A citation-based method for searching scientific literature

Hiroyuki Hirose, Takashi Arayama, Junko Takita, Takashi Igarashi, Yasuhide Hayashi, Yoshiro Nagao. Int J Mol Med 2003
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


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
87

Clinical spectrum of episodic ataxia type 2.
J Jen, G W Kim, R W Baloh. Neurology 2004
179
75

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, D W Stockton, C Amos, W B Dobyns, S H Subramony, H Y Zoghbi, C C Lee. Nat Genet 1997
50

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
145
50

Hereditary paroxysmal ataxia: response to acetazolamide.
R C Griggs, R T Moxley, R A Lafrance, J McQuillen. Neurology 1978
159
37

Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel.
A Jouvenceau, L H Eunson, A Spauschus, V Ramesh, S M Zuberi, D M Kullmann, M G Hanna. Lancet 2001
261
37

Neurotological findings in a family with episodic ataxia.
Osamu Sasaki, Joanna C Jen, Robert W Baloh, Gilbert W Kim, Manami Isawa, Shin-Ichi Usami. J Neurol 2003
8
37

Absence epilepsy in tottering mutant mice is associated with calcium channel defects.
C F Fletcher, C M Lutz, T N O'Sullivan, J D Shaughnessy, R Hawkes, W N Frankel, N G Copeland, N A Jenkins. Cell 1996
583
37

Reduced voltage sensitivity of activation of P/Q-type Ca2+ channels is associated with the ataxic mouse mutation rolling Nagoya (tg(rol)).
Y Mori, M Wakamori, S Oda, C F Fletcher, N Sekiguchi, E Mori, N G Copeland, N A Jenkins, K Matsushita, Z Matsuyama,[...]. J Neurosci 2000
131
37

Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2.
S Guida, F Trettel, S Pagnutti, E Mantuano, A Tottene, L Veneziano, T Fellin, M Spadaro, K Stauderman, M Williams,[...]. Am J Hum Genet 2001
109
37

Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia.
Paola Imbrici, Stephen L Jaffe, Louise H Eunson, Nicholas P Davies, Colin Herd, Robert Robertson, Dimitri M Kullmann, Michael G Hanna. Brain 2004
149
37

Episodic ataxia type 2.
Michael Strupp, Andreas Zwergal, Thomas Brandt. Neurotherapeutics 2007
96
37

Episodic ataxias as channelopathies.
R C Griggs, J G Nutt. Ann Neurol 1995
95
25


Treatment of downbeat nystagmus with 3,4-diaminopyridine: a placebo-controlled study.
M Strupp, O Schüler, S Krafczyk, K Jahn, F Schautzer, U Büttner, T Brandt. Neurology 2003
156
25

Novel splice site CACNA1A mutation causing episodic ataxia type 2.
M A Kaunisto, H Harno, M Kallela, H Somer, R Sallinen, E Hämäläinen, P J Miettinen, J Vesa, A Orpana, A Palotie,[...]. Neurogenetics 2004
20
25

Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family.
Isabel Alonso, José Barros, Assunção Tuna, João Coelho, Jorge Sequeiros, Isabel Silveira, Paula Coutinho. Arch Neurol 2003
59
25

Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.
Kaate R J Vanmolkot, Esther E Kors, Jouke-Jan Hottenga, Gisela M Terwindt, Joost Haan, Wil A J Hoefnagels, David F Black, Lodewijk A Sandkuijl, Rune R Frants, Michel D Ferrari,[...]. Ann Neurol 2003
246
25

Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23.
Roberto Marconi, Maurizio De Fusco, Paolo Aridon, Katrin Plewnia, Maja Rossi, Sadia Carapelli, Andrea Ballabio, Letterio Morgante, Rosa Musolino, Antonio Epifanio,[...]. Ann Neurol 2003
64
25

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2.
M A Kaunisto, H Harno, K R J Vanmolkot, J J Gargus, G Sun, E Hämäläinen, E Liukkonen, M Kallela, A M J M van den Maagdenberg, R R Frants,[...]. Neurogenetics 2004
48
25

Absence of known familial hemiplegic migraine (FHM) mutations in the CACNA1A gene in patients with common migraine: implications for genetic testing.
Thomas Wieser, Christoph Mueller, Stefan Evers, Stephan Zierz, Thomas Deufel. Clin Chem Lab Med 2003
24
25

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
A Ducros, C Denier, A Joutel, M Cecillon, C Lescoat, K Vahedi, F Darcel, E Vicaut, M G Bousser, E Tournier-Lasserve. N Engl J Med 2001
363
25

Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine.
E E Kors, J Haan, N J Giffin, L Pazdera, C Schnittger, G G Lennox, G M Terwindt, F L M J Vermeulen, A M J M Van den Maagdenberg, R R Frants,[...]. Arch Neurol 2003
67
25

Sporadic hemiplegic migraine is an aetiologically heterogeneous disorder.
L L Thomsen, E Ostergaard, S F Romer, I Andersen, M K Eriksen, J Olesen, M B Russell. Cephalalgia 2003
26
25

Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsy.
Barry Chioza, Abena Osei-Lah, Lina Nashef, Blanca Suarez-Merino, Hazel Wilkie, Pak Sham, Jo Knight, Philip Asherson, Andrew J Makoff. Eur J Hum Genet 2002
22
25

Novel CACNA1A mutation causes febrile episodic ataxia with interictal cerebellar deficits.
S H Subramony, Kelly Schott, Robert S Raike, Joel Callahan, Leigh R Langford, Peka S Christova, John H Anderson, Christopher M Gomez. Ann Neurol 2003
30
25

Evidence for a separate type of migraine with aura: sporadic hemiplegic migraine.
Lise L Thomsen, Elsebet Ostergaard, Jes Olesen, Michael B Russell. Neurology 2003
93
25

A novel insertion mutation of acetazolamide-responsive episodic ataxia in a Japanese family.
Zenjiro Matsuyama, Masahiko Murase, Hirotaka Shimizu, Yoko Aoki, Misato Hayashi, Isao Hozumi, Takashi Inuzuka. J Neurol Sci 2003
12
25

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.
Maurizio De Fusco, Roberto Marconi, Laura Silvestri, Luigia Atorino, Luca Rampoldi, Letterio Morgante, Andrea Ballabio, Paolo Aridon, Giorgio Casari. Nat Genet 2003
637
25

Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity.
C F Fletcher, A Tottene, V A Lennon, S M Wilson, S J Dubel, R Paylor, D A Hosford, L Tessarollo, M W McEnery, D Pietrobon,[...]. FASEB J 2001
136
25

High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2.
C Denier, A Ducros, K Vahedi, A Joutel, P Thierry, A Ritz, G Castelnovo, T Deonna, P Gérard, J L Devoize,[...]. Neurology 1999
146
25

Hereditary paroxysmal ataxia with mental retardation: a clinicopathological study in relation to episodic ataxia type 2.
Y Mochizuki, A Kawata, T Mizutani, K Takamoto, H Hayashi, K Taki, Y Morimatsu. Acta Neuropathol 2004
7
28

Clusters of non-truncating mutations of P/Q type Ca2+ channel subunit Ca(v)2.1 causing episodic ataxia 2.
E Mantuano, L Veneziano, M Spadaro, P Giunti, S Guida, M G Leggio, L Verriello, N Wood, C Jodice, M Frontali. J Med Genet 2004
34
25

Altered calcium channel currents in Purkinje cells of the neurological mutant mouse leaner.
N M Lorenzon, C M Lutz, W N Frankel, K G Beam. J Neurosci 1998
128
25

Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons.
Angelita Tottene, Tommaso Fellin, Stefano Pagnutti, Siro Luvisetto, Joerg Striessnig, Colin Fletcher, Daniela Pietrobon. Proc Natl Acad Sci U S A 2002
181
25

Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit.
K Jun, E S Piedras-Rentería, S M Smith, D B Wheeler, S B Lee, T G Lee, H Chin, M E Adams, R H Scheller, R W Tsien,[...]. Proc Natl Acad Sci U S A 1999
353
25


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
140
25

CACNA1A mutations causing episodic and progressive ataxia alter channel trafficking and kinetics.
J Wan, R Khanna, M Sandusky, D M Papazian, J C Jen, R W Baloh. Neurology 2005
39
25

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
37
25

Two novel CACNA1A gene mutations associated with episodic ataxia type 2 and interictal dystonia.
Sian D Spacey, Luke A Materek, Blajez I Szczygielski, Thomas D Bird. Arch Neurol 2005
43
25

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
270
25

An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus.
J L Steckley, G C Ebers, M Z Cader, R S McLachlan. Neurology 2001
48
25

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
25

Acetazolamide-responsive episodic ataxia syndrome.
N L Zasorin, R W Baloh, L B Myers. Neurology 1983
68
25

Episodic ataxia type 1: a neuronal potassium channelopathy.
Sanjeev Rajakulendran, Stephanie Schorge, Dimitri M Kullmann, Michael G Hanna. Neurotherapeutics 2007
64
25

Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p.
C Jodice, E Mantuano, L Veneziano, F Trettel, G Sabbadini, L Calandriello, A Francia, M Spadaro, F Pierelli, F Salvi,[...]. Hum Mol Genet 1997
212
25

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
81
25

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1.
D L Browne, S T Gancher, J G Nutt, E R Brunt, E A Smith, P Kramer, M Litt. Nat Genet 1994
581
25

New calcium channel mutations predict aberrant RNA splicing in episodic ataxia.
Louise H Eunson, Tracey D Graves, Michael G Hanna. Neurology 2005
25
25


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.