About

Biography

I am the associate director of the Cincinnati Children's Research Foundation and a professor of pediatrics at the University of Cincinnati College of Medicine. I received my medical degree, cum laude, from Jefferson Medical College in Philadelphia, PA. I completed my residency in pediatrics at the Johns Hopkins Hospital in Baltimore, MD, and a fellowship in child neurology at The Children’s Hospital of Philadelphia, University of Pennsylvania in Philadelphia, PA. I also completed a National Institute of Neurological Disorders and Stroke research fellowship in pediatric neurology and was a fellow in epilepsy and electroencephalography at St. Louis Children’s Hospital, Washington University School of Medicine in St. Louis, Missouri.

I have authored and co-authored more than 130 articles and book chapters, been involved with the development of six evidence-based guidelines about epilepsy therapy, and given over 150 invited lectures throughout the world. I have been the principal investigator on multiple NIH grants. Currently, I direct the NIH-funded Childhood Absence Epilepsy clinical trial involving 32 pediatric centers around the United States. My fields of expertise are pediatric neurology, pediatric epilepsy, clinical pharmacology, and pharmacogenetics.

MD: Jefferson Medical College, Philadelphia, PA, 1985.

Residency: Johns Hopkins Hospital, Baltimore, MD.

Fellowship: St. Louis Children's Hospital, St. Louis, MO.

Certification: Pediatrics, 1990; Neurology (with special competence in child neurology), 1991.

Interests

Epilepsy; pharmacogenetics; clinical pharmacology

Services and Specialties

Neurology, Epilepsy

Interests

Clinical pharmacology; pharmacogenetics; antiepileptic clinical trials

Research Areas

Neurology, Clinical Pharmacology, Genomics

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Publications

Selected

Development of information sharing in language neocortex in childhood-onset drug-resistant epilepsy. Arya, R; Ervin, B; Wilson, JA; Byars, AW; Rozhkov, L; Buroker, J; Horn, PS; Scholle, C; Fujiwara, H; Greiner, HM; Leach, JL; Rose, DF; Mangano, FT; Glauser, TA; Holland, KD. Epilepsia. 2019; 60:393-405.

Selected

Pretreatment behavior and subsequent medication effects in childhood absence epilepsy. Shinnar, RC; Shinnar, S; Cnaan, A; Clark, P; Dlugos, D; Hirtz, DG; Hu, F; Liu, C; Masur, D; Weiss, EF; Glauser, TA; Study, CA E. Neurology. 2017; 89:1698-1706.

Selected

Pretreatment seizure semiology in childhood absence epilepsy. Kessler, SK; Shinnar, S; Cnaan, A; Dlugos, D; Conry, J; Hirtz, DG; Hu, F; Liu, C; Mizrahi, EM; Moshe, SL; Clark, P; Glauser, TA; Childhood, AE S G. Neurology. 2017; 89:673-679.

Selected

Pharmacogenetics of antiepileptic drug efficacy in childhood absence epilepsy. Glauser, TA; Holland, K; O'Brien, VP; Keddache, M; Martin, LJ; Clark, PO; Cnaan, A; Dlugos, D; Hirtz, DG; Shinnar, S; Grabowski, G; Study, CA E. Annals of Neurology. 2017; 81:444-453.

Selected

Second monotherapy in childhood absence epilepsy. Cnaan, A; Shinnar, S; Arya, R; Adamson, PC; Clark, PO; Dlugos, D; Hirtz, DG; Masur, D; Glauser, TA; Study, CA E. Neurology. 2017; 88:182-190.

Selected

Long-term outcomes of generalized tonic-clonic seizures in a childhood absence epilepsy trial. Shinnar, S; Cnaan, A; Hu, F; Clark, P; Dlugos, D; Hirtz, DG; Masur, D; Mizrahi, EM; Moshe, SL; Glauser, TA; Study, CA E. Neurology. 2015; 85:1108-1114.

Selected

Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy: initial monotherapy outcomes at 12 months. Glauser, TA; Cnaan, A; Shinnar, S; Hirtz, DG; Dlugos, D; Masur, D; Clark, PO; Adamson, PC; Study, CA E. Epilepsia. 2013; 54:141-155.

Selected

Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy. Glauser, TA; Cnaan, A; Shinnar, S; Hirtz, DG; Dlugos, D; Masur, D; Clark, PO; Capparelli, EV; Adamson, PC; Study, CA E. The New England Journal of Medicine. 2010; 362:790-799.

A call for solutions-oriented research and policy to protect children from the effects of climate change. Ryan, PH; Newman, N; Yolton, K; Meinzen-Derr, J; Glauser, T; Cheng, TL. Pediatric Research. 2024; 96:1532-1534.

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes. Berkovic, SF; Neale, BM; Zsurka, G; Zizovic, M; Zimprich, F; Zara, F; Zahnert, F; Zagaglia, S; Yücesan, E; Yolken, R; Ramirez-Hamouz, B; Ragona, F; Rademacher, A; Privitera, M. Nature Neuroscience. 2024; 27:1864-1879.

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