Dopamine D2 Receptors Regulate the Anatomical and Functional Balance of Basal Ganglia Circuitry

Parallel organization of functionally segregated circuits linking basal ganglia and cortex

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The functional anatomy of basal ganglia disorders

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A gene expression atlas of the central nervous system based on bacterial artificial chromosomes

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By Carrot or by Stick: Cognitive Reinforcement Learning in Parkinsonism

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Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry

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Modulation of Striatal Projection Systems by Dopamine

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Role of the Basal Ganglia in the Control of Purposive Saccadic Eye Movements

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Concurrent activation of striatal direct and indirect pathways during action initiation

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Striatal Plasticity and Basal Ganglia Circuit Function

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The basal ganglia

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A biologically constrained spiking neural network model of the primate basal ganglia with overlapping pathways exhibits action selection

Girard, B., Liénard, J., Gutierrez, C. E., Delord, B., & Doya, K. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14869 · Cited by 25

A Circuit-Based Information Approach to Substance Abuse Research

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A non-canonical striatopallidal Go pathway that supports motor control

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Contributions of the basal ganglia to action sequence learning and performance

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Neuroepigenetics of psychiatric disorders: Focus on lncRNA

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Can we use mice to study schizophrenia?

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To Do or Not to Do: Dopamine, Affordability and the Economics of Opportunity

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The Basal Ganglia and Hierarchical Control in Voluntary Behavior

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From "bedside" to "bench" and back: A translational approach to studying dopamine dysfunction in schizophrenia.

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Excessive firing of dyskinesia-associated striatal direct pathway neurons is gated by dopamine and excitatory synaptic input

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Early GABAergic transmission defects in the external globus pallidus and rest/activity rhythm alteration in a mouse model of Huntington’s disease

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Role of Neurochemicals in Schizophrenia

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Intrinsic Connectivity of the Globus Pallidus: An Uncharted Marker of Functional Prognosis in People With First-Episode Schizophrenia

Tarcijonas, G., Foran, W., Haas, G. L., Luna, B., & Sarpal, D. K. (2019) · Schizophrenia Bulletin · doi:10.1093/schbul/sbz034 · Cited by 23

The impact of motivation on cognitive performance in an animal model of the negative and cognitive symptoms of schizophrenia.

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Interneuron Progenitor Transplantation to Treat CNS Dysfunction

Chohan, M. O., & Moore, H. M. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00064 · Cited by 23

The presence of cortical neurons in striatal-cortical co-cultures alters the effects of dopamine and BDNF on medium spiny neuron dendritic development

Penrod, R. D., Campagna, J., Panneck, T., Preese, L., & Lanier, L. M. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00269 · Cited by 26

Evolutionary conservations, changes of circadian rhythms and their effect on circadian disturbances and therapeutic approaches

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Overlapping Projections of Neighboring Direct and Indirect Pathway Neostriatal Neurons to Globus Pallidus External Segment

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Substance P effects exclusively on prototypic neurons in mouse globus pallidus

Mizutani, K., TAKAHASHI, S. Y., Okamoto, S., Karube, F., & Fujiyama, F. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1453-8 · Cited by 20

Contributions of Basal Ganglia Circuits to Perception, Attention, and Consciousness

Redinbaugh, M. J., & Saalmann, Y. B. (2024) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_02177 · Cited by 20

The Addiction-Susceptibility TaqIA/Ankk1 Controls Reward and Metabolism Through D2 Receptor-Expressing Neurons

Montalban, E., Walle, R., Castel, J., Ansoult, A., Hassouna, R., Foppen, E., Fang, X., Hutelin, Z., Mickus, S., Perszyk, E. E., et al. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.02.010 · Cited by 20

Multiple dynamic interactions from basal ganglia direct and indirect pathways mediate action selection

Li, H., & Jin, X. (2023) · eLife · doi:10.7554/elife.87644 · Cited by 22

Differential enhancement of ERK, PKA and Ca2+ signaling in direct and indirect striatal neurons of Parkinsonian mice

Mariani, L., Longueville, S., Girault, J., Hervé, D., & Gervasi, N. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.104506 · Cited by 17

External segment of the globus pallidus in health and disease: Its interactions with the striatum and subthalamic nucleus

Nambu, A., & Chiken, S. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106362 · Cited by 15

Histone deacetylase inhibitors reverse age-related increases in side effects of haloperidol in mice

Montalvo‐Ortiz, J. L., Fisher, D. W., Rodríguez, G., Fang, D., Csernansky, J. G., & Dong, H. (2017) · Psychopharmacology · doi:10.1007/s00213-017-4629-2 · Cited by 17

Quantitative Susceptibility Mapping MRI in Deep-Brain Nuclei in First-Episode Psychosis

Saborit, M. G., Jara, A., Muñoz, N., Milovic, C., Tepper, Á., Alliende, L. M., Mena, C., Iruretagoyena, B., Ramírez-Mahaluf, J. P., Díaz, C., et al. (2023) · Schizophrenia Bulletin · doi:10.1093/schbul/sbad041 · Cited by 15

D2 dopamine receptors and the striatopallidal pathway modulate L-DOPA-induced dyskinesia in the mouse

Sáez, M., Keifman, E., Alberquilla, S., Coll, C., Reig, R., Murer, M. G., & Moratalla, R. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106278 · Cited by 17

The influence of Parkinson's disease on the functional connectivity of the motor loop of human basal ganglia

Rodriguez‐Sabate, C., Moráles, I., Montón, F., & Rodrı́guez, M. (2019) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2019.02.031 · Cited by 16

Beta-band bursting activity in computational model of heterogeneous external globus pallidus circuits

Wang, X., Yu, Y., Han, F., & Wang, Q. (2022) · Communications in Nonlinear Science and Numerical Simulation · doi:10.1016/j.cnsns.2022.106388 · Cited by 16

Chronic treatment with D2-antagonist haloperidol leads to inhibitory/excitatory imbalance in striatal D1-neurons

Santa, C., Rodrigues, D., Coelho, J. F., Anjo, S. I., Mendes, V. M., Bessa‐Neto, D., Dunn, M. J., Cotter, D., Baltazar, G., Monteiro, P., et al. (2023) · Translational Psychiatry · doi:10.1038/s41398-023-02609-w · Cited by 15

The use of chemogenetic approaches in alcohol use disorder research and treatment

Cheng, Y., & Wang, J. (2018) · Alcohol · doi:10.1016/j.alcohol.2018.05.012 · Cited by 15

−NMDA R/+VDR pharmacological phenotype as a novel therapeutic target in relieving motor–cognitive impairments in Parkinsonism

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Ablation of striatal somatostatin interneurons affects MSN morphology and electrophysiological properties, and increases cocaine‐induced hyperlocomotion in mice

Gazan, A., Rial, D., & Schiffmann, S. N. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14581 · Cited by 13

Arkypallidal neurons in basal ganglia circuits: Unveiling novel pallidostriatal loops?

Guilhemsang, L., & Mallet, N. P. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102814 · Cited by 12

Pharmacogenetic and optical dissection for mechanistic understanding of Parkinson's disease: Potential utilities revealed through behavioural assessment

Sharma, P., & Pienaar, I. S. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.07.026 · Cited by 13

Physiology and Pathology of Neuroimmunology: Role of Inflammation in Parkinson’s Disease

Ortíz, G. G., González-Usigli, H., Pacheco-Moisés, F. P., Mireles-Ramírez, M. A., Sánchez-López, A. L., Torres-Sánchez, E. D., González-Renovato, E. D., Flores-Alvarado, L. J., Macías-Islas, M. Á., Rivero-Moragrega, P., et al. (2017) · InTech eBooks · doi:10.5772/intechopen.70377 · Cited by 13

The organization of the basal ganglia functional connectivity network is non-linear in Parkinson's disease

Rodriguez‐Sabate, C., Moráles, I., Lorenzo, J. N., & Rodrı́guez, M. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.101708 · Cited by 13

Proof-of-Mechanism Study of the Phosphodiesterase 10 Inhibitor RG7203 in Patients With Schizophrenia and Negative Symptoms

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Common therapeutic mechanisms of pallidal deep brain stimulation for hypo- and hyperkinetic movement disorders

McCairn, K. W., Iriki, A., & Isoda, M. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00223.2015 · Cited by 12

Axonal degeneration in Parkinson's disease – Basal ganglia circuitry and D2 receptor availability

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Exercise improves behavioral dysfunction and inhibits the spontaneous excitatory postsynaptic current of D2-medium spiny neurons

Zhao, G., Zhang, D., Qiao, D., & Liu, X. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1001256 · Cited by 11

Neuroprotective Effects of P-Coumaric Acid on Haloperidol-Induced Catalepsy Through Ameliorating Oxidative Stress and Brain Dopamine Level

Pathan, A. S., Jain, P. G., Kumawat, V. S., Katolkar, U. N., & Surana, S. J. (2022) · Journal of Pharmacology and Pharmacotherapeutics · doi:10.1177/0976500x221150837 · Cited by 11

A Dual Hit Model for Dopamine in Schizophrenia

Abi‐Dargham, A. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.10.008 · Cited by 10

Dynamic Changes in the Bridging Collaterals of the Basal Ganglia Circuitry Control Stress-Related Behaviors in Mice.

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Morphological Plasticity in the Striatum Associated With Dopamine Dysfunction

Moratalla, R., Solís, Ó., & Suárez, L. M. (2016) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-802206-1.00037-4 · Cited by 9

A diffusion weighted imaging study of basal ganglia in schizophrenia

Delvecchio, G., Pigoni, A., Perlini, C., Barillari, M., Versace, A., Ruggeri, M., Altamura, A. C., Bellani, M., & Brambilla, P. (2017) · International Journal of Psychiatry in Clinical Practice · doi:10.1080/13651501.2017.1340650 · Cited by 9

Increasing dopamine synthesis in nigrostriatal circuits increases phasic dopamine release and alters dorsal striatal connectivity: implications for schizophrenia

Srivastav, S., Cui, X., Varela, R. B., Kesby, J. P., & Eyles, D. W. (2023) · Schizophrenia · doi:10.1038/s41537-023-00397-2 · Cited by 8

The Primate Basal Ganglia Connectome As Revealed By Single-Axon Tracing

Parent, M., & Parent, A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-801393-9.00002-5 · Cited by 8

Cell Types in the Different Nuclei of the Basal Ganglia

Oorschot, D. E. (2016) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-802206-1.00005-2 · Cited by 8

Cell-specific effects of Dyt1 knock-out on sensory processing, network-level connectivity, and motor deficits

Wilkes, B. J., DeSimone, J. C., Liu, Y., Chu, W. T., Coombes, S. A., Li, Y., & Vaillancourt, D. E. (2021) · Experimental Neurology · doi:10.1016/j.expneurol.2021.113783 · Cited by 8

Comparative analysis of resting-state EEG-based multiscale entropy between schizophrenia and bipolar disorder

Hwang, H.-H., Choi, K., Im, C., Yang, C., Kim, S., & Lee, S. (2024) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2024.111048 · Cited by 7

Three paradoxes related to the mode of action of pramipexole: The path from D2/D3 dopamine receptor stimulation to modification of dopamine-modulated functions

Szabadi, E. (2024) · Journal of Psychopharmacology · doi:10.1177/02698811241261022 · Cited by 8

NEUROTRANSMITTER AND BRAIN PARTS INVOLVED IN SCHIZOPHRENIA

Arya, A., Sindhwani, G., & Kadian, R. (2018) · Asian Journal of Pharmaceutical and Clinical Research · doi:10.22159/ajpcr.2018.v11i6.24557 · Cited by 8

Recent Advances in Dopamine D3 Receptor Heterodimers: Focus on Dopamine D3 and D1 Receptor–Receptor Interaction and Striatal Function

Bono, F., Mutti, V., Tomasoni, Z., Sbrini, G., Missale, C., & Fiorentini, C. (2022) · Current topics in behavioral neurosciences · doi:10.1007/7854_2022_353 · Cited by 8

Globus pallidus is not independent from striatal direct pathway neurons: an up-to-date review

Fujiyama, F., Karube, F., & Hirai, Y. (2024) · Molecular Brain · doi:10.1186/s13041-024-01107-4 · Cited by 6

Early Sensory Deprivation Leads to Differential Inhibitory Changes in the Striatum During Learning

Paraouty, N., & Mowery, T. M. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.670858 · Cited by 6

The critical balance between dopamine D2 receptor and RGS for the sensitive detection of a transient decay in dopamine signal

Urakubo, H., Yagishita, S., Kasai, H., Kubota, Y., & Ishii, S. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009364 · Cited by 6

Genetic tools to study complexity of striatal function

Ciriachi, C., Svane‐Petersen, D., & Rickhag, M. (2019) · Journal of Neuroscience Research · doi:10.1002/jnr.24479 · Cited by 5

Beta-Band Oscillations without Segregated Pathways: the opposing Roles of D2 and D5 Receptors in the Basal GangliaPreprint

Liénard, J., Aubin, L., Cos, I., & Girard, B. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/161661 · Cited by 5

Treatment Response and GWAS Risk Allele rs2514218 (C) of the Dopamine D2 Receptor Gene in Inpatients with Schizophrenia

Ma, M., Lezheiko, T., Lepilkina, T. A., Burminskiy, D. S., Potanin, S. S., Герович, Б. А., Rupchev, G. E., & Голимбет, В. Е. (2021) · Neuropsychobiology · doi:10.1159/000519155 · Cited by 4

Direct and indirect pathways of the basal ganglia: opponents or collaborators?

Wang, K. S., McClure, J. P., Alselehdar, S. K., & Kanta, V. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00020 · Cited by 4

The dynamic of basal ganglia activity with a multiple covariance method: influences of Parkinson’s disease

Rodriguez‐Sabate, C., Moráles, I., Puertas‐Avendaño, R., & Rodrı́guez, M. (2019) · Brain Communications · doi:10.1093/braincomms/fcz044 · Cited by 4

Optogenetic Analysis of Striatal Connections to Determine Functional Connectomes

Chuhma, N. (2015) · Springer eBooks · doi:10.1007/978-4-431-55516-2_18 · Cited by 3

The Use of DREADDs for Dissecting the Contribution of Cellular and Neural Circuit Mechanisms in Models of Neurodegenerative Disease

Sharma, P., & Pienaar, I. S. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-804078-2.00024-6 · Cited by 3

The Delta-Opioid System in the Brain: A Neglected Element in Parkinson’s Disease?

Chao, D., & Xia, Y. (2015) · Springer eBooks · doi:10.1007/978-3-319-25495-1_14 · Cited by 3

Adiposity covaries with signatures of asymmetric feedback learning during adaptive decisions

Verstynen, T., Dunovan, K., Walsh, C. P., Kuan, C.-H., Manuck, S. B., & Gianaros, P. J. (2020) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsaa088 · Cited by 3

Targeting the ventral pallidum in obesity

Fang, L. Z., & Vachez, Y. M. (2024) · Addiction Neuroscience · doi:10.1016/j.addicn.2024.100179 · Cited by 2

The Integrative Brain: Functional Units in Predictive Processing

Phillips, M. C. L. (2025) · Journal of Integrative Neuroscience · doi:10.31083/jin39640 · Cited by 4

The effect of the feedback inhibition of heterogeneous external globus pallidus on beta oscillations in an extended basal ganglia network

Li, Z., Shi, X., & Bai, B. (2025) · Electronic Research Archive · doi:10.3934/era.2025270 · Cited by 2

The causal interaction in human basal ganglia

Rodriguez‐Sabate, C., González, A., Pérez, J. C., Moráles, I., & Rodrı́guez, M. (2021) · Scientific Reports · doi:10.1038/s41598-021-92490-8 · Cited by 2

Persistent extrasynaptic hyperdopaminergia in the mouse hippocampus induces plasticity and recognition memory deficits reversed by the atypical antipsychotic sulpiride

Rocchetti, J., Fasano, C., Bo, G. D., Guma, E., Mestikawy, S. E., Wong, T. P., Fakhfouri, G., & Giros, B. (2023) · PLoS ONE · doi:10.1371/journal.pone.0289770 · Cited by 2

Correlation of repetitive behaviors in deer mice with striatal mRNA expression of endogenous opioids and mu, delta, kappa, and dopamine receptors: A preliminary report

Augustine, F., Doss, S. M., Pellicciotti, J., Mahate, S., & Singer, H. S. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.01.005 · Cited by 2

Basal ganglia circuits

Gittis, A. H., Hooks, B. M., & Gerfen, C. R. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814411-4.00010-x · Cited by 4

Behavioral Phenotypes of Genetic Mouse Models

Moran, P. M. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-801829-3.00029-x · Cited by 2

Anatomy and Function of the Direct and Indirect Striatal Pathways

Soghomonian, J. (2016) · Innovations in cognitive neuroscience · doi:10.1007/978-3-319-42743-0_3 · Cited by 2

Striatal circuit development and synapse maturation

Peixoto, R. T., & Kozorovitskiy, Y. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-823672-7.00021-1 · Cited by 2

Functional Connectome Analysis of the Striatum with Optogenetics

Chuhma, N. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-8763-4_27 · Cited by 2

The Indirect Pathway of the Basal Ganglia Promotes Negative Reinforcement, But Not Motor SuppressionPreprint

Isett, B. R., Nguyen, K. P., Schwenk, J. C., Snyder, C. N., Adegbesan, K., Ziausyte, U., & Gittis, A. H. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.05.18.492478 · Cited by 2

Prenatal Ethanol Exposure Results in Cell Type, Age, and Sex-Dependent Differences in the Neonatal Striatum That Coincide with Early Motor Deficits

Tousley, A. R., Deykin, I., Koc, B., Yeh, P. W. L., & Yeh, H. H. (2025) · eNeuro · doi:10.1523/eneuro.0448-24.2025 · Cited by 1

Halved Dose of Antipsychotics Versus High-Dose Antipsychotic Therapy for Relapse in Patients with Schizophrenia Receiving High-Dose Antipsychotic Therapy: A Randomized Single-Blind Trial

Ataniya, R., Koike, T., & Inamoto, A. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26094003 · Cited by 1

Regional heterogeneity of striatal cholinergic interneurons: setting the stage for diverse behavioral repertoires

Lemos, J. C., Duhne, M., & Chuhma, N. (2026) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2026.1718947 · Cited by 1

MSK1 mediates BDNF-dependent MeCP2-S421 phosphorylation in postnatal striatal development and psychiatric-relevant behaviours

Varela-Andrés, N., Caño, C. H.-D., Cebrián-León, A., Blanco, A., de Pariza, I. L. A. L., del Campo, I. S. F., García-Losada, S., Arévalo, J. C., Sánchez-Martín, M., Bajo‐Grañeras, R., et al. (2026) · Molecular Psychiatry · doi:10.1038/s41380-026-03630-3 · Cited by 1

Cognitive functions of the GPe

O'Berry, K., & Gittis, A. H. (2026) · Trends in Neurosciences · doi:10.1016/j.tins.2026.05.005 · Cited by 1

Regulation of Corticostriatal Synaptic Plasticity in Physiological and Pathological Conditions

Filippo, M. D., & Calabresi, P. (2016) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-802206-1.00023-4 · Cited by 2

Dopamine D2R upregulation in ventral striatopallidal neurons does not affect Pavlovian or go/no-go learning.

Martyniuk, K. M., Dandeneau, M., Balsam, P. D., & Kellendonk, C. (2021) · Behavioral Neuroscience · doi:10.1037/bne0000403 · Cited by 1

The external pallidum: think locally, act globallyPreprint

Courtney, C. D., Pamukcu, A., & Chan, C. S. (2021) · arXiv (Cornell University) · doi:10.48550/arxiv.2104.10795 · Cited by 2

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