 2010;51:191-197.
Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+.
Poduri A, Wang Y, Gordon D, Barral-Rodriguez S, Barker-Cummings C, Ulgen A, Chitsazzadeh V, et al.
Neurology 2009;73:1264-1272.
Penetrance of LGI1 mutations in autosomal dominant partial epilepsy with auditory features.
Rosanoff MJ, Ottman R.
Neurology 2008;71:567-571.
Phenotypic concordance in 70 families with IGE-implications for genetic studies of epilepsy.
Kinirons P, Rabinowitz D, Gravel M, Long J, Winawer M, Senechal G, Ottman R, et al.
Epilepsy Research 2008;82:21-28.
Ethical, legal, and social dimensions of epilepsy genetics.
Shostak S, Ottman R.
Epilepsia 2006;47:1595-1602.
Classification of partial seizure symptoms in genetic studies of the epilepsies.
Choi H, Winawer MR, Kalachikov S, Pedley TA, Hauser WA, Ottman R.
Neurology 2006;66:1648-1653.
Familial clustering of seizure types within the idiopathic generalized epilepsies.
Winawer MR, Marini C, Grinton BE, Rabinowitz D, Berkovic SF, Scheffer IE, Ottman R.
Neurology 2005;65:523-528.
Recruitment of families for genetic studies of epilepsy.
Ottman R, Berenson K, Barker-Cummings C. Epilepsia 2005;46:290-297.
Analysis of genetically complex epilepsies. Ottman R.
Epilepsia 2005;46 Suppl 10:7-14.
LGI1 mutations in autosomal dominant partial epilepsy with auditory features.
Ottman R, Winawer MR, Kalachikov S, Barker-Cummings C, Gilliam TC, Pedley TA, Hauser WA.
Neurology 2004;62:1120-1126.
Genetic influences on myoclonic and absence seizures.
Winawer MR, Rabinowitz D, Pedley TA, Hauser WA, Ottman R.
Neurology 2003;61:1576-1581.
Evidence for distinct genetic influences on generalized and localization-related epilepsy.
Winawer MR, Rabinowitz D, Barker-Cummings C, Scheuer ML, Pedley TA, Hauser WA, Ottman R.
Epilepsia 2003;44:1176-1182.
Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24.
Winawer MR, Martinelli Boneschi F, Barker-Cummings C, Lee JH, Liu J, Mekios C, Gilliam TC, et al.
Epilepsia 2002;43:60-67.
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features.
Kalachikov S, Evgrafov O, Ross B, Winawer M, Barker-Cummings C, Martinelli Boneschi F, Choi C, et al.
Nature Genetics 2002;30:335-341.
ILAE genetics commission conference report: molecular analysis of complex genetic epilepsies.
Anderson E, Berkovic S, Dulac O, Gardiner M, Jain S, Laue Friis M, Lindhout D, et al.
Epilepsia 2002;43:1262-1267.
Autosomal dominant partial epilepsy with auditory features: defining the phenotype.
Winawer MR, Ottman R, Hauser WA, Pedley TA.
Neurology 2000;54:2173-2176.
Are generalized and localization-related epilepsies genetically distinct?
Ottman R, Lee JH, Hauser WA, Risch N.
Archives of Neurology 1998;55:339-344.
Genetic epidemiology of epilepsy.
Ottman R.
Epidemiologic Reviews 1997;19:120-128.
Is the comorbidity of epilepsy and migraine due to a shared genetic susceptibility?
Ottman R, Lipton RB.
Neurology 1996;47:918-924.
Clinical indicators of genetic susceptibility to epilepsy.
Ottman R, Lee JH, Risch N, Hauser WA, Susser M.
Epilepsia 1996;37:353-361.
Relations of genetic and environmental factors in the etiology of epilepsy.
Ottman R, Annegers JF, Risch N, Hauser WA, Susser M.
Annals of Neurology 1996;39:442-449.
