A citation-based method for searching scientific literature

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, Stefan Herlitze. J Neurosci 2011
Times Cited: 58







List of co-cited articles
805 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
41


CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
132
27

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
24

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
267
22

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
581
20

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
257
20

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
20

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
134
17

Purkinje cell-specific ablation of Cav2.1 channels is sufficient to cause cerebellar ataxia in mice.
Boyan Todorov, Lieke Kros, Reinald Shyti, Petra Plak, Elize D Haasdijk, Robert S Raike, Rune R Frants, Ellen J Hess, Freek E Hoebeek, Chris I De Zeeuw,[...]. Cerebellum 2012
23
43

High cortical spreading depression susceptibility and migraine-associated symptoms in Ca(v)2.1 S218L mice.
Arn M J M van den Maagdenberg, Tommaso Pizzorusso, Simon Kaja, Nicole Terpolilli, Maryna Shapovalova, Freek E Hoebeek, Curtis F Barrett, Lisa Gherardini, Rob C G van de Ven, Boyan Todorov,[...]. Ann Neurol 2010
140
15

Silencing the majority of cerebellar granule cells uncovers their essential role in motor learning and consolidation.
Elisa Galliano, Zhenyu Gao, Martijn Schonewille, Boyan Todorov, Esther Simons, Andreea S Pop, Egidio D'Angelo, Arn M J M van den Maagdenberg, Freek E Hoebeek, Chris I De Zeeuw. Cell Rep 2013
81
15

CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.
Lena Damaj, Alexis Lupien-Meilleur, Anne Lortie, Émilie Riou, Luis H Ospina, Louise Gagnon, Catherine Vanasse, Elsa Rossignol. Eur J Hum Genet 2015
81
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
13

Calcium control of transmitter release at a cerebellar synapse.
I M Mintz, B L Sabatini, W G Regehr. Neuron 1995
425
13

KCa channels as therapeutic targets in episodic ataxia type-2.
Karina Alviña, Kamran Khodakhah. J Neurosci 2010
72
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
144
13


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
103
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


Conditional inactivation of the Cacna1a gene in transgenic mice.
Boyan Todorov, Rob C G van de Ven, Simon Kaja, Ludo A M Broos, Sjef J Verbeek, Jaap J Plomp, Michel D Ferrari, Rune R Frants, Arn M J M van den Maagdenberg. Genesis 2006
21
33

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
18

Developmental changes in calcium channel types mediating central synaptic transmission.
S Iwasaki, A Momiyama, O D Uchitel, T Takahashi. J Neurosci 2000
198
12

Calcium channel regulation and presynaptic plasticity.
William A Catterall, Alexandra P Few. Neuron 2008
404
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
83
12


α2δ expression sets presynaptic calcium channel abundance and release probability.
Michael B Hoppa, Beatrice Lana, Wojciech Margas, Annette C Dolphin, Timothy A Ryan. Nature 2012
226
12


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
265
12

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
12

Knockdown of Cav2.1 calcium channels is sufficient to induce neurological disorders observed in natural occurring Cacna1a mutants in mice.
Hiromitsu Saito, Motohiro Okada, Takafumi Miki, Minoru Wakamori, Akira Futatsugi, Yasuo Mori, Katsuhiko Mikoshiba, Noboru Suzuki. Biochem Biophys Res Commun 2009
15
46

CaV 2.1 ablation in cortical interneurons selectively impairs fast-spiking basket cells and causes generalized seizures.
Elsa Rossignol, Illya Kruglikov, Arn M J M van den Maagdenberg, Bernardo Rudy, Gord Fishell. Ann Neurol 2013
63
12


De novo mutations in epileptic encephalopathies.
Andrew S Allen, Samuel F Berkovic, Patrick Cossette, Norman Delanty, Dennis Dlugos, Evan E Eichler, Michael P Epstein, Tracy Glauser, David B Goldstein, Yujun Han,[...]. Nature 2013
898
12

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
51
13


Paroxysmal dyskinesias in mice.
Thomas L Shirley, Lekha M Rao, Ellen J Hess, H A Jinnah. Mov Disord 2008
31
19

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
10

P-type calcium channels blocked by the spider toxin omega-Aga-IVA.
I M Mintz, V J Venema, K M Swiderek, T D Lee, B P Bean, M E Adams. Nature 1992
796
10

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
10

The therapeutic mode of action of 4-aminopyridine in cerebellar ataxia.
Karina Alviña, Kamran Khodakhah. J Neurosci 2010
111
10

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
450
10

Gamma-band deficiency and abnormal thalamocortical activity in P/Q-type channel mutant mice.
Rodolfo R Llinás, Soonwook Choi, Francisco J Urbano, Hee-Sup Shin. Proc Natl Acad Sci U S A 2007
71
10



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
10

BKCa-Cav channel complexes mediate rapid and localized Ca2+-activated K+ signaling.
Henrike Berkefeld, Claudia A Sailer, Wolfgang Bildl, Volker Rohde, Jörg-Oliver Thumfart, Silke Eble, Norbert Klugbauer, Ellen Reisinger, Josef Bischofberger, Dominik Oliver,[...]. Science 2006
249
10

Properties of human Cav2.1 channel with a spinocerebellar ataxia type 6 mutation expressed in Purkinje cells.
Hironao Saegusa, Minoru Wakamori, Yoshihiro Matsuda, Junyang Wang, Yasuo Mori, Shuqin Zong, Tsutomu Tanabe. Mol Cell Neurosci 2007
48
12



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.