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Toward a neurobiology of delusions
Open accessAbstract
Delusions are the false and often incorrigible beliefs that can cause severe suffering in mental illness. We cannot yet explain them in terms of underlying neurobiological abnormalities. However, by drawing on recent advances in the biological, computational and psychological processes of reinforcement learning, memory, and perception it may be feasible to account for delusions in terms of cognition and brain function. The account focuses on a particular parameter, prediction error--the mismatch between expectation and experience--that provides a computational mechanism common to cortical hierarchies, fronto-striatal circuits and the amygdala as well as parietal cortices. We suggest that delusions result from aberrations in how brain circuits specify hierarchical predictions, and how they compute and respond to prediction errors. Defects in these fundamental brain mechanisms can vitiate perception, memory, bodily agency and social learning such that individuals with delusions experience an internal and external world that healthy individuals would find difficult to comprehend. The present model attempts to provide a framework through which we can build a mechanistic and translational understanding of these puzzling symptoms.
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“the learning function of dopamine may nonetheless mediate the transition from disordered perception to delusion. In this view, dopamine-modulated learning underlies the re-sculpting of generative models to accommodate persistently elevated prediction error signals (Corlett et al., 2010).”
From An Interoceptive Predictive Coding Model of Conscious Presence (2012) · cites this paper as Corlett et al., 2010
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Importantly, NMDAR dependent signaling is thought to be essential for updating and encoding representations of beliefs (Corlett et al., 2010; Vinckier et al., 2016).”
From Allostatic Self-efficacy: A Metacognitive Theory of Dyshomeostasis-Induced Fatigue and Depression (2016) · cites this paper as Corlett et al., 2010
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Evidence from anatomical and physiological studies has established bridges between the computational and physiological components of this hierarchical precision-weighted message passing: prediction error signaling via forward connections likely rests on glutamatergic (AMPA and NMDA) receptors, prediction signaling via backward connections probably exclusively on NMDA receptors, while precision”
From Allostatic Self-efficacy: A Metacognitive Theory of Dyshomeostasis-Induced Fatigue and Depression (2016) · cites this paper as Corlett et al., 2010
Experimental — accuracy not yet measuredIn the citing paper
“Predictive coding models explain these experiences as attempts to account for and minimise uncertainty.10”
From Computational psychiatry: a Rosetta Stone linking the brain to mental illness (2014) · cites this paper as [10]
In the citing paper
“we propose that anomalies in the genesis of prediction error, its nature, and our responses to it can explain the emergence of psychosis.”
From Computational psychiatry: a Rosetta Stone linking the brain to mental illness (2014) · cites this paper as [10]
In the citing paper
“Disruptions to both processes (prediction error and attentional salience attribution) can manifest in behaviour as aberrant learning and, ultimately, delusional beliefs.10”
From Computational psychiatry: a Rosetta Stone linking the brain to mental illness (2014) · cites this paper as [10]
In the citing paper
“A patient might experience delusions because of a disruption to either system.10”
From Computational psychiatry: a Rosetta Stone linking the brain to mental illness (2014) · cites this paper as [10]
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Citations
Cites
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
Reinforcement Learning: An Introduction
Sutton, R. S., & Barto, A. (2005) · IEEE Transactions on Neural Networks · doi:10.1109/tnn.2004.842673 · Cited by 25,268
Hume, D. A. (1739) · Cambridge University Press eBooks · doi:10.1017/cbo9780511620409.040 · Cited by 9,910
Hebb, D. O. (2005) · doi:10.4324/9781410612403 · Cited by 9,825
A neural substrate of prediction and reward
Schultz, W., Dayan, P., & Montague, P. R. (1997) · Science · doi:10.1126/science.275.5306.1593 · Cited by 9,388
The free-energy principle: a unified brain theory?
Friston, K. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2787 · Cited by 8,120 · cited 3×
“Bayesian learning, predictive coding and information theory – the concept that intersects all of these is surprise or prediction error (Friston, 2010) and our model implicates aberrant prediction in the pathophysiology of delusions.”
BackgroundInfluentialRescorla, R. A. (1972) · Medical Entomology and Zoology · Cited by 7,268
indicated, N. A. (1950) · Journal of Consulting Psychology · doi:10.1037/h0049612 · Cited by 6,984
Rao, R. P. N., & Ballard, D. H. (1999) · Nature Neuroscience · doi:10.1038/4580 · Cited by 5,483 · cited 3×
“Here, prediction errors encode information that remains to be explained by top-down predictions (Rao and Ballard, 1999).”
BackgroundInfluentialThe Organization of Behavior; A Neuropsychological Theory.
Attneave, F., B., M., & Hebb, D. O. (1950) · The American Journal of Psychology · doi:10.2307/1418888 · Cited by 5,146
Action recognition in the premotor cortex
Gallese, V., Fadiga, L., Fogassi, L., & Rizzolatti, G. (1996) · Brain · doi:10.1093/brain/119.2.593 · Cited by 4,968
Premotor cortex and the recognition of motor actions
Rizzolatti, G., Fadiga, L., Gallese, V., & Fogassi, L. (1996) · Cognitive Brain Research · doi:10.1016/0926-6410(95)00038-0 · Cited by 4,870
A theory of cortical responses.
Friston, K. (2005) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2005.1622 · Cited by 4,578
Predictive reward signal of dopamine neurons
Schultz, W. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.1.1 · Cited by 4,564
Classical conditioning II: Current research and theory.
Black, A. H., & Prokasy, W. F. (1972) · Appleton-Century-Crofts eBooks · Cited by 4,449
Rubber hands ‘feel’ touch that eyes see
Botvinick, M., & Cohen, J. (1998) · Nature · doi:10.1038/35784 · Cited by 4,410
An internal model for sensorimotor integration
Wolpert, D. M., Ghahramani, Z., & Jordan, M. I. (1995) · Science · doi:10.1126/science.7569931 · Cited by 3,553
Krystal, J. H. (1994) · Archives of General Psychiatry · doi:10.1001/archpsyc.1994.03950030035004 · Cited by 3,330
Self-citationPearce, J. M., & Hall, G. (1980) · Psychological Review · doi:10.1037/0033-295x.87.6.532 · Cited by 3,023
Bayes, T. (1763) · Philosophical Transactions of the Royal Society of London · doi:10.1098/rstl.1763.0053 · Cited by 3,023
AN ESSAY TOWARDS SOLVING A PROBLEM IN THE DOCTRINE OF CHANCES
BAYES (1958) · Biometrika · doi:10.1093/biomet/45.3-4.296 · Cited by 2,939
Kapur, S. (2003) · American Journal of Psychiatry · doi:10.1176/appi.ajp.160.1.13 · Cited by 2,813
A theory of attention: Variations in the associability of stimuli with reinforcement
Mackintosh, N. J. (1975) · Psychological Review · doi:10.1037/h0076778 · Cited by 2,733
Fear memories require protein synthesis in the amygdala for reconsolidation after retrieval
Nader, K., Schafe, G. E., & Le Doux, J. E. (2000) · Nature · doi:10.1038/35021052 · Cited by 2,706
Daw, N. D., Niv, Y., & Dayan, P. (2005) · Nature Neuroscience · doi:10.1038/nn1560 · Cited by 2,533
Top-Down Versus Bottom-Up Control of Attention in the Prefrontal and Posterior Parietal Cortices
Buschman, T. J., & Miller, E. K. (2007) · Science · doi:10.1126/science.1138071 · Cited by 2,380
The debate over dopamine’s role in reward: the case for incentive salience
Berridge, K. C. (2007) · Psychopharmacology · doi:10.1007/s00213-006-0578-x · Cited by 2,347
Forward Models for Physiological Motor Control
Miall, R. C., & Wolpert, D. M. (1996) · Neural Networks · doi:10.1016/s0893-6080(96)00035-4 · Cited by 2,260
A unifying view of the basis of social cognition
GALLESE, V, KEYSERS, C., & RIZZOLATTI, G. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.07.002 · Cited by 2,236
Whalen, P. J., Rauch, S. L., Etcoff, N. L., McInerney, S. C., Lee, M. B., & Jenike, M. A. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-01-00411.1998 · Cited by 2,205
Abnormal neural oscillations and synchrony in schizophrenia
Uhlhaas, P. J., & Singer, W. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2774 · Cited by 2,120
Discrete coding of reward probability and uncertainty by dopamine neurons
Fiorillo, C. D., Tobler, P. N., & Schultz, W. (2003) · Science · doi:10.1126/science.1077349 · Cited by 2,085
A framework for mesencephalic dopamine systems based on predictive Hebbian learning
Montague, P., Dayan, P., & Sejnowski, T. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-05-01936.1996 · Cited by 2,066
The hippocampal-VTA loop: controlling the entry of information into long-term memory
Lisman, J. E., & Grace, A. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.002 · Cited by 1,983
Neurophysiological and Computational Principles of Cortical Rhythms in Cognition
Wang, X.-J. (2010) · Physiological Reviews · doi:10.1152/physrev.00035.2008 · Cited by 1,939
Self-citationKoch, S., & Albert, E. (1962) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-196210000-00015 · Cited by 1,936
The Prefrontal Cortex—An Update
Fuster, J. M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00285-9 · Cited by 1,837
Metaplasticity: the plasticity of synaptic plasticity
Abraham, W. C., & Bear, M. F. (1996) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)80018-x · Cited by 1,833
Grace, A. A. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90196-u · Cited by 1,831
The free-energy principle: a rough guide to the brain?
Friston, K. (2009) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2009.04.005 · Cited by 1,831
Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia
Walsh, T., McClellan, J. M., McCarthy, S. E., Addington, A. M., Pierce, S. B., Cooper, G. M., Nord, A. S., Kusenda, M., Malhotra, D., Bhandari, A., et al. (2008) · Science · doi:10.1126/science.1155174 · Cited by 1,800
Uncertainty, Neuromodulation, and Attention
Yu, A. J., & Dayan, P. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.026 · Cited by 1,774
Neurons in the orbitofrontal cortex encode economic value
Padoa-Schioppa, C., & Assad, J. A. (2006) · Nature · doi:10.1038/nature04676 · Cited by 1,598
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
Dopamine-dependent prediction errors underpin reward-seeking behaviour in humans
Pessiglione, M., Seymour, B., Flandin, G., Dolan, R. J., & Frith, C. D. (2006) · Nature · doi:10.1038/nature05051 · Cited by 1,584
Cellular and network mechanisms of rhythmic recurrent activity in neocortex
Sanchez-Vives, M. V., & McCormick, D. A. (2000) · Nature Neuroscience · doi:10.1038/79848 · Cited by 1,539
Synaptic Modification by Correlated Activity: Hebb's Postulate Revisited
Bi, G., & Poo, M. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.139 · Cited by 1,525
The primate basal ganglia: Parallel and integrative networks
Haber, S. N. (2003) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2003.10.003 · Cited by 1,479
Perceiving is believing: a Bayesian approach to explaining the positive symptoms of schizophrenia
Fletcher, P. C., & Frith, C. D. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2536 · Cited by 1,462
Self-citationBayesian inference with probabilistic population codes
Ma, W. J., Beck, J. M., Latham, P. E., & Pouget, A. (2006) · Nature Neuroscience · doi:10.1038/nn1790 · Cited by 1,457
Skinner, B. F. (1948) · Journal of Experimental Psychology · doi:10.1037/h0055873 · Cited by 1,456 · cited 2×
“superstitious instrumental conditioning (Skinner, 1948), in which”
BackgroundNeuronal Coding of Prediction Errors
Schultz, W., & Dickinson, A. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.473 · Cited by 1,427
Unilateral Neglect of Representational Space
Bisiach, E., & Luzzatti, C. (1978) · Cortex · doi:10.1016/s0010-9452(78)80016-1 · Cited by 1,390
Frontal lobes and human memory: Insights from functional neuroimaging
Fletcher, P. C. (2001) · Brain · doi:10.1093/brain/124.5.849 · Cited by 1,386
Self-citationTwo types of dopamine neuron distinctly convey positive and negative motivational signals
Matsumoto, M., & Hikosaka, O. (2009) · Nature · doi:10.1038/nature08028 · Cited by 1,378
The neuropsychology of schizophrenia
Gray, J. A., Feldon, J., Rawlins, J. N. P., Hemsley, D. R., & Smith, A. D. (1991) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00065055 · Cited by 1,350
The rubber hand illusion revisited: visuotactile integration and self-attribution
Tsakiris, M., & Haggard, P. (2005) · Journal of Experimental Psychology: Human Perception and Performance · doi:10.1037/0096-1523.31.1.80 · Cited by 1,328
(1995) · PubMed · Cited by 1,320
Lateral habenula as a source of negative reward signals in dopamine neurons
Matsumoto, M., & Hikosaka, O. (2007) · Nature · doi:10.1038/nature05860 · Cited by 1,292
Schultz, W., Apicella, P., & Ljungberg, T. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-03-00900.1993 · Cited by 1,291
A new intellectual framework for psychiatry
Kandel, E. R. (1998) · American Journal of Psychiatry · doi:10.1176/ajp.155.4.457 · Cited by 1,271
Abnormalities in the awareness and control of action
Frith, C., Blakemore, S., & Wolpert, D. M. (2000) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2000.0734 · Cited by 1,258
Yin, H. H., Knowlton, B. J., & Balleine, B. W. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03095.x · Cited by 1,226
Disorders of attention and perception in early schizophrenia
McGhie, A., & Chapman, J. (1961) · British Journal of Medical Psychology · doi:10.1111/j.2044-8341.1961.tb00936.x · Cited by 1,195
Predictive coding: an account of the mirror neuron system
Kilner, J. M., Friston, K. J., & Frith, C. D. (2007) · Cognitive Processing · doi:10.1007/s10339-007-0170-2 · Cited by 1,134
Lacking control increases illusory pattern perception
Whitson, J. A., & Galinsky, A. D. (2008) · Science · doi:10.1126/science.1159845 · Cited by 1,119
Relations between the central Nervous System and the peripheral organs
Holst, E. V. (1954) · The British Journal of Animal Behaviour · doi:10.1016/s0950-5601(54)80044-x · Cited by 1,104
Regulation of firing of dopaminergic neurons and control of goal-directed behaviors
Grace, A. A., Floresco, S. B., Goto, Y., & Lodge, D. J. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.003 · Cited by 1,034
Information Processing in Animals: Memory Mechanisms.
indicated, N. A. (1986) · Contemporary Psychology · doi:10.1037/024459 · Cited by 1,021
Dopamine responses comply with basic assumptions of formal learning theory
Waelti, P., Dickinson, A., & Schultz, W. (2001) · Nature · doi:10.1038/35083500 · Cited by 1,018
Entrainment of Neocortical Neurons and Gamma Oscillations by the Hippocampal Theta Rhythm
Sirota, A., Montgomery, S., Fujisawa, S., Isomura, Y., Zugaro, M., & Buzsáki, G. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.014 · Cited by 1,015
Stengel, E. (1960) · BMJ · doi:10.1136/bmj.1.5178.1031-b · Cited by 988
An essay towards solving a problem in the doctrine of chances
Bayes, T. (2003) · Resonance · doi:10.1007/bf02883540 · Cited by 987
Cortico-Basal Ganglia Reward Network: Microcircuitry
Sesack, S. R., & Grace, A. A. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.93 · Cited by 985
Haider, B., Duque, A., Hasenstaub, A. R., & McCormick, D. A. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.5297-05.2006 · Cited by 962
Abnormalities in the awareness of action.
Blakemore, S.-J., Wolpert, D. M., & Frith, C. D. (2002) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(02)01907-1 · Cited by 947
The Human Amygdala: An Evolved System for Relevance Detection
Sander, D., Grafman, J., & Zalla, T. (2003) · Reviews in the Neurosciences · doi:10.1515/revneuro.2003.14.4.303 · Cited by 944 · cited 1×
“The link between fear and uncertainty is emphasized by theorists who posit that the amygdala is also engaged during conditions of uncertainty about biologically relevant stimuli that warrant vigilance (Sander et al., 2003; Whalen et al., 1998).”
BackgroundAssociative learning of social value
Behrens, T. E. J., Hunt, L. T., Woolrich, M. W., & Rushworth, M. F. S. (2008) · Nature · doi:10.1038/nature07538 · Cited by 925
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 · cited 2×
“However, its role may not be limited to fear; the amygdala is involved in coding, processing and learning about salient stimuli (Balleine and Killcross, 2006; Paton et al., 2006).”
BackgroundWhy canʼt you tickle yourself?
Blakemore, S.-J., Wolpert, D., & Frith, C. (2000) · NeuroReport · doi:10.1097/00001756-200008030-00002 · Cited by 904
Information Processing in Animals
(2014) · Psychology Press eBooks · doi:10.4324/9781315798820 · Cited by 902
A Quantitative Map of the Circuit of Cat Primary Visual Cortex
Binzegger, T., Douglas, R. J., & Martin, K. A. C. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1400-04.2004 · Cited by 893
A cognitive model of persecutory delusions
Freeman, D., Garety, P. A., Kuipers, E., Fowler, D., & Bebbington, P. E. (2002) · British Journal of Clinical Psychology · doi:10.1348/014466502760387461 · Cited by 888 · cited 3×
“Some argue that perceptual aberrations are all that is required for a delusion to form (Gerrans, 2002; Maher, 1974), others that delusions result from top-down reasoning impairments (Freeman et al., 2002; Garety, 1991; Garety and Freeman, 1999), others still posit some combination of both factors, a two-factor approac…”
BackgroundPERSECUTORY DELUSIONS: A REVIEW AND THEORETICAL INTEGRATION
Bentall, R. P., Corcoran, R., Howard, R. J., Blackwood, N., & Kinderman, P. (2001) · Clinical Psychology Review · doi:10.1016/s0272-7358(01)00106-4 · Cited by 876
Misanin, J. R., Miller, R. R., & Lewis, D. J. (1968) · Science · doi:10.1126/science.160.3827.554 · Cited by 872
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 851
Synaptic plasticity and dysconnection in schizophrenia
Stephan, K. E., Baldeweg, T., & Friston, K. J. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.10.005 · Cited by 841
Spatio-Temporal Prediction Modulates the Perception of Self-Produced Stimuli
Blakemore, S.-J., Frith, C. D., & Wolpert, D. M. (1999) · Journal of Cognitive Neuroscience · doi:10.1162/089892999563607 · Cited by 829
Keysers, C. (2004) · doi:10.1016/s0896-6273(04)00156-4 · Cited by 806
Coherence of gamma-band EEG activity as a basis for associative learning
Miltner, W. H. R., Braun, C., Arnold, M., Witte, H., & Taub, E. (1999) · Nature · doi:10.1038/17126 · Cited by 798
Cognitive approaches to delusions: a critical review of theories and evidence.
Garety, P. A., & Freeman, D. (1999) · British Journal of Clinical Psychology · doi:10.1348/014466599162700 · Cited by 794 · cited 3×
“Some argue that perceptual aberrations are all that is required for a delusion to form (Gerrans, 2002; Maher, 1974), others that delusions result from top-down reasoning impairments (Freeman et al., 2002; Garety, 1991; Garety and Freeman, 1999), others still posit some combination of both factors, a two-factor approac…”
BackgroundCircuits for local and global signal integration in primary visual cortex
Angelucci, A., Levitt, J. B., Walton, E. J. S., Hupé, J.-M., Bullier, J., & Lund, J. S. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-19-08633.2002 · Cited by 789
Explaining the symptoms of schizophrenia: abnormalities in the awareness of action.
Frith, C. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00052-1 · Cited by 782
Bilder, R. M., Volavka, J., Lachman, H. M., & Grace, A. A. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300542 · Cited by 769
A specific role for posterior dorsolateral striatum in human habit learning
Tricomi, E., Balleine, B. W., & O’Doherty, J. P. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06796.x · Cited by 769
The short-latency dopamine signal: a role in discovering novel actions?
Redgrave, P., & Gurney, K. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn2022 · Cited by 762
On the actions that one nerve cell can have on another: distinguishing “drivers” from “modulators”
Sherman, S. M., & Guillery, R. W. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.12.7121 · Cited by 746 · cited 1×
“At a given level, any mismatch between expectancy and experience is transmitted up the cortical hierarchy to the level above via AMPA receptor signaling (Angelucci et al., 2002a,b; Friston, 2005b, 2009; Sherman and Guillery, 1998).”
BackgroundElevated Striatal Dopamine Function Linked to Prodromal Signs of Schizophrenia
Howes, O. D., Montgomery, A. J., Asselin, M.-C., Murray, R. M., Valli, I., Tabraham, P., Bramon-Bosch, E., Valmaggia, L., Johns, L., Broome, M., et al. (2009) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2008.514 · Cited by 744
Interactions between monoamines, glutamate, and GABA in schizophrenia: new evidence.
Carlsson, A., Waters, N., Holm-Waters, S., Tedroff, J., Nilsson, M., & Carlsson, M. (2001) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.41.1.237 · Cited by 742
Neural circuitry underlying the regulation of conditioned fear and its relation to extinction
Delgado, M. R., Nearing, K. I., LeDoux, J. E., & Phelps, E. A. (2008) · Neuron · doi:10.1016/j.neuron.2008.06.029 · Cited by 716
Genetic triple dissociation reveals multiple roles for dopamine in reinforcement learning
Frank, M. J., Moustafa, A. A., Haughey, H. M., Curran, T., & Hutchison, K. E. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706111104 · Cited by 696
Phantoms in the brain: probing the mysteries of the human mind
(1999) · Choice Reviews Online · doi:10.5860/choice.36-3941 · Cited by 695
Neural differentiation of expected reward and risk in human subcortical structures
Preuschoff, K., Bossaerts, P., & Quartz, S. R. (2006) · Neuron · doi:10.1016/j.neuron.2006.06.024 · Cited by 692
Haber, S. N., Kim, K.-S., Mailly, P., & Calzavara, R. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.0271-06.2006 · Cited by 686
Conditioned Reflexes and Neuron Organization.
(1949) · Annals of Internal Medicine · doi:10.7326/0003-4819-31-6-1133_1 · Cited by 685
Patterning and plasticity of the cerebral cortex
Sur, M., & Rubenstein, J. L. R. (2005) · Science · doi:10.1126/science.1112070 · Cited by 677
Statistically optimal perception and learning: from behavior to neural representations
Fiser, J., Berkes, P., Orbán, G., & Lengyel, M. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.01.003 · Cited by 672
ON THE PERCEPTION OF INCONGRUITY: A PARADIGM
Bruner, J. S., & Postman, L. J. (1949) · Journal of Personality · doi:10.1111/j.1467-6494.1949.tb01241.x · Cited by 663
A functional MRI study of human amygdala responses to facial expressions of fear versus anger.
Whalen, P. J., Shin, L. M., McInerney, S. C., Fischer, H., Wright, C. I., & Rauch, S. L. (2001) · Emotion · doi:10.1037/1528-3542.1.1.70 · Cited by 660
Hasselmo, M. E., Rolls, E. T., & Baylis, G. C. (1989) · Behavioural Brain Research · doi:10.1016/s0166-4328(89)80054-3 · Cited by 657
Uhlhaas, P. J., Haenschel, C., Nikolic, D., & Singer, W. (2008) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn062 · Cited by 629
Parallel incentive processing: an integrated view of amygdala function
Balleine, B. W., & Killcross, S. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.03.002 · Cited by 622
Alloy, L. B., & Kayne, N. T. (1984) · Psychological Review · doi:10.1037/0033-295x.91.1.112 · Cited by 616
Amygdala circuitry in attentional and representational processes
Holland, P. C., & Gallagher, M. (1999) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(98)01271-6 · Cited by 614
Hornak, J., O'Doherty, J., Bramham, J., Rolls, E. T., Morris, R. G., Bullock, P. R., & Polkey, C. E. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/089892904322926791 · Cited by 603
The Left Striato-pallidal Hyperactivity Model of Schizophrenia
Early, T. S., Haller, J., Posner, M. I., & Raichle, M. (2019) · Psychology Press eBooks · doi:10.4324/9781315785004-2 · Cited by 598
Mellor, C. S. (1970) · The British Journal of Psychiatry · doi:10.1192/s0007125000192116 · Cited by 596
Cognitive modulation of olfactory processing
de Araujo, I. E., Rolls, E. T., Velazco, M. I., Margot, C., & Cayeux, I. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.021 · Cited by 590
The cerebellum is involved in predicting the sensory consequences of action
Blakemore, S.-J., Frith, C. D., & Wolpert, D. M. (2001) · Neuroreport · doi:10.1097/00001756-200107030-00023 · Cited by 587
Cortical remodelling induced by activity of ventral tegmental dopamine neurons
Bao, S., Chan, V. T., & Merzenich, M. M. (2001) · Nature · doi:10.1038/35083586 · Cited by 569
Sleep-dependent memory consolidation and reconsolidation
Stickgold, R., & Walker, M. P. (2007) · Sleep Medicine · doi:10.1016/j.sleep.2007.03.011 · Cited by 567
Addiction as a Computational Process Gone Awry
Redish, A. D. (2004) · Science · doi:10.1126/science.1102384 · Cited by 556
Human oscillatory brain activity near 40 Hz coexists with cognitive temporal binding.
Joliot, M., Ribary, U., & Llinas, R. H. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.24.11748 · Cited by 552
Midbrain Dopamine Neurons Signal Preference for Advance Information about Upcoming Rewards
Bromberg-Martin, E. S., & Hikosaka, O. (2009) · Neuron · doi:10.1016/j.neuron.2009.06.009 · Cited by 548
Accounting for Delusional Misidentifications
Ellis, H. D., & Young, A. W. (1990) · The British Journal of Psychiatry · doi:10.1192/bjp.157.2.239 · Cited by 547
Evidence of Mirror Neurons in Human Inferior Frontal Gyrus
Kilner, J. M., Neal, A., Weiskopf, N., Friston, K. J., & Frith, C. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2668-09.2009 · Cited by 537
Substantia nigra/ventral tegmental reward prediction error disruption in psychosis
Murray, G. K., Corlett, P. R., Clark, L., Pessiglione, M., Blackwell, A. D., Honey, G., Jones, P. B., Bullmore, E. T., Robbins, T. W., & Fletcher, P. C. (2008) · Molecular Psychiatry · doi:10.1038/sj.mp.4002058 · Cited by 532
On the other hand: Dummy hands and peripersonal space
Makin, T. R., Holmes, N. P., & Ehrsson, H. H. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.02.041 · Cited by 530
Diagnostic criteria for psychosis in Parkinson's disease: Report of an NINDS, NIMH work group
Ravina, B., Marder, K., Fernandez, H. H., Friedman, J. H., McDonald, W., Murphy, D., Aarsland, D., Babcock, D., Cummings, J., Endicott, J., et al. (2007) · Movement Disorders · doi:10.1002/mds.21382 · Cited by 528
Neural correlates of mentalizing-related computations during strategic interactions in humans
Hampton, A. N., Bossaerts, P. L., & O’Doherty, J. P. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711099105 · Cited by 522
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
The Cutaneous "Rabbit": A Perceptual Illusion
Geldard, F. A., & Sherrick, C. E. (1972) · Science · doi:10.1126/science.178.4057.178 · Cited by 517
Delusional thinking and perceptual disorder.
Maher, B. A. (1974) · PubMed · Cited by 515
BLAKEMORE, S.-J., SMITH, J., STEEL, R., JOHNSTONE, E. C., & FRITH, C. D. (2000) · Psychological Medicine · doi:10.1017/s0033291799002676 · Cited by 497
Motor functions of the parietal lobe
Fogassi, L., & Luppino, G. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.10.015 · Cited by 488
A Role for the Human Dorsal Anterior Cingulate Cortex in Fear Expression
Milad, M. R., Quirk, G. J., Pitman, R. K., Orr, S. P., Fischl, B., & Rauch, S. L. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.04.032 · Cited by 485
Spence, S. (1997) · Brain · doi:10.1093/brain/120.11.1997 · Cited by 473
Somatoparaphrenia: a body delusion. A review of the neuropsychological literature
Vallar, G., & Ronchi, R. (2008) · Experimental Brain Research · doi:10.1007/s00221-008-1562-y · Cited by 469
A Neural Coding Scheme Formed by the Combined Function of Gamma and Theta Oscillations
Lisman, J. E., & Buzsáki, G. (2008) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn060 · Cited by 468
Disrupted prediction-error signal in psychosis: Evidence for an associative account of delusions
Corlett, P. R., Murray, G. K., Honey, G. D., Aitken, M. R. F., Shanks, D. R., Robbins, T. W., Bullmore, E. T., Dickinson, A., & Fletcher, P. C. (2007) · Brain · doi:10.1093/brain/awm173 · Cited by 460
Self-citationAcetylcholine contributes through muscarinic receptors to attentional modulation in V1
Herrero, J. L., Roberts, M. J., Delicato, L. S., Gieselmann, M. A., Dayan, P., & Thiele, A. (2008) · Nature · doi:10.1038/nature07141 · Cited by 459
Bayesian theories of conditioning in a changing world
Courville, A. C., Daw, N. D., & Touretzky, D. S. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.05.004 · Cited by 457
Steriade, M., Dossi, R. C., Paré, D., & Oakson, G. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.10.4396 · Cited by 455
Dysfunctional Long-Range Coordination of Neural Activity during Gestalt Perception in Schizophrenia
Uhlhaas, P. J., Linden, D. E. J., Singer, W., Haenschel, C., Lindner, M., Maurer, K., & Rodríguez, E. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2002-06.2006 · Cited by 455
Movement and thought: identical control mechanisms by the cerebellum
Ito, M. (1993) · Trends in Neurosciences · doi:10.1016/0166-2236(93)90073-u · Cited by 453
Amphetamine Exposure Enhances Habit Formation
Nelson, A., & Killcross, S. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4305-05.2006 · Cited by 445
Convergence of biological and psychological perspectives on cognitive coordination in schizophrenia
Phillips, W. A., & Silverstein, S. M. (2003) · Behavioral and Brain Sciences · doi:10.1017/s0140525x03000025 · Cited by 445
Reinforcement learning or active inference?
Friston, K. J., Daunizeau, J., & Kiebel, S. J. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006421 · Cited by 443
Critchley, H. D., Mathias, C. J., & Dolan, R. J. (2002) · Neuron · doi:10.1016/s0896-6273(02)00588-3 · Cited by 441
First Rank Symptoms of Schizophrenia
Mellor, C. S. (1970) · The British Journal of Psychiatry · doi:10.1192/bjp.117.536.15 · Cited by 437
Glutamate, Dopamine, and Schizophrenia: From Pathophysiology to Treatment
LARUELLE, M., KEGELES, L. S., & ABI‐DARGHAM, A. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1300.063 · Cited by 437
Habenula: crossroad between the basal ganglia and the limbic system
Hikosaka, O., Sesack, S. R., Lecourtier, L., & Shepard, P. D. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.3463-08.2008 · Cited by 432
Jackson, M. E., Homayoun, H., & Moghaddam, B. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308455101 · Cited by 430
Effects of ketamine on sensory perception: evidence for a role of N-methyl-D-aspartate receptors.
Øye, I., Paulsen, O., & Maurset, A. (1992) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)11430-4 · Cited by 430
From Fear to Safety and Back: Reversal of Fear in the Human Brain
Schiller, D., Levy, I., Niv, Y., LeDoux, J. E., & Phelps, E. A. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2265-08.2008 · Cited by 429
Dopamine gates LTP induction in lateral amygdala by suppressing feedforward inhibition
Bissière, S., Humeau, Y., & Lüthi, A. (2003) · Nature Neuroscience · doi:10.1038/nn1058 · Cited by 427
Serotonin research: contributions to understanding psychoses
GEYER, M., & VOLLENWEIDER, F. (2008) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2008.06.006 · Cited by 427
Memory reconsolidation mediates the strengthening of memories by additional learning
Lee, J. L. C. (2008) · Nature Neuroscience · doi:10.1038/nn.2205 · Cited by 420
Modulating the sense of agency with external cues
Moore, J. W., Wegner, D. M., & Haggard, P. (2009) · Consciousness and Cognition · doi:10.1016/j.concog.2009.05.004 · Cited by 413
Graziano, M. A., & Gross, C. (1993) · Experimental Brain Research · doi:10.1007/bf00228820 · Cited by 408
The Computation of Social Behavior
Behrens, T. E. J., Hunt, L. T., & Rushworth, M. F. S. (2009) · Science · doi:10.1126/science.1169694 · Cited by 407 · cited 5×
“…learning circuits are engaged when human subjects make social value judgments and a further network of brain regions is engaged when subjects make judgments about the intentions of others – including the superior temporal sulcus/temporoparietal junction (STS/TPJ) (Behrens et al., 2009).”
BackgroundInfluentialN-Acetylcysteine reverses cocaine-induced metaplasticity
Moussawi, K., Pacchioni, A. M., Moran, M., Olive, M. F., Gass, J. T., Lavín, A., & Kalivas, P. W. (2009) · Nature Neuroscience · doi:10.1038/nn.2250 · Cited by 403
The Angular Gyrus Computes Action Awareness Representations
Farrer, C., Frey, S. H., Horn, J. D. V., Tunik, E., Turk, D. J., Inati, S., & Grafton, S. T. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm050 · Cited by 386
Schobel, S., Lewandowski, N., Corcoran, C., Moore, H., Brown, T., Malaspina, D., & Small, S. (2009) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2009.115 · Cited by 384
Grossberg, S. (1982) · Psychological Review · doi:10.1037/0033-295x.89.5.529 · Cited by 377
Brain Representation of Active and Passive Movements
Weiller, C., Jüptner, M., Fellows, S. J., Rijntjes, M., Leonhardt, G., Kiebel, S. J., Müller, S., Diener, H., & Thilmann, A. F. (1996) · NeuroImage · doi:10.1006/nimg.1996.0034 · Cited by 367
From drugs to deprivation: A Bayesian framework for understanding models of psychosis
Corlett, P. R., Frith, C. D., & Fletcher, P. C. (2009) · Psychopharmacology · doi:10.1007/s00213-009-1561-0 · Cited by 367 · cited 22×
“…cues, the world seems to have changed, it feels strange and sinister, such signals and experiences provide an impetus for new learning which updates the world model inappropriately, manifest as a delusion (Corlett et al., 2009a, 2007a; Gray, 2004; Gray et al., 1991; Hemsley, 1994; Kapur, 2003).”
BackgroundInfluentialMilad, M. R., Vidal-Gonzalez, I., & Quirk, G. J. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.2.389 · Cited by 354
Dopamine and N-Methyl-D- Aspartate Receptor Interactions in the Neostriatum
Cepeda, C., & Levine, M. S. (1998) · Developmental Neuroscience · doi:10.1159/000017294 · Cited by 350
Expectation modulates neural responses to pleasant and aversive stimuli in primate amygdala
Belova, M. A., Paton, J. J., Morrison, S. E., & Salzman, C. D. (2007) · Neuron · doi:10.1016/j.neuron.2007.08.004 · Cited by 349
The laterodorsal tegmentum is essential for burst firing of ventral tegmental area dopamine neurons
Lodge, D. J., & Grace, A. A. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510715103 · Cited by 349
WEINER, H. (1964) · Psychosomatic Medicine · doi:10.1097/00006842-196403000-00011 · Cited by 349
fMRI Adaptation Reveals Mirror Neurons in Human Inferior Parietal Cortex
Chong, T. T. ‐., Cunnington, R., Williams, M., Kanwisher, N., & Mattingley, J. B. (2008) · Current Biology · doi:10.1016/j.cub.2008.08.068 · Cited by 344
Schizophrenia: A Subcortical Neurotransmitter Imbalance Syndrome?
Carlsson, M. L., & Carlsson, A. C. (1990) · Schizophrenia Bulletin · doi:10.1093/schbul/16.3.425 · Cited by 341
Grabenhorst, F., Rolls, E. T., & Bilderbeck, A. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm185 · Cited by 337
Buhl, E. H., Tamás, G., & Fisahn, A. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.117by.x · Cited by 337
The role of the striatum in aversive learning and aversive prediction errors
Delgado, M. R., Li, J., Schiller, D., & Phelps, E. A. (2008) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2008.0161 · Cited by 328
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
Perceptual Anomalies in Schizophrenia: Integrating Phenomenology and Cognitive Neuroscience
Uhlhaas, P. J., & Mishara, A. L. (2006) · Schizophrenia Bulletin · doi:10.1093/schbul/sbl047 · Cited by 321
Die Beginnende Schizophrenie. By K. Conrad Georg Thieme, Stuttgart, 1958.
Fish, F. (1960) · Journal of Mental Science · doi:10.1192/bjp.106.445.1595 · Cited by 320
Game theory and neural basis of social decision making
Lee, D. (2008) · Nature Neuroscience · doi:10.1038/nn2065 · Cited by 316
The Self in Neuroscience and Psychiatry
David, A., & Kircher, T. (2003) · Cambridge University Press eBooks · doi:10.1017/cbo9780511543708 · Cited by 313
Diverse Psychotomimetics Act Through a Common Signaling Pathway
Svenningsson, P., Tzavara, E. T., Carruthers, R., Rachleff, I., Wattler, S., Nehls, M. C., McKinzie, D. L., Fienberg, A. A., Nomikos, G. G., & Greengard, P. (2003) · Science · doi:10.1126/science.1089681 · Cited by 313
A Dual Role for Prediction Error in Associative Learning
den Ouden, H. E. M., Friston, K. J., Daw, N. D., McIntosh, A. R., & Stephan, K. E. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn161 · Cited by 306
Cannabis and psychosis/schizophrenia: human studies
D’Souza, D. C., Sewell, R. A., & Ranganathan, M. (2009) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-009-0024-2 · Cited by 306
Striatal Prediction Error Modulates Cortical Coupling
den Ouden, H. E. M., Daunizeau, J., Roiser, J., Friston, K. J., & Stephan, K. E. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4458-09.2010 · Cited by 304
Prediction, sequences and the hippocampus
Lisman, J. E., & Redish, A. D. (2009) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0316 · Cited by 299
Mather, M., Schacter, D. L., & Scarry, E. (2001) · The American Journal of Psychology · doi:10.2307/1423692 · Cited by 297
Wang, J.-F. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.5.452 · Cited by 296
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 293
Categorical versus coordinate spatial relations: Computational analyses and computer simulations.
Kosslyn, S. M., Chabris, C. F., Marsolek, C. J., et al. (1992) · Journal of Experimental Psychology Human Perception & Performance · doi:10.1037//0096-1523.18.2.562 · Cited by 292
The mirror-neuron system: a Bayesian perspective
Kilner, J. M., Friston, K. J., & Frith, C. (2007) · Neuroreport · doi:10.1097/wnr.0b013e3281139ed0 · Cited by 291
Magnetic resonance imaging of cerebellar–prefrontal and cerebellar–parietal functional connectivity
Allen, G., McColl, R. W., Barnard, H. D., Ringe, W. K., Fleckenstein, J. R., & Cullum, C. M. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.06.013 · Cited by 288
How visual stimuli activate dopaminergic neurons at short latency
Dommett, E., Coizet, V., Blaha, C. D., Martindale, J., Lefebvre, V., Walton, N., Mayhew, J. E. W., Overton, P. G., & Redgrave, P. (2005) · Science · doi:10.1126/science.1107026 · Cited by 285
Preliminary Observations on Tickling Oneself
Weiskrantz, L., Elliott, J. M., & Darlington, C. D. (1971) · Nature · doi:10.1038/230598a0 · Cited by 283
Lodge, D. J., & Grace, A. A. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300963 · Cited by 280
Delusions of alien control in the normal brain
Blakemore, S., Oakley, D. A., & Frith, C. (2003) · Neuropsychologia · doi:10.1016/s0028-3932(02)00313-5 · Cited by 277
Learning: From Association to Cognition
Shanks, D. R. (2009) · Annual Review of Psychology · doi:10.1146/annurev.psych.093008.100519 · Cited by 272
Cortical Pruning and the Development of Schizophrenia: A Computer Model
Hoffman, R. E., & Dobscha, S. K. (1989) · Schizophrenia Bulletin · doi:10.1093/schbul/15.3.477 · Cited by 270
Corollary discharge dysfunction in schizophrenia: Can it explain auditory hallucinations?
Ford, J. M., & Mathalon, D. H. (2005) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2005.01.014 · Cited by 267
Research works printed but not linked: 7
- Bleuler, 1908, Die Prognose der Dementia praecox (Schizophreniegruppe), Allgemeine Zeitschrift für Psychiatrie und psychischgerichtliche Medizin, 65, 436
- Capgras, 1923, L’illusion des “soises” dans un delire systematise, Bull. Soc. Clin. Med. Mentale, 11, 6
- Cotard, 1880, Du délire hypocondriaque dans une forme grave de la melancolie anxieuse. Memoire lu à la Société médicopsychologique dans la Séance du 28 Juin 1880, Ann. Medico-Psychol. Med., 168
- Hemsley, 1986, The formation of maintenance of delusions: a Bayesian analysis, Br. J. Psychiatry, 149, 51, 10.1192/bjp.149.1.51 · DOI
- Lasegue, 1877, La folie a deux (ou folie communiquee), Ann. Med. Psychol., 18, 321
- Seashore, 1895, Measurements of illusions and hallucinations in normal life, Stud. Yale Psychol. Lab., 3, 1
- Thiebierge, 1894, Les acaraphobes, Ann. Dermatol. Syphiligraphie, 3, 730
Cited by
Sorted by citations
Whatever next? Predictive brains, situated agents, and the future of cognitive science
Clark, A. (2013) · Behavioral and Brain Sciences · doi:10.1017/s0140525x12000477 · Cited by 5,924
An Interoceptive Predictive Coding Model of Conscious Presence
Seth, A. K., Suzuki, K., & Critchley, H. D. (2012) · Frontiers in Psychology · doi:10.3389/fpsyg.2011.00395 · Cited by 950
“Rather, presence depends on a match between informative interoceptive signals and top-down predictions arising from a dynamically evolving brain–body–world interaction.”
BackgroundThe Predictive Coding Account of Psychosis
Sterzer, P., Adams, R. A., Fletcher, P., Frith, C., Lawrie, S. M., Muckli, L., Petrovic, P., Uhlhaas, P., Voss, M., & Corlett, P. R. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.05.015 · Cited by 941
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Edwards, M. J., Adams, R. A., Brown, H., Parees, I., & Friston, K. J. (2012) · Brain · doi:10.1093/brain/aws129 · Cited by 825
Allostatic Self-efficacy: A Metacognitive Theory of Dyshomeostasis-Induced Fatigue and Depression
Stephan, K. E., Manjaly, Z. M., Mathys, C. D., Weber, L. A. E., Paliwal, S., Gard, T., Tittgemeyer, M., Fleming, S. M., Haker, H., Seth, A. K., et al. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00550 · Cited by 437
“Importantly, NMDAR dependent signaling is thought to be essential for updating and encoding representations of beliefs (Corlett et al., 2010; Vinckier et al., 2016).”
BackgroundInfluential
Metadata
- Authors
- Corlett, P. R., Taylor, J. R., Wang, X.-J., Fletcher, P. C., & Krystal, J. H.
- Affiliations
- Yale University (US)
- University of Cambridge (GB)
- Corresponding author
- Corlett, P.R.
- Venue
- Progress in Neurobiology
- Publisher
- Elsevier BV
- Published
- 2010-11
- Volume
- 92
- Issue
- 3
- Pages
- 345-369
- ISSN
- 0301-0082 (ISSN-L)
- PMC
- PMC3676875
- OpenAlex
- W2018699045
- Cited by
- 394
- References
- 438
- Citations by year
- 2026: 31 · 2025: 16 · 2024: 24 · 2023: 20 · 2022: 29 · 2021: 30 · 2020: 33 · 2019: 22 · 2018: 20 · 2017: 35 · 2016: 27 · 2015: 32 · 2014: 25 · 2013: 22 · 2012: 21
- FWCI
- 34.61
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Progress in Neurobiology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Wellcome Trust (064351)
- National Institute on Drug Abuse (R01DA011717, R01DA015222)
- Topics
- Social Sciences › Arts and Humanities › Philosophy › Mental Health and Psychiatry
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Neuroscience › Cognitive Neuroscience › Embodied and Extended Cognition
- Keywords
- delusions, prediction error, reinforcement learning, hierarchical prediction, frontostriatal circuits, amygdala, parietal cortex, memory, perception, bodily agency, social learning, computational psychiatry
- MeSH terms
- Brain, Cognition, Computer Simulation, Culture, Delusions, Humans, Learning, Memory, Models, Neurological, Nervous System Diseases, Neurobiology, Perception
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