A citation-based method for searching scientific literature

Brandy E Fureman, H A Jinnah, Ellen J Hess. Pharmacol Biochem Behav 2002
Times Cited: 43







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



Times Cited
  Times     Co-cited
Similarity


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
55


Abnormal cerebellar signaling induces dystonia in mice.
Carolyn E Pizoli, H A Jinnah, Melvin L Billingsley, Ellen J Hess. J Neurosci 2002
112
37

Paroxysmal dyskinesias in mice.
Thomas L Shirley, Lekha M Rao, Ellen J Hess, H A Jinnah. Mov Disord 2008
32
50


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
30

Calcium channel agonists and dystonia in the mouse.
H A Jinnah, J P Sepkuty, T Ho, S Yitta, T Drew, J D Rothstein, E J Hess. Mov Disord 2000
43
30

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
30



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
270
27

The basal ganglia and cerebellum interact in the expression of dystonic movement.
Vladimir K Neychev, Xueliang Fan, V I Mitev, Ellen J Hess, H A Jinnah. Brain 2008
193
27


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
352
23

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
23

Benign paroxysmal torticollis of infancy: four new cases and linkage to CACNA1A mutation.
N J Giffin, S Benton, P J Goadsby. Dev Med Child Neurol 2002
97
23

Characterization of the rat mutant dystonic (dt): a new animal model of dystonia musculorum deformans.
J F Lorden, T W McKeon, H J Baker, N Cox, S U Walkley. J Neurosci 1984
69
23

Rodent models for dystonia research: characteristics, evaluation, and utility.
H A Jinnah, Ellen J Hess, Mark S Ledoux, Nutan Sharma, Mark G Baxter, Mahlon R Delong. Mov Disord 2005
53
23

Two novel CACNA1A gene mutations associated with episodic ataxia type 2 and interictal dystonia.
Sian D Spacey, Luke A Materek, Blajez I Szczygielski, Thomas D Bird. Arch Neurol 2005
43
23

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
20


Potassium channel blockers inhibit the triggers of attacks in the calcium channel mouse mutant tottering.
Catherine J C Weisz, Robert S Raike, Luis E Soria-Jasso, Ellen J Hess. J Neurosci 2005
48
20

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
198
20

The neural substrates of rapid-onset Dystonia-Parkinsonism.
D Paola Calderon, Rachel Fremont, Franca Kraenzlin, Kamran Khodakhah. Nat Neurosci 2011
145
20


Paroxysmal dyskinesias: clinical features and classification.
M Demirkiran, J Jankovic. Ann Neurol 1995
349
16

Spontaneous polyspike discharges in an epileptic mutant mouse (tottering).
B J Kaplan, T N Seyfried, G H Glaser. Exp Neurol 1979
62
16

Episodic movement disorders as channelopathies.
Kailash P Bhatia, Robert C Griggs, Louis J Ptáček. Mov Disord 2000
19
36


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
16

Selective elimination of cerebellar output in the genetically dystonic rat.
M S LeDoux, J F Lorden, J Meinzen-Derr. Brain Res 1995
41
17

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

Animal models of generalized dystonia.
Robert S Raike, H A Jinnah, Ellen J Hess. NeuroRx 2005
46
16

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
16

Neuroanatomical substrates for paroxysmal dyskinesia in lethargic mice.
Rajiv Devanagondi, Kiyoshi Egami, Mark S LeDoux, Ellen J Hess, H A Jinnah. Neurobiol Dis 2007
18
38

Cerebellothalamocortical connectivity regulates penetrance in dystonia.
Miklos Argyelan, Maren Carbon, Martin Niethammer, Aziz M Ulug, Henning U Voss, Susan B Bressman, Vijay Dhawan, David Eidelberg. J Neurosci 2009
195
16

Low-frequency oscillations in the cerebellar cortex of the tottering mouse.
Gang Chen, Laurentiu S Popa, Xinming Wang, Wangcai Gao, Justin Barnes, Claudia M Hendrix, Ellen J Hess, Timothy J Ebner. J Neurophysiol 2009
41
17

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
260
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


Paroxysmal dyskinesias in the lethargic mouse mutant.
Zubair Khan, H A Jinnah. J Neurosci 2002
19
31

The pathophysiology of primary dystonia.
A Berardelli, J C Rothwell, M Hallett, P D Thompson, M Manfredi, C D Marsden. Brain 1998
593
13

Functional brain networks in DYT1 dystonia.
D Eidelberg, J R Moeller, A Antonini, K Kazumata, T Nakamura, V Dhawan, P Spetsieris, D deLeon, S B Bressman, S Fahn. Ann Neurol 1998
223
13

The sz mutant hamster: a genetic model of epilepsy or of paroxysmal dystonia?
W Löscher, J E Fisher, D Schmidt, G Fredow, D Hönack, W B Iturrian. Mov Disord 1989
92
13

The metabolic topography of essential blepharospasm: a focal dystonia with general implications.
M Hutchinson, T Nakamura, J R Moeller, A Antonini, A Belakhlef, V Dhawan, D Eidelberg. Neurology 2000
108
13


Changes in perfusion pattern using ECD-SPECT indicate frontal lobe and cerebellar involvement in exercise-induced paroxysmal dystonia.
A Kluge, B Kettner, R Zschenderlein, D Sandrock, D L Munz, S Hesse, H Meierkord. Mov Disord 1998
43
13





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.