A citation-based method for searching scientific literature

Massimo Mantegazza, Sandrine Cestèle, William A Catterall. Physiol Rev 2021
Times Cited: 7







List of co-cited articles
41 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
653
42

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
59
42

A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.
Arn M J M van den Maagdenberg, Daniela Pietrobon, Tommaso Pizzorusso, Simon Kaja, Ludo A M Broos, Tiziana Cesetti, Rob C G van de Ven, Angelita Tottene, Jos van der Kaa, Jaap J Plomp,[...]. Neuron 2004
460
42


Modeling cortical spreading depression induced by the hyperactivity of interneurons.
Mathieu Desroches, Olivier Faugeras, Martin Krupa, Massimo Mantegazza. J Comput Neurosci 2019
8
42

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
58
42

Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2.
Loredana Leo, Lisa Gherardini, Virginia Barone, Maurizio De Fusco, Daniela Pietrobon, Tommaso Pizzorusso, Giorgio Casari. PLoS Genet 2011
128
42

First FHM3 mouse model shows spontaneous cortical spreading depolarizations.
Nico A Jansen, Anisa Dehghani, Margot M L Linssen, Cor Breukel, Else A Tolner, Arn M J M van den Maagdenberg. Ann Clin Transl Neurol 2020
16
42

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
77
42

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
795
28

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
699
28

A toolbox of Cre-dependent optogenetic transgenic mice for light-induced activation and silencing.
Linda Madisen, Tianyi Mao, Henner Koch, Jia-min Zhuo, Antal Berenyi, Shigeyoshi Fujisawa, Yun-Wei A Hsu, Alfredo J Garcia, Xuan Gu, Sebastien Zanella,[...]. Nat Neurosci 2012
714
28

Self-limited hyperexcitability: functional effect of a familial hemiplegic migraine mutation of the Nav1.1 (SCN1A) Na+ channel.
Sandrine Cestèle, Paolo Scalmani, Raffaella Rusconi, Benedetta Terragni, Silvana Franceschetti, Massimo Mantegazza. J Neurosci 2008
81
28

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
Martin Dichgans, Tobias Freilinger, Gertrud Eckstein, Elena Babini, Bettina Lorenz-Depiereux, Saskia Biskup, Michel D Ferrari, Jürgen Herzog, Arn M J M van den Maagdenberg, Michael Pusch,[...]. Lancet 2005
531
28

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
41
28


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
511
28

Cholinergic modulation inhibits cortical spreading depression in mouse neocortex through activation of muscarinic receptors and decreased excitatory/inhibitory drive.
Sarah Zerimech, Oana Chever, Paolo Scalmani, Lara Pizzamiglio, Fabrice Duprat, Massimo Mantegazza. Neuropharmacology 2020
5
40



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
754
28

Nonfunctional NaV1.1 familial hemiplegic migraine mutant transformed into gain of function by partial rescue of folding defects.
Sandrine Cestèle, Emanuele Schiavon, Raffaella Rusconi, Silvana Franceschetti, Massimo Mantegazza. Proc Natl Acad Sci U S A 2013
57
28

Mechanisms of firing patterns in fast-spiking cortical interneurons.
David Golomb, Karnit Donner, Liron Shacham, Dan Shlosberg, Yael Amitai, David Hansel. PLoS Comput Biol 2007
66
28


Migraine pathophysiology: lessons from mouse models and human genetics.
Michel D Ferrari, Roselin R Klever, Gisela M Terwindt, Cenk Ayata, Arn M J M van den Maagdenberg. Lancet Neurol 2015
197
28

Pathophysiological mechanisms of migraine and epilepsy: Similarities and differences.
Massimo Mantegazza, Sandrine Cestèle. Neurosci Lett 2018
26
28

The stroke-migraine depolarization continuum.
Jens P Dreier, Clemens Reiffurth. Neuron 2015
179
28

Chronically epileptic human and rat neocortex display a similar resistance against spreading depolarization in vitro.
Anna Maslarova, Mesbah Alam, Clemens Reiffurth, Ezequiel Lapilover, Ali Gorji, Jens P Dreier. Stroke 2011
33
28

Recording, analysis, and interpretation of spreading depolarizations in neurointensive care: Review and recommendations of the COSBID research group.
Jens P Dreier, Martin Fabricius, Cenk Ayata, Oliver W Sakowitz, C William Shuttleworth, Christian Dohmen, Rudolf Graf, Peter Vajkoczy, Raimund Helbok, Michiyasu Suzuki,[...]. J Cereb Blood Flow Metab 2017
147
28

Gain of Function for the SCN1A/hNav1.1-L1670W Mutation Responsible for Familial Hemiplegic Migraine.
Sandra Dhifallah, Eric Lancaster, Shana Merrill, Nathalie Leroudier, Massimo Mantegazza, Sandrine Cestèle. Front Mol Neurosci 2018
18
28

Green fluorescent protein expression and colocalization with calretinin, parvalbumin, and somatostatin in the GAD67-GFP knock-in mouse.
Nobuaki Tamamaki, Yuchio Yanagawa, Ryohei Tomioka, Jun-Ichi Miyazaki, Kunihiko Obata, Takeshi Kaneko. J Comp Neurol 2003
937
28

Gain of function of sporadic/familial hemiplegic migraine-causing SCN1A mutations: Use of an optimized cDNA.
Sara Bertelli, Raffaella Barbieri, Michael Pusch, Paola Gavazzo. Cephalalgia 2019
12
28

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
162
28

Defective glutamate and K+ clearance by cortical astrocytes in familial hemiplegic migraine type 2.
Clizia Capuani, Marcello Melone, Angelita Tottene, Luca Bragina, Giovanna Crivellaro, Mirko Santello, Giorgio Casari, Fiorenzo Conti, Daniela Pietrobon. EMBO Mol Med 2016
63
28

Hyperexcitable interneurons trigger cortical spreading depression in an Scn1a migraine model.
Eva Auffenberg, Ulrike Bs Hedrich, Raffaella Barbieri, Daniela Miely, Bernhard Groschup, Thomas V Wuttke, Niklas Vogel, Philipp Lührs, Ilaria Zanardi, Sara Bertelli,[...]. J Clin Invest 2021
2
100

Enhanced excitatory transmission at cortical synapses as the basis for facilitated spreading depression in Ca(v)2.1 knockin migraine mice.
Angelita Tottene, Rossella Conti, Alessandra Fabbro, Dania Vecchia, Maryna Shapovalova, Mirko Santello, Arn M J M van den Maagdenberg, Michel D Ferrari, Daniela Pietrobon. Neuron 2009
218
28

Migraine: a disorder of brain excitatory-inhibitory balance?
Dania Vecchia, Daniela Pietrobon. Trends Neurosci 2012
137
28



Sodium Channelopathies of Skeletal Muscle.
Stephen C Cannon. Handb Exp Pharmacol 2018
62
28

Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome.
N M Plaster, R Tawil, M Tristani-Firouzi, S Canún, S Bendahhou, A Tsunoda, M R Donaldson, S T Iannaccone, E Brunt, R Barohn,[...]. Cell 2001
653
28

Neddylation inhibition impairs spine development, destabilizes synapses and deteriorates cognition.
Annette M Vogl, Marisa M Brockmann, Sebastian A Giusti, Giuseppina Maccarrone, Claudia A Vercelli, Corinna A Bauder, Julia S Richter, Francesco Roselli, Anne-Sophie Hafner, Nina Dedic,[...]. Nat Neurosci 2015
55
14

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
58
14

Accumulation of NEDD8 in neuronal and glial inclusions of neurodegenerative disorders.
F Mori, M Nishie, Y-S Piao, K Kito, T Kamitani, H Takahashi, K Wakabayashi. Neuropathol Appl Neurobiol 2005
77
14

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
100
14

Noninactivating voltage-gated sodium channels in severe myoclonic epilepsy of infancy.
Thomas H Rhodes, Christoph Lossin, Carlos G Vanoye, Dao W Wang, Alfred L George. Proc Natl Acad Sci U S A 2004
134
14

Neddylation stabilizes Nav1.1 to maintain interneuron excitability and prevent seizures in murine epilepsy models.
Wenbing Chen, Bin Luo, Nannan Gao, Haiwen Li, Hongsheng Wang, Lei Li, Wanpeng Cui, Lei Zhang, Dong Sun, Fang Liu,[...]. J Clin Invest 2021
2
50

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
92
14

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
173
14

H2O2 regulates lung epithelial sodium channel (ENaC) via ubiquitin-like protein Nedd8.
Charles A Downs, Amrita Kumar, Lisa H Kreiner, Nicholle M Johnson, My N Helms. J Biol Chem 2013
33
14


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.