A citation-based method for searching scientific literature

David Bearden, Alanna Strong, Jessica Ehnot, Marissa DiGiovine, Dennis Dlugos, Ethan M Goldberg. Ann Neurol 2014
Times Cited: 125







List of co-cited articles
1051 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Quinidine in the treatment of KCNT1-positive epilepsies.
Mohamad A Mikati, Yong-Hui Jiang, Michael Carboni, Vandana Shashi, Slave Petrovski, Rebecca Spillmann, Carol J Milligan, Melody Li, Annette Grefe, Allyn McConkie,[...]. Ann Neurol 2015
102
61

KCNT1 gain of function in 2 epilepsy phenotypes is reversed by quinidine.
Carol J Milligan, Melody Li, Elena V Gazina, Sarah E Heron, Umesh Nair, Chantel Trager, Christopher A Reid, Anu Venkat, Donald P Younkin, Dennis J Dlugos,[...]. Ann Neurol 2014
141
56

De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy.
Giulia Barcia, Matthew R Fleming, Aline Deligniere, Valeswara-Rao Gazula, Maile R Brown, Maeva Langouet, Haijun Chen, Jack Kronengold, Avinash Abhyankar, Roberta Cilio,[...]. Nat Genet 2012
267
50

Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy.
Sarah E Heron, Katherine R Smith, Melanie Bahlo, Lino Nobili, Esther Kahana, Laura Licchetta, Karen L Oliver, Aziz Mazarib, Zaid Afawi, Amos Korczyn,[...]. Nat Genet 2012
213
41

Ineffective quinidine therapy in early onset epileptic encephalopathy with KCNT1 mutation.
Pin Fee Chong, Ryoko Nakamura, Hirotomo Saitsu, Naomichi Matsumoto, Ryutaro Kira. Ann Neurol 2016
46
80

GRIN2A mutation and early-onset epileptic encephalopathy: personalized therapy with memantine.
Tyler Mark Pierson, Hongjie Yuan, Eric D Marsh, Karin Fuentes-Fajardo, David R Adams, Thomas Markello, Gretchen Golas, Dimitre R Simeonov, Conisha Holloman, Anel Tankovic,[...]. Ann Clin Transl Neurol 2014
143
29

Precision therapy for epilepsy due to KCNT1 mutations: A randomized trial of oral quinidine.
Saul A Mullen, Patrick W Carney, Annie Roten, Michael Ching, Paul A Lightfoot, Leonid Churilov, Umesh Nair, Melody Li, Samuel F Berkovic, Steven Petrou,[...]. Neurology 2018
51
56

Mutations in KCNT1 cause a spectrum of focal epilepsies.
Rikke S Møller, Sarah E Heron, Line H G Larsen, Chiao Xin Lim, Michael G Ricos, Marta A Bayly, Marjan J A van Kempen, Sylvia Klinkenberg, Ian Andrews, Kent Kelley,[...]. Epilepsia 2015
69
40

De novo mutations in epileptic encephalopathies.
Andrew S Allen, Samuel F Berkovic, Patrick Cossette, Norman Delanty, Dennis Dlugos, Evan E Eichler, Michael P Epstein, Tracy Glauser, David B Goldstein, Yujun Han,[...]. Nature 2013
935
26

Human slack potassium channel mutations increase positive cooperativity between individual channels.
Grace E Kim, Jack Kronengold, Giulia Barcia, Imran H Quraishi, Hilary C Martin, Edward Blair, Jenny C Taylor, Olivier Dulac, Laurence Colleaux, Rima Nabbout,[...]. Cell Rep 2014
58
39

Adjunctive everolimus therapy for treatment-resistant focal-onset seizures associated with tuberous sclerosis (EXIST-3): a phase 3, randomised, double-blind, placebo-controlled study.
Jacqueline A French, John A Lawson, Zuhal Yapici, Hiroko Ikeda, Tilman Polster, Rima Nabbout, Paolo Curatolo, Petrus J de Vries, Dennis J Dlugos, Noah Berkowitz,[...]. Lancet 2016
302
23

Quinidine therapy for West syndrome with KCNTI mutation: A case report.
Masataka Fukuoka, Ichiro Kuki, Hisashi Kawawaki, Shin Okazaki, Kiyohiro Kim, Yuka Hattori, Hitomi Tsuji, Megumi Nukui, Takeshi Inoue, Yoko Yoshida,[...]. Brain Dev 2017
30
76

Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy.
Amy McTague, Umesh Nair, Sony Malhotra, Esther Meyer, Natalie Trump, Elena V Gazina, Apostolos Papandreou, Adeline Ngoh, Sally Ackermann, Gautam Ambegaonkar,[...]. Neurology 2018
42
54

De novo KCNT1 mutations in early-onset epileptic encephalopathy.
Chihiro Ohba, Mitsuhiro Kato, Nobuya Takahashi, Hitoshi Osaka, Takashi Shiihara, Jun Tohyama, Shin Nabatame, Junji Azuma, Yuji Fujii, Munetsugu Hara,[...]. Epilepsia 2015
57
38

Migrating partial seizures in infancy: a malignant disorder with developmental arrest.
G Coppola, P Plouin, C Chiron, O Robain, O Dulac. Epilepsia 1995
156
21

Early and effective treatment of KCNQ2 encephalopathy.
Tiziana Pisano, Adam L Numis, Sinéad B Heavin, Sarah Weckhuysen, Marco Angriman, Arvid Suls, Barbara Podesta, Ronald L Thibert, Kevin A Shapiro, Renzo Guerrini,[...]. Epilepsia 2015
111
21

KCNT1 mutations in seizure disorders: the phenotypic spectrum and functional effects.
Chiao Xin Lim, Michael G Ricos, Leanne M Dibbens, Sarah E Heron. J Med Genet 2016
48
43

Does age affect response to quinidine in patients with KCNT1 mutations? Report of three new cases and review of the literature.
Elie Abdelnour, William Gallentine, Marie McDonald, Monisha Sachdev, Yong-Hui Jiang, Mohamad A Mikati. Seizure 2018
27
77

Pharmacological activation and inhibition of Slack (Slo2.2) channels.
Bo Yang, Valentin K Gribkoff, Jennifer Pan, Veronique Damagnez, Steven I Dworetzky, Christopher G Boissard, Arin Bhattacharjee, Yangyang Yan, Fred J Sigworth, Leonard K Kaczmarek. Neuropharmacology 2006
56
35

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.
Markus Wolff, Katrine M Johannesen, Ulrike B S Hedrich, Silvia Masnada, Guido Rubboli, Elena Gardella, Gaetan Lesca, Dorothée Ville, Mathieu Milh, Laurent Villard,[...]. Brain 2017
212
20

Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis.
Hilary C Martin, Grace E Kim, Alistair T Pagnamenta, Yoshiko Murakami, Gemma L Carvill, Esther Meyer, Richard R Copley, Andrew Rimmer, Giulia Barcia, Matthew R Fleming,[...]. Hum Mol Genet 2014
157
19

Remarkable Phenytoin Sensitivity in 4 Children with SCN8A-related Epilepsy: A Molecular Neuropharmacological Approach.
Ragna S Boerma, Kees P Braun, Marcel P H van den Broek, Frederique M C van Berkestijn, Marielle E Swinkels, Eveline O Hagebeuk, Dick Lindhout, Marjan van Kempen, Maartje Boon, Joost Nicolai,[...]. Neurotherapeutics 2016
81
23

KCNQ2 encephalopathy: Features, mutational hot spots, and ezogabine treatment of 11 patients.
John J Millichap, Kristen L Park, Tammy Tsuchida, Bruria Ben-Zeev, Lionel Carmant, Robert Flamini, Nishtha Joshi, Paul M Levisohn, Eric Marsh, Srishti Nangia,[...]. Neurol Genet 2016
99
19

Characterization of two de novoKCNT1 mutations in children with malignant migrating partial seizures in infancy.
Francesca Rizzo, Paolo Ambrosino, Anna Guacci, Massimiliano Chetta, Giovanna Marchese, Teresa Rocco, Maria Virginia Soldovieri, Laura Manocchio, Ilaria Mosca, Gianluca Casara,[...]. Mol Cell Neurosci 2016
35
54

Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum.
Amy McTague, Richard Appleton, Shivaram Avula, J Helen Cross, Mary D King, Thomas S Jacques, Sanjay Bhate, Anthony Cronin, Andrew Curran, Archana Desurkar,[...]. Brain 2013
82
21

SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizures.
Katherine B Howell, Jacinta M McMahon, Gemma L Carvill, Dimira Tambunan, Mark T Mackay, Victoria Rodriguez-Casero, Richard Webster, Damian Clark, Jeremy L Freeman, Sophie Calvert,[...]. Neurology 2015
131
18

Lack of response to quinidine in KCNT1-related neonatal epilepsy.
Adam L Numis, Umesh Nair, Anita N Datta, Tristan T Sands, Michael S Oldham, Akash Patel, Melody Li, Elena Gazina, Steven Petrou, Maria Roberta Cilio. Epilepsia 2018
27
66

Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations: Functional Studies, Clinical Responses, and Critical Issues for Personalized Therapy.
Robertino Dilena, Jacopo C DiFrancesco, Maria Virginia Soldovieri, Antonella Giacobbe, Paolo Ambrosino, Ilaria Mosca, Maria Albina Galli, Sophie Guez, Monica Fumagalli, Francesco Miceli,[...]. Neurotherapeutics 2018
26
65


De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.
Steffen Syrbe, Ulrike B S Hedrich, Erik Riesch, Tania Djémié, Stephan Müller, Rikke S Møller, Bridget Maher, Laura Hernandez-Hernandez, Matthis Synofzik, Hande S Caglayan,[...]. Nat Genet 2015
144
16

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.
Ingrid E Scheffer, Samuel Berkovic, Giuseppe Capovilla, Mary B Connolly, Jacqueline French, Laura Guilhoto, Edouard Hirsch, Satish Jain, Gary W Mathern, Solomon L Moshé,[...]. Epilepsia 2017
16

A quinidine non responsive novel KCNT1 mutation in an Indian infant with epilepsy of infancy with migrating focal seizures.
Priyanka Madaan, Prashant Jauhari, Aparajita Gupta, Biswaroop Chakrabarty, Sheffali Gulati. Brain Dev 2018
20
80

Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients.
Sarah Weckhuysen, Vanja Ivanovic, Rik Hendrickx, Rudy Van Coster, Helle Hjalgrim, Rikke S Møller, Sabine Grønborg, An-Sofie Schoonjans, Berten Ceulemans, Sinead B Heavin,[...]. Neurology 2013
130
15

A recurrent KCNT1 mutation in two sporadic cases with malignant migrating partial seizures in infancy.
Atsushi Ishii, Mutsuki Shioda, Akihisa Okumura, Hiroyuki Kidokoro, Masako Sakauchi, Shino Shimada, Toshiaki Shimizu, Makiko Osawa, Shinichi Hirose, Toshiyuki Yamamoto. Gene 2013
54
27

Dominant-negative effects of KCNQ2 mutations are associated with epileptic encephalopathy.
Gökce Orhan, Merle Bock, Dorien Schepers, Elena I Ilina, Stephanie Nadine Reichel, Heidi Löffler, Nicole Jezutkovic, Sarah Weckhuysen, Simone Mandelstam, Arvid Suls,[...]. Ann Neurol 2014
124
14

Identification of a novel de novo p.Phe932Ile KCNT1 mutation in a patient with leukoencephalopathy and severe epilepsy.
Adeline Vanderver, Cas Simons, Johanna L Schmidt, Philip L Pearl, Miriam Bloom, Bennett Lavenstein, David Miller, Sean M Grimmond, Ryan J Taft. Pediatr Neurol 2014
42
33

The genetic landscape of the epileptic encephalopathies of infancy and childhood.
Amy McTague, Katherine B Howell, J Helen Cross, Manju A Kurian, Ingrid E Scheffer. Lancet Neurol 2016
258
14

For K+ channels, Na+ is the new Ca2+.
Arin Bhattacharjee, Leonard K Kaczmarek. Trends Neurosci 2005
152
14

The phenotypic spectrum of SCN8A encephalopathy.
Jan Larsen, Gemma L Carvill, Elena Gardella, Gerhard Kluger, Gudrun Schmiedel, Nina Barisic, Christel Depienne, Eva Brilstra, Yuan Mang, Jens Erik Klint Nielsen,[...]. Neurology 2015
167
14

GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers.
Dong Li, Hongjie Yuan, Xilma R Ortiz-Gonzalez, Eric D Marsh, Lifeng Tian, Elizabeth M McCormick, Gabrielle J Kosobucki, Wenjuan Chen, Anthony J Schulien, Rosetta Chiavacci,[...]. Am J Hum Genet 2016
100
14

Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009.
Anne T Berg, Samuel F Berkovic, Martin J Brodie, Jeffrey Buchhalter, J Helen Cross, Walter van Emde Boas, Jerome Engel, Jacqueline French, Tracy A Glauser, Gary W Mathern,[...]. Epilepsia 2010
13

KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.
Sarah Weckhuysen, Simone Mandelstam, Arvid Suls, Dominique Audenaert, Tine Deconinck, Lieve R F Claes, Liesbet Deprez, Katrien Smets, Dimitrina Hristova, Iglika Yordanova,[...]. Ann Neurol 2012
290
13

Localization of the Slack potassium channel in the rat central nervous system.
Arin Bhattacharjee, Li Gan, Leonard K Kaczmarek. J Comp Neurol 2002
118
13

Drug screening in Scn1a zebrafish mutant identifies clemizole as a potential Dravet syndrome treatment.
Scott C Baraban, Matthew T Dinday, Gabriela A Hortopan. Nat Commun 2013
214
13

Emerging role of the KCNT1 Slack channel in intellectual disability.
Grace E Kim, Leonard K Kaczmarek. Front Cell Neurosci 2014
45
26

Precision medicine in genetic epilepsies: break of dawn?
Philipp Sebastian Reif, Meng-Han Tsai, Ingo Helbig, Felix Rosenow, Karl Martin Klein. Expert Rev Neurother 2017
39
30

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.
N A Singh, C Charlier, D Stauffer, B R DuPont, R J Leach, R Melis, G M Ronen, I Bjerre, T Quattlebaum, J V Murphy,[...]. Nat Genet 1998
876
11

Formation of intermediate-conductance calcium-activated potassium channels by interaction of Slack and Slo subunits.
W J Joiner, M D Tang, L Y Wang, S I Dworetzky, C G Boissard, L Gan, V K Gribkoff, L K Kaczmarek. Nat Neurosci 1998
123
11

Slick (Slo2.1), a rapidly-gating sodium-activated potassium channel inhibited by ATP.
Arin Bhattacharjee, William J Joiner, Meilin Wu, Youshan Yang, Fred J Sigworth, Leonard K Kaczmarek. J Neurosci 2003
142
11

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy.
Mikko Muona, Samuel F Berkovic, Leanne M Dibbens, Karen L Oliver, Snezana Maljevic, Marta A Bayly, Tarja Joensuu, Laura Canafoglia, Silvana Franceschetti, Roberto Michelucci,[...]. Nat Genet 2015
152
11


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.