Multiple Dopamine Functions at Different Time Courses

Theory of games and economic behavior

Garcia, S. R., & Miller, S. J. (2019) · American Mathematical Society eBooks · doi:10.1090/mbk/121/32 · Cited by 16,777

A neural substrate of prediction and reward

Schultz, W., Dayan, P., & Montague, P. R. (1997) · Science · doi:10.1126/science.275.5306.1593 · Cited by 9,388

Predictive reward signal of dopamine neurons

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

What is the role of dopamine in reward: hedonic impact, reward learning, or incentive salience?

Berridge, K. C., & Robinson, T. E. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(98)00019-8 · Cited by 4,127

Theory of Games and Economic Behavior

Hawkins, D. (1945) · Philosophy of Science · doi:10.1086/286866 · Cited by 3,970

A model for Pavlovian learning: Variations in the effectiveness of conditioned but not of unconditioned stimuli.

Pearce, J. M., & Hall, G. (1980) · Psychological Review · doi:10.1037/0033-295x.87.6.532 · Cited by 3,023

Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex

Funahashi, S., Bruce, C. J., & Goldman-Rakic, P. S. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.2.331 · Cited by 2,685

A primate model of parkinsonism: selective destruction of dopaminergic neurons in the pars compacta of the substantia nigra by N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine.

Burns, R. S., Chiueh, C. C., Markey, S. P., Ebert, M. H., Jacobowitz, D. M., & Kopin, I. J. (1983) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.80.14.4546 · Cited by 2,149

On the relations between the direction of two-dimensional arm movements and cell discharge in primate motor cortex

Georgopoulos, A. P., Kalaska, J. F., Caminiti, R., & Massey, J. (1982) · Journal of Neuroscience · doi:10.1523/jneurosci.02-11-01527.1982 · Cited by 2,133

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

The Neurobiology of Social Affiliation and Pair Bonding

Carter, C. S., & Keverne, E. B. (2009) · Elsevier eBooks · doi:10.1016/b978-008088783-8.00004-8 · Cited by 130

Molecular mechanisms of stress-induced prefrontal cortical impairment: Implications for mental illness

Hains, A. B., & Arnsten, A. F. T. (2008) · Learning & Memory · doi:10.1101/lm.921708 · Cited by 127

Simultaneous assessment of rodent behavior and neurochemistry using a miniature positron emission tomograph

Schulz, D., Southekal, S. S., Junnarkar, S. S., Pratte, J. ‐., Purschke, M. L., Stoll, S. P., Ravindranath, B., Maramraju, S. H., Krishnamoorthy, S., Henn, F. A., et al. (2011) · Nature Methods · doi:10.1038/nmeth.1582 · Cited by 127

Orexin/Hypocretin Modulates Response of Ventral Tegmental Dopamine Neurons to Prefrontal Activation: Diurnal Influences

Moorman, D. E., & Aston‐Jones, G. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2871-10.2010 · Cited by 129

Neural encoding of cocaine‐seeking behavior is coincident with phasic dopamine release in the accumbens core and shell

Owesson‐White, C. A., Ariansen, J., Stuber, G. D., Cleaveland, N. A., Cheer, J. F., Mark Wightman, R., & Carelli, R. M. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06916.x · Cited by 126

Dopamine synapse is a neuroligin-2–mediated contact between dopaminergic presynaptic and GABAergic postsynaptic structures

Uchigashima, M., Ohtsuka, T., Kobayashi, K., & Watanabe, M. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1514074113 · Cited by 126

Role of nicotinic acetylcholine receptors in regulating dopamine neuron activity

Faure, P., Tolu, S., Valverde, S., & Naudé, J. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.05.040 · Cited by 125

Presynaptic Opioid and Nicotinic Receptor Modulation of Dopamine Overflow in the Nucleus Accumbens

Britt, J. P., & McGehee, D. S. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4275-07.2008 · Cited by 130

The central executive as a search process: Priming exploration and exploitation across domains.

Hills, T. T., Todd, P. M., & Goldstone, R. L. (2010) · Journal of Experimental Psychology General · doi:10.1037/a0020666 · Cited by 133

What neurobiology cannot tell us about addiction

Kalant, H. (2009) · Addiction · doi:10.1111/j.1360-0443.2009.02739.x · Cited by 132

Striatum on the anxiety map: Small detours into adolescence

Lago, T. R., Davis, A. A., Grillon, C., & Ernst, M. (2016) · Brain Research · doi:10.1016/j.brainres.2016.06.006 · Cited by 128

Dynamic Nigrostriatal Dopamine Biases Action Selection

Howard, C. D., Li, H., Geddes, C. E., & Jin, X. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.029 · Cited by 125

Existing and future drugs for the treatment of the dark side of addiction

Koob, G. F., & Mason, B. J. (2016) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-010715-103143 · Cited by 121

Neuromodulation of Innate Behaviors in Drosophila

Kim, S. M., Su, C., & Wang, J. W. (2017) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-072116-031558 · Cited by 121

Task-related dissociation in ERN amplitude as a function of obsessive-compulsive symptoms

Gründler, T. O. J., Cavanagh, J. F., Figueroa, C. M., Frank, M. J., & Allen, J. J. B. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.03.010 · Cited by 119

Synaptic computation underlying probabilistic inference

Soltani, A., & Wang, X. (2009) · Nature Neuroscience · doi:10.1038/nn.2450 · Cited by 123

Convergent evidence for abnormal striatal synaptic plasticity in dystonia

Peterson, D. A., B, T. J. S. A., & Howard Poizner, A. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.12.003 · Cited by 120

The pharmacology of effort-related choice behavior: Dopamine, depression, and individual differences

Salamone, J. D., Correa, M., Yohn, S. E., López‐Cruz, L., Miguel, N. S., & Alatorre, L. F. (2016) · Behavioural Processes · doi:10.1016/j.beproc.2016.02.008 · Cited by 130

Tannic acid post-treatment of enzymatically crosslinked chitosan-alginate hydrogels for biomedical applications

Jafari, H., Ghaffari‐Bohlouli, P., Podstawczyk, D. A., Nie, L., & Shavandi, A. (2022) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2022.119844 · Cited by 117

Implantable microelectrode arrays for simultaneous electrophysiological and neurochemical recordings

Johnson, M. D., Franklin, R. K., Gibson, M. D., Brown, R. B., & Kipke, D. R. (2008) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2008.06.036 · Cited by 118

Convergent Processing of Both Positive and Negative Motivational Signals by the VTA Dopamine Neuronal Populations

Wang, D. V., & Tsien, J. Z. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017047 · Cited by 116

Impaired Neurocognitive Functions Affect Social Learning Processes in Oppositional Defiant Disorder and Conduct Disorder: Implications for Interventions

Matthys, W., Vanderschuren, L. J. M. J., Schutter, D. J. L. G., & Lochman, J. E. (2012) · Clinical Child and Family Psychology Review · doi:10.1007/s10567-012-0118-7 · Cited by 123

Dynamic mesolimbic dopamine signaling during action sequence learning and expectation violation

Collins, A. L., Greenfield, V. Y., Bye, J. K., Linker, K. E., Wang, A. S., & Wassum, K. M. (2016) · Scientific Reports · doi:10.1038/srep20231 · Cited by 125

Memory and Reward-Based Learning: A Value-Directed Remembering Perspective

Knowlton, B. J., & Castel, A. D. (2022) · Annual Review of Psychology · doi:10.1146/annurev-psych-032921-050951 · Cited by 115

Event-related EEG responses to anticipation and delivery of monetary and social reward

Flores, A., Münte, T. F., & Doñamayor, N. (2015) · Biological Psychology · doi:10.1016/j.biopsycho.2015.04.005 · Cited by 120

Habitual responding for alcohol depends upon both AMPA and D2 receptor signaling in the dorsolateral striatum

Corbit, L. H., Nie, H., & Janak, P. H. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00301 · Cited by 115

Tonic or Phasic Stimulation of Dopaminergic Projections to Prefrontal Cortex Causes Mice to Maintain or Deviate from Previously Learned Behavioral Strategies

Ellwood, I. T., Patel, T., Wadia, V., Lee, A. T., Liptak, A. T., Bender, K. J., & Sohal, V. S. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1221-17.2017 · Cited by 132

Why do we move to the beat? A multi-scale approach, from physical principles to brain dynamics

Damm, L., Varoqui, D., Cock, V. C. D., Bella, S. D., & Bardy, B. G. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.12.024 · Cited by 121

The Hippocampus and Nucleus Accumbens as Potential Therapeutic Targets for Neurosurgical Intervention in Schizophrenia

Mikell, C. B., McKhann, G. M., Segal, S., McGovern, R. A., Wallenstein, M. B., & Moore, H. M. (2009) · Stereotactic and Functional Neurosurgery · doi:10.1159/000225979 · Cited by 118

In Vivo Monitoring of Dopamine by Microdialysis with 1 min Temporal Resolution Using Online Capillary Liquid Chromatography with Electrochemical Detection

Gu, H. C., Varner, E. L., Groskreutz, S. R., Michael, A. C., & Weber, S. G. (2015) · Analytical Chemistry · doi:10.1021/acs.analchem.5b00633 · Cited by 113

A Paranigral VTA Nociceptin Circuit that Constrains Motivation for Reward

Parker, K. E., Pedersen, C. E., Gomez, A. M., Spangler, S. M., Walicki, M. C., Feng, S., Stewart, S., Otis, J. M., Al‐Hasani, R., McCall, J. G., et al. (2019) · Cell · doi:10.1016/j.cell.2019.06.034 · Cited by 113

Role for the Membrane Receptor Guanylyl Cyclase-C in Attention Deficiency and Hyperactive Behavior

Gong, R., Ding, C., Hu, J., Lu, Y., Liu, F., Mann, E. A., Xu, F., Cohen, M. B., & Luo, M. (2011) · Science · doi:10.1126/science.1207675 · Cited by 115

Divergent medial amygdala projections regulate approach–avoidance conflict behavior

Miller, S. M., Marcotulli, D., Shen, A., & Zweifel, L. S. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0337-z · Cited by 119

Drosophila D1 dopamine receptor mediates caffeine-induced arousal

Waldowski, R. A., Kim, Y.-C., Jones, F. S., Han, K., & Greenspan, R. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806776105 · Cited by 111

Modelling ADHD: A review of ADHD theories through their predictions for computational models of decision-making and reinforcement learning

Ziegler, S., Pedersen, M. L., Mowinckel, A. M., & Biele, G. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.09.002 · Cited by 110

GABAB Receptors in Reward Processes

Vlachou, S., & Markou, A. (2010) · Advances in pharmacology · doi:10.1016/s1054-3589(10)58013-x · Cited by 110

Dopaminergic Meso-Cortical Projections to M1: Role in Motor Learning and Motor Cortex Plasticity

Hosp, J. A., & Luft, A. R. (2013) · Frontiers in Neurology · doi:10.3389/fneur.2013.00145 · Cited by 110

Molecular substrates of action control in cortico-striatal circuits

Shiflett, M. W., & Balleine, B. W. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.05.007 · Cited by 120

Does the kappa opioid receptor system contribute to pain aversion?

Cahill, C. M., Taylor, A. M. W., Cook, C., Ong, E., Morón, J. A., & Evans, C. J. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00253 · Cited by 105

Genetic variation in dopamine moderates neural response during reward anticipation and delivery: Evidence from event‐related potentials

Foti, D., & Hajcak, G. (2012) · Psychophysiology · doi:10.1111/j.1469-8986.2011.01343.x · Cited by 109

Behavioral Phenotyping and Pathological Indicators of Parkinson's Disease in C. elegans Models

Maulik, M., Mitra, S., Bult‐Ito, A., Taylor, B. E., & Vayndorf, E. M. (2017) · Frontiers in Genetics · doi:10.3389/fgene.2017.00077 · Cited by 110

Altered function of ventral striatum during reward-based decision making in old age

Mell, T. (2009) · Frontiers in Human Neuroscience · doi:10.3389/neuro.09.034.2009 · Cited by 109

An integrative framework for perceptual disturbances in psychosis

Horga, G., & Abi-Dargham, A. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0234-1 · Cited by 103

Neuroanatomy of Dopamine: Reward and Addiction

Taber, K. H., Black, D. N., Porrino, L. J., & Hurley, R. A. (2012) · Journal of Neuropsychiatry · doi:10.1176/appi.neuropsych.24.1.1 · Cited by 111

Tracking tonic dopamine levels in vivo using multiple cyclic square wave voltammetry

Oh, Y., Heien, M. L., Park, C., Kang, Y. M., Kim, J., Boschen, S. L., Shin, H., Cho, H. U., Blaha, C. D., Bennet, K. E., et al. (2018) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2018.08.034 · Cited by 103

Cerebral interactions of pain and reward and their relevance for chronic pain

Becker, S., Gandhi, W., & Schweinhardt, P. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.03.013 · Cited by 103

The Feeling of Action Tendencies: On the Emotional Regulation of Goal-Directed Behavior

Lowe, R. J., & Ziemke, T. (2011) · Frontiers in Psychology · doi:10.3389/fpsyg.2011.00346 · Cited by 111

Motor signs in the prodromal phase of Parkinson's disease

Maetzler, W., & Hausdorff, J. M. (2012) · Movement Disorders · doi:10.1002/mds.24973 · Cited by 102

Multiphasic Temporal Dynamics in Responses of Midbrain Dopamine Neurons to Appetitive and Aversive Stimuli

Fiorillo, C. D., Song, M. R., & Yun, S. R. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3883-12.2013 · Cited by 98

Triple reuptake inhibitors for treating subtypes of major depressive disorder: the monoamine hypothesis revisited

Prins, J., Olivier, B., & Korte, S. M. (2011) · Expert Opinion on Investigational Drugs · doi:10.1517/13543784.2011.594039 · Cited by 106

Cognitive Neurostimulation: Learning to Volitionally Sustain Ventral Tegmental Area Activation

MacInnes, J., Dickerson, K. C., Chen, N., & Adcock, R. A. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.002 · Cited by 100

Probabilistic Reinforcement Learning in Patients With Schizophrenia: Relationships to Anhedonia and Avolition

Dowd, E. C., Frank, M. J., Collins, A. G. E., Gold, J. M., & Barch, D. M. (2016) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2016.05.005 · Cited by 101

Metaplasticity as a Neural Substrate for Adaptive Learning and Choice under Uncertainty

Farashahi, S. G., Donahue, C. H., Khorsand, P., Seo, H., Lee, D., & Soltani, A. (2017) · Neuron · doi:10.1016/j.neuron.2017.03.044 · Cited by 106

The role of dopamine in modulating the structure and function of striatal circuits

Surmeier, D. J., Shen, W., Day, M., Gertler, T. S., Chan, C. S., Tian, X., & Plotkin, J. L. (2010) · Progress in brain research · doi:10.1016/s0079-6123(10)83008-0 · Cited by 97

De Novo Expression of Dopamine D2 Receptors on Microglia after Stroke

Huck, J. H. J., Freyer, D., Böttcher, C., Mladinov, M., Muselmann, C., Thielke, M., Gladow, N., Bloomquist, D., Mergenthaler, P., & Priller, J. (2015) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2015.128 · Cited by 97

Individual dopamine midbrain neurons: Functional diversity and flexibility in health and disease

Liss, B., & Roeper, J. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.10.004 · Cited by 97

Reward Systems in the Brain and Nutrition

Rolls, E. T. (2016) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-071715-050725 · Cited by 102

Ventral striatal hypoactivation is associated with apathy but not diminished expression in patients with schizophrenia

Kirschner, M., Hager, O. M., Bischof, M., Hartmann-Riemer, M. N., Kluge, A., Seifritz, E., Tobler, P. N., & Kaiser, S. (2016) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.140383 · Cited by 96

Short-term atrazine exposure causes behavioral deficits and disrupts monoaminergic systems in male C57BL/6 mice

Lin, Z., Dodd, C. A., & Filipov, N. M. (2013) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2013.06.002 · Cited by 97

Value Learning through Reinforcement

Daw, N. D., & Tobler, P. N. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-416008-8.00015-2 · Cited by 109

Influence of Neuronal Nicotinic Receptors over Nicotine Addiction and Withdrawal

De Biasi, M., & Salas, R. (2008) · Experimental Biology and Medicine · doi:10.3181/0712-mr-355 · Cited by 95

O-GlcNAcylation regulates dopamine neuron function, survival and degeneration in Parkinson disease

Lee, B. E., Kim, H. Y., Kim, H., Jeong, H., Kim, B., Lee, H.-E., Lee, J., Kim, H. B., Lee, S. E., Yang, Y. R., et al. (2020) · Brain · doi:10.1093/brain/awaa320 · Cited by 97

Fast dopamine release events in the nucleus accumbens of early adolescent rats

Robinson, D. L., Zitzman, D. L., Smith, K. J., & Spear, L. P. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2010.12.016 · Cited by 94

Representing Something Out of Nothing: The Dawning of Zero

Nieder, A. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2016.08.008 · Cited by 94

Representation of Reward Feedback in Primate Auditory Cortex

Brosch, M., Selezneva, E., & Scheich, H. (2011) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2011.00005 · Cited by 94

The Role of Dopamine in the Prelimbic Cortex and the Dorsomedial Striatum in Instrumental Conditioning

Lex, B., & Hauber, W. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp151 · Cited by 100

RASGRF2 regulates alcohol-induced reinforcement by influencing mesolimbic dopamine neuron activity and dopamine release

Stacey, D., Bilbao, A., Maroteaux, M. J., Jia, T., Easton, A. C., Longueville, S., Nymberg, C., Banaschewski, T., Barker, G. J., Büchel, C., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1211844110 · Cited by 95

Measuring reinforcement learning and motivation constructs in experimental animals: Relevance to the negative symptoms of schizophrenia

Markou, A., Salamone, J. D., Bussey, T. J., Mar, A. C., Brunner, D., Gilmour, G., & Balsam, P. D. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.08.007 · Cited by 95

The neurotoxicology of uranium

Dinocourt, C., Legrand, M., Dublineau, I., & Lestaevel, P. (2015) · Toxicology · doi:10.1016/j.tox.2015.08.004 · Cited by 97

Why Should We Keep the Cerebellum in Mind When Thinking About Addiction?

Miquel, M., Toledo‐Cárdenas, M. R., García, L. I., Coria‐Ávila, G. A., & Manzo, J. (2009) · Current Drug Abuse Reviews · doi:10.2174/1874473710902010026 · Cited by 96

Explicit and implicit reinforcement learning across the psychosis spectrum.

Barch, D. M., Carter, C. S., Gold, J. M., Johnson, S. L., Kring, A. M., MacDonald, A. W., Pizzagalli, D. A., Ragland, J. D., Silverstein, S. M., & Strauss, M. E. (2017) · Journal of Abnormal Psychology · doi:10.1037/abn0000259 · Cited by 97

Direct in Vivo Electrochemical Detection of Resting Dopamine Using Poly(3,4-ethylenedioxythiophene)/Carbon Nanotube Functionalized Microelectrodes

Taylor, I. M., Patel, N., Freedman, N. C., Castagnola, E., & Cui, X. T. (2019) · Analytical Chemistry · doi:10.1021/acs.analchem.9b02904 · Cited by 93

Dopaminergic signals in primary motor cortex

Luft, A. R., & Schwarz, S. (2009) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2009.05.004 · Cited by 99

The role of state uncertainty in the dynamics of dopamine

Mikhael, J. G., Kim, H. R., Uchida, N., & Gershman, S. J. (2022) · Current Biology · doi:10.1016/j.cub.2022.01.025 · Cited by 88

Illicit dopamine transients: reconciling actions of abused drugs

Covey, D. P., Roitman, M. F., & Garris, P. A. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.02.002 · Cited by 90

Executive control of gaze by the frontal lobes

Schall, J. D., & Boucher, L. (2007) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/cabn.7.4.396 · Cited by 91

An n-3 fatty acid deficiency impairs rat spatial learning in the Barnes maze.

Fedorova, I., Hussein, N., Baumann, M. H., Martino, C., & Salem, N. (2009) · Behavioral Neuroscience · doi:10.1037/a0013801 · Cited by 97

Mesolimbic Dopamine Transients in Motivated Behaviors: Focus on Maternal Behavior

Robinson, D. L., Zitzman, D. L., & Williams, S. K. (2011) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2011.00023 · Cited by 89

Recent advances in understanding the role of phasic dopamine activity

Schultz, W. (2019) · F1000Research · doi:10.12688/f1000research.19793.1 · Cited by 94

NF-κB in neurodegenerative diseases: Recent evidence from human genetics

Kaltschmidt, B., Helweg, L. P., Greiner, J. F. W., & Kaltschmidt, C. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.954541 · Cited by 92

Genetic Variability in the Dopamine System (Dopamine Receptor D4, Catechol-O-Methyltransferase) Modulates Neurophysiological Responses to Gains and Losses

Marco‐Pallarés, J., Cucurell, D., Toni Cunillera, B., Krämer, U. M., Càmara, E., Nager, W., Bauer, P., Schüle, R., Schöls, L. J., Münte, T. F., et al. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.01.006 · Cited by 92

The coaction of tonic and phasic dopamine dynamics

Atcherley, C. W., Wood, K. M., Parent, K. L., Hashemi, P., & Heien, M. L. (2014) · Chemical Communications · doi:10.1039/c4cc06165a · Cited by 89

Dopamine Receptors Differentially Enhance Rule Coding in Primate Prefrontal Cortex Neurons

Ott, T., Jacob, S. N., & Nieder, A. (2014) · Neuron · doi:10.1016/j.neuron.2014.11.012 · Cited by 93

Dopamine Modulation of Prefrontal Cortex Activity Is Manifold and Operates at Multiple Temporal and Spatial Scales

Lohani, S., Martig, A. K., Deisseroth, K. A., Witten, I. B., & Moghaddam, B. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.03.012 · Cited by 99

To Choose or to Avoid: Age Differences in Learning from Positive and Negative Feedback

Eppinger, B., & Kray, J. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21364 · Cited by 88

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

Task-Load-Dependent Activation of Dopaminergic Midbrain Areas in the Absence of Reward

Boehler, C. N., Hopf, J., Krebs, R. M., Stoppel, C. M., Schoenfeld, M. A., Heinze, H., & Noesselt, T. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4845-10.2011 · Cited by 86

Neural Mechanisms for Evaluating Environmental Variability in Caenorhabditis elegans

Calhoun, A. J., Tong, A., Pokala, N., Fitzpatrick, J. A. J., Sharpee, T. O., & Chalasani, S. H. (2015) · Neuron · doi:10.1016/j.neuron.2015.03.026 · Cited by 90

Anatomy of a songbird basal ganglia circuit essential for vocal learning and plasticity

Gale, S. D., & Perkel, D. J. (2009) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2009.07.003 · Cited by 89

Optical Control of Dopamine Receptors Using a Photoswitchable Tethered Inverse Agonist

Donthamsetti, P., Winter, N., Schönberger, M., Levitz, J., Stanley, C., Javitch, J. A., Isacoff, E. Y., & Trauner, D. H. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b07659 · Cited by 90

The pathophysiological basis of sensory disturbances in Parkinson's disease

Carlos Juri, C., Rodríguez-Oroz, M. C., & Obeso, J. A. (2009) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2009.08.018 · Cited by 85

Origin and Evolution of the Neuroendocrine Control of Reproduction in Vertebrates, With Special Focus on Genome and Gene Duplications

Dufour, S., Quérat, B., Tostivint, H., Pasqualini, C., Vaudry, H., & Rousseau, K. (2019) · Physiological Reviews · doi:10.1152/physrev.00009.2019 · Cited by 88

Predictive and Reactive Mechanisms in Smile Reciprocity

Heerey, E. A., & Crossley, H. M. (2013) · Psychological Science · doi:10.1177/0956797612472203 · Cited by 84

Dopaminergic neurotransmission dysfunction induced by amyloid-β transforms cortical long-term potentiation into long-term depression and produces memory impairment

Moreno-Castilla, P., Rodriguez-Duran, L. F., Guzman-Ramos, K., Barcenas-Femat, A., Escobar, M. L., & Bermudez-Rattoni, F. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.02.021 · Cited by 84

On the nature of extraversion: variation in conditioned contextual activation of dopamine-facilitated affective, cognitive, and motor processes

Depue, R. A., & Fu, Y. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00288 · Cited by 90

Molecular basis of dopamine replacement therapy and its side effects in Parkinson’s disease

You, H., Mariani, L., Mangone, G., de Nailly, D. L. F., Charbonnier‐Beaupel, F., & Corvol, J. (2018) · Cell and Tissue Research · doi:10.1007/s00441-018-2813-2 · Cited by 92

Chronic atrazine exposure causes disruption of the spontaneous locomotor activity and alters the striatal dopaminergic system of the male Sprague–Dawley rat

Bardullas, U., Giòrdano, M., & Rodríguez, V. M. (2010) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2010.09.001 · Cited by 84

The relevance of reward pathways for schizophrenia

Ziauddeen, H., & Murray, G. K. (2010) · Current Opinion in Psychiatry · doi:10.1097/yco.0b013e328336661b · Cited by 85

Theta and high-beta networks for feedback processing: a simultaneous EEG–fMRI study in healthy male subjects

Andreou, C., Frielinghaus, H., Rauh, J., Mußmann, M., Vauth, S., Braun, P., Leicht, G., & Mulert, C. (2017) · Translational Psychiatry · doi:10.1038/tp.2016.287 · Cited by 90

Midbrain dopaminergic innervation of the hippocampus is sufficient to modulate formation of aversive memories

Tsetsenis, T., Badyna, J. K., Wilson, J., Zhang, X., Krizman, E. N., Subramaniyan, M., Yang, K., THOMAS, S. A., & Dani, J. A. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2111069118 · Cited by 84

Behavioral dopamine signals.

Schultz, W. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.007 · Cited by 1,028

Behavior-related activity of primate dopamine neurons.

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

Multiple functions of dopamine neurons

Schultz, W. (2010) · F1000 Biology Reports · doi:10.3410/b2-2 · Cited by 59

Dopamine Neurons: Reward and Uncertainty

Schultz, W. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.01299-7 · Cited by 2

Midbrain dopamine neurons control judgment of time

Soares, S., Atallah, B. V., & Paton, J. J. (2016) · Science · doi:10.1126/science.aah5234 · Cited by 365