A citation-based method for searching scientific literature

Yi-Chung Lee, Ming-Jen Lee, Hsiang-Yu Yu, Chien Chen, Chang-Hung Hsu, Kon-Ping Lin, Kwong-Kum Liao, Ming-Hong Chang, Yi-Chu Liao, Bing-Wen Soong. PLoS One 2012
Times Cited: 92







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



Times Cited
  Times     Co-cited
Similarity


Clinical and genetic spectrum of SCN2A-associated episodic ataxia.
N Schwarz, T Bast, E Gaily, G Golla, K M Gorman, L R Griffiths, A Hahn, J Hukin, M King, C Korff,[...]. Eur J Paediatr Neurol 2019
26
3

Knock-in mouse model of alternating hemiplegia of childhood: behavioral and electrophysiologic characterization.
Arsen S Hunanyan, Nina A Fainberg, Molly Linabarger, Eric Arehart, A Soren Leonard, Syed M Adil, Ashley R Helseth, Amanda K Swearingen, Stacy L Forbes, Ramona M Rodriguiz,[...]. Epilepsia 2015
52
1

Cognitive impairment in children with CACNA1A mutations.
Veronique Humbertclaude, Florence Riant, Benjamin Krams, Valerie Zimmermann, Nicolas Nagot, Daniel Annequin, Bernard Echenne, Elisabeth Tournier-Lasserve, Agathe Roubertie. Dev Med Child Neurol 2020
20
5

Valproate-induced reversible hemichorea.
Sheila Srinivasan, Au Wing Lok. Mov Disord 2010
12
8

Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.
Patricia de Carvalho Aguiar, Kathleen J Sweadner, John T Penniston, Jacek Zaremba, Liu Liu, Marsha Caton, Gurutz Linazasoro, Michel Borg, Marina A J Tijssen, Susan B Bressman,[...]. Neuron 2004
337
1

CHRNA4 variant causes paroxysmal kinesigenic dyskinesia and genetic epilepsy with febrile seizures plus?
Yong-Li Jiang, Fang Yuan, Ying Yang, Xiao-Long Sun, Lu Song, Wen Jiang. Seizure 2018
16
6

Mechanisms of increased hippocampal excitability in the Mashl+/- mouse model of Na+ /K+ -ATPase dysfunction.
Arsen S Hunanyan, Ashley R Helseth, Elie Abdelnour, Bassil Kherallah, Monisha Sachdev, Leeyup Chung, Melanie Masoud, Jordan Richardson, Qiang Li, J Victor Nadler,[...]. Epilepsia 2018
30
3

GNAO1-related movement disorder with life-threatening exacerbations: movement phenomenology and response to DBS.
Michaela Waak, Shekeeb S Mohammad, David Coman, Kate Sinclair, Lisa Copeland, Peter Silburn, Terry Coyne, Jim McGill, Mary O'Regan, Richard Selway,[...]. J Neurol Neurosurg Psychiatry 2018
36
2

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
4

Benefit of carbamazepine in a patient with hemiplegic migraine associated with PRRT2 mutation.
Russell C Dale, Alice Gardiner, Joceline A Branson, Henry Houlden. Dev Med Child Neurol 2014
16
6

Anticonvulsant-induced dyskinesias: a comparison with dyskinesias induced by neuroleptics.
D Chadwick, E H Reynolds, C D Marsden. J Neurol Neurosurg Psychiatry 1976
167
1

Magnetic resonance imaging volumetric analysis in patients with Alternating hemiplegia of childhood: A pilot study.
Ryan Ghusayni, Jordan P Richardson, Julie Uchitel, Elie Abdelnour, Melissa McLean, Lyndsey Prange, Tavis Abrahamsen, Allen Song, Jeffrey R Petrella, Mohamad A Mikati. Eur J Paediatr Neurol 2020
6
16

The phenotypic spectrum of SCN2A-related epilepsy.
Claire Reynolds, Mary D King, Kathleen M Gorman. Eur J Paediatr Neurol 2020
30
3

Beyond Dystonia-Parkinsonism: Chorea and Ataxia with ATP1A3 Mutations.
Claudio M de Gusmao, Marisela Dy, Nutan Sharma. Mov Disord Clin Pract 2016
11
9

Benign pediatric localization-related epilepsies.
Lama M Chahine, Mohamad A Mikati. Epileptic Disord 2006
26
3

An Atypical Rett Syndrome Phenotype Due to a Novel Missense Mutation in CACNA1A.
Madison V Epperson, Michael E Haws, Shannon M Standridge, Donald L Gilbert. J Child Neurol 2018
14
7


Striatal spreading depolarization: Possible implication in levodopa-induced dyskinetic-like behavior.
Antonio de Iure, Francesco Napolitano, Goichi Beck, Ana Quiroga Varela, Valentina Durante, Miriam Sciaccaluga, Petra Mazzocchetti, Alfredo Megaro, Michela Tantucci, Antonella Cardinale,[...]. Mov Disord 2019
4
25

Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy.
Mark A Corbett, Susannah T Bellows, Melody Li, Renée Carroll, Silvana Micallef, Gemma L Carvill, Candace T Myers, Katherine B Howell, Snezana Maljevic, Holger Lerche,[...]. Neurology 2016
48
2

Late-onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A.
P Imbrici, L H Eunson, T D Graves, K P Bhatia, N H Wadia, D M Kullmann, M G Hanna. Neurology 2005
39
2

Harry Lee Parker and paroxysmal dysarthria and ataxia.
James P Klaas, David B Burkholder, Wolfgang Singer, Christopher J Boes. Neurology 2013
18
5

A Gain-of-Function Mutation in KCNMA1 Causes Dystonia Spells Controlled With Stimulant Therapy.
Guohui Zhang, Rebecca A Gibson, Marie McDonald, Pengfei Liang, Po Wei Kang, Jingyi Shi, Huanghe Yang, Jianmin Cui, Mohamad A Mikati. Mov Disord 2020
10
10

Familial periodic ataxia.
J R Donat, R Auger. Arch Neurol 1979
56
1

Contractures, continuous muscle discharges, and titubation.
P A Hanson, L B Martinez, R Cassidy. Ann Neurol 1977
40
2

Clinical Course of Six Children With GNAO1 Mutations Causing a Severe and Distinctive Movement Disorder.
Amitha L Ananth, Amy Robichaux-Viehoever, Young-Min Kim, Andrea Hanson-Kahn, Rachel Cox, Gregory M Enns, Jonathan Strober, Marcia Willing, Bradley L Schlaggar, Yvonne W Wu,[...]. Pediatr Neurol 2016
52
1

Pyruvate dehydrogenase complex-E2 deficiency causes paroxysmal exercise-induced dyskinesia.
Jennifer Friedman, Annette Feigenbaum, Nathaniel Chuang, Jennifer Silhavy, Joseph G Gleeson. Neurology 2017
16
6

Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutation.
A H Stam, G-J Luijckx, B T Poll-Thé, I B Ginjaar, R R Frants, J Haan, M D Ferrari, G M Terwindt, A M J M van den Maagdenberg. J Neurol Neurosurg Psychiatry 2009
69
1

Hereditary myokymia and periodic ataxia.
D H VanDyke, R C Griggs, M J Murphy, M N Goldstein. J Neurol Sci 1975
108
1



Hypothermia-induced dystonia and abnormal cerebellar activity in a mouse model with a single disease-mutation in the sodium-potassium pump.
Toke Jost Isaksen, Lieke Kros, Natascia Vedovato, Thomas Hellesøe Holm, Ariel Vitenzon, David C Gadsby, Kamran Khodakhah, Karin Lykke-Hartmann. PLoS Genet 2017
30
3

De Novo mutations in GNAO1, encoding a Gαo subunit of heterotrimeric G proteins, cause epileptic encephalopathy.
Kazuyuki Nakamura, Hirofumi Kodera, Tenpei Akita, Masaaki Shiina, Mitsuhiro Kato, Hideki Hoshino, Hiroshi Terashima, Hitoshi Osaka, Shinichi Nakamura, Jun Tohyama,[...]. Am J Hum Genet 2013
131
1

Ineffectiveness of diamox in the treatment of childhood epilepsy.
S LIVINGSTON, D PETERSON, L BOKS. Pediatrics 1956
11
9

A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p.
K Vahedi, A Joutel, P Van Bogaert, A Ducros, J Maciazeck, J F Bach, M G Bousser, E Tournier-Lasserve. Ann Neurol 1995
108
1

Eye movement disorders are an early manifestation of CACNA1A mutations in children.
Esther M Tantsis, Deepak Gill, Lyn Griffiths, Sachin Gupta, John Lawson, Neven Maksemous, Robert Ouvrier, Florence Riant, Robert Smith, Christopher Troedson,[...]. Dev Med Child Neurol 2016
42
2

A novel recurrent mutation in ATP1A3 causes CAPOS syndrome.
Michelle K Demos, Clara Dm van Karnebeek, Colin Jd Ross, Shelin Adam, Yaoqing Shen, Shing Hei Zhan, Casper Shyr, Gabriella Horvath, Mohnish Suri, Alan Fryer,[...]. Orphanet J Rare Dis 2014
130
1

Use of antiepileptic drugs for hyperkinetic movement disorders.
A Siniscalchi, L Gallelli, G De Sarro. Curr Neuropharmacol 2010
20
5

Ketogenic dietary therapies in adults with epilepsy: a practical guide.
Natasha E Schoeler, J Helen Cross. Pract Neurol 2016
21
4

Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies.
Silvia Masnada, Ulrike B S Hedrich, Elena Gardella, Julian Schubert, Charu Kaiwar, Eric W Klee, Brendan C Lanpher, Ralitza H Gavrilova, Matthis Synofzik, Thomas Bast,[...]. Brain 2017
71
1

Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy.
Sanjeev Rajakulendran, Tracey D Graves, Robyn W Labrum, Dimitrios Kotzadimitriou, Louise Eunson, Mary B Davis, Rosalyn Davies, Nicholas W Wood, Dimitri M Kullmann, Michael G Hanna,[...]. J Physiol 2010
59
1

A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy.
S M Zuberi, L H Eunson, A Spauschus, R De Silva, J Tolmie, N W Wood, R C McWilliam, J B Stephenson, D M Kullmann, M G Hanna. Brain 1999
258
1

SEIZURES INDUCED BY MOVEMENT: A FORM OF REFLEX EPILEPSY.
C W WHITTY, W A LISHMAN, J P FITZGIBBON. Lancet 1964
30
3

Paroxysmal eye-head movements in Glut1 deficiency syndrome.
Toni S Pearson, Roser Pons, Kristin Engelstad, Steven A Kane, Michael E Goldberg, Darryl C De Vivo. Neurology 2017
23
4

Missense Variants in RHOBTB2 Cause a Developmental and Epileptic Encephalopathy in Humans, and Altered Levels Cause Neurological Defects in Drosophila.
Jonas Straub, Enrico D H Konrad, Johanna Grüner, Annick Toutain, Levinus A Bok, Megan T Cho, Heather P Crawford, Holly Dubbs, Ganka Douglas, Rebekah Jobling,[...]. Am J Hum Genet 2018
37
2

Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition.
Elena Arystarkhova, Ihtsham U Haq, Timothy Luebbert, Fanny Mochel, Rachel Saunders-Pullman, Susan B Bressman, Polina Feschenko, Cynthia Salazar, Jared F Cook, Scott Demarest,[...]. Neurobiol Dis 2019
20
5

Paroxysmal kinesigenic choreoathetosis. Report of a case relieved by L-dopa.
S C Loong, Y Y Ong. J Neurol Neurosurg Psychiatry 1973
46
2

Alternating hemiplegia of childhood: clinical manifestations and long-term outcome.
M A Mikati, U Kramer, M L Zupanc, R J Shanahan. Pediatr Neurol 2000
130
1

Paroxysmal exercise-induced dystonia due to GLUT1 mutation can be responsive to levodopa: a case report.
Francesca Baschieri, Amit Batla, Roberto Erro, Christos Ganos, Carla Cordivari, Kailash P Bhatia. J Neurol 2014
11
9

Identification of a human synaptotagmin-1 mutation that perturbs synaptic vesicle cycling.
Kate Baker, Sarah L Gordon, Detelina Grozeva, Margriet van Kogelenberg, Nicola Y Roberts, Michael Pike, Edward Blair, Matthew E Hurles, W Kling Chong, Torsten Baldeweg,[...]. J Clin Invest 2015
66
1

Familial frontal lobe epilepsy and its relationship with other nocturnal paroxysmal events.
Paolo Tinuper, Francesca Bisulli, Federica Provini, Elio Lugaresi. Epilepsia 2010
7
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.