A citation-based method for searching scientific literature

Alexandre Mezghrani, Arnaud Monteil, Katrin Watschinger, Martina J Sinnegger-Brauns, Christian Barrère, Emmanuel Bourinet, Joël Nargeot, Jörg Striessnig, Philippe Lory. J Neurosci 2008
Times Cited: 58







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



Times Cited
  Times     Co-cited
Similarity


N terminus is key to the dominant negative suppression of Ca(V)2 calcium channels: implications for episodic ataxia type 2.
Karen M Page, Fay Heblich, Wojciech Margas, Wendy S Pratt, Manuela Nieto-Rostro, Kanchan Chaggar, Kieran Sandhu, Anthony Davies, Annette C Dolphin. J Biol Chem 2010
41
60

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
41


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
32

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
31

CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
134
29

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
37
37

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
66

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
22

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.
Igor Splawski, Katherine W Timothy, Leah M Sharpe, Niels Decher, Pradeep Kumar, Raffaella Bloise, Carlo Napolitano, Peter J Schwartz, Robert M Joseph, Karen Condouris,[...]. Cell 2004
976
22

Clinical spectrum of episodic ataxia type 2.
J Jen, G W Kim, R W Baloh. Neurology 2004
175
22

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
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
20

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
20

Structure and regulation of voltage-gated Ca2+ channels.
W A Catterall. Annu Rev Cell Dev Biol 2000
18

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
267
18

Dominant-negative synthesis suppression of voltage-gated calcium channel Cav2.2 induced by truncated constructs.
A Raghib, F Bertaso, A Davies, K M Page, A Meir, Y Bogdanov, A C Dolphin. J Neurosci 2001
74
17

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
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
15

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
15

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
15

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
15

Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations.
Igor Splawski, Katherine W Timothy, Niels Decher, Pradeep Kumar, Frank B Sachse, Alan H Beggs, Michael C Sanguinetti, Mark T Keating. Proc Natl Acad Sci U S A 2005
404
15

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
144
13

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
13

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
13

Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels.
J Platzer, J Engel, A Schrott-Fischer, K Stephan, S Bova, H Chen, H Zheng, J Striessnig. Cell 2000
609
13

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

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
13

Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2.
Elide Mantuano, Silvia Romano, Liana Veneziano, Cinzia Gellera, Barbara Castellotti, Sara Caimi, Daniela Testa, Margherita Estienne, Giovanna Zorzi, Marianna Bugiani,[...]. J Neurol Sci 2010
48
16

Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness.
Shahid M Baig, Alexandra Koschak, Andreas Lieb, Mathias Gebhart, Claudia Dafinger, Gudrun Nürnberg, Amjad Ali, Ilyas Ahmad, Martina J Sinnegger-Brauns, Niels Brandt,[...]. Nat Neurosci 2011
169
13

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
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
12

Role of hippocampal Cav1.2 Ca2+ channels in NMDA receptor-independent synaptic plasticity and spatial memory.
Sven Moosmang, Nicole Haider, Norbert Klugbauer, Helmuth Adelsberger, Nicolas Langwieser, Jochen Müller, Michael Stiess, Else Marais, Verena Schulla, Lubica Lacinova,[...]. J Neurosci 2005
294
12

International Union of Pharmacology. XLVIII. Nomenclature and structure-function relationships of voltage-gated calcium channels.
William A Catterall, Edward Perez-Reyes, Terrance P Snutch, Joerg Striessnig. Pharmacol Rev 2005
829
12


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
12

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
12

Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels.
Kei Watase, Curtis F Barrett, Taisuke Miyazaki, Taro Ishiguro, Kinya Ishikawa, Yuanxin Hu, Toshinori Unno, Yaling Sun, Sayumi Kasai, Masahiko Watanabe,[...]. Proc Natl Acad Sci U S A 2008
104
12

Identification of CACNA1A large deletions in four patients with episodic ataxia.
Florence Riant, Christelle Lescoat, Katayoun Vahedi, Elsa Kaphan, Annick Toutain, Thierry Soisson, Sylvette R Wiener-Vacher, Elisabeth Tournier-Lasserve. Neurogenetics 2010
26
26

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
12

Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing.
R W Labrum, S Rajakulendran, T D Graves, L H Eunson, R Bevan, M G Sweeney, S R Hammans, N Tubridy, T Britton, L J Carr,[...]. J Med Genet 2009
37
18

Calcium channel beta-subunit binds to a conserved motif in the I-II cytoplasmic linker of the alpha 1-subunit.
M Pragnell, M De Waard, Y Mori, T Tanabe, T P Snutch, K P Campbell. Nature 1994
534
12

Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death.
Charles Antzelevitch, Guido D Pollevick, Jonathan M Cordeiro, Oscar Casis, Michael C Sanguinetti, Yoshiyasu Aizawa, Alejandra Guerchicoff, Ryan Pfeiffer, Antonio Oliva, Bernd Wollnik,[...]. Circulation 2007
583
12


The Cavβ subunit prevents RFP2-mediated ubiquitination and proteasomal degradation of L-type channels.
Christophe Altier, Agustin Garcia-Caballero, Brett Simms, Haitao You, Lina Chen, Jan Walcher, H William Tedford, Tamara Hermosilla, Gerald W Zamponi. Nat Neurosci 2011
172
12

Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.
Sanjeev Rajakulendran, Diego Kaski, Michael G Hanna. Nat Rev Neurol 2012
85
12

The Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic Potential.
Gerald W Zamponi, Joerg Striessnig, Alexandra Koschak, Annette C Dolphin. Pharmacol Rev 2015
442
12

Unified mechanisms of Ca2+ regulation across the Ca2+ channel family.
Haoya Liang, Carla D DeMaria, Michael G Erickson, Masayuki X Mori, Badr A Alseikhan, David T Yue. Neuron 2003
246
10

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
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.