A citation-based method for searching scientific literature

Sophie Sakkaki, Sylvain Barrière, Alex C Bender, Rod C Scott, Pierre-Pascal Lenck-Santini. Cereb Cortex 2020
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


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
66

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
50

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
50

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
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
35
50

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
121
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
7
50

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
157
33

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
33

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
33

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
19
33

The core Dravet syndrome phenotype.
Charlotte Dravet. Epilepsia 2011
276
33

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
50
33

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
148
33

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
47
33

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
33

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
594
33

Altered sleep regulation in a mouse model of SCN1A-derived genetic epilepsy with febrile seizures plus (GEFS+).
Ligia A Papale, Christopher D Makinson, J Christopher Ehlen, Sergio Tufik, Michael J Decker, Ketema N Paul, Andrew Escayg. Epilepsia 2013
33
33

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
15
33


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
380
33

Theta Rhythmopathy as a Cause of Cognitive Disability in TLE.
Tristan Shuman, Benjamin Amendolara, Peyman Golshani. Epilepsy Curr 2017
20
33

Altered Oscillatory Dynamics of CA1 Parvalbumin Basket Cells during Theta-Gamma Rhythmopathies of Temporal Lobe Epilepsy.
Diego Lopez-Pigozzi, François Laurent, Jorge R Brotons-Mas, Mario Valderrama, Manuel Valero, Ivan Fernandez-Lamo, Elena Cid, Daniel Gomez-Dominguez, Beatriz Gal, Liset Menendez de la Prida. eNeuro 2016
29
33

Involvement of fast-spiking cells in ictal sequences during spontaneous seizures in rats with chronic temporal lobe epilepsy.
Adam R Neumann, Robrecht Raedt, Hendrik W Steenland, Mathieu Sprengers, Katarzyna Bzymek, Zaneta Navratilova, Lilia Mesina, Jeanne Xie, Valerie Lapointe, Fabian Kloosterman,[...]. Brain 2017
20
33

Impaired θ-γ Coupling Indicates Inhibitory Dysfunction and Seizure Risk in a Dravet Syndrome Mouse Model.
Nico A Jansen, Carlos Perez, Maarten Schenke, Anouk W van Beurden, Anisa Dehghani, Rob A Voskuyl, Roland D Thijs, Ghanim Ullah, Arn M J M van den Maagdenberg, Else A Tolner. J Neurosci 2021
5
40

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
50
33

Scn8a Antisense Oligonucleotide Is Protective in Mouse Models of SCN8A Encephalopathy and Dravet Syndrome.
Guy M Lenk, Paymaan Jafar-Nejad, Sophie F Hill, Lucas D Huffman, Corrine E Smolen, Jacy L Wagnon, Hayley Petit, Wenxi Yu, Julie Ziobro, Kritika Bhatia,[...]. Ann Neurol 2020
31
33

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
33

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
33

Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures.
Massimo Mantegazza, Antonio Gambardella, Raffaella Rusconi, Emanuele Schiavon, Ferdinanda Annesi, Rita Restano Cassulini, Angelo Labate, Sara Carrideo, Rosanna Chifari, Maria Paola Canevini,[...]. Proc Natl Acad Sci U S A 2005
131
33

Dravet Syndrome: A Sodium Channel Interneuronopathy.
William A Catterall. Curr Opin Physiol 2018
45
33

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
33

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
33

NaV1.1 channels and epilepsy.
William A Catterall, Franck Kalume, John C Oakley. J Physiol 2010
246
33

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
33

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
33

Divergent sodium channel defects in familial hemiplegic migraine.
Kristopher M Kahlig, Thomas H Rhodes, Michael Pusch, Tobias Freilinger, José M Pereira-Monteiro, Michel D Ferrari, Arn M J M van den Maagdenberg, Martin Dichgans, Alfred L George. Proc Natl Acad Sci U S A 2008
72
33

First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.
M-J Castro, A H Stam, C Lemos, B de Vries, K R J Vanmolkot, J Barros, G M Terwindt, R R Frants, J Sequeiros, M D Ferrari,[...]. Cephalalgia 2009
63
33


Focal and generalized seizure activity after local hippocampal or cortical ablation of NaV 1.1 channels in mice.
Nico A Jansen, Anisa Dehghani, Cor Breukel, Else A Tolner, Arn M J M van den Maagdenberg. Epilepsia 2020
4
25

Electroencephalographic characteristics of Dravet syndrome.
Michelle Bureau, Bernardo Dalla Bernardina. Epilepsia 2011
52
16

Functional MRI in chronic epilepsy: associations with cognitive impairment.
Marielle Cg Vlooswijk, Jacobus Fa Jansen, Marc Cftm de Krom, Hj Marian Majoie, Paul Am Hofman, Walter H Backes, Albert P Aldenkamp. Lancet Neurol 2010
45
16

Balancing plasticity/stability across brain development.
Anne E Takesian, Takao K Hensch. Prog Brain Res 2013
269
16

Entrainment of neocortical neurons and gamma oscillations by the hippocampal theta rhythm.
Anton Sirota, Sean Montgomery, Shigeyoshi Fujisawa, Yoshikazu Isomura, Michael Zugaro, György Buzsáki. Neuron 2008
571
16

Impaired hippocampal rhythmogenesis in a mouse model of mesial temporal lobe epilepsy.
Tamar Dugladze, Imre Vida, Adriano B Tort, Anna Gross, Jacub Otahal, Uwe Heinemann, Nancy J Kopell, Tengis Gloveli. Proc Natl Acad Sci U S A 2007
94
16

Optimizing the Diagnosis and Management of Dravet Syndrome: Recommendations From a North American Consensus Panel.
Elaine C Wirrell, Linda Laux, Elizabeth Donner, Nathalie Jette, Kelly Knupp, Mary Anne Meskis, Ian Miller, Joseph Sullivan, Michelle Welborn, Anne T Berg. Pediatr Neurol 2017
105
16

Surviving CA1 pyramidal cells receive intact perisomatic inhibitory input in the human epileptic hippocampus.
L Wittner, L Eross, S Czirják, P Halász, T F Freund, Zs Maglóczky. Brain 2005
79
16

Hippocampal network patterns of activity in the mouse.
G Buzsáki, D L Buhl, K D Harris, J Csicsvari, B Czéh, A Morozov. Neuroscience 2003
291
16

Epileptic high-frequency network activity in a model of non-lesional temporal lobe epilepsy.
Premysl Jiruska, Gerald T Finnerty, Andrew D Powell, Noosheen Lofti, Roman Cmejla, John G R Jefferys. Brain 2010
58
16


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.