A citation-based method for searching scientific literature

Antara Das, Bingyao Zhu, Yunyao Xie, Lisha Zeng, An T Pham, Jonathan C Neumann, Olga Safrina, Daniel R Benavides, Grant R MacGregor, Soleil S Schutte, Robert F Hunt, Diane K O'Dowd. eNeuro 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


High-resolution molecular genomic autopsy reveals complex sudden unexpected death in epilepsy risk profile.
Tara L Klassen, Valerie C Bomben, Ankita Patel, Janice Drabek, Tim T Chen, Wenli Gu, Feng Zhang, Kevin Chapman, James R Lupski, Jeffrey L Noebels,[...]. Epilepsia 2014
58
100

Epilepsy-associated dysfunction in the voltage-gated neuronal sodium channel SCN1A.
Christoph Lossin, Thomas H Rhodes, Reshma R Desai, Carlos G Vanoye, Dao Wang, Sanda Carniciu, Orrin Devinsky, Alfred L George. J Neurosci 2003
132
100

Comparisons of dual isogenic human iPSC pairs identify functional alterations directly caused by an epilepsy associated SCN1A mutation.
Yunyao Xie, Nathan N Ng, Olga S Safrina, Carmen M Ramos, Kevin C Ess, Philip H Schwartz, Martin A Smith, Diane K O'Dowd. Neurobiol Dis 2020
8
100

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
100

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
95
100


Developmental alterations in firing properties of hippocampal CA1 inhibitory and excitatory neurons in a mouse model of Dravet syndrome.
Yael Almog, Saja Fadila, Marina Brusel, Anat Mavashov, Karen Anderson, Moran Rubinstein. Neurobiol Dis 2021
4
100

An epilepsy mutation in the sodium channel SCN1A that decreases channel excitability.
Arthur J Barela, Salina P Waddy, Jay G Lickfett, Jessica Hunter, Aimee Anido, Sandra L Helmers, Alan L Goldin, Andrew Escayg. J Neurosci 2006
59
100

Minimal Hodgkin-Huxley type models for different classes of cortical and thalamic neurons.
Martin Pospischil, Maria Toledo-Rodriguez, Cyril Monier, Zuzanna Piwkowska, Thierry Bal, Yves Frégnac, Henry Markram, Alain Destexhe. Biol Cybern 2008
115
100

A Study among the Genotype, Functional Alternations, and Phenotype of 9 SCN1A Mutations in Epilepsy Patients.
Daniela Kluckova, Miriam Kolnikova, Lubica Lacinova, Bohumila Jurkovicova-Tarabova, Tomas Foltan, Viktor Demko, Ludevit Kadasi, Andrej Ficek, Andrea Soltysova. Sci Rep 2020
5
100

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
100

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
100


Genotype-phenotype associations in SCN1A-related epilepsies.
S M Zuberi, A Brunklaus, R Birch, E Reavey, J Duncan, G H Forbes. Neurology 2011
147
100

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
100

New insights into the early mechanisms of epileptogenesis in a zebrafish model of Dravet syndrome.
Ettore Tiraboschi, Silvia Martina, Wietske van der Ent, Kamil Grzyb, Kinga Gawel, Maria Lorena Cordero-Maldonado, Suresh Kumar Poovathingal, Sarah Heintz, Somisetty Venkata Satheesh, Jarle Brattespe,[...]. Epilepsia 2020
21
100

Pure haploinsufficiency for Dravet syndrome Na(V)1.1 (SCN1A) sodium channel truncating mutations.
Giulia Bechi, Paolo Scalmani, Emanuele Schiavon, Raffaella Rusconi, Silvana Franceschetti, Massimo Mantegazza. Epilepsia 2012
36
100

Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients.
C Depienne, O Trouillard, C Saint-Martin, I Gourfinkel-An, D Bouteiller, W Carpentier, B Keren, B Abert, A Gautier, S Baulac,[...]. J Med Genet 2009
226
100

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
17
100

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
100

A taxonomy of transcriptomic cell types across the isocortex and hippocampal formation.
Zizhen Yao, Cindy T J van Velthoven, Thuc Nghi Nguyen, Jeff Goldy, Adriana E Sedeno-Cortes, Fahimeh Baftizadeh, Darren Bertagnolli, Tamara Casper, Megan Chiang, Kirsten Crichton,[...]. Cell 2021
42
100

NaV1.1 channels and epilepsy.
William A Catterall, Franck Kalume, John C Oakley. J Physiol 2010
246
100

Correlations in timing of sodium channel expression, epilepsy, and sudden death in Dravet syndrome.
Christine S Cheah, Ruth E Westenbroek, William H Roden, Franck Kalume, John C Oakley, Laura A Jansen, William A Catterall. Channels (Austin) 2013
36
100

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
17
100

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
23
100

A novel epilepsy mutation in the sodium channel SCN1A identifies a cytoplasmic domain for beta subunit interaction.
J Spampanato, J A Kearney, G de Haan, D P McEwen, A Escayg, I Aradi, B T MacDonald, S I Levin, I Soltesz, P Benna,[...]. J Neurosci 2004
117
100

The genetics of Dravet syndrome.
Carla Marini, Ingrid E Scheffer, Rima Nabbout, Arvid Suls, Peter De Jonghe, Federico Zara, Renzo Guerrini. Epilepsia 2011
155
100

Inherited neuronal ion channelopathies: new windows on complex neurological diseases.
William A Catterall, Sulayman Dib-Hajj, Miriam H Meisler, Daniela Pietrobon. J Neurosci 2008
155
100


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
100

Clinical spectrum of SCN1A mutations.
Antonio Gambardella, Carla Marini. Epilepsia 2009
63
100

Nontruncating SCN1A mutations associated with severe myoclonic epilepsy of infancy impair cell surface expression.
Christopher H Thompson, J Christopher Porter, Kristopher M Kahlig, Melissa A Daniels, Alfred L George. J Biol Chem 2012
27
100

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
100

Influence of common SCN1A promoter variants on the severity of SCN1A-related phenotypes.
Iris M de Lange, Wout Weuring, Ruben van 't Slot, Boudewijn Gunning, Anja C M Sonsma, Mark McCormack, Carolien de Kovel, Lisette J J M van Gemert, Flip Mulder, Marjan J A van Kempen,[...]. Mol Genet Genomic Med 2019
5
100


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.