Orbitofrontal cortex, associative learning and expectancies

Different contributions of the human amygdala and ventromedial prefrontal cortex to decision-making

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Circuitry of Primate Prefrontal Cortex and Regulation of Behavior by Representational Memory

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Relative reward preference in primate orbitofrontal cortex

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Encoding Predictive Reward Value in Human Amygdala and Orbitofrontal Cortex

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Neural responses during anticipation of a primary taste reward

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Neural Economics and the Biological Substrates of Valuation

Montague, P. R., & Berns, G. S. (2002) · Neuron · doi:10.1016/s0896-6273(02)00974-1 · Cited by 994 · 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

The Involvement of the Orbitofrontal Cortex in the Experience of Regret

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Contrasting Roles of Basolateral Amygdala and Orbitofrontal Cortex in Impulsive Choice

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Orbitofrontal Cortex and Representation of Incentive Value in Associative Learning

Gallagher, M., McMahan, R. W., & Schoenbaum, G. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-15-06610.1999 · Cited by 593 · see citing works

Bilateral orbital prefrontal cortex lesions in rhesus monkeys disrupt choices guided by both reward value and reward contingency

Izquierdo, A., Suda, R. K., & Murray, E. A. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1921-04.2004 · Cited by 588 · 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

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

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A reexamination of the evidence for the somatic marker hypothesis: What participants really know in the Iowa gambling task

Maia, T. V., & McClelland, J. L. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0406666101 · Cited by 541 · see citing works

Neuronal Activity Related to Reward Value and Motivation in Primate Frontal Cortex

Roesch, M. R., & Olson, C. R. (2004) · Science · doi:10.1126/science.1093223 · Cited by 535 · 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

Contemporary Learning Theories: Pavlovian Conditioning and the Status of Traditional Learning Theory

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Effects of lesions of the orbitofrontal cortex on sensitivity to delayed and probabilistic reinforcement

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Different Roles for Orbitofrontal Cortex and Basolateral Amygdala in a Reinforcer Devaluation Task

Pickens, C. L., Saddoris, M. P., Setlow, B., Gallagher, M., Holland, P. C., & Schoenbaum, G. M. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-35-11078.2003 · Cited by 379 · see citing works

Dissociable Contributions of the Human Amygdala and Orbitofrontal Cortex to Incentive Motivation and Goal Selection

Arana, F. S., Parkinson, J. A., Hinton, E. C., Holland, A. J., Owen, A. M., & Roberts, A. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-29-09632.2003 · Cited by 342 · see citing works

Lesions of orbitofrontal cortex and basolateral amygdala complex disrupt acquisition of odor-guided discriminations and reversals.Preprint

Schoenbaum, G., Setlow, B., Nugent, S. L., Saddoris, M. P., & Gallagher, M. (2003) · Learning & memory (Cold Spring Harbor, N.Y.) · doi:10.1101/lm.55203 · Cited by 317 · see citing works

Excitotoxic lesions of the amygdala fail to produce impairment in visual learning for auditory secondary reinforcement but interfere with reinforcer devaluation effects in rhesus monkeys

Málková, L., Gaffan, D., & Murray, E. A. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-15-06011.1997 · Cited by 295 · see citing works

Orbitofrontal cortex is activated during breaches of expectation in tasks of visual attention

Nobre, A. C., Coull, J. T., Frith, C., & Mesulam, M. M. (1999) · Nature Neuroscience · doi:10.1038/4513 · Cited by 249 · 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

Lesions of the Orbitofrontal but not Medial Prefrontal Cortex Disrupt Conditioned Reinforcement in Primates

Pears, A., Parkinson, J. A., Hopewell, L. J., Everitt, B. J., & Roberts, A. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-35-11189.2003 · Cited by 136 · see citing works

The basolateral complex of the amygdala is necessary for acquisition but not expression of CS motivational value in appetitive Pavlovian second‐order conditioning

Setlow, B., Gallagher, M., & Holland, P. C. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02010.x · Cited by 115 · see citing works

The Role of the Primate Amygdala in Conditioned Reinforcement

Parkinson, J. A., Crofts, H. S., McGuigan, M., Tomic, D. L., Everitt, B. J., & Roberts, A. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-19-07770.2001 · Cited by 100 · see citing works

Neural substrates of olfactory discrimination learning with auditory secondary reinforcement. I. Contributions of the basolateral amygdaloid complex and orbitofrontal cortex

Cousens, G. A., & Otto, T. (2003) · Integrative Psychological and Behavioral Science · doi:10.1007/bf02688858 · Cited by 22 · see citing works

NEURAL MECHANISMS OF ADDICTION: The Role of Reward-Related Learning and Memory

Hyman, S. E., Malenka, R. C., & Nestler, E. J. (2006) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.113009 · Cited by 2,647 · see citing works

A framework for studying the neurobiology of value-based decision making

Rangel, A., Camerer, C., & Montague, P. R. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2357 · Cited by 2,184 · see citing works

Pleasure Systems in the Brain

Berridge, K. C., & Kringelbach, M. L. (2015) · Neuron · doi:10.1016/j.neuron.2015.02.018 · Cited by 1,730 · see citing works

Brain on stress: how the social environment gets under the skin

McEwen, B. S. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1121254109 · Cited by 1,200 · see citing works

Neuromarketing: the hope and hype of neuroimaging in business

Dan Ariely, C., & Berns, G. S. (2010) · Nature reviews. Neuroscience · doi:10.1038/nrn2795 · Cited by 1,112 · see citing works

Neural ensembles in CA3 transiently encode paths forward of the animal at a decision point

Johnson, A., & Redish, A. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3761-07.2007 · Cited by 1,003 · see citing works

Goals and Habits in the Brain

Dolan, R. J., & Dayan, P. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.007 · Cited by 977 · see citing works

Common and distinct networks underlying reward valence and processing stages: A meta-analysis of functional neuroimaging studies

Liu, X., Hairston, J., Schrier, M., & Fan, J. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.12.012 · Cited by 916 · see citing works

Orbitofrontal Cortex Encodes Willingness to Pay in Everyday Economic Transactions

Plassmann, H., O'Doherty, J., & Rangel, A. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2131-07.2007 · Cited by 855 · see citing works

Optogenetic investigation of neural circuits underlying brain disease in animal models

Tye, K. M., & Deisseroth, K. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3171 · Cited by 745 · see citing works

The amygdala and ventromedial prefrontal cortex in morality and psychopathy

Blair, R. J. R. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.07.003 · Cited by 742 · see citing works

Norepinephrine ignites local hotspots of neuronal excitation: How arousal amplifies selectivity in perception and memory

Mather, M., Clewett, D., Sakaki, M., & Harley, C. W. (2016) · Behavioral and Brain Sciences · doi:10.1017/s0140525x15000667 · Cited by 695 · see citing works

Impulsivity, frontal lobes and risk for addiction

Crews, F. T., & Boettiger, C. A. (2009) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2009.04.018 · Cited by 679 · 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

The neurobiology of psychopathic traits in youths

Blair, J. (2013) · Nature reviews. Neuroscience · doi:10.1038/nrn3577 · Cited by 620 · see citing works

Effort-Based Cost–Benefit Valuation and the Human Brain

Croxson, P. L., Walton, M. E., O'Reilly, J. X., Behrens, T. E. J., & Rushworth, M. F. S. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.4515-08.2009 · Cited by 560 · 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

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

Separate neural pathways process different decision costs

Rudebeck, P. H., Walton, M. E., Smyth, A. N., Bannerman, D. M., & Rushworth, M. F. S. (2006) · Nature Neuroscience · doi:10.1038/nn1756 · Cited by 580 · see citing works

Neurochemical Modulation of Response Inhibition and Probabilistic Learning in Humans

Chamberlain, S. R., Müller, U., Blackwell, A. D., Clark, L., Robbins, T. W., & Sahakian, B. J. (2006) · Science · doi:10.1126/science.1121218 · Cited by 573 · see citing works

Determining the neural substrates of goal-directed learning in the human brain

Valentin, V. V., Dickinson, A., & O'Doherty, J. P. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.0564-07.2007 · Cited by 529 · see citing works

Reward Processing in Schizophrenia: A Deficit in the Representation of Value

Gold, J. M., Waltz, J. A., Prentice, K. J., Morris, S. E., & Heerey, E. A. (2008) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn068 · Cited by 521 · see citing works

Parallel and interactive learning processes within the basal ganglia: relevance for the understanding of addiction

Belin, D., Jonkman, S., Dickinson, A., Robbins, T. W., & Everitt, B. J. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.09.027 · Cited by 520 · 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

Is Avoiding an Aversive Outcome Rewarding? Neural Substrates of Avoidance Learning in the Human Brain

Kim, H., Shimojo, S., & O’Doherty, J. P. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040233 · Cited by 447 · see citing works

A Review of Reward Processing and Motivational Impairment in Schizophrenia

Strauss, G. P., Waltz, J. A., & Gold, J. M. (2013) · Schizophrenia Bulletin · doi:10.1093/schbul/sbt197 · Cited by 447 · see citing works

Food Reward in the Absence of Taste Receptor Signaling

de Araujo, I. E., Oliveira-Maia, A. J., Sotnikova, T. D., Gainetdinov, R. R., Caron, M. G., Nicolelis, M. A. L., & Simon, S. A. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.032 · Cited by 431 · see citing works

Decision Making and Sequential Sampling from Memory

Shadlen, M. N., & Shohamy, D. (2016) · Neuron · doi:10.1016/j.neuron.2016.04.036 · Cited by 412 · see citing works

The Orbitofrontal Oracle: Cortical Mechanisms for the Prediction and Evaluation of Specific Behavioral Outcomes

Rudebeck, P. H., & Murray, E. A. (2014) · Neuron · doi:10.1016/j.neuron.2014.10.049 · Cited by 405 · see citing works

Early Tagging of Cortical Networks Is Required for the Formation of Enduring Associative Memory

Lesburguères, E., Gobbo, O. L., Alaux‐Cantin, S., Hambücken, A., Trifilieff, P., & Bontempi, B. (2011) · Science · doi:10.1126/science.1196164 · Cited by 390 · 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 · see citing works

Frontal cortex subregions play distinct roles in choices between actions and stimuli

Rudebeck, P. H., Behrens, T. E., Kennerley, S. W., Baxter, M. G., Buckley, M. J., Walton, M. E., & Rushworth, M. F. S. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.3541-08.2008 · Cited by 350 · see citing works

Double dissociation of the effects of medial and orbital prefrontal cortical lesions on attentional and affective shifts in mice

Bissonette, G. B., Martins, G. J., Franz, T. M., Harper, E. S., Schoenbaum, G., & Powell, E. M. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2820-08.2008 · Cited by 353 · see citing works

Over the river, through the woods: cognitive maps in the hippocampus and orbitofrontal cortex

Wikenheiser, A. M., & Schoenbaum, G. M. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.56 · Cited by 353 · see citing works

Neural substrates of choice selection in adults and adolescents: development of the ventrolateral prefrontal and anterior cingulate cortices

Eshel, N., Nelson, E. E., Blair, R. J., Pine, D. S., & Ernst, M. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.10.004 · Cited by 355 · see citing works

The amygdala and ventromedial prefrontal cortex: functional contributions and dysfunction in psychopathy

Blair, J. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0027 · Cited by 343 · see citing works

Probing perceptual decisions in rodents

Carandini, M., & Churchland, A. K. (2013) · Nature Neuroscience · doi:10.1038/nn.3410 · Cited by 323 · see citing works

Pavlovian to instrumental transfer: a neurobehavioural perspective.

Holmes, N. M., Marchand, A., & Coutureau, E. (2010) · Neuroscience and Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.03.007 · Cited by 327 · see citing works

Probabilistic reversal learning impairments in schizophrenia: Further evidence of orbitofrontal dysfunction

Waltz, J. A., & Gold, J. M. (2007) · Schizophrenia Research · doi:10.1016/j.schres.2007.03.010 · Cited by 331 · see citing works

Anterolateral prefrontal cortex mediates the analgesic effect of expected and perceived control over pain

Wiech, K., Kalisch, R., Weiskopf, N., Pleger, B., Stephan, K. E., & Dolan, R. J. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.2568-06.2006 · Cited by 323 · see citing works

Selective Reinforcement Learning Deficits in Schizophrenia Support Predictions from Computational Models of Striatal-Cortical Dysfunction

Waltz, J. A., Frank, M. J., Robinson, B. M., & Gold, J. M. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.09.042 · Cited by 326 · see citing works

Negative Symptoms and the Failure to Represent the Expected Reward Value of Actions

Gold, J. M. (2012) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2011.1269 · Cited by 319 · see citing works

Neural and psychological mechanisms underlying compulsive drug seeking habits and drug memories – indications for novel treatments of addiction

Everitt, B. J. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12644 · Cited by 318 · see citing works

The Role of Orbitofrontal Cortex in Drug Addiction: A Review of Preclinical Studies

Schoenbaum, G. M., & Shaham, Y. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.06.003 · Cited by 314 · see citing works

The Role of the Orbitofrontal Cortex in Anxiety Disorders

Milad, M. R., & Rauch, S. L. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.006 · Cited by 313 · see citing works

A Role for the Macaque Anterior Cingulate Gyrus in Social Valuation

Rudebeck, P. H., Buckley, M. J., Walton, M. E., & Rushworth, M. F. S. (2006) · Science · doi:10.1126/science.1128197 · Cited by 312 · see citing works

A computational framework for the study of confidence in humans and animals

Kepecs, A., & Mainen, Z. F. (2012) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2012.0037 · Cited by 305 · see citing works

A Neural Computational Model of Incentive Salience

Zhang, J., Berridge, K. C., Tindell, A. J., Smith, K. S., & Aldridge, J. W. (2009) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000437 · Cited by 299 · see citing works

Immediate Reward Bias in Humans: Fronto-Parietal Networks and a Role for the Catechol-<i>O</i>-Methyltransferase 158^Val/ValGenotype

Boettiger, C. A., Mitchell, J. M., Tavares, V. C., Robertson, M., Joslyn, G., D'Esposito, M., & Fields, H. L. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2551-07.2007 · Cited by 300 · see citing works

Encoding of Time-Discounted Rewards in Orbitofrontal Cortex Is Independent of Value Representation

Roesch, M. R., Taylor, A. R., & Schoenbaum, G. (2006) · Neuron · doi:10.1016/j.neuron.2006.06.027 · Cited by 297 · see citing works

Recognizing resilience: Learning from the effects of stress on the brain

McEwen, B. S., Gray, J. D., & Nasca, C. (2015) · Neurobiology of Stress · doi:10.1016/j.ynstr.2014.09.001 · Cited by 292 · see citing works

Integrating hippocampus and striatum in decision-making

Johnson, A. C., van der Meer, M. A. A., & Redish, A. D. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.01.003 · Cited by 254 · see citing works

Projections of the medial orbital and ventral orbital cortex in the rat

Hoover, W. B., & Vertes, R. P. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22733 · Cited by 251 · see citing works

Disrupted Reinforcement Signaling in the Orbitofrontal Cortex and Caudate in Youths With Conduct Disorder or Oppositional Defiant Disorder and a High Level of Psychopathic Traits

Finger, E. C., Marsh, A. A., Blair, K. S., Reid, M. E., Sims, C., Ng, P., Pine, D. S., & Blair, J. (2010) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2010.10010129 · Cited by 253 · see citing works

Neurobiology of empathy and callousness: Implications for the development of antisocial behavior

Shirtcliff, E. A., Vitacco, M. J., Graf, A., Gostisha, A. J., Merz, J., & Zahn‐Waxler, C. (2009) · Behavioral Sciences & the Law · doi:10.1002/bsl.862 · Cited by 244 · see citing works

Psychopathy, frustration, and reactive aggression: The role of ventromedial prefrontal cortex

Blair, J. (2009) · British Journal of Psychology · doi:10.1348/000712609x418480 · Cited by 237 · see citing works

The Neurobiology of Impulsive Aggression

Blair, R. J. R. (2016) · Journal of Child and Adolescent Psychopharmacology · doi:10.1089/cap.2015.0088 · Cited by 235 · see citing works

The nexus between decision making and emotion regulation: A review of convergent neurocognitive substrates

Mitchell, D. G. V. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.10.030 · Cited by 219 · see citing works

Orbitofrontal Cortex Is Required for Optimal Waiting Based on Decision Confidence

Lak, A., Costa, G. M., Romberg, E., Koulakov, A. A., Mainen, Z. F., & Kepecs, A. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.039 · Cited by 209 · see citing works

Dissociable effects of lesions to orbitofrontal cortex subregions on impulsive choice in the rat

Mar, A. C., Walker, A. L. J., Theobald, D. E., Eagle, D. M., & Robbins, T. W. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.6620-10.2011 · Cited by 206 · see citing works

Differential Involvement of the Basolateral Amygdala and Mediodorsal Thalamus in Instrumental Action Selection

Ostlund, S. B., & Balleine, B. W. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.5472-07.2008 · Cited by 198 · see citing works

Neural structures underlying set-shifting: Roles of medial prefrontal cortex and anterior cingulate cortex

Bissonette, G. B., Powell, E. M., & Roesch, M. R. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.04.037 · Cited by 189 · see citing works

Reinforcement learning, conditioning, and the brain: Successes and challenges

Maia, T. V. (2009) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/cabn.9.4.343 · Cited by 184 · see citing works

A prefrontal non-opioid mechanism in placebo analgesia

Petrovic, P., Kalso, E., Petersson, K. M., Andersson, J., Fransson, P., & Ingvar, M. (2010) · Pain · doi:10.1016/j.pain.2010.03.011 · Cited by 182 · see citing works

The Affective Core of Emotion: Linking Pleasure, Subjective Well-Being, and Optimal Metastability in the Brain

Kringelbach, M. L., & Berridge, K. C. (2017) · Emotion Review · doi:10.1177/1754073916684558 · Cited by 187 · see citing works

Appetitive conditioning: Neural bases and implications for psychopathology

Martin-Söelch, C., Linthicum, J., & Ernst, M. (2007) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2006.11.002 · Cited by 185 · see citing works

Role of Orbitofrontal Cortex Connections in Emotion

Rempel-Clower, N. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.026 · Cited by 181 · see citing works

Prefrontal cortex and drug abuse vulnerability: Translation to prevention and treatment interventions

Perry, J. L., Joseph, J. E., Jiang, Y., Zimmerman, R. S., Kelly, T. H., Darna, M., Huettl, P., Dwoskin, L. P., & Bardo, M. T. (2011) · Brain Research Reviews · doi:10.1016/j.brainresrev.2010.09.001 · Cited by 180 · see citing works

Top-Down Dysregulation—From ADHD to Emotional Instability

Petrovic, P., & Castellanos, F. X. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2016.00070 · Cited by 179 · see citing works

Dissociable Effects of Subtotal Lesions within the Macaque Orbital Prefrontal Cortex on Reward-Guided Behavior

Rudebeck, P. H., & Murray, E. A. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0091-11.2011 · Cited by 179 · 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

The contribution of distinct subregions of the ventromedial frontal cortex to emotion, social behavior, and decision making

Rudebeck, P. H., Bannerman, D. M., & Rushworth, M. F. S. (2008) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/cabn.8.4.485 · Cited by 172 · see citing works

Behavioral States, Network States, and Sensory Response Variability

Fontanini, A., & Katz, D. B. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90592.2008 · Cited by 170 · see citing works

Reduced amygdala–orbitofrontal connectivity during moral judgments in youths with disruptive behavior disorders and psychopathic traits

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Neural substrates of reward magnitude, probability, and risk during a wheel of fortune decision-making task

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