A citation-based method for searching scientific literature

J Spillane, D M Kullmann, M G Hanna. J Neurol Neurosurg Psychiatry 2016
Times Cited: 54







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



Times Cited
  Times     Co-cited
Similarity


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
636
9

Painful neuropathies: the emerging role of sodium channelopathies.
Brigitte A Brouwer, Ingemar S J Merkies, Monique M Gerrits, Stephen G Waxman, Janneke G J Hoeijmakers, Catharina G Faber. J Peripher Nerv Syst 2014
66
7


Sodium channel SCN1A and epilepsy: mutations and mechanisms.
Andrew Escayg, Alan L Goldin. Epilepsia 2010
207
7

Channelopathies.
June-Bum Kim. Korean J Pediatr 2014
72
7

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
Martin Dichgans, Tobias Freilinger, Gertrud Eckstein, Elena Babini, Bettina Lorenz-Depiereux, Saskia Biskup, Michel D Ferrari, Jürgen Herzog, Arn M J M van den Maagdenberg, Michael Pusch,[...]. Lancet 2005
529
5

Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19.
Anna Duarri, Justyna Jezierska, Michiel Fokkens, Michel Meijer, Helenius J Schelhaas, Wilfred F A den Dunnen, Freerk van Dijk, Corien Verschuuren-Bemelmans, Gerard Hageman, Pieter van de Vlies,[...]. Ann Neurol 2012
86
5

Mutations in KCND3 cause spinocerebellar ataxia type 22.
Yi-Chung Lee, Alexandra Durr, Karen Majczenko, Yen-Hua Huang, Yu-Chao Liu, Cheng-Chang Lien, Pei-Chien Tsai, Yaeko Ichikawa, Jun Goto, Marie-Lorraine Monin,[...]. Ann Neurol 2012
98
5

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.
Igor Splawski, Katherine W Timothy, Leah M Sharpe, Niels Decher, Pradeep Kumar, Raffaella Bloise, Carlo Napolitano, Peter J Schwartz, Robert M Joseph, Karen Condouris,[...]. Cell 2004
983
5

Inwardly rectifying potassium channels: their structure, function, and physiological roles.
Hiroshi Hibino, Atsushi Inanobe, Kazuharu Furutani, Shingo Murakami, Ian Findlay, Yoshihisa Kurachi. Physiol Rev 2010
834
5


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
138
5

Gain of function Naν1.7 mutations in idiopathic small fiber neuropathy.
Catharina G Faber, Janneke G J Hoeijmakers, Hye-Sook Ahn, Xiaoyang Cheng, Chongyang Han, Jin-Sung Choi, Mark Estacion, Giuseppe Lauria, Els K Vanhoutte, Monique M Gerrits,[...]. Ann Neurol 2012
332
5

Gain-of-function Nav1.8 mutations in painful neuropathy.
Catharina G Faber, Giuseppe Lauria, Ingemar S J Merkies, Xiaoyang Cheng, Chongyang Han, Hye-Sook Ahn, Anna-Karin Persson, Janneke G J Hoeijmakers, Monique M Gerrits, Tiziana Pierro,[...]. Proc Natl Acad Sci U S A 2012
246
5

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
R A Ophoff, G M Terwindt, M N Vergouwe, R van Eijk, P J Oefner, S M Hoffman, J E Lamerdin, H W Mohrenweiser, D E Bulman, M Ferrari,[...]. Cell 1996
5

Migraine pathophysiology: lessons from mouse models and human genetics.
Michel D Ferrari, Roselin R Klever, Gisela M Terwindt, Cenk Ayata, Arn M J M van den Maagdenberg. Lancet Neurol 2015
191
5


Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder.
Wei Du, Jocelyn F Bautista, Huanghe Yang, Ana Diez-Sampedro, Sun-Ah You, Lejin Wang, Prakash Kotagal, Hans O Lüders, Jingyi Shi, Jianmin Cui,[...]. Nat Genet 2005
368
5

Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy.
Tara Klassen, Caleb Davis, Alica Goldman, Dan Burgess, Tim Chen, David Wheeler, John McPherson, Traci Bourquin, Lora Lewis, Donna Villasana,[...]. Cell 2011
215
5

Potassium Channels and Human Epileptic Phenotypes: An Updated Overview.
Chiara Villa, Romina Combi. Front Cell Neurosci 2016
57
5

Advancing epilepsy genetics in the genomic era.
Candace T Myers, Heather C Mefford. Genome Med 2015
97
5

Neurological channelopathies.
Dimitri M Kullmann. Annu Rev Neurosci 2010
79
5

Spreading convulsions, spreading depolarization and epileptogenesis in human cerebral cortex.
Jens P Dreier, Sebastian Major, Heinz-Wolfgang Pannek, Johannes Woitzik, Michael Scheel, Dirk Wiesenthal, Peter Martus, Maren K L Winkler, Jed A Hartings, Martin Fabricius,[...]. Brain 2012
151
5

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
5

Neurogenic radial glia in the outer subventricular zone of human neocortex.
David V Hansen, Jan H Lui, Philip R L Parker, Arnold R Kriegstein. Nature 2010
720
5

Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development.
Richard S Smith, Connor J Kenny, Vijay Ganesh, Ahram Jang, Rebeca Borges-Monroy, Jennifer N Partlow, R Sean Hill, Taehwan Shin, Allen Y Chen, Ryan N Doan,[...]. Neuron 2018
52
5

Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca2+-Activated K+ Channel SK3 Cause Zimmermann-Laband Syndrome.
Christiane K Bauer, Pauline E Schneeberger, Fanny Kortüm, Janine Altmüller, Fernando Santos-Simarro, Laura Baker, Jennifer Keller-Ramey, Susan M White, Philippe M Campeau, Karen W Gripp,[...]. Am J Hum Genet 2019
16
18

Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis.
Devon P Ryan, Magnus R Dias da Silva, Tuck Wah Soong, Bertrand Fontaine, Matt R Donaldson, Annie W C Kung, Wallaya Jongjaroenprasert, Mui Cheng Liang, Daphne H C Khoo, Jin Seng Cheah,[...]. Cell 2010
157
3



Gain-of-function mutations in SCN11A cause familial episodic pain.
Xiang Yang Zhang, Jingmin Wen, Wei Yang, Cheng Wang, Luna Gao, Liang Hong Zheng, Tao Wang, Kaikai Ran, Yulei Li, Xiangyang Li,[...]. Am J Hum Genet 2013
117
3

A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome.
Barbara Kremeyer, Francisco Lopera, James J Cox, Aliakmal Momin, Francois Rugiero, Steve Marsh, C Geoffrey Woods, Nicholas G Jones, Kathryn J Paterson, Florence R Fricker,[...]. Neuron 2010
269
3

Pathophysiology of migraine.
Daniela Pietrobon, Michael A Moskowitz. Annu Rev Physiol 2013
340
3

An SCN9A channelopathy causes congenital inability to experience pain.
James J Cox, Frank Reimann, Adeline K Nicholas, Gemma Thornton, Emma Roberts, Kelly Springell, Gulshan Karbani, Hussain Jafri, Jovaria Mannan, Yasmin Raashid,[...]. Nature 2006
940
3

Association between genetic variation of CACNA1H and childhood absence epilepsy.
Yucai Chen, Jianjun Lu, Hong Pan, Yuehua Zhang, Husheng Wu, Keming Xu, Xiaoyan Liu, Yuwu Jiang, Xinhua Bao, Zhijian Yao,[...]. Ann Neurol 2003
256
3

Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features.
R Tawil, L J Ptacek, S G Pavlakis, D C DeVivo, A S Penn, C Ozdemir, R C Griggs. Ann Neurol 1994
229
3

Ca2+ toxicity due to reverse Na+/Ca2+ exchange contributes to degeneration of neurites of DRG neurons induced by a neuropathy-associated Nav1.7 mutation.
M Estacion, B P S Vohra, S Liu, J Hoeijmakers, C G Faber, I S J Merkies, G Lauria, J A Black, S G Waxman. J Neurophysiol 2015
30
6

SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes.
Caroline R Fertleman, Mark D Baker, Keith A Parker, Sarah Moffatt, Frances V Elmslie, Bjarke Abrahamsen, Johan Ostman, Norbert Klugbauer, John N Wood, R Mark Gardiner,[...]. Neuron 2006
486
3

The role of the KATP channel in glucose homeostasis in health and disease: more than meets the islet.
James S McTaggart, Rebecca H Clark, Frances M Ashcroft. J Physiol 2010
110
3

Dissecting the phenotypes of Dravet syndrome by gene deletion.
Moran Rubinstein, Sung Han, Chao Tai, Ruth E Westenbroek, Avery Hunker, Todd Scheuer, William A Catterall. Brain 2015
55
3

Primary episodic ataxias: diagnosis, pathogenesis and treatment.
J C Jen, T D Graves, E J Hess, M G Hanna, R C Griggs, R W Baloh. Brain 2007
198
3

Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia.
Y Yang, Y Wang, S Li, Z Xu, H Li, L Ma, J Fan, D Bu, B Liu, Z Fan,[...]. J Med Genet 2004
504
3

ClC-1 chloride channels: state-of-the-art research and future challenges.
Paola Imbrici, Concetta Altamura, Mauro Pessia, Renato Mantegazza, Jean-François Desaphy, Diana Conte Camerino. Front Cell Neurosci 2015
38
5

Channelopathies of skeletal muscle excitability.
Stephen C Cannon. Compr Physiol 2015
109
3

Early-onset epileptic encephalopathy caused by gain-of-function mutations in the voltage sensor of Kv7.2 and Kv7.3 potassium channel subunits.
Francesco Miceli, Maria Virginia Soldovieri, Paolo Ambrosino, Michela De Maria, Michele Migliore, Rosanna Migliore, Maurizio Taglialatela. J Neurosci 2015
86
3


Identification and functional characterization of Kir2.6 mutations associated with non-familial hypokalemic periodic paralysis.
Chih-Jen Cheng, Shih-Hua Lin, Yi-Fen Lo, Sung-Sen Yang, Yu-Juei Hsu, Stephen C Cannon, Chou-Long Huang. J Biol Chem 2011
43
4

Novel SCN3A variants associated with focal epilepsy in children.
Carlos G Vanoye, Christina A Gurnett, Katherine D Holland, Alfred L George, Jennifer A Kearney. Neurobiol Dis 2014
49
4

Sodium channel genes in pain-related disorders: phenotype-genotype associations and recommendations for clinical use.
Stephen G Waxman, Ingemar S J Merkies, Monique M Gerrits, Sulayman D Dib-Hajj, Giuseppe Lauria, James J Cox, John N Wood, C Geoffrey Woods, Joost P H Drenth, Catharina G Faber. Lancet Neurol 2014
113
3

Pharmacotherapy for neuropathic pain in adults: a systematic review and meta-analysis.
Nanna B Finnerup, Nadine Attal, Simon Haroutounian, Ewan McNicol, Ralf Baron, Robert H Dworkin, Ian Gilron, Maija Haanpää, Per Hansson, Troels S Jensen,[...]. Lancet Neurol 2015
3


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.