A citation-based method for searching scientific literature


List of co-cited articles
1021 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity




Selective increase in T-type calcium conductance of reticular thalamic neurons in a rat model of absence epilepsy.
E Tsakiridou, L Bertollini, M de Curtis, G Avanzini, H C Pape. J Neurosci 1995
283
6

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.
R H Wallace, D W Wang, R Singh, I E Scheffer, A L George, H A Phillips, K Saar, A Reis, E W Johnson, G R Sutherland,[...]. Nat Genet 1998
774
6

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
69
8

beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brain.
D L Burgess, G H Biddlecome, S I McDonough, M E Diaz, C A Zilinski, B P Bean, K P Campbell, J L Noebels. Mol Cell Neurosci 1999
78
7

Primary structure of the receptor for calcium channel blockers from skeletal muscle.
T Tanabe, H Takeshima, A Mikami, V Flockerzi, H Takahashi, K Kangawa, M Kojima, H Matsuo, T Hirose, S Numa. Nature 1987
6

P/Q-type Ca2+ channel defects in migraine, ataxia and epilepsy.
R A Ophoff, G M Terwindt, R R Frants, M D Ferrari. Trends Pharmacol Sci 1998
46
13

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia.
S Battistini, S Stenirri, M Piatti, C Gelfi, P G Righetti, R Rocchi, F Giannini, N Battistini, G C Guazzi, M Ferrari,[...]. Neurology 1999
138
6

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
6



Altered pain responses in mice lacking alpha 1E subunit of the voltage-dependent Ca2+ channel.
H Saegusa, T Kurihara, S Zong, O Minowa, A Kazuno, W Han, Y Matsuda, H Yamanaka, M Osanai, T Noda,[...]. Proc Natl Acad Sci U S A 2000
173
6

The status of voltage-dependent calcium channels in alpha 1E knock-out mice.
S M Wilson, P T Toth, S B Oh, S E Gillard, S Volsen, D Ren, L H Philipson, E C Lee, C F Fletcher, L Tessarollo,[...]. J Neurosci 2000
115
6

Three new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kinetics.
R L Kraus, M J Sinnegger, A Koschak, H Glossmann, S Stenirri, P Carrera, J Striessnig. J Biol Chem 2000
107
6

Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission.
J Jen, J Wan, M Graves, H Yu, A F Mock, C J Coulin, G Kim, Q Yue, D M Papazian, R W Baloh. Neurology 2001
101
6

Altered calcium homeostasis in cerebellar Purkinje cells of leaner mutant mice.
L S Dove, S S Nahm, D Murchison, L C Abbott, W H Griffith. J Neurophysiol 2000
46
13


Calcium-channel antibodies in the Lambert-Eaton syndrome and other paraneoplastic syndromes.
V A Lennon, T J Kryzer, G E Griesmann, P E O'Suilleabhain, A J Windebank, A Woppmann, G P Miljanich, E H Lambert. N Engl J Med 1995
406
6

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
6


Functional consequences of P/Q-type Ca2+ channel Cav2.1 missense mutations associated with episodic ataxia type 2 and progressive ataxia.
Edwin Wappl, Alexandra Koschak, Michael Poteser, Martina J Sinnegger, Doris Walter, Andreas Eberhart, Klaus Groschner, Hartmut Glossmann, Richard L Kraus, Manfred Grabner,[...]. J Biol Chem 2002
76
7

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
121
6

Decreases in the precision of Purkinje cell pacemaking cause cerebellar dysfunction and ataxia.
Joy T Walter, Karina Alviña, Mary D Womack, Carolyn Chevez, Kamran Khodakhah. Nat Neurosci 2006
274
6

Human autoantibodies specific for the alpha1A calcium channel subunit reduce both P-type and Q-type calcium currents in cerebellar neurons.
A Pinto, S Gillard, F Moss, K Whyte, P Brust, M Williams, K Stauderman, M Harpold, B Lang, J Newsom-Davis,[...]. Proc Natl Acad Sci U S A 1998
81
6




Experimental studies of "lethargic" mutant mice.
H C Dung, R H Swigart. Tex Rep Biol Med 1971
26
19

Beta subunit heterogeneity in neuronal L-type Ca2+ channels.
M Pichler, T N Cassidy, D Reimer, H Haase, R Kraus, D Ostler, J Striessnig. J Biol Chem 1997
94
5

Differential distribution of three members of a gene family encoding low voltage-activated (T-type) calcium channels.
E M Talley, L L Cribbs, J H Lee, A Daud, E Perez-Reyes, D A Bayliss. J Neurosci 1999
582
5

Roles of a membrane-localized beta subunit in the formation and targeting of functional L-type Ca2+ channels.
A J Chien, X Zhao, R E Shirokov, T S Puri, C F Chang, D Sun, E Rios, M M Hosey. J Biol Chem 1995
227
5


Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp.
S E Fisher, A Ciccodicola, K Tanaka, A Curci, S Desicato, M D'urso, I W Craig. Genomics 1997
34
14

Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice.
G A Cox, C M Lutz, C L Yang, D Biemesderfer, R T Bronson, A Fu, P S Aronson, J L Noebels, W N Frankel. Cell 1997
215
5

SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel gene.
O Riess, L Schöls, H Bottger, D Nolte, A M Vieira-Saecker, C Schimming, F Kreuz, M Macek, A Krebsová, Macek M Sen,[...]. Hum Mol Genet 1997
101
5

A potassium channel mutation in neonatal human epilepsy.
C Biervert, B C Schroeder, C Kubisch, S F Berkovic, P Propping, T J Jentsch, O K Steinlein. Science 1998
791
5

A calcium channel mutation causing hypokalemic periodic paralysis.
K Jurkat-Rott, F Lehmann-Horn, A Elbaz, R Heine, R G Gregg, K Hogan, P A Powers, P Lapie, J E Vale-Santos, J Weissenbach. Hum Mol Genet 1994
246
5

Identification of a mutation in the gene causing hyperkalemic periodic paralysis.
L J Ptácek, A L George, R C Griggs, R Tawil, R G Kallen, R L Barchi, M Robertson, M F Leppert. Cell 1991
332
5

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.
Q Wang, M E Curran, I Splawski, T C Burn, J M Millholland, T J VanRaay, J Shen, K W Timothy, G M Vincent, T de Jager,[...]. Nat Genet 1996
5

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
6

Direct binding of G-protein betagamma complex to voltage-dependent calcium channels.
M De Waard, H Liu, D Walker, V E Scott, C A Gurnett, K P Campbell. Nature 1997
345
5

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome.
Q Wang, J Shen, I Splawski, D Atkinson, Z Li, J L Robinson, A J Moss, J A Towbin, M T Keating. Cell 1995
5

The skeletal muscle chloride channel in dominant and recessive human myotonia.
M C Koch, K Steinmeyer, C Lorenz, K Ricker, F Wolf, M Otto, B Zoll, F Lehmann-Horn, K H Grzeschik, T J Jentsch. Science 1992
592
5

T-type Ca2+ current properties are not modified by Ca2+ channel beta subunit depletion in nodosus ganglion neurons.
R C Lambert, Y Maulet, J Mouton, R Beattie, S Volsen, M De Waard, A Feltz. J Neurosci 1997
62
8

Cloning and expression of a novel member of the low voltage-activated T-type calcium channel family.
J H Lee, A N Daud, L L Cribbs, A E Lacerda, A Pereverzev, U Klöckner, T Schneider, E Perez-Reyes. J Neurosci 1999
366
5


Familial hemiplegic migraine in The Netherlands. Dutch Migraine Genetics Research Group.
J Haan, G M Terwindt, P L Bos, R A Ophoff, R R Frants, M D Ferrari. Clin Neurol Neurosurg 1994
43
11




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.