A citation-based method for searching scientific literature

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
Times Cited: 636







List of co-cited articles
1214 articles co-cited >1



Times Cited
  Times     Co-cited
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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
494
55

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
167
30

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
109
29

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
368
27

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
49

The core Dravet syndrome phenotype.
Charlotte Dravet. Epilepsia 2011
257
25

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
780
24

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
88
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
98
16

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
55
29

Temperature- and age-dependent seizures in a mouse model of severe myoclonic epilepsy in infancy.
John C Oakley, Franck Kalume, Frank H Yu, Todd Scheuer, William A Catterall. Proc Natl Acad Sci U S A 2009
139
15

A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients.
Yishan Sun, Sergiu P Paşca, Thomas Portmann, Carleton Goold, Kathleen A Worringer, Wendy Guan, Karen C Chan, Hui Gai, Daniel Vogt, Ying-Jiun J Chen,[...]. Elife 2016
63
22

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
146
14

Sodium channel SCN1A and epilepsy: mutations and mechanisms.
Andrew Escayg, Alan L Goldin. Epilepsia 2010
207
14

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.
Markus Wolff, Katrine M Johannesen, Ulrike B S Hedrich, Silvia Masnada, Guido Rubboli, Elena Gardella, Gaetan Lesca, Dorothée Ville, Mathieu Milh, Laurent Villard,[...]. Brain 2017
200
14

NaV1.1 channels and epilepsy.
William A Catterall, Franck Kalume, John C Oakley. J Physiol 2010
237
14

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
65
21

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
168
13

The genetics of Dravet syndrome.
Carla Marini, Ingrid E Scheffer, Rima Nabbout, Arvid Suls, Peter De Jonghe, Federico Zara, Renzo Guerrini. Epilepsia 2011
149
12

Incidence of Dravet Syndrome in a US Population.
Yvonne W Wu, Joseph Sullivan, Sharon S McDaniel, Miriam H Meisler, Eileen M Walsh, Sherian Xu Li, Michael W Kuzniewicz. Pediatrics 2015
89
13

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
75
16

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
149
12

Selective NaV1.1 activation rescues Dravet syndrome mice from seizures and premature death.
Kay L Richards, Carol J Milligan, Robert J Richardson, Nikola Jancovski, Morten Grunnet, Laura H Jacobson, Eivind A B Undheim, Mehdi Mobli, Chun Yuen Chow, Volker Herzig,[...]. Proc Natl Acad Sci U S A 2018
50
24

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
71
15

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
11

A human Dravet syndrome model from patient induced pluripotent stem cells.
Norimichi Higurashi, Taku Uchida, Christoph Lossin, Yoshio Misumi, Yohei Okada, Wado Akamatsu, Yoichi Imaizumi, Bo Zhang, Kazuki Nabeshima, Masayuki X Mori,[...]. Mol Brain 2013
71
14

Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome.
A Brunklaus, R Ellis, E Reavey, G H Forbes, S M Zuberi. Brain 2012
172
10

The SCN1A mutation database: updating information and analysis of the relationships among genotype, functional alteration, and phenotype.
Heng Meng, Hai-Qing Xu, Lu Yu, Guo-Wang Lin, Na He, Tao Su, Yi-Wu Shi, Bin Li, Jie Wang, Xiao-Rong Liu,[...]. Hum Mutat 2015
93
10

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
692
10

Preclinical Animal Models for Dravet Syndrome: Seizure Phenotypes, Comorbidities and Drug Screening.
Aliesha Griffin, Kyla R Hamling, SoonGweon Hong, Mana Anvar, Luke P Lee, Scott C Baraban. Front Pharmacol 2018
38
26

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
45
22


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
344
9

Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients.
C Depienne, O Trouillard, C Saint-Martin, I Gourfinkel-An, D Bouteiller, W Carpentier, B Keren, B Abert, A Gautier, S Baulac,[...]. J Med Genet 2009
223
9

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
59
15

Genotype-phenotype associations in SCN1A-related epilepsies.
S M Zuberi, A Brunklaus, R Birch, E Reavey, J Duncan, G H Forbes. Neurology 2011
142
9

Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome.
Orrin Devinsky, J Helen Cross, Linda Laux, Eric Marsh, Ian Miller, Rima Nabbout, Ingrid E Scheffer, Elizabeth A Thiele, Stephen Wright. N Engl J Med 2017
556
9

A long-term follow-up study of Dravet syndrome up to adulthood.
Mari Akiyama, Katsuhiro Kobayashi, Harumi Yoshinaga, Yoko Ohtsuka. Epilepsia 2010
109
9

A catalog of SCN1A variants.
Christoph Lossin. Brain Dev 2009
141
9

The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy.
Melinda S Martin, Bin Tang, Ligia A Papale, Frank H Yu, William A Catterall, Andrew Escayg. Hum Mol Genet 2007
141
9

Inhibitory interneuron deficit links altered network activity and cognitive dysfunction in Alzheimer model.
Laure Verret, Edward O Mann, Giao B Hang, Albert M I Barth, Inma Cobos, Kaitlyn Ho, Nino Devidze, Eliezer Masliah, Anatol C Kreitzer, Istvan Mody,[...]. Cell 2012
558
9

Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.
Hsiao-Tuan Chao, Hongmei Chen, Rodney C Samaco, Mingshan Xue, Maria Chahrour, Jong Yoo, Jeffrey L Neul, Shiaoching Gong, Hui-Chen Lu, Nathaniel Heintz,[...]. Nature 2010
738
9

GABRA1 and STXBP1: novel genetic causes of Dravet syndrome.
Gemma L Carvill, Sarah Weckhuysen, Jacinta M McMahon, Corinna Hartmann, Rikke S Møller, Helle Hjalgrim, Joseph Cook, Eileen Geraghty, Brian J O'Roak, Steve Petrou,[...]. Neurology 2014
147
9

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
36
25

Unaltered Network Activity and Interneuronal Firing During Spontaneous Cortical Dynamics In Vivo in a Mouse Model of Severe Myoclonic Epilepsy of Infancy.
Angela Michela De Stasi, Pasqualina Farisello, Iacopo Marcon, Stefano Cavallari, Angelo Forli, Dania Vecchia, Gabriele Losi, Massimo Mantegazza, Stefano Panzeri, Giorgio Carmignoto,[...]. Cereb Cortex 2016
35
25

Hippocampal deletion of NaV1.1 channels in mice causes thermal seizures and cognitive deficit characteristic of Dravet Syndrome.
Rachael E Stein, Joshua S Kaplan, Jin Li, William A Catterall. Proc Natl Acad Sci U S A 2019
13
69

Optimizing the Diagnosis and Management of Dravet Syndrome: Recommendations From a North American Consensus Panel.
Elaine C Wirrell, Linda Laux, Elizabeth Donner, Nathalie Jette, Kelly Knupp, Mary Anne Meskis, Ian Miller, Joseph Sullivan, Michelle Welborn, Anne T Berg. Pediatr Neurol 2017
100
9

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, Jacinta M McMahon, Brian J O'Roak, Joseph Cook, Adiba Khan, Michael O Dorschner, Molly Weaver, Sophie Calvert,[...]. Nat Genet 2013
402
8

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
159
8

De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP.
Krishna R Veeramah, Janelle E O'Brien, Miriam H Meisler, Xiaoyang Cheng, Sulayman D Dib-Hajj, Stephen G Waxman, Dinesh Talwar, Santhosh Girirajan, Evan E Eichler, Linda L Restifo,[...]. Am J Hum Genet 2012
251
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.