A citation-based method for searching scientific literature

Jacy L Wagnon, Miriam H Meisler. Front Neurol 2015
Times Cited: 81







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



Times Cited
  Times     Co-cited
Similarity


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
178
65

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
267
61

Convulsive seizures and SUDEP in a mouse model of SCN8A epileptic encephalopathy.
Jacy L Wagnon, Matthew J Korn, Rachel Parent, Taylor A Tarpey, Julie M Jones, Michael F Hammer, Geoffrey G Murphy, Jack M Parent, Miriam H Meisler. Hum Mol Genet 2015
87
37

De novo gain-of-function and loss-of-function mutations of SCN8A in patients with intellectual disabilities and epilepsy.
Maxime G Blanchard, Marjolein H Willemsen, Jaclyn B Walker, Sulayman D Dib-Hajj, Stephen G Waxman, Marjolijn C J Jongmans, Tjitske Kleefstra, Bart P van de Warrenburg, Peter Praamstra, Joost Nicolai,[...]. J Med Genet 2015
85
35

SCN8A encephalopathy: Research progress and prospects.
Miriam H Meisler, Guy Helman, Michael F Hammer, Brandy E Fureman, William D Gaillard, Alan L Goldin, Shinichi Hirose, Atsushi Ishii, Barbara L Kroner, Christoph Lossin,[...]. Epilepsia 2016
80
36

A novel de novo mutation of SCN8A (Nav1.6) with enhanced channel activation in a child with epileptic encephalopathy.
Mark Estacion, Janelle E O'Brien, Allison Conravey, Michael F Hammer, Stephen G Waxman, Sulayman D Dib-Hajj, Miriam H Meisler. Neurobiol Dis 2014
74
37

Pathogenic mechanism of recurrent mutations of SCN8A in epileptic encephalopathy.
Jacy L Wagnon, Bryan S Barker, James A Hounshell, Charlotte A Haaxma, Amy Shealy, Timothy Moss, Sumit Parikh, Ricka D Messer, Manoj K Patel, Miriam H Meisler. Ann Clin Transl Neurol 2015
69
39

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
84
27

Characterization of a de novo SCN8A mutation in a patient with epileptic encephalopathy.
Carolien G F de Kovel, Miriam H Meisler, Eva H Brilstra, Frederique M C van Berkestijn, Ruben van 't Slot, Stef van Lieshout, Isaac J Nijman, Janelle E O'Brien, Michael F Hammer, Mark Estacion,[...]. Epilepsy Res 2014
69
31

Early onset epileptic encephalopathy caused by de novo SCN8A mutations.
Chihiro Ohba, Mitsuhiro Kato, Satoru Takahashi, Tally Lerman-Sagie, Dorit Lev, Hiroshi Terashima, Masaya Kubota, Hisashi Kawawaki, Mayumi Matsufuji, Yasuko Kojima,[...]. Epilepsia 2014
91
25

Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation.
Elena Gardella, Felicitas Becker, Rikke S Møller, Julian Schubert, Johannes R Lemke, Line H G Larsen, Hans Eiberg, Michael Nothnagel, Holger Thiele, Janine Altmüller,[...]. Ann Neurol 2016
106
24


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
955
22

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.
Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, Jacinta M McMahon, Brian J O'Roak, Joseph Cook, Adiba Khan, Michael O Dorschner, Molly Weaver, Sophie Calvert,[...]. Nat Genet 2013
422
20

Sodium channel Na(v)1.6 is localized at nodes of ranvier, dendrites, and synapses.
J H Caldwell, K L Schaller, R S Lasher, E Peles, S R Levinson. Proc Natl Acad Sci U S A 2000
473
19

SCN8A mutations in Chinese children with early onset epilepsy and intellectual disability.
Weijing Kong, Yujia Zhang, Yang Gao, Xiaoyan Liu, Kai Gao, Han Xie, Jingmin Wang, Ye Wu, Yuehua Zhang, Xiru Wu,[...]. Epilepsia 2015
46
32

De novo SCN8A mutation identified by whole-exome sequencing in a boy with neonatal epileptic encephalopathy, multiple congenital anomalies, and movement disorders.
Ulvi Vaher, Margit Nõukas, Tiit Nikopensius, Mart Kals, Tarmo Annilo, Mari Nelis, Katrin Ounap, Tiia Reimand, Inga Talvik, Pilvi Ilves,[...]. J Child Neurol 2014
49
30

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
676
17

Early-onset movement disorder and epileptic encephalopathy due to de novo dominant SCN8A mutation.
R Singh, S Jayapal, S Goyal, H Jungbluth, K Lascelles. Seizure 2015
22
63

The phenotype of SCN8A developmental and epileptic encephalopathy.
Elena Gardella, Carla Marini, Marina Trivisano, Mark P Fitzgerald, Michael Alber, Katherine B Howell, Francesca Darra, Sabrina Siliquini, Bigna K Bölsterli, Silva Masnada,[...]. Neurology 2018
72
19

Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability.
Yuanyuan Liu, Julian Schubert, Lukas Sonnenberg, Katherine L Helbig, Christina E Hoei-Hansen, Mahmoud Koko, Maert Rannap, Stephan Lauxmann, Mahbubul Huq, Michael C Schneider,[...]. Brain 2019
44
31

Distinct contributions of Na(v)1.6 and Na(v)1.2 in action potential initiation and backpropagation.
Wenqin Hu, Cuiping Tian, Tun Li, Mingpo Yang, Han Hou, Yousheng Shu. Nat Neurosci 2009
410
16


The SCN8A encephalopathy mutation p.Ile1327Val displays elevated sensitivity to the anticonvulsant phenytoin.
Bryan S Barker, Matteo Ottolini, Jacy L Wagnon, Rachel M Hollander, Miriam H Meisler, Manoj K Patel. Epilepsia 2016
31
41

The voltage-gated sodium channel Scn8a is a genetic modifier of severe myoclonic epilepsy of infancy.
Melinda S Martin, Bin Tang, Ligia A Papale, Frank H Yu, William A Catterall, Andrew Escayg. Hum Mol Genet 2007
145
16

Prominent role of forebrain excitatory neurons in SCN8A encephalopathy.
Rosie K A Bunton-Stasyshyn, Jacy L Wagnon, Eric R Wengert, Bryan S Barker, Alexa Faulkner, Pravin K Wagley, Kritika Bhatia, Julie M Jones, Marissa R Maniaci, Jack M Parent,[...]. Brain 2019
44
29

Diagnostic yield of genetic testing in epileptic encephalopathy in childhood.
Saadet Mercimek-Mahmutoglu, Jaina Patel, Dawn Cordeiro, Stacy Hewson, David Callen, Elizabeth J Donner, Cecil D Hahn, Peter Kannu, Jeff Kobayashi, Berge A Minassian,[...]. Epilepsia 2015
136
14

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
14

Neuronal hyperexcitability in a mouse model of SCN8A epileptic encephalopathy.
Luis F Lopez-Santiago, Yukun Yuan, Jacy L Wagnon, Jacob M Hull, Chad R Frasier, Heather A O'Malley, Miriam H Meisler, Lori L Isom. Proc Natl Acad Sci U S A 2017
45
26

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
236
14

Mutation of a new sodium channel gene, Scn8a, in the mouse mutant 'motor endplate disease'.
D L Burgess, D C Kohrman, J Galt, N W Plummer, J M Jones, B Spear, M H Meisler. Nat Genet 1995
248
13

Sodium channel mutations in epilepsy and other neurological disorders.
Miriam H Meisler, Jennifer A Kearney. J Clin Invest 2005
343
13

Electroclinical features of epileptic encephalopathy caused by SCN8A mutation.
Satoru Takahashi, Shiho Yamamoto, Akie Okayama, Akiko Araki, Hirotomo Saitsu, Naomichi Matsumoto, Hiroshi Azuma. Pediatr Int 2015
13
84

Role of the hippocampus in Nav1.6 (Scn8a) mediated seizure resistance.
Christopher D Makinson, Brian S Tanaka, Tyra Lamar, Alan L Goldin, Andrew Escayg. Neurobiol Dis 2014
31
35

Loss-of-function variants of SCN8A in intellectual disability without seizures.
Jacy L Wagnon, Bryan S Barker, Matteo Ottolini, Young Park, Alicia Volkheimer, Purnima Valdez, Marielle E M Swinkels, Manoj K Patel, Miriam H Meisler. Neurol Genet 2017
41
26

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
818
12

Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome.
Kazuyuki Nakamura, Mitsuhiro Kato, Hitoshi Osaka, Sumimasa Yamashita, Eiji Nakagawa, Kazuhiro Haginoya, Jun Tohyama, Mitsuko Okuda, Takahito Wada, Shuichi Shimakawa,[...]. Neurology 2013
135
12

Molecular and pathological effects of a modifier gene on deficiency of the sodium channel Scn8a (Na(v)1.6).
Jennifer A Kearney, David A Buchner, Georgius De Haan, Maja Adamska, Stephen I Levin, Amy R Furay, Roger L Albin, Julie M Jones, Mauricio Montal, Martin J Stevens,[...]. Hum Mol Genet 2002
82
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
137
11

Autosomal dominant SCN8A mutation with an unusually mild phenotype.
G Anand, F Collett-White, A Orsini, S Thomas, S Jayapal, N Trump, Z Zaiwalla, S Jayawant. Eur J Paediatr Neurol 2016
27
33

Partial loss-of-function of sodium channel SCN8A in familial isolated myoclonus.
Jacy L Wagnon, Niccolò E Mencacci, Bryan S Barker, Eric R Wengert, Kailash P Bhatia, Bettina Balint, Miryam Carecchio, Nicholas W Wood, Manoj K Patel, Miriam H Meisler. Hum Mutat 2018
21
42

Aberrant Sodium Channel Currents and Hyperexcitability of Medial Entorhinal Cortex Neurons in a Mouse Model of SCN8A Encephalopathy.
Matteo Ottolini, Bryan S Barker, Ronald P Gaykema, Miriam H Meisler, Manoj K Patel. J Neurosci 2017
31
29

Early mortality in SCN8A-related epilepsies.
Katrine M Johannesen, Elena Gardella, Ingrid Scheffer, Katherine Howell, Douglas M Smith, Ingo Helbig, Rikke S Møller, Guido Rubboli. Epilepsy Res 2018
32
28

Role of axonal NaV1.6 sodium channels in action potential initiation of CA1 pyramidal neurons.
Michel Royeck, Marie-Therese Horstmann, Stefan Remy, Margit Reitze, Yoel Yaari, Heinz Beck. J Neurophysiol 2008
126
9

Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice.
Ligia A Papale, Barbara Beyer, Julie M Jones, Lisa M Sharkey, Sergio Tufik, Michael Epstein, Verity A Letts, Miriam H Meisler, Wayne N Frankel, Andrew Escayg. Hum Mol Genet 2009
82
9

Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism.
Yu Liu, Luis F Lopez-Santiago, Yukun Yuan, Julie M Jones, Helen Zhang, Heather A O'Malley, Gustavo A Patino, Janelle E O'Brien, Raffaella Rusconi, Ajay Gupta,[...]. Ann Neurol 2013
154
9

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
525
9

Sodium channel SCN1A and epilepsy: mutations and mechanisms.
Andrew Escayg, Alan L Goldin. Epilepsia 2010
224
9


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.