A citation-based method for searching scientific literature

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
Times Cited: 401







List of co-cited articles
1011 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
676
37

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
525
27

Neocortical excitation/inhibition balance in information processing and social dysfunction.
Ofer Yizhar, Lief E Fenno, Matthias Prigge, Franziska Schneider, Thomas J Davidson, Daniel J O'Shea, Vikaas S Sohal, Inbal Goshen, Joel Finkelstein, Jeanne T Paz,[...]. Nature 2011
20

The core Dravet syndrome phenotype.
Charlotte Dravet. Epilepsia 2011
293
19

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
131
17


Model of autism: increased ratio of excitation/inhibition in key neural systems.
J L R Rubenstein, M M Merzenich. Genes Brain Behav 2003
16

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
770
16

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
66
22

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
65
23

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
177
15

Increased Excitation-Inhibition Ratio Stabilizes Synapse and Circuit Excitability in Four Autism Mouse Models.
Michelle W Antoine, Tomer Langberg, Philipp Schnepel, Daniel E Feldman. Neuron 2019
135
14


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
180
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
78
16

Excitation/Inhibition Imbalance in Animal Models of Autism Spectrum Disorders.
Eunee Lee, Jiseok Lee, Eunjoon Kim. Biol Psychiatry 2017
205
13

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
818
13

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
98
12

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
165
12

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction.
João Peça, Cátia Feliciano, Jonathan T Ting, Wenting Wang, Michael F Wells, Talaignair N Venkatraman, Christopher D Lascola, Zhanyan Fu, Guoping Feng. Nature 2011
856
12

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
64
17

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
148
11

Behavioural phenotyping assays for mouse models of autism.
Jill L Silverman, Mu Yang, Catherine Lord, Jacqueline N Crawley. Nat Rev Neurosci 2010
895
11

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
11

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.
Olga Peñagarikano, Brett S Abrahams, Edward I Herman, Kellen D Winden, Amos Gdalyahu, Hongmei Dong, Lisa I Sonnenblick, Robin Gruver, Joel Almajano, Anatol Bragin,[...]. Cell 2011
613
11

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
28
35

A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice.
Katsuhiko Tabuchi, Jacqueline Blundell, Mark R Etherton, Robert E Hammer, Xinran Liu, Craig M Powell, Thomas C Südhof. Science 2007
648
10

NaV1.1 channels and epilepsy.
William A Catterall, Franck Kalume, John C Oakley. J Physiol 2010
259
10

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
10

Common circuit defect of excitatory-inhibitory balance in mouse models of autism.
Nadine Gogolla, Jocelyn J Leblanc, Kathleen B Quast, Thomas C Südhof, Michela Fagiolini, Takao K Hensch. J Neurodev Disord 2009
395
10

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
164
10

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
524
10

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
104
9

Mortality in Dravet syndrome.
Monica S Cooper, Anne Mcintosh, Douglas E Crompton, Jacinta M McMahon, Amy Schneider, Kevin Farrell, Vijeya Ganesan, Deepak Gill, Sara Kivity, Tally Lerman-Sagie,[...]. Epilepsy Res 2016
125
9

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
21
42


GABA(A) receptor downregulation in brains of subjects with autism.
S Hossein Fatemi, Teri J Reutiman, Timothy D Folsom, Paul D Thuras. J Autism Dev Disord 2009
277
9

A two-hit story: Seizures and genetic mutation interaction sets phenotype severity in SCN1A epilepsies.
Ana Rita Salgueiro-Pereira, Fabrice Duprat, Paula A Pousinha, Alexandre Loucif, Vincent Douchamps, Cristina Regondi, Marion Ayrault, Martine Eugie, Marion I Stunault, Andrew Escayg,[...]. Neurobiol Dis 2019
25
36

The genetics of Dravet syndrome.
Carla Marini, Ingrid E Scheffer, Rima Nabbout, Arvid Suls, Peter De Jonghe, Federico Zara, Renzo Guerrini. Epilepsia 2011
162
8

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
83
9

Autism and behavior in adult patients with Dravet syndrome (DS).
J J L Berkvens, I Veugen, M J B M Veendrick-Meekes, F M Snoeijen-Schouwenaars, H J Schelhaas, M H Willemsen, I Y Tan, A P Aldenkamp. Epilepsy Behav 2015
37
21

Dravet syndrome: the long-term outcome.
Pierre Genton, Reana Velizarova, Charlotte Dravet. Epilepsia 2011
151
8

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
69
11

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
45
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
43
18

The Number of Parvalbumin-Expressing Interneurons Is Decreased in the Prefrontal Cortex in Autism.
Ezzat Hashemi, Jeanelle Ariza, Haille Rogers, Stephen C Noctor, Verónica Martínez-Cerdeño. Cereb Cortex 2017
161
8

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
A Jeremy Willsey, Stephan J Sanders, Mingfeng Li, Shan Dong, Andrew T Tebbenkamp, Rebecca A Muhle, Steven K Reilly, Leon Lin, Sofia Fertuzinhos, Jeremy A Miller,[...]. Cell 2013
517
8

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
639
8

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
61
13

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
410
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.