A citation-based method for searching scientific literature

R A Maselli, J Wan, V Dunne, M Graves, R W Baloh, R L Wollmann, J Jen. Neurology 2003
Times Cited: 30







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



Times Cited
  Times     Co-cited
Similarity


Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability.
L H Eunson, R Rea, S M Zuberi, S Youroukos, C P Panayiotopoulos, R Liguori, P Avoni, R C McWilliam, J B Stephenson, M G Hanna,[...]. Ann Neurol 2000
169
16

Dominant-negative effects of human P/Q-type Ca2+ channel mutations associated with episodic ataxia type 2.
Chung-Jiuan Jeng, Yu-Ting Chen, Yi-Wen Chen, Chih-Yung Tang. Am J Physiol Cell Physiol 2006
38
16

Episodic ataxia type 2.
Michael Strupp, Andreas Zwergal, Thomas Brandt. Neurotherapeutics 2007
96
16

Dominant-negative suppression of Cav2.1 currents by alpha(1)2.1 truncations requires the conserved interaction domain for beta subunits.
Robert S Raike, Holly B Kordasiewicz, Randall M Thompson, Christopher M Gomez. Mol Cell Neurosci 2007
21
23

Severely impaired neuromuscular synaptic transmission causes muscle weakness in the Cacna1a-mutant mouse rolling Nagoya.
Simon Kaja, Rob C G van de Ven, J Gert van Dijk, Jan J G M Verschuuren, Kiichi Arahata, Rune R Frants, Michel D Ferrari, Arn M J M van den Maagdenberg, Jaap J Plomp. Eur J Neurosci 2007
40
16

CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
134
16

Transmitter release deficits at the neuromuscular synapse of mice with mutations in the Cav2.1 (alpha1A) subunit of the P/Q-type Ca2+ channel.
J J Plomp, A M van den Maagdenberg, M D Ferrari, R R Frants, P C Molenaar. Ann N Y Acad Sci 2003
7
57



Primary structure and functional expression from complementary DNA of a brain calcium channel.
Y Mori, T Friedrich, M S Kim, A Mikami, J Nakai, P Ruth, E Bosse, F Hofmann, V Flockerzi, T Furuichi. Nature 1991
760
13

Structure and regulation of voltage-gated Ca2+ channels.
W A Catterall. Annu Rev Cell Dev Biol 2000
13



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
13


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
13

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
13

Potassium channel blockers inhibit the triggers of attacks in the calcium channel mouse mutant tottering.
Catherine J C Weisz, Robert S Raike, Luis E Soria-Jasso, Ellen J Hess. J Neurosci 2005
48
13

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
13

Rocker is a new variant of the voltage-dependent calcium channel gene Cacna1a.
T A Zwingman, P E Neumann, J L Noebels, K Herrup. J Neurosci 2001
110
13

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
60
13


Systematic identification of splice variants in human P/Q-type channel alpha1(2.1) subunits: implications for current density and Ca2+-dependent inactivation.
Tuck Wah Soong, Carla D DeMaria, Rebecca S Alvania, Larry S Zweifel, Mui Cheng Liang, Scott Mittman, William S Agnew, David T Yue. J Neurosci 2002
108
13

Dominant-negative calcium channel suppression by truncated constructs involves a kinase implicated in the unfolded protein response.
Karen M Page, Fay Heblich, Anthony Davies, Adrian J Butcher, Jerôme Leroy, Federica Bertaso, Wendy S Pratt, Annette C Dolphin. J Neurosci 2004
69
13

A destructive interaction mechanism accounts for dominant-negative effects of misfolded mutants of voltage-gated calcium channels.
Alexandre Mezghrani, Arnaud Monteil, Katrin Watschinger, Martina J Sinnegger-Brauns, Christian Barrère, Emmanuel Bourinet, Joël Nargeot, Jörg Striessnig, Philippe Lory. J Neurosci 2008
58
13


Reduced ACh release at neuromuscular synapses of heterozygous leaner Ca(v)2.1-mutant mice.
Simon Kaja, Rob C G Van De Ven, Rune R Frants, Michel D Ferrari, Arn M J M Van Den Maagdenberg, Jaap J Plomp. Synapse 2008
10
40

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
27
14

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
53
13


Neuromuscular transmission in SCA6.
H Jurgen Schelhaas, Bart P C Van de Warrenburg, Hubertus P H Kremer, Machiel J Zwarts. Ann Neurol 2004
8
37




Ca2+/calmodulin binds to and modulates P/Q-type calcium channels.
A Lee, S T Wong, D Gallagher, B Li, D R Storm, T Scheuer, W A Catterall. Nature 1999
394
10


Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.
C M Gomez, R M Thompson, J T Gammack, S L Perlman, W B Dobyns, C L Truwit, D S Zee, H B Clark, J H Anderson. Ann Neurol 1997
201
10


Multiple types of Ca2+ channels in mouse motor nerve terminals.
M J Lin, S Y Lin-Shiau. Eur J Neurosci 1997
29
10

Functional compensation of P/Q by N-type channels blocks short-term plasticity at the calyx of Held presynaptic terminal.
Carlota González Inchauspe, Francisco J Martini, Ian D Forsythe, Osvaldo D Uchitel. J Neurosci 2004
105
10


P/Q-type calcium channels mediate the activity-dependent feedback of syntaxin-1A.
K G Sutton, J E McRory, H Guthrie, T H Murphy, T P Snutch. Nature 1999
120
10

Episodic ataxias as channelopathies.
R C Griggs, J G Nutt. Ann Neurol 1995
95
10

Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p.
B von Brederlow, A F Hahn, W J Koopman, G C Ebers, D E Bulman. Hum Mol Genet 1995
78
10

Acetazolamide-responsive episodic ataxia in an Italian family refines gene mapping on chromosome 19p13.
L Calandriello, L Veneziano, A Francia, G Sabbadini, C Colonnese, E Mantuano, C Jodice, F Trettel, P Viviani, M Manfredi,[...]. Brain 1997
20
15

Episodic ataxia type 1: a neuronal potassium channelopathy.
Sanjeev Rajakulendran, Stephanie Schorge, Dimitri M Kullmann, Michael G Hanna. Neurotherapeutics 2007
64
10


Hereditary paroxysmal ataxia with neuromyotonia.
J Vaamonde, J Artieda, J A Obeso. Mov Disord 1991
25
12


Specific kinetic alterations of human CaV2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma.
Angelita Tottene, Francesca Pivotto, Tommaso Fellin, Tiziana Cesetti, Arn M J M van den Maagdenberg, Daniela Pietrobon. J Biol Chem 2005
99
10


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.