Escayg, Andrew

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

Escayg, A., MacDonald, B. T., Meisler, M. H., Baulac, S., Huberfeld, G., An-Gourfinkel, I., Brice, A., LeGuern, E., Moulard, B., Chaigne, D., et al. (2000) · Nature Genetics

Epilepsy research and treatmentIon channel regulation and function

Cited by 996

Impaired Action Potential Initiation in GABAergic Interneurons Causes Hyperexcitable Networks in an Epileptic Mouse Model Carrying a Human NaV1.1 Mutation

Hedrich, U. B. S., Liautard, C., Kirschenbaum, D., Pofahl, M., Lavigne, J., Liu, Y., Theiss, S., Slotta, J., Escayg, A., Dihné, M., et al. (2014) · The Journal of Neuroscience

Epilepsy research and treatmentIon channel regulation and function

Cited by 164

Preferential inactivation of Scn1a in parvalbumin interneurons increases seizure susceptibility

Dutton, S. B., Makinson, C. D., Papale, L. A., Shankar, A., Balakrishnan, B., Nakazawa, K., & Escayg, A. (2013) · Neurobiology of Disease

Epilepsy research and treatmentIon channel regulation and function

Cited by 128

Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice

Papale, L. A., Beyer, B., Jones, J. M., Sharkey, L. M., Tufik, S., Epstein, M., Letts, V. A., Meisler, M. H., Frankel, W. N., & Escayg, A. (2009) · Human Molecular Genetics

Epilepsy research and treatmentIon channel regulation and function

Cited by 127

Sodium Channels and Neurological Disease: Insights from Scn8a Mutations in the Mouse

Meisler, M. H., Kearney, J., Escayg, A., Macdonald, B. T., & Sprunger, L. K. (2001) · The Neuroscientist

Ion channel regulation and functionHereditary Neurological Disorders

Cited by 68

Stress and epilepsy: multiple models, multiple outcomes.

Sawyer, N. T., & Escayg, A. (2010) · Journal of Clinical Neurophysiology

Epilepsy research and treatmentStress Responses and Cortisol

Cited by 47