Orbitofrontal cortex, decision-making and drug addiction
Open accessAbstract
The orbitofrontal cortex, as a part of prefrontal cortex, is implicated in executive function. However, within this broad region, the orbitofrontal cortex is distinguished by its unique pattern of connections with crucial subcortical associative learning nodes, such as basolateral amygdala and nucleus accumbens. By virtue of these connections, the orbitofrontal cortex is uniquely positioned to use associative information to project into the future, and to use the value of perceived or expected outcomes to guide decisions. This review will discuss recent evidence that supports this proposal and will examine evidence that loss of this signal, as the result of drug-induced changes in these brain circuits, might account for the maladaptive decision-making that characterizes drug addiction.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The behavioral pattern after orbitofrontal cortex damage in humans, non-human primates, and rodents closely resembles addictive behavior.
“Thus, the pattern of behavior seen with OFC damage in humans, as well as in non-human primates and rodents (Bechara, 2005; Schoenbaum et al., 2006), is highly reminiscent of addictive behavior.”
From Impulsivity, frontal lobes and risk for addiction (2009) · cites this paper as Schoenbaum et al., 2006
An essential orbitofrontal cortex function is flexible assignment of value to environmental stimuli, which determines how stimuli influence actions.
“an essential function of the OFC is the flexible assignment of value to environmental stimuli, which critically determines how such stimuli influence our actions (Schoenbaum et al., 2006).”
From Impulsivity, frontal lobes and risk for addiction (2009) · cites this paper as Schoenbaum et al., 2006
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Diagnostic and Statistical Manual of Mental Disorders
Williams, J. B. W., & First, M. B. (2013) · Oxford University Press eBooks · doi:10.1093/acrefore/9780199975839.013.104 · Cited by 109,841 · see citing works
(1996) · Cited by 3,692 · see citing works
Ongur, D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.206 · Cited by 2,627 · see citing works
Fuster, J. M. (1997) · Cited by 2,095 · see citing works
Different contributions of the human amygdala and ventromedial prefrontal cortex to decision-making
Bechara, A., Damasio, H., Damasio, A. R., & Lee, G. P. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-13-05473.1999 · Cited by 2,001 · see citing works
Circuitry of Primate Prefrontal Cortex and Regulation of Behavior by Representational Memory
Goldman‐Rakic, P. S. (1987) · Comprehensive Physiology · doi:10.1002/cphy.cp010509 · Cited by 1,960 · see citing works
Preliminary analysis of functions of the temporal lobes in monkeys
KLÜVER, H. (1939) · Archives of Neurology And Psychiatry · doi:10.1001/archneurpsyc.1939.02270240017001 · Cited by 1,696 · see citing works
The amygdala: Neurobiological aspects of emotion, memory, and mental dysfunction.
Aggleton, J. P. (1992) · Wiley-Liss eBooks · Cited by 1,536 · 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
Relative reward preference in primate orbitofrontal cortex
Tremblay, L., & Schultz, W. (1999) · Nature · doi:10.1038/19525 · Cited by 1,314 · see citing works
The cortical projections of the mediodorsal nucleus and adjacent thalamic nuclei in the rat
Krettek, J. E., & Price, J. L. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901710204 · Cited by 1,277 · see citing works
Acute effects of cocaine on human brain activity and emotion
Breiter, H. C., Gollub, R. L., Weisskoff, R. M., Kennedy, D. N., Makris, N., Berke, J. D., Goodman, J. M., Kantor, H. L., Gastfriend, D. R., Riorden, J. P., et al. (1997) · Neuron · doi:10.1016/s0896-6273(00)80374-8 · Cited by 1,270 · see citing works
Addiction, a disease of compulsion and drive: involvement of the orbitofrontal cortex
Volkow, N. D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.318 · Cited by 1,240 · see citing works
Baxter, M. G., & Murray, E. A. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn875 · Cited by 1,200 · see citing works
Bechara, A., Dolan, S. L., Denburg, N. L., Hindes, A. R., Anderson, S. W., & Nathan, P. E. (2001) · Neuropsychologia · doi:10.1016/s0028-3932(00)00136-6 · Cited by 1,168 · 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
Rogers, R. (1999) · Neuropsychopharmacology · doi:10.1016/s0893-133x(98)00091-8 · Cited by 1,101 · see citing works
Neural responses during anticipation of a primary taste reward
O'Doherty, J. P., Deichmann, R., Critchley, H. D., & Dolan, R. J. (2002) · Neuron · doi:10.1016/s0896-6273(02)00603-7 · Cited by 1,076 · see citing works
Rolls, E. T., Hornak, J., Wade, D., & McGrath, J. (1994) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.57.12.1518 · Cited by 1,005 · see citing works
The Amygdala: a functional analysis
Aggleton, J. P. (2000) · Cited by 964 · see citing works
Bechara, A., & Damasio, H. (2002) · Neuropsychologia · doi:10.1016/s0028-3932(02)00015-5 · Cited by 889 · see citing works
Functions of the frontal cortex of the rat: A comparative review
Kolb, B. E. (1984) · Brain Research Reviews · doi:10.1016/0165-0173(84)90018-3 · Cited by 882 · see citing works
Groenewegen, H. J., Vermeulen‐Vanderzee, E., Kortschot, A. T., & Witter, M. P. (1987) · Neuroscience · doi:10.1016/0306-4522(87)90275-2 · Cited by 867 · see citing works
Limbic lesions and the problem of stimulus--reinforcement associations.
Jones, B., & Mishkin, M. (1972) · Experimental Neurology · doi:10.1016/0014-4886(72)90030-1 · Cited by 864 · see citing works
Leonard, C. M. (1969) · Brain Research · doi:10.1016/0006-8993(69)90003-1 · Cited by 850 · 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
Behavioral changes associated with ablation of the amygdaloid complex in monkeys.
Weiskrantz, L. (1956) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0088009 · Cited by 837 · 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
Projections from the amygdaloid complex to the cerebral cortex and thalamus in the rat and cat
Krettek, J. E., & Price, J. L. (1977) · Journal of Comparative Neurology · doi:10.1002/cne.901720408 · Cited by 785 · see citing works
Drug Seeking Becomes Compulsive After Prolonged Cocaine Self-Administration
Vanderschuren, L. J. M. J., & Everitt, B. J. (2004) · Science · doi:10.1126/science.1098975 · Cited by 733 · see citing works
Groenewegen, H. J. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90339-9 · Cited by 732 · see citing works
Robinson, T. E., & Kolb, B. E. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00576.x · Cited by 726 · see citing works
The Involvement of the Orbitofrontal Cortex in the Experience of Regret
Camille, N., Coricelli, G., Sallet, J., Pradat-Diehl, P., Duhamel, J.-R., & Sirigu, A. (2004) · Science · doi:10.1126/science.1094550 · Cited by 716 · 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
The primate mediodorsal (MD) nucleus and its projection to the frontal lobe
Goldman‐Rakic, P. S., & Porrino, L. J. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902420406 · Cited by 666 · see citing works
Impulsivity and rapid discounting of delayed hypothetical rewards in cocaine-dependent individuals.
Coffey, S., Gudleski, G., Saladin, M., & Brady, K. (2003) · Experimental and clinical psychopharmacology · doi:10.1037//1064-1297.11.1.18 · Cited by 655 · see citing works
Fellows, L. K. (2003) · Brain · doi:10.1093/brain/awg180 · Cited by 631 · see citing works
Drug abusers show impaired performance in a laboratory test of decision making
Grant, S. (2000) · Neuropsychologia · doi:10.1016/s0028-3932(99)00158-x · Cited by 625 · see citing works
Impulsivity and rapid discounting of delayed hypothetical rewards in cocaine-dependent individuals.
Coffey, S. F., Gudleski, G. D., Saladin, M. E., & Brady, K. T. (2003) · Experimental and Clinical Psychopharmacology · doi:10.1037/1064-1297.11.1.18 · Cited by 625 · see citing works
Amygdala circuitry in attentional and representational processes.
Holland, P., & Gallagher, M. (1999) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(98)01271-6 · Cited by 613 · see citing works
The orbital and medial prefrontal circuit through the primate basal ganglia
Haber, S., Kunishio, K., Mizobuchi, M., & Lynd-Balta, E. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-07-04851.1995 · Cited by 605 · see citing works
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
Self-citationIzquierdo, 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
Baxter, M. G., Parker, A., Lindner, C. C. C., Izquierdo, A. D., & Murray, E. A. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-11-04311.2000 · Cited by 582 · see citing works
Decision-making and addiction (part II): myopia for the future or hypersensitivity to reward?
Bechara, A., Dolan, S., & Hindes, A. (2002) · Neuropsychologia · doi:10.1016/s0028-3932(02)00016-7 · Cited by 580 · see citing works
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
Chudasama, Y., & Robbins, T. W. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-25-08771.2003 · Cited by 543 · 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
Groenewegen, H. J., Berendse, H. W., Wolters, J. G., & Lohman, A. H. M. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)62677-1 · Cited by 506 · see citing works
Organization of the thalamo-cortical connexions to the frontal lobe in the rhesus monkey
Kievit, J., & Kuypers, H. G. J. M. (1977) · Experimental Brain Research · doi:10.1007/bf00236173 · Cited by 497 · see citing works
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
Kehoe, E. J., Klein, S. B., & Mowrer, R. R. (1991) · The American Journal of Psychology · doi:10.2307/1423162 · Cited by 483 · see citing works
Gottfried, J. A., O’Doherty, J. P., & Dolan, R. J. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-24-10829.2002 · Cited by 474 · see citing works
Organization of amygdaloid projections to the prefrontal cortex and associated striatum in the rat
McDonald, A. J. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90247-l · Cited by 463 · see citing works
Wyvell, C. L., & Berridge, K. C. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-19-07831.2001 · Cited by 436 · see citing works
Functional Magnetic Resonance Imaging of Human Brain Activation During Cue-Induced Cocaine Craving
Maas, L. C., Lukas, S. E., Kaufman, M. J., Weiss, R. D., Daniels, S. L., Rogers, V. W., Kukes, T. J., & Renshaw, P. F. (1998) · American Journal of Psychiatry · doi:10.1176/ajp.155.1.124 · Cited by 434 · see citing works
Russchen, F. T., Amaral, D. G., & Price, J. L. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902560202 · Cited by 416 · see citing works
The role of the amygdala in conditioned and unconditioned fear and anxiety
Davis, M. (2000) · The Amygdala · doi:10.1093/oso/9780198505013.003.0006 · Cited by 384 · see citing works
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
The orbitofrontal cortex and its connections with the mediodorsal nucleus in rabbit, sheep and cat.
ROSE, J. E., & Woolsey, C. N. (1948) · PubMed · Cited by 374 · see citing works
Orbitofrontal Cortex and Human Drug Abuse: Functional Imaging
London, E. D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.334 · Cited by 360 · see citing works
Amygdaloid projections to the frontal cortex and the striatum in the rat
Kita, H., & Kitai, S. T. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902980104 · Cited by 351 · see citing works
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
Schoenbaum, G. M., & Eichenbaum, H. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.74.2.733 · Cited by 329 · see citing works
Ray, J. P., & Price, J. L. (1992) · Journal of Comparative Neurology · doi:10.1002/cne.903230204 · Cited by 326 · see citing works
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
Ladpli, R., & Brodal, A. (1968) · Brain Research · doi:10.1016/0006-8993(68)90173-x · Cited by 299 · see citing works
Jentsch, D. (2002) · Neuropsychopharmacology · doi:10.1016/s0893-133x(01)00355-4 · Cited by 278 · see citing works
Preexposure sensitizes rats to the rewarding effects of cocaine
Horger, B. A., Shelton, K. L., & Schenk, S. (1990) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(90)90552-s · Cited by 271 · see citing works
XI. An investigation into the functions of the occipital and temporal lobes of the monkey's brain
Brown, S., & Schäfer, E. A. (1888) · Philosophical Transactions of the Royal Society of London (B ) · doi:10.1098/rstb.1888.0011 · Cited by 263 · 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
Dom, G., Sabbe, B., Hulstijn, W., & van Den Brink, W. (2005) · British Journal of Psychiatry · doi:10.1192/bjp.187.3.209 · 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
Schoenbaum, G. M., Saddoris, M. P., Ramus, S. J., Shaham, Y., & Setlow, B. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03274.x · Cited by 192 · see citing works
Crombag, H. S. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh136 · Cited by 178 · see citing works
Oral cocaine seeking by rats: Action or habit?
Miles, F. J., Everitt, B. J., & Dickinson, A. (2003) · Behavioral Neuroscience · doi:10.1037/0735-7044.117.5.927 · Cited by 175 · see citing works
Gaffan, D., & Murray, E. A. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-11-03479.1990 · Cited by 168 · see citing works
Cajal on the Cerebral Cortex: An Annotated Translation of the Complete Writings
Glickstein, M. (1989) · Annals of Internal Medicine · doi:10.7326/0003-4819-110-10-851_3 · Cited by 166 · see citing works
Schoenbaum, G. M., & Setlow, B. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh216 · Cited by 161 · see citing works
Orbital and Medial Prefrontal Cortex and Psychostimulant Abuse: Studies in Animal Models
Porrino, L. J. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.326 · Cited by 155 · see citing works
Neuronal Activity in Primate Orbitofrontal Cortex Reflects the Value of Time
Roesch, M. R., & Olson, C. R. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00373.2005 · Cited by 155 · see citing works
Taylor, J. R., & Horger, B. A. (1999) · Psychopharmacology · doi:10.1007/s002130050859 · Cited by 137 · see citing works
Information coding in the rodent prefrontal cortex. II. Ensemble activity in orbitofrontal cortex
Schoenbaum, G. M., & Eichenbaum, H. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.74.2.751 · Cited by 125 · see citing works
Schoenbaum, G. M., & Setlow, B. (2001) · Learning & Memory · doi:10.1101/lm.39901 · Cited by 123 · see citing works
Neural Correlates of Olfactory Recognition Memory in the Rat Orbitofrontal Cortex
Ramus, S. J., & Eichenbaum, H. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-21-08199.2000 · Cited by 122 · see citing works
Enhanced appetitive conditioning following repeated pretreatment with d-amphetamine
Harmer, C. J., & Phillips, G. D. (1998) · Behavioural Pharmacology · doi:10.1097/00008877-199807000-00001 · Cited by 107 · see citing works
Taylor, J. R., & Jentsch, J. D. (2001) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01106-4 · Cited by 106 · see citing works
Crossmodal Associative Memory Representations in Rodent Orbitofrontal Cortex
Lipton, P. A., Alvarez, P., & Eichenbaum, H. (1999) · Neuron · doi:10.1016/s0896-6273(00)81095-8 · Cited by 101 · see citing works
Encoding Changes in Orbitofrontal Cortex in Reversal-Impaired Aged Rats
Schoenbaum, G. M., Setlow, B., Saddoris, M. P., & Gallagher, M. (2005) · Journal of Neurophysiology · doi:10.1152/jn.01052.2005 · Cited by 83 · see citing works
Ensemble coding in the nucleus accumbens
O’Donnell, P. (1999) · Psychobiology · doi:10.3758/bf03332113 · Cited by 58 · see citing works
Phillips, G., Harmer, C., & Hitchcott, P. (2002) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00034-7 · Cited by 24 · see citing works
The amygdala and associative learning
Gallagher, M. (2000) · doi:10.1093/oso/9780198505013.003.0008 · Cited by 24 · see citing works
Flagged first, then by citations
2 of the 95 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- [52]Stalnaker TA, et al. Abstract Viewer and Itinerary Planner. Society for Neuroscience; 2005. Orbitofrontal cortex fails to represent bad outcomes after cocaine exposure. Program number 112.2. Online ( http://sfn.scholarone.com/) [Google Scholar]
Cited by
Sorted by citations
On the relationship between emotion and cognition
Pessoa, L. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2317 · Cited by 2,350 · see citing works
Frames, Biases, and Rational Decision-Making in the Human Brain
de Martino, B., Kumaran, D., Seymour, B., & Dolan, R. (2006) · Science · doi:10.1126/science.1128356 · Cited by 1,623 · see citing works
Affective neuroscience of pleasure: reward in humans and animals
Berridge, K. C., & Kringelbach, M. L. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1099-6 · Cited by 1,254 · see citing works
Mental fatigue: Costs and benefits
Boksem, M. A. S., & Tops, M. (2008) · Brain Research Reviews · doi:10.1016/j.brainresrev.2008.07.001 · Cited by 1,142 · 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
Interoception in anxiety and depression
Paulus, M. P., & Stein, M. B. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0258-9 · Cited by 952 · see citing works
Everitt, B. J., Belin, D., Economidou, D., Pelloux, Y., Dalley, J. W., & Robbins, T. W. (2008) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2008.0089 · Cited by 974 · 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
Anterior Prefrontal Function and the Limits of Human Decision-Making
Koechlin, É., & Hyafil, A. (2007) · Science · doi:10.1126/science.1142995 · Cited by 750 · see citing works
From reinforcement learning models to psychiatric and neurological disorders
Maia, T. V., & Frank, M. J. (2011) · Nature Neuroscience · doi:10.1038/nn.2723 · Cited by 715 · see citing works
Belin, D., & Everitt, B. J. (2008) · Neuron · doi:10.1016/j.neuron.2007.12.019 · Cited by 697 · see citing works
From the ventral to the dorsal striatum: devolving views of their roles in drug addiction
Everitt, B. J., & Robbins, T. W. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.02.010 · Cited by 675 · 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
“Once dlPFC focuses attention on activity it activates OFC to use associative information and project future outcomes (Schoenbaum et al., 2006).”
BackgroundInfluentialNeuroimaging of child abuse: a critical review
Hart, H., & Rubia, K. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00052 · Cited by 660 · see citing works
Jasinska, A. J., Stein, E. A., Kaiser, J., Naumer, M. J., & Yalachkov, Y. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.10.013 · Cited by 513 · see citing works
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
Cubillo, A., Halari, R., Smith, A., Taylor, E., & Rubia, K. (2012) · Cortex · doi:10.1016/j.cortex.2011.04.007 · Cited by 505 · 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
Logue, S. F., & Gould, T. J. (2014) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.08.007 · Cited by 477 · see citing works
Stress-induced prefrontal reorganization and executive dysfunction in rodents
Holmes, A., & Wellman, C. L. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.11.005 · Cited by 469 · see citing works
Rubia, K. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.09.023 · Cited by 440 · see citing works
Internet and Gaming Addiction: A Systematic Literature Review of Neuroimaging Studies
Kuss, D. J., & Griffiths, M. D. (2012) · Brain Sciences · doi:10.3390/brainsci2030347 · Cited by 437 · 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
Walton, M. E., Behrens, T. E. J., Buckley, M. J., Rudebeck, P. H., & Rushworth, M. F. S. (2010) · Neuron · doi:10.1016/j.neuron.2010.02.027 · Cited by 397 · see citing works
Rubia, K., Halari, R., Cubillo, A., Mohammad, A.-M., Brammer, M., & Taylor, E. (2009) · Neuropharmacology · doi:10.1016/j.neuropharm.2009.08.013 · Cited by 393 · see citing works
Alterations in brain structure and functional connectivity in prescription opioid-dependent patients
Upadhyay, J., Maleki, N., Potter, J. S., Elman, I., Rudrauf, D., Knudsen, J., Wallin, D. J., Pendse, G., McDonald, L., Griffin, M. L., et al. (2010) · Brain · doi:10.1093/brain/awq138 · Cited by 394 · see citing works
Distinct Roles of Rodent Orbitofrontal and Medial Prefrontal Cortex in Decision Making
Sul, J. H., Kim, H., Huh, N., Lee, D., & Jung, M. W. (2010) · Neuron · doi:10.1016/j.neuron.2010.03.033 · Cited by 372 · see citing works
Internet addiction in adolescence: neurobiological, psychosocial and clinical issues
Cerniglia, L., Zoratto, F., Cimino, S., Laviola, G., Ammaniti, M., & Adriani, W. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.12.024 · Cited by 371 · see citing works
Circuit-Based Corticostriatal Homologies Between Rat and Primate
Heilbronner, S. R., Rodríguez-Romaguera, J., Quirk, G. J., Groenewegen, H. J., & Haber, S. N. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.05.012 · Cited by 321 · see citing works
The role of neuroimmune signaling in alcoholism
Crews, F. T., Lawrimore, C. J., Walter, T. J., & Coleman, L. G. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.01.031 · Cited by 321 · 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
Younger, J., Aron, A., Parke, S., Chatterjee, N., & Mackey, S. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013309 · Cited by 314 · see citing works
George, O., & Koob, G. F. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.05.002 · Cited by 312 · see citing works
Rubia, K., Halari, R., Christakou, A., & Taylor, E. (2009) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2009.0014 · Cited by 310 · see citing works
Induction of innate immune genes in brain create the neurobiology of addiction
Crews, F. T., Zou, J., & Qin, L. (2011) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2011.03.003 · Cited by 313 · 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
Self-citationFeil, J., Sheppard, D., Fitzgerald, P. B., Yücel, M., Lubman, D. I., & Bradshaw, J. L. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.03.001 · Cited by 342 · see citing works
Covert expectation-of-reward in rat ventral striatum at decision points
van der Meer, M. A. A. (2009) · Frontiers in Integrative Neuroscience · doi:10.3389/neuro.07.001.2009 · Cited by 296 · see citing works
The drift diffusion model as the choice rule in reinforcement learning
Pedersen, M. L., Frank, M. J., & Biele, G. (2016) · Psychonomic Bulletin & Review · doi:10.3758/s13423-016-1199-y · Cited by 272 · see citing works
Impulsivity is associated with behavioral decision-making deficits.
Franken, I., Strien, J. W. V., Nijs, I., & Muris, P. (2008) · Psychiatry Research · doi:10.1016/j.psychres.2007.06.002 · Cited by 308 · see citing works
Reduced hippocampal volume correlates with executive dysfunctioning in major depression
Frodl, T., Schaub, A., Banac, S., Charypar, M., Jäger, M., Kümmler, P., Ronald Bottlender, A., Zetzsche, T., Born, C., Leinsinger, G. L., et al. (2006) · Journal of Psychiatry and Neuroscience · doi:10.1139/jpn.0636 · Cited by 280 · see citing works
Lin, F., Zhou, Y. F., Du, Y., Qin, L.-D., Zhao, Z., Jian-rong, X., & Lei, H. C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030253 · Cited by 278 · see citing works
Christakou, A., Brammer, M., & Rubia, K. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.08.067 · Cited by 266 · 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
A voxel‐based morphometry study of frontal gray matter correlates of impulsivity
Matsuo, K., Nicoletti, M., Nemoto, K., Hatch, J. P., Peluso, M. A. M., Nery, F. G., & Soares, J. C. (2008) · Human Brain Mapping · doi:10.1002/hbm.20588 · Cited by 253 · 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
Myopic Discounting of Future Rewards after Medial Orbitofrontal Damage in Humans
Sellitto, M., Ciaramelli, E., & di Pellegrino, G. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2516-10.2010 · Cited by 229 · see citing works
Haber, S. N., & Behrens, T. E. J. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.031 · Cited by 230 · see citing works
Medial orbitofrontal cortex gray matter is reduced in abstinent substance dependent individuals
Tanabe, J., Tregellas, J., Dalwani, M., Thompson, L., Owens, E., Crowley, T., & Banich, M. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.07.030 · Cited by 238 · see citing works
The Neurobiology of Addiction: Implications for Voluntary Control of Behavior
Hyman, S. E. (2007) · The American Journal of Bioethics · doi:10.1080/15265160601063969 · Cited by 223 · see citing works
Role of rodent secondary motor cortex in value-based action selection
Sul, J. H., Jo, S., Lee, D., & Jung, M. W. (2011) · Nature Neuroscience · doi:10.1038/nn.2881 · Cited by 221 · see citing works
The Social Determinants of Mental Health: Implications for Research and Health Promotion
Fisher, M., & Baum, F. E. (2010) · Australian & New Zealand Journal of Psychiatry · doi:10.3109/00048674.2010.509311 · Cited by 218 · see citing works
Li, J., Duan, X., Cui, Q., Chen, H., & Liao, W. (2019) · Psychological Medicine · doi:10.1017/s0033291718001502 · Cited by 208 · see citing works
A Genetically Mediated Bias in Decision Making Driven by Failure of Amygdala Control
Roiser, J. P., Martino, B. D., Tan, G. C.-Y., Kumaran, D., Seymour, B., Wood, N. W., & Dolan, R. J. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0407-09.2009 · Cited by 199 · see citing works
McCracken, C. B., & Grace, A. A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3750-07.2007 · Cited by 195 · see citing works
Weber, M. J., Messing, S. B., Rao, H., Detre, J. A., & Thompson‐Schill, S. L. (2014) · Human Brain Mapping · doi:10.1002/hbm.22429 · Cited by 183 · see citing works
Cortical Thickness Abnormalities in Late Adolescence with Online Gaming Addiction
Yuan, K., Cheng, P., Dong, T., Bi, Y., Xing, L., Yu, D., Zhao, L., Dong, M., von Deneen, K. M., Liu, Y., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0053055 · Cited by 185 · see citing works
Rubia, K., Halari, R., Cubillo, A., Smith, A. B., Mohammad, A.-M., Brammer, M., & Taylor, E. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.30 · Cited by 184 · see citing works
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
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
Rubenstein, J. L. R. (2010) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2010.02307.x · Cited by 170 · see citing works
Impulsivity, compulsivity, and habit: the role of orbitofrontal cortex revisited.
Torregrossa, M., Quinn, J., & Taylor, J. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.11.014 · Cited by 163 · see citing works
Diekhof, E. K., Falkai, P., & Gruber, O. (2008) · Brain Research Reviews · doi:10.1016/j.brainresrev.2008.07.004 · Cited by 165 · see citing works
George, O., Mandyam, C. D., Wee, S., & Koob, G. F. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301626 · Cited by 160 · see citing works
Neural correlates of cognitive control in gambling disorder: a systematic review of fMRI studies
Moccia, L., Pettorruso, M., De Crescenzo, F., De Risio, L., di Nuzzo, L., Martinotti, G., Bifone, A., Janiri, L., & Di Nicola, M. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.04.025 · Cited by 158 · see citing works
Toll-like receptor signaling and stages of addiction
Crews, F. T., Walter, T. J., Coleman, L. G., & Vetreno, R. P. (2017) · Psychopharmacology · doi:10.1007/s00213-017-4560-6 · Cited by 159 · see citing works
The human amygdala and orbital prefrontal cortex in behavioural regulation
Dolan, R. J. (2007) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2007.2088 · Cited by 150 · see citing works
Totah, N. K. B., Kim, Y. B., Homayoun, H., & Moghaddam, B. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1142-09.2009 · Cited by 151 · see citing works
Neural substrates of cognitive inflexibility after chronic cocaine exposure
Stalnaker, T. A., Takahashi, Y. K., Roesch, M. R., & Schoenbaum, G. M. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.07.019 · Cited by 151 · see citing works
Schoenbaum, G. M., Saddoris, M. P., & Stalnaker, T. A. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.001 · Cited by 150 · see citing works
Temporal isolation of neural processes underlying face preference decisions
Kim, H., Adolphs, R., O’Doherty, J. P., & Shinsuke Shimojo, A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703101104 · Cited by 150 · see citing works
Group II metabotropic glutamate receptors (mGlu2/3) in drug addiction
Moussawi, K., & Kalivas, P. W. (2010) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2010.01.030 · Cited by 146 · see citing works
Calu, D. J., Stalnaker, T. A., Franz, T. M., Singh, T., Shaham, Y., & Schoenbaum, G. M. (2007) · Learning & Memory · doi:10.1101/lm.534807 · Cited by 146 · see citing works
ΔFosB Induction in Orbitofrontal Cortex Mediates Tolerance to Cocaine-Induced Cognitive Dysfunction
Winstanley, C., LaPlant, Q., Theobald, D., Green, T., Bachtell, R., Perrotti, L., DiLeone, R., Russo, S., Garth, W. J., Self, D., et al. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2566-07.2007 · Cited by 149 · see citing works
Cohen, A., Najolia, G. M., Brown, L., & Minor, K. S. (2011) · Clinical Psychology Review · doi:10.1016/j.cpr.2010.11.001 · Cited by 149 · see citing works
Interactions between the prefrontal cortex and amygdala during delay discounting and reversal.
Churchwell, J. C., Morris, A. M., Heurtelou, N. M., & Kesner, R. P. (2009) · Behavioral Neuroscience · doi:10.1037/a0017734 · Cited by 141 · see citing works
Cholinergic circuits in cognitive flexibility
Prado, V. F., Janíčková, H., Al‐Onaizi, M., & Prado, M. A. M. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.09.013 · Cited by 143 · see citing works
Dong, G., Wang, L., Du, X., & Potenza, M. N. (2018) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsy084 · Cited by 141 · see citing works
The Orbital Prefrontal Cortex and Drug Addiction in Laboratory Animals and Humans
Everitt, B. J., Hutcheson, D. M., Ersche, K. D., Pelloux, Y., Dalley, J. W., & Robbins, T. W. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.022 · Cited by 139 · see citing works
León Méndez, M., Padrón, I., Fumero, A., & Marrero, R. J. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105572 · Cited by 148 · see citing works
“This is because the OFC is connected to some striatal regions, including the caudate and nucleus accumbens, which associate it with reward function (Schoenbaum et al., 2006).”
BackgroundErsche, K. D., Roiser, J. P., Abbott, S., Craig, K. J., Müller, U., Suckling, J., Ooi, C., Shabbir, S. S., Clark, L., Sahakian, B. J., et al. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.06.033 · Cited by 128 · see citing works
Walton, M. E., Groves, J., Jennings, K. A., Croxson, P. L., Sharp, T., Rushworth, M. F. S., & Bannerman, D. M. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06726.x · Cited by 129 · see citing works
Zernig, G., Ahmed, S. H., Cardinal, R. N., Morgan, D., Acquas, E., Foltin, R. W., Vezina, P., Negus, S. S., Crespo, J. A., Stöckl, P., et al. (2007) · Pharmacology · doi:10.1159/000103923 · Cited by 131 · see citing works
Jin, C., Zhang, T., Cai, C., Bi, Y., Li, Y., Yu, D., Zhang, M., & Yuan, K. (2015) · Brain Imaging and Behavior · doi:10.1007/s11682-015-9439-8 · Cited by 125 · see citing works
Kumari, V., Barkataki, I., Goswami, S., Flora, S., Das, M., & Taylor, P. (2009) · Psychiatry Research · doi:10.1016/j.pscychresns.2008.09.003 · Cited by 118 · see citing works
Shared gray matter alterations in subtypes of addiction: a voxel-wise meta-analysis
Zhang, M., Gao, X., Yang, Z., Wen, M., Huang, H., Zheng, R., Wang, W., Wei, Y., Cheng, J., Han, S., et al. (2021) · Psychopharmacology · doi:10.1007/s00213-021-05920-w · Cited by 123 · see citing works
Previous Cocaine Exposure Makes Rats Hypersensitive to Both Delay and Reward Magnitude
Roesch, M. R., Takahashi, Y. K., Gugsa, N., Bissonette, G. B., & Schoenbaum, G. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4080-06.2007 · Cited by 119 · see citing works
Fritz, M., Rawas, R. E., Salti, A., Klement, S., Bardo, M. T., Kemmler, G., Dechant, G., Saria, A., & Zernig, G. (2011) · Addiction Biology · doi:10.1111/j.1369-1600.2010.00285.x · Cited by 117 · see citing works
The role of the orbitofrontal cortex in alcohol use, abuse, and dependence
Moorman, D. E. (2018) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2018.01.010 · Cited by 109 · see citing works
Pharmacological Enhancement of Memory and Executive Functioning in Laboratory Animals
Floresco, S., & Jentsch, J. D. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.158 · Cited by 109 · see citing works
Behavior- and Modality-General Representation of Confidence in Orbitofrontal Cortex
Masset, P., Ott, T., Lak, A., Hirokawa, J., & Kepecs, A. (2020) · Cell · doi:10.1016/j.cell.2020.05.022 · Cited by 109 · see citing works
Early and Late Components of Error Monitoring in Violent Offenders with Psychopathy
Brazil, I. A., de Bruijn, E. R. A., Bulten, B. H., von Borries, A. K. L., van Lankveld, J. J. D. M., Buitelaar, J. K., & Verkes, R. J. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.08.011 · Cited by 108 · see citing works
Li, Y., Yuan, K., Cai, C., Feng, D., Yin, J., Bi, Y., Shi, S., Yu, D., Jin, C., von Deneen, K. M., et al. (2015) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2015.03.023 · Cited by 104 · see citing works
Reward and Social Valuation Deficits following Ventromedial Prefrontal Damage
Moretti, L., Dragone, D., & di Pellegrino, G. (2008) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21011 · Cited by 108 · see citing works
Divergent Plasticity of Prefrontal Cortex Networks
Moghaddam, B., & Homayoun, H. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301554 · Cited by 104 · see citing works
Shirayama, Y., Obata, T., Matsuzawa, D., Nonaka, H., Kanazawa, Y., Yoshitome, E., Ikehira, H., Hashimoto, K., & Iyo, M. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.10.031 · Cited by 103 · see citing works
Placebo analgesia: findings from brain imaging studies and emerging hypotheses
Kong, J., Kaptchuk, T. J., Polich, G., Kirsch, I., & Gollub, R. L. (2007) · Reviews in the Neurosciences · doi:10.1515/revneuro.2007.18.3-4.173 · Cited by 97 · see citing works
Lovell, M. E., Akhurst, J., Padgett, C. R., Garry, M. I., & Matthews, A. J. (2019) · Experimental and Clinical Psychopharmacology · doi:10.1037/pha0000326 · Cited by 101 · see citing works
Drug use and addiction: evolutionary perspective
Durrant, R., Adamson, S. J., Todd, F. C., & Sellman, D. (2009) · Australian & New Zealand Journal of Psychiatry · doi:10.1080/00048670903270449 · Cited by 99 · see citing works
Truitt, W. A., Johnson, P. L., Dietrich, A. D., Fitz, S. D., & Shekhar, A. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.01.083 · Cited by 98 · see citing works
- Authors
- Schoenbaum, G., Roesch, M. R., & Stalnaker, T. A.
- Affiliations
- University of Maryland, Baltimore (US)
- Corresponding author
- Schoenbaum, Geoffrey
- Venue
- Trends in Neurosciences
- Publisher
- Elsevier BV
- Published
- 2006-02
- Volume
- 29
- Issue
- 2
- Pages
- 116-124
- ISSN
- 0166-2236 (ISSN-L)
- PMC
- PMC2430629
- OpenAlex
- W2099221443
- Cited by
- 499
- References
- 95
- Citations by year
- 2026: 11 · 2025: 18 · 2024: 18 · 2023: 15 · 2022: 18 · 2021: 21 · 2020: 60 · 2019: 28 · 2018: 19 · 2017: 24 · 2016: 22 · 2015: 16 · 2014: 18 · 2013: 27 · 2012: 21
- FWCI
- 2.92
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Trends in Neurosciences (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Drug Abuse (R01DA015718)
- National Institute on Deafness and Other Communication Disorders (T32 DC 00054, T32DC000054)
- National Institute of Neurological Disorders and Stroke (T32 NS07375, T32NS007375)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Social Sciences › Decision Sciences › General Decision Sciences › Decision-Making and Behavioral Economics
- Keywords
- orbitofrontal cortex, decision-making, drug addiction, prefrontal cortex, executive function, associative learning, basolateral amygdala, nucleus accumbens, outcome value, maladaptive decision-making
- MeSH terms
- Animals, Decision Making, Humans, Neural Pathways, Orbit, Prefrontal Cortex, Substance-Related Disorders
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review