A citation-based method for searching scientific literature

Giulia Barcia, Matthew R Fleming, Aline Deligniere, Valeswara-Rao Gazula, Maile R Brown, Maeva Langouet, Haijun Chen, Jack Kronengold, Avinash Abhyankar, Roberta Cilio, Patrick Nitschke, Anna Kaminska, Nathalie Boddaert, Jean-Laurent Casanova, Isabelle Desguerre, Arnold Munnich, Olivier Dulac, Leonard K Kaczmarek, Laurence Colleaux, Rima Nabbout. Nat Genet 2012
Times Cited: 265







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



Times Cited
  Times     Co-cited
Similarity


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
210
45

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
136
35

Targeted treatment of migrating partial seizures of infancy with quinidine.
David Bearden, Alanna Strong, Jessica Ehnot, Marissa DiGiovine, Dennis Dlugos, Ethan M Goldberg. Ann Neurol 2014
125
34

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
32

Migrating partial seizures in infancy: a malignant disorder with developmental arrest.
G Coppola, P Plouin, C Chiron, O Robain, O Dulac. Epilepsia 1995
155
25

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
66
37

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
55
45

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
25

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
925
23

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
47
46

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
57
38

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
201
21

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
41
51

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
43

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
49
40

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
20

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
53
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
247
17

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
79
21

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
40

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
142
16

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
33
48

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
16

Localization of the Slack potassium channel in the rat central nervous system.
Arin Bhattacharjee, Li Gan, Leonard K Kaczmarek. J Comp Neurol 2002
117
15

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
57

STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy.
Hannah Stamberger, Marina Nikanorova, Marjolein H Willemsen, Patrizia Accorsi, Marco Angriman, Hartmut Baier, Ira Benkel-Herrenbrueck, Valérie Benoit, Mauro Budetta, Almuth Caliebe,[...]. Neurology 2016
131
14

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
284
13

De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP.
Krishna R Veeramah, Janelle E O'Brien, Miriam H Meisler, Xiaoyang Cheng, Sulayman D Dib-Hajj, Stephen G Waxman, Dinesh Talwar, Santhosh Girirajan, Evan E Eichler, Linda L Restifo,[...]. Am J Hum Genet 2012
254
13

Emerging role of the KCNT1 Slack channel in intellectual disability.
Grace E Kim, Leonard K Kaczmarek. Front Cell Neurosci 2014
45
28

For K+ channels, Na+ is the new Ca2+.
Arin Bhattacharjee, Leonard K Kaczmarek. Trends Neurosci 2005
152
13

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
48

An Epilepsy-Associated KCNT1 Mutation Enhances Excitability of Human iPSC-Derived Neurons by Increasing Slack KNa Currents.
Imran H Quraishi, Shani Stern, Kile P Mangan, Yalan Zhang, Syed R Ali, Michael R Mercier, Maria C Marchetto, Michael J McLachlan, Eugenia M Jones, Fred H Gage,[...]. J Neurosci 2019
19
68

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
29
41

Slack, Slick and Sodium-Activated Potassium Channels.
Leonard K Kaczmarek. ISRN Neurosci 2013
69
17

Epilepsy-Related Slack Channel Mutants Lead to Channel Over-Activity by Two Different Mechanisms.
Qiong-Yao Tang, Fei-Fei Zhang, Jie Xu, Ran Wang, Jian Chen, Diomedes E Logothetis, Zhe Zhang. Cell Rep 2016
26
46

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
26
46

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
60

De novo KCNB1 mutations in epileptic encephalopathy.
Ali Torkamani, Kevin Bersell, Benjamin S Jorge, Robert L Bjork, Jennifer R Friedman, Cinnamon S Bloss, Julie Cohen, Siddharth Gupta, Sakkubai Naidu, Carlos G Vanoye,[...]. Ann Neurol 2014
77
14

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
785
11

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
126
11

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
19

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
11

Treatment Responsiveness in KCNT1-Related Epilepsy.
Mark P Fitzgerald, Martina Fiannacca, Douglas M Smith, Tracy S Gertler, Boudewijn Gunning, Steffen Syrbe, Nienke Verbeek, Hannah Stamberger, Sarah Weckhuysen, Berten Ceulemans,[...]. Neurotherapeutics 2019
19
57

The spectrum of SCN1A-related infantile epileptic encephalopathies.
Louise A Harkin, Jacinta M McMahon, Xenia Iona, Leanne Dibbens, James T Pelekanos, Sameer M Zuberi, Lynette G Sadleir, Eva Andermann, Deepak Gill, Kevin Farrell,[...]. Brain 2007
345
10

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
108
10

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
871
10

Three Cases of KCNT1 Mutations: Malignant Migrating Partial Seizures in Infancy with Massive Systemic to Pulmonary Collateral Arteries.
Yuki Kawasaki, Ichiro Kuki, Eiji Ehara, Yosuke Murakami, Shin Okazaki, Hisashi Kawawaki, Munetsugu Hara, Yoriko Watanabe, Shintaro Kishimoto, Kenji Suda,[...]. J Pediatr 2017
13
76

The sodium-activated potassium channel is encoded by a member of the Slo gene family.
Alex Yuan, Celia M Santi, Aguan Wei, Zhao Wen Wang, Kelly Pollak, Michael Nonet, Leonard Kaczmarek, C Michael Crowder, Lawrence Salkoff. Neuron 2003
170
10

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
123
10

Opposite regulation of Slick and Slack K+ channels by neuromodulators.
Celia M Santi, Gonzalo Ferreira, Bo Yang, Valeswara-Rao Gazula, Alice Butler, Aguan Wei, Leonard K Kaczmarek, Lawrence Salkoff. J Neurosci 2006
73
13


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.