A citation-based method for searching scientific literature

Robert S Raike, Catherine Weisz, Freek E Hoebeek, Matthew C Terzi, Chris I De Zeeuw, Arn M van den Maagdenberg, H A Jinnah, Ellen J Hess. Neurobiol Dis 2013
Times Cited: 17







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



Times Cited
  Times     Co-cited
Similarity


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
47

Abnormal cerebellar signaling induces dystonia in mice.
Carolyn E Pizoli, H A Jinnah, Melvin L Billingsley, Ellen J Hess. J Neurosci 2002
113
41

The neural substrates of rapid-onset Dystonia-Parkinsonism.
D Paola Calderon, Rachel Fremont, Franca Kraenzlin, Kamran Khodakhah. Nat Neurosci 2011
148
41

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
35

Limited regional cerebellar dysfunction induces focal dystonia in mice.
Robert S Raike, Carolyn E Pizoli, Catherine Weisz, Arn M J M van den Maagdenberg, H A Jinnah, Ellen J Hess. Neurobiol Dis 2013
48
35


Hereditary dystonia as a neurodevelopmental circuit disorder: Evidence from neuroimaging.
Martin Niethammer, Maren Carbon, Miklos Argyelan, David Eidelberg. Neurobiol Dis 2011
111
29

Cerebellothalamocortical pathway abnormalities in torsinA DYT1 knock-in mice.
Aziz M Uluğ, An Vo, Miklos Argyelan, Lauren Tanabe, Wynne K Schiffer, Stephen Dewey, William T Dauer, David Eidelberg. Proc Natl Acad Sci U S A 2011
84
29



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
194
29

The functional neuroanatomy of dystonia.
Vladimir K Neychev, Robert E Gross, Stephane Lehéricy, Ellen J Hess, H A Jinnah. Neurobiol Dis 2011
266
29


KCa channels as therapeutic targets in episodic ataxia type-2.
Karina Alviña, Kamran Khodakhah. J Neurosci 2010
74
29

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
200
29

Altered dendritic morphology of Purkinje cells in Dyt1 ΔGAG knock-in and purkinje cell-specific Dyt1 conditional knockout mice.
Lin Zhang, Fumiaki Yokoi, Yuan-Hu Jin, Mark P DeAndrade, Kenji Hashimoto, David G Standaert, Yuqing Li. PLoS One 2011
50
23


The cerebellum communicates with the basal ganglia.
Eiji Hoshi, Léon Tremblay, Jean Féger, Peter L Carras, Peter L Strick. Nat Neurosci 2005
492
23



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
196
23

Prolonged generalized dystonia after chronic cerebellar application of kainic acid.
Daniel Alvarez-Fischer, Michael Grundmann, Lixia Lu, Birgit Samans, Brita Fritsch, J Carsten Möller, Martin K-H Schaefer, Andreas Hartmann, Wolfgang H Oertel, Oliver Bandmann. Brain Res 2012
23
23

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
225
23


CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
136
23

Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.
Sanjeev Rajakulendran, Diego Kaski, Michael G Hanna. Nat Rev Neurol 2012
88
23

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
23

Paroxysmal dyskinesias in mice.
Thomas L Shirley, Lekha M Rao, Ellen J Hess, H A Jinnah. Mov Disord 2008
32
23

IP3R1 deficiency in the cerebellum/brainstem causes basal ganglia-independent dystonia by triggering tonic Purkinje cell firings in mice.
Chihiro Hisatsune, Hiroyuki Miyamoto, Moritoshi Hirono, Naohide Yamaguchi, Takeyuki Sugawara, Naoko Ogawa, Etsuko Ebisui, Toshio Ohshima, Masahisa Yamada, Takao K Hensch,[...]. Front Neural Circuits 2013
33
23

Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia.
Chang-Hyun Song, Xueliang Fan, Cicely J Exeter, Ellen J Hess, H A Jinnah. Neurobiol Dis 2012
72
17



The anatomical basis of symptomatic hemidystonia.
C D Marsden, J A Obeso, J J Zarranz, A E Lang. Brain 1985
509
17

Neuropathology of cervical dystonia.
C N Prudente, C A Pardo, J Xiao, J Hanfelt, E J Hess, M S Ledoux, H A Jinnah. Exp Neurol 2013
79
17

Structural, functional and molecular imaging of the brain in primary focal dystonia--a review.
E Zoons, J Booij, A J Nederveen, J M Dijk, M A J Tijssen. Neuroimage 2011
95
17

Caytaxin deficiency causes generalized dystonia in rats.
Jianfeng Xiao, Mark S Ledoux. Brain Res Mol Brain Res 2005
30
17


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
17

Neurophysiological evidence for cerebellar dysfunction in primary focal dystonia.
J T H Teo, B P C van de Warrenburg, S A Schneider, J C Rothwell, K P Bhatia. J Neurol Neurosurg Psychiatry 2009
81
17

Animal models for dystonia.
Bethany K Wilson, Ellen J Hess. Mov Disord 2013
37
17

The anatomical basis of dystonia: current view using neuroimaging.
Stéphane Lehéricy, Marina A J Tijssen, Marie Vidailhet, Ryuji Kaji, Sabine Meunier. Mov Disord 2013
117
17

Structural abnormalities in the cerebellum and sensorimotor circuit in writer's cramp.
C Delmaire, M Vidailhet, A Elbaz, F Bourdain, J P Bleton, S Sangla, S Meunier, A Terrier, S Lehéricy. Neurology 2007
122
17

Episodic ataxias 1 and 2.
Robert W Baloh. Handb Clin Neurol 2012
22
17

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
61
17

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
146
17

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
17

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
17

Phenomenology and classification of dystonia: a consensus update.
Alberto Albanese, Kailash Bhatia, Susan B Bressman, Mahlon R Delong, Stanley Fahn, Victor S C Fung, Mark Hallett, Joseph Jankovic, Hyder A Jinnah, Christine Klein,[...]. Mov Disord 2013
17

TorsinA hypofunction causes abnormal twisting movements and sensorimotor circuit neurodegeneration.
Chun-Chi Liang, Lauren M Tanabe, Stephanie Jou, Frank Chi, William T Dauer. J Clin Invest 2014
93
17

Short latency cerebellar modulation of the basal ganglia.
Christopher H Chen, Rachel Fremont, Eduardo E Arteaga-Bracho, Kamran Khodakhah. Nat Neurosci 2014
152
17


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.