Neuronal responses in the ventral striatum of the behaving macaque

Functional architecture of basal ganglia circuits: neural substrates of parallel processing

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From motivation to action: Functional interface between the limbic system and the motor system

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Amphetamine and apomorphine responses in the rat following 6-OHDA lesions of the nucleus accumbens septi and corpus striatum

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THE CORTICO-STRIATE PROJECTION IN THE MONKEY

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The mesolimbic dopamine system : from motivation to action

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A Theory of Emotion, and its Application to Understanding the Neural Basis of Emotion

Rolls, E. (1990) · Cognition & Emotion · doi:10.1080/02699939008410795 · Cited by 411

Ventral striatum and ventral pallidum

Heimer, L., Switzer, R. D., & Hoesen, G. W. V. (1982) · Trends in Neurosciences · doi:10.1016/0166-2236(82)90037-6 · Cited by 401

Neurons in the amygdala of the monkey with responses selective for faces.

Leonard, C. M., Rolls, E. T., Wilson, F. A., & Baylis, G. C. (1985) · Behavioural Brain Research · doi:10.1016/0166-4328(85)90062-2 · Cited by 396

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

The Orbitofrontal Cortex and Reward

Rolls, E. T. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.284 · Cited by 1,595

Visual Object Recognition

Logothetis, N. K., & Sheinberg, D. L. (1996) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.19.030196.003045 · Cited by 1,374

The functions of the orbitofrontal cortex

Rolls, E. T. (2004) · Brain and Cognition · doi:10.1016/s0278-2626(03)00277-x · Cited by 1,327

Multiple reward signals in the brain

Schultz, W. (2000) · Nature Reviews Neuroscience · doi:10.1038/35044563 · Cited by 1,303

The ventral visual pathway: an expanded neural framework for the processing of object quality

Kravitz, D. J., Saleem, K. S., Baker, C. I., Ungerleider, L. G., & Mishkin, M. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.10.011 · Cited by 1,204

Dopamine neurons report an error in the temporal prediction of reward during learning

Hollerman, J. R., & Schultz, W. (1998) · Nature Neuroscience · doi:10.1038/1124 · Cited by 1,161

Imaging dopamine's role in drug abuse and addiction

Volkow, N. D., Fowler, J. S., Wang, G. J., Baler, R., & Telang, F. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.05.022 · Cited by 988

Dopamine neurons and their role in reward mechanisms

Schultz, W. (1997) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(97)80007-4 · Cited by 809

The orbitofrontal cortex

Rolls, E. T. (1996) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1996.0128 · Cited by 755

The hippocampal formation participates in novel picture encoding: evidence from functional magnetic resonance imaging.

Stern, C. E., Corkin, S., González, R. G., Guimarães, A. R., Baker, J. R., Jennings, P. J., Carr, C. A., Sugiura, R., Vedantham, V., & Rosen, B. R. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.16.8660 · Cited by 645

Dissociation in Effects of Lesions of the Nucleus Accumbens Core and Shell on Appetitive Pavlovian Approach Behavior and the Potentiation of Conditioned Reinforcement and Locomotor Activity byd-Amphetamine

Parkinson, J. A., Olmstead, M. C., Burns, L. H., Robbins, T. W., & Everitt, B. J. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-06-02401.1999 · Cited by 555

Computational Neuroscience of Vision

Rolls, E. T., & Deco, G. (2001) · doi:10.1093/acprof:oso/9780198524885.001.0001 · Cited by 554

Neural Correlates of Face and Object Recognition in Young Children with Autism Spectrum Disorder, Developmental Delay, and Typical Development

Dawson, G., Carver, L., Meltzoff, A. N., Panagiotides, H., McPartland, J., & Webb, S. J. (2002) · Child Development · doi:10.1111/1467-8624.00433 · Cited by 523

The orbitofrontal cortex: reward, emotion and depression

Rolls, E. T., Cheng, W., & Feng, J. (2020) · Brain Communications · doi:10.1093/braincomms/fcaa196 · Cited by 474

Human Striatal Responses to Monetary Reward Depend On Saliency

Zink, C. F., Pagnoni, G., Martin-Skurski, M. E., Chappelow, J., & Berns, G. S. (2004) · Neuron · doi:10.1016/s0896-6273(04)00183-7 · Cited by 432

Experience-dependent neural integration of taste and smell in the human brain

Small, D. M., Voss, J., Mak, Y. E., Simmons, K. B., Parrish, T., & Gitelman, D. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00050.2004 · Cited by 398

Précis of The brain and emotion

Rolls, E. T. (2000) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00002429 · Cited by 397

An ERP index of task relevance evaluation of visual stimuli

Potts, G. F. (2004) · Brain and Cognition · doi:10.1016/j.bandc.2004.03.006 · Cited by 375

Specific cognitive deficits in mild frontal variant frontotemporal dementia

Rahman, S., Sahakian, B. J., Hodges, J. R., Rogers, R. D., & Robbins, T. W. (1999) · Brain · doi:10.1093/brain/122.8.1469 · Cited by 374

Memory Systems in the Brain

Rolls, E. T. (2000) · Annual Review of Psychology · doi:10.1146/annurev.psych.51.1.599 · Cited by 354

Emotion, motivation, decision-making, the orbitofrontal cortex, anterior cingulate cortex, and the amygdala

Rolls, E. T. (2023) · Brain Structure and Function · doi:10.1007/s00429-023-02644-9 · Cited by 356

Disconnection of the anterior cingulate cortex and nucleus accumbens core impairs Pavlovian approach behavior: Further evidence for limbic cortical-ventral striatopallidal systems.

Parkinson, J. A., Willoughby, P. J., Robbins, T. W., & Everitt, B. J. (2000) · Behavioral Neuroscience · doi:10.1037//0735-7044.114.1.42 · Cited by 309

Human striatal response to salient nonrewarding stimuli

Zink, C. F., Pagnoni, G., Martin, M. E., Dhamala, M., & Berns, G. S. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-22-08092.2003 · Cited by 312

Functions of the Primate Temporal Lobe Cortical Visual Areas in Invariant Visual Object and Face Recognition

Rolls, E. T. (2000) · Neuron · doi:10.1016/s0896-6273(00)00030-1 · Cited by 303

Taste, olfactory, and food reward value processing in the brain

Rolls, E. T. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.03.002 · Cited by 308

Disconnection of the anterior cingulate cortex and nucleus accumbens core impairs Pavlovian approach behavior: further evidence for limbic cortical–ventral striatopallidal systems

Parkinson, J. A., Willoughby, P. J., Robbins, T. W., & Everitt, B. J. (2000) · Behavioral Neuroscience · doi:10.1037/0735-7044.114.1.42 · Cited by 314

Neural responses associated with cue evoked emotional states and heroin in opiate addicts

Sell, L., Morris, J. S., Bearn, J., Frackowiak, R. S. J., Friston, K. J., & Dolan, R. J. (2000) · Drug and Alcohol Dependence · doi:10.1016/s0376-8716(99)00158-1 · Cited by 235

Expected Value, Reward Outcome, and Temporal Difference Error Representations in a Probabilistic Decision Task

Rolls, E. T., McCabe, C., & Redouté, J. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm097 · Cited by 251

Food for thought: hedonic experience beyond homeostasis in the human brain

Kringelbach, M. L. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.04.035 · Cited by 236

Neural Encoding in Ventral Striatum during Olfactory Discrimination Learning

Setlow, B., Schoenbaum, G. M., & Gallagher, M. (2003) · Neuron · doi:10.1016/s0896-6273(03)00264-2 · Cited by 220

Encoding of Palatability and Appetitive Behaviors by Distinct Neuronal Populations in the Nucleus Accumbens

Taha, S. A., & Fields, H. L. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3975-04.2005 · Cited by 217

Dopamine gating of glutamatergic sensorimotor and incentive motivational input signals to the striatum

Horvitz, J. C. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00285-1 · Cited by 205

Cue-Evoked Firing of Nucleus Accumbens Neurons Encodes Motivational Significance During a Discriminative Stimulus Task

Nicola, S. M., Yun, I. A., Wakabayashi, K. T., & Fields, H. L. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00657.2003 · Cited by 196

Cerebral cortex : principles of operation

Rolls, E. T. (2016) · doi:10.82444/warw.33712699 · Cited by 187

Heterogeneous Coding of Temporally Discounted Values in the Dorsal and Ventral Striatum during Intertemporal Choice

Cai, X., Kim, S., & Lee, D. (2011) · Neuron · doi:10.1016/j.neuron.2010.11.041 · Cited by 185

Separate brain regions code for salience vs. valence during reward prediction in humans

Jensen, J., Smith, A. J., Willeit, M., Crawley, A. P., Mikulis, D. J., Vitcu, I., & Kapur, S. (2006) · Human Brain Mapping · doi:10.1002/hbm.20274 · Cited by 184

Comparison of learning‐related neuronal activity in the dorsal premotor cortex and striatum

Brasted, P. J., & Wise, S. P. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2003.03181.x · Cited by 171

Cholinergic interneurons in the dorsal and ventral striatum: anatomical and functional considerations in normal and diseased conditions

Gonzales, K. K., & Smith, Y. (2015) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12762 · Cited by 175

Disconnection of the basolateral amygdala complex and nucleus accumbens impairs appetitive Pavlovian second-order conditioned responses.

Setlow, B., Holland, P. C., & Gallagher, M. (2002) · Behavioral Neuroscience · doi:10.1037//0735-7044.116.2.267 · Cited by 160

Convergence of sensory systems in the orbitofrontal cortex in primates and brain design for emotion.

Rolls, E. (2004) · Anatomical Record Part A-discoveries in Molecular Cellular and Evolutionary Biology · doi:10.1002/ar.a.20126 · Cited by 170

P300 amplitude variation is related to ventral striatum BOLD response during gain and loss anticipation: An EEG and fMRI experiment

Pfabigan, D. M., Seidel, E., Sladky, R., Hahn, A., Paul, K., Grahl, A., Küblböck, M., Kraus, C., Hummer, A., Kranz, G. S., et al. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.03.077 · Cited by 166

The influence of stress on neuroinflammation and alterations in brain structure and function in major depressive disorder

Kim, Y., & Won, E. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.04.020 · Cited by 160

The representation of information about faces in the temporal and frontal lobes

Rolls, E. T. (2006) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.04.019 · Cited by 150

Activation of reward circuitry in human opiate addicts

Sell, L., Morris, J., Bearn, J., Frackowiak, R. S. J., Friston, K. J., & Dolan, R. J. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00522.x · Cited by 146

Taste and smell processing in the brain

Rolls, E. T. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63855-7.00007-1 · Cited by 150

The functions of the orbitofrontal cortex.

Rolls, E. (1999) · Brain and Cognition · doi:10.1080/13554799908411984 · Cited by 1,505

Lesions of Nucleus Accumbens Disrupt Learning about Aversive Outcomes

Schoenbaum, G. M., & Setlow, B. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-30-09833.2003 · Cited by 137

Disconnection of the basolateral amygdala complex and nucleus accumbens impairs appetitive pavlovian second-order conditioned responses

Setlow, B., Holland, P. C., & Gallagher, M. (2002) · Behavioral Neuroscience · doi:10.1037/0735-7044.116.2.267 · Cited by 160

The Olfactory Tubercle Encodes Odor Valence in Behaving Mice

Gadziola, M. A., Tylicki, K. A., Christian, D. L., & Wesson, D. W. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4750-14.2015 · Cited by 137

Response Differences in Monkey TE and Perirhinal Cortex: Stimulus Association Related to Reward Schedules

Liu, Z., & Richmond, B. J. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.3.1677 · Cited by 132

IS FACE RECOGNITION NOT SO UNIQUE AFTER ALL?

Gauthier, L., & Logothetis, N. K. (2000) · Cognitive Neuropsychology · doi:10.1080/026432900380535 · Cited by 133

The nucleus accumbens and reward: neurophysiological investigations in behaving animals

Carelli, R. M. (2002) · Behavioral and Cognitive Neuroscience Reviews · doi:10.1177/1534582302238338 · Cited by 131

The bivalent side of the nucleus accumbens

Levita, L., Hare, T. A., Voss, H. U., Glover, G., Ballon, D. J., & Casey, B. J. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.09.039 · Cited by 117

Responses of Tonically Active Neurons in the Monkey Striatum Discriminate between Motivationally Opposing Stimuli

Ravel, S., Legallet, E., & Apicella, P. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-24-08489.2003 · Cited by 118

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 122

Brain mechanisms for invariant visual recognition and learning

Rolls, E. T. (1994) · Behavioural Processes · doi:10.1016/0376-6357(94)90062-0 · Cited by 116

Responses of Primate Taste Cortex Neurons to the Astringent Tastant Tannic Acid

Critchley, H., & Rolls, E. T. (1996) · Chemical Senses · doi:10.1093/chemse/21.2.135 · Cited by 113

Responses of neurons in the primate taste cortex to the glutamate ion and to inosine 5′-monophosphate

Rolls, E. T. (1996) · Physiology & Behavior · doi:10.1016/0031-9384(95)02178-7 · Cited by 107

Impact of instructed relevance on the visual ERP

Potts, G. F., Patel, S. H., & Azzam, P. N. (2004) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2003.10.005 · Cited by 104

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

The von Restorff Effect in Visual Object Recognition Memory in Humans and Monkeys: The Role of Frontal/Perirhinal Interaction

Parker, A. J., Wilding, E. L., & Akerman, C. J. (1998) · Journal of Cognitive Neuroscience · doi:10.1162/089892998563103 · Cited by 86

Brain activation during human defensive behaviour: A systematic review and preliminary meta-analysis

Patrick, F., Kempton, M. J., Marwood, L., Williams, S., Young, A. H., & Perkins, A. M. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.12.028 · Cited by 82

Cocaine exposure shifts the balance of associative encoding from ventral to dorsolateral striatum

Takahashi, Y. K. (2007) · Frontiers in Integrative Neuroscience · doi:10.3389/neuro.07.011.2007 · Cited by 82

Object vision and visual awareness

Logethetis, N. (1998) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(98)80043-3 · Cited by 82

The nucleus accumbens in monkeys (Macaca fascicularis)

Stern, C., & Passingham, R. E. (1995) · Experimental Brain Research · doi:10.1007/bf00241119 · Cited by 76

Selective excitotoxic lesions of the nucleus accumbens core and shell differentially affect aversive Pavlovian conditioning to discrete and contextual cues

Parkinson, J. A., Robbins, T. W., & Everitt, B. J. (1999) · Psychobiology · doi:10.3758/bf03332119 · Cited by 74

Expectancies in decision making, reinforcement learning, and ventral striatum

van der Meer, M. A. A. (2010) · Frontiers in Neuroscience · doi:10.3389/neuro.01.006.2010 · Cited by 72

The cholinergic system and neostriatal memory functions

Havekes, R., Abel, T. G., & van der Zee, E. A. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.11.047 · Cited by 69

The roles of the orbitofrontal cortex via the habenula in non-reward and depression, and in the responses of serotonin and dopamine neurons

Rolls, E. T. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.02.013 · Cited by 62

The neuroscience of emotional disorders.

Rolls, E. (2021) · Handbook of Clinical Neurology · doi:10.1016/b978-0-12-822290-4.00002-5 · Cited by 29

Memory reactivation and consolidation during sleep: from cellular mechanisms to human performance

Pennartz, C. M. A., Uylings, H. B. M., Barnes, C. A., & McNaughton, B. L. (2002) · Progress in brain research · doi:10.1016/s0079-6123(02)38076-2 · Cited by 59

The neurophysiology and functions of the orbitofrontal cortex

Rolls, E. T. (2006) · doi:10.1093/acprof:oso/9780198565741.003.0005 · Cited by 57

Studies on the involvement of the dopaminergic system in the 5-HT2 agonist (DOI)-induced premature responding in a five-choice serial reaction time task

Koskinen, T., & Sirviö, J. (2001) · Brain Research Bulletin · doi:10.1016/s0361-9230(00)00425-1 · Cited by 56

Rapid Rule-Based Reward Reversal and the Lateral Orbitofrontal Cortex

Rolls, E. T., Vatansever, D., Li, Y., Cheng, W., & Feng, J. (2020) · Cerebral Cortex Communications · doi:10.1093/texcom/tgaa087 · Cited by 56

The prototype effect revisited: Evidence for an abstract feature model of face recognition

Wallis, G. M., Siebeck, U. E., Swann, K., Blanz, V., & Bülthoff, H. (2008) · Journal of Vision · doi:10.1167/8.3.20 · Cited by 56

The neural control of feeding in primates

Rolls, E. T. (1993) · Elsevier eBooks · doi:10.1016/b978-0-08-041988-6.50013-4 · Cited by 55

The Tubular Striatum

Wesson, D. W. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1109-20.2020 · Cited by 50

Comparative Cognitive Neuropsychological Studies of Frontal Lobe Function: Implications for Therapeutic Strategies in Frontal Variant Frontotemporal Dementia

Rahman, S., Robbins, T. W., & Sahakian, B. J. (1999) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000051207 · Cited by 54

Role of a lateralized parietal-basal ganglia circuit in hierarchical pattern perception: Evidence from Parkinson's disease.

Schendan, H. E., Amick, M. M., & Cronin‐Golomb, A. (2009) · Behavioral Neuroscience · doi:10.1037/a0013734 · Cited by 50

Firing Patterns of Accumbal Neurons During a Pavlovian-Conditioned Approach Task

Wan, X., & Peoples, L. L. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00068.2006 · Cited by 50

Understanding the attraction process

Montoya, R. M., & Horton, R. S. (2020) · Social and Personality Psychology Compass · doi:10.1111/spc3.12526 · Cited by 49

The Neural Representation of Goal-Directed Actions and Outcomes in the Ventral Striatum's Olfactory Tubercle

Gadziola, M. A., & Wesson, D. W. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3328-15.2016 · Cited by 52

Two what, two where, visual cortical streams in humans

Rolls, E. T. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105650 · Cited by 48

Differential Changes in Signal and Background Firing of Accumbal Neurons During Cocaine Self-Administration

Peoples, L. L., & Cavanaugh, D. J. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00849.2002 · Cited by 45

Integrating early results on ventral striatal gamma oscillations in the rat

van der Meer, M. A. A. (2010) · Frontiers in Neuroscience · doi:10.3389/fnins.2010.00028 · Cited by 43

Neural correlates of insomnia with depression and anxiety from a neuroimaging perspective: A systematic review

Chen, P., Wang, K., Wang, J., Wassing, R., Eickhoff, S. B., Tahmasian, M., & Ji, C. (2025) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2025.102093 · Cited by 46

Different representation of forthcoming reward in nucleus accumbens and medial prefrontal cortex

Miyazaki, K., Miyazaki, K. W., & Matsumoto, G. (2004) · Neuroreport · doi:10.1097/00001756-200403220-00030 · Cited by 40

The nucleus accumbens in monkeys (Macaca fascicularis): II. Emotion and motivation

Stern, C. E., & Passingham, R. E. (1996) · Behavioural Brain Research · doi:10.1016/0166-4328(96)00169-6 · Cited by 37

Omega-3 Fatty Acid Deficiency and Behavior

Reisbick, S., & Neuringer, M. D. (1997) · Humana Press eBooks · doi:10.1007/978-1-4757-2582-7_17 · Cited by 35

Response in taste circuitry is not modulated by hunger and satiety in women remitted from bulimia nervosa

Ely, A. V., Wierenga, C., Bischoff-Grethe, A., Bailer, U., Berner, L. A., Fudge, J., Paulus, M., & Kaye, W. (2017) · Journal of Abnormal Psychology · doi:10.1037/abn0000218 · Cited by 30

Taste, Olfactory, Visual, and Somatosensory Representations of the Sensory Properties of Foods in the Brain, and Their Relation to the Control of Food Intake

Rolls, E. T. (1999) · CRC Press eBooks · doi:10.1201/9781420048933.sec3 · Cited by 32

The glutamate hypothesis of reinforcement learning

Pennartz, C. M. A., McNaughton, B. L., & Mulder, A. B. (2000) · Progress in brain research · doi:10.1016/s0079-6123(00)26017-2 · Cited by 33

Invariant Representations of Objects in Natural Scenes in the Temporal Cortex Visual Areas

Rolls, E. T. (2007) · Springer eBooks · doi:10.1007/978-4-431-73021-7_3 · Cited by 31

Disruption of self‐organized actions in monkeys with progressive MPTP‐induced parkinsonism: II. Effects of reward preference

Pessiglione, M., Guehl, D., Jan, C., François, C., Hirsch, É. C., Féger, J., & Tremblay, L. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2003.03089.x · Cited by 31

Rat Nucleus Accumbens Neurons Predominantly Respond to the Outcome-Related Properties of Conditioned Stimuli Rather Than Their Behavioral-Switching Properties

Wilson, D. I. G., & Bowman, E. M. (2005) · Journal of Neurophysiology · doi:10.1152/jn.01332.2004 · Cited by 29

A Comparison of Reward‐Contingent Neuronal Activity in Monkey Orbitofrontal Cortex and Ventral Striatum

Simmons, J. M., Ravel, S., Shidara, M., & Richmond, B. J. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.028 · Cited by 33

Face processing in different brain areas, and critical band masking

Rolls, E. T. (2008) · Journal of Neuropsychology · doi:10.1348/174866407x258903 · Cited by 28

New directions in modelling dysregulated reward seeking for food and drugs

Brown, R. M., Dayas, C. V., James, M. H., & Smith, R. J. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.10.043 · Cited by 27

Responses of striatal neurons in the behaving monkey. 1. Head of the caudate nucleus

Rolls, E. T., Thorpe, S. J., & Maddison, S. P. (1983) · Behavioural Brain Research · doi:10.1016/0166-4328(83)90191-2 · Cited by 256

Responses of cells in the tail of the caudate nucleus during visual discrimination learning

Brown, V. J., Desimone, R., & Mishkin, M. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.74.3.1083 · Cited by 90

Responses of Tonic Striatal Neurons to Conditioned Stimuli in Behaving Monkeys

Apicella, P., Legallet, E., & Trouche, E. (1996) · Advances in behavioral biology · doi:10.1007/978-1-4899-0194-1_27 · Cited by 2

Responses to reward in monkey dorsal and ventral striatum

Apicella, P., Ljungberg, T., Scarnati, E., & Schultz, W. (1991) · Experimental Brain Research · doi:10.1007/bf00231732 · Cited by 369

Elsevier Responses of Striatal Neurons in the Behaving Monkey. 2. Visual Processing in the

Neostriatum, C., Caan, W., Perrett, D. I., & Rolls, E. T. (1983)