Neural mechanisms of reward-related motor learning

Predictive reward signal of dopamine neurons

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

Learning and Memory Functions of the Basal Ganglia

Packard, M. G., & Knowlton, B. J. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142937 · Cited by 1,717 · see citing works

Dissociation of reward anticipation and outcome with event-related fMRI

Knutson, B., Fong, G. W., Adams, C. M., Varner, J. L., & Hommer, D. (2001) · Neuroreport · doi:10.1097/00001756-200112040-00016 · Cited by 1,300 · 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

Tracking the Hemodynamic Responses to Reward and Punishment in the Striatum

Delgado, M. R., Nystrom, L. E., Fissell, C., Noll, D. C., & Fiez, J. A. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.6.3072 · Cited by 1,116 · see citing works

Subsecond dopamine release promotes cocaine seeking

Phillips, P. E. M., Stuber, G. D., Heien, M. L. A. V., Wightman, R. M., & Carelli, R. M. (2003) · Nature · doi:10.1038/nature01476 · Cited by 1,113 · see citing works

A triple dissociation of memory systems: Hippocampus, amygdala, and dorsal striatum.

McDonald, R. J., & White, N. M. (1993) · Behavioral Neuroscience · doi:10.1037/0735-7044.107.1.3 · Cited by 885 · see citing works

A cellular mechanism of reward-related learning

Reynolds, J. N. J., Hyland, B. I., & Wickens, J. R. (2001) · Nature · doi:10.1038/35092560 · Cited by 879 · see citing works

Building neural representations of habits.

Jog, M. S., Kubota, Y., Connolly, C. I., Hillegaart, V., & Graybiel, A. M. (1999) · Science · doi:10.1126/science.286.5445.1745 · Cited by 834 · see citing works

Expectation of reward modulates cognitive signals in the basal ganglia

Kawagoe, R., Takikawa, Y., & Hikosaka, O. (1998) · Nature Neuroscience · doi:10.1038/1625 · Cited by 632 · see citing works

Responses of tonically active neurons in the primate's striatum undergo systematic changes during behavioral sensorimotor conditioning

Aosaki, T., Tsubokawa, H., Ishida, A., Watanabe, K., Graybiel, A. M., & Kimura, M. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-06-03969.1994 · Cited by 600 · see citing works

Dopamine-dependent plasticity of corticostriatal synapses

Reynolds, J. N. J., & Wickens, J. R. (2002) · Neural Networks · doi:10.1016/s0893-6080(02)00045-x · Cited by 528 · see citing works

Differential Response Patterns in the Striatum and Orbitofrontal Cortex to Financial Reward in Humans: A Parametric Functional Magnetic Resonance Imaging Study

Elliott, R., Newman, J. L., Longe, O. A., & Deakin, J. F. W. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-01-00303.2003 · Cited by 515 · see citing works

Firing modes of midbrain dopamine cells in the freely moving rat

Hyland, B. I., Reynolds, J. N. J., HAY, J. G., Perk, C. G., & Miller, R. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00267-1 · Cited by 487 · see citing works

Probabilistic learning and reversal deficits in patients with Parkinson’s disease or frontal or temporal lobe lesions: possible adverse effects of dopaminergic medication

Swainson, R., Rogers, R. D., Sahakian, B. J., Summers, B. A., Polkey, C. E., & Robbins, T. W. (2000) · Neuropsychologia · doi:10.1016/s0028-3932(99)00103-7 · Cited by 486 · see citing works

The corticostriatal projection: from synaptic plasticity to dysfunctions of the basal ganglia

Calabresi, P., Pisani, A., Mercuri, N. B., & Bernardi, G. (1996) · Trends in Neurosciences · doi:10.1016/0166-2236(96)81862-5 · Cited by 462 · see citing works

Effect of the nigrostriatal dopamine system on acquired neural responses in the striatum of behaving monkeys

Aosaki, T., Graybiel, A. M., & Kimura, M. (1994) · Science · doi:10.1126/science.8023166 · Cited by 427 · see citing works

Long‐term Potentiation in the Striatum is Unmasked by Removing the Voltage‐dependent Magnesium Block of NMDA Receptor Channels

Calabresi, P., Pisani, A., Mercuri, N. B., & Bernardi, G. (1992) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1992.tb00119.x · Cited by 418 · see citing works

A neural correlate of response bias in monkey caudate nucleus

Lauwereyns, J., Watanabe, K., Coe, B. C., & Hikosaka, O. (2002) · Nature · doi:10.1038/nature00892 · Cited by 415 · see citing works

Responses of midbrain dopamine neurons to behavioral trigger stimuli in the monkey

Schultz, W. (1986) · Journal of Neurophysiology · doi:10.1152/jn.1986.56.5.1439 · Cited by 390 · cited 1× · see citing works

Dopamine D-1/D-5 Receptor Activation Is Required for Long-Term Potentiation in the Rat Neostriatum In Vitro

Kerr, J. N. D., & Wickens, J. R. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.1.117 · Cited by 384 · see citing works

Dopamine neurons of the monkey midbrain: contingencies of responses to active touch during self-initiated arm movements

Romo, R., & Schultz, W. (1990) · Journal of Neurophysiology · doi:10.1152/jn.1990.63.3.592 · Cited by 353 · cited 1× · see citing works

Operant Reward Learning in <i>Aplysia</i> : Neuronal Correlates and Mechanisms

Brembs, B., Lorenzetti, F. D., Reyes, F. D., Baxter, D. A., & Byrne, J. H. (2002) · Science · doi:10.1126/science.1069434 · Cited by 338 · see citing works

Dissociation of dopamine release in the nucleus accumbens from intracranial self-stimulation

Garris, P. A., Kilpatrick, M., Bunin, M. A., Michael, D., Walker, Q. D., & Wightman, R. M. (1999) · Nature · doi:10.1038/18019 · Cited by 327 · see citing works

Inhibitory Interactions Between Spiny Projection Neurons in the Rat Striatum

Tunstall, M. J., Oorschot, D. E., Kean, A., & Wickens, J. R. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.88.3.1263 · Cited by 311 · see citing works

Dopamine reverses the depression of rat corticostriatal synapses which normally follows high-frequency stimulation of cortex In vitro

Wickens, J. R., Begg, A., & Arbuthnott, G. W. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00436-m · Cited by 294 · see citing works

Tonically discharging putamen neurons exhibit set-dependent responses.

Kimura, M., Rajkowski, J., & Evarts, E. V. (1984) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.81.15.4998 · Cited by 276 · see citing works

Modifications of Reward Expectation-Related Neuronal Activity During Learning in Primate Striatum

Tremblay, L., Hollerman, J. R., & Schultz, W. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.2.964 · Cited by 267 · see citing works

Intracranial self-stimulation in relation to the ascending dopaminergic systems of the midbrain: A moveable electrode mapping study

Corbett, D., & Wise, R. A. (1980) · Brain Research · doi:10.1016/0006-8993(80)90666-6 · Cited by 264 · see citing works

Differential activation of monkey striatal neurons in the early and late stages of procedural learning

Miyachi, S., Hikosaka, O., & Lu, X. (2002) · Experimental Brain Research · doi:10.1007/s00221-002-1213-7 · Cited by 262 · see citing works

Behavioral correlates of dopaminergic unit activity in freely moving cats

Steinfels, G. F., Heym, J., Strecker, R. E., & Jacobs, B. L. (1983) · Brain Research · doi:10.1016/0006-8993(83)91145-9 · Cited by 261 · see citing works

Relations between movement and single cell discharge in the substantia nigra of the behaving monkey

DeLong, M., Crutcher, M., & Georgopoulos, A. (1983) · The Journal of Neuroscience · doi:10.1523/jneurosci.03-08-01599.1983 · Cited by 247 · see citing works

Modulation of Hippocampal and Amygdalar-Evoked Activity of Nucleus Accumbens Neurons by Dopamine: Cellular Mechanisms of Input Selection

Floresco, S., Blaha, C. D., Yang, C. R., & Phillips, A. G. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-08-02851.2001 · Cited by 242 · see citing works

Behaviorally contingent property of movement-related activity of the primate putamen

Kimura, M. (1990) · Journal of Neurophysiology · doi:10.1152/jn.1990.63.6.1277 · Cited by 226 · see citing works

Changes in behavior-related neuronal activity in the striatum during learning

Schultz, W. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00122-x · Cited by 225 · see citing works

Regional and Postnatal Heterogeneity of Activity-Dependent Long-Term Changes in Synaptic Efficacy in the Dorsal Striatum

Partridge, J. G., Tang, K., & Lovinger, D. M. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.3.1422 · Cited by 213 · see citing works

Activity of A9 and A10 dopaminergic neurons in unrestrained rats: further characterization and effects of apomorphine and cholecystokinin

Freeman, A. S., & Bunney, B. S. (1987) · Brain Research · doi:10.1016/0006-8993(87)90988-7 · Cited by 162 · see citing works

Dopamine-Dependent Synaptic Plasticity in the Striatal Cholinergic Interneurons

Suzuki, T., Miura, M., Nishimura, K., & Aosaki, T. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-17-06492.2001 · Cited by 151 · see citing works

A triple dissociation of memory systems: Hippocampus, amygdala, and dorsal striatum.

McDonald, R., & White, N. (1993) · Behavioral Neuroscience · doi:10.1037/a0034883 · Cited by 146 · see citing works

The activity of pars compacta neurons of the monkey substantia nigra in relation to motor activation

Schultz, W., Ruffieux, A., & Aebischer, P. (1983) · Experimental Brain Research · doi:10.1007/bf00237874 · Cited by 136 · see citing works

Substantia nigra dopamine regulates synaptic plasticity and membrane potential fluctuations in the rat neostriatum, in vivo

Reynolds, J. N. J., & Wickens, J. R. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00273-6 · Cited by 131 · see citing works

Responses of monkey midbrain dopamine neurons during delayed alternation performance

Ljungberg, T., Apicella, P., & Schultz, W. (1991) · Brain Research · doi:10.1016/0006-8993(91)90816-e · Cited by 128 · see citing works

Feature-Based Anticipation of Cues that Predict Reward in Monkey Caudate Nucleus

Lauwereyns, J., Takikawa, Y., Kawagoe, R., Kobayashi, S., Koizumi, M., Coe, B. C., Sakagami, M., & Hikosaka, O. (2002) · Neuron · doi:10.1016/s0896-6273(02)00571-8 · Cited by 123 · see citing works

Disfacilitation and long-lasting inhibition of neostriatal neurons in the rat

Wilson, C. J., Chang, H. T., & Kitai, S. T. (1983) · Experimental Brain Research · doi:10.1007/bf00237198 · Cited by 121 · see citing works

Effects of US devaluation on win-stay and win-shift radial maze performance in rats.

Sage, J. R., & Knowlton, B. J. (2000) · Behavioral Neuroscience · doi:10.1037//0735-7044.114.2.295 · Cited by 90 · see citing works

Reduced reward processing in the brains of Parkinsonian patients

Künig, G., Leenders, K. L., Martin-Söelch, C., Missimer, J. H., Magyar‐Lehmann, S., & Schultz, W. (2000) · Neuroreport · doi:10.1097/00001756-200011270-00019 · Cited by 85 · see citing works

Dendritic Calcium Encodes Striatal Neuron Output during Up-States

Kerr, J. N. D., & Plenz, D. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-05-01499.2002 · Cited by 83 · see citing works

Extracellular dopamine dynamics in rat caudate–putamen during experimenter-delivered and intracranial self-stimulation

Kilpatrick, M., Rooney, M. B., MICHAEL, D., & Wightman, R. M. (2000) · Neuroscience · doi:10.1016/s0306-4522(99)00578-3 · Cited by 80 · see citing works

Effects of US devaluation on win–stay and win–shift radial maze performance in rats.

Sage, J. R., & Knowlton, B. J. (2000) · Behavioral Neuroscience · doi:10.1037/0735-7044.114.2.295 · Cited by 74 · see citing works

Impulse activity of ventral tegmental area neurons during heroin self-administration in rats

Kiyatkin, E. A., & Rebec, G. V. (2001) · Neuroscience · doi:10.1016/s0306-4522(00)00492-9 · Cited by 66 · see citing works

A theory of the action of the after-effects of a connection upon it.

Thorndike, E. L. (1933) · Psychological Review · doi:10.1037/h0071025 · Cited by 61 · see citing works

Regional differences in the expression of corticostriatal synaptic plasticity

Smith, R. B., Musleh, W., Akopian, G. K., Buckwalter, J. G., & Walsh, J. P. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00260-3 · Cited by 44 · see citing works

Distribution of the histamine H2 receptor in monkey brain and its mRNA localization in monkey and human brain

Honrubia, M., Vilar�, M. T., Palacios, J. M., & Mengod, G. (2000) · Synapse · doi:10.1002/1098-2396(20001201)38:3 · Cited by 36 · see citing works

Impaired Incentive Learning in Treated Parkinson’s Disease

Charbonneau, D., Riopelle, R. J., & Beninger, R. J. (1996) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s031716710003821x · Cited by 28 · see citing works

Stimulus frequency, calcium levels and striatal synaptic plasticity

Bonsi, P., Pisani, A., Bernardi, G., & Calabresi, P. (2003) · Neuroreport · doi:10.1097/00001756-200303030-00024 · Cited by 24 · see citing works

The use of two operants to examine the nature of pimozide-induced decreases in responding for brain stimulation

Beninger, R. J., & Freedman, N. L. (1982) · Physiological Psychology · doi:10.3758/bf03332973 · Cited by 21 · see citing works

Brain Dynamics and the Striatal Complex

Wickens, J. R. (2000) · Taylor & Francis eBooks · doi:10.4324/9780203304914 · Cited by 19 · see citing works

The debate over dopamine’s role in reward: the case for incentive salience

Berridge, K. C. (2007) · Psychopharmacology · doi:10.1007/s00213-006-0578-x · Cited by 2,347 · see citing works

D1 and D2 dopamine-receptor modulation of striatal glutamatergic signaling in striatal medium spiny neurons

Surmeier, D. J., Ding, J., Day, M., Wang, Z., & Shen, W. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.008 · Cited by 1,203 · see citing works

Representation of Action-Specific Reward Values in the Striatum

Samejima, K., Ueda, Y., Doya, K., & Kimura, M. (2005) · Science · doi:10.1126/science.1115270 · Cited by 939 · see citing works

Dopamine-mediated regulation of corticostriatal synaptic plasticity

Calabresi, P., Picconi, B., Tozzi, A., & Di Filippo, M. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.001 · Cited by 865 · see citing works

Memory and Addiction

Kelley, A. E. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.016 · Cited by 773 · see citing works

The short-latency dopamine signal: a role in discovering novel actions?

Redgrave, P., & Gurney, K. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn2022 · Cited by 762 · see citing works

Corticostriatal-hypothalamic circuitry and food motivation: Integration of energy, action and reward

Kelley, A. E., Baldo, B. A., Pratt, W. E., & Will, M. J. (2005) · Physiology & Behavior · doi:10.1016/j.physbeh.2005.08.066 · Cited by 752 · see citing works

Decision Making in Recurrent Neuronal Circuits

Wang, X.-J. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.034 · Cited by 679 · 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

Distinct Roles of Synaptic Transmission in Direct and Indirect Striatal Pathways to Reward and Aversive Behavior

Hikida, T., Kimura, K., Wada, N., Funabiki, K., & Nakanishi, S. (2010) · Neuron · doi:10.1016/j.neuron.2010.05.011 · Cited by 592 · see citing works

Dopaminergic neurons inhibit striatal output through non-canonical release of GABA

Tritsch, N. X., Ding, J. B., & Sabatini, B. L. (2012) · Nature · doi:10.1038/nature11466 · Cited by 576 · see citing works

Principles of Neurorehabilitation After Stroke Based on Motor Learning and Brain Plasticity Mechanisms

Maier, M., Ballester, B. R., & Verschure, P. F. M. J. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2019.00074 · Cited by 528 · see citing works

A unified framework for addiction: Vulnerabilities in the decision process

Redish, A. D., Jensen, S., & Johnson, A. (2008) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0800472x · Cited by 501 · see citing works

Cortical and basal ganglia contributions to habit learning and automaticity

Ashby, F. G., Turner, B. O., & Horvitz, J. C. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.02.001 · Cited by 481 · see citing works

Learning from Sensory and Reward Prediction Errors during Motor Adaptation

Izawa, J., & Shadmehr, R. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002012 · Cited by 474 · see citing works

Dopamine and Addiction

Wise, R. A., & Robble, M. A. (2020) · Annual Review of Psychology · doi:10.1146/annurev-psych-010418-103337 · Cited by 418 · see citing works

Adenosine A2A receptors and basal ganglia physiology

Schiffmann, S. N., Fisone, G., Moresco, R. M., Cunha, R. A., & Ferré, S. (2007) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2007.05.001 · Cited by 393 · see citing works

Reinforcement Learning in Multidimensional Environments Relies on Attention Mechanisms

Niv, Y., Daniel, R., Geana, A., Gershman, S. J., Leong, Y. C., Radulescu, A., & Wilson, R. C. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.2978-14.2015 · Cited by 362 · see citing works

Dopamine Modulation of State-Dependent Endocannabinoid Release and Long-Term Depression in the Striatum

Kreitzer, A. C., & Malenka, R. C. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2959-05.2005 · Cited by 358 · see citing works

Neural prediction errors reveal a risk-sensitive reinforcement-learning process in the human brain

Niv, Y., Edlund, J. A., Dayan, P., & O'Doherty, J. P. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.5498-10.2012 · Cited by 356 · see citing works

A proposed hypothalamic–thalamic–striatal axis for the integration of energy balance, arousal, and food reward

Kelley, A. E., Baldo, B. A., & Pratt, W. E. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20769 · Cited by 352 · see citing works

Research Review: Dopamine transfer deficit: a neurobiological theory of altered reinforcement mechanisms in ADHD

Tripp, G., & Wickens, J. R. (2008) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2007.01851.x · Cited by 346 · see citing works

An fMRI study of reward-related probability learning

Delgado, M. R., Miller, M. M., Inati, S., & Phelps, E. A. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.10.002 · Cited by 337 · see citing works

Human category learning 2.0

Ashby, F. G., & Maddox, W. T. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05874.x · Cited by 319 · see citing works

Discrete neurochemical coding of distinguishable motivational processes: insights from nucleus accumbens control of feeding

Baldo, B. A., & Kelley, A. E. (2007) · Psychopharmacology · doi:10.1007/s00213-007-0741-z · Cited by 312 · see citing works

Reward Improves Long-Term Retention of a Motor Memory through Induction of Offline Memory Gains

Abe, M., Schambra, H., Wassermann, E. M., Luckenbaugh, D., Schweighofer, N., & Cohen, L. G. (2011) · Current Biology · doi:10.1016/j.cub.2011.02.030 · Cited by 313 · see citing works

Switching from automatic to controlled behavior: cortico-basal ganglia mechanisms

Hikosaka, O., & Isoda, M. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.01.006 · Cited by 304 · see citing works

What is reinforced by phasic dopamine signals?

Redgrave, P., GURNEY, K. N., & Reynolds, J. N. J. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.10.007 · Cited by 254 · see citing works

Basal Ganglia Circuits for Reward Value–Guided Behavior

Hikosaka, O., Kim, H. F., Yasuda, M., & Yamamoto, S. (2014) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071013-013924 · Cited by 259 · see citing works

Presynaptic nicotinic receptors: a dynamic and diverse cholinergic filter of striatal dopamine neurotransmission

Exley, R. A., & Cragg, S. J. (2007) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0707510 · Cited by 249 · see citing works

M4 Muscarinic Receptor Signaling Ameliorates Striatal Plasticity Deficits in Models of L-DOPA-Induced Dyskinesia

Shen, W., Plotkin, J. L., Francardo, V., Ko, W. K. D., Xie, Z., Li, Q., Fieblinger, T., Wess, J., Neubig, R. R., Lindsley, C. W., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.10.039 · Cited by 713 · see citing works

Meaningful silences: how dopamine listens to the ACh pause

Cragg, S. J. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.01.003 · Cited by 245 · see citing works

Selective enhancement of associative learning by microstimulation of the anterior caudate

Williams, Z. M., & Eskandar, E. N. (2006) · Nature Neuroscience · doi:10.1038/nn1662 · Cited by 235 · see citing works

Dopamine Signaling in Dorsal Versus Ventral Striatum: The Dynamic Role of Cholinergic Interneurons

Threlfell, S., & Cragg, S. J. (2011) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2011.00011 · Cited by 195 · see citing works

Neurogenetics and Pharmacology of Learning, Motivation, and Cognition

Frank, M. J., & Fossella, J. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.96 · Cited by 191 · see citing works

Dopamine: the salient issue

Ungless, M. A. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.10.001 · Cited by 190 · see citing works

Functional properties of the basal ganglia's re-entrant loop architecture: selection and reinforcement

Redgrave, P., Vautrelle, N., & Reynolds, J. N. J. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.07.060 · Cited by 183 · see citing works

Influence of reward motivation on human declarative memory

Lombard, E., Bavelier, D., & Schwartz, S. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.11.015 · Cited by 174 · see citing works

Striatal Contributions to Reward and Decision Making: Making Sense of Regional Variations in a Reiterated Processing Matrix

WICKENS, J. R., BUDD, C. S., HYLAND, B. I., & ARBUTHNOTT, G. W. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1390.016 · Cited by 165 · see citing works

Subcortical contributions to large-scale network communication

Bell, P. T., & Shine, J. M. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.08.036 · Cited by 163 · see citing works

Dopamine Antagonism Decreases Willingness to Expend Physical, But Not Cognitive, Effort: A Comparison of Two Rodent Cost/Benefit Decision-Making Tasks

Hosking, J. G., Floresco, S., & Winstanley, C. A. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.285 · Cited by 154 · see citing works

A psychological and neuroanatomical model of obsessive-compulsive disorder

Huey, E. D., Zahn, R., Krueger, F., Moll, J., Kapogiannis, D., Wassermann, E. M., & Grafman, J. (2008) · The Journal of Neuropsychiatry and Clinical Neurosciences · doi:10.1176/jnp.2008.20.4.390 · Cited by 152 · see citing works

Extrastriatal dopaminergic circuits of the basal ganglia

Rommelfanger, K. S. (2010) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2010.00139 · Cited by 150 · see citing works

Ethanol Action on Dopaminergic Neurons in the Ventral Tegmental Area

Morikawa, H., & Morrisett, R. A. (2010) · International review of neurobiology · doi:10.1016/s0074-7742(10)91008-8 · Cited by 139 · see citing works

Vagus nerve stimulation drives selective circuit modulation through cholinergic reinforcement

Bowles, S. G., Hickman, J. L., Peng, X., Williamson, W. R., Huang, R., Washington, K. A., Donegan, D., & Welle, C. G. (2022) · Neuron · doi:10.1016/j.neuron.2022.06.017 · Cited by 137 · see citing works

Where Do You Think You Are Going? The NMDA-D1 Receptor Trap

Cepeda, C., & Levine, M. S. (2006) · Science's STKE · doi:10.1126/stke.3332006pe20 · Cited by 136 · see citing works

Meaning and the brain: The neurosemantics of referential, interactive, and combinatorial knowledge

Friedemann Pulvermüller, A. (2011) · Journal of Neurolinguistics · doi:10.1016/j.jneuroling.2011.03.004 · Cited by 131 · see citing works

Parallel associative processing in the dorsal striatum: Segregation of stimulus–response and cognitive control subregions

Devan, B. D., Hong, N. S., & McDonald, R. J. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.06.002 · Cited by 130 · see citing works

Dysregulated Information Processing by Medium Spiny Neurons in Striatum of Freely Behaving Mouse Models of Huntington's Disease

Miller, B., Walker, A. G., Shah, A. S., Barton, S. J., & Rebec, G. V. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90606.2008 · Cited by 122 · see citing works

Transient Calcium and Dopamine Increase PKA Activity and DARPP-32 Phosphorylation

Lindskog, M., Kim, M., Wikström, M. A., Blackwell, K. T., & Kotaleski, J. H. (2006) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0020119 · Cited by 119 · see citing works

Reward Value-Contingent Changes of Visual Responses in the Primate Caudate Tail Associated with a Visuomotor Skill

Yamamoto, S., Kim, H. F., & Hikosaka, O. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0318-13.2013 · Cited by 118 · see citing works

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 · see citing works

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 118 · see citing works

Silencing the critics: understanding the effects of cocaine sensitization on dorsolateral and ventral striatum in the context of an actor/critic model

Takahashi, Y. K. (2008) · Frontiers in Neuroscience · doi:10.3389/neuro.01.014.2008 · Cited by 115 · see citing works

Pathway-specific control of reward learning and its flexibility via selective dopamine receptors in the nucleus accumbens

Yawata, S., Yamaguchi, T., Danjo, T., Hikida, T., & Nakanishi, S. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1210797109 · Cited by 112 · see citing works

Hormones that increase maternal responsiveness affect accumbal dopaminergic responses to pup- and food-stimuli in the female rat

Afonso, V. M., King, S., Chatterjee, D., & Fleming, A. S. (2009) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.02.003 · Cited by 112 · see citing works

Semaphorin 3E–Plexin-D1 signaling controls pathway-specific synapse formation in the striatum

Ding, J., Oh, W., Sabatini, B. L., & Gu, C. (2011) · Nature Neuroscience · doi:10.1038/nn.3003 · Cited by 110 · see citing works

Dopamine, Prediction Error and Beyond

Diederen, K. M. J., & Fletcher, P. C. (2021) · The Neuroscientist · doi:10.1177/1073858420907591 · Cited by 106 · see citing works

Robust Representation of Stable Object Values in the Oculomotor Basal Ganglia

Yasuda, M., Yamamoto, S., & Hikosaka, O. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3438-12.2012 · Cited by 103 · see citing works

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 · see citing works

Basal ganglia output to the thalamus: still a paradox

Goldberg, J. H., Farries, M. A., & Fee, M. S. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.09.001 · Cited by 93 · see citing works

The Neuropsychology of Anxiety

McNaughton, N., & Gray, J. A. (2024) · doi:10.1093/oso/9780198843313.001.0001 · Cited by 98 · see citing works

Science-Based Neurorehabilitation: Recommendations for Neurorehabilitation From Basic Science

Nielsen, J. B., Willerslev‐Olsen, M., Christiansen, L., Lundbye‐Jensen, J., & Lorentzen, J. (2015) · Journal of Motor Behavior · doi:10.1080/00222895.2014.931273 · Cited by 96 · see citing works

Striatal GPR88 expression is confined to the whole projection neuron population and is regulated by dopaminergic and glutamatergic afferents

Massart, R., Guilloux, J., Mignon, V., Sokoloff, P., & Díaz, J. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06842.x · Cited by 96 · see citing works

Activation of the dopaminergic pathway from VTA to the medial olfactory tubercle generates odor-preference and reward

Zhang, Z., Liu, Q., Wen, P., Zhang, J., Rao, X., Zhou, Z., Zhang, H., He, X., Li, J., Zhou, Z., et al. (2017) · eLife · doi:10.7554/elife.25423 · Cited by 89 · see citing works

Corticostriatal plasticity: life after the depression

Mahon, S., Deniau, J., & Charpier, S. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.06.010 · Cited by 90 · see citing works

Therapeutic potential of targeting G protein-gated inwardly rectifying potassium (GIRK) channels in the central nervous system

Jeremic, D., Sanchez-Rodriguez, I., Jimenez-Diaz, L., & Navarro-Lopez, J. D. (2021) · Pharmacology &amp; Therapeutics · doi:10.1016/j.pharmthera.2021.107808 · Cited by 89 · see citing works

Potential benefits of music playing in stroke upper limb motor rehabilitation

Grau‐Sánchez, J., Münte, T. F., ALTENMÜLLER, E. O., Duarte, E., & Rodríguez‐Fornells, A. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.02.027 · Cited by 88 · see citing works

Dyskinesia in Parkinson's disease: mechanisms and current non‐pharmacological interventions

Heumann, R., Moratalla, R., Herrero, M. T., Chakrabarty, K., Drucker-Colı́n, R., García-Montes, J. R., Simola, N., & Morelli, M. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.12751 · Cited by 86 · see citing works

Cell-Type-Specific Outcome Representation in the Primary Motor Cortex

Levy, S., Lavzin, M., Benisty, H., Ghanayim, A., Dubin, U., Achvat, S., Brosh, Z., Aeed, F., Mensh, B. D., Schiller, Y., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.06.006 · Cited by 88 · see citing works

Interpreting the role of the striatum during multiple phases of motor learning

Cataldi, S., Stanley, A. T., Miniaci, M. C., & Sulzer, D. L. (2021) · FEBS Journal · doi:10.1111/febs.15908 · Cited by 83 · see citing works

Efficient reinforcement learning: computational theories, neuroscience and robotics

Kawato, M., & Samejima, K. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.03.004 · 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

How may the basal ganglia contribute to auditory categorization and speech perception?

Lim, S.-J., Fiez, J. A., & Holt, L. L. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00230 · Cited by 75 · see citing works

Cortico‐basal ganglia mechanisms for overcoming innate, habitual and motivational behaviors

Isoda, M., & Hikosaka, O. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07698.x · Cited by 76 · see citing works

Reward Prediction Error Computation in the Pedunculopontine Tegmental Nucleus Neurons

Kobayashi, Y., & Okada, K. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1390.003 · Cited by 75 · see citing works

Cocaine sensitization and dopamine mediation of cue effects in rodents, monkeys, and humans: areas of agreement, disagreement, and implications for addiction

Bradberry, C. (2007) · Psychopharmacology · doi:10.1007/s00213-006-0561-6 · Cited by 76 · see citing works

Short-term memory traces for action bias in human reinforcement learning

Bogacz, R., McClure, S. M., Li, J., Cohen, J. D., & Montague, P. R. (2007) · Brain Research · doi:10.1016/j.brainres.2007.03.057 · Cited by 74 · see citing works

Dual Role of Medial A10 Dopamine Neurons in Affective Encoding

Liu, Z., Shin, R. S., & Ikemoto, S. (2008) · Neuropsychopharmacology · doi:10.1038/npp.2008.4 · Cited by 73 · see citing works

rTMS with motor training modulates cortico-basal ganglia-thalamocortical circuits in stroke patients

Chang, W. H., Kim, Y., Yoo, W., Goo, K.-H., Park, C.-H., Kim, S. T., & Pascual‐Leone, Á. (2012) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-2012-110162 · Cited by 72 · see citing works

Short-Latency Activation of Striatal Spiny Neurons via Subcortical Visual Pathways

Schulz, J. M., Redgrave, P., Mehring, C., Aertsen, A., Clements, K. M., Wickens, J. R., & Reynolds, J. N. J. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4815-08.2009 · Cited by 68 · see citing works

Dopamine-dependent long term potentiation in the dorsal striatum is reduced in the R6/2 mouse model of Huntington’s disease

Kung, V., Hassam, R., Morton, A. J., & Jones, S. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.03.036 · Cited by 72 · see citing works

Age-related reduction in motor adaptation: brain structural correlates and the role of explicit memory

Wolpe, N., Ingram, J. N., Tsvetanov, K. A., Henson, R. N., Wolpert, D. M., TYLER, L. K., Brayne, C., Bullmore, E. T., Calder, A. C., Cusack, R., et al. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.02.016 · Cited by 69 · see citing works

Dopamine transporter glycosylation correlates with the vulnerability of midbrain dopaminergic cells in Parkinson's disease

Afonso‐Oramas, D., Cruz‐Muros, I., de la Rosa, D. Á., Abreu, P. M., Giráldez, T., Castro‐Hernández, J., Salas-Hernández, J., Lanciego, J. L., Rodrı́guez, M., & González‐Hernández, T. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.09.002 · Cited by 70 · see citing works

Vulnerability of mesostriatal dopaminergic neurons in Parkinson’s disease

González-Hernández, T. (2010) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2010.00140 · Cited by 65 · see citing works

PKA-Dependent Phosphorylation of Ribosomal Protein S6 Does Not Correlate with Translation Efficiency in Striatonigral and Striatopallidal Medium-Sized Spiny Neurons

Biever, A., Puighermanal, E., Nishi, A., David, A., Panciatici, C., Longueville, S., Xirodimas, D. P., Gangarossa, G., Meyuhas, O., Hervé, D., et al. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3288-14.2015 · Cited by 63 · 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

Instrumental learning, but not performance, requires dopamine D1-receptor activation in the amygdala

Andrzejewski, M. E., Spencer, R. C., & Kelley, A. E. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.06.038 · Cited by 59 · see citing works

The impact of music interventions on motor rehabilitation following stroke in elderly

ALTENMÜLLER, E. O., & James, C. E. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-817422-7.00016-x · Cited by 60 · see citing works

Learning processing in the basal ganglia: A mosaic of broken mirrors

Cunha, C. D., Lovato, E. C. W., Dombrowski, P. A., Bortolanza, M., dos Santos, L. M., Boschen, S. L., & Miyoshi, E. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.10.001 · Cited by 59 · see citing works

The neuronal nicotinic acetylcholine receptors α4* and α6* differentially modulate dopamine release in mouse striatal slices

Meyer, E. L., Yoshikami, D., & McIntosh, J. M. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05266.x · Cited by 58 · see citing works

Stimulus-response and response-outcome learning mechanisms in the striatum

Horvitz, J. C. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.12.014 · Cited by 58 · see citing works

A subcortical circuit linking the cerebellum to the basal ganglia engaged in vocal learning

Pidoux, L., Leblanc-Veyrac, P., Lévénès, C., & Leblois, A. (2018) · eLife · doi:10.7554/elife.32167 · Cited by 57 · see citing works

Speech-induced striatal dopamine release is left lateralized and coupled to functional striatal circuits in healthy humans: A combined PET, fMRI and DTI study

Simonyan, K., Herscovitch, P., & Horwitz, B. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.12.042 · Cited by 57 · see citing works

Learning Similar Actions by Reinforcement or Sensory-Prediction Errors Rely on Distinct Physiological Mechanisms

Uehara, S., Mawase, F., & Celnik, P. A. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx214 · Cited by 52 · see citing works

Auditory Thalamostriatal and Corticostriatal Pathways Convey Complementary Information about Sound Features

Ponvert, N. D., & Jaramillo, S. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1188-18.2018 · Cited by 53 · see citing works

Intrinsically motivated action–outcome learning and goal-based action recall: A system-level bio-constrained computational model

Baldassarre, G., Mannella, F., Fiore, V. G., Redgrave, P., GURNEY, K. N., & Mirolli, M. (2012) · Neural Networks · doi:10.1016/j.neunet.2012.09.015 · Cited by 52 · see citing works

Establishing causality for dopamine in neural function and behavior with optogenetics

Steinberg, E. E., & Janak, P. H. (2012) · Brain Research · doi:10.1016/j.brainres.2012.09.036 · Cited by 52 · see citing works

Endogenous 17β-estradiol is required for activity-dependent long-term potentiation in the striatum: interaction with the dopaminergic system

Tozzi, A., de Iure, A., Tantucci, M., Durante, V., Quiroga‐Varela, A., Giampà, C., Mauro, M. D., Mazzocchetti, P., Costa, C., Filippo, M. D., et al. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00192 · Cited by 49 · see citing works

Lack of depotentiation at basal ganglia output neurons in PD patients with levodopa-induced dyskinesia

Prescott, I. A., Liu, L. D., Dostrovsky, J. O., Hodaie, M., Lozano, A. M., & Hutchison, W. D. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.08.002 · Cited by 49 · see citing works

Striatal Dopamine Signals and Reward Learning

Bech, P., Crochet, S., Dard, R. F., Ghaderi, P., Liu, Y., Malekzadeh, M., Petersen, C. C. H., Pulin, M., Renard, A., & Sourmpis, C. (2023) · Function · doi:10.1093/function/zqad056 · Cited by 25 · see citing works

Striatal action-learning based on dopamine concentration

Morris, G., Schmidt, R., & Bergman, H. (2009) · Experimental Brain Research · doi:10.1007/s00221-009-2060-6 · Cited by 32 · see citing works

DOI 10.1007/s00221-009-2060-6REVIEW Striatal action-learning based on dopamine concentration

Res, E. B., Morris, G., Schmidt, R., & Bergman, H. (2014)

Dopamine’s Effects on Corticostriatal Synapses during Reward-Based Behaviors

Bamford, N. S., Wightman, R. M., & Sulzer, D. (2018) · Neuron · doi:10.1016/j.neuron.2018.01.006 · Cited by 137 · see citing works

Signaling pathways underlying striatal synaptic plasticity and reward learning

Blackwell, K. T. (2008) · BMC Neuroscience · doi:10.1186/1471-2202-9-s1-l3