A citation-based method for searching scientific literature

Susumu Ito, Ikuo Ogiwara, Kazuyuki Yamada, Hiroyuki Miyamoto, Takao K Hensch, Makiko Osawa, Kazuhiro Yamakawa. Neurobiol Dis 2013
Times Cited: 61







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



Times Cited
  Times     Co-cited
Similarity


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
75

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
70

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
63

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
42

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
36

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
31

The core Dravet syndrome phenotype.
Charlotte Dravet. Epilepsia 2011
262
31

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
141
29

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
29

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
26

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
24

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
22

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
21

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
173
19

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
26

Impairments in social novelty recognition and spatial memory in mice with conditional deletion of Scn1a in parvalbumin-expressing cells.
Tetsuya Tatsukawa, Ikuo Ogiwara, Emi Mazaki, Atsushi Shimohata, Kazuhiro Yamakawa. Neurobiol Dis 2018
26
46

Severe myoclonic epilepsy of infants (Dravet syndrome): natural history and neuropsychological findings.
Markus Wolff, Catherine Cassé-Perrot, Charlotte Dravet. Epilepsia 2006
174
18

NaV1.1 channels and epilepsy.
William A Catterall, Franck Kalume, John C Oakley. J Physiol 2010
238
18

Dravet syndrome: the long-term outcome.
Pierre Genton, Reana Velizarova, Charlotte Dravet. Epilepsia 2011
139
18

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
18

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
19

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
16

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
26

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
14

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
225
14

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
14

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
14

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

Sodium channel SCN1A and epilepsy: mutations and mechanisms.
Andrew Escayg, Alan L Goldin. Epilepsia 2010
208
13

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
13

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
13

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
13

Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009.
Anne T Berg, Samuel F Berkovic, Martin J Brodie, Jeffrey Buchhalter, J Helen Cross, Walter van Emde Boas, Jerome Engel, Jacqueline French, Tracy A Glauser, Gary W Mathern,[...]. Epilepsia 2010
13

Focal Scn1a knockdown induces cognitive impairment without seizures.
Alex C Bender, Heather Natola, Christian Ndong, Gregory L Holmes, Rod C Scott, Pierre-Pascal Lenck-Santini. Neurobiol Dis 2013
53
15

Correlations in timing of sodium channel expression, epilepsy, and sudden death in Dravet syndrome.
Christine S Cheah, Ruth E Westenbroek, William H Roden, Franck Kalume, John C Oakley, Laura A Jansen, William A Catterall. Channels (Austin) 2013
33
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
72
13

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
16

Fine Mapping of a Dravet Syndrome Modifier Locus on Mouse Chromosome 5 and Candidate Gene Analysis by RNA-Seq.
Nicole A Hawkins, Nicole J Zachwieja, Alison R Miller, Lyndsey L Anderson, Jennifer A Kearney. PLoS Genet 2016
42
19

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
13

SCN1A mutations in Dravet syndrome: impact of interneuron dysfunction on neural networks and cognitive outcome.
Alex C Bender, Richard P Morse, Rod C Scott, Gregory L Holmes, Pierre-Pascal Lenck-Santini. Epilepsy Behav 2012
50
14

Behavioural phenotyping assays for mouse models of autism.
Jill L Silverman, Mu Yang, Catherine Lord, Jacqueline N Crawley. Nat Rev Neurosci 2010
861
11

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
24

Encephalopathy in children with Dravet syndrome is not a pure consequence of epilepsy.
Rima Nabbout, Nicole Chemaly, Mathilde Chipaux, Giulia Barcia, Charles Bouis, Celia Dubouch, Dorothee Leunen, Isabelle Jambaqué, Olivier Dulac, Georges Dellatolas,[...]. Orphanet J Rare Dis 2013
88
11

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
65
11

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
18

Pure haploinsufficiency for Dravet syndrome Na(V)1.1 (SCN1A) sodium channel truncating mutations.
Giulia Bechi, Paolo Scalmani, Emanuele Schiavon, Raffaella Rusconi, Silvana Franceschetti, Massimo Mantegazza. Epilepsia 2012
34
17

The genetics of Dravet syndrome.
Carla Marini, Ingrid E Scheffer, Rima Nabbout, Arvid Suls, Peter De Jonghe, Federico Zara, Renzo Guerrini. Epilepsia 2011
152
9

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
9

A long-term follow-up study of Dravet syndrome up to adulthood.
Mari Akiyama, Katsuhiro Kobayashi, Harumi Yoshinaga, Yoko Ohtsuka. Epilepsia 2010
111
9

Deletions of SCN1A 5' genomic region with promoter activity in Dravet syndrome.
Tojo Nakayama, Ikuo Ogiwara, Koichi Ito, Makoto Kaneda, Emi Mazaki, Hitoshi Osaka, Hideyuki Ohtani, Yushi Inoue, Tateki Fujiwara, Mitsugu Uematsu,[...]. Hum Mutat 2010
34
17


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.