The phasic reward signal of primate dopamine neurons

A theory of Pavlovian conditioning : Variations in the effectiveness of reinforcement and nonreinforcement

Rescorla, R. A. (1972) · Medical Entomology and Zoology · Cited by 7,268 · see citing works

Classical conditioning II: Current research and theory.

Black, A. H., & Prokasy, W. F. (1972) · Appleton-Century-Crofts eBooks · Cited by 4,449 · see citing works

Toward a modern theory of adaptive networks: Expectation and prediction.

Sutton, R. S., & Barto, A. G. (1981) · Psychological Review · doi:10.1037/0033-295x.88.2.135 · Cited by 1,450 · see citing works

Responses of monkey dopamine neurons to reward and conditioned stimuli during successive steps of learning a delayed response task

Schultz, W., Apicella, P., & Ljungberg, T. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-03-00900.1993 · Cited by 1,291 · see citing works

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 · see citing works

Preferential activation of midbrain dopamine neurons by appetitive rather than aversive stimuli

Mirenowicz, J., & Schultz, W. (1996) · Nature · doi:10.1038/379449a0 · Cited by 829 · see citing works

Stress signalling pathways that impair prefrontal cortex structure and function

Arnsten, A. F. T. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2648 · Cited by 3,299 · see citing works

Autoradiographic localization of dopamine D1 and D2 receptors in rat nucleus accumbens: Resistance to differential rearing conditions

Bardo, M. T., & Hammer, R. P. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90226-e · Cited by 3,229 · see citing works

Addiction, Dopamine, and the Molecular Mechanisms of Memory

Berke, J. D., & Hyman, S. E. (2000) · Neuron · doi:10.1016/s0896-6273(00)81056-9 · Cited by 1,167 · see citing works

Cortico-Basal Ganglia Reward Network: Microcircuitry

Sesack, S. R., & Grace, A. A. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.93 · Cited by 985 · see citing works

The Neuropsychopharmacology of Fronto-Executive Function: Monoaminergic Modulation

Robbins, T. W., & Arnsten, A. F. T. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135535 · Cited by 957 · see citing works

Dopamine system dysregulation in major depressive disorders

Belujon, P., & Grace, A. A. (2017) · International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyx056 · Cited by 754 · see citing works

Reward‐Related Responses in the Human Striatum

DELGADO, M. R. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1390.002 · Cited by 736 · see citing works

Behavioral functions of the mesolimbic dopaminergic system: An affective neuroethological perspective

Alcaro, A., Huber, R., & Panksepp, J. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.07.014 · Cited by 614 · see citing works

Catecholamine modulation of prefrontal cortical cognitive function

Arnsten, A. F. T. (1998) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(98)01240-6 · Cited by 608 · see citing works

Integrating Memories in the Human Brain: Hippocampal-Midbrain Encoding of Overlapping Events

Daphna Shohamy, A., & Wagner, A. D. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.023 · Cited by 525 · see citing works

Neuromodulation of thought: flexibilities and vulnerabilities in prefrontal cortical network synapses

Arnsten, A. F. T., Wang, M. J., & Paspalas, C. D. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.038 · Cited by 538 · see citing works

Catecholamine Influences on Dorsolateral Prefrontal Cortical Networks

Arnsten, A. F. T. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.01.027 · Cited by 493 · see citing works

Reward-guided learning beyond dopamine in the nucleus accumbens: the integrative functions of cortico-basal ganglia networks

Yin, H. H., Ostlund, S. B., & Balleine, B. W. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06422.x · Cited by 416 · see citing works

Catecholamine influences on prefrontal cortical function: Relevance to treatment of attention deficit/hyperactivity disorder and related disorders

Arnsten, A. F. T., & Pliszka, S. R. (2011) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2011.01.020 · Cited by 383 · see citing works

Liking vs. wanting food: Importance for human appetite control and weight regulation

Finlayson, G., King, N. A., & Blundell, J. E. (2007) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2007.03.004 · Cited by 376 · see citing works

Attention-Deficit/Hyperactivity Disorder and Attention Networks

Bush, G. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.120 · Cited by 358 · see citing works

Dysfunctional reward processing in depression

Admon, R., & Pizzagalli, D. A. (2015) · Current Opinion in Psychology · doi:10.1016/j.copsyc.2014.12.011 · Cited by 343 · see citing works

Cingulate, Frontal, and Parietal Cortical Dysfunction in Attention-Deficit/Hyperactivity Disorder

Bush, G. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.01.022 · Cited by 304 · see citing works

Sufficiency of Mesolimbic Dopamine Neuron Stimulation for the Progression to Addiction

Pascoli, V., Terrier, J. E., Hiver, A., & Lüscher, C. (2015) · Neuron · doi:10.1016/j.neuron.2015.10.017 · Cited by 291 · see citing works

The Dopamine Hypothesis of Drug Addiction: Hypodopaminergic State

Melis, M., Spiga, S., & Diana, M. (2005) · International review of neurobiology · doi:10.1016/s0074-7742(05)63005-x · Cited by 271 · see citing works

<i>Neuronal Mechanisms Underlying Attention Deficit Hyperactivity Disorder</i>: <i>The Influence of Arousal on Prefrontal Cortical Function</i>

Brennan, A. R., & Arnsten, A. F. T. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1417.007 · Cited by 267 · see citing works

Pathophysiology of Parkinson's Disease: The MPTP Primate Model of the Human Disorder

Wichmann, T., & DeLong, M. R. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07477.x · Cited by 255 · see citing works

Mechanisms of Dopaminergic and Serotonergic Neurotransmission in Tourette Syndrome: Clues from an In Vivo Neurochemistry Study with PET

Wong, D. F., Brašić, J. R., Singer, H. S., Schretlen, D. J., Kuwabara, H., Zhou, Y., Nandi, A., Maris, M. A., Alexander, M., Ye, W., et al. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301528 · Cited by 253 · see citing works

Increased phasic dopamine signaling in the mesolimbic pathway during social defeat in rats

Anstrom, K. K., Miczek, K. A., & Budygin, E. A. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.03.023 · Cited by 246 · see citing works

Anhedonia and the Brain Reward Circuitry in Depression

Heshmati, M., & Russo, S. J. (2015) · Current Behavioral Neuroscience Reports · doi:10.1007/s40473-015-0044-3 · Cited by 236 · see citing works

From prediction error to psychosis: Ketamine as a pharmacological model of delusions

Corlett, P. R., Honey, G. D., & Fletcher, P. C. (2007) · Journal of Psychopharmacology · doi:10.1177/0269881107077716 · Cited by 227 · see citing works

Basal ganglia and dopamine contributions to probabilistic category learning

Daphna Shohamy, A., Myers, C. E., Kalanithi, J., & Gluck, M. A. (2007) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2007.07.008 · Cited by 216 · see citing works

Characterizing anhedonia: A systematic review of neuroimaging across the subtypes of reward processing deficits in depression

Borsini, A., Wallis, A. S. J., Zunszain, P., Pariante, C. M., & Kempton, M. J. (2020) · Cognitive, Affective, &amp; Behavioral Neuroscience · doi:10.3758/s13415-020-00804-6 · Cited by 207 · see citing works

Catecholamine and second messenger influences on prefrontal cortical networks of “representational knowledge”: a rational bridge between genetics and the symptoms of mental illness

Arnsten, A. F. T. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm033 · Cited by 200 · see citing works

Frontal Responses During Learning Predict Vulnerability to the Psychotogenic Effects of Ketamine: Linking Cognition, Brain Activity, and Psychosis

Corlett, P. R., Honey, G. D., Aitken, M. R. F., Dickinson, A., Shanks, D. R., Absalom, A. R., Lee, M., Pomarol-Clotet, E., Murray, G. K., McKenna, P. J., et al. (2006) · Archives of General Psychiatry · doi:10.1001/archpsyc.63.6.611 · Cited by 182 · see citing works

Medial prefrontal cortex and striatum mediate the influence of social comparison on the decision process

Bault, N., Joffily, M., Rustichini, A., & Coricelli, G. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1100892108 · Cited by 162 · see citing works

The ability of the mesocortical dopamine system to operate in distinct temporal modes

Lapish, C. C., Kroener, S., Durstewitz, D., Lavı́n, A., & Seamans, J. K. (2006) · Psychopharmacology · doi:10.1007/s00213-006-0527-8 · Cited by 153 · see citing works

Dopamine and addiction: what have we learned from 40 years of research

Solinas, M., Belujon, P., Fernagut, P., Jaber, M., & Thiriet, N. (2018) · Journal of Neural Transmission · doi:10.1007/s00702-018-1957-2 · Cited by 155 · see citing works

Dopamine’s Actions in Primate Prefrontal Cortex: Challenges for Treating Cognitive Disorders

Arnsten, A. F. T., Wang, M., & Paspalas, C. D. (2015) · Pharmacological Reviews · doi:10.1124/pr.115.010512 · Cited by 149 · see citing works

Beyond reward prediction errors: the role of dopamine in movement kinematics

Barter, J. W., Li, S., Lu, D., Bartholomew, R. A., Rossi, M. A., Shoemaker, C. T., Salas-Meza, D., Gaidis, E., & Yin, H. H. (2015) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2015.00039 · Cited by 137 · see citing works

The novelty exploration bonus and its attentional modulation☆

Krebs, R. M., Schott, B. H., Schütze, H., & Düzel, E. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.01.015 · Cited by 127 · see citing works

Central fatigue theory and endurance exercise: Toward an interoceptive model

McMorris, T., Barwood, M. J., & Corbett, J. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.03.024 · Cited by 131 · see citing works

Personality traits are differentially associated with patterns of reward and novelty processing in the human substantia nigra/ventral tegmental area

Krebs, R. M., Schott, B. H., & Düzel, E. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.08.019 · Cited by 129 · see citing works

Ventral Pallidal Representation of Pavlovian Cues and Reward: Population and Rate Codes

Tindell, A. J., Berridge, K. C., & Aldridge, J. W. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1437-03.2004 · Cited by 128 · see citing works

The heterogeneity of ventral tegmental area neurons: Projection functions in a mood-related context

Walsh, J. J., & Han, M. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.06.006 · Cited by 106 · see citing works

Psychostimulants and motivated behavior: Arousal and cognition

Berridge, C. W., & Arnsten, A. F. T. (2013) · Neuroscience &amp; Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.11.005 · Cited by 104 · see citing works

The Cognitive Neuroscience of Motivation and Learning

Daw, N. D., & Daphna Shohamy, A. (2008) · Social Cognition · doi:10.1521/soco.2008.26.5.593 · Cited by 103 · see citing works

Which Way Do I Go? Neural Activation in Response to Feedback and Spatial Processing in a Virtual T-Maze

Baker, T. E., & Holroyd, C. B. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn223 · Cited by 96 · see citing works

Differential actions of dizocilpine (MK-801) on the mesolimbic and mesocortical dopamine systems: role of neuronal activity

Mathé, J. M., Nomikos, G. G., Blakeman, K. H., & Svensson, T. H. (1999) · Neuropharmacology · doi:10.1016/s0028-3908(98)00163-4 · Cited by 99 · see citing works

Dopamine System Dysregulation by the Ventral Subiculum as the Common Pathophysiological Basis for Schizophrenia Psychosis, Psychostimulant Abuse, and Stress

Grace, A. A. (2010) · Neurotoxicity Research · doi:10.1007/s12640-010-9154-6 · Cited by 96 · see citing works

Linking neuroscience with modern concepts of impulse control disorders in Parkinson's disease

Napier, T. C., Corvol, J., Grace, A. A., Roitman, J. D., Rowe, J. B., Voon, V., & Strafella, A. P. (2014) · Movement Disorders · doi:10.1002/mds.26068 · Cited by 94 · see citing works

The infralimbic cortex bidirectionally modulates mesolimbic dopamine neuron activity via distinct neural pathways

Patton, M. H., Bizup, B. T., & Grace, A. A. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.2449-13.2013 · Cited by 94 · see citing works

Dopaminergic Enhancement of Cognitive Function

Mehta, M. A., & Riedel, W. J. (2006) · Current Pharmaceutical Design · doi:10.2174/138161206777698891 · Cited by 91 · see citing works

The basal ganglia: anatomy, physiology, and pharmacology

Tisch, S. H., Silberstein, P., Limousin, P. D., & Jahanshahi, M. (2004) · Psychiatric Clinics of North America · doi:10.1016/j.psc.2004.06.004 · Cited by 92 · see citing works

Modulatory effects of cannabinoids on brain neurotransmission

Cohen, K., Weizman, A., & Weinstein, A. M. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14407 · Cited by 92 · see citing works

Peroxisome Proliferator-Activated Receptors-Alpha Modulate Dopamine Cell Activity Through Nicotinic Receptors

Melis, M., Carta, S., Fattore, L., Tolu, S., Yasar, S., Goldberg, S. R., Fratta, W., Maskos, U., & Pistis, M. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.04.016 · Cited by 89 · see citing works

Handbook of Reward and Decision Making

Dreher, J., & Tremblay, L. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374620-7.x0001-5 · Cited by 88 · see citing works

Neurobiology of ADHD: A Review

Mehta, T., Monegro, A. F., Nene, Y., Fayyaz, M., & Bollu, P. C. (2019) · Current Developmental Disorders Reports · doi:10.1007/s40474-019-00182-w · Cited by 86 · see citing works

The use of α-2A adrenergic agonists for the treatment of attention-deficit/hyperactivity disorder

Arnsten, A. (2010) · Expert Review of Neurotherapeutics · doi:10.1586/ern.10.133 · Cited by 80 · see citing works

Molecular Influences on Working Memory Circuits in Dorsolateral Prefrontal Cortex

Arnsten, A. F. T., & Jin, L. E. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-420170-5.00008-8 · Cited by 79 · see citing works

The role of the cerebellum in preparing responses to predictable sensory events

Nixon, P. D. (2003) · The Cerebellum · doi:10.1080/14734220309410 · Cited by 80 · see citing works

Instrumental learning in hyperdopaminergic mice

Yin, H. H., Zhuang, X., & Balleine, B. W. (2006) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.12.001 · Cited by 77 · see citing works

Dopamine vs Noradrenaline: Inverted-U Effects and ADHD Theories

Lévy, F. (2009) · Australian & New Zealand Journal of Psychiatry · doi:10.1080/00048670802607238 · Cited by 77 · see citing works

Loss of UBE3A from TH-expressing neurons suppresses GABA co-release and enhances VTA-NAc optical self-stimulation

Wallace, J. B., Stamatakis, A. M., Kantak, P. A., McElligott, Z. A., Judson, M. C., Aita, M., Rougié, M., Stuber, G. D., & Philpot, B. D. (2016) · Nature Communications · doi:10.1038/ncomms10702 · Cited by 76 · see citing works

Neural systems analysis of decision making during goal-directed navigation

Penner, M. R., & Mizumori, S. J. Y. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.08.010 · Cited by 72 · see citing works

GABAergic circuits in the basal ganglia and movement disorders

Galván, A., & Wichmann, T. (2007) · Progress in brain research · doi:10.1016/s0079-6123(06)60017-4 · Cited by 70 · see citing works

Roles of centromedian parafascicular nuclei of thalamus and cholinergic interneurons in the dorsal striatum in associative learning of environmental events

Yamanaka, K., Hori, Y., Minamimoto, T., Yamada, H., Matsumoto, N., Enomoto, K., Aosaki, T., Graybiel, A. M., & Kimura, M. (2017) · Journal of Neural Transmission · doi:10.1007/s00702-017-1713-z · Cited by 67 · see citing works

Neural signals of extinction in the inhibitory microcircuit of the ventral midbrain

Pan, W. X., Brown, J., & Dudman, J. T. (2012) · Nature Neuroscience · doi:10.1038/nn.3283 · Cited by 65 · see citing works

Role of tonically-active neurons in the control of striatal function: Cellular mechanisms and behavioral correlates

Pisani, A., Bonsi, P., Picconi, B., Tolu, M., Giacomini, P., & Scarnati, E. (2001) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(00)00153-6 · Cited by 65 · see citing works

The Role of Feedback in Learning and Motivation

Tricomi, E. M., & DePasque, S. (2016) · Advances in motivation and achievement · doi:10.1108/s0749-742320160000019015 · Cited by 68 · see citing works

Momentary reward induce changes in excitability of primary motor cortex

Thabit, M. N., Nakatsuka, M., Koganemaru, S., Fawi, G., Fukuyama, H., & Mima, T. (2011) · Clinical Neurophysiology · doi:10.1016/j.clinph.2011.02.021 · Cited by 59 · see citing works

Decision neuroscience: neuroeconomics

Smith, D. V., & Huettel, S. A. (2010) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.73 · Cited by 62 · see citing works

Integration of reward signalling and appetite regulating peptide systems in the control of food‐cue responses

Reichelt, A. C., Westbrook, R. F., & Morris, M. J. (2015) · British Journal of Pharmacology · doi:10.1111/bph.13321 · Cited by 62 · see citing works

Catecholamine receptors differentially mediate impulsive choice in the medial prefrontal and orbitofrontal cortex

Pardey, M. C., Kumar, N. N., Goodchild, A. K., & Cornish, J. L. (2012) · Journal of Psychopharmacology · doi:10.1177/0269881112465497 · Cited by 61 · see citing works

The effects of acute tyrosine and phenylalanine depletion on spatial working memory and planning in healthy volunteers are predicted by changes in striatal dopamine levels

Mehta, M. A., Gumaste, D., Montgomery, A. J., McTavish, S. F. B., & Grasby, P. M. (2005) · Psychopharmacology · doi:10.1007/s00213-004-2128-8 · Cited by 58 · see citing works

Research on eating disorders: current status and future prospects

Vitiello, B., & Lederhendler, I. I. (2000) · Biological Psychiatry · doi:10.1016/s0006-3223(99)00319-4 · Cited by 59 · see citing works

Physiology of the normal and dopamine-depleted basal ganglia: Insights into levodopa pharmacotherapy

Grace, A. A. (2008) · Movement Disorders · doi:10.1002/mds.22020 · Cited by 57 · see citing works

Ventral tegmental area dopamine projections to the hippocampus trigger long-term potentiation and contextual learning

Sayegh, F. J. P., Moulédous, L., Macri, C., Macedo, J. P., Lejards, C., Rampon, C., Verret, L., & Dahan, L. (2024) · Nature Communications · doi:10.1038/s41467-024-47481-4 · Cited by 54 · see citing works

The neural coding of expected and unexpected monetary performance outcomes: Dissociations between active and observational learning

Bellebaum, C., Jokisch, D., Gizewski, E. R., Forsting, M., & Daum, I. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.10.042 · Cited by 46 · see citing works

An extended reinforcement learning model of basal ganglia to understand the contributions of serotonin and dopamine in risk-based decision making, reward prediction, and punishment learning

Balasubramani, P. P., Chakravarthy, V. S., Ravindran, B., & Moustafa, A. A. (2014) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2014.00047 · Cited by 42 · see citing works

Dopaminergic Balance between Reward Maximization and Policy Complexity

Parush, N., Tishby, N., & Bergman, H. (2011) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2011.00022 · Cited by 37 · see citing works

Mesolimbic Dopamine and Habenulo-Interpeduncular Pathways in Nicotine Withdrawal

Dani, J. A., & De Biasi, M. (2013) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a012138 · Cited by 34 · see citing works

Acute D3 Antagonist GSK598809 Selectively Enhances Neural Response During Monetary Reward Anticipation in Drug and Alcohol Dependence

Platform, I., Murphy, A., Nestor, L. J., McGonigle, J., Paterson, L. M., Boyapati, V., Ersche, K. D., Flechais, R., Kuchibatla, S., Metastasio, A., et al. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2016.289 · Cited by 33 · see citing works

Erratum: Acute D3 Antagonist GSK598809 Selectively Enhances Neural Response During Monetary Reward Anticipation in Drug and Alcohol Dependence

Platform, I., Murphy, A., Nestor, L. J., McGonigle, J., Paterson, L. M., Boyapati, V., Ersche, K. D., Flechais, R., Kuchibatla, S., Metastasio, A., et al. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.99 · Cited by 33 · see citing works

The Neuroscience of Freedom and Creativity: Our Predictive Brain

Fuster, J. M. (2013) · Cited by 31 · see citing works

D1 Dopamine Receptor Activation Induces Neuronal eEF2 Pathway-Dependent Protein Synthesis

David, O., Barrera, I., Gould, N. L., Gal-Ben-Ari, S., & Rosenblum, K. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00067 · Cited by 29 · see citing works

Ameliorating prefrontal cortical dysfunction in mental illness: inhibition of phosphotidyl inositol-protein kinase C signaling

Arnsten, A. F. T. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1274-9 · Cited by 31 · see citing works

Neuronal activity in the subthalamic nucleus modulates the release of dopamine in the monkey striatum

Shimo, Y., & Wichmann, T. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06565.x · Cited by 30 · see citing works

Critical periods for the neurodevelopmental processes of externalizing and internalizing

Tucker, D. M., Poulsen, C., & Luu, P. (2015) · Development and Psychopathology · doi:10.1017/s0954579415000024 · Cited by 26 · see citing works

Processing of action- but not stimulus-related prediction errors differs between active and observational feedback learning

Kobza, S., & Bellebaum, C. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.10.036 · Cited by 23 · see citing works

Medial septum differentially regulates dopamine neuron activity in the rat ventral tegmental area and substantia nigra via distinct pathways

Bortz, D. M., & Grace, A. A. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0048-2 · Cited by 24 · see citing works

Different corticostriatal patterns of L-DOPA utilization in patients with untreated schizophrenia and patients treated with classical antipsychotics or clozapine.

Gefvert, O., Lindström, L., Waters, N., Waters, S., Carlsson, A., & Tedroff, J. (2003) · Scandinavian Journal of Psychology · doi:10.1111/1467-9450.00347 · Cited by 27 · see citing works

5.3 Dopamine’s Influence on Prefrontal Cortical Cognition: Actions and Circuits in Behaving Primates

Arnsten, A. F. T., Vijayraghavan, S., Wang, M., Gamo, N. J., & Paspalas, C. D. (2009) · Dopamine Handbook · doi:10.1093/acprof:oso/9780195373035.003.0016 · Cited by 23 · see citing works

α7 nicotinic receptor full agonist reverse basolateral amygdala hyperactivity and attenuation of dopaminergic neuron activity in rats exposed to chronic mild stress

Neves, G. A., & Grace, A. A. (2019) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2019.09.009 · Cited by 22 · see citing works

The incentive amplifying effects of nicotine are reduced by selective and non-selective dopamine antagonists in rats

Palmatier, M. I., Kellicut, M. R., Brianna Sheppard, A., Brown, R. W., & Robinson, D. L. (2014) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2014.08.012 · Cited by 21 · see citing works

Solving the Credit Assignment Problem With the Prefrontal Cortex

Stolyarova, A. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00182 · Cited by 22 · see citing works

Photoperiod Impacts Nucleus Accumbens Dopamine Dynamics

Jameson, A. N., Siemann, J. K., Melchior, J. R., Calipari, E. S., McMahon, D. G., & Grueter, B. A. (2023) · eNeuro · doi:10.1523/eneuro.0361-22.2023 · Cited by 19 · see citing works

Dopamine Neurons in the Ventral Tegmental Area: Drug-induced Synaptic Plasticity and Its Role in Relapse to Drug-seeking Behavior

Sun, W. (2011) · Current Drug Abuse Reviews · doi:10.2174/1874473711104040270 · Cited by 20 · see citing works

Cell-type specific increases in female hamster nucleus accumbens spine density following female sexual experience

Staffend, N. A., Hedges, V. L., Chemel, B. R., Watts, V. J., & Meisel, R. L. (2013) · Brain Structure and Function · doi:10.1007/s00429-013-0624-5 · Cited by 20 · see citing works

Changes in nucleus accumbens dopamine transmission associated with fixed‐ and variable‐time schedule‐induced feeding

Richardson, N. R., & Gratton, A. P. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06236.x · Cited by 19 · see citing works

Individual Differences in Impulsivity Predict Anticipatory Eye Movements

Cirilli, L., de Timary, P., Lefèvre, P., & Missal, M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026699 · Cited by 19 · see citing works

Pathophysiological Considerations in Basal Ganglia Surgery: Role of the Basal Ganglia in Hypokinetic and Hyperkinetic Movement Disorders

Wichmann, T., DeLong, M. R., & Vitek, J. L. (2000) · KARGER eBooks · doi:10.1159/000062035 · Cited by 19 · see citing works

Off the Beaten Path: Drug Addiction and the Pontine Laterodorsal Tegmentum

Kohlmeier, K. A. (2013) · ISRN Neuroscience · doi:10.1155/2013/604847 · Cited by 17 · see citing works

Effects of restraint and haloperidol on sensory gating in the midbrain of awake rats

Anstrom, K. K., Cromwell, H. C., & Woodward, D. J. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.01.060 · Cited by 16 · see citing works

Cost-benefit analysis: the first real rule of fight club?

Hillman, K. L. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00248 · Cited by 16 · see citing works

Preferential activation of midbrain dopamine neurons by appetitive rather than aversive stimuli

Mirenowicz, J., & Schultz, W. (1996) · Nature · doi:10.1038/379449a0 · Cited by 829 · see citing works

Adaptive Dopaminergic Neurons Report the Appetitive Value of Environmental Stimuli

Schultz, W. (1997) · Advances in psychology · doi:10.1016/s0166-4115(97)80103-3 · Cited by 7 · see citing works

Activity of dopamine neurons in the behaving primate

Schultz, W. (1992) · Seminars in Neuroscience · doi:10.1016/1044-5765(92)90011-p · Cited by 178 · see citing works

Dopamine signals for reward value and risk: basic and recent data

Schultz, W. (2010) · Behavioral and Brain Functions · doi:10.1186/1744-9081-6-24 · Cited by 653 · see citing works

Behavior-related activity of primate dopamine neurons.

Schultz, W. (1995) · PubMed · Cited by 74 · see citing works