A citation-based method for searching scientific literature

Nicola Specchio, Paolo Curatolo. Brain 2021
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity



Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology.
Robert S Fisher, J Helen Cross, Jacqueline A French, Norimichi Higurashi, Edouard Hirsch, Floor E Jansen, Lieven Lagae, Solomon L Moshé, Jukka Peltola, Eliane Roulet Perez,[...]. Epilepsia 2017
999
28


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
81
28

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
28


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
28


CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development.
Scott T Demarest, Heather E Olson, Angela Moss, Elia Pestana-Knight, Xiaoming Zhang, Sumit Parikh, Lindsay C Swanson, Katherine D Riley, Grace A Bazin, Katie Angione,[...]. Epilepsia 2019
37
28

Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis.
Natalie Trump, Amy McTague, Helen Brittain, Apostolos Papandreou, Esther Meyer, Adeline Ngoh, Rodger Palmer, Deborah Morrogh, Christopher Boustred, Jane A Hurst,[...]. J Med Genet 2016
120
14


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
37
14

The ion channel inverse problem: neuroinformatics meets biophysics.
Robert C Cannon, Giampaolo D'Alessandro. PLoS Comput Biol 2006
23
14

SCN8A encephalopathy: Mechanisms and models.
Miriam H Meisler. Epilepsia 2019
16
14

Nanoscale Architecture of the Axon Initial Segment Reveals an Organized and Robust Scaffold.
Christophe Leterrier, Jean Potier, Ghislaine Caillol, Claire Debarnot, Fanny Rueda Boroni, Bénédicte Dargent. Cell Rep 2015
111
14

Cerebellum-related characteristics of Scn8a-mutant mice.
Kejian Chen, Donald A Godfrey, Omer Ilyas, Jiansong Xu, Todd W Preston. Cerebellum 2009
9
14

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
105
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
14

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
29
14

Clinical study of 19 patients with SCN8A-related epilepsy: Two modes of onset regarding EEG and seizures.
Julien Denis, Nathalie Villeneuve, Pierre Cacciagli, Cecile Mignon-Ravix, Caroline Lacoste, Jeremie Lefranc, Sylvia Napuri, Lena Damaj, Frederic Villega, Jean-Michel Pedespan,[...]. Epilepsia 2019
14
14


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
66
14

The effect of phenytoin on glutamate and GABA transport.
P T Wong, W L Teo. Neurochem Res 1986
11
14

Nav1.1 is predominantly expressed in nodes of Ranvier and axon initial segments.
Amandine Duflocq, Barbara Le Bras, Erika Bullier, François Couraud, Marc Davenne. Mol Cell Neurosci 2008
110
14


The synergistic inhibitory actions of oxcarbazepine on voltage-gated sodium and potassium currents in differentiated NG108-15 neuronal cells and model neurons.
Chin-Wei Huang, Chao-Ching Huang, Ming-Wei Lin, Jing-Jane Tsai, Sheng-Nan Wu. Int J Neuropsychopharmacol 2008
33
14

Ion channel associated diseases: overview of molecular mechanisms.
Mark A Zaydman, Jonathan R Silva, Jianmin Cui. Chem Rev 2012
25
14

SCN8A: When Neurons Are So Excited, They Just Can't Hide It.
Tracy S Gertler, Gemma L Carvill. Epilepsy Curr 2019
4
25

Differential targeting and functional specialization of sodium channels in cultured cerebellar granule cells.
Nancy Osorio, Gisèle Alcaraz, Françoise Padilla, François Couraud, Patrick Delmas, Marcel Crest. J Physiol 2005
41
14


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
38
14


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
14

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
89
14

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
81
14

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
259
14

Oxcarbazepine monotherapy for partial-onset seizures: a multicenter, double-blind, clinical trial.
A Beydoun, R C Sachdeo, W E Rosenfeld, G L Krauss, N Sessler, P Mesenbrink, L Kramer, J D'Souza. Neurology 2000
122
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


A novel, abundant sodium channel expressed in neurons and glia.
K L Schaller, D M Krzemien, P J Yarowsky, B K Krueger, J H Caldwell. J Neurosci 1995
202
14

Persistent Nav1.6 current at axon initial segments tunes spike timing of cerebellar granule cells.
Nancy Osorio, Laurence Cathala, Miriam H Meisler, Marcel Crest, Jacopo Magistretti, Patrick Delmas. J Physiol 2010
51
14


Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato,[...]. Lancet 2012
677
14

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
14

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
14


Impaired motor function in mice with cell-specific knockout of sodium channel Scn8a (NaV1.6) in cerebellar purkinje neurons and granule cells.
Stephen I Levin, Zayd M Khaliq, Teresa K Aman, Tina M Grieco, Jennifer A Kearney, Indira M Raman, Miriam H Meisler. J Neurophysiol 2006
91
14

Predicting functional effects of missense variants in voltage-gated sodium and calcium channels.
Henrike O Heyne, David Baez-Nieto, Sumaiya Iqbal, Duncan S Palmer, Andreas Brunklaus, Patrick May, Katrine M Johannesen, Stephan Lauxmann, Johannes R Lemke, Rikke S Møller,[...]. Sci Transl Med 2020
19
14

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
14

An ankyrinG-binding motif is necessary and sufficient for targeting Nav1.6 sodium channels to axon initial segments and nodes of Ranvier.
Andreas Gasser, Tammy Szu-Yu Ho, Xiaoyang Cheng, Kae-Jiun Chang, Stephen G Waxman, Matthew N Rasband, Sulayman D Dib-Hajj. J Neurosci 2012
84
14


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.