Otto, James F; Singh, Nanda A; Dahle, E Jill et al. (2009) Electroconvulsive seizure thresholds and kindling acquisition rates are altered in mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions. Epilepsia 50:1752-9
|
Singh, Nanda A; Pappas, Chris; Dahle, E Jill et al. (2009) A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome. PLoS Genet 5:e1000649
|
Singh, Nanda A; Otto, James F; Dahle, E Jill et al. (2008) Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization. J Physiol 586:3405-23
|
Singh, Nanda A; Westenskow, Peter; Charlier, Carole et al. (2003) KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum. Brain 126:2726-37
|
Singh, N; Charlier, C; Peiffer, A et al. (1999) Genes for rare idiopathic generalized epilepsies: BFNC. Adv Neurol 79:341-50
|
Singh, N A; Charlier, C; Stauffer, D et al. (1998) A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns. Nat Genet 18:25-9
|
Charlier, C; Singh, N A; Ryan, S G et al. (1998) A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family. Nat Genet 18:53-5
|