A citation-based method for searching scientific literature

Jaap J Plomp, Arn M J M van den Maagdenberg, Simon Kaja. Cerebellum 2009
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


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
56

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
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
460
31


Severely impaired neuromuscular synaptic transmission causes muscle weakness in the Cacna1a-mutant mouse rolling Nagoya.
Simon Kaja, Rob C G van de Ven, J Gert van Dijk, Jan J G M Verschuuren, Kiichi Arahata, Rune R Frants, Michel D Ferrari, Arn M J M van den Maagdenberg, Jaap J Plomp. Eur J Neurosci 2007
40
31

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
147
31


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
25

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
261
25

SCA1 transgenic mice: a model for neurodegeneration caused by an expanded CAG trinucleotide repeat.
E N Burright, H B Clark, A Servadio, T Matilla, R M Feddersen, W S Yunis, L A Duvick, H Y Zoghbi, H T Orr. Cell 1995
461
18


Neurodegeneration in Lurcher mice caused by mutation in delta2 glutamate receptor gene.
J Zuo, P L De Jager, K A Takahashi, W Jiang, D J Linden, N Heintz. Nature 1997
419
18


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
583
18

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
105
18

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
233
18

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
18

Forward genetic screen of mouse reveals dominant missense mutation in the P/Q-type voltage-dependent calcium channel, CACNA1A.
G Xie, S J Clapcote, B J Nieman, T Tallerico, Y Huang, I Vukobradovic, S P Cordes, L R Osborne, J Rossant, J G Sled,[...]. Genes Brain Behav 2007
29
18

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
172
18

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
450
18

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
149
18

Cerebellar cell degeneration in the leaner mutant mouse.
K Herrup, S L Wilczynski. Neuroscience 1982
144
18




Recovery from polyglutamine-induced neurodegeneration in conditional SCA1 transgenic mice.
Tao Zu, Lisa A Duvick, Michael D Kaytor, Michael S Berlinger, Huda Y Zoghbi, H Brent Clark, Harry T Orr. J Neurosci 2004
191
12

Behavioural characterisation of the robotic mouse mutant.
Peter L Oliver, David A Keays, Kay E Davies. Behav Brain Res 2007
17
12

Cerebellum and nonmotor function.
Peter L Strick, Richard P Dum, Julie A Fiez. Annu Rev Neurosci 2009
934
12


Clinical, genetic, molecular, and pathophysiological insights into spinocerebellar ataxia type 1.
Antoni Matilla-Dueñas, Robert Goold, Paola Giunti. Cerebellum 2008
67
12



Spinocerebellar ataxia 8: variable phenotype and unique pathogenesis.
Amitabh Gupta, Joseph Jankovic. Parkinsonism Relat Disord 2009
17
12

Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans.
Joyce van de Leemput, Jayanth Chandran, Melanie A Knight, Lynne A Holtzclaw, Sonja Scholz, Mark R Cookson, Henry Houlden, Katrina Gwinn-Hardy, Hon-Chung Fung, Xian Lin,[...]. PLoS Genet 2007
194
12

Bidirectional expression of the SCA8 expansion mutation: one mutation, two genes.
Yoshio Ikeda, Randy S Daughters, Laura P W Ranum. Cerebellum 2008
58
12

Molecular pathogenesis of spinocerebellar ataxias.
Antoni Matilla Dueñas, Robert Goold, Paola Giunti. Brain 2006
156
12

Ataxia with loss of Purkinje cells in a mouse model for Refsum disease.
Sacha Ferdinandusse, Anna W M Zomer, Jasper C Komen, Christina E van den Brink, Melissa Thanos, Frank P T Hamers, Ronald J A Wanders, Paul T van der Saag, Bwee Tien Poll-The, Pedro Brites. Proc Natl Acad Sci U S A 2008
76
12

Molecular genetics and biomarkers of polyglutamine diseases.
Masahisa Katsuno, Haruhiko Banno, Keisuke Suzuki, Yu Takeuchi, Motoshi Kawashima, Fumiaki Tanaka, Hiroaki Adachi, Gen Sobue. Curr Mol Med 2008
36
12

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
55
12


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
12

Presynaptic failure of neuromuscular transmission and synaptic remodeling in EA2.
R A Maselli, J Wan, V Dunne, M Graves, R W Baloh, R L Wollmann, J Jen. Neurology 2003
30
12


The genetic spectrum of a population-based sample of familial hemiplegic migraine.
L L Thomsen, M Kirchmann, A Bjornsson, H Stefansson, R M Jensen, A C Fasquel, H Petursson, M Stefansson, M L Frigge, A Kong,[...]. Brain 2007
100
12

Mouse Zic1 is involved in cerebellar development.
J Aruga, O Minowa, H Yaginuma, J Kuno, T Nagai, T Noda, K Mikoshiba. J Neurosci 1998
150
12

Motor coordination impairment in aged heterozygous rolling Nagoya, Cav2.1 mutant mice.
Eiki Takahashi, Kimie Niimi, Chitoshi Itakura. Brain Res 2009
25
12

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
50
12

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