A citation-based method for searching scientific literature

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, N G Copeland, N A Jenkins. FASEB J 2001
Times Cited: 135







List of co-cited articles
1071 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
67

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
46

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
582
43

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
37

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
32

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
31

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
27


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
178
22

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
22

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
21

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
21

Structure and regulation of voltage-gated Ca2+ channels.
W A Catterall. Annu Rev Cell Dev Biol 2000
19

Altered properties of quantal neurotransmitter release at endplates of mice lacking P/Q-type Ca2+ channels.
Francisco J Urbano, Erika S Piedras-Rentería, Kisun Jun, Hee-Sup Shin, Osvaldo D Uchitel, Richard W Tsien. Proc Natl Acad Sci U S A 2003
103
19

Presynaptic Ca2+ channels compete for channel type-preferring slots in altered neurotransmission arising from Ca2+ channelopathy.
Yu-Qing Cao, Erika S Piedras-Rentería, Geoffrey B Smith, Gong Chen, Nobutoshi C Harata, Richard W Tsien. Neuron 2004
124
19

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
19




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
16

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
98
16

Splicing of alpha 1A subunit gene generates phenotypic variants of P- and Q-type calcium channels.
E Bourinet, T W Soong, K Sutton, S Slaymaker, E Mathews, A Monteil, G W Zamponi, J Nargeot, T P Snutch. Nat Neurosci 1999
329
16

Neurobiology of migraine.
Daniela Pietrobon, Jörg Striessnig. Nat Rev Neurosci 2003
383
15

Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine.
M Hans, S Luvisetto, M E Williams, M Spagnolo, A Urrutia, A Tottene, P F Brust, E C Johnson, M M Harpold, K A Stauderman,[...]. J Neurosci 1999
189
15


Clinical spectrum of episodic ataxia type 2.
J Jen, G W Kim, R W Baloh. Neurology 2004
175
15

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
74
20

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
107
15

Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics.
R L Kraus, M J Sinnegger, H Glossmann, S Hering, J Striessnig. J Biol Chem 1998
155
14

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
14


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
13


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
104
13


Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine.
E E Kors, G M Terwindt, F L Vermeulen, R B Fitzsimons, P E Jardine, P Heywood, S Love, A M van den Maagdenberg, J Haan, R R Frants,[...]. Ann Neurol 2001
232
13

Cerebellar cell degeneration in the leaner mutant mouse.
K Herrup, S L Wilczynski. Neuroscience 1982
144
13

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
13

P-type voltage-dependent calcium channel mediates presynaptic calcium influx and transmitter release in mammalian synapses.
O D Uchitel, D A Protti, V Sanchez, B D Cherksey, M Sugimori, R Llinás. Proc Natl Acad Sci U S A 1992
338
12

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
16

Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model.
Hayrunnisa Bolay, Uwe Reuter, Andrew K Dunn, Zhihong Huang, David A Boas, Michael A Moskowitz. Nat Med 2002
769
12

P-type calcium channels in rat central and peripheral neurons.
I M Mintz, M E Adams, B P Bean. Neuron 1992
720
12

Pain sensitivity in mice lacking the Ca(v)2.1alpha1 subunit of P/Q-type Ca2+ channels.
S Luvisetto, S Marinelli, M S Panasiti, F R D'Amato, C F Fletcher, F Pavone, D Pietrobon. Neuroscience 2006
50
24

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

CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
134
12

Localization and functional properties of a rat brain alpha 1A calcium channel reflect similarities to neuronal Q- and P-type channels.
A Stea, W J Tomlinson, T W Soong, E Bourinet, S J Dubel, S R Vincent, T P Snutch. Proc Natl Acad Sci U S A 1994
310
11


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
98
11


Functional implications of a novel EA2 mutation in the P/Q-type calcium channel.
Sian D Spacey, Michael E Hildebrand, Luke A Materek, Thomas D Bird, Terrance P Snutch. Ann Neurol 2004
53
20


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.