Expectancy, ambiguity, and behavioral flexibility: separable and complementary roles of the orbital frontal cortex and amygdala in processing reward expectancies

Reinforcement Learning: An Introduction

Sutton, R. S., & Barto, A. G. (1998) · IEEE Transactions on Neural Networks · doi:10.1109/tnn.1998.712192 · Cited by 27,225 · see citing works

Reinforcement Learning: An Introduction

Sutton, R. S., & Barto, A. (2005) · IEEE Transactions on Neural Networks · doi:10.1109/tnn.2004.842673 · Cited by 25,263 · see citing works

Untitled work

(1994) · DigitalGeorgetown (Georgetown University Library) · Cited by 10,542 · see citing works

Parallel organization of functionally segregated circuits linking basal ganglia and cortex

Alexander, G. E., DeLong, M. R., & Strick, P. L. (1986) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.09.030186.002041 · Cited by 8,527 · see citing works

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

Introduction to Reinforcement Learning

Sutton, R. S., & Barto, A. G. (1998) · The MIT Press eBooks · Cited by 6,855 · see citing works

Learning to predict by the methods of temporal differences

Sutton, R. S. (1988) · Machine Learning · doi:10.1007/bf00115009 · Cited by 5,148 · see citing works

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

Neural systems of reinforcement for drug addiction: from actions to habits to compulsion

Everitt, B. J., & Robbins, T. W. (2005) · Nature Neuroscience · doi:10.1038/nn1579 · Cited by 3,785 · see citing works

The Organization of Networks within the Orbital and Medial Prefrontal Cortex of Rats, Monkeys and Humans

Ongur, D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.206 · Cited by 2,627 · see citing works

THE BASAL GANGLIA: FOCUSED SELECTION AND INHIBITION OF COMPETING MOTOR PROGRAMS

Mink, J. W. (1996) · Progress in Neurobiology · doi:10.1016/s0301-0082(96)00042-1 · Cited by 2,478 · see citing works

Simplified neuron model as a principal component analyzer

Oja, E. (1982) · Journal of Mathematical Biology · doi:10.1007/bf00275687 · Cited by 2,309 · see citing works

Emotion and motivation: the role of the amygdala, ventral striatum, and prefrontal cortex

Cardinal, R. N., Parkinson, J. A., Hall, J., & Everitt, B. J. (2002) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(02)00007-6 · Cited by 2,129 · see citing works

By Carrot or by Stick: Cognitive Reinforcement Learning in Parkinsonism

Frank, M. J., Seeberger, L. C., & O'Reilly, R. C. (2004) · Science · doi:10.1126/science.1102941 · Cited by 1,964 · see citing works

The principal features and mechanisms of dopamine modulation in the prefrontal cortex

Seamans, J. K., & Yang, C. R. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.05.006 · Cited by 1,592 · see citing works

Dissociation in prefrontal cortex of affective and attentional shifts

Dias, R., Robbins, T. W., & Roberts, A. C. (1996) · Nature · doi:10.1038/380069a0 · Cited by 1,527 · see citing works

Descartes' Error: Emotion, Reason, and the Human Brain

Joynt, R. J. (1995) · JAMA · doi:10.1001/jama.1995.03520420079045 · Cited by 1,447 · see citing works

The Role of the Dorsal Striatum in Reward and Decision-Making: Figure 1.

Balleine, B. W., Delgado, M. R., & Hikosaka, O. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1554-07.2007 · Cited by 1,390 · see citing works

The organization of the projection from the cerebral cortex to the striatum in the rat

McGeorge, A. J., & Faull, R. L. M. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90128-0 · Cited by 1,345 · 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

The amygdala: Neurobiological aspects of emotion, memory and mental dysfunction

Scheel-Krüger, J. (1993) · Journal of Chemical Neuroanatomy · doi:10.1016/0891-0618(93)90037-5 · Cited by 1,277 · see citing works

Models of Information Processing in the Basal Ganglia

(1994) · doi:10.7551/mitpress/4708.001.0001 · Cited by 1,190 · see citing works

Dichotomous dopaminergic control of striatal synaptic plasticity

Shen, W., Flajolet, M., Greengard, P., & Surmeier, D. J. (2008) · Science · doi:10.1126/science.1160575 · Cited by 1,190 · see citing works

Encoding Predictive Reward Value in Human Amygdala and Orbitofrontal Cortex

Gottfried, J. A., O'Doherty, J., & Dolan, R. J. (2003) · Science · doi:10.1126/science.1087919 · Cited by 1,165 · see citing works

Fear and the human amygdala

Adolphs, R., Tranel, D., Damasio, H., & Damasio, A. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-09-05879.1995 · Cited by 1,138 · see citing works

Tonic dopamine: Opportunity costs and the control of response vigor

Niv, Y., Daw, N. D., Joel, D., & Dayan, P. (2007) · Psychopharmacology · doi:10.1007/s00213-006-0502-4 · Cited by 1,133 · see citing works

Afferent modulation of dopamine neuron firing differentially regulates tonic and phasic dopamine transmission

Floresco, S. B., West, A. R., Ash, B., Moore, H., & Grace, A. A. (2003) · Nature Neuroscience · doi:10.1038/nn1103 · Cited by 1,106 · see citing works

The role of the dorsomedial striatum in instrumental conditioning

Yin, H. H., Ostlund, S. B., Knowlton, B. J., & Balleine, B. W. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04218.x · Cited by 1,099 · see citing works

Cortical mechanisms of action selection: the affordance competition hypothesis

Cisek, P. (2007) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2007.2054 · Cited by 1,077 · see citing works

Making Working Memory Work: A Computational Model of Learning in the Prefrontal Cortex and Basal Ganglia

O’Reilly, R. C., & Frank, M. J. (2005) · Neural Computation · doi:10.1162/089976606775093909 · Cited by 1,066 · see citing works

Architectonic subdivision of the human orbital and medial prefrontal cortex

Öngür, D., Ferry, A. T., & Price, J. L. (2003) · Journal of Comparative Neurology · doi:10.1002/cne.10609 · Cited by 944 · see citing works

Orbitofrontal cortex and its contribution to decision-making.

Wallis, J. D. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094334 · Cited by 938 · see citing works

Dopaminergic modulation of neuronal excitability in the striatum and nucleus accumbens

Nicola, S. M., Surmeier, D. J., & Malenka, R. C. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.185 · Cited by 931 · see citing works

Dynamic Dopamine Modulation in the Basal Ganglia: A Neurocomputational Account of Cognitive Deficits in Medicated and Nonmedicated Parkinsonism

Frank, M. J. (2005) · Journal of Cognitive Neuroscience · doi:10.1162/0898929052880093 · Cited by 925 · see citing works

The primate amygdala represents the positive and negative value of visual stimuli during learning

Paton, J. J., Belova, M. A., Morrison, S. E., & Salzman, C. D. (2006) · Nature · doi:10.1038/nature04490 · Cited by 917 · see citing works

Why We Think Plasticity Underlying Pavlovian Fear Conditioning Occurs in the Basolateral Amygdala

Fanselow, M. S., & LeDoux, J. E. (1999) · Neuron · doi:10.1016/s0896-6273(00)80775-8 · Cited by 914 · see citing works

Dissociable functions in the medial and lateral orbitofrontal cortex: Evidence from human neuroimaging studies

Elliott, R. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.308 · Cited by 887 · see citing works

Interactions between frontal cortex and basal ganglia in working memory: A computational model

FRANK, M. J., LOUGHRY, B., & O'REILLY, R. C. (2001) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.1.2.137 · Cited by 879 · see citing works

Synaptic basis of cortical persistent activity: the importance of NMDA receptors to working memory

Wang, X.-J. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-21-09587.1999 · Cited by 859 · see citing works

Orbitofrontal cortex and basolateral amygdala encode expected outcomes during learning

Schoenbaum, G. M., Chiba, A. A., & Gallagher, M. (1998) · Nature Neuroscience · doi:10.1038/407 · Cited by 849 · see citing works

Untitled work

(1964) · McGraw-Hill eBooks · Cited by 838 · see citing works

The orbitofrontal cortex: Neuronal activity in the behaving monkey

Thorpe, S. J., Rolls, E. T., & Maddison, S. (1983) · Experimental Brain Research · doi:10.1007/bf00235545 · Cited by 836 · see citing works

The orbitofrontal cortex and beyond: From affect to decision-making

Rolls, E. T., & Fabian Grabenhorst, B. (2008) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2008.09.001 · Cited by 808 · see citing works

Fear conditioning enhances short-latency auditory responses of lateral amygdala neurons: Parallel recordings in the freely behaving rat

Quirk, G. J., Repa, J. C., & LeDoux, J. E. (1995) · Neuron · doi:10.1016/0896-6273(95)90092-6 · Cited by 808 · see citing works

Dissociating the role of the orbitofrontal cortex and the striatum in the computation of goal values and prediction errors

Hare, T. A., O'Doherty, J., Camerer, C. F., Schultz, W., & Rangel, A. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1309-08.2008 · Cited by 792 · see citing works

Pathways for emotion: interactions of prefrontal and anterior temporal pathways in the amygdala of the rhesus monkey

Ghashghaei, H. T., & Barbas, H. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00446-3 · Cited by 785 · see citing works

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 · see citing works

Neurocomputational models of working memory

Durstewitz, D., Seamans, J. K., & B, T. J. S. A. (2000) · Nature Neuroscience · doi:10.1038/81460 · Cited by 710 · see citing works

The frontal granular cortex and behavior

Pribram, K. H. (1965) · Neuropsychologia · doi:10.1016/0028-3932(65)90022-9 · Cited by 705 · see citing works

The amygdala, reward and emotion

Murray, E. A. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.08.013 · Cited by 679 · see citing works

Do Rats Have Prefrontal Cortex? The Rose-Woolsey-Akert Program Reconsidered

Preuss, T. M. (1995) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1995.7.1.1 · Cited by 666 · see citing works

Basal Ganglia Output and Cognition: Evidence from Anatomical, Behavioral, and Clinical Studies

Middleton, F. A., & Strick, P. L. (2000) · Brain and Cognition · doi:10.1006/brcg.1999.1099 · Cited by 657 · see citing works

A computational model of action selection in the basal ganglia. I. A new functional anatomy

GURNEY, K. N., Prescott, T. J., & Redgrave, P. (2001) · Biological Cybernetics · doi:10.1007/pl00007984 · Cited by 633 · see citing works

Untitled work

(1992) · Cited by 626 · see citing works

The connections of the dopaminergic system with the striatum in rats and primates: an analysis with respect to the functional and compartmental organization of the striatum

Joel, D., & Weiner, I. (2000) · Neuroscience · doi:10.1016/s0306-4522(99)00575-8 · Cited by 614 · see citing works

The Cognitive Neuroscience of Emotion

Watt, D. F. (2001) · Neuropsychoanalysis · doi:10.1080/15294145.2001.10773346 · Cited by 610 · see citing works

Feature Article: Distributed Modular Architectures Linking Basal Ganglia, Cerebellum, and Cerebral Cortex: Their Role in Planning and Controlling Action

Houk, J. C., & Wise, S. P. (1995) · Cerebral Cortex · doi:10.1093/cercor/5.2.95 · Cited by 594 · see citing works

A new perspective on the role of the orbitofrontal cortex in adaptive behaviour

Schoenbaum, G., Roesch, M. R., Stalnaker, T. A., & Takahashi, Y. K. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2753 · Cited by 585 · see citing works

Neural Encoding in Orbitofrontal Cortex and Basolateral Amygdala during Olfactory Discrimination Learning

Schoenbaum, G., Chiba, A. A., & Gallagher, M. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-05-01876.1999 · Cited by 579 · see citing works

Basal ganglia functional connectivity based on a meta-analysis of 126 positron emission tomography and functional magnetic resonance imaging publications

Postuma, R. B., & Dagher, A. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhj088 · Cited by 579 · see citing works

Anatomy of a decision: Striato-orbitofrontal interactions in reinforcement learning, decision making, and reversal.

Frank, M. J., & Claus, E. D. (2006) · Psychological Review · doi:10.1037/0033-295x.113.2.300 · Cited by 578 · see citing works

Computational Explorations in Cognitive Neuroscience

O’Reilly, R. C., & Munakata, Y. (2000) · The MIT Press eBooks · doi:10.7551/mitpress/2014.001.0001 · Cited by 564 · see citing works

A Model of How the Basal Ganglia Generate and Use Neural Signals That Predict Reinforcement

Houk, J. C., Adams, J. L., & Barto, A. G. (1994) · The MIT Press eBooks · doi:10.7551/mitpress/4708.003.0020 · Cited by 555 · see citing works

Neurotoxic lesions of basolateral, but not central, amygdala interfere with Pavlovian second-order conditioning and reinforcer devaluation effects

Hatfield, T., Han, J.-S., Conley, M., Gallagher, M., & Holland, P. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05256.1996 · Cited by 555 · see citing works

Afferent connections of the laterodorsal and the pedunculopontine tegmental nuclei in the rat: A retro‐ and antero‐grade transport and immunohistochemical study

Semba, K., & Fibiger, H. C. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903230307 · Cited by 544 · see citing works

Contrasting roles for cingulate and orbitofrontal cortex in decisions and social behaviour

Rushworth, M. F. S., Behrens, T. E. J., Rudebeck, P. H., & Walton, M. E. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.01.004 · Cited by 507 · see citing works

D1Receptor Activation Enhances Evoked Discharge in Neostriatal Medium Spiny Neurons by Modulating an L-Type Ca2+Conductance

Hernández‐López, S., Bargas, J., Surmeier, D. J., Reyes, A., & Galarraga, E. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-09-03334.1997 · Cited by 495 · see citing works

Encoding predicted outcome and acquired value in orbitofrontal cortex during cue sampling depends upon input from basolateral amygdala.

Schoenbaum, G., Setlow, B., Saddoris, M. P., & Gallagher, M. (2003) · Neuron · doi:10.1016/s0896-6273(03)00474-4 · Cited by 484 · see citing works

Towards an executive without a homunculus: computational models of the prefrontal cortex/basal ganglia system

Hazy, T. E., Frank, M. J., & O’Reilly, R. C. (2007) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2007.2055 · Cited by 450 · see citing works

Biologically Based Computational Models of High-Level Cognition

O’Reilly, R. C. (2006) · Science · doi:10.1126/science.1127242 · Cited by 447 · see citing works

A role for NMDA-receptor channels in working memory

Lisman, J. E., Fellous, J., & Wang, X. (1998) · Nature Neuroscience · doi:10.1038/1086 · Cited by 438 · see citing works

How does PKMζ maintain long-term memory?

Sacktor, T. C. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn2949 · Cited by 431 · see citing works

Orbitofrontal cortex, associative learning and expectancies

Schoenbaum, G., & Roesch, M. (2005) · Neuron · doi:10.1016/j.neuron.2005.07.018 · Cited by 404 · see citing works

Stop-Signal Reaction-Time Task Performance: Role of Prefrontal Cortex and Subthalamic Nucleus

Eagle, D. M., Baunez, C., Hutcheson, D. M., Lehmann, O., Shah, A. P., & Robbins, T. W. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm044 · Cited by 404 · see citing works

Amygdala–frontal interactions and reward expectancy

Holland, P. C., & Gallagher, M. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.03.007 · Cited by 390 · see citing works

Banishing the homunculus: Making working memory work

Hazy, T. E., Frank, M. J., & O’Reilly, R. C. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.04.067 · Cited by 385 · see citing works

Orbitofrontal Cortex Mediates Outcome Encoding in Pavlovian But Not Instrumental Conditioning

Ostlund, S. B., & Balleine, B. W. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5443-06.2007 · Cited by 379 · cited 1× · see citing works

A Physiologically Plausible Model of Action Selection and Oscillatory Activity in the Basal Ganglia

Humphries, M. D., Stewart, R. D., & GURNEY, K. N. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3486-06.2006 · Cited by 364 · see citing works

Biologically plausible error-driven learning using local activation differences: the generalized recirculation algorithm

O'Reilly, R. C. (1996) · Neural Computation · doi:10.1162/neco.1996.8.5.895 · Cited by 352 · see citing works

Molecular effects of dopamine on striatal-projection pathways

Gerfen, C. R. (2000) · Trends in Neurosciences · doi:10.1016/s1471-1931(00)00019-7 · Cited by 341 · see citing works

Separate value comparison and learning mechanisms in macaque medial and lateral orbitofrontal cortex

Noonan, M. P., Walton, M. E., Behrens, T. E. J., Sallet, J., Buckley, M. J., & Rushworth, M. F. S. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1012246107 · Cited by 340 · see citing works

The amygdala, fear, and memory

FANSELOW, M. S., & GALE, G. D. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07077.x · Cited by 299 · see citing works

Ventral Tegmental Area Afferents to the Prefrontal Cortex Maintain Membrane Potential 'Up' States in Pyramidal Neurons via D1 Dopamine Receptors

Lewis, B. L. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.12.1168 · Cited by 287 · see citing works

The Orbitofrontal Cortex and Ventral Tegmental Area Are Necessary for Learning from Unexpected Outcomes

Takahashi, Y. K., Roesch, M. R., Stalnaker, T. A., Haney, R. Z., Calu, D. J., Taylor, A. R., Burke, K. A., & Schoenbaum, G. M. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.005 · Cited by 284 · see citing works

Models of information processing in the basal ganglia

Alexander, G. E. (1996) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0921-884x(96)89703-7 · Cited by 278 · see citing works

Lesions of the medial striatum in monkeys produce perseverative impairments during reversal learning similar to those produced by lesions of the orbitofrontal cortex

Clarke, H. F., Robbins, T. W., & Roberts, A. C. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1521-08.2008 · Cited by 263 · see citing works

How laminar frontal cortex and basal ganglia circuits interact to control planned and reactive saccades

Brown, J. W., Bullock, D. H., & Grossberg, S. (2003) · Neural Networks · doi:10.1016/j.neunet.2003.08.006 · Cited by 263 · see citing works

Active versus latent representations: A neural network model of perseveration, dissociation, and decalage

Morton, J. B., & Munakata, Y. (2002) · Developmental Psychobiology · doi:10.1002/dev.10033 · Cited by 260 · see citing works

Surround inhibition among projection neurons is weak or nonexistent in the rat neostriatum

Jaeger, D., Kita, H., & Wilson, C. J. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.72.5.2555 · Cited by 232 · see citing works

A Computational Model of How the Basal Ganglia Produce Sequences

Berns, G. S., & B, T. J. S. A. (1998) · Journal of Cognitive Neuroscience · doi:10.1162/089892998563815 · Cited by 231 · see citing works

Rapid Associative Encoding in Basolateral Amygdala Depends on Connections with Orbitofrontal Cortex

Saddoris, M. P., Gallagher, M., & Schoenbaum, G. M. (2005) · Neuron · doi:10.1016/j.neuron.2005.02.018 · Cited by 214 · see citing works

Cognitive-Emotional Interactions: Listen to the Brain

LeDoux, J. E. (1999) · doi:10.1093/oso/9780195118889.003.0007 · Cited by 210 · see citing works

Action selection and refinement in subcortical loops through basal ganglia and cerebellum

Houk, J. C., Bastianen, C., Fansler, D., Fishbach, A., Fraser, D. A., Reber, P. J., Roy, S. A., & Simó, L. S. (2007) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2007.2063 · Cited by 196 · see citing works

A Model of Corticostriatal Plasticity for Learning Oculomotor Associations and Sequences

Dominey, P. F., Arbib, M. A., & Joseph, J. (1995) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1995.7.3.311 · Cited by 191 · see citing works

Lesions of mediodorsal thalamus and anterior thalamic nuclei produce dissociable effects on instrumental conditioning in rats

Corbit, L. H., Muir, J. L., & Balleine, B. W. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02833.x · Cited by 186 · see citing works

Basolateral Amygdala Lesions Abolish Orbitofrontal-Dependent Reversal Impairments

Stalnaker, T. A., Franz, T. M., Singh, T., & Schoenbaum, G. M. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.014 · Cited by 178 · see citing works

Dopamine D1/D5 Receptor Activation Modulates a Persistent Sodium Current in Rat Prefrontal Cortical Neurons In Vitro

Gorelova, N. A., & Yang, C. R. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.1.75 · Cited by 162 · see citing works

A Theory of the Striatum

(1993) · Elsevier eBooks · doi:10.1016/c2009-0-35344-1 · Cited by 161 · see citing works

PVLV: The Primary Value and Learned Value Pavlovian Learning Algorithm.

O’Reilly, R. C., Frank, M. J., Hazy, T. E., & Watz, B. (2007) · Behavioral Neuroscience · doi:10.1037/0735-7044.121.1.31 · Cited by 144 · see citing works

The central nucleus of the amygdala projection to dopamine subpopulations in primates

Fudge, J. L., & Haber, S. N. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00092-0 · Cited by 138 · see citing works

Representation of olfactory information in the primate orbitofrontal cortex

Rolls, E. T., Critchley, H., & Treves, A. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.75.5.1982 · Cited by 136 · see citing works

Generalization in Interactive Networks: The Benefits of Inhibitory Competition and Hebbian Learning

O’Reilly, R. C. (2001) · Neural Computation · doi:10.1162/08997660152002834 · Cited by 133 · see citing works

Dissociable contributions of the orbitofrontal and lateral prefrontal cortex of the marmoset to performance on a detour reaching task

Wallis, J. D., Dias, R. S., Robbins, T. W., & Roberts, A. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01546.x · Cited by 113 · see citing works

Neural mechanisms of acquired phasic dopamine responses in learning

Hazy, T. E., Frank, M. J., & O’Reilly, R. C. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.11.019 · Cited by 103 · see citing works

Dorsal striatum and stimulus–response learning: lesions of the dorsolateral, but not dorsomedial, striatum impair acquisition of a simple discrimination task

Featherstone, R. E., & McDonald, R. J. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(03)00218-3 · Cited by 98 · see citing works

Abnormal associative encoding in orbitofrontal neurons in cocaine‐experienced rats during decision‐making

Stalnaker, T. A., Roesch, M. R., Franz, T. M., Burke, K. A., & Schoenbaum, G. M. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05128.x · Cited by 83 · see citing works

Functional and Anatomical Relationships among the Amygdala, Basal Forebrain, Ventral Striatum, and Cortex: An Integrative Discussion

Gray, T. S. (1999) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1999.tb09281.x · Cited by 69 · see citing works

Independent modulation of basal and feeding-evoked dopamine efflux in the nucleus accumbens and medial prefrontal cortex by the central and basolateral amygdalar nuclei in the rat.

Ahn, S., & Phillips, A. G. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00551-1 · Cited by 68 · see citing works

Place and contingency differential responses of monkey septal neurons during conditional place-object discrimination

Toshiaki, K. I. T. A., Nishijo, H., Eifuku, S., TERASAWA, K., & Ono, T. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-03-01683.1995 · Cited by 64 · see citing works

Effects of local connectivity on striatal function: Simulation and analysis of a model

Wickens, J. R., Kötter, R., & Alexander, M. E. (1995) · Synapse · doi:10.1002/syn.890200402 · Cited by 64 · see citing works

Rhesus Monkeys with Orbital Prefrontal Cortex Lesions Can Learn to Inhibit Prepotent Responses in the Reversed Reward Contingency Task

Chudasama, Y., Kralik, J. D., & Murray, E. A. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhl025 · Cited by 59 · see citing works

The contribution of NMDA receptors in the dorsolateral striatum to egocentric response learning.

Palencia, C. A., & Ragozzino, M. E. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.4.953 · Cited by 49 · see citing works

Reward sensitivity modulates connectivity among reward brain areas during processing of anticipatory reward cues

Costumero, V., Barrós‐Loscertales, A., Bustamante, J. C., Ventura‐Campos, N., Fuentes‐Claramonte, P., & Ávila, C. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12234 · Cited by 44 · see citing works

Effects of electrical stimulation of the central nucleus of the amygdala on the in vivo electrophysiological activity of rat nigral dopaminergic neurons

Rouillard, C., & Freeman, A. S. (1995) · Synapse · doi:10.1002/syn.890210410 · Cited by 16 · see citing works

Effects of dopaminergic modulation of persistent sodium currents on the excitability of prefrontal cortical neurons: A computational study

Dilmore, J. G., Gutkin, B. S., & Ermentrout, G. B. (1999) · Neurocomputing · doi:10.1016/s0925-2312(99)00005-3 · Cited by 13 · see citing works

Feedback Blunting: Total Sleep Deprivation Impairs Decision Making that Requires Updating Based on Feedback

Whitney, P. J., Hinson, J. M., Jackson, M. L., & Dongen, H. P. A. V. (2015) · SLEEP · doi:10.5665/sleep.4668 · Cited by 145 · see citing works

Orbitofrontal cortex volume and brain reward response in obesity

Shott, M. E., Cornier, M.-A., Mittal, V. A., Pryor, T. L., Orr, J. M., Brown, M. S., & Frank, G. (2014) · International Journal of Obesity · doi:10.1038/ijo.2014.121 · Cited by 129 · see citing works

Unraveling the Mysteries of Motivation

O’Reilly, R. C. (2020) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2020.03.001 · Cited by 48 · see citing works

Reward Sensitivity Is Associated with Brain Activity during Erotic Stimulus Processing

Costumero, V., Barrós-Loscertales, A., Bustamante, J. C., Ventura-Campos, N., Fuentes, P., Rosell-Negre, P., & Ávila, C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0066940 · Cited by 45 · see citing works

Reward sensitivity modulates connectivity among reward brain areas during processing of anticipatory reward cues

Costumero, V., Barrós‐Loscertales, A., Bustamante, J. C., Ventura‐Campos, N., Fuentes‐Claramonte, P., & Ávila, C. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12234 · Cited by 44 · see citing works

Inhibiting PKMζ reveals dorsal lateral and dorsal medial striatum store the different memories needed to support adaptive behaviorPreprint

Pauli, W. M., Clark, A. D., Guenther, H. J., O’Reilly, R. C., & Rudy, J. W. (2012) · Learning & Memory · doi:10.1101/lm.025148.111 · Cited by 44 · see citing works

The Leabra Cognitive Architecture: How to Play 20 Principles with Nature and Win!

O’Reilly, R. C., Hazy, T. E., & Herd, S. A. (2012) · Cited by 39 · see citing works

A pavlovian model of the amygdala and its influence within the medial temporal lobe

Carrere, M., & Alexandre, F. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00041 · Cited by 36 · see citing works

Multilevel models from biology to psychology: Mission impossible?

Bilder, R. M., Howe, A. G., & Sabb, F. W. (2013) · Journal of Abnormal Psychology · doi:10.1037/a0032263 · Cited by 36 · see citing works

Sleep loss, executive function, and decision-making

Satterfield, B. C., & Killgore, W. D. S. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-815373-4.00026-5 · Cited by 35 · see citing works

Goal-Driven Cognition in the Brain: A Computational FrameworkPreprint

O’Reilly, R. C., Hazy, T. E., Mollick, J., Mackie, P., & Herd, S. A. (2014) · arXiv (Cornell University) · doi:10.48550/arxiv.1404.7591 · Cited by 45 · see citing works

Higher Adherence to the Mediterranean Diet Is Associated With Preserved White Matter Integrity and Altered Structural Connectivity

Rodrigues, B., Coelho, A., Portugal‐Nunes, C., Magalhães, R. J. D. S., Moreira, P. S., Castanho, T. C., Amorim, L., Marques, P., Soares, J. M., Sousa, N., et al. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00786 · Cited by 32 · see citing works

Functional neuroimaging of visuospatial working memory tasks enables accurate detection of attention deficit and hyperactivity disorder

Hammer, R., Cooke, G. E., Stein, M. A., & Booth, J. R. (2015) · NeuroImage: Clinical · doi:10.1016/j.nicl.2015.08.015 · Cited by 25 · see citing works

A Systems-Neuroscience Model of Phasic Dopamine

Mollick, J., Hazy, T., Krueger, K. A., Nair, A., Mackie, P., Herd, S. A., & O'Reilly, R. (2020) · Psychology Review · doi:10.1037/rev0000199 · Cited by 20 · see citing works

Feedback associated with expectation for larger-reward improves visuospatial working memory performances in children with ADHD

Hammer, R., Tennekoon, M., Cooke, G. E., Gayda, J., Stein, M. A., & Booth, J. R. (2015) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2015.06.002 · Cited by 21 · see citing works

Test–retest reliability of the prefrontal response to affective pictures based on functional near-infrared spectroscopy

Huang, Y., Mao, M., Zong, Z., Zhou, H., Zhao, Y., Duan, L. F., Kreplin, U., & Xiao, X. N. (2017) · Journal of Biomedical Optics · doi:10.1117/1.jbo.22.1.016011 · Cited by 22 · see citing works

Understanding Neuronal Architecture in Obesity through Analysis of White Matter Connection Strength

Riederer, J., Shott, M. E., DeGuzman, M. C., Pryor, T. L., & Frank, G. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00271 · Cited by 20 · see citing works

Computational approaches to habits in a model-free world

Pauli, W. M., Cockburn, J., Pool, E. R., Perez, O. D., & O’Doherty, J. P. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.12.001 · Cited by 16 · see citing works

On the Complexity of Brain Disorders: A Symptom-Based Approach

Moustafa, A. A., Phillips, J. R., Kéri, S., Misiak, B., & Frydecka, D. (2016) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2016.00016 · Cited by 14 · see citing works

Neural Responses to Smoking Stimuli Are Influenced by Smokers' Attitudes towards Their Own Smoking Behaviour

Stippekohl, B., Winkler, M. H., Walter, B., Kagerer, S., Mucha, R. F., Pauli, P., Vaitl, D., & Stark, R. M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046782 · Cited by 12 · see citing works

A comparison of implicit and explicit reward learning in low risk alcohol users versus people who binge drink and people with alcohol dependence

Paelecke–Habermann, Y., Paelecke, M., Mauth, J., Tschisgale, J., Lindenmeyer, J., & Kübler, A. (2019) · Addictive Behaviors Reports · doi:10.1016/j.abrep.2019.100178 · Cited by 11 · see citing works

Control of goal-directed and inflexible actions by dorsal striatal melanocortin systems, in coordination with the central nucleus of the amygdala

Heaton, E. C., Seo, E. H., Butkovich, L. M., Yount, S. T., & Gourley, S. L. (2024) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2024.102629 · Cited by 8 · see citing works

Altered connectivity patterns of medial and lateral orbitofrontal cortex underlie the severity of bulimic symptoms

Li, W., Chen, X., Luo, Y., Xiao, M., Liu, Y., & Chen, H. (2024) · International Journal of Clinical and Health Psychology · doi:10.1016/j.ijchp.2024.100439 · Cited by 8 · see citing works

Low-intensity focused ultrasound to human amygdala reveals a causal role in ambiguous emotion processing and alters local and network activity

Algermissen, J., Rascu, M., Weber, L. A. E., den Boer, T., Martin, E. M., Treeby, B. E., Gray, M. D., Cleveland, R. O., Wittmann, M. K., Clarke, W. T., et al. (2026) · Neuron · doi:10.1016/j.neuron.2026.03.009 · Cited by 7 · see citing works

Computational models of motivated frontal function

O’Reilly, R. C., Russin, J., & Herd, S. A. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-12-804281-6.00017-3 · Cited by 7 · see citing works

Modeling Neuromodulation as a Framework to Integrate Uncertainty in General Cognitive Architectures

Alexandre, F., & Carrere, M. (2016) · Lecture notes in computer science · doi:10.1007/978-3-319-41649-6_33 · Cited by 5 · see citing works

Selective disruption of gray matter volume covariance in orbitofrontal cortex subregions among patients with functional constipation

Su, Q., Liu, L., Hua, T., Gong, J., Tian, H., Yun, J., & Cai, W. (2025) · Scientific Reports · doi:10.1038/s41598-025-00148-6 · Cited by 1 · see citing works

Differentiating the abnormalities of food and monetary reward cue processing associated with overweight/obesity: an ALE meta-analysis

Wang, N., Xiao, M., Hou, X., Lu, C., Yuan, R., Lam, C., Chen, H., & Cao, B. (2026) · International Journal of Obesity · doi:10.1038/s41366-026-02026-1 · Cited by 1 · see citing works

Modeling pavlovian conditioning with multiple neuronal populations

Carrere, M., & Alexandre, F. (2015) · International Joint Conference on Neural Networks (IJCNN) · doi:10.1109/ijcnn.2015.7280716

Computational Link Between Motivational Factors and Cognitive Deficits in Depression

Stolicyn, A., Romaniuk, L., Lawrie, S. M., & Seriès, P. (2026) · Cognitive Computation · doi:10.1101/2025.05.30.25328678

Sleep loss, decision-making, and executive function

Fluke, S. K., Satterfield, B. C., & Killgore, W. D. S. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-13954-3.00028-0

Low-intensity focused ultrasound to human amygdala reveals a causal role in ambiguous emotion processing and alters local and network activityPreprint

Algermissen, J., Weber, L. A. E., Rascu, M., & Klein-Flügge, M. C. (2025) · doi:10.17605/osf.io/wq7cg

Expectancy, Ambiguity, and Behavioral Flexibility: Separable and Complementary Roles of the Orbital Frontal Cortex and Amygdala in Processing Reward

Pauli, W. M., Hazy, T. E., & Oʼreilly, A. C. (2012)

Distinct roles for the amygdala and orbitofrontal cortex in representing the relative amount of expected reward

Saez, R. A., Saez, A., Paton, J. J., Lau, B., & Salzman, C. D. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.012 · Cited by 75 · see citing works

A Neural Mechanism of Cue-Outcome Expectancy Generated by the Interaction Between Orbitofrontal Cortex and Amygdala

Takei, K., Fujita, K., & Kashimori, Y. (2019) · Chemical Senses · doi:10.1093/chemse/bjz066 · Cited by 3 · see citing works

Functional Roles of Amygdala and Orbitofrontal Cortex in Adaptive Behavior

Antaket, L. C., Hamada, K., & Kashimori, Y. (2023) · Lecture notes in computer science · doi:10.1007/978-3-031-30108-7_7

Amygdala–frontal interactions and reward expectancy

Holland, P. C., & Gallagher, M. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.03.007 · Cited by 390 · see citing works