A citation-based method for searching scientific literature

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
Times Cited: 582







List of co-cited articles
1121 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
351
25


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
22

Single tottering mutations responsible for the neuropathic phenotype of the P-type calcium channel.
M Wakamori, K Yamazaki, H Matsunodaira, T Teramoto, I Tanaka, T Niidome, K Sawada, Y Nishizawa, N Sekiguchi, E Mori,[...]. J Biol Chem 1998
170
18

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
259
18

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
17


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
15

Role of the alpha1G T-type calcium channel in spontaneous absence seizures in mutant mice.
Inseon Song, Daesoo Kim, Soonwook Choi, Minjeong Sun, Yeongin Kim, Hee-Sup Shin. J Neurosci 2004
100
15

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
15

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
269
14

CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
134
13


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
147
13

Reduced cortical inhibition in a mouse model of familial childhood absence epilepsy.
Heneu O Tan, Christopher A Reid, Frank N Single, Philip J Davies, Cindy Chiu, Susan Murphy, Alison L Clarke, Leanne Dibbens, Heinz Krestel, John C Mulley,[...]. Proc Natl Acad Sci U S A 2007
140
13

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
135
13

Excitatory but not inhibitory synaptic transmission is reduced in lethargic (Cacnb4(lh)) and tottering (Cacna1atg) mouse thalami.
S J Caddick, C Wang, C F Fletcher, N A Jenkins, N G Copeland, D A Hosford. J Neurophysiol 1999
96
12


Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies.
T Miki, T A Zwingman, M Wakamori, C M Lutz, S A Cook, D A Hosford, K Herrup, C F Fletcher, Y Mori, W N Frankel,[...]. Neuroscience 2008
37
32

Cortical focus drives widespread corticothalamic networks during spontaneous absence seizures in rats.
Hanneke K M Meeren, Jan Pieter M Pijn, Egidius L J M Van Luijtelaar, Anton M L Coenen, Fernando H Lopes da Silva. J Neurosci 2002
573
12

Delayed postnatal loss of P/Q-type calcium channels recapitulates the absence epilepsy, dyskinesia, and ataxia phenotypes of genomic Cacna1a mutations.
Melanie D Mark, Takashi Maejima, Denise Kuckelsberg, Jong W Yoo, Robert A Hyde, Viral Shah, Davina Gutierrez, Rosa L Moreno, Wolfgang Kruse, Jeffrey L Noebels,[...]. J Neurosci 2011
60
20

Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells.
J Barclay, N Balaguero, M Mione, S L Ackerman, V A Letts, J Brodbeck, C Canti, A Meir, K M Page, K Kusumi,[...]. J Neurosci 2001
200
11

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
127
10

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
197
10

Childhood absence epilepsy: genes, channels, neurons and networks.
Vincenzo Crunelli, Nathalie Leresche. Nat Rev Neurosci 2002
393
10

A Cav3.2 T-type calcium channel point mutation has splice-variant-specific effects on function and segregates with seizure expression in a polygenic rat model of absence epilepsy.
Kim L Powell, Stuart M Cain, Caroline Ng, Shreerang Sirdesai, Laurence S David, Mervyn Kyi, Esperanza Garcia, John R Tyson, Christopher A Reid, Melanie Bahlo,[...]. J Neurosci 2009
121
10


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
10

Immunochemical identification and subcellular distribution of the alpha 1A subunits of brain calcium channels.
R E Westenbroek, T Sakurai, E M Elliott, J W Hell, T V Starr, T P Snutch, W A Catterall. J Neurosci 1995
448
10

Deep layer somatosensory cortical neurons initiate spike-and-wave discharges in a genetic model of absence seizures.
Pierre-Olivier Polack, Isabelle Guillemain, Emilie Hu, Colin Deransart, Antoine Depaulis, Stéphane Charpier. J Neurosci 2007
246
10

Bidirectional alterations in cerebellar synaptic transmission of tottering and rolling Ca2+ channel mutant mice.
Kaori Matsushita, Minoru Wakamori, Im Joo Rhyu, Tatsuo Arii, Sen-Ichi Oda, Yasuo Mori, Keiji Imoto. J Neurosci 2002
72
12

The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.
V A Letts, R Felix, G H Biddlecome, J Arikkath, C L Mahaffey, A Valenzuela, F S Bartlett, Y Mori, K P Campbell, W N Frankel. Nat Genet 1998
446
9

A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.
Arn M J M van den Maagdenberg, Daniela Pietrobon, Tommaso Pizzorusso, Simon Kaja, Ludo A M Broos, Tiziana Cesetti, Rob C G van de Ven, Angelita Tottene, Jos van der Kaa, Jaap J Plomp,[...]. Neuron 2004
455
9

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
359
9

Deletion of the K(V)1.1 potassium channel causes epilepsy in mice.
S L Smart, V Lopantsev, C L Zhang, C A Robbins, H Wang, S Y Chiu, P A Schwartzkroin, A Messing, B L Tempel. Neuron 1998
420
9

Pathophysiological mechanisms of genetic absence epilepsy in the rat.
L Danober, C Deransart, A Depaulis, M Vergnes, C Marescaux. Prog Neurobiol 1998
392
9



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
281
9

Paroxysmal dyskinesias in mice.
Thomas L Shirley, Lekha M Rao, Ellen J Hess, H A Jinnah. Mov Disord 2008
32
28

Triggers of paroxysmal dyskinesia in the calcium channel mouse mutant tottering.
Brandy E Fureman, H A Jinnah, Ellen J Hess. Pharmacol Biochem Behav 2002
43
20

Increased noise level of purkinje cell activities minimizes impact of their modulation during sensorimotor control.
F E Hoebeek, J S Stahl, A M van Alphen, M Schonewille, C Luo, M Rutteman, A M J M van den Maagdenberg, P C Molenaar, H H L M Goossens, M A Frens,[...]. Neuron 2005
107
8

Impaired feedforward inhibition of the thalamocortical projection in epileptic Ca2+ channel mutant mice, tottering.
Sachie Sasaki, Kadrul Huda, Tsuyoshi Inoue, Mariko Miyata, Keiji Imoto. J Neurosci 2006
33
24

Absence epilepsy and sinus dysrhythmia in mice lacking the pacemaker channel HCN2.
Andreas Ludwig, Thomas Budde, Juliane Stieber, Sven Moosmang, Christian Wahl, Knut Holthoff, Anke Langebartels, Carsten Wotjak, Thomas Munsch, Xiangang Zong,[...]. EMBO J 2003
369
8

Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures.
R H Wallace, C Marini, S Petrou, L A Harkin, D N Bowser, R G Panchal, D A Williams, G R Sutherland, J C Mulley, I E Scheffer,[...]. Nat Genet 2001
567
8

Gating effects of mutations in the Cav3.2 T-type calcium channel associated with childhood absence epilepsy.
Houman Khosravani, Christophe Altier, Brett Simms, Kevin S Hamming, Terrance P Snutch, Janette Mezeyova, John E McRory, Gerald W Zamponi. J Biol Chem 2004
128
8

Structure and regulation of voltage-gated Ca2+ channels.
W A Catterall. Annu Rev Cell Dev Biol 2000
8

The neural substrates of rapid-onset Dystonia-Parkinsonism.
D Paola Calderon, Rachel Fremont, Franca Kraenzlin, Kamran Khodakhah. Nat Neurosci 2011
144
8


The ß subunit of voltage-gated Ca2+ channels.
Zafir Buraei, Jian Yang. Physiol Rev 2010
236
8


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.