The brain’s reward system in health and disease

Ghrelin induces adiposity in rodents

Tschöp, M., Smiley, D. L., & Heiman, M. L. (2000) · Nature · doi:10.1038/35038090 · Cited by 3,949 · see citing works

Anorexigenic and Orexigenic Hormone Modulation of Mammalian Target of Rapamycin Complex 1 Activity and the Regulation of Hypothalamic Agouti-Related Protein mRNA Expression

Watterson, K. R., Bestow, D., Gallagher, J. R., Hamilton, D. L., Ashford, F. B., Meakin, P. J., & Ashford, M. L. J. (2012) · Neurosignals · doi:10.1159/000334144 · Cited by 3,395 · see citing works

Molecular Bases for Circadian Clocks

Dunlap, J. C. (1999) · Cell · doi:10.1016/s0092-8674(00)80566-8 · Cited by 2,900 · see citing works

Obesity and Metabolic Syndrome in Circadian <i>Clock</i> Mutant Mice

Turek, F. W., Joshu, C., Kohsaka, A., Lin, E., Ivanova, G., McDearmon, E., Laposky, A., Losee-Olson, S., Easton, A., Jensen, D. R., et al. (2005) · Science · doi:10.1126/science.1108750 · Cited by 2,485 · see citing works

Neurobiologic advances from the brain disease model of addiction

Volkow, N. D., Koob, G. F., & McLellan, A. T. (2016) · New England Journal of Medicine · doi:10.1056/nejmra1511480 · Cited by 2,008 · see citing works

Brain dopamine and obesity

Wang, G.-J., Volkow, N. D., Logan, J., Pappas, N. R., Wong, C. T., Zhu, W., Netusll, N., & Fowler, J. S. (2001) · The Lancet · doi:10.1016/s0140-6736(00)03643-6 · Cited by 1,864 · see citing works

The incentive sensitization theory of addiction: some current issues

Robinson, T. E., & Berridge, K. C. (2008) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2008.0093 · Cited by 1,717 · see citing works

Interacting Appetite-Regulating Pathways in the Hypothalamic Regulation of Body Weight

Kalra, S. P., Dube, M. G., Pu, S., Xu, B., Horváth, T. L., & Kalra, P. S. (1999) · Endocrine Reviews · doi:10.1210/edrv.20.1.0357 · Cited by 1,556 · see citing works

Relationship of smartphone use severity with sleep quality, depression, and anxiety in university students

Demirci, K., Akgönül, M., & Akpinar, A. (2015) · Journal of Behavioral Addictions · doi:10.1556/2006.4.2015.010 · Cited by 1,529 · see citing works

Dopamine D2 receptors in addiction-like reward dysfunction and compulsive eating in obese rats

Johnson, P. M., & Kenny, P. J. (2010) · Nature Neuroscience · doi:10.1038/nn.2519 · Cited by 1,495 · see citing works

The role of leptin and ghrelin in the regulation of food intake and body weight in humans: a review

Klok, M. D., Jakobsdottir, S., & Drent, M. L. (2007) · Obesity Reviews · doi:10.1111/j.1467-789x.2006.00270.x · Cited by 1,442 · see citing works

The Role of the Dorsal Striatum in Reward and Decision-Making: Figure 1.

Balleine, B. W., Delgado, M. R., & Hikosaka, O. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1554-07.2007 · Cited by 1,390 · see citing works

Neurobehavioural mechanisms of reward and motivation

Robbins, T. W., & Everitt, B. J. (1996) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(96)80077-8 · Cited by 1,187 · see citing works

Theory and measurement of generalized problematic internet use : A two-step approach

Caplan, S. E. (2010) · Computers in Human Behavior · doi:10.1016/j.chb.2010.03.012 · Cited by 1,061 · see citing works

Modeling habitual and addictive smartphone behavior

van Deursen, A. J. A. M., Bolle, C. L., Hegner, S. M., & Kommers, P. A. M. (2015) · Computers in Human Behavior · doi:10.1016/j.chb.2014.12.039 · Cited by 1,031 · see citing works

Ghrelin modulates the activity and synaptic input organization of midbrain dopamine neurons while promoting appetite

Abizaid, A., Liu, Z.-W., Andrews, Z. B., Shanabrough, M., Borok, E., Elsworth, J. D., Roth, R. H., Sleeman, M. W., Picciotto, M. R., Tschöp, M. H., et al. (2006) · Journal of Clinical Investigation · doi:10.1172/jci29867 · Cited by 984 · see citing works

Adolescents’ electronic media use at night, sleep disturbance, and depressive symptoms in the smartphone age

Lemola, S., Perkinson-Gloor, N., Brand, S., Dewald-Kaufmann, J. F., & Grob, A. (2015) · Journal of Youth and Adolescence · doi:10.1007/s10964-014-0176-x · Cited by 940 · see citing works

Peroxiredoxins are conserved markers of circadian rhythms

Edgar, R. S., Green, E. W., Zhao, Y., Gerben Van Ooijen, A., Olmedo, M., Qin, X., Xu, Y. Q., Pan, M., Valekunja, U. K., Feeney, K. A., et al. (2012) · Nature · doi:10.1038/nature11088 · Cited by 915 · see citing works

Circadian food-anticipatory activity: Formal models and physiological mechanisms

Mistlberger, R. E. (1994) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(94)90023-x · Cited by 857 · see citing works

Processing of Social and Monetary Rewards in the Human Striatum

Izuma, K., Saito, D. N., & Sadato, N. (2008) · Neuron · doi:10.1016/j.neuron.2008.03.020 · Cited by 855 · 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

Effects of light on human circadian rhythms, sleep and mood

Blume, C., Garbazza, C., & Spitschan, M. (2019) · Somnologie · doi:10.1007/s11818-019-00215-x · Cited by 695 · cited 1× · see citing works

The structure of the caudate nucleus of the cat: light and electron microscopy

Kemp, J. M., & Powell, T. P. S. (1971) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1971.0102 · Cited by 672 · see citing works

Sexual motivation: a neural and behavioural analysis of the mechanisms underlying appetitive and copulatory responses of male rats

Everitt, B. J. (1990) · Neuroscience &amp; Biobehavioral Reviews · doi:10.1016/s0149-7634(05)80222-2 · Cited by 650 · see citing works

Feeding-induced dopamine release in dorsal striatum correlates with meal pleasantness ratings in healthy human volunteers

Small, D. M., Jones-Gotman, M., & Dagher, A. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00253-2 · Cited by 632 · see citing works

Food reward and cocaine increase extracellular dopamine in the nucleus accumbens as measured by microdialysis

Hernandez, L., & Hoebel, B. G. (1988) · Life Sciences · doi:10.1016/0024-3205(88)90036-7 · Cited by 627 · see citing works

Reward deficiency syndrome: genetic aspects of behavioral disorders

Comings, D. E., & Blum, K. (2000) · Progress in Brain Research · doi:10.1016/s0079-6123(00)26022-6 · Cited by 621 · see citing works

Intense Sweetness Surpasses Cocaine Reward

Lenoir, M., Serre, F., Cantin, L., & Ahmed, S. H. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000698 · Cited by 608 · see citing works

Daily bingeing on sugar repeatedly releases dopamine in the accumbens shell

Rada, P. V., Avena, N. M., & Hoebel, B. G. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.04.043 · Cited by 542 · see citing works

Addiction: Decreased reward sensitivity and increased expectation sensitivity conspire to overwhelm the brain's control circuit

Volkow, N. D., Wang, G., Fowler, J. S., Tomasi, D., Telang, F., & Baler, R. (2010) · BioEssays · doi:10.1002/bies.201000042 · Cited by 532 · see citing works

Food and Drug Reward: Overlapping Circuits in Human Obesity and Addiction

Volkow, N. D., Wang, G. J., Fowler, J. S., Tomasi, D., & Baler, R. (2011) · Current Topics in Behavioral Neurosciences · doi:10.1007/7854_2011_169 · Cited by 525 · see citing works

Regulation of dopaminergic transmission and cocaine reward by the <i>Clock</i> gene

McClung, C. A., Sidiropoulou, K., Vitaterna, M., Takahashi, J. S., White, F. J., Cooper, D. C., & Nestler, E. J. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0503584102 · Cited by 493 · see citing works

Expression of receptors for insulin and leptin in the ventral tegmental area/substantia nigra (VTA/SN) of the rat

Figlewicz, D. P., Evans, S. B., Murphy, J., Hoen, M., & Baskin, D. G. (2003) · Brain Research · doi:10.1016/s0006-8993(02)04087-8 · Cited by 482 · see citing works

Expression of muscarinic acetylcholine and dopamine receptor mRNAs in rat basal ganglia.

Weiner, D. M., Levey, A. I., & Brann, M. R. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.18.7050 · Cited by 481 · see citing works

Metabolic Consequences of Sleep and Circadian Disorders

Depner, C. M., Stothard, E. R., & Wright, K. P. (2014) · Current Diabetes Reports · doi:10.1007/s11892-014-0507-z · Cited by 481 · see citing works

Cocaine sensitization and reward are under the influence of circadian genes and rhythm

Abarca, C., Albrecht, U., & Spanagel, R. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.142039099 · Cited by 472 · see citing works

Genetic deletion of ghrelin does not decrease food intake but influences metabolic fuel preference

Wortley, K. E., Anderson, K. D., García, K., Murray, J. D., Malinova, L., Liu, R., Moncrieffe, M., Thabet, K., Cox, H. J., Yancopoulos, G. D., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402763101 · Cited by 471 · see citing works

Dopamine and sexual behavior

Melis, M. R., & Argiolas, A. (1995) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(94)00020-2 · Cited by 428 · see citing works

Regulation of Monoamine Oxidase A by Circadian-Clock Components Implies Clock Influence on Mood

Hampp, G., Ripperger, J. A., Houben, T., Schmutz, I., Blex, C., Perreau‐Lenz, S., Brunk, I., Spanagel, R., Ahnert‐Hilger, G., Meijer, J. H., et al. (2008) · Current Biology · doi:10.1016/j.cub.2008.04.012 · Cited by 419 · see citing works

Ghrelin directly interacts with neuropeptide-Y-containing neurons in the rat arcuate nucleus: Ca2+ signaling via protein kinase A and N-type channel-dependent mechanisms and cross-talk with leptin and orexin.

Kohno, D., Gao, H.-Z., Muroya, S., Kikuyama, S., & Yada, T. (2003) · Diabetes · doi:10.2337/diabetes.52.4.948 · Cited by 390 · see citing works

Neuropharmacological Mechanisms of Drug Reward: Beyond Dopamine in the Nucleus Accumbens

Bardo, M. T. (1998) · Critical Reviews in Neurobiology · doi:10.1615/critrevneurobiol.v12.i1-2.30 · Cited by 383 · see citing works

Distinct Roles of GABAergic Interneurons in the Regulation of Striatal Output Pathways

Gittis, A. H., Nelson, A., Thwin, M. T., Palop, J. J., & Kreitzer, A. C. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4870-09.2010 · Cited by 364 · see citing works

Dopamine Production in the Caudate Putamen Restores Feeding in Dopamine-Deficient Mice

Szczypka, M. S., Kwok, K., Brot, M. D., Marck, B. T., Matsumoto, A. M., Donahue, B. A., & Palmiter, R. D. (2001) · Neuron · doi:10.1016/s0896-6273(01)00319-1 · Cited by 354 · see citing works

Blue light from light-emitting diodes elicits a dose-dependent suppression of melatonin in humans

West, K., Jablonski, M., Warfield, B., Cecil, K. S., James, M. E., Ayers, M. A., Maida, J. C., Bowen, C. K., Sliney, D. H., Rollag, M. D., et al. (2010) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01413.2009 · Cited by 344 · see citing works

The Time of Day of Food Intake Influences Overall Intake in Humans

de Castro, J. M. (2004) · The Journal of Nutrition · doi:10.1093/jn/134.1.104 · Cited by 329 · see citing works

The frequency and distribution of medium-sized neurons with indented nuclei in the primate and rodent neostriatum

Graveland, G. A., & DiFiglia, M. (1985) · Brain Research · doi:10.1016/0006-8993(85)91524-0 · Cited by 323 · see citing works

The Association Between Use of Electronic Media in Bed Before Going to Sleep and Insomnia Symptoms, Daytime Sleepiness, Morningness, and Chronotype

Fossum, I. N., Nordnes, L. T., Storemark, S. S., Bjorvatn, B., & Pallesen, S. (2013) · Behavioral Sleep Medicine · doi:10.1080/15402002.2013.819468 · Cited by 307 · see citing works

Dopamine D1-like Receptors and Reward-related Incentive Learning

Beninger, R. J. (1998) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(97)00019-5 · Cited by 299 · see citing works

Impact of Circadian Nuclear Receptor REV-ERBα on Midbrain Dopamine Production and Mood Regulation

Chung, S., Lee, E. J., Yun, S., Choe, H. K., Park, S., Son, H. J., Kim, K., Dluzen, D. E., Lee, I., Hwang, O., et al. (2014) · Cell · doi:10.1016/j.cell.2014.03.039 · Cited by 298 · see citing works

The internal circadian clock increases hunger and appetite in the evening independent of food intake and other behaviors

Scheer, F. A. J. L., Morris, C. J., & Shea, S. A. (2013) · Obesity · doi:10.1002/oby.20351 · Cited by 296 · see citing works

Behavioral characterization of neuropeptide Y knockout mice

Bannon, A. W., Seda, J., Carmouché, M., Francis, J. M., Norman, M. H., Karbon, B., & McCaleb, M. L. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02285-x · Cited by 288 · see citing works

Effect of Fasting, Refeeding, and Dietary Fat Restriction on Plasma Leptin Levels

Weigle, D. S. (1997) · Journal of Clinical Endocrinology &amp; Metabolism · doi:10.1210/jc.82.2.561 · Cited by 287 · see citing works

Neurotransmitters in key neurons of the hypothalamus that regulate feeding behavior and body weight

Meister, B. (2007) · Physiology & Behavior · doi:10.1016/j.physbeh.2007.05.021 · Cited by 284 · see citing works

Circadian rhythms of dopamine, glutamate and GABA in the striatum and nucleus accumbens of the awake rat: modulation by light

Castañeda, T. R., de Prado, B. M., Prieto, D., & Mora, F. (2004) · Journal of Pineal Research · doi:10.1046/j.1600-079x.2003.00114.x · Cited by 276 · see citing works

Chronotype and psychiatric disorders

Kivelä, L., Papadopoulos, M. R., & Antypa, N. (2018) · Current Sleep Medicine Reports · doi:10.1007/s40675-018-0113-8 · Cited by 273 · see citing works

Pineal Melatonin Rhythm: Reduction in Aging Syrian Hamsters

Reiter, R. J., Richardson, B. A., Johnson, L. Y., Ferguson, B. N., & Dinh, D. T. (1980) · Science · doi:10.1126/science.7434032 · Cited by 251 · see citing works

Endogenous Dopamine Regulates the Rhythm of Expression of the Clock Protein PER2 in the Rat Dorsal Striatum via Daily Activation of D₂Dopamine Receptors

Hood, S., Cassidy, P., Cossette, M.-P., Weigl, Y., Verwey, M., Robinson, B., Stewart, J., & Amir, S. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.2128-10.2010 · Cited by 246 · see citing works

From ventral-medial to dorsal-lateral striatum: neural correlates of reward-guided decision-making

Burton, A. C., Nakamura, K., & Roesch, M. R. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.05.003 · Cited by 238 · see citing works

Evening types are prone to depression

Merikanto, I., Lahti, T., Kronholm, E., Peltonen, M., Laatikainen, T., Vartiainen, E., Salomaa, V., & Partonen, T. (2013) · Chronobiology International · doi:10.3109/07420528.2013.784770 · Cited by 237 · see citing works

Daily rhythms of food-anticipatory behavioral activity do not require the known circadian clock

Storch, K.-F., & Weitz, C. J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0902063106 · Cited by 222 · see citing works

Homeostatic reinforcement learning for integrating reward collection and physiological stability

Keramati, M., & Gutkin, B. (2014) · eLife · doi:10.7554/elife.04811 · Cited by 218 · see citing works

A universal role of the ventral striatum in reward-based learning: Evidence from human studies

Daniel, R., & Pollmann, S. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.05.002 · Cited by 209 · see citing works

The role of dopamine in the nucleus accumbens and striatum during sexual behavior in the female rat

Becker, J. B., Rudick, C. N., & Jenkins, W. J. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-09-03236.2001 · Cited by 206 · see citing works

Leptin Modulates the Intrinsic Excitability of AgRP/NPY Neurons in the Arcuate Nucleus of the Hypothalamus

Baver, S. B., Hope, K., Guyot, S., Bjørbaek, C., Kaczorowski, C., & O'Connell, K. M. S. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.4861-12.2014 · Cited by 203 · see citing works

Dorsal Striatal Circuits for Habits, Compulsions and Addictions

Lipton, D. M., Gonzales, B. J., & Citri, A. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2019.00028 · Cited by 197 · see citing works

Impact of Sleep and Circadian Rhythms on Addiction Vulnerability in Adolescents

Logan, R. W., Hasler, B. P., Forbes, E. E., Franzen, P. L., Torregrossa, M. M., Huang, Y. H., Buysse, D. J., Clark, D. B., & McClung, C. A. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.11.035 · Cited by 194 · see citing works

Dopamine transporters govern diurnal variation in extracellular dopamine tone

Ferris, M. J., España, R. A., Locke, J. L., Konstantopoulos, J. K., Rose, J. H., Chen, R., & Jones, S. R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1407935111 · Cited by 192 · see citing works

Striatal microcircuitry and movement disorders

Gittis, A. H., & Kreitzer, A. C. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.06.008 · Cited by 188 · see citing works

Circadian rhythms of dopamine in mouse retina: The role of melatonin

Doyle, S. E., Grace, M. S., McIvor, W. E., & Menaker, M. (2002) · Visual Neuroscience · doi:10.1017/s0952523802195058 · Cited by 182 · see citing works

The circadian clock of CD8 T cells modulates their early response to vaccination and the rhythmicity of related signaling pathways

Nobis, C. C., Laramée, G. D., Kervezee, L., Sousa, D. M. D., Labrecque, N., & Cermakian, N. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1905080116 · Cited by 180 · see citing works

Sexual Behavior and Sex-Associated Environmental Cues Activate the Mesolimbic System in Male Rats

Balfour, M. E., Yu, L., & Coolen, L. M. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300350 · Cited by 177 · see citing works

Environmental enrichment during early stages of life reduces the behavioral, neurochemical, and molecular effects of cocaine

Solinas, M., Thiriet, N., Rawas, R. E., Lardeux, V., & Jaber, M. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2008.51 · Cited by 175 · see citing works

The clock gene, brain and muscle Arnt‐like 1, regulates adipogenesis via Wnt signaling pathway

Guo, B., Chatterjee, S., Li, L., Kim, J. M., Lee, J., Yechoor, V. K., Minze, L. J., Hsueh, W. A., & Ma, K. (2012) · The FASEB Journal · doi:10.1096/fj.12-205781 · Cited by 168 · see citing works

Consequences of Circadian Disruption on Cardiometabolic Health

Reutrakul, S., & Knutson, K. L. (2015) · Sleep Medicine Clinics · doi:10.1016/j.jsmc.2015.07.005 · Cited by 163 · see citing works

Physiological responses to food intake throughout the day

Johnston, J. D. (2014) · Nutrition Research Reviews · doi:10.1017/s0954422414000055 · Cited by 158 · see citing works

Circuit projection from suprachiasmatic nucleus to ventral tegmental area: a novel circadian output pathway

Luo, A. H., & Aston‐Jones, G. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06606.x · Cited by 154 · see citing works

Obesity-driven synaptic remodeling affects endocannabinoid control of orexinergic neurons

Cristino, L., Busetto, G., Imperatore, R., Ferrandino, I., Palomba, L., Silvestri, C., Petrosino, S., Orlando, P., Bentivoglio, M., Mackie, K., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1219485110 · Cited by 143 · see citing works

Dopamine receptor-mediated regulation of neuronal “clock” gene expression

Imbesi, M., Yildiz, S., Arslan, A. D., Sharma, R., Manev, H., & Uz, T. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.10.044 · Cited by 141 · see citing works

Direct Midbrain Dopamine Input to the Suprachiasmatic Nucleus Accelerates Circadian Entrainment

Grippo, R. M., Purohit, A. M., Zhang, Q., Zweifel, L. S., & Güler, A. D. (2017) · Current Biology · doi:10.1016/j.cub.2017.06.084 · Cited by 140 · see citing works

Quantitative microdialysis of dopamine in the striatum: effect of circadian variation

Smith, A. D., Olson, R. J., & Justice, J. B. (1992) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(92)90111-p · Cited by 135 · see citing works

Circadian clock genes: Effects on dopamine, reward and addiction

Parekh, P. K., Ozburn, A. R., & McClung, C. A. (2015) · Alcohol · doi:10.1016/j.alcohol.2014.09.034 · Cited by 132 · see citing works

Diurnal Variations in Natural and Drug Reward, Mesolimbic Tyrosine Hydroxylase, and Clock Gene Expression in the Male Rat

Webb, I. C., Baltazar, R. M., Wang, X., Pitchers, K. K., Coolen, L. M., & Lehman, M. N. (2009) · Journal of Biological Rhythms · doi:10.1177/0748730409346657 · Cited by 130 · see citing works

Enhanced GABA Transmission Drives Bradykinesia Following Loss of Dopamine D2 Receptor Signaling

Lemos, J. C., Friend, D. M., Kaplan, A. R., Shin, J. H., Rubinstein, M., Kravitz, A. V., & Alvarez, V. A. (2016) · Neuron · doi:10.1016/j.neuron.2016.04.040 · Cited by 130 · see citing works

Circadian insights into dopamine mechanisms

Mendoza, J., & Challet, É. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.07.081 · Cited by 124 · see citing works

Role of core circadian clock genes in hormone release and target tissue sensitivity in the reproductive axis

Sen, A., & Hoffmann, H. M. (2019) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2019.110655 · Cited by 123 · see citing works

Obesity – A neuropsychological disease? Systematic review and neuropsychological model

Jauch‐Chara, K., & Oltmanns, K. M. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.12.001 · Cited by 121 · see citing works

The Pineal Gland is Critical for Circadian Period1 Expression in the Striatum and for Circadian Cocaine Sensitization in Mice

Uz, T., Akhisaroğlu, M., Ahmed, R., & Manev, H. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300254 · Cited by 117 · see citing works

Parkinsonism Driven by Antipsychotics Originates from Dopaminergic Control of Striatal Cholinergic Interneurons

Kharkwal, G., Brami‐Cherrier, K., Lizardi-Ortiz, J. E., Nelson, A., Ramos, M., Barrio, D. D., Sulzer, D. L., Kreitzer, A. C., & Borrelli, E. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.014 · Cited by 113 · see citing works

Dynamics of rapid dopamine release in the nucleus accumbens during goal-directed behaviors for cocaine versus natural rewards

Cameron, C. M., Wightman, R. M., & Carelli, R. M. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.08.006 · Cited by 109 · see citing works

Prolonged High Fat Diet Reduces Dopamine Reuptake without Altering DAT Gene Expression

Cone, J. J., Chartoff, E. H., Potter, D. N., Ebner, S. R., & Roitman, M. F. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058251 · Cited by 108 · see citing works

Individual vulnerability to addiction

Swendsen, J. D., & Moal, M. L. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05894.x · Cited by 106 · see citing works

Sensitized Increase of Period Gene Expression in the Mouse Caudate/Putamen Caused by Repeated Injection of Methamphetamine

Nikaido, T., Akiyama, M., Moriya, T., & Shibata, S. (2001) · Molecular Pharmacology · doi:10.1124/mol.59.4.894 · Cited by 102 · see citing works

Effect of meal frequency and timing on physical performance

Hawley, J. A., & Burke, L. M. (1997) · British Journal of Nutrition · doi:10.1079/bjn19970107 · Cited by 99 · see citing works

Chronobiological Influence Over Cardiovascular Function

Rana, S., Prabhu, S. D., & Young, M. E. (2020) · Circulation Research · doi:10.1161/circresaha.119.313349 · Cited by 99 · see citing works

Dopamine receptor 1 neurons in the dorsal striatum regulate food anticipatory circadian activity rhythms in mice

Gallardo, C. M., Darvas, M., Oviatt, M., Chang, C. H., Michalik, M. J., Huddy, T. F., Meyer, E. E., Shuster, S. A., Aguayo, A., Hill, E. M., et al. (2014) · eLife · doi:10.7554/elife.03781 · Cited by 98 · see citing works

Definition of the developmental transition from dopaminergic to photic regulation of c-fos gene expression in the rat suprachiasmatic nucleus

Weaver, D. R., & Reppert, S. M. (1995) · Molecular Brain Research · doi:10.1016/0169-328x(95)00117-b · Cited by 94 · see citing works

Clock Genes and the Long‐Term Regulation of Prolactin Secretion: Evidence for a Photoperiod/Circannual Timer in the Pars Tuberalis

Lincoln, G. A., Andersson, H., & Hazlerigg, D. G. (2003) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2003.00990.x · Cited by 92 · see citing works

Social interactions impact on the dopaminergic system and drive individuality

Torquet, N., Marti, F., Campart, C., Tolu, S., Nguyen, C., Oberto, V. J., Benallaoua, M., Naudé, J., Didienne, S., Debray, N., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05526-5 · Cited by 88 · see citing works

Gene profiling the response to repeated cocaine self-administration in dorsal striatum: A focus on circadian genes

Lynch, W. J., Girgenti, M. J., Breslin, F. J., Newton, S. S., & Taylor, J. R. (2008) · Brain Research · doi:10.1016/j.brainres.2008.02.106 · Cited by 87 · see citing works

Cocaine self-administration behaviors in ClockΔ19 mice

Ozburn, A. R., Larson, E. B., Self, D. W., & McClung, C. A. (2012) · Psychopharmacology · doi:10.1007/s00213-012-2704-2 · Cited by 85 · see citing works

Measuring Television Addiction

Horvath, C. W. (2004) · Journal of Broadcasting & Electronic Media · doi:10.1207/s15506878jobem4803_3 · Cited by 82 · see citing works

Department of Defense influenza and other respiratory disease surveillance during the 2009 pandemic

Burke, R. L., Vest, K. G., Eick, A. A., Sánchez, J. L., Johns, M. C., Pavlin, J. A., Jarman, R. G., Mothershead, J. L., Quintana, M., Palys, T. J., et al. (2011) · BMC Public Health · doi:10.1186/1471-2458-11-s2-s6 · Cited by 81 · see citing works

Effects of cocaine on extracellular dopamine and serotonin levels in the nucleus accumbens

Andrews, C. M., & Lucki, I. (2001) · Psychopharmacology · doi:10.1007/s002130100704 · Cited by 81 · see citing works

Neural basis of reward and craving - a homeostatic point of view

Paulus, M. P. (2007) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2007.9.4/mpaulus · Cited by 79 · see citing works

Meal Timing in Humans during Isolation without Time Cues

Aschoff, J., von Goetz, C., Wildgruber, C., & Wever, R. A. (1986) · Journal of Biological Rhythms · doi:10.1177/074873048600100206 · Cited by 75 · see citing works

PER1 Phosphorylation Specifies Feeding Rhythm in Mice

Liu, Z., Huang, M., Wu, X., Shi, G., Xing, L., Dong, Z., Qu, Z., Yan, J., Yang, L., Panda, S., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.04.032 · Cited by 73 · see citing works

The circadian Per1 and Per2 genes influence alcohol intake, reinforcement, and blood alcohol levels

Gamsby, J. J., Templeton, E. L., Bonvini, L., Wang, W., Loros, J., Dunlap, J., Green, A. I., & Gulick, D. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.04.016 · Cited by 72 · see citing works

Impaired light masking in dopamine D2 receptor–null mice

Doi, M., Yujnovsky, I., Hirayama, J., Malerba, M., Tirotta, E., Sassone‐Corsi, P., & Borrelli, E. (2006) · Nature Neuroscience · doi:10.1038/nn1711 · Cited by 71 · see citing works

Regional Differences in the Effects of Amphetamine Withdrawal on Dopamine Dynamics in the Striatum Analysis of Circadian Patterns Using Automated On-Line Microdialysis

Paulson, P. E. (1996) · Neuropsychopharmacology · doi:10.1016/0893-133x(95)00141-y · Cited by 70 · see citing works

Using electronic media before sleep can curtail sleep time and result in self-perceived insufficient sleep

Suganuma, N., KIKUCHI, T., YANAGI, K., Yamamura, S., Morishima, H., Adachi, H., Kumano‐go, T., Mikami, A., Sugita, Y., & Takeda, M. (2007) · Sleep and Biological Rhythms · doi:10.1111/j.1479-8425.2007.00276.x · Cited by 70 · see citing works

Molecular Clocks in Pharmacology

Musiek, E. S., & FitzGerald, G. A. (2013) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-25950-0_10 · Cited by 69 · see citing works

Characterization of Cocaine Self-Administration and Pharmacokinetics as a Function of Time of Day in the Rat

Baird, T. J., & Gauvin, D. V. (2000) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(99)00207-5 · Cited by 67 · see citing works

Neural basis of reward anticipation and its genetic determinants

Jia, T., Macare, C., Desrivières, S., Gonzalez, D. A., Tao, C., Ji, X., Ruggeri, B., Nees, F., Banaschewski, T., Barker, G. J., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1503252113 · Cited by 66 · see citing works

Centrally Administered Ghrelin Acutely Influences Food Choice in Rodents

Schéle, E., Bake, T., Rabasa, C., & Dickson, S. L. (2016) · PLoS ONE · doi:10.1371/journal.pone.0149456 · Cited by 65 · see citing works

Effects of enriched environment on morphine-induced reward in mice

Xu, Z., Hou, B., Gao, Y., He, F., & Zhang, C. (2007) · Experimental Neurology · doi:10.1016/j.expneurol.2006.12.027 · Cited by 63 · see citing works

Simultaneous absence of dopamine D1 and D2 receptor-mediated signaling is lethal in mice

Kobayashi, M., Iaccarino, C., Saiardi, A., Heidt, V., Bozzi, Y., Picetti, R., Vitale, C., Westphal, H., Drago, J., & Borrelli, E. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402028101 · Cited by 61 · see citing works

Socio-demographic, psychosocial and home-environmental attributes associated with adults' domestic screen time

Dyck, D. V., Cardon, G., Deforche, B. I., Owen, N. G., Cocker, K. A. D., Wijndaele, K., & Bourdeaudhuij, I. D. (2011) · BMC Public Health · doi:10.1186/1471-2458-11-668 · Cited by 60 · see citing works

Single prenatal injections of melatonin or the D1-dopamine receptor agonist SKF 38393 to pregnant hamsters sets the offsprings' circadian rhythms to phases 180° apart

Viswanathan, N., & Davis, F. C. (1997) · Journal of Comparative Physiology A · doi:10.1007/s003590050053 · Cited by 59 · see citing works

Circadian Rhythms and Substance Abuse: Chronobiological Considerations for the Treatment of Addiction

Webb, I. C. (2017) · Current Psychiatry Reports · doi:10.1007/s11920-017-0764-z · Cited by 57 · see citing works

The Effects of Methamphetamine on Serotonin Transporter Activity

Haughey, H. M., Fleckenstein, A. E., Metzger, R. R., & Hanson, G. R. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0751608.x · Cited by 55 · see citing works

Altered Sexual Behavior in Dopamine Transporter (DAT) Knockout Male Rats: A Behavioral, Neurochemical and Intracerebral Microdialysis Study

Sanna, F., Bratzu, J., Serra, M. P., Leo, D., Quartu, M., Boi, M., Espinoza, S., Gainetdinov, R. R., Melis, M. R., & Argiolas, A. (2020) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2020.00058 · Cited by 52 · see citing works

Common problems in patients recovering from chemical dependency.

Jones, E. M., Knutson, D., & Haines, D. (2003) · PubMed · Cited by 47 · see citing works

Dopamine D2 receptors in striatal output neurons enable the psychomotor effects of cocaine

Kharkwal, G., Radl, D. B., Lewis, R. G., & Borrelli, E. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1608362113 · Cited by 45 · see citing works

Biochemistry of Biogenic Amines

(1975) · Springer eBooks · doi:10.1007/978-1-4684-3171-1 · Cited by 44 · see citing works

Periodicity of Presentations of Drugs of Abuse and Overdose in an Emergency Department

Raymond, R. C., Warren, M., Morris, R. W., & Leikin, J. B. (1992) · Journal of Toxicology Clinical Toxicology · doi:10.3109/15563659209021561 · Cited by 44 · see citing works

Dopamine 2 Receptor Activation Entrains Circadian Clocks in Mouse Retinal Pigment Epithelium

Baba, K., DeBruyne, J. P., & Tosini, G. (2017) · Scientific Reports · doi:10.1038/s41598-017-05394-x · Cited by 44 · see citing works

The impact of meal timing on performance, sleepiness, gastric upset, and hunger during simulated night shift

GRANT, C. L., Dorrian, J., Coates, A. M., Pajcin, M., Kennaway, D. J., Wittert, G., Heilbronn, L. K., Vedova, C. B. D., Gupta, C. C., & Banks, S. (2017) · Industrial Health · doi:10.2486/indhealth.2017-0047 · Cited by 43 · see citing works

A High-Fat Meal, or Intraperitoneal Administration of a Fat Emulsion, Increases Extracellular Dopamine in the Nucleus Accumbens

Rada, P. V., Avena, N. M., Barson, J. R., Hoebel, B. G., & LEIBOWITZ, S. F. (2012) · Brain Sciences · doi:10.3390/brainsci2020242 · Cited by 42 · see citing works

Time for sex: nycthemeral distribution of human sexual behavior

Refinetti, R. (2005) · Journal of Circadian Rhythms · doi:10.1186/1740-3391-3-4 · Cited by 41 · see citing works

Dietary intakes and leptin concentrations.

Izadi, V., Saraf‐Bank, S., & Azadbakht, L. (2014) · PubMed Central · Cited by 39 · see citing works

Differences between Dorsal and Ventral Striatum in the Sensitivity of Tonically Active Neurons to Rewarding Events

Marche, K., Martel, A., & Apicella, P. (2017) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2017.00052 · Cited by 39 · see citing works

The percentage of interneurons in the dorsal striatum of the rat, cat, monkey and human: A critique of the evidence

Oorschot, D. E. (2012) · Basal Ganglia · doi:10.1016/j.baga.2012.11.001 · Cited by 34 · see citing works

Dopaminergic Control of Striatal Cholinergic Interneurons Underlies Cocaine-Induced Psychostimulation

Lewis, R. G., Serra, M., Radl, D. B., Gori, M., Tran, C., Michalak, S. E., Vanderwal, C. D., & Borrelli, E. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107527 · Cited by 34 · see citing works

Enhanced reward-related responding following cholera toxin infusion into the nucleus accumbens

Kelley, A. E., & Holahan, M. R. (1997) · Synapse · doi:10.1002/(sici)1098-2396(199705)26:1 · Cited by 31 · see citing works

Phase-dependent phase shift of methamphetamine-induced circadian rhythm by haloperidol in SCN-lesioned rats

Honma, S., & Honma, K.-I. (1995) · Brain Research · doi:10.1016/0006-8993(95)00027-n · Cited by 30 · see citing works

Circadian Effects of Timed Meals (and Other Rewards)

Davidson, A. J., Tataroğlu, Ö., & Menaker, M. (2005) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(05)93026-7 · Cited by 29 · see citing works

Dopamine Signaling in Circadian Photoentrainment: Consequences of Desynchrony.

Grippo, R. M., & Güler, A. D. (2019) · PubMed Central · Cited by 29 · see citing works

Adaptation to daily meal-timing and its effect on circadian temperature rhythms in two inbred strains of mice

Hotz, M. M., Connolly, M. S., & Lynch, C. B. (1987) · Behavior Genetics · doi:10.1007/bf01066009 · Cited by 24 · see citing works

Active Time-Restricted Feeding Improved Sleep-Wake Cycle in db/db Mice

Hou, T., Wang, C., Joshi, S., O’Hara, B. F., Gong, M. C., & Guo, Z. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00969 · Cited by 24 · see citing works

Palatable food consumption in children: interplay between (food) reward motivation and the home food environment

Decker, A. D., Verbeken, S., Sioen, I., Lippevelde, W. V., Braet, C., Eiben, G., Pala, V. M., Reish, L. A., & Henauw, S. D. (2017) · European Journal of Pediatrics · doi:10.1007/s00431-017-2857-4 · Cited by 22 · see citing works

Scheduled Daily Mating Induces Circadian Anticipatory Activity Rhythms in the Male Rat

Landry, G. J., Opiol, H., Marchant, E. G., Pavlovski, I., Mear, R. J., Hamson, D. K., & Mistlberger, R. E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040895 · Cited by 21 · see citing works

Circadian and circannual rhythms of emergency room drug-overdose admissions.

Morris, R. W. (1987) · PubMed · Cited by 18 · see citing works

mPer1 promotes morphine-induced locomotor sensitization and conditioned place preference via histone deacetylase activity

Perreau‐Lenz, S., Hoelters, L.-S., Leixner, S., Sanchis‐Segura, C., Hansson, A. C., Bilbao, A., & Spanagel, R. (2017) · Psychopharmacology · doi:10.1007/s00213-017-4574-0 · Cited by 17 · see citing works

Brain Imaging in Behavioral Neuroscience

Carter, C., & Dalley, J. (2012) · Current topics in behavioral neurosciences · doi:10.1007/978-3-642-28711-4 · Cited by 13 · see citing works

Glucagon-like peptide 1 agonist and effects on reward behaviour: A systematic review

Badulescu, S., Tabassum, A., Le, G. H., Wong, S., Phan, L., Gill, H., Llach, C.-D., McIntyre, R. S., Rosenblat, J., & Mansur, R. (2024) · Physiology &amp; Behavior · doi:10.1016/j.physbeh.2024.114622 · Cited by 90 · see citing works

Social Media Algorithms and Teen Addiction: Neurophysiological Impact and Ethical Considerations

De, D., El Jamal, M., Aydemir, E., & Khera, A. (2025) · Cureus · doi:10.7759/cureus.77145 · Cited by 54 · see citing works

Cell therapy for neurological disorders

Svendsen, S. P., & Svendsen, C. N. (2024) · Nature Medicine · doi:10.1038/s41591-024-03281-3 · Cited by 43 · see citing works

From Reward to Anhedonia-Dopamine Function in the Global Mental Health Context

Dresp, B. (2023) · Biomedicines · doi:10.3390/biomedicines11092469 · Cited by 49 · see citing works

Drug addiction and treatment: An epigenetic perspective

Koijam, A. S., Singh, K. D., Singh, N. B., Haobam, R., & Rajashekar, Y. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115951 · Cited by 43 · see citing works

Food Cravings and Obesity in Women with Polycystic Ovary Syndrome: Pathophysiological and Therapeutic Considerations

Stefanaki, K., Karagiannakis, D. S., Peppa, Μ., Vryonidou, A., Kalantaridou, S., Goulis, D. G., Ψαλτοπούλου, Θ., & Paschou, S. Α. (2024) · Nutrients · doi:10.3390/nu16071049 · Cited by 26 · see citing works

An organic brain-inspired platform with neurotransmitter closed-loop control, actuation and reinforcement learning

Bruno, U., Rana, D., Ausilio, C., Mariano, A., Bettucci, O., Musall, S., Lubrano, C., & Santoro, F. (2024) · Materials Horizons · doi:10.1039/d3mh02202a · Cited by 25 · see citing works

Glucagon-Like Peptide 1: An Introduction and Possible Implications for Neuropsychiatry

López-Ojeda, W., & Hurley, R. A. (2024) · Journal of Neuropsychiatry · doi:10.1176/appi.neuropsych.20230226 · Cited by 24 · see citing works

The Relationship between Canine Behavioral Disorders and Gut Microbiome and Future Therapeutic Perspectives

Kiełbik, P., & Witkowska‐Piłaszewicz, O. (2024) · Animals · doi:10.3390/ani14142048 · Cited by 24 · see citing works

Pharmacological strategies for sexual recovery in men undergoing antipsychotic treatment

Jannini, T. B., Sansone, A., Rossi, R., Lorenzo, G. D., Toscano, M., Siracusano, A., & Jannini, E. A. (2022) · Expert Opinion on Pharmacotherapy · doi:10.1080/14656566.2022.2071124 · Cited by 21 · see citing works

Multisensory stimulation reduces neuropsychiatric symptoms and enhances cognitive function in older adults with dementia: A meta-analysis of randomized controlled trials

Octary, T., Fajarini, M., Arifin, H., Chen, R., Sung, C., Chang, L., Wang, C., Banda, K. J., & Chou, K. (2025) · The Journal of Prevention of Alzheimer s Disease · doi:10.1016/j.tjpad.2025.100091 · Cited by 20 · see citing works

Deficiency of the Circadian Clock Gene Rev-Erbα Induces Mood Disorders and Dysregulation of the Serotonergic System in Mice

Otsuka, T., Le, H. T., Thein, Z. L., Ihara, H., Sato, F., Nakao, T., & Kohsaka, A. (2022) · Physiology & Behavior · doi:10.1016/j.physbeh.2022.113960 · Cited by 20 · see citing works

Impaired interhemispheric synchrony in Parkinson's disease patients with apathy

Zhang, H., Shan, A., Gan, C., Zhang, L., Wang, L., Sun, H., Yuan, Y., & Zhang, K. (2022) · Journal of Affective Disorders · doi:10.1016/j.jad.2022.09.006 · Cited by 19 · see citing works

IUPHAR review: Recent progress in the development of Mu opioid receptor modulators to treat opioid use disorders

Pagare, P. P., Flammia, R., & Zhang, Y. (2023) · Pharmacological Research · doi:10.1016/j.phrs.2023.107023 · Cited by 18 · see citing works

Screen use and sleep duration and quality at 15 years old: Cohort study

Echevarria, P., Del‐Ponte, B., Tovo‐Rodrigues, L., Matijasevich, A., Halal, C. S. E., & Santos, I. S. (2023) · Sleep Medicine X · doi:10.1016/j.sleepx.2023.100073 · Cited by 18 · see citing works

Sex differences in glutamate transmission and plasticity in reward related regions

Kniffin, A. R., & Briand, L. A. (2024) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2024.1455478 · Cited by 17 · see citing works

Gene expression differences associated with alcohol use disorder in human brain

Willis, C., White, J. D., Minto, M. S., Quach, B. C., Han, S., Tao, R., Shin, J. H., Deep‐Soboslay, A., Hyde, T. M., Mayfield, R. D., et al. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02777-1 · Cited by 15 · see citing works

A holistic exploration of the psychosocial, environmental, neurobiological, and individual factors influencing children’s food choices: a narrative review

Albardan, L., & Platat, C. (2025) · Frontiers in Nutrition · doi:10.3389/fnut.2025.1645293 · Cited by 12 · see citing works

Repeated binge‐like eating episodes in female rats alter adenosine A2A and dopamine D2 receptor genes regulation in the brain reward system

Mercante, F., Bonaventura, E. M. D., Pucci, M., Botticelli, L., Cifani, C., D’Addario, C., & Bonaventura, M. V. M. D. (2024) · International Journal of Eating Disorders · doi:10.1002/eat.24216 · Cited by 12 · see citing works

The Effects of Obesity on the Inflammatory, Cardiovascular, and Neurobiological Responses to Exercise in Older Adults

Fico, B. G., Maharaj, A., Pena, G. S., & Huang, C. (2023) · Biology · doi:10.3390/biology12060865 · Cited by 14 · see citing works

Exploring the association between melatonin and nicotine dependence (Review)

GEORGAKOPOULOU, V. E., Sklapani, P., Τράκας, Ν., Reiter, R. J., & Spandidos, D. A. (2024) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2024.5406 · Cited by 12 · see citing works

Interconnections of screen time with neuroinflammation

Verma, A., Kumar, A., Chauhan, S. S., Sharma, N., Kalani, A., & Gupta, P. C. (2024) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-024-05123-9 · Cited by 11 · see citing works

Early Life Stress and Gut Microbiome Dysbiosis: A Narrative Review

Borrego-Ruiz, A., & Borrego, J. J. (2025) · Stresses · doi:10.3390/stresses5020038 · Cited by 11 · see citing works

The role of BDNF on food intake and overweight: Linking neuroplasticity and obesity

Sequeira‐Cordero, A., Brenes, J. C., & Vindas-Smith, R. (2025) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2025.111457 · Cited by 13 · see citing works

Catecholamine Variations in Pediatric Gastrointestinal Disorders and Their Neuropsychiatric Expression

Matiș, L., Alexandru, B. A., & Ghitea, T. C. (2023) · Biomedicines · doi:10.3390/biomedicines11102600 · Cited by 10 · see citing works

Implications of Kynurenine Pathway Metabolism for the Immune System, Hypothalamic–Pituitary–Adrenal Axis, and Neurotransmission in Alcohol Use Disorder

Osuch, B., Misztal, T., Pałatyńska, K., & Tomaszewska-Zaremba, D. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25094845 · Cited by 10 · see citing works

The endocannabinoid and paracannabinoid systems in natural reward processes: possible pharmacological targets?

Friuli, M., Eramo, B., Sepe, C., Kiani, M., Casolini, P., & Zuena, A. R. (2025) · Physiology & Behavior · doi:10.1016/j.physbeh.2025.114929 · Cited by 11 · see citing works

The Interplay Between Psychological and Neurobiological Predictors of Weight Regain: A Narrative Review

Moszak, M., Marcickiewicz, J., Pelczyńska, M., & Bogdański, P. (2025) · Nutrients · doi:10.3390/nu17101662 · Cited by 9 · see citing works

Novel neurotherapeutic targets for substance use disorders: Neuroplasticity, neuroinflammation, gasotransmitters and non-canonical organ systems

Sharma, P., Sawaya, M. F., Dumitrescu, A. M., Kolluru, G. K., Schmoutz, C. D., Salinas, A. G., Cannon, C. E., Kumbhare, D., Korneeva, N. L., Vest, M. F., et al. (2025) · Neurotherapeutics · doi:10.1016/j.neurot.2025.e00770 · Cited by 11 · see citing works

Framing decision-making: the role of executive functions, cognitive bias and reward

Rovelli, K., & Allegretta, R. A. (2023) · Neuropsychological Trends · doi:10.7358/neur-2023-033-rove · Cited by 9 · see citing works

Fractional amplitude of low-frequency fluctuations associated with μ-opioid and dopamine receptor distributions in the central nervous system after high-intensity exercise bouts

Boecker, H., Maurer, A., Daamen, M., Bodensohn, L., Werkhausen, J., Lohaus, M., Manunzio, C., Manunzio, U., Radbruch, A., Attenberger, U. I., et al. (2024) · Frontiers in Neuroimaging · doi:10.3389/fnimg.2024.1332384 · Cited by 9 · see citing works

Abnormal voxel‐mirrored homotopic connectivity in first‐episode, drug‐naïve patients with obsessive–compulsive disorder

Xu, Y., & Zhang, Y. (2023) · European Journal of Neuroscience · doi:10.1111/ejn.16117 · Cited by 8 · see citing works

Intranasal administration of the essential oil from Perillae Folium ameliorates social defeat stress-induced behavioral impairments in mice

Nguyen, L. T. H., Nguyen, N. P. K., Tran, K. N., Shin, H., & Yang, I. (2024) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2024.117775 · Cited by 8 · see citing works

Disrupted Resting-State Functional Connectivity and Effective Connectivity of the Nucleus Accumbens in Chronic Low Back Pain: A Cross-Sectional Study

Zhang, B., Guo, M., Dong, T., Yang, H., Zhang, Q., Yang, Q., Zhou, X., Mao, C., & Zhang, M. (2024) · Journal of Pain Research · doi:10.2147/jpr.s455239 · Cited by 8 · see citing works

The interaction effects between opioidergic and D1-like dopamine receptors in the nucleus accumbens on pain-related behaviors in the animal model of acute pain

Shahani, P., Abolghasemi, H., Abtin, S., Mozafari, R., Barikrow, N., Yekta, B. G., & Haghparast, A. (2024) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2024.173911 · Cited by 8 · see citing works

Pathophysiological and therapeutic implications of neuropeptide S system in neurological disorders

Shirasath, K. R., Patil, V. K., Awathale, S. N., Goyal, S. N., & Nakhate, K. T. (2024) · Peptides · doi:10.1016/j.peptides.2024.171167 · Cited by 7 · see citing works

Contribution of the subthalamic nucleus to motor, cognitive and limbic processes: an electrophysiological and stimulation study in monkeys

Bertrand, M., Chabardès, S., Fontanier, V., Procyk, E., Bastin, J., & Piallat, B. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1257579 · Cited by 7 · see citing works

Astrocyte Ca2+ in the dorsal striatum suppresses neuronal activity to oppose cue-induced reinstatement of cocaine seeking

Tavakoli, N. S., Malone, S. G., Anderson, T. L., Neeley, R. E., Asadipooya, A., Bardo, M. T., & Ortinski, P. I. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1347491 · Cited by 7 · see citing works

The Effects of Osteopathic Manipulative Treatment on Brain Activity: A Scoping Review of MRI and EEG Studies

Bonanno, M., Papa, G. F. S., Ruffoni, P., Catalioto, E., Luca, R. D., Maggio, M. G., & Calabrò, R. S. (2024) · Healthcare · doi:10.3390/healthcare12131353 · Cited by 7 · see citing works

The role of emotional eating as relief mechanism from psychological distress and its impact on overall wellbeing

Jurek, J. M., & Maruda, A. (2024) · Debates em Psiquiatria · doi:10.25118/2763-9037.2024.v14.1268 · Cited by 10 · see citing works

Differences in resting-state functional connectivity between depressed bipolar and major depressive disorder patients: A machine learning study

Calesella, F., Serra, E., Palladini, M., Colombo, F., Bravi, B., Fortaner-Uyà, L., Monopoli, C., Tassi, E., Brambilla, P., Colombo, C., et al. (2025) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2025.05.011 · Cited by 7 · see citing works

Bridging Genetic Insights with Neuroimaging in Autism Spectrum Disorder—A Systematic Review

Vilela, J. E. R., Rasga, C., Santos, J. X., Martiniano, H., Marques, A. R., Oliveira, G., & Vicente, A. M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25094938 · Cited by 7 · see citing works

Antiobesity Pharmacotherapy for Patients With Genetic Obesity Due to Defects in the Leptin-Melanocortin Pathway

Welling, M. S., van Rossum, E. F. C., & van den Akker, E. L. T. (2025) · Endocrine Reviews · doi:10.1210/endrev/bnaf004 · Cited by 6 · see citing works

Federated Learning: Attacks and Defenses, Rewards, Energy Efficiency: Past, Present and Future

Karydas, D., & Leligou, H. C. (2024) · WSEAS Transactions on Computers archive · doi:10.37394/23205.2024.23.10 · Cited by 6 · see citing works

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 5 · see citing works

Social interaction-induced fear memory reduction: exploring the influence of dopamine and oxytocin receptors on memory updating

Pérez, A. D. A., Kautzmann, A. S., & Alvares, L. D. O. (2024) · Translational Psychiatry · doi:10.1038/s41398-024-02955-3 · Cited by 5 · see citing works

A systematic review and meta-analysis of group-based trajectory modeling of sleep duration across age groups and in relation to health outcomes

Wang, W., Cheung, S. H., Cheung, S. F., Sun, R. W., Hui, C.-C. H., Ma, H. Y. D., & Lau, E. Y. Y. (2025) · SLEEP · doi:10.1093/sleep/zsaf021 · Cited by 5 · see citing works

Liraglutide alleviated alpha-pyrrolidinovalerophenone (α-PVP) induced cognitive deficits in rats by modifying brain mitochondrial impairment

Noruzi, M., Behmadi, H., Sabzevari, O., Foroumadi, A., Ghahremani, M. H., Pourahmad, J., Hassani, S., Baeeri, M., Gholami, M., Ghahremanian, A., et al. (2024) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2024.176776 · Cited by 5 · see citing works

Bipolar electrochemical sensor with perylene diimide-based cathodic luminophore for dopamine detection and imaging

Iwama, T., Komatsu, M., Inoue, K. Y., Kubota, K., Ito‐Sasaki, T., & Shiku, H. (2024) · Talanta · doi:10.1016/j.talanta.2024.126509 · Cited by 5 · see citing works

Carnosine Mitigates Cognitive Impairment and Dopamine Release in an Okadaic Acid-Induced Zebrafish Model with Alzheimer’s Disease-like Symptoms

Chern, H., Caruso, G., Desaire, H., & Jarošová, R. (2025) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.4c00596 · Cited by 6 · see citing works

Is interesting knowledge a reward? An integrative model of emotion, reward and appraisal frameworks of epistemic curiosity.Preprint

Erdemli, A., Audrin, C., & Sander, D. (2024) · doi:10.31234/osf.io/kz2a7 · Cited by 6 · see citing works

Biopsychosocial and Environmental Factors That Impact Brain-Gut-Microbiome Interactions in Obesity

Sood, R., Kilpatrick, L. A., Keefer, L., & Church, A. (2025) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2025.07.045 · Cited by 4 · see citing works

Coadministration antagonist dopamine receptor D4 with CB2 receptor agonist decreases binge-like intake of palatable food in mice

Rodríguez–Serrano, L. M., López-Castillo, A. P., Cabrera-Mejía, M. C., Cedillo-Figueroa, A. S., Zepeda-Ortigosa, N., Carregha-Lozano, C., & Chávez–Hernández, M. E. (2025) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2025.1572374 · Cited by 4 · see citing works

Eveningness and distinctness of the circadian rhythm in men are related to altered neural responses to gain and loss

Scislewska, P., Zareba, M., Lengier, J., Schirmer, A. E., Bębas, P., & Szatkowska, I. (2025) · Scientific Reports · doi:10.1038/s41598-025-07049-8 · Cited by 3 · see citing works

Reward-related neural activation during social media exposure in young women with non-suicidal self-injury: evidence for a continuum of severity in the reward network

Nicolaou, S., Julià, A., Otero, D., Schmidt, C., Pascual, J. C., Soler, J., Marco‐Pallarés, J., & Vega, D. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03536-8 · Cited by 5 · see citing works

Semaglutide for Craving Reduction in a Cocaine Dependent Patient: A Case Report

Sileoni, A. M., Turco, E. T., Semeraro, F., Cavallotto, C., Mosca, A., Chiappini, S., & Martinotti, G. (2025) · Clinical Neuropsychopharmacology and Addiction · doi:10.53941/cna.2025.100003 · Cited by 4 · see citing works

Astrocyte-Neuron Interactions in Substance Use Disorders

Harder, E. V., Franklin, J. P., VanRyzin, J. W., & Reissner, K. J. (2024) · Advances in neurobiology · doi:10.1007/978-3-031-64839-7_7 · Cited by 4 · see citing works

Combined Chronic Oral Methylphenidate and Fluoxetine Decreases D2R Levels in the Caudate Putamen and Nucleus Accumbens

Lagamjis, G., Lu, H., Roeder, N. M., Richardson, B., Marion, M., Quattrin, T., Mastrandrea, L. D., Hadjiargyrou, M., Komatsu, D. E., & Thanos, P. K. (2025) · Neurochemical Research · doi:10.1007/s11064-025-04481-0 · Cited by 4 · see citing works

The neurobiology of love and addiction: Central nervous system signaling and energy metabolism

Esch, T., & Stefano, G. B. (2025) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-025-01333-w · Cited by 3 · see citing works

Inflammation-Associated Mechanisms of Blood–Brain Barrier Disruption and Depression Pathogenesis in People with and Without HIV

Hills, C., Hernandez, C. A., Gabbay, V., & Berman, J. W. (2026) · Cells · doi:10.3390/cells15050399 · Cited by 3 · see citing works

Maternal immune activation with high molecular weight poly (I:C) induces selective depressive-like phenotype in adult offspring

Santoni, M., Mastio, A., Concas, L., Mostallino, R., Herres, A., Sagheddu, C., Castelli, M. P., Frau, R., Muntoni, A. L., & Pistis, M. (2026) · Translational Psychiatry · doi:10.1038/s41398-026-03926-6 · Cited by 3 · see citing works

Cannabidiol Plays a Modulatory Function on the Methamphetamine-Induced Reward Through Hippocampal D2-Like Dopamine Receptors

Mohammadi, M., Omidiani, S. E., Azizbeigi, R., & Haghparast, A. (2024) · Neurochemical Research · doi:10.1007/s11064-024-04256-z · Cited by 4 · see citing works

Maternal exposure to dim light at night induces behavioral alterations in the adolescent and adult offspring Wistar rat

González‐González, S., Gutiérrez‐Pérez, M., Guzmán‐Ruiz, M. A., Espítia‐Bautista, E., Pavón, R. M., Estrada‐Rodriguez, K. P., Alejandro Díaz-Infante, R., Gándara, C. G. G., Escobar, C., & Guerrero‐Vargas, N. N. (2025) · Frontiers in Physiology · doi:10.3389/fphys.2024.1520160 · Cited by 3 · see citing works

Healthcare resource utilization and costs of using cariprazine as the first versus subsequent adjunctive therapy for major depressive disorder

Masand, P. S., Clayton, A. H., Parikh, M., Laliberté, F., Germain, G., Mahendran, M., Martínez, C., & Nabulsi, N. A. (2025) · Journal of Medical Economics · doi:10.1080/13696998.2025.2457872 · Cited by 3 · see citing works

The Anatomical and Evolutionary Impact of Pain, Pleasure, Motivation, and Cognition: Integrating Energy Metabolism and the Mind–Body BERN (Behavior, Exercise, Relaxation, and Nutrition) Framework

Stefano, G. B., Büttiker, P., Michaelsen, M. M., & Esch, T. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26125491 · Cited by 6 · see citing works

Enhancement of Electrochemiluminescence by Au Paste Electrode for Bipolar Electroanalysis

Ayane, E. N. D. O., Kubota, K., Ito‐Sasaki, T., Komatsu, M., Iwama, T., Shiku, H., & Inoue, K. Y. (2023) · Electrochemistry · doi:10.5796/electrochemistry.23-68114 · Cited by 3 · see citing works

Unlocking the neural mechanisms of consumer loan evaluations: an fNIRS and ML-based consumer neuroscience study

Çakar, T. E., Son-Turan, S., Girişken, Y., Sayar, A., Ertuğrul, S., Filiz, G., & Tuna, E. (2024) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2024.1286918 · Cited by 3 · see citing works

Investigating the impact of microbiome-changing interventions on food decision-making: MIFOOD study protocol

Vartanian, M., Endres, K. J., Lee, Y. T., Friedrich, S., Meemken, M.-T., Schamarek, I., Rohde‐Zimmermann, K., Schürfeld, R., Eisenberg, L., Hilbert, A., et al. (2025) · BMC Nutrition · doi:10.1186/s40795-024-00971-6 · Cited by 4 · see citing works

Disordered Eating Behaviors in Individuals With Physical Disabilities: A Narrative Review

Raffman, E. S., & Jayabalan, P. S. (2025) · American Journal of Lifestyle Medicine · doi:10.1177/15598276251363516 · Cited by 3 · see citing works

Algorithmic dopamine economies: emerging psychiatric challenges in an artificial-intelligence-mediated attention ecology

Jose, A., Mathew, S., & Arvind, T. (2026) · The British Journal of Psychiatry · doi:10.1192/bjp.2026.10557 · Cited by 2 · see citing works

Big tech, the state, or you? Who is responsible for generative AI addiction?

Stahl, B. C., Ali, R., Hitcham, L., Liebherr, M., Murray, R., Vallejos, E. P., & Yankouskaya, A. (2026) · Behaviour and Information Technology · doi:10.1080/0144929x.2026.2663509 · Cited by 2 · see citing works

Neuroendocrine Control of the Vascular System

Dalmasso, C., & Loria, A. S. (2023) · Masterclass in neuroendocrinology · doi:10.1007/978-3-031-39995-4_3 · Cited by 2 · see citing works

Breaking the Chains: Advances in Substance Addiction Research through Single-Cell Sequencing, Epigenetics, and Epitranscriptomic

Filošević, A., Matić, I. S., Martinović, L. S., & Pavlić, S. D. (2024) · Future Pharmacology · doi:10.3390/futurepharmacol4010009 · Cited by 2 · see citing works

Effects of prenatal cannabinoid use on the monoamine system in the fetoplacental unit: A systematic review of animal and human studies

Portillo, R., Synova, T., & Štaud, F. (2025) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2025.112579 · Cited by 2 · see citing works

Habit loop in addictive behaviors formation among adolescents: The mediating role of impulsivity

Vazifehkhorani, A. K., & Hekmati, I. (2025) · Current Psychology · doi:10.1007/s12144-025-07480-0 · Cited by 2 · see citing works

Neurobiological Mechanisms of Ketamine Use, its Addiction, and Withdrawal: A Mini Review

Ng, S. H., Lee, Y. Z., Hong, M. Y., Kow, A. S. F., d’Arqom, A., Tham, C. L., Ho, Y., & Lee, M. T. (2025) · Current Clinical Pharmacology · doi:10.2174/0127724328362434250224105609 · Cited by 2 · see citing works

Dissecting the shared molecular mechanisms underlying polycystic ovary syndrome and schizophrenia etiology: a translational integrative approach

Pirim, D., & Bağcı, F. A. (2025) · Systems Biology in Reproductive Medicine · doi:10.1080/19396368.2025.2499475 · Cited by 2 · see citing works

Chronic Pain and Substance Use Disorders: A Brief Narrative Review of Genetic, Neurobiological, and Environmental Contributions to Comorbidity

Villela, P. N. R., & Johnson, E. C. (2025) · Journal of Psychiatry and Brain Science · doi:10.20900/jpbs.20250003 · Cited by 2 · see citing works

Fronto-striato network function is reduced in major depressive disorder

Kijima, R., Watanabe, K., Okamoto, N., Ikenouchi, A., Tesen, H., Kakeda, S., & Yoshimura, R. (2024) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2024.1336370 · Cited by 2 · see citing works

Exploring the Art and Experiences of Painters with Epilepsy

Gomes, M. D. M. (2024) · Revista brasileira de neurologia · doi:10.46979/rbn.v59i4.63113 · Cited by 2 · see citing works

Reward network modulation while learning movements to music during weekly multisensory training program for people with Parkinson’s disease: mood effects over 7-yrsPreprint

D’Alessandro, E. M., Karimi, A., Bearss, K. A., Bar, R. J., & DeSouza, J. F. X. (2025) · medRxiv · doi:10.1101/2025.07.19.25331836 · Cited by 2 · see citing works

Reward circuit local field potential modulations precede risk taking

Hughes, N., Qian, H., Doss, D. J., Makhoul, G. S., Zargari, M., Zhao, Z., Singh, B., Wang, Z., Fulton, J. N., Johnson, G. W., et al. (2025) · Brain · doi:10.1093/brain/awaf107 · Cited by 1 · see citing works

Circadian photoreception influences loss aversion

Lander, A. C., Burge, M. T., Thomas, B. G., Phillips, A. J. K., McGlashan, E. M., & Cain, S. W. (2025) · Scientific Reports · doi:10.1038/s41598-025-97370-z · Cited by 1 · see citing works

Underexplored Connections Between Diabetes, Hypomanic States and Insecure Attachment

Bogdanova, D., Maes, M. H. J., & Stoyanov, D. (2025) · Psychology Research and Behavior Management · doi:10.2147/prbm.s524823 · Cited by 1 · see citing works

The gut and heart’s role in reward processing

Arinel, M., & Abdelaal, K. (2025) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2025.1479923 · Cited by 1 · see citing works

PET/fMRI demonstrates that bariatric surgery may reverse striatal dopaminergic dysfunction in women with obesity

Pais, M. L., Crisóstomo, J., Abrunhosa, A., & Castelo-Branco, M. S. (2025) · Communications Medicine · doi:10.1038/s43856-025-01079-z · Cited by 1 · see citing works

Juvenile Rats Exposed to Antibiotics Early in Life Display Sexual Dimorphisms on Social Behaviour and Sex Hormone Deconjugating Activity

Kuehnel, I. M., González‐Irarrázabal, C. E., Pardo, R., Julio‐Pieper, M., & Bravo, J. A. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70224 · Cited by 1 · see citing works

D1 / D5 receptor activation promotes long‐term potentiation and synaptic tagging/capture in hippocampal area CA2

Chua, K., Chong, Y. S., & Sajikumar, S. (2025) · FEBS Journal · doi:10.1111/febs.70266 · Cited by 1 · see citing works

Grief-Related Psychopathology from Complicated Grief to DSM-5-TR Prolonged Grief Disorder: A Systematic Review of Biochemical Findings

Pedrinelli, V., Rimoldi, B., Conti, L., Bordacchini, A., Parrini, L., Betti, L., Giannaccini, G., Dell’Oste, V., & Carmassi, C. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262411835 · Cited by 4 · see citing works

Developmental differences in reward-learning and its connection to resting-state functional connectivity modeled using a hierarchical Bayesian model

Karlócai, Z., Vegelius, J. R., Widegren, E., Kleberg, J. L., Fällmar, D., Kroemer, N. B., Gingnell, M., & Frick, A. (2025) · Behavioural Brain Research · doi:10.1016/j.bbr.2025.116008 · Cited by 1 · see citing works

Neuroanatomical correlates of communication apprehension in young adults using voxel-based morphometry

Bai, C., Tian, Q., Chen, J., Li, C., Liu, X., Wei, D., Zhu, X., & Wang, K. (2026) · Scientific Reports · doi:10.1038/s41598-025-34598-9 · Cited by 1 · see citing works

Pharmacological inhibition of O-GlcNAcase reduces pS129-α-synuclein positive aggregates in the substantia nigra of mThy1-hSNCA mice

Yue, J., Jones, B., Tran, K. H., Deen, M. C., Holicek, V., Cheng, W. H., Michalik, M. J., Power, S. C., Wellington, C. L., Watson, N. V., et al. (2026) · Journal of Parkinson s Disease · doi:10.1177/1877718x251410291 · Cited by 1 · see citing works

The Impact of Smartphone Use on Brain Function in Adolescence: A Scoping Review

Marks, A., Berthelot, M., Jones, H., Taylor, A. K., Chang, K. K.-F., Crozier, S., & Cosper, S. M. (2026) · Pediatric Reports · doi:10.3390/pediatric18020043 · Cited by 4 · see citing works

Transcranial alternating current stimulation over left DLPFC modulates feedback processing: a simultaneous tACS-fMRI study

Debnath, R., Lenz, E., Tobelander, J., Schweppe, P. C., Renner, V., & Mulert, C. (2026) · Translational Psychiatry · doi:10.1038/s41398-026-03942-6 · Cited by 1 · see citing works

Neurocognitive factors predicting BMI changes from adolescence to young adulthood

Reyes, S., Peirano, P. D., Gahagan, S., Blanco, E., & Algarín, C. R. (2024) · Obesity · doi:10.1002/oby.23978 · Cited by 1 · see citing works

Exploring Decision-Making Processes in Neuroeconomics

Jacob, L., & Reddy, K. J. (2024) · Advances in finance, accounting, and economics book series · doi:10.4018/979-8-3693-6055-2.ch005 · Cited by 1 · see citing works

Neurobiologia do condicionamento pavloviano e condicionamento operante – Revisão narrativa

Silva, W. D. S. (2024) · Research Society and Development · doi:10.33448/rsd-v13i11.47523 · Cited by 1 · see citing works

Exploring the Risks of General-Purpose AI: The Role of the Brain’s Reward Mechanism and Nearsighted Goals in Processes of Decision-Makings

Oliveira, D. G. D. S. (2024) · Communications in computer and information science · doi:10.1007/978-3-031-74627-7_19 · Cited by 1 · see citing works

Functional magnetic resonance imaging in prurigo nodularis: A call to study neural sensitization phenomena

Zhao, X., Mueller, J. M., & Mueller, S. M. (2025) · Clinics in Dermatology · doi:10.1016/j.clindermatol.2025.03.005 · Cited by 1 · see citing works

Prefrontal cortex activation during daily movements and its association with clinical symptoms in knee osteoarthritis

Lee, S., Kim, E., Cha, B., Ferre, C. L., Yücel, M. A., & Kumar, D. (2025) · Osteoarthritis and Cartilage Open · doi:10.1016/j.ocarto.2025.100615 · Cited by 1 · see citing works

Racing and Pacing in the Reward System: A Multi-Clock Circadian Control Over Dopaminergic Signalling

Pradel, K., Drwiȩga, G., Chrobok, Ł., & Błasiak, T. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.932378 · Cited by 15 · see citing works

Circadian insights into dopamine mechanisms

Mendoza, J., & Challet, É. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.07.081 · Cited by 124 · see citing works

Dopamine systems and biological rhythms: Let’s get a move on

Tang, Q., Assali, D. R., Güler, A. D., & Steele, A. D. (2022) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2022.957193 · Cited by 25 · see citing works

Dopamine: A Modulator of Circadian Rhythms in the Central Nervous System

Korshunov, K. S., Blakemore, L. J., & Trombley, P. Q. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00091 · Cited by 173 · see citing works

Dopamine: a modulator of circadian rhythms/biological clock

Kant, R., Meena, M. K., & Pathania, M. (2021) · International Journal of Advances in Medicine · doi:10.18203/2349-3933.ijam20210285 · Cited by 10 · see citing works