How Visual Stimuli Activate Dopaminergic Neurons at Short Latency

Predictive reward signal of dopamine neurons

Schultz, W. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.1.1 · Cited by 4,564

The rat nervous system

Paxinos, G. (1985) · Cited by 3,715

Discrete coding of reward probability and uncertainty by dopamine neurons

Fiorillo, C. D., Tobler, P. N., & Schultz, W. (2003) · Science · doi:10.1126/science.1077349 · Cited by 2,085

A framework for mesencephalic dopamine systems based on predictive Hebbian learning

Montague, P., Dayan, P., & Sejnowski, T. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-05-01936.1996 · Cited by 2,066

Neuronal Coding of Prediction Errors

Schultz, W., & Dickinson, A. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.473 · Cited by 1,427

Inducible and constitutive transcription factors in the mammalian nervous system: control of gene expression by Jun, Fos and Krox, and CREB/ATF proteins

Herdegen, T., & Leah, J. D. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(98)00018-6 · Cited by 1,369

Mesolimbocortical and nigrostriatal dopamine responses to salient non-reward events

Horvitz, J. C. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00019-1 · Cited by 967

Visual-Motor Function of the Primate Superior Colliculus

Wurtz, R. H., & Albano, J. E. (1980) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.03.030180.001201 · Cited by 904

Translation of sensory signals into commands for control of saccadic eye movements: role of primate superior colliculus

Sparks, D. L. (1986) · Physiological Reviews · doi:10.1152/physrev.1986.66.1.118 · Cited by 824

Uniform Inhibition of Dopamine Neurons in the Ventral Tegmental Area by Aversive Stimuli

Ungless, M. A., Magill, P. J., & Bolam, J. P. (2004) · Science · doi:10.1126/science.1093360 · Cited by 782

Amperometric Monitoring of Sensory-Evoked Dopamine Release in Awake Larval Zebrafish

Shang, C., Li, X., Chen, Y., Liu, B., Wang, Y., Zhou, Z., & Du, J. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3050-15.2015 · Cited by 11

Identifying non-toxic doses of manganese for manganese-enhanced magnetic resonance imaging to map brain areas activated by operant behavior in trained rats

Gálosi, R., Szalay, C., Aradi, M., Perlaki, G., Pál, J., Steier, R., Lénárd, L., & Karádi, Z. (2016) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2016.11.017 · Cited by 11

Human subcortical pathways automatically detect collision trajectory without attention and awareness

Guo, F., Zou, J., Wang, Y., Fang, B., Zhou, H., Wang, D., He, S., & Zhang, P. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002375 · Cited by 11

The path to learning: Action acquisition is impaired when visual reinforcement signals must first access cortex

Thirkettle, M., Walton, T., Shah, A., GURNEY, K. N., Redgrave, P., & Stafford, T. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.01.023 · Cited by 10

Intersection of effort and risk: ethological and neurobiological perspectives

Miller, M. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00208 · Cited by 11

Biological Cumulative Learning through Intrinsic Motivations: A Simulated Robotic Study on the Development of Visually-Guided Reaching.

Santucci, V. G., Baldassarre, G., & Mirolli, M. (2010) · Cited by 10

From hardware and software to kernels and envelopes: a concept shift for robotics, developmental psychology, and brain sciences

Kaplan, F., & Oudeyer, P. (2011) · Cambridge University Press eBooks · doi:10.1017/cbo9780511994838.011 · Cited by 10

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Jiang, H., Stein, B. E., & McHaffie, J. G. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.213553 · Cited by 10

Glutamate and dopamine in the VTA participate differently in the acute and chronic effect of methylphenidate

Floren, S. A., King, N., Carrasco, A., & Dafny, N. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112390 · Cited by 10

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Silkis, I. G. (2008) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-008-0057-4 · Cited by 10

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Weber, C., Elshaw, M., Wermter, S., Triesch, J., & Willmot, C. (2008) · doi:10.5772/5278 · Cited by 9

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Silkis, I. G. (2007) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-007-0082-8 · Cited by 9

Superior Colliculus Projections Drive Dopamine Neuron Activity and Movement But Not Value

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Auditory responses in a rodent model of Attention Deficit Hyperactivity Disorder

Brace, L. R., Kraev, I., Rostron, C. L., Stewart, M. G., Overton, P. G., & Dommett, E. J. (2015) · Brain Research · doi:10.1016/j.brainres.2015.09.038 · Cited by 8

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Takakuwa, N., Redgrave, P., & Isa, T. (2018) · Scientific Reports · doi:10.1038/s41598-018-33335-9 · Cited by 8

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Liss, B., & Roeper, J. (2009) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195373035.003.0009 · Cited by 8

Electrophysiological registration of phonological perception in the subthalamic nucleus of patients with Parkinson’s Disease

Letter, M. D., Aerts, A., Borsel, J. V., Vanhoutte, S., Taeye, L. D., Raedt, R., van Mierlo, P., Boon, P., Roost, D. V., & Santens, P. (2014) · Brain and Language · doi:10.1016/j.bandl.2014.08.008 · Cited by 7

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Sandberg, S. G., & Garris, P. A. (2010) · Frontiers in neuroscience · doi:10.1201/9781420007350-c3 · Cited by 7

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Li, P.-Y., Jing, M., Cun, X.-F., Wu, N., Li, J., & Song, R. (2024) · Neuroscience Letters · doi:10.1016/j.neulet.2024.137997 · Cited by 6

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Ihezie, S. A., Thomas, M. M., & Dafny, N. (2019) · Journal of Neural Transmission · doi:10.1007/s00702-018-1963-4 · Cited by 6

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Sandberg, S. G., & Garris, P. A. (2010) · CRC Press/Taylor & Francis, Boca Raton (FL) eBooks · Cited by 6

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Rossini, L., & Rossini, P. (2006) · Cited by 6

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Huang, X., Wang, S., Chen, Z., Qu, W., Song, L., Hu, Z., Xi, Y., Yang, Y., Hong, W.-H., Lin, S., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115865 · Cited by 5

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Pautrat, A., Tannir, R. A., Pernet‐Gallay, K., Soutrenon, R., Vendramini, E., Sinniger, V., Overton, P. G., Olivier David, A., & Coizet, V. (2023) · npj Parkinson s Disease · doi:10.1038/s41531-023-00516-x · Cited by 5

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Redgrave, P., Vautrelle, N., Overton, P. G., & Reynolds, J. N. J. (2016) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-802206-1.00034-9 · Cited by 5

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Stewart, R. D., & Dommett, E. J. (2006) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2006.08.010 · Cited by 5

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Savidge, L. E., & Bales, K. L. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105317 · Cited by 4

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Redgrave, P., Coizet, V., & Reynolds, J. N. J. (2010) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-374767-9.00031-7 · Cited by 4

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Visuomotor coordination and cognitive capacity in blindsight

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Turner, A. C., Kraev, I., Stewart, M., Stramek, A., Overton, P., & Dommett, E. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.05.033 · Cited by 2

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Vassilis Cutsuridis, A. (2008) · Lecture notes in computer science · doi:10.1007/978-3-540-87559-8_26 · Cited by 4

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Tobler, P. N., & Kobayashi, S. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374620-7.00002-9 · Cited by 4

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Solié, C., Contestabile, A., Espinosa, P., Musardo, S., Bariselli, S., Huber, C., Carleton, A., & Bellone, C. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/735340 · Cited by 4

The reasons for the preferable use of A2A receptor antagonists for improvement of locomotor activity and learning

Silkis, I. (2014) · Neurochemical Journal · doi:10.1134/s1819712414040072 · Cited by 3

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Berényi, A., Gombkötő, P., Farkas, Á., Paróczy, Z., Márkus, Z., Averkin, R. G., Benedek, G., & Nagy, A. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.07.031 · Cited by 3

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Aboitiz, F. (2008) · Springer eBooks · doi:10.1007/978-3-540-70573-4_10 · Cited by 3

The role of neural synchrony and rate in high-dimensional input systems. The Antennal Lobe: A case study

Lechón, M., Martinez, D., Verschure, P. F. M. J., & Badia, S. B. I. (2010) · International Joint Conference on Neural Networks (IJCNN) · doi:10.1109/ijcnn.2010.5596749 · Cited by 3

Sensory Reinforced Corticostriatal Plasticity

Vautrelle, N., Coizet, V., Leriche, M., Dahan, L., Schulz, J. M., Zhang, Y.-F., Zeghbib, A., Overton, P. G., Bracci, E., Redgrave, P., et al. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230801110359 · Cited by 3

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Zhang, Y.-F., & Reynolds, J. N. J. (2024) · Current Neuropharmacology · doi:10.2174/1570159x22666231115151403 · Cited by 2

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Watabe-Uchida, M., & Amo, R. (2025) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-443-29867-7.00009-8 · Cited by 3

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Coizet, V., Tannir, R. A., Pautrat, A., & Overton, P. G. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230818154903 · Cited by 2

Rapid dopaminergic signatures in movement: Reach vigor reflects reward prediction error and learned expectation

Korbisch, C. C., & Ahmed, A. A. (2026) · Science Advances · doi:10.1126/sciadv.adz9361 · Cited by 2

Cambios del EEG por habituación y condicionamiento en niños de tres a 15 años que acuden al Instituto Nacional de Rehabilitación (INR)

Brust-Carmona, H., Ramírez-Aboytes, F., Sánchez, A., Martínez, J., Miguel, Á. R., Flores-Ávalos, B., & Yáñez-Suárez, Ó. (2009) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · Cited by 2

Generation of Ponto-Geniculo-Occipital (PGO) Waves as a Possible Cause of Impairments to Visual Perception during Microsleep

Silkis, I. G. (2013) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-012-9701-0 · Cited by 2

Instrumental Conditioning Driven by Apparently Neutral Stimuli: A Model Tested with a Simulated Robotic Rat

Fiore, V. G., Mannella, F., Mirolli, M., Gurney, K. R., & Baldassarre, G. (2008) · Cited by 2

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Rashidi, M., Schmitgen, M. M., Weisbrod, M., Schnell, K., Wolf, R. C., & Whittington, M. A. (2021) · Journal of Neurophysiology · doi:10.1152/jn.00640.2020 · Cited by 2

The contribution of dopamine to the functioning of the hippocampus during spatial learning (a hypothetical mechanism)

Silkis, I. G. (2016) · Neurochemical Journal · doi:10.1134/s181971241601013x · Cited by 2

Lateral habenula neurons transmit negative value signals to midbrain dopamine neurons

Matsumoto, M. (2013) · Japanese Journal of Animal Psychology · doi:10.2502/janip.63.1.1 · Cited by 1

The superior colliculus gates dopamine responses to conditioned stimuli in visual classical conditioning

Zhang, Y.-F., Dufour, J.-P., Zatka-Haas, P., Redgrave, P., Black, M. J., Lak, A., Mann, E., Cragg, S. J., Abraham, W. C., & Reynolds, J. N. J. (2026) · Nature Communications · doi:10.1038/s41467-026-72167-4 · Cited by 1

Instrumentation for electrochemical performance characterization of neural electrodes

Marsh, M. P., Kruchowski, J., Hara, S. A., McIntosh, M. B., Forsman, R. M., Reed, T. L., Kimble, C. J., Lee, K. H., Bennet, K. E., & Tomshine, J. R. (2017) · Review of Scientific Instruments · doi:10.1063/1.4993796 · Cited by 1

Chronic amphetamine treatment affects collicular‐dependent behaviour

Turner, A. C., Stramek, A., Kraev, I., Stewart, M., Overton, P., & Dommett, E. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.01.028 · Cited by 2

Primate superior colliculus neurons activated by unexpected sensation

Mikulić, A., & Hoffmann, K. (2016) · Experimental Brain Research · doi:10.1007/s00221-016-4745-y · Cited by 1

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Smith, Y. (2011) · Parkinson s Disease · doi:10.1002/9781444397970.ch4 · Cited by 1

Untitled work

(2012) · Figshare

Dopamine Modulation of Choice Behavior Following Unexpected Reward Omission

Porter‐Stransky, K. A. (2014) · Deep Blue (University of Michigan)

Effets motivationnels de la nicotine chez le rat. Implication des endocannabinoïdes et d'autres systèmes de neurotransmission.

Forget, B. (2007) · HAL

Hypocretin (Orexin), Dopamine, and Goal-Directed Behavior

Muschamp, J. W. (2007)

Projeções diferenciadas da habênula lateral para o núcleo tegmental rostromedial e área tegmental ventral no rato.

Gonçalves, L. (2013) · doi:10.11606/t.42.2013.tde-20092013-105631

Cellular and Chemical Dynamics Within the Nucleus Accumbens During Reward-related Learning and Decision Making

Day, J. J. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/s1tk-dq52

Integration of appetitive and aversive reinforcers and the neuromodulation of reward seeking and pain avoidance

Ilango, A. (2010) · Digitalen Hochschulbibliothek Sachsen-Anhalt (Universitäts- und Landesbibliothek Sachsen-Anhalt) · doi:10.25673/5073

Anatomy and Synaptic Connectivity of the Basal Ganglia

Smith, Y. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4160-5316-3.00074-5

Obesity

Kral, J. G. (2005) · CRC Press eBooks · doi:10.3109/9780203025758-2

Chapter 19 Electrochemical Measurement of Neurochemical Concentrations

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Shah, A. (2014)

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Saites, L. (2018) · doi:10.21007/etd.cghs.201.0456

Faculty Opinions recommendation of Dopamine in motivational control: rewarding, aversive, and alerting.

Frank, M. J. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.7340957.7601055

Decision letter: Ventral striatum dopamine release encodes unique properties of visual stimuli in mice

(2023) · eLife · doi:10.7554/elife.85064.sa1

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Gonzalez, L. S., Fisher, A. A., Grover, K. E., & Robinson, J. E. (2025) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2025.1568878

Reward-associated cues reduce H-current amplitude in midbrain dopamine neurons

Calo‐Guadalupe, C., Bosque-Cordero, K. Y., Capella-Muñiz, J., Consuegra‐García, D., Vázquez‐Torres, R., Vélez‐Acevedo, O., Laboy-Juárez, K. J., Sanabria, P., & Jiménez‐Rivera, C. A. (2025) · Neuropharmacology · doi:10.1016/j.neuropharm.2025.110699

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Totah, N. K. B. (2012) · D-Scholarship@Pitt (University of Pittsburgh)

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Li, X., Zhang, J., & Wu, J. (2026) · Chinese Chemical Letters · doi:10.1016/j.cclet.2026.113404

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Whitaker, G. A., Poliakoff, E., Martin, S. L., Neill, J. C., Silverdale, M., Kobylecki, C., & El‐Deredy, W. (2026) · Experimental Brain Research · doi:10.1007/s00221-026-07355-1

Dopamine, Reward, and Attention

(2005) · Science s STKE · doi:10.1126/stke.2742005tw93

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Bertram, C., Dahan, L., Boorman, L. W., Harris, S., Vautrelle, N., Leriche, M., Redgrave, P., & Overton, P. G. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00329.2013 · Cited by 18

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Coizet, V., Comoli, E., Westby, G. W. M., & Redgrave, P. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02415.x · Cited by 70

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Bertram, C. (2011) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York)

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