A citation-based method for searching scientific literature

John C Oakley, Franck Kalume, Frank H Yu, Todd Scheuer, William A Catterall. Proc Natl Acad Sci U S A 2009
Times Cited: 141







List of co-cited articles
927 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy.
Frank H Yu, Massimo Mantegazza, Ruth E Westenbroek, Carol A Robbins, Franck Kalume, Kimberly A Burton, William J Spain, G Stanley McKnight, Todd Scheuer, William A Catterall. Nat Neurosci 2006
643
71

Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation.
Ikuo Ogiwara, Hiroyuki Miyamoto, Noriyuki Morita, Nafiseh Atapour, Emi Mazaki, Ikuyo Inoue, Tamaki Takeuchi, Shigeyoshi Itohara, Yuchio Yanagawa, Kunihiko Obata,[...]. J Neurosci 2007
499
56

Autistic-like behaviour in Scn1a+/- mice and rescue by enhanced GABA-mediated neurotransmission.
Sung Han, Chao Tai, Ruth E Westenbroek, Frank H Yu, Christine S Cheah, Gregory B Potter, John L Rubenstein, Todd Scheuer, Horacio O de la Iglesia, William A Catterall. Nature 2012
372
39

Specific deletion of NaV1.1 sodium channels in inhibitory interneurons causes seizures and premature death in a mouse model of Dravet syndrome.
Christine S Cheah, Frank H Yu, Ruth E Westenbroek, Franck K Kalume, John C Oakley, Gregory B Potter, John L Rubenstein, William A Catterall. Proc Natl Acad Sci U S A 2012
168
33

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
L Claes, J Del-Favero, B Ceulemans, L Lagae, C Van Broeckhoven, P De Jonghe. Am J Hum Genet 2001
785
32

Sudden unexpected death in a mouse model of Dravet syndrome.
Franck Kalume, Ruth E Westenbroek, Christine S Cheah, Frank H Yu, John C Oakley, Todd Scheuer, William A Catterall. J Clin Invest 2013
152
28

NaV1.1 channels and epilepsy.
William A Catterall, Franck Kalume, John C Oakley. J Physiol 2010
238
27

Reduced sodium current in Purkinje neurons from Nav1.1 mutant mice: implications for ataxia in severe myoclonic epilepsy in infancy.
Franck Kalume, Frank H Yu, Ruth E Westenbroek, Todd Scheuer, William A Catterall. J Neurosci 2007
170
27

The core Dravet syndrome phenotype.
Charlotte Dravet. Epilepsia 2011
262
26

Nav1.1 haploinsufficiency in excitatory neurons ameliorates seizure-associated sudden death in a mouse model of Dravet syndrome.
Ikuo Ogiwara, Takuji Iwasato, Hiroyuki Miyamoto, Ryohei Iwata, Tetsushi Yamagata, Emi Mazaki, Yuchio Yanagawa, Nobuaki Tamamaki, Takao K Hensch, Shigeyoshi Itohara,[...]. Hum Mol Genet 2013
99
22

Altered function of the SCN1A voltage-gated sodium channel leads to gamma-aminobutyric acid-ergic (GABAergic) interneuron abnormalities.
Melinda S Martin, Karoni Dutt, Ligia A Papale, Céline M Dubé, Stacey B Dutton, Georgius de Haan, Anupama Shankar, Sergio Tufik, Miriam H Meisler, Tallie Z Baram,[...]. J Biol Chem 2010
147
21

Dravet syndrome: the long-term outcome.
Pierre Genton, Reana Velizarova, Charlotte Dravet. Epilepsia 2011
139
20

Impaired excitability of somatostatin- and parvalbumin-expressing cortical interneurons in a mouse model of Dravet syndrome.
Chao Tai, Yasuyuki Abe, Ruth E Westenbroek, Todd Scheuer, William A Catterall. Proc Natl Acad Sci U S A 2014
112
19

Sodium channel SCN1A and epilepsy: mutations and mechanisms.
Andrew Escayg, Alan L Goldin. Epilepsia 2010
208
18

Mouse with Nav1.1 haploinsufficiency, a model for Dravet syndrome, exhibits lowered sociability and learning impairment.
Susumu Ito, Ikuo Ogiwara, Kazuyuki Yamada, Hiroyuki Miyamoto, Takao K Hensch, Makiko Osawa, Kazuhiro Yamakawa. Neurobiol Dis 2013
61
29

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.
A Escayg, B T MacDonald, M H Meisler, S Baulac, G Huberfeld, I An-Gourfinkel, A Brice, E LeGuern, B Moulard, D Chaigne,[...]. Nat Genet 2000
693
17

Strain- and age-dependent hippocampal neuron sodium currents correlate with epilepsy severity in Dravet syndrome mice.
Akshitkumar M Mistry, Christopher H Thompson, Alison R Miller, Carlos G Vanoye, Alfred L George, Jennifer A Kearney. Neurobiol Dis 2014
90
18

Na(V)1.1 channels are critical for intercellular communication in the suprachiasmatic nucleus and for normal circadian rhythms.
Sung Han, Frank H Yu, Michael D Schwartz, Jonathan D Linton, Martha M Bosma, James B Hurley, William A Catterall, Horacio O de la Iglesia. Proc Natl Acad Sci U S A 2012
66
21

Preferential inactivation of Scn1a in parvalbumin interneurons increases seizure susceptibility.
Stacey B Dutton, Christopher D Makinson, Ligia A Papale, Anupama Shankar, Bindu Balakrishnan, Kazu Nakazawa, Andrew Escayg. Neurobiol Dis 2013
76
18

Hippocampal hyperexcitability and specific epileptiform activity in a mouse model of Dravet syndrome.
Camille Liautard, Paolo Scalmani, Giovanni Carriero, Marco de Curtis, Silvana Franceschetti, Massimo Mantegazza. Epilepsia 2013
38
36

Severe myoclonic epilepsy of infants (Dravet syndrome): natural history and neuropsychological findings.
Markus Wolff, Catherine Cassé-Perrot, Charlotte Dravet. Epilepsia 2006
174
13

Severe myoclonic epilepsy in infancy: Dravet syndrome.
Charlotte Dravet, Michelle Bureau, Hirokazu Oguni, Yukio Fukuyama, Ozlem Cokar. Adv Neurol 2005
181
13

Synergistic GABA-enhancing therapy against seizures in a mouse model of Dravet syndrome.
John C Oakley, Alvin R Cho, Christine S Cheah, Todd Scheuer, William A Catterall. J Pharmacol Exp Ther 2013
33
39

Autism in Dravet syndrome: prevalence, features, and relationship to the clinical characteristics of epilepsy and mental retardation.
Bing-Mei Li, Xiao-Rong Liu, Yong-Hong Yi, Yu-Hong Deng, Tao Su, Xin Zou, Wei-Ping Liao. Epilepsy Behav 2011
66
18

The genetics of Dravet syndrome.
Carla Marini, Ingrid E Scheffer, Rima Nabbout, Arvid Suls, Peter De Jonghe, Federico Zara, Renzo Guerrini. Epilepsia 2011
152
12

Efficacy of stiripentol in hyperthermia-induced seizures in a mouse model of Dravet syndrome.
Dezhi Cao, Hideyuki Ohtani, Ikuo Ogiwara, Sanae Ohtani, Yukitoshi Takahashi, Kazuhiro Yamakawa, Yushi Inoue. Epilepsia 2012
29
41

Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism.
Yu Liu, Luis F Lopez-Santiago, Yukun Yuan, Julie M Jones, Helen Zhang, Heather A O'Malley, Gustavo A Patino, Janelle E O'Brien, Raffaella Rusconi, Ajay Gupta,[...]. Ann Neurol 2013
148
12

A BAC transgenic mouse model reveals neuron subtype-specific effects of a Generalized Epilepsy with Febrile Seizures Plus (GEFS+) mutation.
Bin Tang, Karoni Dutt, Ligia Papale, Raffaella Rusconi, Anupama Shankar, Jessica Hunter, Sergio Tufik, Frank H Yu, William A Catterall, Massimo Mantegazza,[...]. Neurobiol Dis 2009
72
15

The pharmacologic treatment of Dravet syndrome.
Catherine Chiron, Olivier Dulac. Epilepsia 2011
87
12

Mice lacking sodium channel beta1 subunits display defects in neuronal excitability, sodium channel expression, and nodal architecture.
Chunling Chen, Ruth E Westenbroek, Xiaorong Xu, Chris A Edwards, Dorothy R Sorenson, Yuan Chen, Dyke P McEwen, Heather A O'Malley, Vandana Bharucha, Laurence S Meadows,[...]. J Neurosci 2004
182
11

Mapping genetic modifiers of survival in a mouse model of Dravet syndrome.
A R Miller, N A Hawkins, C E McCollom, J A Kearney. Genes Brain Behav 2014
67
16

Drug screening in Scn1a zebrafish mutant identifies clemizole as a potential Dravet syndrome treatment.
Scott C Baraban, Matthew T Dinday, Gabriela A Hortopan. Nat Commun 2013
208
10

Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome.
Moran Rubinstein, Ruth E Westenbroek, Frank H Yu, Christina J Jones, Todd Scheuer, William A Catterall. Neurobiol Dis 2015
46
21

Dissecting the phenotypes of Dravet syndrome by gene deletion.
Moran Rubinstein, Sung Han, Chao Tai, Ruth E Westenbroek, Avery Hunker, Todd Scheuer, William A Catterall. Brain 2015
57
17

SCN1A mutations and epilepsy.
John C Mulley, Ingrid E Scheffer, Steven Petrou, Leanne M Dibbens, Samuel F Berkovic, Louise A Harkin. Hum Mutat 2005
242
9

Lamotrigine and seizure aggravation in severe myoclonic epilepsy.
R Guerrini, C Dravet, P Genton, A Belmonte, A Kaminska, O Dulac. Epilepsia 1998
311
9



The spectrum of SCN1A-related infantile epileptic encephalopathies.
Louise A Harkin, Jacinta M McMahon, Xenia Iona, Leanne Dibbens, James T Pelekanos, Sameer M Zuberi, Lynette G Sadleir, Eva Andermann, Deepak Gill, Kevin Farrell,[...]. Brain 2007
345
9

A functional null mutation of SCN1B in a patient with Dravet syndrome.
Gustavo A Patino, Lieve R F Claes, Luis F Lopez-Santiago, Emily A Slat, Raja S R Dondeti, Chunling Chen, Heather A O'Malley, Charles B B Gray, Haruko Miyazaki, Nobuyuki Nukina,[...]. J Neurosci 2009
160
9

A catalog of SCN1A variants.
Christoph Lossin. Brain Dev 2009
142
9

De novo mutations in epileptic encephalopathies.
Andrew S Allen, Samuel F Berkovic, Patrick Cossette, Norman Delanty, Dennis Dlugos, Evan E Eichler, Michael P Epstein, Tracy Glauser, David B Goldstein, Yujun Han,[...]. Nature 2013
925
9

Sleep impairment and reduced interneuron excitability in a mouse model of Dravet Syndrome.
Franck Kalume, John C Oakley, Ruth E Westenbroek, Jennifer Gile, Horacio O de la Iglesia, Todd Scheuer, William A Catterall. Neurobiol Dis 2015
48
18

Impaired action potential initiation in GABAergic interneurons causes hyperexcitable networks in an epileptic mouse model carrying a human Na(V)1.1 mutation.
Ulrike B S Hedrich, Camille Liautard, Daniel Kirschenbaum, Martin Pofahl, Jennifer Lavigne, Yuanyuan Liu, Stephan Theiss, Johannes Slotta, Andrew Escayg, Marcel Dihné,[...]. J Neurosci 2014
72
12

Screening of conventional anticonvulsants in a genetic mouse model of epilepsy.
Nicole A Hawkins, Lyndsey L Anderson, Tracy S Gertler, Linda Laux, Alfred L George, Jennifer A Kearney. Ann Clin Transl Neurol 2017
38
23

Cannabidiol attenuates seizures and social deficits in a mouse model of Dravet syndrome.
Joshua S Kaplan, Nephi Stella, William A Catterall, Ruth E Westenbroek. Proc Natl Acad Sci U S A 2017
144
9

A Transient Developmental Window of Fast-Spiking Interneuron Dysfunction in a Mouse Model of Dravet Syndrome.
Morgana Favero, Nathaniel P Sotuyo, Emily Lopez, Jennifer A Kearney, Ethan M Goldberg. J Neurosci 2018
53
16

Dravet syndrome and parent associations: the IDEA League experience with comorbid conditions, mortality, management, adaptation, and grief.
Joan V Skluzacek, Kathryn P Watts, Olivier Parsy, Beverly Wical, Peter Camfield. Epilepsia 2011
87
9

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.
Claudia B Catarino, Joan Y W Liu, Ioannis Liagkouras, Vaneesha S Gibbons, Robyn W Labrum, Rachael Ellis, Cathy Woodward, Mary B Davis, Shelagh J Smith, J Helen Cross,[...]. Brain 2011
119
8



Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.