Cited by 371Neurotransmitter Receptor Influence on BehaviorDeep Brain Stimulation and Movement DisordersNeural and Behavioral Psychology Studies

The DOI matches its Crossref record; 102 of the 104 references it cites were found in a registry or an index.

The place of dopamine in the cortico-basal ganglia circuit

Open access

Haber, S.N.·2014·Neuroscience

DOI 10.1016/j.neuroscience.2014.10.008PMC PMC5484174

Open this paper in CoChat — free account

Abstract

The midbrain dopamine (DA) neurons play a central role in developing appropriate goal-directed behaviors, including the motivation and cognition to develop appropriate actions to obtain a specific outcome. Indeed, subpopulations of DA neurons have been associated with these different functions: the mesolimbic, mesocortical, and nigrostriatal pathways. The mesolimbic and nigrostriatal pathways are an integral part of the basal ganglia through its reciprocal connections to the ventral and dorsal striatum respectively. This chapter reviews the connections of the midbrain DA cells and their role in integrating information across limbic, cognitive and motor functions. Emphasis is placed on the interface between these functional domains within the striatum through corticostriatal connections, through the striato-nigro-striatal connection, and through the lateral habenula projection to the midbrain.

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

Crossref · 10.1016/j.neuroscience.2014.10.008

Cites

102 of 102 references verified0 citation errors · 0 not checkable

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Dopamine, learning and motivation.
Wise, R. A. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1406 · Cited by 3,379 · cited 1×
“Indeed, subpopulations of DA neurons have been associated with these different functions: the mesolimbic, mesocortical, and nigrostriatal pathways, respectively (Wullner et al., 1994; Sawaguchi, 1995; Goldman-Rakic, 1998; Wise, 2004).”
Autoradiographic localization of dopamine D1 and D2 receptors in rat nucleus accumbens: Resistance to differential rearing conditions
Bardo, M. T., & Hammer, R. P. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90226-e · Cited by 3,229
Getting formal with dopamine and reward
Schultz, W. (2002) · Neuron · doi:10.1016/s0896-6273(02)00967-4 · Cited by 2,574
Basal ganglia-thalamocortical circuits: parallel substrates for motor, oculomotor, "prefrontal" and "limbic" functions.
Alexander, G. E., Crutcher, M. D., & DeLong, M. R. (1990) · PubMed · Cited by 2,422
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
Chapter 6 Basal ganglia-thalamocortical circuits: Parallel substrates for motor, oculomotor, “prefrontal” and “limbic” functions
(1991) · Progress in Brain Research · doi:10.1016/s0079-6123(08)62678-3 · Cited by 1,961
Verteilung Von Noradrenalin Und Dopamin (3-Hydroxytyramin) Im Gehirn Des Menschen Und Ihr Verhalten Bei Erkrankungen Des Extrapyramidalen Systems
Ehringer, H., & Hornykiewicz, O. (1960) · Journal of Molecular Medicine · doi:10.1007/bf01485901 · Cited by 1,875
Striatonigrostriatal pathways in primates form an ascending spiral from the shell to the dorsolateral striatum
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
Self-citation
Lateral habenula as a source of negative reward signals in dopamine neurons
Matsumoto, M., & Hikosaka, O. (2007) · Nature · doi:10.1038/nature05860 · Cited by 1,292
Cocaine cues and dopamine in dorsal striatum: mechanism of craving in cocaine addiction
Volkow, N. D., Wang, G.-J., Telang, F., Fowler, J. S., Logan, J., Childress, A.-R., Jayne, M., Ma, Y., & Wong, C. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1544-06.2006 · Cited by 1,164
Longitudinal topography and interdigitation of corticostriatal projections in the rhesus monkey
Selemon, L. D., & Goldman-Rakic, P. S. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-03-00776.1985 · Cited by 1,074
Motivational control of goal-directed action
Dickinson, A., & Balleine, B. (1994) · Animal Learning & Behavior · doi:10.3758/bf03199951 · Cited by 995
Cytoarchitecture of the Human Brain Stem.
Boyd, J. D. (1955) · Archives of Ophthalmology · doi:10.1001/archopht.1955.00930010774037 · Cited by 897
Efferent connections of the habenular nuclei in the rat
Herkenham, M. A., & Nauta, W. J. H. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901870103 · Cited by 855
Prediction of immediate and future rewards differentially recruits cortico-basal ganglia loops
Tanaka, S. C., Doya, K., Okada, G., Ueda, K., Okamoto, Y., & Yamawaki, S. (2004) · Nature Neuroscience · doi:10.1038/nn1279 · Cited by 779
Bilateral projections from precentral motor cortex to the putamen and other parts of the basal ganglia. An autoradiographic study inMacaca fascicularis
Künzle, H. (1975) · Brain Research · doi:10.1016/0006-8993(75)90384-4 · Cited by 714
Different time courses of learning-related activity in the prefrontal cortex and striatum.
Pasupathy, A., & Miller, E. K. (2005) · Nature · doi:10.1038/nature03287 · Cited by 712
Cocaine seeking habits depend upon dopamine-dependent serial connectivity linking the ventral with the dorsal striatum
Belin, D., & Everitt, B. J. (2008) · Neuron · doi:10.1016/j.neuron.2007.12.019 · Cited by 697
The rostromedial tegmental nucleus (RMTg), a GABAergic afferent to midbrain dopamine neurons, encodes aversive stimuli and inhibits motor responses.
Jhou, T. C., Fields, H. L., Baxter, M. G., Saper, C. B., & Holland, P. C. (2009) · Neuron · doi:10.1016/j.neuron.2009.02.001 · Cited by 696
Reward-related cortical inputs define a large striatal region in primates that interface with associative cortical connections, providing a substrate for incentive-based learning.
Haber, S. N., Kim, K.-S., Mailly, P., & Calzavara, R. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.0271-06.2006 · Cited by 686
Self-citation
The basal ganglia: learning new tricks and loving it
Graybiel, A. M. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.10.006 · Cited by 678
Cortico-striate projections in the rhesus monkey: The organization of certain cortico-caudate connections
Yeterian, E. H., & Hoesen, G. W. V. (1978) · Brain Research · doi:10.1016/0006-8993(78)90059-8 · Cited by 641
Distinct basal ganglia territories are engaged in early and advanced motor sequence learning
Lehéricy, S., Benali, H., Van de Moortele, P.-F., Pélégrini-Issac, M., Waechter, T., Ugurbil, K., & Doyon, J. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0502762102 · Cited by 634
Remission of major depression under deep brain stimulation of the lateral habenula in a therapy-refractory patient
Sartorius, A., Kiening, K. L., Kirsch, P., von Gall, C. C., Haberkorn, U., Unterberg, A. W., Henn, F. A., & Meyer-Lindenberg, A. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.08.027 · Cited by 611
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
Self-citation
An Autoradiographic Analysis of the Efferent Connections from Premotor and Adjacent Prefrontal Regions (Areas 6 and 9) in Macaca fascicularis; pp. 185–209
Künzle, H. (2008) · Brain Behavior and Evolution · doi:10.1159/000123779 · Cited by 559
Parallel and interactive learning processes within the basal ganglia: relevance for the understanding of addiction
Belin, D., Jonkman, S., Dickinson, A., Robbins, T. W., & Everitt, B. J. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.09.027 · Cited by 520
Error Monitoring Using External Feedback: Specific Roles of the Habenular Complex, the Reward System, and the Cingulate Motor Area Revealed by Functional Magnetic Resonance Imaging
Ullsperger, M., & von Cramon, D. Y. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-10-04308.2003 · Cited by 484
Efferent connections of the ventral pallidum: Evidence of a dual striato pallidofugal pathway
Haber, S. N., Groenewegen, H. J., Grove, E. A., & Nauta, W. J. H. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902350304 · Cited by 432
Self-citation
Stimulation of the lateral habenula inhibits dopamine-containing neurons in the substantia nigra and ventral tegmental area of the rat
Christoph, G., Leonzio, R., & Wilcox, K. (1986) · The Journal of Neuroscience · doi:10.1523/jneurosci.06-03-00613.1986 · Cited by 418
Distribution of dopaminergic receptors in the primate cerebral cortex: Quantitative autoradiographic analysis using [3H]raclopride, [3H]spiperone and [3H]SCH23390
Lidow, M. S., Goldman-Rakic, P. S., Gallager, D. W., & Rakic, P. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90003-7 · Cited by 394
The Cortical Dopamine System: Role in Memory and Cognition
Goldman, P. S. (1997) · Advances in pharmacology · doi:10.1016/s1054-3589(08)60846-7 · Cited by 393
Negative Reward Signals from the Lateral Habenula to Dopamine Neurons Are Mediated by Rostromedial Tegmental Nucleus in Primates
Hong, S., Jhou, T. C., Smith, M., Saleem, K. S., & Hikosaka, O. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.1384-11.2011 · Cited by 390
Lateral Habenula Stimulation Inhibits Rat Midbrain Dopamine Neurons through a GABAA Receptor-Mediated Mechanism
Ji, H., & Shepard, P. D. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0958-07.2007 · Cited by 388
The precise localization of nigral afferents in the rat as determined by a retrograde tracing technique
Bunney, B. S., & Aghajanian, G. K. (1976) · Brain Research · doi:10.1016/0006-8993(76)90751-4 · Cited by 373
Brainstem innervation of prefrontal and anterior cingulate cortex in the rhesus monkey revealed by retrograde transport of HRP
Porrino, L. J., & Goldman, P. S. (1982) · The Journal of Comparative Neurology · doi:10.1002/cne.902050107 · Cited by 357
The globus pallidus sends reward-related signals to the lateral habenula
Hong, S., & Hikosaka, O. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.035 · Cited by 346
Insular Cortical Projections to Functional Regions of the Striatum Correlate with Cortical Cytoarchitectonic Organization in the Primate
Chikama, M., Mcfarland, N. R., Amaral, D., & Haber, S. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-24-09686.1997 · Cited by 333
Self-citation
The distribution of tyrosine hydroxylase-immunoreactive fibers in primate neocortex is widespread but regionally specific
Lewis, D., Campbell, M., Foote, S., Goldstein, M., & Morrison, J. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-01-00279.1987 · Cited by 325
Pedunculopontine nucleus in the squirrel monkey: Projections to the basal ganglia as revealed by anterograde tract‐tracing methods
Lavoie, B. A., & Parent, A. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903440204 · Cited by 321
Comparative neurobiology of the basal ganglia
Parent, A. (1986) · Cited by 313
Cytoarchitecture of the Human Brain Stem
Bandler, R. J. (1983) · Pathology · doi:10.1016/s0031-3025(16)37288-9 · Cited by 300
Biochemistry and pharmacology of the basal ganglia
Yahr, M. D. (1965) · International Journal of Neuropharmacology · doi:10.1016/0028-3908(65)90018-3 · Cited by 294
Topographic organization of the ventral striatal efferent projections in the rhesus monkey: An anterograde tracing study
Haber, S. N., Lynd‐Balta, E., Klein, C. M., & Groenewegen, H. J. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902930210 · Cited by 291
Self-citation
Primate cingulostriatal projection: Limbic striatal versus sensorimotor striatal input
Kunishio, K., & Haber, S. N. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903500302 · Cited by 290
Self-citation
The Olfactory Cortex and the Ventral Striatum
Heimer, L. (1978) · Springer eBooks · doi:10.1007/978-1-4757-0716-8_7 · Cited by 283
Differential activation of the caudate nucleus in primates performing spatial and nonspatial working memory tasks
Levy, R., Friedman, H. R., Davachi, L., & Goldman-Rakic, P. S. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-10-03870.1997 · Cited by 279
Cocaine self-administration produces a progressive involvement of limbic, association, and sensorimotor striatal domains
Porrino, L. J., Lyons, D., Smith, H. R., Daunais, J. B., & Nader, M. A. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.5578-03.2004 · Cited by 276
Influence of Expectation of Different Rewards on Behavior-Related Neuronal Activity in the Striatum
Hassani, O. K., Cromwell, H. C., & Schultz, W. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.6.2477 · Cited by 257
Glutamatergic axons from the lateral habenula mainly terminate on GABAergic neurons of the ventral midbrain
Brinschwitz, K., Dittgen, A., Madai, V. I., Lommel, R., Geisler, S., & Veh, R. W. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.03.050 · Cited by 240
The organization of midbrain projections to the striatum in the primate: sensorimotor-related striatum versus ventral striatum
Lynd-Balta, E., & Haber, S. N. (1994) · Neuroscience · doi:10.1016/0306-4522(94)90182-1 · Cited by 233
Self-citation
The subcortical afferents to caudate nucleus and putamen in primate: A fluorescence retrograde double labeling study
Parent, A., Mackey, A., & Bellefeuille, L. D. (1983) · Neuroscience · doi:10.1016/0306-4522(83)90104-5 · Cited by 233
The Neural Network Underlying Incentive-Based Learning: Implications for Interpreting Circuit Disruptions in Psychiatric Disorders
Haber, S. N., & Behrens, T. E. J. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.031 · Cited by 230
Self-citation
Amygdaloid projections to ventromedial striatal subterritories in the primate
Fudge, J. L., Kunishio, K., Walsh, P., Richard, C., & Haber, S. N. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00546-2 · Cited by 226
Self-citation
Corticostriatal Interactions during Learning, Memory Processing, and Decision Making
Pennartz, C. M. A., Berke, J. D., Graybiel, A. M., Ito, R., Lansink, C. S., van der Meer, M., Redish, A. D., Smith, K. S., & Voorn, P. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.3177-09.2009 · Cited by 213
Region‐specific distribution of catecholamine afferents in primate cerebral cortex: A fluorescence histochemical analysis
Levitt, P. R., RAKIC, P. T., & Goldman, P. S. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902270105 · Cited by 190
Subsets of midbrain dopaminergic neurons in monkeys are distinguished by different levels of mRNA for the dopamine transporter: Comparison with the mRNA for the D2 receptor, tyrosine hydroxylase and calbindin immunoreactivity
Haber, S. N., Ryoo, H., Cox, C., & Lu, W. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903620308 · Cited by 188
Self-citation
Topography and collateralization of the dopaminergic projections to motor and lateral prefrontal cortex in owl monkeys
Gaspar, P., Stepniewska, I., & Kaas, J. H. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903250102 · Cited by 187
A Pallidus-Habenula-Dopamine Pathway Signals Inferred Stimulus Values
Bromberg-Martin, E. S., Matsumoto, M., Hong, S., & Hikosaka, O. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00158.2010 · Cited by 186
The organization of the descending ventral pallidal projections in the monkey
Haber, S., Lynd-Balta, E., & Mitchell, S. (1993) · The Journal of comparative neurology · doi:10.1002/cne.903290108 · Cited by 184
Self-citation
Evidence for structural abnormalities of the human habenular complex in affective disorders but not in schizophrenia
Ranft, K., Dobrowolny, H., Krell, D., Bielau, H., Bogerts, B., & Bernstein, H.-G. (2010) · Psychological Medicine · doi:10.1017/s0033291709990821 · Cited by 183
Habenula Volume in Bipolar Disorder and Major Depressive Disorder: A High-Resolution Magnetic Resonance Imaging Study
Savitz, J. B., Nugent, A. C., Bogers, W., Roiser, J. P., Bain, E., Neumeister, A., Zarate, C. A., Manji, H. K., Cannon, D. M., Marrett, S., et al. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.09.027 · Cited by 182
The effects of cocaine: A shifting target over the course of addiction
Porrino, L. J., Smith, H. R., Nader, M. A., & Beveridge, T. J. R. (2007) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2007.08.040 · Cited by 180
Estimates of projection overlap and zones of convergence within frontal-striatal circuits
Averbeck, B. B., Lehman, J., Jacobson, M., & Haber, S. N. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.5806-12.2014 · Cited by 179
Self-citation
The ventral pallidal projection to the mediodorsal thalamus: a study with fluorescent retrograde tracers and immunohistofluorescence
Young, W. S., Alheid, G., & Heimer, L. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-06-01626.1984 · Cited by 179
Relationship between the corticostriatal terminals from areas 9 and 46, and those from area 8A, dorsal and rostral premotor cortex and area 24c: an anatomical substrate for cognition to action
Calzavara, R., Mailly, P., & Haber, S. N. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05825.x · Cited by 170
Self-citation
Parallel processing in the basal ganglia: up to a point
Percheron, G., & Filion, M. (1991) · Trends in Neurosciences · doi:10.1016/0166-2236(91)90020-u · Cited by 168
Monoamine Innervation of Cerebral Cortex and a Theory of the Role of Monoamines in Cerebral Cortex and Basal Ganglia
Fallon, J. H., & Loughlin, S. E. (1932) · Cerebral cortex · doi:10.1007/978-1-4615-6616-8_2 · Cited by 166
Dopaminergic neurons expressing calbindin in normal and parkinsonian monkeys
Lavoie, B. A., & Parent, A. (1991) · Neuroreport · doi:10.1097/00001756-199110000-00012 · Cited by 165
The efferent projections of the medial prefrontal cortex in the squirrel monkey (Saimiri sciureus)
Leichnetz, G. R., & Astruc, J. A. (1976) · Brain Research · doi:10.1016/0006-8993(76)90027-5 · Cited by 164
Primate striatonigral projections: A comparison of the sensorimotor‐related striatum and the ventral striatum
Lynd‐Balta, E., & Haber, S. N. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903450407 · Cited by 164
Self-citation
The efferent projections of the rat lateral habenular nucleus revealed by the PHA-L anterograde tracing method
Araki, M., McGeer, P. L., & Kimura, H. (1988) · Brain Research · doi:10.1016/0006-8993(88)91410-2 · Cited by 163
Signals in Human Striatum Are Appropriate for Policy Update Rather than Value Prediction
Li, J., & Daw, N. D. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6316-10.2011 · Cited by 159
Reward-Modulated Motor Information in Identified Striatum Neurons
Isomura, Y., Takekawa, T., Harukuni, R., Handa, T., Aizawa, H., Takada, M., & Fukai, T. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0381-13.2013 · Cited by 157
Comparative anatomy of the ventromedial mesencephalic tegmentum in the rat, cat, monkey and human
Halliday, G. M., & Törk, I. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902520402 · Cited by 147
Pharmacological inhibition of the lateral habenula improves depressive-like behavior in an animal model of treatment resistant depression
Winter, C., Vollmayr, B., Djodari-Irani, A., Klein, J., & Sartorius, A. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.07.034 · Cited by 145
Electrical stimulation of the lateral habenula produces enduring inhibitory effect on cocaine seeking behavior
Friedman, A., Lax, E., Dikshtein, Y., Abraham, L., Flaumenhaft, Y., Sudai, E., Ben‐Tzion, M., Ami-Ad, L., Yaka, R., & Yadid, G. (2010) · Neuropharmacology · doi:10.1016/j.neuropharm.2010.06.008 · Cited by 145
Comparative morphology of the substantia nigra and ventral tegmental area in the monkey, cat and rat
POIRIER, L. J., Giguère, M., & Marchand, R. (1983) · Brain Research Bulletin · doi:10.1016/0361-9230(83)90173-9 · Cited by 142
Prefrontal Cortical Projections to the Midbrain in Primates: Evidence for a Sparse Connection
Frankle, W., Laruelle, M., & Haber, S. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300990 · Cited by 141
Self-citation
Schizophrenia in Translation: The Presence of Absence: Habenular Regulation of Dopamine Neurons and the Encoding of Negative Outcomes
Shepard, D. S., Holcomb, H. H., & Gold, J. M. (2005) · Schizophrenia Bulletin · doi:10.1093/schbul/sbj083 · Cited by 140
Chemotherapy in psychiatry : principles and practice
Baldessarini, R. J. (1985) · Medical Entomology and Zoology · Cited by 135
BOLD responses to negative reward prediction errors in human habenula
Salas (2010) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2010.00036 · Cited by 131
The cortico-nigral projection: reduced glutamate content in the substantia nigra following frontal cortex ablation in the rat
Kornhuber, J., Kim, J.-S., Kornhuber, M. E., & Kornhuber, H. H. (1984) · Brain Research · doi:10.1016/0006-8993(84)91189-2 · Cited by 130
Comparative neurobiology of the basal ganglia
Reiner, A. J. (1987) · Trends in Neurosciences · doi:10.1016/0166-2236(87)90019-1 · Cited by 129
Chemotherapy in Psychiatry: Principles and Practice
Seelye, E. E. (1986) · American Journal of Psychotherapy · doi:10.1176/appi.psychotherapy.1986.40.4.614 · Cited by 129
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
Neural Correlates of Rewarded and Unrewarded Eye Movements in the Primate Caudate Nucleus
Watanabe, K., Lauwereyns, J., & Hikosaka, O. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-31-10052.2003 · Cited by 118
The origin of forebrain afferents to the habenula in rat, cat and monkey
Parent, A., Gravel, S., & Boucher, R. (1981) · Brain Research Bulletin · doi:10.1016/s0361-9230(81)80066-4 · Cited by 117
Human Dorsal Striatum Encodes Prediction Errors during Observational Learning of Instrumental Actions
Cooper, J. C., Dunne, S., Furey, T., & O'Doherty, J. P. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00114 · Cited by 101
Studies on neuromelanin
Bazelon, M., Fenichel, G. M., & Randall, J. O. (1967) · Neurology · doi:10.1212/wnl.17.5.512 · Cited by 101
The Basal Ganglia
Haber, S. N., Adler, A., & Bergman, H. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-374236-0.10020-3 · Cited by 94
Self-citation
Catecholaminergic innervation of the hippocampus in the cynomolgus monkey
Samson, Y., Wu, J. J., Friedman, A. H., & Davis, J. N. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902980209 · Cited by 64
The Ventral Striato-Pallidal Pathway Mediates the Effect of Predictive Learning on Choice between Goal-Directed Actions
Leung, B. K., & Balleine, B. W. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1697-13.2013 · Cited by 60
Calbindin D28k-containing neurons are restricted to the medial substantia nigra in humans
McRitchie, D. A., & Halliday, G. M. (1995) · Neuroscience · doi:10.1016/0306-4522(94)00483-l · Cited by 54
A histological atlas of the macaque (Macaca, mulatta) substantia nigra in ventricular coordinates
François, C., Percheron, G., Yelnik, J., & Heyner, S. (1985) · Brain Research Bulletin · doi:10.1016/0361-9230(85)90196-0 · Cited by 53
Functions of the Cortico-Basal Ganglia Loop
Kimura, M., & Graybiel, A. M. (1995) · Springer eBooks · doi:10.1007/978-4-431-68547-0 · Cited by 53
Dopamine Terminal Loss and Onset of Motor Symptoms in MPTP-Treated Monkeys: A Positron Emission Tomography Study with 11C-CFT
Wüllner, U., Pakzaban, P., Brownell, A.-L., Hantraye, P., Burns, L. H., Shoup, T. M., Elmaleh, D. R., Petto, A. J., Spealman, R. D., Brownell, G. L., et al. (1994) · Experimental Neurology · doi:10.1006/exnr.1994.1069 · Cited by 51
The heterogeneity of the mesostriatal dopaminergic system as revealed in normal and parkinsonian monkeys.
Parent, A., & Lavoie, B. A. (1993) · PubMed · Cited by 50
The cortico-nigral fibre tract. An experimental Fink-Heimer study in cats.
Afifi, A. K., Bahuth, N. B., Kaelber, W. W., Mikhael, E. M., & Nassar, S. (1974) · Europe PMC (PubMed Central) · Cited by 42
Strionigral and Nigrostriatal Connections
Szabó, J. (1979) · Stereotactic and Functional Neurosurgery · doi:10.1159/000102324 · Cited by 31
The Role of Dopamine in Frontal Motor Cortical Functions of Monkeys
Sawaguchi, T. (1995) · Springer eBooks · doi:10.1007/978-4-431-68547-0_11 · Cited by 4
Untitled work
Yeterian (1998) · doi:10.1002/(sici)1096-9861(19980928)399:3

Research works printed but not linked: 3

Bremer, 1920, Encephalite lethargique avec syndrome Parkinsonien et catatonie, Rev Neurol, 27, 770
Carter, 1980, Glutamatergic pathways from the medial pre-frontal cortex to the anterior striatum, nucleus accumbens and substantia nigra, Br J Pharmacol, 70, 50
Hassler, 1939, Zur pathologischen anatomie des senilen und des parkinsonistischen tremor, J Psychol Neurol, 13

Sorted by citations

Prefrontal cortex as a meta-reinforcement learning system
Wang, J. X., Kurth-Nelson, Z., Kumaran, D., Tirumala, D., Soyer, H., Leibo, J. Z., Hassabis, D., & Botvinick, M. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0147-8 · Cited by 596
Pathophysiological and cognitive mechanisms of fatigue in multiple sclerosis
Manjaly, Z., Harrison, N. A., Critchley, H., Tri, C., Stefanics, G., Wenderoth, N., Lutterotti, A., Müller, A. E., & Stephan, K. E. (2019) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2018-320050 · Cited by 358
Dopamine neurons projecting to the posterior striatum form an anatomically distinct subclass
Menegas, W., Bergan, J. F., Ogawa, S. K., Isogai, Y., Venkataraju, K. U., Osten, P., Uchida, N., & Watabe‐Uchida, M. (2015) · eLife · doi:10.7554/elife.10032 · Cited by 335
A Dopamine Hypothesis of Autism Spectrum Disorder
Pavăl, D. (2017) · Developmental Neuroscience · doi:10.1159/000478725 · Cited by 316
Specialized astrocytes mediate glutamatergic gliotransmission in the CNS
Ceglia, R. D., Ledonne, A., Litvin, D. G., Lind, B. L., Carriero, G., Latagliata, E. C., Bindocci, E., Castro, M. A. D., Savtchouk, I., Vitali, I., et al. (2023) · Nature · doi:10.1038/s41586-023-06502-w · Cited by 297

See all 371

Authors: Haber, S. N.
Affiliations: University of Rochester Medicine (US)
Corresponding author: Haber, S.N.
ORCID: Haber, S.N.
Venue: Neuroscience
Publisher: Elsevier BV
Published: 2014-12
Volume: 282
Pages: 248-257
ISSN: 0306-4522 (ISSN-L)
DOI: 10.1016/j.neuroscience.2014.10.008
PMC: PMC5484174
OpenAlex: W2029942338
Cited by: 364
References: 104
Citations by year: 2026: 26 · 2025: 28 · 2024: 26 · 2023: 32 · 2022: 30 · 2021: 46 · 2020: 34 · 2019: 36 · 2018: 32 · 2017: 32 · 2016: 20 · 2015: 21 · 2014: 1
FWCI: 2.84
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Neuroscience (publishedVersion)
PubMed (publishedVersion)
Europe PMC (PubMed Central) (acceptedVersion)
PubMed Central (acceptedVersion)
Funders: NIMH (MH045573-24)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
Health Sciences › Medicine › Clinical Neurology › Deep Brain Stimulation and Movement Disorders
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
Keywords: dopamine, midbrain dopaminergic neurons, cortico-basal ganglia circuits, mesolimbic system, mesocortical pathway, nigrostriatal pathway, ventral striatum, dorsal striatum, corticostriatal connections, lateral habenula, goal-directed behavior, motivation, cognitive function, motor function, functional integration
MeSH terms: Animals, Basal Ganglia, Cerebral Cortex, Dopamine, Mesencephalon, Neural Pathways, Dopaminergic Neurons

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

The place of dopamine in the cortico-basal ganglia circuit

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks