The nucleus accumbens as a nexus between values and goals in goal-directed behavior: a review and a new hypothesis
Open accessAbstract
Goal-directed behavior is a fundamental means by which animals can flexibly solve the challenges posed by variable external and internal conditions. Recently, the processes and brain mechanisms underlying such behavior have been extensively studied from behavioral, neuroscientific and computational perspectives. This research has highlighted the processes underlying goal-directed behavior and associated brain systems including prefrontal cortex, basal ganglia and, in particular therein, the nucleus accumbens (NAcc). This paper focusses on one particular process at the core of goal-directed behavior: how motivational value is assigned to goals on the basis of internal states and environmental stimuli, and how this supports goal selection processes. Various biological and computational accounts have been given of this problem and of related multiple neural and behavior phenomena, but we still lack an integrated hypothesis on the generation and use of value for goal selection. This paper proposes an hypothesis that aims to solve this problem and is based on this key elements: (a) amygdala and hippocampus establish the motivational value of stimuli and goals; (b) prefrontal cortex encodes various types of action outcomes; (c) NAcc integrates different sources of value, representing them in terms of a common currency with the aid of dopamine, and thereby plays a major role in selecting action outcomes within prefrontal cortex. The "goals" pursued by the organism are the outcomes selected by these processes. The hypothesis is developed in the context of a critical review of relevant biological and computational literature which offer it support. The paper shows how the hypothesis has the potential to integrate existing interpretations of motivational value and goal selection.
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 dorsolateral striatum is more involved in stimulus-response learning and habitual control, the dorsomedial striatum is linked to action-outcome learning and goal-directed action, and ventral striatum to Pavlovian values.
“For example, the dorsolateral striatum is thought to be more involved in stimulus-response learning and habitual control, the dorsomedial striatum has been linked to action-outcome learning and goal-directed action, and ventral striatum to Pavlovian values (Glascher et al., 2010, Liljeholm and O’Doherty, 2012, Mannella et al., 2013, O’Doherty et al., 2004).”
From Active Inference, homeostatic regulation and adaptive behavioural control (2015) · cites this paper as Mannella et al., 2013
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
Reinforcement Learning: An Introduction
Sutton, R. S., & Barto, A. G. (1998) · IEEE Transactions on Neural Networks · doi:10.1109/tnn.1998.712192 · Cited by 27,225 · see citing works
Reinforcement Learning: An Introduction
Sutton, R. S., & Barto, A. (2005) · IEEE Transactions on Neural Networks · doi:10.1109/tnn.2004.842673 · Cited by 25,263 · see citing works
Watkins, C., & Dayan, P. (1992) · Machine-mediated learning · doi:10.1023/a:1022676722315 · Cited by 14,277 · see citing works
An Integrative Theory of Prefrontal Cortex Function
Miller, E. K., & Cohen, J. D. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.167 · Cited by 12,803 · see citing works
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 · see citing works
Watkins, C. J. C. H., & Dayan, P. (1992) · Machine Learning · doi:10.1007/bf00992698 · Cited by 9,083 · see citing works
Parallel organization of functionally segregated circuits linking basal ganglia and cortex
Alexander, G. E., DeLong, M. R., & Strick, P. L. (1986) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.09.030186.002041 · Cited by 8,527 · see citing works
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010 · see citing works
Rizzolatti, G., & Craighero, L. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144230 · Cited by 7,433 · see citing works
Separate visual pathways for perception and action
Goodale, M. A., & Milner, A. D. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90344-8 · Cited by 6,519 · see citing works
McClelland, J. L., McNaughton, B. L., & O'Reilly, R. C. (1995) · Psychological Review · doi:10.1037/0033-295x.102.3.419 · Cited by 5,256 · see citing works
The Neural Basis of Decision Making
Gold, J. I., & Shadlen, M. N. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.113038 · Cited by 3,764 · see citing works
Cattaneo, L., & Rizzolatti, G. (2009) · Archives of Neurology · doi:10.1001/archneurol.2009.41 · Cited by 3,137 · see citing works
Gerfen, C. R., Engber, T. M., Mahan, L. C., Susel, Z., Chase, T. N., Monsma, F. J., & Sibley, D. R. (1990) · Science · doi:10.1126/science.2147780 · Cited by 2,967 · see citing works
The amygdala: vigilance and emotion
Davis, M., & Whalen, P. J. (2001) · Molecular Psychiatry · doi:10.1038/sj.mp.4000812 · Cited by 2,882 · see citing works
Getting formal with dopamine and reward
Schultz, W. (2002) · Neuron · doi:10.1016/s0896-6273(02)00967-4 · Cited by 2,574 · see citing works
Daw, N. D., Niv, Y., & Dayan, P. (2005) · Nature Neuroscience · doi:10.1038/nn1560 · Cited by 2,533 · see citing works
THE BASAL GANGLIA: FOCUSED SELECTION AND INHIBITION OF COMPETING MOTOR PROGRAMS
Mink, J. W. (1996) · Progress in Neurobiology · doi:10.1016/s0301-0082(96)00042-1 · Cited by 2,478 · see citing works
The role of the basal ganglia in habit formation
Yin, H. H., & Knowlton, B. J. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1919 · Cited by 2,402 · see citing works
The Hippocampus as a Cognitive Map
Ranck, J. B. (1979) · American Journal of Psychiatry · doi:10.1176/ajp.136.10.1353 · Cited by 2,373 · see citing works
The Prefrontal Cortex: Anatomy, Physiology, and Neuropsychology of the Frontal Lobe
Fuster, J. M. (1980) · Cited by 2,367 · see citing works
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 · see citing works
From motivation to action: Functional interface between the limbic system and the motor system
MOGENSON, G., JONES, D., & YIM, C. (1980) · Progress in Neurobiology · doi:10.1016/0301-0082(80)90018-0 · Cited by 2,331 · see citing works
The organization of recent and remote memories
Frankland, P. W., & Bontempi, B. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1607 · Cited by 2,138 · see citing works
Emotion and motivation: the role of the amygdala, ventral striatum, and prefrontal cortex
Cardinal, R. N., Parkinson, J. A., Hall, J., & Everitt, B. J. (2002) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(02)00007-6 · Cited by 2,129 · see citing works
Parietal Lobe: From Action Organization to Intention Understanding
Fogassi, L., Ferrari, P. F., Gesierich, B., Rozzi, S., Chersi, F., & Rizzolatti, G. (2005) · Science · doi:10.1126/science.1106138 · Cited by 1,990 · see citing works
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 · see citing works
KRINGELBACH, M. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.03.006 · Cited by 1,977 · see citing works
Functional role of the supplementary and pre-supplementary motor areas
Nachev, P., Kennard, C., & Husain, M. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2478 · Cited by 1,928 · see citing works
Neural Basis of a Perceptual Decision in the Parietal Cortex (Area LIP) of the Rhesus Monkey
Shadlen, M. N., & Newsome, W. T. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.4.1916 · Cited by 1,755 · see citing works
Learning and Memory Functions of the Basal Ganglia
Packard, M. G., & Knowlton, B. J. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142937 · Cited by 1,717 · see citing works
Neural Mechanisms of Extinction Learning and Retrieval
Quirk, G. J., & Mueller, D. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301555 · Cited by 1,645 · see citing works
Haber, S. N., Fudge, J. L., & McFarland, N. R. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-06-02369.2000 · Cited by 1,610 · see citing works
The Orbitofrontal Cortex and Reward
Rolls, E. T. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.284 · Cited by 1,595 · see citing works
Sesack, S. R., Deutch, A. Y., Roth, R. H., & Bunney, B. S. (1989) · Journal of Comparative Neurology · doi:10.1002/cne.902900205 · Cited by 1,568 · see citing works
Differential projections of the infralimbic and prelimbic cortex in the rat
Vertes, R. P. (2004) · Synapse · doi:10.1002/syn.10279 · Cited by 1,550 · see citing works
Goal-directed instrumental action: contingency and incentive learning and their cortical substrates
Balleine, B. W., & Dickinson, A. (1998) · Neuropharmacology · doi:10.1016/s0028-3908(98)00033-1 · Cited by 1,541 · see citing works
The role of medial prefrontal cortex in memory and decision making
Euston, D. R., Gruber, A. J., & McNaughton, B. L. (2012) · Neuron · doi:10.1016/j.neuron.2012.12.002 · Cited by 1,541 · see citing works
Grasping objects: the cortical mechanisms of visuomotor transformation
Jeannerod, M., Arbib, M. A., Rizzolatti, G., & Sakata, H. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)93921-j · Cited by 1,399 · see citing works
The Role of the Dorsal Striatum in Reward and Decision-Making: Figure 1.
Balleine, B. W., Delgado, M. R., & Hikosaka, O. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1554-07.2007 · Cited by 1,390 · see citing works
Dynamic Programming: Deterministic and Stochastic Models
Bertsekas, D. P. (1987) · Medical Entomology and Zoology · Cited by 1,348 · see citing works
Prefrontal executive and cognitive functions in rodents: neural and neurochemical substrates
Dalley, J. W., Cardinal, R. N., & Robbins, T. W. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.09.006 · Cited by 1,329 · see citing works
The functions of the orbitofrontal cortex
Rolls, E. T. (2004) · Brain and Cognition · doi:10.1016/s0278-2626(03)00277-x · Cited by 1,327 · see citing works
The hippocampus and memory: insights from spatial processing
Bird, C. M., & Burgess, N. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2335 · Cited by 1,313 · see citing works
Motivation concepts in behavioral neuroscience
Berridge, K. C. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.02.004 · Cited by 1,302 · see citing works
Role of the Basal Ganglia in the Control of Purposive Saccadic Eye Movements
Hikosaka, O., Takikawa, Y., & Kawagoe, R. (2000) · Physiological Reviews · doi:10.1152/physrev.2000.80.3.953 · Cited by 1,287 · see citing works
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 · see citing works
The basal ganglia: a vertebrate solution to the selection problem?
Redgrave, P., Prescott, T. J., & Gurney, K. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00319-4 · Cited by 1,199 · see citing works
Self-citationModels of Information Processing in the Basal Ganglia
(1994) · doi:10.7551/mitpress/4708.001.0001 · Cited by 1,190 · see citing works
Putting a spin on the dorsal-ventral divide of the striatum
Voorn, P., Vanderschuren, L. J. M. J., Groenewegen, H. J., Robbins, T. W., & Pennartz, C. M. A. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.06.006 · Cited by 1,188 · see citing works
Geometric determinants of the place fields of hippocampal neurons
O'Keefe, J., & Burgess, N. (1996) · Nature · doi:10.1038/381425a0 · Cited by 1,166 · see citing works
Goal-directed and habitual control in the basal ganglia: implications for Parkinson's disease
Redgrave, P., Rodriguez, M., Smith, Y., Rodriguez-Oroz, M. C., Lehericy, S., Bergman, H., Agid, Y., DeLong, M. R., & Obeso, J. A. (2010) · Nature reviews. Neuroscience · doi:10.1038/nrn2915 · Cited by 1,134 · see citing works
Tonic dopamine: Opportunity costs and the control of response vigor
Niv, Y., Daw, N. D., Joel, D., & Dayan, P. (2007) · Psychopharmacology · doi:10.1007/s00213-006-0502-4 · Cited by 1,133 · see citing works
Floresco, S. B., West, A. R., Ash, B., Moore, H., & Grace, A. A. (2003) · Nature Neuroscience · doi:10.1038/nn1103 · Cited by 1,106 · see citing works
The role of the dorsomedial striatum in instrumental conditioning
Yin, H. H., Ostlund, S. B., Knowlton, B. J., & Balleine, B. W. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04218.x · Cited by 1,099 · see citing works
Cortical mechanisms of action selection: the affordance competition hypothesis
Cisek, P. (2007) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2007.2054 · Cited by 1,077 · see citing works
O’Reilly, R. C., & Frank, M. J. (2005) · Neural Computation · doi:10.1162/089976606775093909 · Cited by 1,066 · see citing works
The Hippocampus, Memory, and Place Cells
Eichenbaum, H., Dudchenko, P., Wood, E., Shapiro, M., & Tanila, H. (1999) · Neuron · doi:10.1016/s0896-6273(00)80773-4 · Cited by 1,064 · see citing works
Neuroeconomics: decision making and the brain
(2014) · Choice Reviews Online · doi:10.5860/choice.51-5702 · Cited by 1,020 · 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
Medial prefrontal cortex as an action-outcome predictor
Alexander, W. H., & Brown, J. W. (2011) · Nature Neuroscience · doi:10.1038/nn.2921 · Cited by 1,000 · see citing works
Motivational control of goal-directed action
Dickinson, A., & Balleine, B. (1994) · Animal Learning & Behavior · doi:10.3758/bf03199951 · Cited by 995 · see citing works
Pape, H.-C., & Pare, D. (2010) · Physiological Reviews · doi:10.1152/physrev.00037.2009 · Cited by 994 · see citing works
Mesolimbocortical and nigrostriatal dopamine responses to salient non-reward events
Horvitz, J. C. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00019-1 · Cited by 967 · see citing works
Computational roles for dopamine in behavioural control
Montague, P. R., Hyman, S. E., & Cohen, J. D. (2004) · Nature · doi:10.1038/nature03015 · Cited by 966 · see citing works
Disinhibition as a basic process in the expression of striatal functions.
Chevalier, G., & Deniau, J. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90109-n · Cited by 965 · see citing works
The role of ventromedial prefrontal cortex in the recovery of extinguished fear
Quirk, G. J., Russo, G. K., Barron, J. L., & Lebron, K. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-16-06225.2000 · Cited by 957 · cited 1× · see citing works
“In terms of connectivity, in rats NaccSh targets the AIC, the PL and the IL. IL plays a role in inhibiting instrumental behaviors and in the extinction of Pavlovian processes (Quirk et al., 2000; Coutureau and Killcross, 2003; Rhodes and Killcross, 2004; Sotres-Bayon and Quirk, 2010).”
Quirk, G. J., Likhtik, E., Pelletier, J. G., & Paré, D. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-25-08800.2003 · Cited by 927 · see citing works
A triple dissociation of memory systems: Hippocampus, amygdala, and dorsal striatum.
McDonald, R. J., & White, N. M. (1993) · Behavioral Neuroscience · doi:10.1037/0735-7044.107.1.3 · Cited by 885 · see citing works
Neural Networks and Brain Function
Rolls, E. T., & Treves, A. (1997) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198524328.001.0001 · Cited by 885 · see citing works
Functional characteristics of the midbrain periaqueductal gray.
Behbehani, M. M. (1995) · Progress in Neurobiology · doi:10.1016/0301-0082(95)00009-k · Cited by 879 · 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
Latent inhibition: The effect of nonreinforced pre-exposure to the conditional stimulus.
Lubow, R. E., & Moore, A. U. (1959) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0046700 · Cited by 806 · see citing works
Neural mechanisms for detecting and remembering novel events
Ranganath, C., & Rainer, G. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1052 · Cited by 779 · see citing works
Short latency inhibition of human hand motor cortex by somatosensory input from the hand
Tokimura, H., Lazzaro, V. D., Tokimura, Y., Oliviero, A., Profice, P., Insola, A., Mazzone, P., Tonali, P., & Rothwell, J. C. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.t01-1-00503.x · Cited by 771 · see citing works
Wyvell, C. L., & Berridge, K. C. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-21-08122.2000 · Cited by 764 · see citing works
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 · see citing works
Self-citationO’Donnell, P., & Grace, A. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-05-03622.1995 · Cited by 760 · see citing works
Dopamine operates as a subsecond modulator of food seeking
Roitman, M. F., Stuber, G. D., Phillips, P. E. M., Wightman, R. M., & Carelli, R. M. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.3823-03.2004 · Cited by 718 · see citing works
Neuroeconomics: Decision Making and the Brain
Rushworth, M. F. S., & Walton, M. E. (2009) · Neuron · doi:10.1016/j.neuron.2009.07.005 · Cited by 669 · 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
Hierarchically organized behavior and its neural foundations: A reinforcement learning perspective
Botvinick, M. M., Niv, Y., & Barto, A. G. (2009) · Cognition · doi:10.1016/j.cognition.2008.08.011 · Cited by 646 · see citing works
A computational model of action selection in the basal ganglia. I. A new functional anatomy
GURNEY, K. N., Prescott, T. J., & Redgrave, P. (2001) · Biological Cybernetics · doi:10.1007/pl00007984 · Cited by 633 · see citing works
Self-citationPrefrontal control of fear: more than just extinction
Sotres-Bayon, F., & Quirk, G. J. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.02.005 · Cited by 625 · cited 1× · see citing works
“In terms of connectivity, in rats NaccSh targets the AIC, the PL and the IL. IL plays a role in inhibiting instrumental behaviors and in the extinction of Pavlovian processes (Quirk et al., 2000; Coutureau and Killcross, 2003; Rhodes and Killcross, 2004; Sotres-Bayon and Quirk, 2010).”
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 · 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
Detecting Subsecond Dopamine Release with Fast-Scan Cyclic Voltammetry in Vivo
Robinson, D. L., Venton, B. J., Heien, M. L., & Wightman, R. M. (2003) · Clinical Chemistry · doi:10.1373/49.10.1763 · Cited by 602 · see citing works
Corbit, L. H., & Balleine, B. W. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.4507-04.2005 · Cited by 589 · see citing works
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
Central circuits mediating patterned autonomic activity during active vs. passive emotional coping
Bandler, R., Keay, K. A., Floyd, N., & Price, J. (2000) · Brain Research Bulletin · doi:10.1016/s0361-9230(00)00313-0 · Cited by 582 · see citing works
Frank, M. J., & Claus, E. D. (2006) · Psychological Review · doi:10.1037/0033-295x.113.2.300 · Cited by 578 · see citing works
Dopaminergic modulation of limbic and cortical drive of nucleus accumbens in goal-directed behavior
Goto, Y., & Grace, A. A. (2005) · Nature Neuroscience · doi:10.1038/nn1471 · Cited by 576 · see citing works
Corbit, L. H., Muir, J. L., & Balleine, B. W. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-09-03251.2001 · Cited by 564 · see citing works
A Model of How the Basal Ganglia Generate and Use Neural Signals That Predict Reinforcement
Houk, J. C., Adams, J. L., & Barto, A. G. (1994) · The MIT Press eBooks · doi:10.7551/mitpress/4708.003.0020 · Cited by 555 · see citing works
Hatfield, T., Han, J.-S., Conley, M., Gallagher, M., & Holland, P. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05256.1996 · Cited by 555 · see citing works
Infralimbic Prefrontal Cortex Is Responsible for Inhibiting Cocaine Seeking in Extinguished Rats
Peters, J., LaLumiere, R. T., & Kalivas, P. W. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1045-08.2008 · Cited by 537 · see citing works
Midbrain dopamine neurons encode decisions for future action
Morris, G., Nevet, A., Arkadir, D., Vaadia, E., & Bergman, H. (2006) · Nature Neuroscience · doi:10.1038/nn1743 · Cited by 503 · see citing works
Actor–critic models of the basal ganglia: new anatomical and computational perspectives
Joel, D., Niv, Y., & Ruppin, E. (2002) · Neural Networks · doi:10.1016/s0893-6080(02)00047-3 · Cited by 500 · see citing works
Afferent connections of the medial frontal cortex of the rat. II. Cortical and subcortical afferents
Condé, F., Maire-Lepoivre, E., Audinat, É., & Crépel, F. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903520407 · Cited by 494 · see citing works
Neuronal mechanisms of executive control by the prefrontal cortex
Funahashi, S. (2001) · Neuroscience Research · doi:10.1016/s0168-0102(00)00224-8 · Cited by 493 · see citing works
Zahm, D. S. (2000) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(99)00065-2 · Cited by 487 · see citing works
RAGOZZINO, M. E. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.013 · Cited by 482 · see citing works
Forward frontal fields: phylogeny and fundamental function
Wise, S. P. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2008.08.008 · Cited by 478 · see citing works
Dopamine: generalization and bonuses
Kakade, S. M., & Dayan, P. (2002) · Neural Networks · doi:10.1016/s0893-6080(02)00048-5 · Cited by 477 · see citing works
A neoHebbian framework for episodic memory; role of dopamine-dependent late LTP
Lisman, J., Grace, A. A., & Duzel, E. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.07.006 · Cited by 465 · see citing works
Hasselmo, M. E., Schnell, E., & Barkai, E. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-07-05249.1995 · Cited by 463 · see citing works
The prefrontal cortex: Anatomy, physiology and neuropsychology of the frontal lobe
Andy, O. J. (1981) · Surgical Neurology · doi:10.1016/0090-3019(81)90062-8 · Cited by 455 · see citing works
Hedonic Hot Spots in the Brain
Peciña, S., Smith, K. S., & Berridge, K. C. (2006) · The Neuroscientist · doi:10.1177/1073858406293154 · Cited by 441 · see citing works
Salamone, J. D., Correa, M., Mingote, S., & Weber, S. M. (2003) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.102.035063 · Cited by 433 · see citing works
The role of prelimbic cortex in instrumental conditioning
Corbit, L. H., & Balleine, B. W. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.09.023 · Cited by 423 · see citing works
The Basal Ganglia and Cortex Implement Optimal Decision Making Between Alternative Actions
Bogacz, R., & GURNEY, K. N. (2007) · Neural Computation · doi:10.1162/neco.2007.19.2.442 · Cited by 417 · see citing works
Self-citationYin, H. H., Ostlund, S. B., & Balleine, B. W. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06422.x · Cited by 416 · see citing works
A computational substrate for incentive salience
McClure, S. M., Daw, N. D., & Montague, P. R. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00177-2 · Cited by 416 · see citing works
The ventral basal ganglia, a selection mechanism at the crossroads of space, strategy, and reward.
Humphries, M. D., & Prescott, T. J. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.11.003 · Cited by 414 · see citing works
Lisman, J. E., & Otmakhova, N. A. (2001) · Hippocampus · doi:10.1002/hipo.1071 · Cited by 402 · see citing works
Lesion to the nigrostriatal dopamine system disrupts stimulus-response habit formation
Faure, A., Haberland, U., Condé, F., & Massioui, N. E. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3894-04.2005 · Cited by 402 · see citing works
Functional correlates of prospective memory in stroke
Kant, N., van den Berg, E., van Zandvoort, M. J. E., Frijns, C. J. M., Kappelle, L. J., & Postma, A. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.05.015 · Cited by 393 · see citing works
Orbitofrontal Cortex Mediates Outcome Encoding in Pavlovian But Not Instrumental Conditioning
Ostlund, S. B., & Balleine, B. W. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5443-06.2007 · Cited by 379 · cited 1× · see citing works
“In contrast, lesions of the orbitofrontal cortex (OFC; Ostlund and Balleine, 2007a,b) or the entorhinal cortex (EC) result in a lack of expression of contingency degradation alone (but not so in primates where OFC is important for instrumental devaluation, Izquierdo et al., 2004; Roberts, 2006).”
Functional correlates of prospective memory in stroke
Kant, N., Van den Berg, E., van Zandvoort, M. J. E., et al. (2010) · Università Politecnica delle Marche (Università Politecnica delle Marche) · doi:10.1016/j.neuropsychologia · Cited by 375 · see citing works
The integrative function of the basal ganglia in instrumental conditioning
Balleine, B. W., Liljeholm, M., & Ostlund, S. B. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.10.034 · Cited by 356 · see citing works
Hall, J., Parkinson, J. A., Connor, T. M., Dickinson, A., & Everitt, B. J. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01577.x · Cited by 355 · see citing works
The effect of lesions of the basolateral amygdala on instrumental conditioning
Balleine, B. W., Killcross, A. S., & Dickinson, A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-02-00666.2003 · Cited by 355 · see citing works
Coutureau, E., & Killcross, S. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.09.025 · Cited by 342 · see citing works
Molecular effects of dopamine on striatal-projection pathways
Gerfen, C. R. (2000) · Trends in Neurosciences · doi:10.1016/s1471-1931(00)00019-7 · Cited by 341 · see citing works
Chikama, M., McFarland, N. R., Amaral, D. G., & Haber, S. N. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-24-09686.1997 · Cited by 341 · see citing works
Projection from the sensory to the motor cortex is important in learning motor skills in the monkey
Pavlides, C., Miyashita, E., & Asanuma, H. (1993) · Journal of Neurophysiology · doi:10.1152/jn.1993.70.2.733 · Cited by 331 · see citing works
The mesoaccumbens dopamine in coping with stress
Cabib, S., & Puglisi-Allegra, S. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.04.012 · Cited by 329 · 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
Parkinson, J. A., Willoughby, P. J., Robbins, T. W., & Everitt, B. J. (2000) · Behavioral Neuroscience · doi:10.1037/0735-7044.114.1.42 · Cited by 314 · see citing works
Insulin, IGF-1 and GLP-1 signaling in neurodegenerative disorders: Targets for disease modification?
Bassil, F., Fernagut, P., Bézard, E., & Meissner, W. G. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2014.02.005 · Cited by 313 · see citing works
Parkinson, J. A., Willoughby, P. J., Robbins, T. W., & Everitt, B. J. (2000) · Behavioral Neuroscience · doi:10.1037//0735-7044.114.1.42 · Cited by 309 · see citing works
Corbit, L. H., & Balleine, B. W. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2711-11.2011 · Cited by 309 · see citing works
Hippocampal place cells, context, and episodic memory
Smith, D. M., & Mizumori, S. J. Y. (2006) · Hippocampus · doi:10.1002/hipo.20208 · Cited by 302 · see citing works
The temporal lobe is a target of output from the basal ganglia.
Middleton, F. A., & Strick, P. L. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.16.8683 · Cited by 301 · see citing works
Chiba, T., Kayahara, T., & Nakano, K. (2001) · Brain Research · doi:10.1016/s0006-8993(00)03013-4 · Cited by 290 · see citing works
The hippocampal-striatal axis in learning, prediction and goal-directed behavior
Pennartz, C. M. A., Ito, R., Verschure, P. F. M. J., Battaglia, F. P., & Robbins, T. W. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.08.001 · Cited by 287 · see citing works
The dopaminergic mesencephalic projections to the hippocampal formation in the rat
Gasbarri, A., Sulli, A., & Packard, M. G. (1997) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(96)00157-1 · Cited by 285 · see citing works
Coding for spatial goals in the prelimbic/infralimbic area of the rat frontal cortex
Hok, V., Save, É., Lenck‐Santini, P., & Poucet, B. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407332102 · Cited by 269 · see citing works
Dissociable roles of the central and basolateral amygdala in appetitive emotional learning
Parkinson, J. A., Robbins, T. W., & Everitt, B. J. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00960.x · Cited by 266 · see citing works
Parallels between cerebellum- and amygdala-dependent conditioning
Medina, J. F., Repa, J. C., Mauk, M. D., & LeDoux, J. E. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn728 · Cited by 265 · see citing works
Anticipation of novelty recruits reward system and hippocampus while promoting recollection
Wittmann, B. C., Bunzeck, N., Dolan, R. J., & Düzel, E. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.06.038 · Cited by 265 · see citing works
Match–Mismatch Processes Underlie Human Hippocampal Responses to Associative Novelty
Kumaran, D., & Maguire, E. A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1677-07.2007 · Cited by 264 · 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
Activity in the lateral prefrontal cortex reflects multiple steps of future events in action plans
Mushiake, H., Saito, N., Sakamoto, K., Itoyama, Y., & Tanji, J. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.045 · Cited by 249 · see citing works
Weak before strong: dissociating synaptic tagging and plasticity-factor accounts of late-LTP
Frey, U., & Morris, R. (1998) · Neuropharmacology · doi:10.1016/s0028-3908(98)00040-9 · Cited by 242 · see citing works
Rebec, G. V., Christensen, J. R. C., Guerra, C., & Bardo, M. T. (1997) · Brain Research · doi:10.1016/s0006-8993(97)01004-4 · Cited by 235 · see citing works
The Nucleus Accumbens and Pavlovian Reward Learning
Day, J. J., & Carelli, R. M. (2007) · The Neuroscientist · doi:10.1177/1073858406295854 · Cited by 235 · see citing works
Corbit, L. H., Janak, P. H., & Balleine, B. W. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05934.x · Cited by 231 · see citing works
Parieto-frontal coding of reaching: an integrated framework
Burnod, Y., Baraduc, P., Battaglia‐Mayer, A., Guigon, E., Koechlin, É., Ferraina, S., Lacquaniti, F., & Caminiti, R. (1999) · Experimental Brain Research · doi:10.1007/s002210050902 · Cited by 230 · see citing works
Fear of novelty in infant rats predicts adult corticosterone dynamics and an early death
Cavigelli, S. A., & McClintock, M. K. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2535721100 · Cited by 226 · see citing works
A Role for Prefrontal Cortex in Memory Storage for Trace Fear Conditioning
Runyan, J. D., Moore, A. N., & Dash, P. K. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.4880-03.2004 · Cited by 224 · see citing works
The Human Hippocampus: Cognitive Maps or Relational Memory?
Kumaran, D., & Maguire, E. A. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1103-05.2005 · Cited by 218 · see citing works
Network Dynamics Underlying the Formation of Sparse, Informative Representations in the Hippocampus
Karlsson, M. P., & Frank, L. M. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4261-08.2008 · Cited by 217 · see citing works
Learning arbitrary visuomotor associations: temporal dynamic of brain activity
Toni, I., Ramnani, N., Josephs, O., Ashburner, J., & Passingham, R. E. (2001) · NeuroImage · doi:10.1006/nimg.2001.0894 · Cited by 210 · see citing works
Cardinal, R. N., Parkinson, J. A., Lachenal, G., Halkerston, K. M., Rudarakanchana, N., Hall, J., Morrison, C. H., Howes, S. R., Robbins, T. W., & Everitt, B. J. (2002) · Behavioral Neuroscience · doi:10.1037//0735-7044.116.4.553 · Cited by 201 · see citing works
Cardinal, R. N., Parkinson, J. A., Lachenal, G., Halkerston, K. M., Rudarakanchana, N., Hall, J., Morrison, C. H., Howes, S. R., Robbins, T. W., & Everitt, B. J. (2002) · Behavioral Neuroscience · doi:10.1037/0735-7044.116.4.553 · Cited by 201 · see citing works
Ostlund, S. B., & Balleine, B. W. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.5472-07.2008 · Cited by 198 · see citing works
Peciña, S., Schulkin, J., & Berridge, K. C. (2006) · BMC Biology · doi:10.1186/1741-7007-4-8 · Cited by 194 · see citing works
Corbit, L. H., Muir, J. L., & Balleine, B. W. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02833.x · Cited by 186 · see citing works
Still at the Choice‐Point: Action Selection and Initiation in Instrumental Conditioning
BALLEINE, B. W., & OSTLUND, S. B. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1390.006 · Cited by 184 · see citing works
Room, P., Russchen, F. T., Groenewegen, H. J., & Lohman, A. H. M. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902420104 · Cited by 181 · see citing works
Solway, A., & Botvinick, M. (2012) · Psychological Review · doi:10.1037/a0026435 · Cited by 180 · see citing works
VanElzakker, M. B., Fevurly, R. D., Breindel, T., & Spencer, R. L. (2008) · Learning & Memory · doi:10.1101/lm.1196508 · Cited by 179 · see citing works
Gruber, A. J., & McDonald, R. J. (2012) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2012.00050 · Cited by 173 · see citing works
TD(λ) Converges with Probability 1
Dayan, P., & B, T. J. S. A. (1994) · Machine Learning · doi:10.1023/a:1022657612745 · Cited by 169 · see citing works
Romanelli, P., Esposito, V., Schaal, D. W., & Heit, G. (2004) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.09.008 · Cited by 163 · see citing works
Pezzulo, G., Rigoli, F., & Chersi, F. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00092 · Cited by 163 · see citing works
Convergence of sensory systems in the orbitofrontal cortex in primates and brain design for emotion
Rolls, E. T. (2004) · The Anatomical Record Part A Discoveries in Molecular Cellular and Evolutionary Biology · doi:10.1002/ar.a.20126 · Cited by 160 · see citing works
Bast, T. (2007) · Reviews in the Neurosciences · doi:10.1515/revneuro.2007.18.3-4.253 · Cited by 149 · see citing works
A triple dissociation of memory systems: Hippocampus, amygdala, and dorsal striatum.
McDonald, R., & White, N. (1993) · Behavioral Neuroscience · doi:10.1037/a0034883 · Cited by 146 · see citing works
Nucleus accumbens neurons encode Pavlovian approach behaviors: evidence from an autoshaping paradigm
Day, J. J., Wheeler, R. A., Roitman, M. F., & Carelli, R. M. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04654.x · Cited by 140 · see citing works
The central nucleus of the amygdala projection to dopamine subpopulations in primates
Fudge, J. L., & Haber, S. N. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00092-0 · Cited by 138 · see citing works
Meeter, M., Murre, J. M. J., & Talamini, L. M. (2004) · Hippocampus · doi:10.1002/hipo.10214 · Cited by 138 · see citing works
TRoPICALS: A computational embodied neuroscience model of compatibility effects.
Caligiore, D., Borghi, A. M., Parisi, D., & Baldassarre, G. (2010) · Psychological Review · doi:10.1037/a0020887 · Cited by 132 · see citing works
Self-citationThe novelty exploration bonus and its attentional modulation☆
Krebs, R. M., Schott, B. H., Schütze, H., & Düzel, E. (2009) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2009.01.015 · Cited by 127 · see citing works
The role of the medial prefrontal cortex in achieving goals
Matsumoto, K., & Tanaka, K. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.03.005 · Cited by 123 · see citing works
Saito, N., Mushiake, H., Sakamoto, K., Itoyama, Y., & Tanji, J. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhi032 · Cited by 121 · see citing works
Khamassi, M., & Humphries, M. D. (2012) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2012.00079 · Cited by 121 · see citing works
Rhodes, S. E. V., & Killcross, S. (2004) · Learning & Memory · doi:10.1101/lm.79704 · Cited by 119 · see citing works
Multiple Forms of Value Learning and the Function of Dopamine
Balleine, B. W., Daw, N. D., & O’Doherty, J. P. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374176-9.00024-5 · Cited by 112 · see citing works
Primate orbitofrontal cortex and adaptive behaviour
Roberts, A. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.12.002 · Cited by 103 · see citing works
Featherstone, R. E., & McDonald, R. J. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2003.10.038 · Cited by 103 · see citing works
The Contribution of Orbitofrontal Cortex to Action Selection
Ostlund, S. B., & Balleine, B. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.033 · Cited by 102 · see citing works
Contextual interaction between novelty and reward processing within the mesolimbic system
Bunzeck, N., Doeller, C. F., Dolan, R. J., & Düzel, E. (2011) · Human Brain Mapping · doi:10.1002/hbm.21288 · Cited by 97 · see citing works
Multiplicity of control in the basal ganglia: computational roles of striatal subregions
Bornstein, A. M., & Daw, N. D. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.02.009 · Cited by 97 · see citing works
Dopaminergic regulation of limbic-striatal interplay
Floresco, S. (2007) · Journal of Psychiatry and Neuroscience · doi:10.1139/jpn.0739 · Cited by 94 · see citing works
The role of intra-thalamic and thalamocortical circuits in action selection
Humphries, M. D., & GURNEY, K. N. (2002) · Network Computation in Neural Systems · doi:10.1080/net.13.1.131.156 · Cited by 93 · see citing works
Self-citationMesolimbic Dopamine Transients in Motivated Behaviors: Focus on Maternal Behavior
Robinson, D. L., Zitzman, D. L., & Williams, S. K. (2011) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2011.00023 · Cited by 89 · see citing works
A Temporal-Difference Model of Classical Conditioning
Sutton, R. S., & Barto, A. G. (1987) · eScholarship (California Digital Library) · Cited by 89 · see citing works
Integration of Reinforcement Learning and Optimal Decision-Making Theories of the Basal Ganglia
Bogacz, R., & Larsen, T. (2011) · Neural Computation · doi:10.1162/neco_a_00103 · Cited by 83 · see citing works
Insulin, IGF-1 and GLP-1 signaling in neurodegenerative disorders: targets for disease modification?
Bassil, F., Fernagut, P., Bézard, E., et al. (2014) · HAL (Le Centre pour la Communication Scientifique Directe) · doi:10.1016/j.pneurobio · Cited by 82 · see citing works
The extended amygdala and the dopamine system: another piece of the dopamine puzzle.
Fudge, J., & Emiliano, A. (2003) · The Journal of Neuropsychiatry and Clinical Neurosciences · doi:10.1176/jnp.15.3.306 · Cited by 79 · see citing works
Neural systems analysis of decision making during goal-directed navigation
Penner, M. R., & Mizumori, S. J. Y. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.08.010 · Cited by 72 · see citing works
Representation of Subjective Value in the Striatum
Knutson, B. D., Delgado, M. R., & Phillips, P. E. M. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374176-9.00025-7 · Cited by 68 · see citing works
Nomifensine amplifies subsecond dopamine signals in the ventral striatum of freely‐moving rats
Robinson, D. L., & Wightman, R. M. (2004) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02559.x · Cited by 67 · see citing works
The associative striatum: cortical and thalamic projections to the dorsocentral striatum in rats
Cheatwood, J. L., Reep, R. L., & Corwin, J. V. (2003) · Brain Research · doi:10.1016/s0006-8993(02)04212-9 · Cited by 66 · see citing works
Timing-dependent limbic-motor synaptic integration in the nucleus accumbens
Goto, Y., & O’Donnell, P. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.202303199 · Cited by 62 · see citing works
Lex, B., & Hauber, W. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2009.11.002 · Cited by 61 · see citing works
Otmakhova, N. A., Düzel, E., Deutch, A. Y., & Lisman, J. E. (2012) · Springer eBooks · doi:10.1007/978-3-642-32375-1_10 · Cited by 57 · see citing works
Baldassarre, G., Mannella, F., Fiore, V. G., Redgrave, P., GURNEY, K. N., & Mirolli, M. (2012) · Neural Networks · doi:10.1016/j.neunet.2012.09.015 · Cited by 52 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
The Nucleus Accumbens: An Interface Between Cognition, Emotion, and Action
Floresco, S. B. (2015) · Annual Review of Psychology · doi:10.1146/annurev-psych-010213-115159 · Cited by 938 · see citing works
Active Inference, homeostatic regulation and adaptive behavioural control
Pezzulo, G., Rigoli, F., & Friston, K. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.09.001 · Cited by 650 · see citing works
“…involved in stimulus-response learning and habitual control, the dorsomedial striatum has been linked to action-outcome learning and goal-directed action, and ventral striatum to Pavlovian values (Glascher et al., 2010; Liljeholm and O’Doherty, 2012; Mannella et al., 2013; O’Doherty et al., 2004).”
Striatal circuits for reward learning and decision-making
Cox, J., & Witten, I. B. (2019) · Nature reviews. Neuroscience · doi:10.1038/s41583-019-0189-2 · Cited by 554 · see citing works
Habitual control of goal selection in humans
Cushman, F. A., & Morris, A. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1506367112 · Cited by 165 · see citing works
Role of Striatal Cholinergic Interneurons in Set-Shifting in the Rat
Aoki, S., Liu, A. W., Zucca, A., Zucca, S., & Wickens, J. R. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0490-15.2015 · Cited by 136 · see citing works
Emotions and motivated behavior converge on an amygdala‐like structure in the zebrafish
von Trotha, J. W., Vernier, P., & Bally‐Cuif, L. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12692 · Cited by 121 · see citing works
Neurobehavioral markers of resilience to depression amongst adolescents exposed to child abuse
Dennison, M. J., Sheridan, M. A., Busso, D. S., Jenness, J. L., Peverill, M., Rosen, M. L., & McLaughlin, K. A. (2016) · Journal of Abnormal Psychology · doi:10.1037/abn0000215 · Cited by 117 · see citing works
Neurobiology of Loneliness, Isolation, and Loss: Integrating Human and Animal Perspectives
Vitale, E. M., & Smith, A. S. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.846315 · Cited by 112 · see citing works
Caligiore, D., Mannella, F., Arbib, M. A., & Baldassarre, G. (2017) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005395 · Cited by 111 · see citing works
Self-citationCaligiore, D., Arbib, M. A., Miall, R. C., & Baldassarre, G. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.02.008 · Cited by 105 · see citing works
Self-citationYoshida, K., Drew, M. R., Mimura, M., & Tanaka, K. F. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0376-5 · Cited by 96 · see citing works
Coordinated Reductions in Excitatory Input to the Nucleus Accumbens Underlie Food Consumption
Reed, S. J., Lafferty, C. K., Mendoza, J. A., Yang, A. K., Davidson, T. J., Grosenick, L., Deisseroth, K. A., & Britt, J. P. (2018) · Neuron · doi:10.1016/j.neuron.2018.07.051 · Cited by 85 · see citing works
Loss of nucleus accumbens low-frequency fluctuations is a signature of chronic pain
Makary, M. M., Polosecki, P. I., Cecchi, G., DeAraujo, I. E., Barron, D. S., Constable, R. T., Whang, P. G., Thomas, D.-A. M., Mowafi, H. O., Small, D. M., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1918682117 · Cited by 90 · see citing works
Special Issue “On Defining Artificial Intelligence”—Commentaries and Author’s Response
Monett, D., Lewis, C. W. P., Þórisson, K. R., Bach, J., Baldassarre, G., Granato, G., Berkeley, I. S. N., Chollet, F., Crosby, M., Shevlin, H., et al. (2020) · Journal of Artificial General Intelligence · doi:10.2478/jagi-2020-0003 · Cited by 98 · see citing works
Self-citationDing, S.-L., Yao, Z., Hirokawa, K. E., Nguyen, T. N., Graybuck, L. T., Fong, O., Bohn, P., Ngo, K., Smith, K. A., Koch, C., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107648 · Cited by 82 · see citing works
Nucleus Accumbens Cell Type- and Input-Specific Suppression of Unproductive Reward Seeking
Lafferty, C. K., Yang, A. K., Mendoza, J. A., & Britt, J. P. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.02.095 · Cited by 76 · see citing works
Obsessive-compulsive disorder: Insights from animal models
Szechtman, H., Ahmari, S. E., Beninger, R. J., Eilam, D., Harvey, B. H., Edemann-Callesen, H., & Winter, C. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.04.019 · Cited by 81 · see citing works
Kroemer, N. B., Guevara, A., Ciocanea Teodorescu, I., Wuttig, F., Kobiella, A., & Smolka, M. N. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.07.060 · Cited by 64 · see citing works
Floresco, S., Montes, D. R., Tse, M., & van Holstein, M. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.3191-17.2018 · Cited by 68 · see citing works
Evolutionarily conserved mechanisms for the selection and maintenance of behavioural activity
Fiore, V. G., Dolan, R., Strausfeld, N., & Hirth, F. (2015) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2015.0053 · Cited by 65 · see citing works
L-DOPA reduces model-free control of behavior by attenuating the transfer of value to action
Kroemer, N. B., Lee, Y., Pooseh, S., Eppinger, B., Goschke, T., & Smolka, M. N. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.10.075 · Cited by 64 · see citing works
Neural Correlates of Sexual Orientation in Heterosexual, Bisexual, and Homosexual Men
Safron, A., Sylva, D., Klimaj, V., Rosenthal, A. M., Li, M., Walter, M., & Bailey, J. M. (2017) · Scientific Reports · doi:10.1038/srep41314 · Cited by 57 · see citing works
Martín‐García, E., Courtin, J., Renault, P., Fiancette, J.-F., Wurtz, H., Simonnet, A., Levet, F., Herry, C., & Deroche‐Gamonet, V. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.66 · Cited by 55 · see citing works
Wagner, G., Schachtzabel, C., Peikert, G., & Bär, K. (2015) · Human Brain Mapping · doi:10.1002/hbm.22807 · Cited by 55 · see citing works
Neural Correlates of Sexual Orientation in Heterosexual, Bisexual, and Homosexual Women
Safron, A., Klimaj, V., Sylva, D., Rosenthal, A. M., Li, M., Walter, M., & Bailey, J. M. (2018) · Scientific Reports · doi:10.1038/s41598-017-18372-0 · Cited by 54 · see citing works
Safron, A. (2021) · Entropy · doi:10.3390/e23060783 · Cited by 52 · see citing works
Köhler, S., Bär, K., & Wagner, G. (2016) · Human Brain Mapping · doi:10.1002/hbm.23173 · Cited by 52 · see citing works
Cell-Type- and Endocannabinoid-Specific Synapse Connectivity in the Adult Nucleus Accumbens Core
Deroche, M. A., Lassalle, O., Castell, L., Valjent, E., & Manzoni, O. J. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1100-19.2019 · Cited by 48 · see citing works
Innate and learned aspects of pheromone-mediated social behaviours
Beny, Y., & Kimchi, T. (2014) · Animal Behaviour · doi:10.1016/j.anbehav.2014.09.014 · Cited by 49 · see citing works
Xia, X., Fan, L., Chen, C., Eickhoff, S. B., Chen, J., Li, H., & Jiang, T. (2017) · Human Brain Mapping · doi:10.1002/hbm.23636 · Cited by 48 · see citing works
Reid, L. B., Sale, M. V., Cunnington, R., Mattingley, J. B., & Rose, S. (2017) · Human Brain Mapping · doi:10.1002/hbm.23514 · Cited by 45 · see citing works
Smith, C. J. W., Mogavero, J. N., Tulimieri, M. T., & Veenema, A. H. (2017) · Hormones and Behavior · doi:10.1016/j.yhbeh.2017.05.005 · Cited by 42 · see citing works
Astrocyte Molecular Clock Function in the Nucleus Accumbens Is Important for Reward-Related Behavior
Becker‐Krail, D. D., Ketchesin, K. D., Burns, J. N., Zong, W., Hildebrand, M. A., DePoy, L. M., Vadnie, C. A., Tseng, G. C., Logan, R. W., Huang, Y. H., et al. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.02.007 · Cited by 42 · see citing works
Engelhardt, K.-A., Fuchs, E., Schwarting, R. K. W., & Wöhr, M. (2017) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2017.01.003 · Cited by 40 · see citing works
Contreras, J. A., Aslanyan, V., Sweeney, M. D., Sanders, L. M. J., Sagare, A. P., Zloković, B. V., Toga, A. W., Han, S. D., Morris, J. C., Fagan, A. M., et al. (2019) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2019.10.013 · Cited by 41 · see citing works
Penrod, R. D., Kumar, J., Smith, L. N., McCalley, D. M., Nentwig, T. B., Hughes, B. W., Barry, G. M., Glover, K., Taniguchi, M., & Cowan, C. W. (2019) · Genes Brain & Behavior · doi:10.1111/gbb.12561 · Cited by 37 · see citing works
Safron, A., & DeYoung, C. G. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819200-9.00010-7 · Cited by 34 · see citing works
Safron, A., Çatal, O., & Verbelen, T. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2022.787659 · Cited by 33 · see citing works
Le Merrer, J., Detraux, B., Gandía, J., De Groote, A., Fonteneau, M., de Kerchove d’Exaerde, A., & Becker, J. A. J. (2024) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.05.008 · Cited by 35 · see citing works
A computational model of language functions in flexible goal-directed behaviour
Granato, G., Borghi, A. M., & Baldassarre, G. (2020) · Scientific Reports · doi:10.1038/s41598-020-78252-y · Cited by 34 · see citing works
Self-citationIntegrated world modeling theory expanded: Implications for the future of consciousness
Safron, A. (2022) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2022.642397 · Cited by 43 · see citing works
Parallel and hierarchical neural mechanisms for adaptive and predictive behavioral control
Macpherson, T., Matsumoto, M., Gomi, H., Morimoto, J., Uchibe, E., & Hikida, T. (2021) · Neural Networks · doi:10.1016/j.neunet.2021.09.009 · Cited by 30 · see citing works
Neurons in the Nucleus Accumbens Promote Selection Bias for Nearer Objects
Morrison, S. E., & Nicola, S. M. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2197-14.2014 · Cited by 32 · see citing works
DNA Epigenetics in Addiction Susceptibility
Kaplan, G., Xu, H., Abreu, K., & Feng, J. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.806685 · Cited by 34 · see citing works
Astrocyte ensembles manipulated with AstroLight tune cue-motivated behavior
Serra, I., Martín-Monteagudo, C., Romero, J. S., Quintanilla, J. P., Ganchala, D., Arévalo, M., García‐Marqués, J., & Navarrete, M. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-01870-0 · Cited by 31 · see citing works
Ojha, A., Parr, A. C., Foran, W., Calabro, F. J., & Luna, B. (2022) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2022.101183 · Cited by 31 · see citing works
Goal-Directed Behavior and Instrumental Devaluation: A Neural System-Level Computational Model
Mannella, F., Mirolli, M., & Baldassarre, G. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2016.00181 · Cited by 30 · see citing works
Self-citationShiohama, T., Ortuğ, A., Warren, J. L. A., Valli, B., Levman, J. E. D., Faja, S., Tsujimura, K., Maunakea, A. K., & Takahashi, E. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab283 · Cited by 29 · see citing works
Nishioka, T., Attachaipanich, S., Hamaguchi, K., Lazarus, M., d’Exaerde, A. D. K., Macpherson, T., & Hikida, T. (2023) · Nature Communications · doi:10.1038/s41467-023-38025-3 · Cited by 29 · see citing works
A hippocampus-accumbens code guides goal-directed appetitive behavior
Barnstedt, O., Mocellin, P., & Remy, S. (2024) · Nature Communications · doi:10.1038/s41467-024-47361-x · Cited by 28 · see citing works
Threat and Bidirectional Valence Signaling in the Nucleus Accumbens Core
Ray, M. H., Moaddab, M., & McDannald, M. A. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1107-21.2021 · Cited by 28 · see citing works
Kroemer, N. B., Burrasch, C., & Hellrung, L. (2016) · Progress in brain research · doi:10.1016/bs.pbr.2016.06.009 · Cited by 29 · see citing works
Know Your Body Through Intrinsic Goals
Mannella, F., Santucci, V. G., Somogyi, E., Jacquey, L., O'Regan, J. K., & Baldassarre, G. (2018) · Frontiers in Neurorobotics · doi:10.3389/fnbot.2018.00030 · Cited by 27 · see citing works
Self-citationToward a systems-oriented approach to the role of the extended amygdala in adaptive responding
Waraczynski, M. A. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.05.015 · Cited by 26 · see citing works
Chamakalayil, S., Strasser, J., Vogel, M., Brand, S., Walter, M., & Dürsteler, K. M. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.540837 · Cited by 26 · see citing works
The computational structure of consummatory anhedonia
Hall, A., Browning, M. D., & Huys, Q. J. M. (2024) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2024.01.006 · Cited by 29 · see citing works
Reyes-Lizaola, S., Luna-Zarate, U., Tendilla‐Beltrán, H., Morales‐Medina, J. C., & Flores, G. (2023) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2023.110876 · Cited by 26 · see citing works
Caligiore, D., Mustile, M., Fineschi, A., Romano, L., Piras, F., Assogna, F., Pontieri, F. E., Spalletta, G., & Baldassarre, G. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2019.00007 · Cited by 24 · see citing works
Self-citationKim, J., Kwon, J. H., Kim, E. J., Kim, E. J., Kim, H. E., Kyeong, S.-H., & Kim, J. (2021) · Scientific Reports · doi:10.1038/s41598-021-94328-9 · Cited by 33 · see citing works
Orchard, E. R., Voigt, K., Chopra, S., Thapa, T., Ward, P. G. D., Egan, G. F., & Jamadar, S. D. (2023) · Scientific Reports · doi:10.1038/s41598-023-31696-4 · Cited by 27 · see citing works
Safron, A., Sylva, D., Klimaj, V., Rosenthal, A. M., & Bailey, J. M. (2019) · Archives of Sexual Behavior · doi:10.1007/s10508-019-01521-z · Cited by 24 · see citing works
Becker, J. A. J., Pellissier, L. P., Corde, Y., Laboute, T., Léauté, A., Gandía, J., & Merrer, J. L. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-00927-x · Cited by 22 · see citing works
Seepanomwan, K., Caligiore, D., Cangelosi, A., & Baldassarre, G. (2015) · Neural Networks · doi:10.1016/j.neunet.2015.09.010 · Cited by 23 · see citing works
Self-citationThe Hidden Life of the Basal Ganglia
Bergman, H. (2021) · The MIT Press eBooks · doi:10.7551/mitpress/14075.001.0001 · Cited by 21 · see citing works
Accumbal Cholinergic Interneurons Differentially Influence Motivation Related to Satiety Signaling
Aitta‐aho, T., Phillips, B. U., Pappa, E., Hay, Y. A., Harnischfeger, F., Heath, C. J., Saksida, L. M., Bussey, T. J., & Apergis‐Schoute, J. (2017) · eNeuro · doi:10.1523/eneuro.0328-16.2017 · Cited by 22 · see citing works
Kang, S., Hong, S., Kang, S., Song, M. R., Yang, M. A., Essa, H., Baker, M. R., Lee, J., Bruce, R. A., Lee, S. W., et al. (2023) · Science Advances · doi:10.1126/sciadv.adh9239 · Cited by 21 · see citing works
Corticolimbic catecholamines in stress: a computational model of the appraisal of controllability
Fiore, V. G., Mannella, F., Mirolli, M., Latagliata, E. C., Valzania, A., Cabib, S., Dolan, R. J., Puglisi‐Allegra, S., & Baldassarre, G. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0727-7 · Cited by 21 · see citing works
Self-citationAstrocyte-neuron interaction in the dorsal striatum-pallidal circuits and alcohol-seeking behaviors
Hong, S., Kang, S., Baker, M. R., & Choi, D. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108759 · Cited by 19 · see citing works
Medial Accumbens Shell Spiny Projection Neurons Encode Relative Reward PreferencePreprint
Pedersen, C. E., Gowrishankar, R., Piantadosi, S. C., Castro, D. C., Hjort, M. M., Zhou, Z. C., Kan, S. A., Murphy, P. J., O’Neill, P., & Bruchas, M. R. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.18.508426 · Cited by 16 · see citing works
Fiore, V. G., Nolte, T., Rigoli, F., Smittenaar, P., Gu, X., & Dolan, R. J. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.02.048 · Cited by 16 · see citing works
Newmyer, B. A., Whindleton, C. M., Klein, P., Beenhakker, M. P., Jones, M., & Scott, M. M. (2019) · JCI Insight · doi:10.1172/jci.insight.126283 · Cited by 15 · see citing works
Carlson, H. N., Murphy, C., & Pratt, W. E. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.112999 · Cited by 15 · see citing works
Autism and Inner Speech: A Computational Model of Language Functions in Autistic Flexible BehaviourPreprint
Granato, G., Borghi, A. M., Mattera, A., & Baldassarre, G. (2021) · doi:10.31234/osf.io/fk5nz · Cited by 15 · see citing works
Self-citationOff-Target Influences of Arch-Mediated Axon Terminal Inhibition on Network Activity and Behavior
Lafferty, C. K., & Britt, J. P. (2020) · Frontiers in Neural Circuits · doi:10.3389/fncir.2020.00010 · Cited by 14 · see citing works
Dream to Explore: 5-HT2a as Adaptive Temperature Parameter for Sophisticated Affective Inference
Safron, A., & Sheikhbahaee, Z. (2021) · Communications in computer and information science · doi:10.1007/978-3-030-93736-2_56 · Cited by 13 · see citing works
Suarez‐Jimenez, B., Lazarov, A., Zhu, X., Pine, D. S., Bar‐Haim, Y., & Neria, Y. (2022) · Psychological Medicine · doi:10.1017/s003329172200157x · Cited by 13 · see citing works
The Use of Physiological Signals in Brainstem/Midbrain fMRI
Schumann, A., Köhler, S., de la Cruz, F., Güllmar, D., Reichenbach, J. R., Wagner, G., & Bär, K. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00718 · Cited by 15 · see citing works
Vasquez, T. E. S., Shah, P., Re, J. D., Laezza, F., & Green, T. A. (2021) · eNeuro · doi:10.1523/eneuro.0136-21.2021 · Cited by 13 · see citing works
Puhlmann, L., Derome, M., Morosan, L., Kilicel, D., Vrtička, P., & Debbané, M. (2021) · Attachment & Human Development · doi:10.1080/14616734.2021.1993628 · Cited by 13 · see citing works
A generative spiking neural-network model of goal-directed behaviour and one-step planning
Basanisi, R., Brovelli, A., Cartoni, E., & Baldassarre, G. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007579 · Cited by 12 · see citing works
Self-citationJorge, H., Duarte, I. C., Paiva, S., Relvas, A. P., & Castelo-Branco, M. S. (2022) · Diabetes & Metabolism Journal · doi:10.4093/dmj.2021.0307 · Cited by 12 · see citing works
Safron, A. (2020) · Communications in computer and information science · doi:10.1007/978-3-030-64919-7_15 · Cited by 13 · see citing works
Baldassarre, G., Santucci, V. G., Cartoni, E., & Caligiore, D. (2017) · Behavioral and Brain Sciences · doi:10.1017/s0140525x17000036 · Cited by 11 · see citing works
Self-citationContext coding in the mouse nucleus accumbens modulates motivationally relevant information
Gmaz, J. M., & van der Meer, M. A. A. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001338 · Cited by 10 · see citing works
Neuroaesthetics: Maladies and Remedies
Kubovy, M. (2019) · Art & Perception · doi:10.1163/22134913-20191138 · Cited by 11 · see citing works
Hatzipantelis, C. J., Langiu, M., Vandekolk, T. H., Pierce, T. L., Nithianantharajah, J., Stewart, G. D., & Langmead, C. J. (2020) · ACS Pharmacology & Translational Science · doi:10.1021/acsptsci.0c00117 · Cited by 12 · see citing works
A global framework for a systemic view of brain modeling
Alexandre, F. (2021) · Brain Informatics · doi:10.1186/s40708-021-00126-4 · Cited by 11 · see citing works
Neudorf, J., Shen, K., & McIntosh, A. R. (2024) · Network Neuroscience · doi:10.1162/netn_a_00377 · Cited by 10 · see citing works
From avoidance to new action: the multifaceted role of the striatal indirect pathway
Lee, J., & Sabatini, B. L. (2025) · Nature reviews. Neuroscience · doi:10.1038/s41583-025-00925-2 · Cited by 10 · see citing works
Parkin regulates drug-taking behavior in rat model of methamphetamine use disorder
SHARMA, A. K., Harutyunyan, A., Schneider, B. L., & Moszczyńska, A. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01387-7 · Cited by 10 · see citing works
Neural activation to loss and reward among alcohol naive adolescents who later initiate alcohol use
Gonçalves, S. F., Turpyn, C. C., Niehaus, C. E., Mauro, K. L., Hinagpis, C. L., Thompson, J. C., & Chaplin, T. M. (2021) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2021.100978 · Cited by 10 · see citing works
Finnell, J. E., & Ferrario, C. R. (2022) · Physiology & Behavior · doi:10.1016/j.physbeh.2022.113892 · Cited by 11 · see citing works
Granato, G., & Baldassarre, G. (2021) · Neural Networks · doi:10.1016/j.neunet.2021.07.013 · Cited by 10 · see citing works
Self-citationGildawie, K. R., Wang, K. L., Budge, K. E., & Byrnes, E. M. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.11.030 · Cited by 8 · see citing works
Simón, M. J., Higuera‐Matas, A., Roura‐Martínez, D., Ucha, M., Santos‐Toscano, R., Garcı́a-Lecumberri, C., Ambrosio, E., & Puerto, A. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.11.007 · Cited by 9 · see citing works
Face-to-trait inferences in patients with Parkinson’s disease
Hirai, M., Sakurada, T., & Muramatsu, S. (2018) · Journal of Clinical and Experimental Neuropsychology · doi:10.1080/13803395.2018.1513452 · Cited by 9 · see citing works
Accumbal Adenosine A2A Receptors Enhance Cognitive Flexibility by Facilitating Strategy Shifting
Zhou, J., Wu, B., Lin, X., Dai, Y., Li, T., Zheng, W., Guo, W. M., Vakal, S., Chen, X., & Chen, J. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00130 · Cited by 9 · see citing works
Antenna movements as a function of odorants’ biological value in honeybees (Apis mellifera L.)
Cholé, H., Merlin, A., Henderson, N., Paupy, E., Mahé, P., Arnold, G., & Sandoz, J. (2022) · Scientific Reports · doi:10.1038/s41598-022-14354-z · Cited by 9 · see citing works
Wolmarans, D. W., Stein, D. J., & Harvey, B. H. (2017) · Current Medicinal Chemistry · doi:10.2174/0929867324666170523125256 · Cited by 9 · see citing works
Silkstone, M., & Brudzyński, S. M. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.01.044 · Cited by 11 · see citing works
- Authors
- Mannella, F., Gurney, K., & Baldassarre, G.
- Affiliations
- National Research Council (IT)
- University of Sheffield (GB)
- Corresponding author
- Mannella, Francesco
- Venue
- Frontiers in Behavioral Neuroscience
- Publisher
- Frontiers Media SA
- Published
- 2013
- Volume
- 7
- Pages
- 135-135
- ISSN
- 1662-5153 (ISSN-L)
- PMC
- PMC3805952
- OpenAlex
- W2165106227
- Cited by
- 166
- References
- 217
- Citations by year
- 2026: 8 · 2025: 13 · 2024: 10 · 2023: 14 · 2022: 18 · 2021: 23 · 2020: 16 · 2019: 18 · 2018: 10 · 2017: 11 · 2016: 10 · 2015: 8 · 2014: 7
- FWCI
- 4.09
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Frontiers in Behavioral Neuroscience (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- White Rose Research Online (University of Leeds, The University of Sheffield, University of York) (acceptedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- European Commission (231722)
- Engineering and Physical Sciences Research Council (EP/I009310/1)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- nucleus accumbens, goal-directed behavior, motivational value, value-based decision making, goal selection, dopamine, amygdala, hippocampus, prefrontal cortex, basal ganglia, value integration
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