Mathern, Gary W.

ILAE official report: a practical clinical definition of epilepsy

Fisher, R. S., Acevedo, C., Arzimanoglou, A., Bogacz, A., Cross, J. H., Elger, C. E., Engel, J., Forsgren, L., French, J. A., Glynn, M., et al. (2014) · Epilepsia

Epilepsy research and treatmentNeurology and Historical Studies

Cited by 6,108

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology

Scheffer, I. E., Berkovic, S., Capovilla, G., Connolly, M. B., French, J., Guilhoto, L., Hirsch, E., Jain, S., Mathern, G. W., Moshé, S. L., et al. (2017) · Epilepsia

Epilepsy research and treatmentNeurology and Historical Studies

Cited by 5,054

Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005–2009

Berg, A. T., Berkovic, S. F., Brodie, M. J., Buchhalter, J., Cross, J. H., Van Emde Boas, W., Engel, J., French, J., Glauser, T. A., Mathern, G. W., et al. (2010) · Epilepsia

Epilepsy research and treatmentNeurology and Historical Studies

Cited by 4,363

Human hippocampal neurogenesis drops sharply in children to undetectable levels in adults

Sorrells, S. F., Paredes, M. F., Cebrian-Silla, A., Sandoval, K., Qi, D., Kelley, K. W., James, D., Mayer, S., Chang, J., Auguste, K. I., et al. (2018) · Nature

Neurogenesis and neuroplasticity mechanismsMemory and Neural Mechanisms

Cited by 1,422

De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly

Lee, J. H., Huynh, M., Silhavy, J. L., Kim, S., Dixon-Salazar, T., Heiberg, A., Scott, E., Bafna, V., Hill, K. J., Collazo, A., et al. (2012) · Nature Genetics

Fetal and Pediatric Neurological DisordersPI3K/AKT/mTOR signaling in cancer

Cited by 703

Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network

McConnell, M. J., Moran, J. V., Abyzov, A., Akbarian, S., Bae, T., Cortes-Ciriano, I., Erwin, J. A., Fasching, L., Flasch, D. A., Freed, D., et al. (2017) · Science

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 262

Noninflammatory Changes of Microglia Are Sufficient to Cause Epilepsy

Zhao, X., Liao, Y., Morgan, S., Mathur, R., Feustel, P., Mazurkiewicz, J., Qian, J., Chang, J., Mathern, G. W., Adamo, M. A., et al. (2018) · Cell Reports

Epilepsy research and treatmentNeuroinflammation and Neurodegeneration Mechanisms

Cited by 190

Brain molecular mechanisms in Rasmussen encephalitis

Leitner, D. F., Lin, Z., Sawaged, Z., Kanshin, E., Friedman, D., Devore, S., Ueberheide, B., Chang, J. W., Mathern, G. W., Anink, J. J., et al. (2023) · Epilepsia

Epilepsy research and treatmentAutoimmune Neurological Disorders and Treatments

Cited by 17

Iconography of abnormal non-neuronal cells in pediatric focal cortical dysplasia type IIb and tuberous sclerosis complex

Zhang, J., Argueta, D., Tong, X., Vinters, H. V., Mathern, G. W., & Cepeda, C. (2025) · Frontiers in Cellular Neuroscience

Tuberous Sclerosis Complex ResearchEpilepsy research and treatment

Cited by 3