A citation-based method for searching scientific literature

Tun Li, Cuiping Tian, Paolo Scalmani, Carolina Frassoni, Massimo Mantegazza, Yonghong Wang, Mingpo Yang, Si Wu, Yousheng Shu. PLoS Biol 2014
Times Cited: 58







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



Times Cited
  Times     Co-cited
Similarity


Distinct contributions of Na(v)1.6 and Na(v)1.2 in action potential initiation and backpropagation.
Wenqin Hu, Cuiping Tian, Tun Li, Mingpo Yang, Han Hou, Yousheng Shu. Nat Neurosci 2009
439
44

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
560
43


Molecular identity of axonal sodium channels in human cortical pyramidal cells.
Cuiping Tian, Kaiyan Wang, Wei Ke, Hui Guo, Yousheng Shu. Front Cell Neurosci 2014
51
31

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
706
24

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
270
24

Opposing Effects on NaV1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile Seizures.
Roy Ben-Shalom, Caroline M Keeshen, Kiara N Berrios, Joon Y An, Stephan J Sanders, Kevin J Bender. Biol Psychiatry 2017
126
22

Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy.
Yunxiang Liao, Liesbet Deprez, Snezana Maljevic, Julika Pitsch, Lieve Claes, Dimitrina Hristova, Albena Jordanova, Sirpa Ala-Mello, Astrid Bellan-Koch, Dragica Blazevic,[...]. Brain 2010
122
20

A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline.
Kazusaku Kamiya, Makoto Kaneda, Takashi Sugawara, Emi Mazaki, Nami Okamura, Mauricio Montal, Naomasa Makita, Masaki Tanaka, Katsuyuki Fukushima, Tateki Fujiwara,[...]. J Neurosci 2004
148
20

Action potential generation requires a high sodium channel density in the axon initial segment.
Maarten H P Kole, Susanne U Ilschner, Björn M Kampa, Stephen R Williams, Peter C Ruben, Greg J Stuart. Nat Neurosci 2008
413
20


Nav1.2 is expressed in caudal ganglionic eminence-derived disinhibitory interneurons: Mutually exclusive distributions of Nav1.1 and Nav1.2.
Tetsushi Yamagata, Ikuo Ogiwara, Emi Mazaki, Yuchio Yanagawa, Kazuhiro Yamakawa. Biochem Biophys Res Commun 2017
26
46

De novo mutations of voltage-gated sodium channel alphaII gene SCN2A in intractable epilepsies.
I Ogiwara, K Ito, Y Sawaishi, H Osaka, E Mazaki, I Inoue, M Montal, T Hashikawa, T Shike, T Fujiwara,[...]. Neurology 2009
146
18

A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction.
T Sugawara, Y Tsurubuchi, K L Agarwala, M Ito, G Fukuma, E Mazaki-Miyazaki, H Nagafuji, M Noda, K Imoto, K Wada,[...]. Proc Natl Acad Sci U S A 2001
301
18


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
137
18

The action potential in mammalian central neurons.
Bruce P Bean. Nat Rev Neurosci 2007
871
17

The physiology of the axon initial segment.
Kevin J Bender, Laurence O Trussell. Annu Rev Neurosci 2012
127
17


De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
17

Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in mice.
Ikuo Ogiwara, Hiroyuki Miyamoto, Tetsuya Tatsukawa, Tetsushi Yamagata, Tojo Nakayama, Nafiseh Atapour, Eriko Miura, Emi Mazaki, Sara J Ernst, Dezhi Cao,[...]. Commun Biol 2018
47
21

Progress in Understanding and Treating SCN2A-Mediated Disorders.
Stephan J Sanders, Arthur J Campbell, Jeffrey R Cottrell, Rikke S Moller, Florence F Wagner, Angie L Auldridge, Raphael A Bernier, William A Catterall, Wendy K Chung, James R Empfield,[...]. Trends Neurosci 2018
127
17

NaV1.1 channels and epilepsy.
William A Catterall, Franck Kalume, John C Oakley. J Physiol 2010
275
15


Sodium-channel defects in benign familial neonatal-infantile seizures.
Sarah E Heron, Kathryn M Crossland, Eva Andermann, Hilary A Phillips, Allison J Hall, Andrew Bleasel, Michael Shevell, Suha Mercho, Marie-Helene Seni, Marie-Christine Guiot,[...]. Lancet 2002
252
15

Neuronal death and perinatal lethality in voltage-gated sodium channel alpha(II)-deficient mice.
R Planells-Cases, M Caprini, J Zhang, E M Rockenstein, R R Rivera, C Murre, E Masliah, M Montal. Biophys J 2000
114
15

GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits.
Robin Tremblay, Soohyun Lee, Bernardo Rudy. Neuron 2016
795
15

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato,[...]. Lancet 2012
712
13

Localization of voltage-gated ion channels in mammalian brain.
James S Trimmer, Kenneth J Rhodes. Annu Rev Physiol 2004
332
13

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
90
13

Three groups of interneurons account for nearly 100% of neocortical GABAergic neurons.
Bernardo Rudy, Gordon Fishell, SooHyun Lee, Jens Hjerling-Leffler. Dev Neurobiol 2011
801
13

Signal processing in the axon initial segment.
Maarten H P Kole, Greg J Stuart. Neuron 2012
262
13

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
71
13

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
71
13

Axon physiology.
Dominique Debanne, Emilie Campanac, Andrzej Bialowas, Edmond Carlier, Gisèle Alcaraz. Physiol Rev 2011
314
12

Molecular identity of dendritic voltage-gated sodium channels.
Andrea Lorincz, Zoltan Nusser. Science 2010
191
12

A resource of Cre driver lines for genetic targeting of GABAergic neurons in cerebral cortex.
Hiroki Taniguchi, Miao He, Priscilla Wu, Sangyong Kim, Raehum Paik, Ken Sugino, Duda Kvitsiani, Yu Fu, Jiangteng Lu, Ying Lin,[...]. Neuron 2011
12

Interneurons of the neocortical inhibitory system.
Henry Markram, Maria Toledo-Rodriguez, Yun Wang, Anirudh Gupta, Gilad Silberberg, Caizhi Wu. Nat Rev Neurosci 2004
12

'Neonatal' Nav1.2 reduces neuronal excitability and affects seizure susceptibility and behaviour.
Elena V Gazina, Bryan T W Leaw, Kay L Richards, Verena C Wimmer, Tae H Kim, Timothy D Aumann, Travis J Featherby, Leonid Churilov, Vicki E Hammond, Christopher A Reid,[...]. Hum Mol Genet 2015
38
18

SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizures.
Katherine B Howell, Jacinta M McMahon, Gemma L Carvill, Dimira Tambunan, Mark T Mackay, Victoria Rodriguez-Casero, Richard Webster, Damian Clark, Jeremy L Freeman, Sophie Calvert,[...]. Neurology 2015
145
12

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
187
12

The Autism-Associated Gene Scn2a Contributes to Dendritic Excitability and Synaptic Function in the Prefrontal Cortex.
Perry W E Spratt, Roy Ben-Shalom, Caroline M Keeshen, Kenneth J Burke, Rebecca L Clarkson, Stephan J Sanders, Kevin J Bender. Neuron 2019
68
12

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
438
10

SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain.
Y Liao, A-K Anttonen, E Liukkonen, E Gaily, S Maljevic, S Schubert, A Bellan-Koch, S Petrou, V E Ahonen, H Lerche,[...]. Neurology 2010
103
10

An SCN2A mutation in a family with infantile seizures from Madagascar reveals an increased subthreshold Na(+) current.
Stephan Lauxmann, Nadia Boutry-Kryza, Clotilde Rivier, Stephan Mueller, Ulrike B S Hedrich, Snezana Maljevic, Pierre Szepetowski, Holger Lerche, Gaetan Lesca. Epilepsia 2013
30
20

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
721
10

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
10

Sodium channel Na(v)1.6 is localized at nodes of ranvier, dendrites, and synapses.
J H Caldwell, K L Schaller, R S Lasher, E Peles, S R Levinson. Proc Natl Acad Sci U S A 2000
486
10

Effects in neocortical neurons of mutations of the Na(v)1.2 Na+ channel causing benign familial neonatal-infantile seizures.
Paolo Scalmani, Raffaella Rusconi, Elena Armatura, Federico Zara, Giuliano Avanzini, Silvana Franceschetti, Massimo Mantegazza. J Neurosci 2006
88
10



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.