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Encoding of action by the Purkinje cells of the cerebellum.
David J Herzfeld, Yoshiko Kojima, Robijanto Soetedjo, Reza Shadmehr. Nature 2015
Times Cited: 114






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List of co-cited articles
1293 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


A theory of cerebellar cortex.
D Marr. J Physiol 1969
1500
35
35

Encoding of error and learning to correct that error by the Purkinje cells of the cerebellum.
David J Herzfeld, Yoshiko Kojima, Robijanto Soetedjo, Reza Shadmehr. Nat Neurosci 2018
58
26
44

Distributed synergistic plasticity and cerebellar learning.
Zhenyu Gao, Boeke J van Beugen, Chris I De Zeeuw. Nat Rev Neurosci 2012
275
24
24

Internal models in the cerebellum.
D M Wolpert, R C Miall, M Kawato. Trends Cogn Sci 1998
951
21
21

Purkinje neuron synchrony elicits time-locked spiking in the cerebellar nuclei.
Abigail L Person, Indira M Raman. Nature 2011
178
18
18

Climbing fibers encode a temporal-difference prediction error during cerebellar learning in mice.
Shogo Ohmae, Javier F Medina. Nat Neurosci 2015
81
18
22

Timing Rules for Synaptic Plasticity Matched to Behavioral Function.
Aparna Suvrathan, Hannah L Payne, Jennifer L Raymond. Neuron 2016
70
18
25

Purkinje-cell plasticity and cerebellar motor learning are graded by complex-spike duration.
Yan Yang, Stephen G Lisberger. Nature 2014
92
18
19

Precise control of movement kinematics by optogenetic inhibition of Purkinje cell activity.
Shane A Heiney, Jinsook Kim, George J Augustine, Javier F Medina. J Neurosci 2014
127
17
17

Links from complex spikes to local plasticity and motor learning in the cerebellum of awake-behaving monkeys.
Javier F Medina, Stephen G Lisberger. Nat Neurosci 2008
162
16
16

Spatiotemporal firing patterns in the cerebellum.
Chris I De Zeeuw, Freek E Hoebeek, Laurens W J Bosman, Martijn Schonewille, Laurens Witter, Sebastiaan K Koekkoek. Nat Rev Neurosci 2011
224
16
16

Evolving Models of Pavlovian Conditioning: Cerebellar Cortical Dynamics in Awake Behaving Mice.
Michiel M ten Brinke, Henk-Jan Boele, Jochen K Spanke, Jan-Willem Potters, Katja Kornysheva, Peer Wulff, Anna C H G IJpelaar, Sebastiaan K E Koekkoek, Chris I De Zeeuw. Cell Rep 2015
99
15
15

Complex spike activity in the oculomotor vermis of the cerebellum: a vectorial error signal for saccade motor learning?
Robijanto Soetedjo, Yoshiko Kojima, Albert F Fuchs. J Neurophysiol 2008
71
14
19

Cerebellar modules operate at different frequencies.
Haibo Zhou, Zhanmin Lin, Kai Voges, Chiheng Ju, Zhenyu Gao, Laurens W J Bosman, Tom J H Ruigrok, Freek E Hoebeek, Chris I De Zeeuw, Martijn Schonewille. Elife 2014
137
14
14

Error correction, sensory prediction, and adaptation in motor control.
Reza Shadmehr, Maurice A Smith, John W Krakauer. Annu Rev Neurosci 2010
706
14
14

The cerebellum linearly encodes whisker position during voluntary movement.
Susu Chen, George J Augustine, Paul Chadderton. Elife 2016
34
14
41

Representation of limb kinematics in Purkinje cell simple spike discharge is conserved across multiple tasks.
Angela L Hewitt, Laurentiu S Popa, Siavash Pasalar, Claudia M Hendrix, Timothy J Ebner. J Neurophysiol 2011
44
13
29

Cerebellar complex spikes encode both destinations and errors in arm movements.
S Kitazawa, T Kimura, P B Yin. Nature 1998
222
13
13

Multiplexed coding by cerebellar Purkinje neurons.
Sungho Hong, Mario Negrello, Marc Junker, Aleksandra Smilgin, Peter Thier, Erik De Schutter. Elife 2016
25
13
52

Computational Principles of Supervised Learning in the Cerebellum.
Jennifer L Raymond, Javier F Medina. Annu Rev Neurosci 2018
46
13
28

Effects of lesions of the oculomotor vermis on eye movements in primate: saccades.
M Takagi, D S Zee, R J Tamargo. J Neurophysiol 1998
243
12
12

Encoding of movement time by populations of cerebellar Purkinje cells.
P Thier, P W Dicke, R Haas, S Barash. Nature 2000
97
12
12

Complex spike activity of purkinje cells in the oculomotor vermis during behavioral adaptation of monkey saccades.
Robijanto Soetedjo, Albert F Fuchs. J Neurosci 2006
73
12
16

Cerebellar contributions to adaptive control of saccades in humans.
Minnan Xu-Wilson, Haiyin Chen-Harris, David S Zee, Reza Shadmehr. J Neurosci 2009
111
12
12

Cerebellar granule cells acquire a widespread predictive feedback signal during motor learning.
Andrea Giovannucci, Aleksandra Badura, Ben Deverett, Farzaneh Najafi, Talmo D Pereira, Zhenyu Gao, Ilker Ozden, Alexander D Kloth, Eftychios Pnevmatikakis, Liam Paninski,[...]. Nat Neurosci 2017
74
12
16

Dynamic modulation of activity in cerebellar nuclei neurons during pavlovian eyeblink conditioning in mice.
Michiel M Ten Brinke, Shane A Heiney, Xiaolu Wang, Martina Proietti-Onori, Henk-Jan Boele, Jacob Bakermans, Javier F Medina, Zhenyu Gao, Chris I De Zeeuw. Elife 2017
39
12
30

Circuit mechanisms underlying motor memory formation in the cerebellum.
Ka Hung Lee, Paul J Mathews, Alexander M B Reeves, Katrina Y Choe, Shekib A Jami, Raul E Serrano, Thomas S Otis. Neuron 2015
70
12
17

Sensory prediction errors drive cerebellum-dependent adaptation of reaching.
Ya-Weng Tseng, Jörn Diedrichsen, John W Krakauer, Reza Shadmehr, Amy J Bastian. J Neurophysiol 2007
446
12
12

Force field effects on cerebellar Purkinje cell discharge with implications for internal models.
S Pasalar, A V Roitman, W K Durfee, T J Ebner. Nat Neurosci 2006
123
11
11

Widespread state-dependent shifts in cerebellar activity in locomoting mice.
Ilker Ozden, Daniel A Dombeck, Tycho M Hoogland, David W Tank, Samuel S-H Wang. PLoS One 2012
68
11
16

Integration of quanta in cerebellar granule cells during sensory processing.
Paul Chadderton, Troy W Margrie, Michael Häusser. Nature 2004
474
11
11

Synaptic diversity enables temporal coding of coincident multisensory inputs in single neurons.
François P Chabrol, Alexander Arenz, Martin T Wiechert, Troy W Margrie, David A DiGregorio. Nat Neurosci 2015
95
11
11

Cerebellar cortical organization: a one-map hypothesis.
Richard Apps, Richard Hawkes. Nat Rev Neurosci 2009
249
11
11

Changes in simple spike activity of some Purkinje cells in the oculomotor vermis during saccade adaptation are appropriate to participate in motor learning.
Yoshiko Kojima, Robijanto Soetedjo, Albert F Fuchs. J Neurosci 2010
56
11
19

Cerebellar-dependent motor learning is based on pruning a Purkinje cell population response.
Nicolas Catz, Peter W Dicke, Peter Thier. Proc Natl Acad Sci U S A 2008
90
11
12

Interacting adaptive processes with different timescales underlie short-term motor learning.
Maurice A Smith, Ali Ghazizadeh, Reza Shadmehr. PLoS Biol 2006
563
11
11

Cerebellum and nonmotor function.
Peter L Strick, Richard P Dum, Julie A Fiez. Annu Rev Neurosci 2009
845
11
11

Variation, signal, and noise in cerebellar sensory-motor processing for smooth-pursuit eye movements.
Javier F Medina, Stephen G Lisberger. J Neurosci 2007
81
11
13

Beyond parallel fiber LTD: the diversity of synaptic and non-synaptic plasticity in the cerebellum.
C Hansel, D J Linden, E D'Angelo. Nat Neurosci 2001
411
11
11

Dendritic excitation-inhibition balance shapes cerebellar output during motor behaviour.
Marta Jelitai, Paolo Puggioni, Taro Ishikawa, Arianna Rinaldi, Ian Duguid. Nat Commun 2016
42
11
26

Cerebellar granule cells encode the expectation of reward.
Mark J Wagner, Tony Hyun Kim, Joan Savall, Mark J Schnitzer, Liqun Luo. Nature 2017
171
11
11

Excitatory Cerebellar Nucleocortical Circuit Provides Internal Amplification during Associative Conditioning.
Zhenyu Gao, Martina Proietti-Onori, Zhanmin Lin, Michiel M Ten Brinke, Henk-Jan Boele, Jan-Willem Potters, Tom J H Ruigrok, Freek E Hoebeek, Chris I De Zeeuw. Neuron 2016
69
11
15

Dynamic organization of motor control within the olivocerebellar system.
J P Welsh, E J Lang, I Suglhara, R Llinás. Nature 1995
414
11
11

A cortico-cerebellar loop for motor planning.
Zhenyu Gao, Courtney Davis, Alyse M Thomas, Michael N Economo, Amada M Abrego, Karel Svoboda, Chris I De Zeeuw, Nuo Li. Nature 2018
79
11
13

Control of mental activities by internal models in the cerebellum.
Masao Ito. Nat Rev Neurosci 2008
559
10
10

Convergence of pontine and proprioceptive streams onto multimodal cerebellar granule cells.
Cheng-Chiu Huang, Ken Sugino, Yasuyuki Shima, Caiying Guo, Suxia Bai, Brett D Mensh, Sacha B Nelson, Adam W Hantman. Elife 2013
114
10
10

The cerebellar microcircuit as an adaptive filter: experimental and computational evidence.
Paul Dean, John Porrill, Carl-Fredrik Ekerot, Henrik Jörntell. Nat Rev Neurosci 2010
202
10
10

Synaptic representation of locomotion in single cerebellar granule cells.
Kate Powell, Alexandre Mathy, Ian Duguid, Michael Häusser. Elife 2015
60
10
16

The contribution of single synapses to sensory representation in vivo.
Alexander Arenz, R Angus Silver, Andreas T Schaefer, Troy W Margrie. Science 2008
129
10
10

Anatomical and physiological foundations of cerebellar information processing.
Richard Apps, Martin Garwicz. Nat Rev Neurosci 2005
284
10
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.

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