A citation-based method for searching scientific literature

Hyo-Jung Kim, Ji-Soo Kim, Jae-Hwan Choi, Jin-Hong Shin, Kwang-Dong Choi, David S Zee. Cerebellum 2014
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


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
181
100

Episodic Ataxia Type 2 due to a Deletion Mutation in the CACNA1A Gene in a Korean Family.
Jeong-Min Kim, Ji Soo Kim, Chang-Seok Ki, Beom-Seok Jeon. J Clin Neurol 2006
8
66

De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia.
Q Yue, J C Jen, M M Thwe, S F Nelson, R W Baloh. Am J Med Genet 1998
49
66

Possible anticipation associated with a novel splice site mutation in episodic ataxia type 2.
Kwang-Dong Choi, Ji-Won Yook, Min-Ji Kim, Hyang-Sook Kim, Young-Eun Park, Ji Soo Kim, Jae-Hwan Choi, Jin-Hong Shin, Dae-Seong Kim. Neurol Sci 2013
7
66

Exercise-induced downbeat nystagmus in a Korean family with a nonsense mutation in CACNA1A.
Jae-Hwan Choi, Jae-Deuk Seo, Yu Ri Choi, Min-Ji Kim, Jin-Hong Shin, Ji Soo Kim, Kwang-Dong Choi. Neurol Sci 2015
6
66

Progressive ataxia due to a missense mutation in a calcium-channel gene.
Q Yue, J C Jen, S F Nelson, R W Baloh. Am J Hum Genet 1997
101
33

Familial periodic cerebellar ataxia: a problem of cerebellar intracellular pH homeostasis.
P G Bain, M D O'Brien, S F Keevil, D A Porter. Ann Neurol 1992
52
33


Corticotropin-releasing factor immunoreactivity increases in the cerebellar climbing fibers in the novel ataxic mutant mouse, pogo.
Y G Jeong, S H Chung, C T Kim, K H Kim, S Y Han, B H Hyun, N S Lee, K Sawada, M H Won, Y Fukui. Anat Histol Embryol 2006
7
33

Stress, caffeine and ethanol trigger transient neurological dysfunction through shared mechanisms in a mouse calcium channelopathy.
Robert S Raike, Catherine Weisz, Freek E Hoebeek, Matthew C Terzi, Chris I De Zeeuw, Arn M van den Maagdenberg, H A Jinnah, Ellen J Hess. Neurobiol Dis 2013
16
33


Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutation.
D I Zafeiriou, F Lehmann-Horn, E Vargiami, E Teflioudi, A Ververi, K Jurkat-Rott. Eur J Paediatr Neurol 2009
10
33


Vertical nystagmus: clinical facts and hypotheses.
C Pierrot-Deseilligny, D Milea. Brain 2005
134
33

Effects of treadmill running on brain activation and the corticotropin-releasing hormone system.
Elena Timofeeva, Qingling Huang, Denis Richard. Neuroendocrinology 2003
53
33

Paroxysmal tonic upward gaze as a presentation of de-novo mutations in CACNA1A.
Lubov Blumkin, Esther Leshinsky-Silver, Marina Michelson, Ayelet Zerem, Sara Kivity, Dorit Lev, Tally Lerman-Sagie. Eur J Paediatr Neurol 2015
18
33

New insights into the pathogenesis and therapeutics of episodic ataxia type 1.
Maria Cristina D'Adamo, Sonia Hasan, Luca Guglielmi, Ilenio Servettini, Marta Cenciarini, Luigi Catacuzzeno, Fabio Franciolini. Front Cell Neurosci 2015
36
33

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
83
33

Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias.
K F Damji, R R Allingham, S C Pollock, K Small, K E Lewis, J M Stajich, L H Yamaoka, J M Vance, M A Pericak-Vance. Arch Neurol 1996
41
33

Episodic ataxia type 1: clinical characterization, quality of life and genotype-phenotype correlation.
Tracey D Graves, Yoon-Hee Cha, Angelika F Hahn, Richard Barohn, Mohammed K Salajegheh, Robert C Griggs, Brian N Bundy, Joanna C Jen, Robert W Baloh, Michael G Hanna. Brain 2014
45
33

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
31
33

Acetazolamide-responsive exercise-induced episodic ataxia associated with a novel homozygous DARS2 mutation.
Matthis Synofzik, Julia Schicks, Tobias Lindig, Saskia Biskup, Thorsten Schmidt, Jochen Hansel, Frank Lehmann-Horn, Ludger Schöls. J Med Genet 2011
31
33

Benign paroxysmal tonic upgaze, benign paroxysmal torticollis, episodic ataxia and CACNA1A mutation in a family.
Agathe Roubertie, Bernard Echenne, Julie Leydet, Sophie Soete, Benjamin Krams, Francois Rivier, Florence Riant, Elisabeth Tournier-Lasserve. J Neurol 2008
44
33

Large CACNA1A deletion in a family with episodic ataxia type 2.
Florence Riant, Reda Mourtada, Pascale Saugier-Veber, Elisabeth Tournier-Lasserve. Arch Neurol 2008
27
33

A three-year-old boy with glucose transporter type 1 deficiency syndrome presenting with episodic ataxia.
Akiko Ohshiro-Sasaki, Hiroko Shimbo, Kyoko Takano, Takahito Wada, Hitoshi Osaka. Pediatr Neurol 2014
10
33

Clinical neurophysiology of the episodic ataxias: insights into ion channel dysfunction in vivo.
Susan E Tomlinson, Michael G Hanna, Dimitri M Kullmann, S Veronica Tan, David Burke. Clin Neurophysiol 2009
25
33

PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.
Alice R Gardiner, Kailash P Bhatia, Maria Stamelou, Russell C Dale, Manju A Kurian, Susanne A Schneider, G M Wali, Tim Counihan, Anthony H Schapira, Sian D Spacey,[...]. Neurology 2012
94
33

Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake.
Boukje de Vries, Hafsa Mamsa, Anine H Stam, Jijun Wan, Stef L M Bakker, Kaate R J Vanmolkot, Joost Haan, Gisela M Terwindt, Elles M J Boon, Bruce D Howard,[...]. Arch Neurol 2009
75
33

Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A gene.
Ester Cuenca-León, Isabel Banchs, Selma A Serra, Pilar Latorre, Noèlia Fernàndez-Castillo, Roser Corominas, Miguel A Valverde, Víctor Volpini, José M Fernández-Fernández, Alfons Macaya,[...]. J Neurol Sci 2009
23
33

Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.
A Escayg, M De Waard, D D Lee, D Bichet, P Wolf, T Mayer, J Johnston, R Baloh, T Sander, M H Meisler. Am J Hum Genet 2000
228
33

A Gain-of-Function Mutation in NALCN in a Child with Intellectual Disability, Ataxia, and Arthrogryposis.
Kyota Aoyagi, Elsa Rossignol, Fadi F Hamdan, Ben Mulcahy, Lin Xie, Shinya Nagamatsu, Guy A Rouleau, Mei Zhen, Jacques L Michaud. Hum Mutat 2015
26
33

An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus.
J L Steckley, G C Ebers, M Z Cader, R S McLachlan. Neurology 2001
38
33

CAOS-Episodic Cerebellar Ataxia, Areflexia, Optic Atrophy, and Sensorineural Hearing Loss: A Third Allelic Disorder of the ATP1A3 Gene.
Gali Heimer, Yair Sadaka, Lori Israelian, Ariel Feiglin, Alessandra Ruggieri, Christian R Marshall, Stephen W Scherer, Esther Ganelin-Cohen, Dina Marek-Yagel, Michal Tzadok,[...]. J Child Neurol 2015
29
33

Large Genomic Deletions in CACNA1A Cause Episodic Ataxia Type 2.
Jijun Wan, Hafsa Mamsa, Janine L Johnston, Elizabeth L Spriggs, Harvey S Singer, David S Zee, Alhamza R Al-Bayati, Robert W Baloh, Joanna C Jen. Front Neurol 2011
27
33

The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway.
Hsien-Yang Lee, Ying Xu, Yong Huang, Andrew H Ahn, Georg W J Auburger, Massimo Pandolfo, Hubert Kwiecinski, David A Grimes, Anthony E Lang, Jorgen E Nielsen,[...]. Hum Mol Genet 2004
88
33


Treatment of episodic ataxia type 2 with the potassium channel blocker 4-aminopyridine.
M Strupp, R Kalla, M Dichgans, T Freilinger, S Glasauer, T Brandt. Neurology 2004
120
33

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
45
33

A new episodic ataxia syndrome with linkage to chromosome 19q13.
Kevin A Kerber, Joanna C Jen, Hane Lee, Stanley F Nelson, Robert W Baloh. Arch Neurol 2007
30
33

A novel locus for episodic ataxia:UBR4 the likely candidate.
Judith Conroy, Paul McGettigan, Raymond Murphy, David Webb, Sinéad M Murphy, Blathnaid McCoy, Christine Albertyn, Dara McCreary, Cara McDonagh, Orla Walsh,[...]. Eur J Hum Genet 2014
36
33

Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures.
J C Jen, J Wan, T P Palos, B D Howard, R W Baloh. Neurology 2005
190
33

A novel frameshift mutation in FGF14 causes an autosomal dominant episodic ataxia.
Karine Choquet, Roberta La Piana, Bernard Brais. Neurogenetics 2015
21
33

Clinical and molecular features of spinocerebellar ataxia type 6.
G Stevanin, A Dürr, G David, O Didierjean, G Cancel, S Rivaud, A Tourbah, J M Warter, Y Agid, A Brice. Neurology 1997
76
33

Dynamic properties of horizontal and vertical eye movements in parkinsonian syndromes.
K G Rottach, D E Riley, A O DiScenna, A Z Zivotofsky, R J Leigh. Ann Neurol 1996
105
33

Ocular motor abnormalities in ataxia telangiectasia.
R F Lewis, H M Lederman, T O Crawford. Ann Neurol 1999
31
33

Huntington's disease: changes in saccades and hand-tapping over 3 years.
Chrystalina A Antoniades, Zheyu Xu, Sarah L Mason, R H S Carpenter, Roger A Barker. J Neurol 2010
26
33

Frequency and phenotypic spectrum of ataxia with oculomotor apraxia 2: a clinical and genetic study in 18 patients.
Isabelle Le Ber, Naïma Bouslam, Sophie Rivaud-Péchoux, João Guimarães, Ali Benomar, Céline Chamayou, Cyril Goizet, Maria-Ceù Moreira, Sandra Klur, Mohamed Yahyaoui,[...]. Brain 2004
118
33

The disturbance of gaze in progressive supranuclear palsy: implications for pathogenesis.
Athena L Chen, David E Riley, Susan A King, Anand C Joshi, Alessandro Serra, Ke Liao, Mark L Cohen, Jorge Otero-Millan, Susana Martinez-Conde, Michael Strupp,[...]. Front Neurol 2010
62
33


Periodic alternating nystagmus with circumscribed nodular lesion.
Y-M Oh, K-D Choi, S-Y Oh, J S Kim. Neurology 2006
12
33


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.