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Dr. Ruth Ottman's research addresses the role of inherited factors in susceptibility to neurologic disorders, primarily focusing on seizure disorders. Her work on epilepsy has included assessment of familial aggregation, phenotype definition, linkage analysis and gene identification. She is currently conducting three different studies of the genetic epidemiology of epilepsy. Dr. Ottman and her colleagues were the first to recognize a syndrome of temporal lobe epilepsy known as autosomal dominant partial epilepsy with auditory symptoms (ADPEAF), and to identify a gene, LGI1, with causative mutations in approximately half of affected families.
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JAMA NEUROLOGYno. 5 (2024): 499-506
Critical reviews in oncology/hematology (2023): 104081-104081
Lorraine N. Clark,Yizhe Gao,Gao T. Wang,Nora Hernandez,Allison Ashley-Koch,Joseph Jankovic,Ruth Ottman,Suzanne M. Leal, Sandra M. Barral Rodriguez,Elan D. Louis
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