Functional Connectivity of the Striatum Links Motivation to Action Control in Humans
Open accessAbstract
Motivation improves the efficiency of intentional behavior, but how this performance modulation is instantiated in the human brain remains unclear. We used a reward-cued antisaccade paradigm to investigate how motivational goals (the expectation of a reward for good performance) modulate patterns of neural activation and functional connectivity to improve preparation for antisaccade performance. Behaviorally, subjects performed better (faster and more accurate antisaccades) when they knew they would be rewarded for good performance. Reward anticipation was associated with increased activation in the ventral and dorsal striatum, and cortical oculomotor regions. Functional connectivity between the caudate nucleus and cortical oculomotor control structures predicted individual differences in the behavioral benefit of reward anticipation. We conclude that although both dorsal and ventral striatal circuitry are involved in the anticipation of reward, only the dorsal striatum and its connected cortical network is involved in the direct modulation of oculomotor behavior by motivational incentive.
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?
Networks associated with attention and dopamine release were largely segregated during control trials but less segregated during reward trials.
“they showed that while those networks were largely segregated during control trials (i.e., they exhibited high within-network connectivity), there was less segregation (i.e., higher between-network connectivity) during reward trials (Harsay et al., 2011; Kinnison, Padmala, Choi, & Pessoa, 2012).”
From Selection history: How reward modulates selectivity of visual attention. (2018) · cites this paper as Harsay et al., 2011
The ‘Functional connectivity between striatal and cortical regions’ section (page not provided) reports higher connectivity between the caudate and oculomotor-control regions during reward anticipation than during no-reward anticipation. It does not report high within-network connectivity or establish that attention and dopamine-release networks were largely segregated during control trials; dopamine release was not measured. (LLM, conf=0.84)
Experimental — accuracy not yet measured
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
1 retracted
Savine, A. C., & Braver, T. S. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2052-10.2010 · Cited by 117 · see citing works
RetractedAdvances in functional and structural MR image analysis and implementation as FSL
Smith, S. M., Jenkinson, M., Woolrich, M. W., Beckmann, C. F., Behrens, T. E. J., Johansen-Berg, H., Bannister, P. R., De Luca, M., Drobnjak, I., Flitney, D. E., et al. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.07.051 · Cited by 13,630 · see citing works
Functional architecture of basal ganglia circuits: neural substrates of parallel processing
Alexander, G. E., & Crutcher, M. D. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90107-l · Cited by 4,131 · see citing works
The reward circuit: linking primate anatomy and human imaging
Haber, S. N., & Knutson, B. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.129 · Cited by 3,718 · see citing works
Psychophysiological and Modulatory Interactions in Neuroimaging
Friston, K. J., Buechel, C., Fink, G. R., Morris, J., Rolls, E., & Dolan, R. J. (1997) · NeuroImage · doi:10.1006/nimg.1997.0291 · Cited by 3,097 · see citing works
Bayesian analysis of neuroimaging data in FSL
Woolrich, M., Jbabdi, S., Patenaude, B., Chappell, M., Makni, S., Behrens, T. E. J., Beckmann, C., Jenkinson, M., & Smith, S. M. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.10.055 · Cited by 2,774 · see citing works
Alexander, G. E., Crutcher, M. D., & DeLong, M. R. (1990) · PubMed · Cited by 2,422 · see citing works
Persistent activity in the prefrontal cortex during working memory
Curtis, C. E., & D'Esposito, M. (2003) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(03)00197-9 · Cited by 2,001 · see citing works
Balleine, B. W., & O'Doherty, J. P. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.131 · Cited by 1,775 · see citing works
A Probabilistic Atlas of the Human Brain: Theory and Rationale for Its Development
Mazziotta, J. C., Toga, A. W., Evans, A., Fox, P. T., & Lancaster, J. L. (1995) · NeuroImage · doi:10.1006/nimg.1995.1012 · Cited by 1,578 · see citing works
Look away: the anti-saccade task and the voluntary control of eye movement
Munoz, D. P., & Everling, S. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1345 · Cited by 1,423 · see citing works
Dissociation of reward anticipation and outcome with event-related fMRI
Knutson, B., Fong, G. W., Adams, C. M., Varner, J. L., & Hommer, D. (2001) · Neuroreport · doi:10.1097/00001756-200112040-00016 · Cited by 1,300 · 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
Primary and secondary saccades to goals defined by instructions
Hallett, P. E. (1978) · Vision Research · doi:10.1016/0042-6989(78)90218-3 · Cited by 1,262 · see citing works
Encoding Predictive Reward Value in Human Amygdala and Orbitofrontal Cortex
Gottfried, J. A., O'Doherty, J., & Dolan, R. J. (2003) · Science · doi:10.1126/science.1087919 · Cited by 1,165 · see citing works
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
Assignment of functional activations to probabilistic cytoarchitectonic areas revisited
Eickhoff, S., Paus, T., Caspers, S., Grosbras, M.-H., Evans, A. C., Zilles, K., & Amunts, K. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.03.060 · Cited by 1,038 · see citing works
The cognitive functions of the caudate nucleus
Grahn, J. A., Parkinson, J. A., & Owen, A. M. (2008) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2008.09.004 · Cited by 942 · see citing works
Reward, Motivation, and Reinforcement Learning
Dayan, P., & Balleine, B. W. (2002) · Neuron · doi:10.1016/s0896-6273(02)00963-7 · Cited by 855 · see citing works
Neuroimaging of cognitive functions in human parietal cortex
Culham, J. C., & Kanwisher, N. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00191-4 · Cited by 825 · see citing works
Location and function of the human frontal eye-field: A selective review
Paus, T. (1996) · Neuropsychologia · doi:10.1016/0028-3932(95)00134-4 · Cited by 746 · see citing works
Neuronal activity in monkey ventral striatum related to the expectation of reward
Schultz, W., Apicella, P., Scarnati, E., & Ljungberg, T. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-12-04595.1992 · Cited by 744 · see citing works
Functional magnetic resonance imaging of reward prediction
Knutson, B., & Cooper, J. C. (2005) · Current Opinion in Neurology · doi:10.1097/01.wco.0000173463.24758.f6 · Cited by 736 · see citing works
Expectation of reward modulates cognitive signals in the basal ganglia
Kawagoe, R., Takikawa, Y., & Hikosaka, O. (1998) · Nature Neuroscience · doi:10.1038/1625 · Cited by 632 · see citing works
Neuronal activity in monkey superior colliculus related to the initiation of saccadic eye movements
Dorris, M. C., Paré, M., & Munoz, D. P. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-21-08566.1997 · Cited by 593 · see citing works
Postuma, R. B., & Dagher, A. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhj088 · Cited by 579 · see citing works
Modulation of Caudate Activity by Action Contingency
Tricomi, E. M., Delgado, M. R., & Fiez, J. A. (2004) · Neuron · doi:10.1016/s0896-6273(03)00848-1 · Cited by 575 · see citing works
Diffusion tensor fiber tracking shows distinct corticostriatal circuits in humans
Lehéricy, S., Ducros, M., Van De Moortele, P., Francois, C., Thivard, L., Poupon, C., Swindale, N., Ugurbil, K., & Kim, D. (2004) · Annals of Neurology · doi:10.1002/ana.20030 · Cited by 542 · see citing works
Dorris, M. C., & Glimcher, P. W. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.009 · Cited by 428 · see citing works
A neural correlate of response bias in monkey caudate nucleus
Lauwereyns, J., Watanabe, K., Coe, B. C., & Hikosaka, O. (2002) · Nature · doi:10.1038/nature00892 · Cited by 415 · see citing works
Basal ganglia orient eyes to reward
Hikosaka, O., Nakamura, K., & Nakahara, H. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00458.2005 · Cited by 377 · see citing works
Human fMRI evidence for the neural correlates of preparatory set
Connolly, J. D., Goodale, M. A., Menon, R. S., & Munoz, D. P. (2002) · Nature Neuroscience · doi:10.1038/nn969 · Cited by 336 · see citing works
Modulation of saccadic eye movements by predicted reward outcome
Takikawa, Y., Kawagoe, R., Itoh, H., Nakahara, H., & Hikosaka, O. (2002) · Experimental Brain Research · doi:10.1007/s00221-001-0928-1 · Cited by 287 · see citing works
Executive control of countermanding saccades by the supplementary eye field
Stuphorn, V., & Schall, J. D. (2006) · Nature Neuroscience · doi:10.1038/nn1714 · Cited by 222 · see citing works
Functional Anatomy of a Prelearned Sequence of Horizontal Saccades in Humans
Petit, L., Orssaud, C., Tzourio‐Mazoyer, N., Crivello, F., Berthoz, A., & Mazoyer, B. M. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-11-03714.1996 · Cited by 214 · see citing works
On your mark, get set: Brainstem circuitry underlying saccadic initiation
Munoz, D. P., Dorris, M. C., Paré, M., & Everling, S. (2000) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-78-11-934 · Cited by 211 · see citing works
Comparison of subcortical connections of inferior temporal and posterior parietal cortex in monkeys
Baizer, J. S., Desimone, R., & Ungerleider, L. G. (1993) · Visual Neuroscience · doi:10.1017/s0952523800003229 · Cited by 209 · see citing works
Cavada, C., & Goldman-Rakic, P. S. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90037-o · Cited by 201 · see citing works
Functional connectivity with anterior cingulate and orbitofrontal cortices during decision-making
Cohen, M. X., Heller, A. S., & Charan Ranganath, A. (2005) · Cognitive Brain Research · doi:10.1016/j.cogbrainres.2005.01.010 · Cited by 198 · see citing works
Self-citationRorie, A. E., Gao, J., McClelland, J. L., & Newsome, W. T. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009308 · Cited by 195 · see citing works
Schott, B. H., Niehaus, L., Wittmann, B. C., Schütze, H., Seidenbecher, C. I., Heinze, H. –., & Düzel, E. (2007) · Brain · doi:10.1093/brain/awm147 · Cited by 193 · see citing works
Role of Primate Substantia Nigra Pars Reticulata in Reward-Oriented Saccadic Eye Movement
Sato, M., & Hikosaka, O. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-06-02363.2002 · Cited by 191 · see citing works
Signal-, Set- and Movement-related Activity in the Human Brain: An Event-related fMRI Study
Toni, I. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.1.35 · Cited by 188 · see citing works
Cortico-cortical networks and cortico-subcortical loops for the higher control of eye movements
Lynch, J. C., & Tian, J. (2005) · Progress in brain research · doi:10.1016/s0079-6123(05)51015-x · Cited by 182 · see citing works
Role of Dopamine in the Primate Caudate Nucleus in Reward Modulation of Saccades
Nakamura, K., & Hikosaka, O. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4853-05.2006 · Cited by 179 · see citing works
Valyear, K. F., Culham, J. C., Sharif, N., Westwood, D. A., & Goodale, M. A. (2005) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2005.05.004 · Cited by 177 · see citing works
Kawagoe, R., Takikawa, Y., & Hikosaka, O. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00721.2003 · Cited by 158 · see citing works
Aarts, E., Roelofs, A., Franke, B., Rijpkema, M., Fernández, G., Helmich, R. C., & Cools, R. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.68 · Cited by 157 · cited 1× · see citing works
“Researchers have recently linked the left dorsolateral prefrontal cortex (Savine and Braver) and genetic polymorphisms of a dopamine transporter gene known to affect caudate dopamine (Aarts et al., 2010) to reward-related improvements in task switching.”
BackgroundCortical control of ocular saccades in humans: a model for motricity
Pierrot‐Deseilligny, C., Müri, R. M., Ploner, C. J., Gaymard, B. M., & Rivaud-Péchoux, S. (2003) · Progress in brain research · doi:10.1016/s0079-6123(03)42003-7 · Cited by 148 · see citing works
Shaping of Motor Responses by Incentive Values through the Basal Ganglia
Pasquereau, B., Nadjar, A., Arkadir, D., Bézard, E., Goillandeau, M., Bioulac, B. H., Gross, C. E., & Boraud, T. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3745-06.2007 · Cited by 146 · see citing works
fMRI Activation in the Human Frontal Eye Field Is Correlated With Saccadic Reaction Time
Connolly, J. D., Goodale, M. A., Goltz, H. C., & Munoz, D. P. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00830.2004 · Cited by 139 · see citing works
The Influence of Expected Value on Saccadic Preparation
Milstein, D. M., & Dorris, M. C. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0577-07.2007 · Cited by 138 · see citing works
On your mark, get set: Brainstem circuitry underlying saccadic initiation
Munoz, D. P., Dorris, M. C., Paré, M., et al. (2000) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y00-062 · Cited by 138 · see citing works
Reward-Dependent Spatial Selectivity of Anticipatory Activity in Monkey Caudate Neurons
Takikawa, Y., Kawagoe, R., & Hikosaka, O. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00288.2001 · Cited by 124 · see citing works
Saccade Preparation Signals in the Human Frontal and Parietal Cortices
Curtis, C. E., & Connolly, J. D. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00899.2007 · Cited by 117 · see citing works
Cohen, M. X., Elger, C. E., & Weber, B. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.10.004 · Cited by 106 · see citing works
Self-citationLeichnetz, G. R., Spencer, R. F., & Smith, D. J. B. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902280306 · Cited by 104 · see citing works
Multiple Movement Representations in the Human Brain: An Event-Related fMRI Study
Toni, I., Shah, N. J., Fink, G. R., Thoenissen, D., Passingham, R. E., & Zilles, K. (2002) · Journal of Cognitive Neuroscience · doi:10.1162/08989290260138663 · Cited by 100 · see citing works
On the Programming and Reprogramming of Actions
Mars, R. B., Piekema, C., COLES, M. G. H., Hulstijn, W., & Toni, I. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm022 · Cited by 97 · see citing works
Self-citationInstructed Delay Activity in the Human Prefrontal Cortex is Modulated by Monetary Reward Expectation
Ramnani, N. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.3.318 · Cited by 91 · see citing works
Law, I. G., Svarer, C., Holm, S., & Paulson, O. B. (1997) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.1997.00207.x · Cited by 69 · see citing works
Pursuit Subregion of the Frontal Eye Field Projects to the Caudate Nucleus in Monkeys
Cui, D.-M., Yan, Y.-J., & Lynch, J. C. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00501.2002 · Cited by 68 · see citing works
Meaningful design and contrast estimability in FMRI
Smith, S. M., Jenkinson, M., Beckmann, C. F., Miller, K. L., & Woolrich, M. W. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.09.019 · Cited by 67 · see citing works
Watanabe, K., & Hikosaka, O. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00012.2005 · Cited by 56 · see citing works
The time of secondary saccades to primary targets
Fischer, B., Weber, H., & Biscaldi, M. (1993) · Experimental Brain Research · doi:10.1007/bf00228706 · Cited by 53 · see citing works
Motor Preparatory Activity in Posterior Parietal Cortex is Modulated by Subjective Absolute Value
Iyer, A., Lindner, A., Kagan, I., & Andersen, R. A. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000444 · Cited by 32 · see citing works
Delay-related cerebral activity and motor preparation
Mars, R. B., COLES, M. G. H., Hulstijn, W., & Toni, I. (2007) · Cortex · doi:10.1016/j.cortex.2007.07.002 · Cited by 32 · see citing works
Self-citationXiong (1999) · doi:10.1002/(sici)1097-0193(1999)8:2/3
Flagged first, then by citations
Cited by
Sorted by citations
Wiers, R. W., Gladwin, T. E., Hofmann, W., Salemink, E., & Ridderinkhof, K. R. (2013) · Clinical Psychological Science · doi:10.1177/2167702612466547 · Cited by 486 · see citing works
Self-citationPerformance Validity and Symptom Validity in Neuropsychological Assessment
Larrabee, G. J. (2012) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617712000240 · Cited by 428 · see citing works
Selection history: How reward modulates selectivity of visual attention.
Failing, M., & Theeuwes, J. (2018) · Psychonomic Bulletin & Review · doi:10.3758/s13423-017-1380-y · Cited by 345 · see citing works
“…they showed that while those networks were largely segregated during control trials (i.e., they exhibited high within-network connectivity), there was less segregation (i.e., higher between-network connectivity) during reward trials (Harsay et al., 2011; Kinnison, Padmala, Choi, & Pessoa, 2012).”
BackgroundSummerfield, C., & Tsetsos, K. (2012) · Frontiers in Neuroscience · doi:10.3389/fnins.2012.00070 · Cited by 167 · see citing works
Network Analysis Reveals Increased Integration during Emotional and Motivational Processing
Kinnison, J., Padmala, S., Choi, J.-M., & Pessoa, L. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0821-12.2012 · Cited by 153 · see citing works
van Heeringen, K., Bijttebier, S., Desmyter, S., Vervaet, M., & Baeken, C. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00824 · Cited by 141 · see citing works
Jamadar, S. D., Fielding, J., & Egan, G. F. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00749 · Cited by 127 · see citing works
A face a mother could love: Depression-related maternal neural responses to infant emotion faces
Laurent, H. K., & Ablow, J. C. (2013) · Social Neuroscience · doi:10.1080/17470919.2012.762039 · Cited by 124 · see citing works
Hagger, M. S., & Chatzisarantis, N. L. D. (2012) · Personality and Social Psychology Bulletin · doi:10.1177/0146167212459912 · Cited by 115 · see citing works
The visual corticostriatal loop through the tail of the caudate: circuitry and function
Seger, C. A. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00104 · Cited by 95 · see citing works
The Potential Role of the Striatum in Antisocial Behavior and Psychopathy
Glenn, A. L., & Yang, Y. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.04.027 · Cited by 94 · see citing works
Précis on <i>The Cognitive-Emotional Brain</i>
Pessoa, L. (2015) · Behavioral and Brain Sciences · doi:10.1017/s0140525x14000120 · Cited by 84 · see citing works
Multiple influences of reward on perception and attention
Pessoa, L. (2014) · Visual Cognition · doi:10.1080/13506285.2014.974729 · Cited by 77 · see citing works
Richey, J. A., Brewer, J. A., Sullivan-Toole, H., Strege, M. V., Kim-Spoon, J., White, S. W., & Ollendick, T. H. (2019) · Clinical Psychology Review · doi:10.1016/j.cpr.2019.101756 · Cited by 79 · see citing works
Specific maternal brain responses to their own child’s face: An fMRI meta-analysis
Rigo, P., Kim, P., Esposito, G., Putnick, D. L., Venuti, P., & Bornstein, M. H. (2018) · Developmental Review · doi:10.1016/j.dr.2018.12.001 · Cited by 73 · see citing works
Motivational Tuning of Fronto-Subthalamic Connectivity Facilitates Control of Action Impulses
Herz, D. M., Christensen, M. S., Brüggemann, N., Hulme, O. J., Ridderinkhof, K. R., Madsen, K. H., & Siebner, H. R. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4081-13.2014 · Cited by 76 · see citing works
Self-citationReward, motivation and brain imaging in human healthy participants – A narrative review
Weinstein, A. M. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2023.1123733 · Cited by 83 · see citing works
Taking subjectivity seriously: towards a unification of phenomenology, psychiatry, and neuroscience
Kyzar, E. J., & Denfield, G. H. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01891-2 · Cited by 71 · see citing works
Cortico-subcortical activation patterns for itch and pain imagery
Mochizuki, H., Baumgärtner, U., Kamping, S., Ruttorf, M., Schad, L. R., Flor, H., Kakigi, R., & Treede, R. (2013) · Pain · doi:10.1016/j.pain.2013.06.007 · Cited by 60 · see citing works
Top-Down Response Suppression Mitigates Action Tendencies Triggered by a Motivating Stimulus
Freeman, S. M., Razhas, I., & Aron, A. R. (2014) · Current Biology · doi:10.1016/j.cub.2013.12.019 · Cited by 58 · see citing works
Neurocognitive mechanisms of perception–action coordination: A review and theoretical integration
Ridderinkhof, K. R. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.05.008 · Cited by 53 · see citing works
Self-citationInteractions between reward and threat during visual processing
Hu, K., Padmala, S., & Pessoa, L. (2013) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2013.05.025 · Cited by 41 · see citing works
Dissociable Effects of Motivation and Expectancy on Conflict Processing: An fMRI Study
Soutschek, A., Stelzel, C., Paschke, L. M., Walter, H., & Schubert, T. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00712 · Cited by 42 · see citing works
van Holst, R. J., Chase, H. W., & Clark, L. (2014) · NeuroImage Clinical · doi:10.1016/j.nicl.2014.06.008 · Cited by 42 · see citing works
Hedonic Hotspots Regulate Cingulate-driven Adaptation to Cognitive Demands
van Steenbergen, H., Band, G. P. H., Hommel, B., Rombouts, S. A. R. B., & Nieuwenhuis, S. (2014) · Cerebral Cortex · doi:10.1093/cercor/bht416 · Cited by 41 · see citing works
Potential reward reduces the adverse impact of negative distractor stimuli
Padmala, S., Sirbu, M., & Pessoa, L. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsx067 · Cited by 37 · see citing works
Brain Processing of Contagious Itch in Patients with Atopic Dermatitis
Schut, C., Mochizuki, H., Grossman, S. K., Lin, A. C., Conklin, C. J., Mohamed, F. B., Gieler, U., Kupfer, J., & Yosipovitch, G. (2017) · Frontiers in Psychology · doi:10.3389/fpsyg.2017.01267 · Cited by 36 · see citing works
Aue, T., Hoeppli, M., Piguet, C., Virginie Sterpenich, A., & Vuilleumier, P. O. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00194 · Cited by 35 · see citing works
van Holst, R. J., van der Meer, J. N., McLaren, D. G., van den Brink, W., Veltman, D. J., & Goudriaan, A. E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049923 · Cited by 33 · see citing works
Platform, I., Murphy, A., Nestor, L. J., McGonigle, J., Paterson, L. M., Boyapati, V., Ersche, K. D., Flechais, R., Kuchibatla, S., Metastasio, A., et al. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2016.289 · Cited by 33 · see citing works
Platform, I., Murphy, A., Nestor, L. J., McGonigle, J., Paterson, L. M., Boyapati, V., Ersche, K. D., Flechais, R., Kuchibatla, S., Metastasio, A., et al. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.99 · Cited by 33 · 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
Harsay, H. A., Cohen, M. X., Spaan, M., Weeda, W. D., Nieuwenhuis, S., & Ridderinkhof, K. R. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.10.030 · Cited by 28 · see citing works
Self-citationGreer, S. M., Goldstein‐Piekarski, A. N., Knutson, B. D., & Walker, M. P. (2016) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00939 · Cited by 27 · see citing works
Neural correlates of reward-directed action and inhibition of action
Le, T. M., Zhang, S., Zhornitsky, S., Wang, W., & Li, C.-S. R. (2019) · Cortex · doi:10.1016/j.cortex.2019.10.007 · Cited by 22 · see citing works
Li, C., Chen, J., & Tsai, C. (2015) · Brain Research · doi:10.1016/j.brainres.2015.10.024 · Cited by 21 · see citing works
Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa
PGC-ED, Walton, E., ENIGMA Genetics Working Group, Hibar, D. P., Yılmaz, Z., Jahanshad, N., Cheung, J. T. P., Batury, V.-L., Seitz, J., Bulik, C. M., et al. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1439-4 · Cited by 19 · see citing works
Cognitive-motivational interactions: Beyond boxes-and-arrows models of the mind-brain.
Pessoa, L. (2017) · Motivation Science · doi:10.1037/mot0000074 · Cited by 18 · see citing works
Brain Processing of Itch and Scratching
Mochizuki, H. (2014) · CRC Press eBooks · doi:10.1201/b16573-27 · Cited by 17 · see citing works
Harnessing Motivation to Alleviate Neglect
Russell, C., Li, K., & Malhotra, P. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00230 · Cited by 17 · see citing works
Otsuka, T., Tanemura, R., Noda, K., Nagao, T., Sakai, H., & Luo, Z.-W. (2015) · Current Alzheimer Research · doi:10.2174/1567205012666150530202335 · Cited by 16 · see citing works
Chung, T. A., Paulsen, D. J., Geier, C. F., Luna, B., & Clark, D. B. (2015) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2015.05.004 · Cited by 15 · see citing works
More than Meets the Eye: Age Differences in the Capture and Suppression of Oculomotor Action
Ridderinkhof, K. R., & Wijnen, J. G. (2011) · Frontiers in Psychology · doi:10.3389/fpsyg.2011.00267 · Cited by 14 · see citing works
Self-citationOvergaauw, S., Jansen, M., Korbee, N. J., & de Bruijn, E. R. A. (2019) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2019.00160 · Cited by 14 · see citing works
How Cognition and Motivation “Freeze” the Motor Behavior in Parkinson’s Disease
Ortelli, P., Ferrazzoli, D., Cian, V., Zarucchi, M., Palamara, G., Giobbia, A., Frazzitta, G., Maestri, R., & Canesi, M. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01302 · Cited by 13 · see citing works
Effects of social and emotional context on neural activation and synchrony during movie viewing
Dziura, S. L., Merchant, J. S., Alkire, D. R., Rashid, A., Shariq, D. A., Moraczewski, D., & Redcay, E. (2021) · Human Brain Mapping · doi:10.1002/hbm.25669 · Cited by 13 · see citing works
Reward sensitivity predicts dopaminergic response in spatial neglect
Li, K., Bentley, P., Nair, A., Halse, O., Barker, G. J., Russell, C., Soto, D., & Malhotra, P. (2018) · Cortex · doi:10.1016/j.cortex.2018.09.002 · Cited by 11 · see citing works
Miller, H. C., Pattison, K. F., Laude, J. R., & Zentall, T. R. (2014) · Behavioural Processes · doi:10.1016/j.beproc.2014.09.030 · Cited by 11 · see citing works
Carbohydrate ingestion but not mouth rinse maintains sustained attention when fasted
Kumar, N., Wheaton, L. A., Snow, T. K., & Millard-Stafford, M. (2015) · Physiology & Behavior · doi:10.1016/j.physbeh.2015.10.023 · Cited by 11 · see citing works
Striatal and Pallidal Activation during Reward Modulated Movement Using a Translational Paradigm
Bischoff‐Grethe, A., Buxton, R. B., Paulus, M. P., Fleisher, A., Yang, T. T., & Brown, G. G. (2015) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617715000491 · Cited by 10 · see citing works
Papazacharias, A., Taurisano, P., Fazio, L., Gelao, B., Giorgio, A. D., Bianco, L. L., Quarto, T., Mancini, M., Porcelli, A., Romano, R., et al. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00097 · Cited by 10 · see citing works
Harsay, H. A., Cohen, M. X., Reneman, L., & Ridderinkhof, K. R. (2011) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2011.06.005 · Cited by 10 · see citing works
Self-citationDopamine-mediated striatal activity and function is enhanced in GlyRα2 knockout animals
Devoght, J., Comhair, J., Morelli, G., Rigo, J., D’Hooge, R., Touma, C., Palme, R., Dewachter, I., vandeVen, M., Harvey, R. J., et al. (2023) · iScience · doi:10.1016/j.isci.2023.107400 · Cited by 9 · see citing works
Lee, H.-J., Lin, F., & Kuo, W. (2017) · Scientific Reports · doi:10.1038/s41598-017-10539-z · Cited by 8 · see citing works
Prolonged fasting impairs neural reactivity to visual stimulation
Kohn, N., Wassenberg, A., Toygar, T., Kellermann, T., Weidenfeld, C., Berthold‐Losleben, M., Chechko, N., Orfanos, S., Vocke, S., Laoutidis, Z. G., et al. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0898-2 · Cited by 8 · see citing works
Neural profiles of observing acceptance and rejection decisions in human mate choice copying
Zhuang, J.-Y., Xie, J., Li, P., Fan, M., & Bode, S. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.117929 · Cited by 7 · see citing works
The cognitive effects of a promised bonus do not depend on dopamine synthesis capacity
Hofmans, L., van den Bosch, R., Määttä, J. I., Verkes, R., Aarts, E., & Cools, R. (2020) · Scientific Reports · doi:10.1038/s41598-020-72329-4 · Cited by 6 · see citing works
Bigler, E. D. (2012) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617712000409 · Cited by 5 · see citing works
Medullary and C3–C4 propriospinal pathways underlying mammalian forelimb movement control
Jindal, V., Grudny, M. M., Wesson, D. W., Vaillancourt, D. E., & Vahdat, S. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2518217123 · Cited by 4 · see citing works
Functional vs anatomical cortico-striatal connectivity in the macaque brain
Tang, W., Monko, M. E., Liu, Z. S.-J., Manea, A. M. G., Aguilar-Ortega, F., Hart, D. W., Zhou, J., Zimmermann, J., & Heilbronner, S. R. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03757-x · Cited by 2 · see citing works
Wyngaarden, J. Β., Nambiar, A., Dennison, J. B., Alloy, L. B., Fareri, D. S., Jarcho, J. M., & Smith, D. V. (2026) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-025-01396-9 · Cited by 2 · see citing works
Cai, W., & Mizuno, Y. (2026) · Translational Psychiatry · doi:10.1038/s41398-026-03972-0 · Cited by 3 · see citing works
Attentional Orienting by Non-informative Cue Is Shaped via Reinforcement Learning
Cho, S. A., & Cho, Y. S. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.02884 · Cited by 2 · see citing works
Chen, Y., & Huang, S. (2024) · Psychophysiology · doi:10.1111/psyp.14501 · Cited by 2 · see citing works
Song, Y., Cawthon, P. M., Zhai, X., Huppert, T. J., Rosso, A. L., Butters, M. A., Chahine, L. M., Lopresti, B. J., Royse, S. K., & Rosano, C. (2026) · American Journal of Geriatric Psychiatry · doi:10.1016/j.jagp.2026.03.210 · Cited by 1 · see citing works
Schlund, M. W., Magee, S. K., & Hudgins, C. D. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.06.018 · Cited by 1 · see citing works
The impacts of sleep and sleep deprivation on human brain and behavioral incentive processing
Greer, S. M. (2014) · eScholarship (California Digital Library)
The development of affective and cognitive striatal neurobiology and connectivity during adolescence
Larsen, B. (2018) · D-Scholarship@Pitt (University of Pittsburgh)
The cognitive effects of a promised bonus do not depend on dopamine synthesis capacityPreprint
Hofmans, L., van den Bosch, R., Määttä, J. I., Verkes, R., Aarts, E., & Cools, R. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.26.264168
Garcia, K. M. (2021) · VTechWorks (Virginia Tech)
Lack of the glycine receptor alpha 2 increases striatal activity and motivated behaviorPreprint
Devoght, J., Comhair, J., Morelli, G., Rigo, J., D’Hooge, R., Touma, C., Palme, R., Dewachter, I., vandeVen, M., Harvey, R. J., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.08.31.506020
The Chemistry of Romantic Love
(2016) · Royal Society of Chemistry eBooks · doi:10.1039/bk9781782621348-00169
Neural and cognitive underpinnings of ball/strike judgments of baseball umpires: An fMRI studyPreprint
Chen, Y., & Huang, S.-K. (2023) · doi:10.22541/au.167907244.45522204/v1
Corbett, J. D., Silvers, J. A., & Wu, R. (2026) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2026.106754
Yang, C., Zhao, H., Huang, J., Xiong, Z., Wei, Z., Feng, T., & Feng, P. (2026) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2026.113463
- Authors
- Harsay, H. A., Cohen, M. X., Oosterhof, N. N., Forstmann, B. U., Mars, R. B., & Ridderinkhof, K. R.
- Affiliations
- University of Amsterdam (NL)
- University of Arizona (US)
- Bangor University (GB)
- Spinoza Centre for Neuroimaging (NL)
- University of Oxford (GB)
- Corresponding author
- Ridderinkhof, K. R.
- Venue
- Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2011-07-20
- Volume
- 31
- Issue
- 29
- Pages
- 10701-10711
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6622616
- OpenAlex
- W2107219405
- Cited by
- 75
- References
- 68
- Citations by year
- 2026: 6 · 2025: 1 · 2024: 1 · 2023: 3 · 2022: 3 · 2021: 3 · 2020: 3 · 2019: 4 · 2018: 4 · 2017: 8 · 2016: 2 · 2015: 6 · 2014: 13 · 2013: 8 · 2012: 8
- FWCI
- 5.04
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- UvA-DARE (University of Amsterdam) (publishedVersion)
- UvA-DARE (University of Amsterdam) (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
- Keywords
- motivation, reward anticipation, functional connectivity, striatum, dorsal striatum, ventral striatum, caudate nucleus, antisaccade task, oculomotor control, action control, individual differences
- MeSH terms
- Analysis of Variance, Attention, Basal Ganglia, Brain Mapping, Caudate Nucleus, Cues, Eye Movements, Female, Humans, Image Processing, Computer-Assisted, Magnetic Resonance Imaging, Male, Motivation, Neural Pathways, Oxygen, Photic Stimulation, Reaction Time, Reward, Serial Learning, Time Factors, Young Adult
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