A citation-based method for searching scientific literature

D L Browne, S T Gancher, J G Nutt, E R Brunt, E A Smith, P Kramer, M Litt. Nat Genet 1994
Times Cited: 577







List of shared articles



Times cited

Paroxysmal Genetic Movement Disorders and Epilepsy.
Claudio M de Gusmão, Lucas Garcia, Mohamad A Mikati, Samantha Su, Laura Silveira-Moriyama. Front Neurol 2021
2

Structural basis of the potency and selectivity of Urotoxin, a potent Kv1 blocker from scorpion venom.
Karen Luna-Ramirez, Agota Csoti, Jeffrey R McArthur, Yanni K Y Chin, Raveendra Anangi, Rosby Del Carmen Najera, Lourival D Possani, Glenn F King, Gyorgy Panyi, Haibo Yu,[...]. Biochem Pharmacol 2020
5


Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies.
Julia Oyrer, Snezana Maljevic, Ingrid E Scheffer, Samuel F Berkovic, Steven Petrou, Christopher A Reid. Pharmacol Rev 2018
75

De novo KCNA1 variants in the PVP motif cause infantile epileptic encephalopathy and cognitive impairment similar to recurrent KCNA2 variants.
Amanda Rogers, Paul Golumbek, Elena Cellini, Viola Doccini, Renzo Guerrini, Carina Wallgren-Pettersson, Ann-Charlotte Thuresson, Christina A Gurnett. Am J Med Genet A 2018
17

Venom-derived peptide inhibitors of voltage-gated potassium channels.
Raymond S Norton, K George Chandy. Neuropharmacology 2017
45

Arthropod toxins acting on neuronal potassium channels.
Juana María Jiménez-Vargas, Lourival D Possani, Karen Luna-Ramírez. Neuropharmacology 2017
17

Potassium Channels and Human Epileptic Phenotypes: An Updated Overview.
Chiara Villa, Romina Combi. Front Cell Neurosci 2016
57

Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy.
Mark A Corbett, Susannah T Bellows, Melody Li, Renée Carroll, Silvana Micallef, Gemma L Carvill, Candace T Myers, Katherine B Howell, Snezana Maljevic, Holger Lerche,[...]. Neurology 2016
41

Genetic neurological channelopathies: molecular genetics and clinical phenotypes.
J Spillane, D M Kullmann, M G Hanna. J Neurol Neurosurg Psychiatry 2016
54

De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.
Steffen Syrbe, Ulrike B S Hedrich, Erik Riesch, Tania Djémié, Stephan Müller, Rikke S Møller, Bridget Maher, Laura Hernandez-Hernandez, Matthis Synofzik, Hande S Caglayan,[...]. Nat Genet 2015
142