A citation-based method for searching scientific literature

Saja Fadila, Shir Quinn, Ana Turchetti Maia, Daniel Yakubovich, Mor Ovadia, Karen L Anderson, Moshe Giladi, Moran Rubinstein. Epilepsia 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


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
75

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
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
525
75

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
67
75

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
75

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
75

Epilepsy and neuropsychiatric comorbidities in mice carrying a recurrent Dravet syndrome SCN1A missense mutation.
Ana Ricobaraza, Lucia Mora-Jimenez, Elena Puerta, Rocio Sanchez-Carpintero, Ana Mingorance, Julio Artieda, Maria Jesus Nicolas, Guillermo Besne, Maria Bunuales, Manuela Gonzalez-Aparicio,[...]. Sci Rep 2019
21
75

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
75

Dravet syndrome (severe myoclonic epilepsy in infancy).
Charlotte Dravet, Hirokazu Oguni. Handb Clin Neurol 2013
82
75

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
75


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
75

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
50

Molecular identity of dendritic voltage-gated sodium channels.
Andrea Lorincz, Zoltan Nusser. Science 2010
180
50

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
50

GluN2A NMDA Receptor Enhancement Improves Brain Oscillations, Synchrony, and Cognitive Functions in Dravet Syndrome and Alzheimer's Disease Models.
Jesse E Hanson, Keran Ma, Justin Elstrott, Martin Weber, Sandrine Saillet, Abdullah S Khan, Jeffrey Simms, Benjamin Liu, Thomas A Kim, Gui-Qiu Yu,[...]. Cell Rep 2020
17
50

Dendritic integration: 60 years of progress.
Greg J Stuart, Nelson Spruston. Nat Neurosci 2015
191
50

Augmented Reticular Thalamic Bursting and Seizures in Scn1a-Dravet Syndrome.
Stefanie Ritter-Makinson, Alexandra Clemente-Perez, Bryan Higashikubo, Frances S Cho, Stephanie S Holden, Eric Bennett, Ana Chkhaidze, Oscar H J Eelkman Rooda, Marie-Coralie Cornet, Freek E Hoebeek,[...]. Cell Rep 2019
18
50

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
49
50

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
50

Gene expression profiling in a mouse model of Dravet syndrome.
Nicole A Hawkins, Jeffrey D Calhoun, Alexandra M Huffman, Jennifer A Kearney. Exp Neurol 2019
16
50

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
50

Impairment of Sharp-Wave Ripples in a Murine Model of Dravet Syndrome.
Christine S Cheah, Brian N Lundstrom, William A Catterall, John C Oakley. J Neurosci 2019
8
50



Interneuron Desynchronization Precedes Seizures in a Mouse Model of Dravet Syndrome.
Conny H Tran, Michael Vaiana, Johan Nakuci, Ala Somarowthu, Kevin M Goff, Nitsan Goldstein, Priya Murthy, Sarah F Muldoon, Ethan M Goldberg. J Neurosci 2020
26
50


Disordered breathing in a mouse model of Dravet syndrome.
Fu-Shan Kuo, Colin M Cleary, Joseph J LoTurco, Xinnian Chen, Daniel K Mulkey. Elife 2019
24
50

In vivo, in vitro and in silico correlations of four de novo SCN1A missense mutations.
Andreea Nissenkorn, Yael Almog, Inbar Adler, Mary Safrin, Marina Brusel, Milit Marom, Shayel Bercovich, Daniel Yakubovich, Michal Tzadok, Bruria Ben-Zeev,[...]. PLoS One 2019
10
50

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
38
50

A blueprint for the spatiotemporal origins of mouse hippocampal interneuron diversity.
Ludovic Tricoire, Kenneth A Pelkey, Brian E Erkkila, Brian W Jeffries, Xiaoqing Yuan, Chris J McBain. J Neurosci 2011
197
50

Single-cell RNA-Seq characterization of anatomically identified OLM interneurons in different transgenic mouse lines.
Jochen Winterer, David Lukacsovich, Lin Que, Andrea M Sartori, Wenshu Luo, Csaba Földy. Eur J Neurosci 2019
16
50

Transient sodium current at subthreshold voltages: activation by EPSP waveforms.
Brett C Carter, Andrew J Giessel, Bernardo L Sabatini, Bruce P Bean. Neuron 2012
60
50


Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant Dravet Syndrome model during development.
Ming-Shian Tsai, Meng-Larn Lee, Chun-Yun Chang, Hsiang-Hsuan Fan, I-Shing Yu, You-Tzung Chen, Jhih-Yi You, Chun-Yu Chen, Fang-Chia Chang, Jane H Hsiao,[...]. Neurobiol Dis 2015
27
50

CRISPR/dCas9-based Scn1a gene activation in inhibitory neurons ameliorates epileptic and behavioral phenotypes of Dravet syndrome model mice.
Tetsushi Yamagata, Matthieu Raveau, Kenta Kobayashi, Hiroyuki Miyamoto, Tetsuya Tatsukawa, Ikuo Ogiwara, Shigeyoshi Itohara, Takao K Hensch, Kazuhiro Yamakawa. Neurobiol Dis 2020
25
50

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
50

The core Dravet syndrome phenotype.
Charlotte Dravet. Epilepsia 2011
293
50

Treatment of Dravet Syndrome.
Elaine C Wirrell. Can J Neurol Sci 2016
56
50

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
99
50

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
50

dCas9-Based Scn1a Gene Activation Restores Inhibitory Interneuron Excitability and Attenuates Seizures in Dravet Syndrome Mice.
Gaia Colasante, Gabriele Lignani, Simone Brusco, Claudia Di Berardino, Jenna Carpenter, Serena Giannelli, Nicholas Valassina, Simone Bido, Raffaele Ricci, Valerio Castoldi,[...]. Mol Ther 2020
65
50

Antisense oligonucleotides increase Scn1a expression and reduce seizures and SUDEP incidence in a mouse model of Dravet syndrome.
Zhou Han, Chunling Chen, Anne Christiansen, Sophina Ji, Qian Lin, Charles Anumonwo, Chante Liu, Steven C Leiser, Meena, Isabel Aznarez,[...]. Sci Transl Med 2020
66
50

Selective spider toxins reveal a role for the Nav1.1 channel in mechanical pain.
Jeremiah D Osteen, Volker Herzig, John Gilchrist, Joshua J Emrick, Chuchu Zhang, Xidao Wang, Joel Castro, Sonia Garcia-Caraballo, Luke Grundy, Grigori Y Rychkov,[...]. Nature 2016
177
50

Antisense oligonucleotide modulation of non-productive alternative splicing upregulates gene expression.
Kian Huat Lim, Zhou Han, Hyun Yong Jeon, Jacob Kach, Enxuan Jing, Sebastien Weyn-Vanhentenryck, Mikaela Downs, Anna Corrionero, Raymond Oh, Juergen Scharner,[...]. Nat Commun 2020
40
50

Upregulation of Haploinsufficient Gene Expression in the Brain by Targeting a Long Non-coding RNA Improves Seizure Phenotype in a Model of Dravet Syndrome.
J Hsiao, T Y Yuan, M S Tsai, C Y Lu, Y C Lin, M L Lee, S W Lin, F C Chang, H Liu Pimentel, C Olive,[...]. EBioMedicine 2016
67
50

Dravet Syndrome: A Sodium Channel Interneuronopathy.
William A Catterall. Curr Opin Physiol 2018
49
50

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
401
50




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.