A citation-based method for searching scientific literature

Joseph D Symonds, Sameer M Zuberi. Neuropharmacology 2018
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity



Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies.
Julia Oyrer, Snezana Maljevic, Ingrid E Scheffer, Samuel F Berkovic, Steven Petrou, Christopher A Reid. Pharmacol Rev 2018
79
25

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
25

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
25

Molecular correlates of age-dependent seizures in an inherited neonatal-infantile epilepsy.
Yunxiang Liao, Liesbet Deprez, Snezana Maljevic, Julika Pitsch, Lieve Claes, Dimitrina Hristova, Albena Jordanova, Sirpa Ala-Mello, Astrid Bellan-Koch, Dragica Blazevic,[...]. Brain 2010
116
25

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
25

Genotype phenotype associations across the voltage-gated sodium channel family.
Andreas Brunklaus, Rachael Ellis, Eleanor Reavey, Christopher Semsarian, Sameer M Zuberi. J Med Genet 2014
47
25

Opposing Effects on NaV1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile Seizures.
Roy Ben-Shalom, Caroline M Keeshen, Kiara N Berrios, Joon Y An, Stephan J Sanders, Kevin J Bender. Biol Psychiatry 2017
104
25

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
25

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
25

The core Dravet syndrome phenotype.
Charlotte Dravet. Epilepsia 2011
276
25

Inhibitory interneuron deficit links altered network activity and cognitive dysfunction in Alzheimer model.
Laure Verret, Edward O Mann, Giao B Hang, Albert M I Barth, Inma Cobos, Kaitlyn Ho, Nino Devidze, Eliezer Masliah, Anatol C Kreitzer, Istvan Mody,[...]. Cell 2012
576
25

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
25

Autistic-like behaviour in Scn1a+/- mice and rescue by enhanced GABA-mediated neurotransmission.
Sung Han, Chao Tai, Ruth E Westenbroek, Frank H Yu, Christine S Cheah, Gregory B Potter, John L Rubenstein, Todd Scheuer, Horacio O de la Iglesia, William A Catterall. Nature 2012
380
25

From genotype to phenotype in Dravet disease.
Svetlana Gataullina, Olivier Dulac. Seizure 2017
65
25

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
25

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
25


Na Channel β Subunits: Overachievers of the Ion Channel Family.
William J Brackenbury, Lori L Isom. Front Pharmacol 2011
187
25

Sodium channel β subunits: emerging targets in channelopathies.
Heather A O'Malley, Lori L Isom. Annu Rev Physiol 2015
127
25

Dravet Syndrome: A Sodium Channel Interneuronopathy.
William A Catterall. Curr Opin Physiol 2018
45
25


Animal toxins for channelopathy treatment.
Sergey Kozlov. Neuropharmacology 2018
9
12


Insights into channel dysfunction from modelling and molecular dynamics simulations.
Maria Musgaard, Teresa Paramo, Laura Domicevica, Ole Juul Andersen, Philip C Biggin. Neuropharmacology 2018
7
14

Autoantibody-mediated diseases of the CNS: Structure, dysfunction and therapy.
James Varley, Jennifer Taylor, Sarosh R Irani. Neuropharmacology 2018
33
12

Post-translational dysfunctions in channelopathies of the nervous system.
Benedetta Terragni, Paolo Scalmani, Silvana Franceschetti, Sandrine Cestèle, Massimo Mantegazza. Neuropharmacology 2018
12
12

Relevance of tissue specific subunit expression in channelopathies.
Hartwig Seitter, Alexandra Koschak. Neuropharmacology 2018
10
12


The therapeutic implication of a novel SCN2A mutation associated early-onset epileptic encephalopathy with Rett-like features.
Jao-Shwann Liang, Li-Ju Lin, Ming-Tao Yang, Jinn-Shyan Wang, Jyh-Feng Lu. Brain Dev 2017
6
16

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
12

Whole genome sequencing identifies SCN2A mutation in monozygotic twins with Ohtahara syndrome and unique neuropathologic findings.
Marlin Touma, Mugdha Joshi, Meghan C Connolly, P Ellen Grant, Anne R Hansen, Omar Khwaja, Gerard T Berry, Hannah C Kinney, Annapurna Poduri, Pankaj B Agrawal. Epilepsia 2013
36
12

A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline.
Kazusaku Kamiya, Makoto Kaneda, Takashi Sugawara, Emi Mazaki, Nami Okamura, Mauricio Montal, Naomasa Makita, Masaki Tanaka, Katsuyuki Fukushima, Tateki Fujiwara,[...]. J Neurosci 2004
142
12

Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy.
Samuel F Berkovic, Sarah E Heron, Lucio Giordano, Carla Marini, Renzo Guerrini, Robert E Kaplan, Antonio Gambardella, Ortrud K Steinlein, Bronwyn E Grinton, Joanne T Dean,[...]. Ann Neurol 2004
175
12

Sodium channel mutations in epilepsy and other neurological disorders.
Miriam H Meisler, Jennifer A Kearney. J Clin Invest 2005
336
12

Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation.
Liam S Carroll, Rebecca Woolf, Yousef Ibrahim, Hywel J Williams, Sarah Dwyer, James Walters, George Kirov, Michael C O'Donovan, Michael J Owen. Psychiatr Genet 2016
27
12

Infantile epileptic encephalopathy, transient choreoathetotic movements, and hypersomnia due to a De Novo missense mutation in the SCN2A gene.
Annette Hackenberg, Alessandra Baumer, Heinrich Sticht, Bernhard Schmitt, Judith Kroell-Seger, David Wille, Pascal Joset, Sorina Papuc, Anita Rauch, Barbara Plecko. Neuropediatrics 2014
22
12

Compromised function in the Na(v)1.2 Dravet syndrome mutation R1312T.
Christoph Lossin, Xiuyu Shi, Michael A Rogawski, Shinichi Hirose. Neurobiol Dis 2012
20
12

Targeted next generation sequencing as a diagnostic tool in epileptic disorders.
Johannes R Lemke, Erik Riesch, Tim Scheurenbrand, Max Schubach, Christian Wilhelm, Isabelle Steiner, Jörg Hansen, Carolina Courage, Sabina Gallati, Sarah Bürki,[...]. Epilepsia 2012
229
12


Exome sequencing identifies a de novo SCN2A mutation in a patient with intractable seizures, severe intellectual disability, optic atrophy, muscular hypotonia, and brain abnormalities.
Anna-Lena Baasch, Irina Hüning, Christian Gilissen, Joerg Klepper, Joris A Veltman, Gabriele Gillessen-Kaesbach, Alexander Hoischen, Katja Lohmann. Epilepsia 2014
46
12

Potassium channel genes and benign familial neonatal epilepsy.
Snezana Maljevic, Holger Lerche. Prog Brain Res 2014
41
12

Letter to the editor: confirming neonatal seizure and late onset ataxia in SCN2A Ala263Val.
Katrine M Johannesen, Maria J Miranda, Holger Lerche, Rikke S Møller. J Neurol 2016
10
12

Lidocaine-dependent early infantile status epilepticus with highly suppressed EEG.
Yukio Sawaishi, Tamami Yano, Masamichi Enoki, Goro Takada. Epilepsia 2002
12
12


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
12

An SCN2A mutation in a family with infantile seizures from Madagascar reveals an increased subthreshold Na(+) current.
Stephan Lauxmann, Nadia Boutry-Kryza, Clotilde Rivier, Stephan Mueller, Ulrike B S Hedrich, Snezana Maljevic, Pierre Szepetowski, Holger Lerche, Gaetan Lesca. Epilepsia 2013
29
12

SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum.
Eric Herlenius, Sarah E Heron, Bronwyn E Grinton, Deborah Keay, Ingrid E Scheffer, John C Mulley, Samuel F Berkovic. Epilepsia 2007
77
12

Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia.
N Schwarz, A Hahn, T Bast, S Müller, H Löffler, S Maljevic, E Gaily, I Prehl, S Biskup, T Joensuu,[...]. J Neurol 2016
50
12

Ion channels in genetic and acquired forms of epilepsy.
Holger Lerche, Mala Shah, Heinz Beck, Jeff Noebels, Dan Johnston, Angela Vincent. J Physiol 2013
83
12


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.