The DOI matches its Crossref record; 10 of the 10 references it cites were found in a registry or an index.
Role of primate basal ganglia and frontal cortex in the internal generation of movements: III. Neuronal activity in the supplementary motor area
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Citations
Cites
Parallel organization of functionally segregated circuits linking basal ganglia and cortex
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Unconscious cerebral initiative and the role of conscious will in voluntary action
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Responses of monkey dopamine neurons during learning of behavioral reactions
Ljungberg, T., Apicella, P., & Schultz, W. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.67.1.145 · Cited by 987
Self-citationThe orbitofrontal cortex: Neuronal activity in the behaving monkey
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The cingulate gyrus and human behaviour
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“They do not show comparable premovement activity (Romo and Schultz 1990) and thus do not actively participate in the development of preparatory activity in loops.”
BackgroundSelf-citationSchultz, W., & Romo, R. (1990) · Journal of Neurophysiology · doi:10.1152/jn.1990.63.3.607 · Cited by 334
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The distinct modes of vision offered by feedforward and recurrent processing
Lamme, V. A. F., & Roelfsema, P. R. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01657-x · Cited by 2,338
Multiple dopamine functions at different time courses
Schultz, W. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135722 · Cited by 1,415
Self-citationSchultz, W., Apicella, P., & Ljungberg, T. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-03-00900.1993 · Cited by 1,291
Self-citationNeuronal Reward and Decision Signals: From Theories to Data
Schultz, W. (2015) · Physiological Reviews · doi:10.1152/physrev.00023.2014 · Cited by 1,126
Self-citationDiamond, A. (2000) · Child Development · doi:10.1111/1467-8624.00117 · Cited by 1,175
Reward processing in primate orbitofrontal cortex and basal ganglia
Schultz, W. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.272 · Cited by 942
Self-citationNeuronal correlates of parametric working memory in the prefrontal cortex
Romo, R., Brody, C. D., Hernández, A., & Lemus, L. (1999) · Nature · doi:10.1038/20939 · Cited by 822
Self-citationComputation Through Neural Population Dynamics
Vyas, S., Golub, M. D., Sussillo, D., & Shenoy, K. V. (2020) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-092619-094115 · Cited by 671
Postuma, R. B., & Dagher, A. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhj088 · Cited by 579
Influence of Reward Expectation on Behavior-Related Neuronal Activity in Primate Striatum
Hollerman, J. R., Tremblay, L., & Schultz, W. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.2.947 · Cited by 380
Self-citationThe role of the striatum in social behavior
Báez-Mendoza, R., & Schultz, W. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00233 · Cited by 312
Self-citationWhat, If, and When to Move: Basal Ganglia Circuits and Self-Paced Action Initiation
Klaus, A., Alves da Silva, J., & Costa, R. M. (2019) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-072116-031033 · Cited by 284
Striatal mechanisms underlying movement, reinforcement, and punishment
Kravitz, A. V., & Kreitzer, A. C. (2012) · Physiology · doi:10.1152/physiol.00004.2012 · Cited by 224
A neural mechanism for sensing and reproducing a time interval
Jazayeri, M., & Shadlen, M. N. (2015) · Current Biology · doi:10.1016/j.cub.2015.08.038 · Cited by 210
In vivo intracellular recording and perturbation of persistent activity in a neural integrator
Aksay, E., Gamkrelidze, G., Seung, H. S., Baker, R., & Tank, D. W. (2001) · Nature Neuroscience · doi:10.1038/84023 · Cited by 201
A cognitive signal for the proactive timing of action in macaque LIP
Maimon, G., & Assad, J. A. (2006) · Nature Neuroscience · doi:10.1038/nn1716 · Cited by 185
Individual Differences in Premotor Brain Systems Underlie Behavioral Apathy
Bonnelle, V., Manohar, S., Behrens, T., & Husain, M. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv247 · Cited by 163
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Smaers, J. B., Schleicher, A., Zilles, K., & Vinicius, L. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009123 · Cited by 81
Differentiating SCT and inattentive symptoms in ADHD using fMRI measures of cognitive control
Fassbender, C., Krafft, C. E., & Schweitzer, J. B. (2015) · NeuroImage: Clinical · doi:10.1016/j.nicl.2015.05.007 · Cited by 72
Extended LATER model can account for trial-by-trial variability of both pre- and post-processes
Nakahara, H., Nakamura, K., & Hikosaka, O. (2006) · Neural Networks · doi:10.1016/j.neunet.2006.07.001 · Cited by 45
Ramp-to-threshold dynamics in a hindbrain population controls the timing of spontaneous saccades
Ramirez, A. D., & Aksay, E. R. F. (2021) · Nature Communications · doi:10.1038/s41467-021-24336-w · Cited by 24
Pre-motion positivity during self-paced movements of finger and mouth
Bortoletto, M., Sarlo, M., Poli, S., & Stegagno, L. (2006) · NeuroReport · doi:10.1097/01.wnr.0000221830.95598.ea · Cited by 9
Metadata
- Authors
- Romo, R., & Schultz, W.
- Venue
- Experimental Brain Research
- Published
- 1992-11
- Volume
- 91
- Issue
- 3
- Pages
- 396-407
- ISSN
- 0014-4819 (ISSN-L)
- 1432-1106
- OpenAlex
- W1579888686
- Cited by
- 270
- References
- 10
- FWCI
- 2.63
- Type
- journal article
- Language
- en
- Open access
- closed
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
