Dopamine transporters govern diurnal variation in extracellular dopamine tone

Activity of norepinephrine-containing locus coeruleus neurons in behaving rats anticipates fluctuations in the sleep-waking cycle

Aston-Jones, G., & Bloom, F. (1981) · The Journal of Neuroscience · doi:10.1523/jneurosci.01-08-00876.1981 · Cited by 1,960

Sleep Cycle Oscillation: Reciprocal Discharge by Two Brainstem Neuronal Groups

Hobson, J. A., McCarley, R. W., & Wyzinski, P. (1975) · Science · doi:10.1126/science.1094539 · Cited by 1,238

Regulation of firing of dopaminergic neurons and control of goal-directed behaviors

Grace, A. A., Floresco, S. B., Goto, Y., & Lodge, D. J. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.003 · Cited by 1,034

Impulse activity of locus coeruleus neurons in awake rats and monkeys is a function of sensory stimulation and arousal

Foote, S. L., Aston-Jones, G., & Bloom, F. E. (1980) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.77.5.3033 · Cited by 857

Dopaminergic Role in Stimulant-Induced Wakefulness

Wisor, J. P., Nishino, S., Sora, I., Uhl, G. R., Mignot, E. J.-M., & Edgar, D. M. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-05-01787.2001 · Cited by 779

Profound neuronal plasticity in response to inactivation of the dopamine transporter

Jones, S. R., Gainetdinov, R. R., Jaber, M., Giros, B., Wightman, R. M., & Caron, M. G. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.7.4029 · Cited by 712

Dopamine Is a Regulator of Arousal in the Fruit Fly

Kume, K., Kume, S., Park, S. K., Hirsh, J., & Jackson, F. R. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2048-05.2005 · Cited by 605

The Dopamine Transporter and Attention-Deficit/Hyperactivity Disorder

Madras, B. K., Miller, G. M., & Fischman, A. J. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.10.011 · Cited by 393

Cocaine supersensitivity and enhanced motivation for reward in mice lacking dopamine D2 autoreceptors

Bello, E. P., Mateo, Y., Gelman, D. M., Noaín, D., Shin, J. H., Low, M. J., Alvarez, V. A., Lovinger, D. M., & Rubinstein, M. (2011) · Nature Neuroscience · doi:10.1038/nn.2862 · Cited by 364

Variations in extracellular levels of dopamine, noradrenaline, glutamate, and aspartate across the sleep–wake cycle in the medial prefrontal cortex and nucleus accumbens of freely moving rats

Léna, I., Parrot, S., Deschaux, O., Muffat‐Joly, S., Sauvinet, V., Renaud, B., Suaud‐Chagny, M. ‐., & Gottesmann, C. (2005) · Journal of Neuroscience Research · doi:10.1002/jnr.20602 · Cited by 322

Emotionally clocked out: cell-type specific regulation of mood and anxiety by the circadian clock system in the brain

Francis, T. C., & Porcu, A. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1188184 · Cited by 15

Disruption of circadian rhythms promotes alcohol use: a systematic review

Nelson, M. J., Soliman, P., Rhew, R. H. H., Cassidy, R. N., & Haass‐Koffler, C. L. (2023) · Alcohol and Alcoholism · doi:10.1093/alcalc/agad083 · Cited by 17

Sleep and Circadian Medicine

Ruben, M. D., Hogenesch, J. B., & Smith, D. F. (2019) · Neurologic Clinics · doi:10.1016/j.ncl.2019.03.004 · Cited by 15

The efficacy of (+)-Naltrexone on alcohol preference and seeking behaviour is dependent on light-cycle

Jacobsen, J. H. W., Buisman‐Pijlman, F. T. A., Mustafa, S., Rice, K. C., & Hutchinson, M. R. (2017) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2017.08.021 · Cited by 15

Objective Measurement and Characterization of Sleep Benefit in Parkinson's Disease

Lee, W., Evans, A. H., & Williams, D. R. (2017) · Movement Disorders Clinical Practice · doi:10.1002/mdc3.12489 · Cited by 12

Chronic abdominal vagus stimulation increased brain metabolic connectivity, reduced striatal dopamine transporter and increased mid-brain serotonin transporter in obese miniature pigs

Malbert, C., Genissel, M., Divoux, J., & Henry, C. (2019) · Journal of Translational Medicine · doi:10.1186/s12967-019-1831-5 · Cited by 13

Dopaminergic Ric GTPase activity impacts amphetamine sensitivity and sleep quality in a dopamine transporter-dependent manner in Drosophila melanogaster

Fagan, R. R., Kearney, P. J., Luethi, D., Bolden, N. C., Sitte, H. H., Emery, P., & Melikian, H. E. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01275-y · Cited by 11

Individual differences in dopamine uptake in the dorsomedial striatum prior to cocaine exposure predict motivation for cocaine in male rats

Shaw, J. K., Alonso, I. P., Lewandowski, S. I., Scott, M. O., O’Connor, B. M., Aggarwal, S., Biasi, M. D., Mortensen, O. V., & España, R. A. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01009-2 · Cited by 11

Delayed circadian rhythms and substance abuse: dopamine transmission’s time has come

Hasler, B. P., & McClung, C. A. (2021) · Journal of Clinical Investigation · doi:10.1172/jci152832 · Cited by 10

The circadian neurobiology of reward

Olejniczak, I., Begemann, K., Wilhelm, I., & Oster, H. (2023) · Acta Physiologica · doi:10.1111/apha.13928 · Cited by 13

Wake up and smell the dopamine: new mechanisms mediating dopamine activity fluctuations related to sleep and psychostimulant sensitivity

Kesner, A. J., & Lovinger, D. M. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-00903-5 · Cited by 11

A proxy measure of striatal dopamine predicts individual differences in temporal precision

Sadibolova, R., Monaldi, L., & Terhune, D. B. (2022) · Psychonomic Bulletin & Review · doi:10.3758/s13423-022-02077-1 · Cited by 10

Motivational and Valence‐Related Modulation of Sleep/Wake Behavior are Mediated by Midbrain Dopamine and Uncoupled from the Homeostatic and Circadian Processes

Fifel, K., Farissi, A. E., Chérasse, Y., & Yanagisawa, M. (2022) · Advanced Science · doi:10.1002/advs.202200640 · Cited by 9

Individual and Familial Susceptibility to MPTP in a Common Marmoset Model for Parkinson's Disease

Franke, S. K., van Kesteren, R. E., Hofman, S., Wubben, J. A. M., Smit, A. B., & Philippens, I. H. C. H. M. (2016) · Neurodegenerative Diseases · doi:10.1159/000442574 · Cited by 10

Comparison of dopamine release and uptake parameters across sex, species and striatal subregions

Kuiper, L. B., Dawes, M. H., West, A. M., DiMarco, E. K., Galante, E. V., Kishida, K. T., & Jones, S. R. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16495 · Cited by 10

Effects of exercise on mental health in mice with circadian rhythm disruption

He, C., Wakayama, M., Jiang, H., Zhao, T., Zhang, Y., Liu, B., & Moriyama, H. (2025) · Journal of Affective Disorders · doi:10.1016/j.jad.2025.119936 · Cited by 9

Sleep Disturbance in Tourette’s Disorder: Potential Underlying Mechanisms

Ricketts, E. J., Swisher, V. S., Greene, D. J., Silverman, D. H. S., Nofzinger, E. A., & Colwell, C. S. (2023) · Current Sleep Medicine Reports · doi:10.1007/s40675-022-00242-5 · Cited by 10

Chronic methamphetamine uncovers a circadian rhythm in multiple-unit neural activity in the dorsal striatum which is independent of the suprachiasmatic nucleus

Miyazaki, S., Tahara, Y., Colwell, C. S., Block, G. D., Nakamura, W., & Nakamura, T. J. (2021) · Neurobiology of Sleep and Circadian Rhythms · doi:10.1016/j.nbscr.2021.100070 · Cited by 9

Influence of DAT1 Promotor Methylation on Sports Performance

Grzywacz, A., Chmielowiec, K., Boroń, A., Michałowska‐Sawczyn, M., Chmielowiec, J., Trybek, G., Mroczek, B., Leźnicka, K., Cięszczyk, P., & Masiak, J. (2021) · Genes · doi:10.3390/genes12091425 · Cited by 9

Chronic modafinil administration to preadolescent rats impairs social play behavior and dopaminergic system

Cid-Jofré, V., Gárate-Pérez, M. F., Clark, P. J., Valero-Jara, V., España, R. A., Sotomayor‐Zárate, R., Cruz, G., & Renard, G. M. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.108404 · Cited by 8

A common alteration in effort-based decision-making in apathy, anhedonia, and late circadian rhythmPreprint

Mehrhof, S. Z., & Nord, C. L. (2024) · eLife · doi:10.7554/elife.96803 · Cited by 11

Synchrony between midbrain gene transcription and dopamine terminal regulation is modulated by chronic alcohol drinking

Farahbakhsh, Z. Z., Holleran, K. M., Sens, J. P., Fordahl, S. C., Mauterer, M. I., López, A. J., Carlson, V. C. C., Kiraly, D. D., Grant, K. A., Jones, S. R., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-56715-y · Cited by 7

Disrupted circadian rhythms and opioid‐mediated adverse effects: Bidirectional relationship and putative mechanisms

Mehranfard, N., Ghasemi, M., & Saboory, E. (2025) · Journal of Neuroendocrinology · doi:10.1111/jne.70065 · Cited by 7

Brain Chemistry: Neurotransmitters

Berger, S. N., & Hashemi, P. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-409547-2.12682-4 · Cited by 8

Hypothalamic A11 Nuclei Regulate the Circadian Rhythm of Spinal Mechanonociception through Dopamine Receptors and Clock Gene Expression

Piña-Leyva, C., Lara-Lozano, M., Rodríguez-Sánchez, M., Vidal‐Cantú, G. C., Zavalza, E. B., Jiménez‐Estrada, I., Delgado‐Lezama, R., Rodríguez‐Sosa, L., Granados‐Soto, V., González-Barrios, J. A., et al. (2022) · Life · doi:10.3390/life12091411 · Cited by 8

The Dopaminergic System Modulates the Electrophysiological Activity of the Suprachiasmatic Nucleus Dependent on the Circadian Cycle

Mesgar, S., Eskandari, K., Karimian-Sani-Varjovi, H., Salemi-Mokri-Boukani, P., & Haghparast, A. (2023) · Neurochemical Research · doi:10.1007/s11064-023-03988-8 · Cited by 8

Cell-type and sex-specific rhythmic gene expression in the nucleus accumbens

DePoy, L. M., Petersen, K. A., Zong, W., Ketchesin, K. D., Matthaei, R. C., Yin, R., Perez, M. S., Vadnie, C. A., Becker‐Krail, D. D., Scott, M. R., et al. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02569-7 · Cited by 8

Melatonin Modulates Interval Timing in Rats: Effect of Pinealectomy

Bussi, I. L., Levin, G. M., Golombek, D. A., & Agostino, P. V. (2015) · International Journal of Comparative Psychology · doi:10.46867/ijcp.2015.28.02.06 · Cited by 6

An earlier time of scan is associated with greater threat-related amygdala reactivity

Baranger, D. A. A., Margolis, S., Hariri, A. R., & Bogdan, R. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsx057 · Cited by 8

Effect of Dopaminergic Therapy on Impulse Control Disorders in Patients With a Prolactinoma

Varan, E. O., & Gurvit, H. I. (2022) · Cognitive and Behavioral Neurology · doi:10.1097/wnn.0000000000000320 · Cited by 6

Evolution of in vivo dopamine monitoring techniques

Yocky, A. G., & Covey, D. P. (2020) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2020.173078 · Cited by 8

Genes, dopamine pathways, and sociality in primates

French, J. A. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1605972113 · Cited by 6

The Orexin System in Addiction: Neuromodulatory Interactions and Therapeutic Potential

Capó, T., Lillo, J., Rebassa, J. B., Badia, P., Raïch, I., Cubeles-Juberias, E., Reyes‐Resina, I., & Navarro, G. (2025) · Brain Sciences · doi:10.3390/brainsci15101105 · Cited by 6

A mathematical model for the role of dopamine-D2 self-regulation in the production of ultradian rhythms

Zhang, A. Q., Ralph, M. R., & Stinchcombe, A. R. (2024) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1012082 · Cited by 5

Circadian Rhythms and Addiction

Barko, K., Shelton, M. A., Seggio, J. A., & Logan, R. W. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812202-0.00013-0 · Cited by 7

Circadian neuromarkers of mood disorders

Agnorelli, C., & Fagiolini, A. M. (2022) · Journal of Affective Disorders Reports · doi:10.1016/j.jadr.2022.100384 · Cited by 6

Striatal astrocytes modulate behavioral flexibility and whole-body metabolism in mice

Montalban, E., Ansoult, A., Chao, D. H. M., Pham, C., Franco, C., Contini, A., Castel, J., Hassouna, R., Hardonk, M. H., Petitbon, A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60968-y · Cited by 6

Effects of age and sex on photoperiod modulation of nucleus accumbens monoamine content and release in adolescence and adulthood

Jameson, A. N., Siemann, J. K., Grueter, C. A., Grueter, B. A., & McMahon, D. G. (2024) · Neurobiology of Sleep and Circadian Rhythms · doi:10.1016/j.nbscr.2024.100103 · Cited by 4

Associations of sympathetic activation with exposure to volatile organic compounds: A cross-sectional study

Stopforth, C. K., Sears, C. G., Gao, H., Riggs, D. W., Srivastava, S., Krivokhizhina, T. V., Hart, J. L., Walker, K. L., Srivastava, S., Bhatnagar, A., et al. (2025) · Environmental Research · doi:10.1016/j.envres.2025.122451 · Cited by 3

Mathematical modeling of dopamine rhythms and timing of dopamine reuptake inhibitors

Yao, T., & Kim, R. (2025) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1013508 · Cited by 3

The Ins and Outs of Dopamine Transporter Gene Manipulation: In Vivo Models of DAT Dysfunction

Stewart, A., & Blakely, R. (2025) · Advances in neurobiology · doi:10.1007/978-3-031-96364-3_10 · Cited by 3

Fast Scan Cyclic Voltammetry to Assess Dopamine Function: From Circuits to Behavior

Clark, P. J., & España, R. A. (2022) · Neuromethods · doi:10.1007/978-1-0716-2799-0_11 · Cited by 3

Behavioral, Biochemical and Molecular Characterization of a Parkinson’s Disease Mouse Model Using the Neurotoxin 2′-CH3-MPTP: A Novel Approach

Herlinger, A. L., Almeida, A. R., Presti‐Silva, S. M., Pereira, E. V., Andrich, F., Pires, R. G. W., & Martins-Silva, C. (2018) · NeuroMolecular Medicine · doi:10.1007/s12017-018-8476-z · Cited by 3

How Psychoactive Drugs and the Circadian Clock Are Enlightening One Another

Engmann, O. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-81147-1_8 · Cited by 3

Melatonin Receptors as Modulators of Methamphetamine-Mediated Behaviors

Clough, S. J., Hutchinson, A. J., & Dubocovich, M. L. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-800212-4.00016-9 · Cited by 3

Nurr1 deficiency shortens free running period, enhances photoentrainment to phase advance, and disrupts circadian cycling of the dopamine neuron phenotype

Partington, H. S., Nutter, J. M., & Eells, J. B. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113347 · Cited by 5

Increased Activity of Tyrosine Hydroxylase Leads to Elevated Amphetamine Response and Markers of Oxidative Stress in Transgenic MicePreprint

Vecchio, L. M., Bermejo, M. K., Dunn, A. R., Milenkovic, M., Urs, N. M., Ramsey, A. J., Miller, G. W., & Salahpour, A. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/188318 · Cited by 3

Overlapping effects of neuropsychiatric symptoms and circadian rhythm on effort-based decision-makingPreprint

Mehrhof, S. Z., & Nord, C. L. (2024) · eLife · doi:10.7554/elife.96803.1 · Cited by 3

The molecular clock drives motivated locomotion and time-of-day-dependent firing patterns in mouse dopaminergic neurons

Swaroop, A., Paul, J. R., McMeekin, L. J., Barnett, A. M., Colafrancesco, A. M., Russell, D. L., Smith, C. M., Simmons, M. S., Volpicelli‐Daley, L. A., Cowell, R. M., et al. (2025) · npj Biological Timing and Sleep · doi:10.1038/s44323-025-00044-2 · Cited by 3

Computational modelling identifies key determinants of subregion-specific dopamine dynamics in the striatum

Ejdrup, A. L., Dreyer, J. K., Lycas, M. D., Jørgensen, S. H., Robbins, T. W., Dalley, J. W., Herborg, F., & Gether, U. (2026) · eLife · doi:10.7554/elife.105214.3 · Cited by 2

Seeing how we smell

Benveniste, H., Lazebnik, Y. A., & Volkow, N. D. (2017) · Journal of Clinical Investigation · doi:10.1172/jci91305 · Cited by 2

Analysis of membrane transport mechanisms of endogenous substrates using chromatographic techniques

Yamaguchi, H., & Mano, N. (2019) · Biomedical Chromatography · doi:10.1002/bmc.4495 · Cited by 2

Long-term effects of adolescent versus adult nicotine self-administration on cholinergic modulation of dopamine in the nucleus accumbens core

Iacino, M. C., Pitts, E. G., Bonsib, A. G., Sexton, L. L., & Ferris, M. J. (2025) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2025.112555 · Cited by 1

Circadian rhythm homeostasis biomarkers: current landscape and emerging frontiers

Li, S., Zhang, C., Lin, Y., & Wang, S. (2025) · Oral Science and Homeostatic Medicine · doi:10.26599/oshm.2025.9610028 · Cited by 1

Sleep in tic disorders and Tourette syndrome

Mingolla, G. P., Vico, I. A. D., & Antelmi, E. (2026) · Handbook of clinical neurology · doi:10.1016/b978-0-443-13554-5.00006-7 · Cited by 1

Zwitterionic Polymer Coating Enabled Chronic Dopamine Sensing and Electrophysiology Recording in Free‐Moving Mice

Wu, B., Thompson, C. H., Deakin, T. P., Xu, Y., McClung, C. A., & Cui, X. T. (2026) · Advanced Healthcare Materials · doi:10.1002/adhm.71688 · Cited by 1

Tonic dopamine sensing reveals a D2 and D3-mediated dopamine response to raclopride in ClockΔ19 mice model

Wu, B., Castagnola, E., Robbins, E. M., Kaminsky, M., Sanker, S., McClung, C. A., & Cui, X. T. (2026) · npj Biosensing · doi:10.1038/s44328-026-00095-w · Cited by 2

Mitochondria-centered neuroenergetic dysfunction in treatment-resistant depression: A conceptual framework for multi-layer nutritional modulation and serum BDNF as a biomarker of systemic recovery

Zhang, R. H. (2026) · Nutritional Psychiatry · doi:10.1016/j.nupsyc.2026.100024

Dopamine tone depends on DAT

Bray, N. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3792 · Cited by 1

Hypothalamic A11 Nuclei Regulate the Circadian Rhythm of the Mechanonociception and the Spinal Clock Gene Transcription through Dopamine Receptor ActivationPreprint

Piña-Leyva, C., Lara-Lozano, M., Rodríguez-Sánchez, M., Vidal‐Cantú, G. C., Zavalza-Barrientos, E., Jiménez‐Estrada, I., Delgado‐Lezama, R., Rodríguez‐Sosa, L., Granados‐Soto, V., Florán, B., et al. (2020) · Preprints.org · doi:10.20944/preprints202009.0188.v1 · Cited by 1

Neuroinflammation, sleep, and autoimmune disease

Zielinski, M. R., & Gibbons, A. J. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-822963-7.00312-1 · Cited by 1

Tonic Dopamine Sensing Reveals a D2/D3 Mediated Dopamine Response to Raclopride in ClockΔ19 Mice ModelPreprint

Wu, B., Castagnola, E., Robbins, E. M., Kaminsky, M., Sanker, S., McClung, C. A., & Cui, X. T. (2025) · Research Square · doi:10.21203/rs.3.rs-7403119/v1 · Cited by 1

Circadian food anticipation in dopamine-1 receptor knockout mice

Michalik, M. J. (2015) · Summit (Simon Fraser University)

Circadian Mechanisms Underlying

Neurophysiology, R.-R., & McClung, C. A. (2016)

Intracerebroventricular administration of dopamine in Parkinson's disease: treatment of motor fluctuations and dyskinesia

Laloux, C., Lachaud, C., Moreau, C., Fisichella, M., Devedjian, J.-C., Duce, J. A., & Devos, D. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-815946-0.00030-2

Neurobehavioral Impact of Disease-Associated Variation in the Dopamine Transporter

Davis, G. L. (2017)

Timing in psychiatry: exploring resonance in biological systems for treatment of mental disorders.Preprint

Argôlo, F. C., Garcia‐Dias, R., Pan, P. M., Gadelha, A., Quarantini, L. D. C., & Bressan, R. A. (2020) · PsyArXiv (OSF Preprints) · doi:10.31234/osf.io/84ndb · Cited by 1

No association of Brain-derived neurotrophic factor with striatal dopamine transporter availability in healthy subjects

Nam, H., Seo, S., Lee, M. J., Kim, K., Kim, I. J., & Pak, K. (2021) · Nuklearmedizin - NuclearMedicine · doi:10.1055/a-1521-8572

小形ノーマルモードヘリカルアンテナの設計法と性能 (ワイヤレスシステムを支える技術を融合するアンテナ・伝搬技術論文特集)

山田, 吉., & 道下, 尚. (2013) · 電子情報通信学会論文誌. B, 通信

Neurochemistry of sleep

Alonso, I. P., & España, R. A. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822963-7.00166-3

Faculty Opinions recommendation of NAD+ cellular redox and SIRT1 regulate the diurnal rhythms of tyrosine hydroxylase and conditioned cocaine reward.

Karatsoreos, I. N. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733181688.793564070

Chronically elevated corticosterone impairs dopaminergic transmission in the dorsomedial striatum by sex-divergent mechanismsPreprint

Holloway, A. L., Schaid, M. D., & Lerner, T. N. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.03.510627

A common alteration in effort-based decision-making in apathy, anhedonia, and late circadian rhythm

Mehrhof, S. Z., & Nord, C. L. (2025) · eLife · doi:10.31234/osf.io/z69w4

Système de récompense et rythmes biologiques

Tebeka, S., Mauries, S., & Geoffroy, P. A. (2023) · Elsevier eBooks · doi:10.1016/b978-2-294-77934-3.00009-3 · Cited by 1

Circadian clock in the lateral habenula affects motor function in mice through the regulation of daily rhythms in the nigrostriatal pathwayPreprint

Goldfarb, C., Baharav, N., Jiang, H., Szubinski, A., Amir, S., & Schöttner, K. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.17.608401

Both neuropsychiatric symptoms and circadian rhythm alter effort-based decision-makingPreprint

Mehrhof, S. Z., & Nord, C. L. (2024) · eLife · doi:10.7554/elife.96803.2 · Cited by 1

A common alteration in effort-based decision-making in apathy, anhedonia, and late circadian rhythmPreprint

Mehrhof, S. Z., & Nord, C. L. (2024) · eLife · doi:10.7554/elife.96803.3 · Cited by 1

Overexpression of α–synuclein in Midbrain Dopamine Neurons Reduces Dopamine Release Without Cell Loss and Drives Mild Motor Deficits in MicePreprint

Barcomb, K., Hsiao, J.-H. T., Lemak, J., Zhuang, X., Coutant, B., Yanez, A., Behal, A., Fu, Y., Lerner, T. N., Nakamura, K., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.17.643840

Identification of photoperiod as a regulator of dopamine-mediated behavior in female mice

Kassaye, B. B., Jameson, A. N., Moore, K., McMahon, D. G., & Grueter, B. A. (2025) · Neurobiology of Sleep and Circadian Rhythms · doi:10.1016/j.nbscr.2025.100135

Restoration of Rapid-Eye Movement Sleep During Cocaine Abstinence Reduces Incubation of Cocaine Seeking and Normalizes Dopamine Transporter FunctionPreprint

Alonso, I. P., Cohen, S. R., Migovich, V. M., & España, R. A. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.12.697196

Palatable food, clock genes and the reward circuitry

Blancas‐Velazquez, A. S. (2018) · theses.fr (ABES) · doi:10.70675/bad46fd4zc72az43cbz991dzc3345213a608

Etude du rôle des altérations des cycles éveil/sommeil dans la progression de la maladie de Parkinson et de l'atrophie multisystématisée

Persillet, M. (2021) · theses.fr (ABES) · doi:10.70675/2e71b554zc94dz40b3za63bz7a6591d0daaf

Régulation du sommeil paradoxal en condition de stress : implication des projections corticales au noyau préoptique ventrolatéral

Chouvaeff, M. (2024) · theses.fr (ABES) · doi:10.70675/53bed38fz9683z4dd1z9e02zce298e901929

Circadian modulation of spontaneous dopamine release shapes reward-evoked signaling in the nucleus accumbensPreprint

Cook, J. N., GEVORGYAN, M., Armitage, J., & Jones, J. R. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.04.22.720003

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