D1 Dopamine Receptors in Prefrontal Cortex: Involvement in Working Memory

Multiple receptors for dopamine

Kebabian, J. W., & Calne, D. B. (1979) · Nature · doi:10.1038/277093a0 · Cited by 3,756

Mnemonic coding of visual space in the monkey's dorsolateral prefrontal cortex

Funahashi, S., Bruce, C. J., & Goldman-Rakic, P. S. (1989) · Journal of Neurophysiology · doi:10.1152/jn.1989.61.2.331 · Cited by 2,685

Cognitive Deficit Caused by Regional Depletion of Dopamine in Prefrontal Cortex of Rhesus Monkey

Brozoski, T. J., Brown, R. M., Rosvold, H. E., & Goldman, P. S. (1979) · Science · doi:10.1126/science.112679 · Cited by 1,500

Specific in vitro and in vivo binding of 3H-raclopride a potent substituted benzamide drug with high affinity for dopamine D-2 receptors in the rat brain

Köhler, C., Hall, H., Ögren, S. O., & Gawell, L. (1985) · Biochemical Pharmacology · doi:10.1016/0006-2952(85)90778-6 · Cited by 505

Catecholamine innervation of the human cerebral cortex as revealed by comparative immunohistochemistry of tyrosine hydroxylase and dopamine-beta-hydroxylase

Gaspar, P., Berger, B., Febvret, A., Vigny, A., & Henry, J. P. (1989) · Journal of Comparative Neurology · doi:10.1002/cne.902790208 · Cited by 395

Injection of solutions into cerebral tissue: Relation between volume and diffusion

Myers, R. D. (1966) · Physiology & Behavior · doi:10.1016/0031-9384(66)90064-3 · Cited by 337

Regional distribution of monoamines in the cerebral cortex and subcortical structures of the rhesus monkey: concentrations and in vivo synthesis rates

Brown, R. M., Crane, A. M., & Goldman, P. S. (1979) · Brain Research · doi:10.1016/0006-8993(79)90132-x · Cited by 327

The distribution of tyrosine hydroxylase-immunoreactive fibers in primate neocortex is widespread but regionally specific

Lewis, D., Campbell, M., Foote, S., Goldstein, M., & Morrison, J. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-01-00279.1987 · Cited by 325

Overlap of dopaminergic, adrenergic, and serotoninergic receptors and complementarity of their subtypes in primate prefrontal cortex

Goldman-Rakic, P. S., Lidow, M. S., & Gallager, D. W. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-07-02125.1990 · Cited by 311

Dopamine receptors in human brain: Autoradiographic distribution of D2 sites

Camps, M., Cortés, R., Gueye, B., Probst, A., & Palacios, J. M. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90179-6 · Cited by 305

The effects of dopamine on digit span in Parkinson’s disease

Warden, C., Hwang, J. J., Marshall, A. J., Fenesy, M. C., & Poston, K. L. (2016) · Journal of Clinical Movement Disorders · doi:10.1186/s40734-016-0033-z · Cited by 27

Advances in Dopamine D1 Receptor Ligands for Neurotherapeutics

Felsing, D. E., Jain, M. K., & Allen, J. (2019) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026619666190712210903 · Cited by 27

Tyrosine supplementation in phenylketonuria: Diurnal blood tyrosine levels and presumptive brain influx of tyrosine and other large neutral amino acids

Kalsner, L. R., Rohr, F., Strauss, K. A., Korson, M. S., & Levy, H. L. (2001) · The Journal of Pediatrics · doi:10.1067/mpd.2001.117576 · Cited by 27

Dopamine D1‐like receptor modulates layer‐ and frequency‐specific short‐term synaptic plasticity in rat prefrontal cortical neurons

Young, C. E., & Yang, C. R. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04161.x · Cited by 27

Intermediate Cognitive Phenotypes Associated with Schizophrenia

Egan, M. F., & Goldberg, T. E. (2003) · Humana Press eBooks · doi:10.1385/1-59259-348-8:163 · Cited by 27

The Schizophrenia Spectrum Personality Disorders

Chemerinski, E., & Siever, L. J. (2010) · Wiley eBooks · doi:10.1002/9781444327298.ch5 · Cited by 27

Dopamine receptor activation regulates reward expectancy signals during cognitive control in primate prefrontal neurons

Ott, T., Stein, A. M., & Nieder, A. (2023) · Nature Communications · doi:10.1038/s41467-023-43271-6 · Cited by 26

Dopamine in socioecological and evolutionary perspectives: implications for psychiatric disorders

Yamaguchi, Y., Lee, Y., & Goto, Y. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00219 · Cited by 26

Chronic haloperidol-induced spatial memory deficits accompany the upregulation of D1 and D2 receptors in the caudate putamen of C57BL/6 mouse

Xu, H., Yang, H.-J., & Rose, G. M. (2012) · Life Sciences · doi:10.1016/j.lfs.2012.07.025 · Cited by 26

Working Memory in Schizophrenia: Behavioral and Neural Evidence for Reduced Susceptibility to Item-Specific Proactive Interference

Kaller, C. P., Loosli, S. V., Rahm, B., Gössel, A., Schieting, S., Hornig, T., Hennig, J., van Elst, L. T., Weiller, C., & Katzev, M. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.03.012 · Cited by 26

Longitudinal Changes in Component Processes of Working Memory

Rieckmann, A., Pudas, S., & Nyberg, L. H. (2017) · eNeuro · doi:10.1523/eneuro.0052-17.2017 · Cited by 26

Distribution of protein phosphatases‐1α and ‐1γ1 and the D1 dopamine receptor in primate prefrontal cortex: Evidence for discrete populations of spines

Muly, E. C., Greengard, P., & Goldman, P. S. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1384 · Cited by 26

Genetic and Molecular Analysis of Drosophila Behavior

Kyriacou, C. P., & Hall, J. C. (1994) · Advances in genetics · doi:10.1016/s0065-2660(08)60397-1 · Cited by 26

l-DOPA produces strong induction of c-fos messenger RNA in dopamine-denervated cortical and striatal areas of the common marmoset

Svenningsson, P., Gunne, L. M., & Andrén, P. E. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00213-x · Cited by 26

The role of executive functions in psychiatric disorders

Testa, R., & Pantelis, C. (2009) · The Neuropsychology of Mental Illness · doi:10.1017/cbo9780511642197.012 · Cited by 25

Ameliorative effect of traditional Japanese medicine yokukansan on age-related impairments of working memory and reversal learning in rats

Mizoguchi, K., Shoji, H., Tanaka, Y., & Tabira, T. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.12.045 · Cited by 25

Psychostimulant Use Disorder, an Unmet Therapeutic Goal: Can Modafinil Narrow the Gap?

Hersey, M., Bacon, A. K., Bailey, L. G., Coggiano, M. A., Newman, A. H., Leggio, L., & Tanda, G. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.656475 · Cited by 25

Defining the interconnectivity of the medial prefrontal cortex and ventral midbrain

Hui, M., & Beier, K. T. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.971349 · Cited by 25

Closing the gap between clinic and cage: Sensori-motor and cognitive behavioural testing regimens in neurotoxin-induced animal models of Parkinson's disease

Pienaar, I. S., Lu, B., & Schallert, T. J. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.07.009 · Cited by 25

Antisaccadic Effects of a Dopamine Agonist as Add-On Therapy in Advanced Parkinson’s Patients

Crevits, L., Versijpt, J. J., Hanse, M. C. J., & Ridder, K. D. (2000) · Neuropsychobiology · doi:10.1159/000026694 · Cited by 25

Nicotine sensitization of monkey striatal dopamine release

Domino, E. F., & Tsukada, H. (2009) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2009.02.011 · Cited by 25

JL 13, An Atypical Antipsychotic: A Preclinical Review

Ellenbroek, B. A., & Liégeois, J. (2003) · CNS Drug Reviews · doi:10.1111/j.1527-3458.2003.tb00243.x · Cited by 25

Tonic activity during visuo-oculomotor behavior in the monkey superior colliculus

Kojima, J., Matsumura, M., Togawa, M., & Hikosaka, O. (1996) · Neuroscience Research · doi:10.1016/0168-0102(96)01067-x · Cited by 25

Maintenance in working memory or response selection?

Lissek, S., & Güntürkün, O. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.01.007 · Cited by 25

GSK ‐3β Interacts with Dopamine D1 Receptor to Regulate Receptor Function: Implication for Prefrontal Cortical D1 Receptor Dysfunction in Schizophrenia

Wang, J., Sun, P., Ren, Z., Meltzer, H. Y., & Zhen, X. (2016) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12664 · Cited by 24

Repeated methamphetamine administration produces cognitive deficits through augmentation of GABAergic synaptic transmission in the prefrontal cortex

Armenta-Reséndiz, M., Assali, A., Tsvetkov, E., Cowan, C. W., & Lavín, A. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01371-9 · Cited by 25

The effect of high-energy protons in the Bragg Peak on the behavior of rats and the exchange of monoamines in some brain structures

Shtemberg, A. S., Kokhan, V. S., Кудрин, В. С., Матвеева, М. И., Lebedeva-Georgievskaya, K. D., Тимошенко, Г. Н., Molokanov, A. G., Krasavin, E. A., Наркевич, В. Б., Михайлович, К. П., et al. (2015) · Neurochemical Journal · doi:10.1134/s1819712415010109 · Cited by 24

Phencyclidine-induced disruption of oscillatory activity in prefrontal cortex: Effects of antipsychotic drugs and receptor ligands

Lladó-Pelfort, L., Troyano‐Rodriguez, E., van den Munkhof, H. E., Cervera‐Ferri, A., Jurado, N., Núñez-Calvet, M., Artigas, F., & Celada, P. (2015) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2015.11.015 · Cited by 24

Serotonin–Dopamine Interaction: Experimental Evidence and Therapeutic Relevance

(2008) · Progress in brain research · doi:10.1016/s0079-6123(08)00935-7 · Cited by 24

N-methyl-d-aspartate antagonists as drug models of schizophrenia: a surprising link to tobacco smoking

Domino, E. F., Mirzoyan, D., & Tsukada, H. (2004) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2004.05.024 · Cited by 24

Dopamine system: manager of neural pathways

Hong, S. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00854 · Cited by 24

Lesion of medial prefrontal dopamine terminals abolishes habituation of accumbens shell dopamine responsiveness to taste stimuli

Bimpisidis, Z., Luca, M. A. D., Pisanu, A., & Chiara, G. D. (2012) · European Journal of Neuroscience · doi:10.1111/ejn.12068 · Cited by 24

Context dependent effects of ventral tegmental area inactivation on spatial working memory

Martig, A. K., Jones, G. L., Smith, K. E., & Mizumori, S. J. Y. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.05.008 · Cited by 24

Different activation of NF‐κB by stimulation of dopamine D2L and D2S receptors through calcineurin activation

Takeuchi, Y., & Fukunaga, K. (2004) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02476.x · Cited by 24

Transcranial direct current stimulation of the prefrontal cortex reduces cigarette craving in not motivated to quit smokers: A randomized, sham-controlled study

Perri, R. L., & Perrotta, D. (2021) · Addictive Behaviors · doi:10.1016/j.addbeh.2021.106956 · Cited by 23

Dopamine Modulates Adaptive Forgetting in Medial Prefrontal Cortex

Gallo, F. T., Zanoni, M. B., Silva, A., Morici, J. F., Miranda, M., Anderson, M. C., Weisstaub, N., & Bekinschtein, P. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.0740-21.2022 · Cited by 23

Dopamine, Salience, and Response Set Shifting in Prefrontal Cortex

Shiner, T., Symmonds, M., Guitart‐Masip, M., Fleming, S. M., Friston, K. J., & Dolan, R. J. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu210 · Cited by 23

Stimulation of dopamine D1 receptors in the avian fronto-striatal system adjusts daily cognitive fluctuations

Herold, C., Diekamp, B., & Güntürkün, O. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.07.017 · Cited by 23

Four facets of a single brain: behaviour, cerebral blood flow/metabolism, neuronal activity and neurotransmitter dynamics

Kéri, S., & Gulyás, B. Z. (2003) · Neuroreport · doi:10.1097/00001756-200306110-00001 · Cited by 23

The Relevance of the Dopamine-D1 Receptor in the Cognitive Symptoms of Schizophrenia

Goldman-Rakic, P. (1999) · Neuropsychopharmacology · doi:10.1016/s0893-133x(99)00107-4 · Cited by 23

Dopamine firing plays a dual role in coding reward prediction errors and signaling motivation in a working memory task

Sarno, S., Beirán, M., Falcó-Roget, J., Diaz-deLeon, G., Rossi-Pool, R., Romo, R., & Parga, N. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2113311119 · Cited by 22

Contributions of COMT Val158Met to cognitive stability and flexibility in infancy

Markant, J. C., Cicchetti, D., Hetzel, S., & Thomas, K. M. (2014) · Developmental Science · doi:10.1111/desc.12128 · Cited by 22

Split–Brain Basics: Relevance for the Concept of One's Other Mind

Bogen, J. E. (2000) · Journal of the American Academy of Psychoanalysis · doi:10.1521/jaap.1.2000.28.2.341 · Cited by 22

New therapeutic strategies targeting D1-type dopamine receptors for neuropsychiatric disease

Kim, Y.-C., Alberico, S. L., Emmons, E. B., & Narayanan, N. S. (2015) · Frontiers in Biology · doi:10.1007/s11515-015-1360-4 · Cited by 23

Genome-Wide Analyses of Working-Memory Ability: A Review

Knowles, E. E. M., Mathias, S. R., McKay, D., Sprooten, E., Blangero, J., Almasy, L. A., & Glahn, D. C. (2014) · Current Behavioral Neuroscience Reports · doi:10.1007/s40473-014-0028-8 · Cited by 22

Clinical significance of knowledge about the structure, function, and impairments of working memory

Bajor, G. (2013) · Medical Science Monitor · doi:10.12659/msm.883900 · Cited by 22

Relationship Between Neuromodulation and Working Memory in the Prefrontal Cortex: It's Complicated

Motley, S. E. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00031 · Cited by 22

Amphetamine Effects on Striatal Neurons: Implications for Models of Dopamine Function

Haracz, J. L. (1998) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(97)00057-2 · Cited by 22

Monoaminergic-Dependent Cognitive Functions of the Prefrontal Cortex in Monkey and Man

Robbins, T. W., Roberts, A., Owen, A. M., Sahakian, B. J., Everitt, B. J., Wilkinson, L., Muir, J. L., Salvia, M. D., & Tovée, M. J. (1994) · Research and perspectives in neurosciences · doi:10.1007/978-3-642-85007-3_6 · Cited by 22

Just do it: A neuropsychological theory of agency, cognition, mood, and dopamine.

Ashby, F. G., Zetzer, H. A., Conoley, C. W., & Pickering, A. D. (2024) · Journal of Experimental Psychology General · doi:10.1037/xge0001587 · Cited by 21

Potential Contribution of Dopaminergic Gene Variants in ADHD Core Traits and Co-Morbidity: A Study on Eastern Indian Probands

Maitra, S., Sarkar, K., Ghosh, P., Karmakar, A., Bhattacharjee, A., Sinha, S., & Mukhopadhyay, K. (2014) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-014-0038-9 · Cited by 21

D1, but not D2, receptor blockade within the infralimbic and medial orbitofrontal cortex impairs cocaine seeking in a region‐specific manner

Cosme, C. V., Gutman, A. L., Worth, W. R., & LaLumiere, R. T. (2016) · Addiction Biology · doi:10.1111/adb.12442 · Cited by 21

Imidazolium Based Surface Active Ionic Liquids as Novel Micellar Media for Simultaneous and Sensitive Electrochemical Detection of Dopamine and Ascorbic Acid

Rather, M. A., Bhat, S. A., Pandit, S. A., Rather, G. M., Khan, K. Z., & Bhat, M. A. (2017) · Electroanalysis · doi:10.1002/elan.201700047 · Cited by 21

Slc20a2-Deficient Mice Exhibit Multisystem Abnormalities and Impaired Spatial Learning Memory and Sensorimotor Gating but Normal Motor Coordination Abilities

Ren, Y., Shen, Y., Si, N., Fan, S., Zhang, Y., Xu, W., Shi, L., & Zhang, X. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.639935 · Cited by 21

Dopaminergic neuromodulation of semantic priming in a cortical network model

Lavigne, F., & Darmon, N. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2008.06.019 · Cited by 21

Chapter 11 Working memory

D’Esposito, M. (2008) · Handbook of clinical neurology · doi:10.1016/s0072-9752(07)88011-0 · Cited by 21

Healthy aging increases the cognitive effects of two genes that influence extracellular dopamine.

Greenwood, P. M., Lin, M., Sundararajan, R., Fryxell, K. J., & Parasuraman, R. (2014) · Psychology and Aging · doi:10.1037/a0036109 · Cited by 21

The contribution of AT1 and AT2 angiotensin receptors to its cognitive effects

Braszko, J. J. (1996) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-1996-1103 · Cited by 21

Activation of the dopaminergic system of medial prefrontal cortex of gerbils during formation of relevant associations for the avoidance strategy in the shuttle-box

Stark, H., Bischof, A., Wagner, T., & Scheich, H. (2001) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(00)00171-8 · Cited by 21

Gq/11-Induced and Spontaneous Waves of Coordinated Network Activation in Developing Frontal Cortex

Calderon, D. P., Leverkova, N., & Peinado, A. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2765-04.2005 · Cited by 21

Plasticity of the Primate Prefrontal Cortex

Amemori, S., & Sawaguchi, T. (2007) · The Neuroscientist · doi:10.1177/1073858406298554 · Cited by 21

Effects of COMT Genotypes on Working Memory Performance in Fibromyalgia Patients

Ferrera, D., Gómez‐Esquer, F., Peláez, I., Barjola, P., Fernandes-Magalhaes, R., Carpio, A., Lahoz, M. E. D., Díaz‐Gil, G., & Mercado, F. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9082479 · Cited by 20

5 Dopaminergic Modulation of Cognition in Human Aging

Li, S., Lindenberger, U., Nyberg, L. H., Heekeren, H. R., & Bäckman, L. (2009) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195328875.003.0005 · Cited by 20

Simultaneous determination of 5-hydroxytryptamine and dopamine using ionic liquid functionalized graphene

Liu, P., Dong, M., Lu, J., Guo, H., Lu, X., & Liu, X. (2014) · Ionics · doi:10.1007/s11581-014-1260-7 · Cited by 20

A Fragile Balance: Perturbation of GABA Mediated Circuit in Prefrontal Cortex Generates High Intraindividual Performance Variability

Pouget, P., Wattiez, N., Rivaud-Péchoux, S., & Gaymard, B. M. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005208 · Cited by 20

Relationship of frontal D2/3 binding potentials to cognition: a study of antipsychotic-naive schizophrenia patients

Fagerlund, B., Pinborg, L. H., Mortensen, E. L., Friberg, L., Baaré, W. F. C., Gade, A., Svarer, C., & Glenthoj, B. Y. (2012) · The International Journal of Neuropsychopharmacology · doi:10.1017/s146114571200003x · Cited by 20

CALCYONgene variation, schizophrenia, and cocaine dependence

Luο, X., Kranzler, H. R., Lappalainen, J., Rosenheck, R. A., Charney, D. S., Zuo, L., Erdos, J., van Kammen, D. P., & Gelernter, J. E. (2003) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.20092 · Cited by 20

No effect of age and estrogen on aromatic L- amino acid decarboxylase activity in rhesus monkey brain

Eberling, J. L. (2002) · Neurobiology of Aging · doi:10.1016/s0197-4580(01)00323-2 · Cited by 20

Combined D1/D2 receptor stimulation under conditions of dopamine depletion impairs spatial working memory performance in humans

Ellis, K. A., Mehta, M. A., Wesnes, K. A., Armstrong, S., & Nathan, P. J. (2005) · Psychopharmacology · doi:10.1007/s00213-005-0019-2 · Cited by 20

Comparative distribution of mRNA encoding the growth hormone secretagogue‐receptor (GHS‐R) in Microcebus murinus (Primate, Lemurian) and rat forebrain and pituitary

Mitchell, V. A., Bouret, S. G., Beauvillain, J., Schilling, A., Perret, M., Kordon, C., & Epelbaum, J. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20010115)429:3 · Cited by 119

Role of Dopamine in the Plasticity of Glutamic Acid Decarboxylase Messenger RNA in the Rat Frontal Cortex and the Nucleus Accumbens

Rétaux, S., Trovero, F., & Besson, M. (1994) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1994.tb00571.x · Cited by 20

Effects of dopamine D1 modulation of the anterior cingulate cortex in a fear conditioning procedure

Pezze, M. A., Marshall, H. J., Domonkos, A., & Cassaday, H. J. (2015) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2015.08.015 · Cited by 19

Hippocampal monoamine receptor complex levels linked to spatial memory decline in the aging C57BL/6J

Saroja, S. R., Kim, E., Shanmugasundaram, B., Höger, H., & Lübec, G. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.01.042 · Cited by 19

Effects of haloperidol on cognition in schizophrenia patients depend on baseline performance: A saccadic eye movement study

Babin, S. L., Hood, A. J., Wassef, A. A., Williams, N., Patel, S. S., & Sereno, A. B. (2011) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2011.06.004 · Cited by 19

Dopaminergic impact on local and global cortical circuit processing during learning

Happel, M. F. K. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.11.016 · Cited by 19

Contribution of non-genetic factors to dopamine and serotonin receptor availability in the adult human brain

Borg, J., Červenka, S., Kuja‐Halkola, R., Matheson, G. J., Jönsson, E. G., Lichtenstein, P., Henningsson, S., Ichimiya, T., Larsson, H., Stenkrona, P., et al. (2015) · Molecular Psychiatry · doi:10.1038/mp.2015.147 · Cited by 19

Cell-based therapies for the treatment of schizophrenia

Donegan, J. J., & Lodge, D. J. (2016) · Brain Research · doi:10.1016/j.brainres.2016.08.010 · Cited by 19

Effects of Amisulpride Adjunctive Therapy on Working Memory and Brain Metabolism in the Frontal Cortex of Patients with Schizophrenia: A Preliminary Positron Emission Tomography/Computerized Tomography Investigation

Park, J. H., Hong, J. S., Kim, S. M., Min, K. J., Chung, U., & Han, D. H. (2019) · Clinical Psychopharmacology and Neuroscience · doi:10.9758/cpn.2019.17.2.250 · Cited by 19

A three-year prospective study of spontaneous eye-blink rate in first-episode schizophrenia: relationship with relapse and neurocognitive function.

Chan, K. K. S., Hui, C. L. M., Lam, M. M. L., Tang, J. Y. ‐., Wong, G. H. Y., Chan, S. K. W., & Chen, E. Y. H. (2010) · PubMed · Cited by 19

PET neuroimaging of extrastriatal dopamine receptors and prefrontal cortex functions

Takahashi, H. (2013) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2013.07.001 · Cited by 19

D1 Dopamine Receptor Signaling Is Modulated by the R7 RGS Protein EAT-16 and the R7 Binding Protein RSBP-1 in Caenoerhabditis elegans Motor Neurons

Wani, K. A., Catanese, M. C., Normantowicz, R., Herd, M., Maher, K. N., & Chase, D. L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037831 · Cited by 19

Trace amine-associated receptor 1 agonism promotes wakefulness without impairment of cognition in Cynomolgus macaques

Goonawardena, A. V., Morairty, S. R., Dell, R., Orellana, G. A., Hoener, M. C., Wallace, T. L., & Kilduff, T. S. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0386-8 · Cited by 19

International Health Practices: A Multidisciplinary Approach to Therapeutic Mediations With an Artistic Medium Based on the Model of Play

Brun, A., Brunet, L., Cerclet, D., Masson, A., Ravit, M., Tassin, J., Zornig, S. M. A.-J., Zurlo, M. C., Guénoun, T., Missonnier, S., et al. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2020.00254 · Cited by 19

Synaptic density of the prefrontal cortex regulated by dopamine instead of serotonin in rats

Sugahara, M., & Shiraishi, H. (1998) · Brain Research · doi:10.1016/s0006-8993(98)01068-3 · Cited by 19

Behavioural relevance modulates access to spatial working memory in humans

Ploner, C. J., Ostendorf, F., Brandt, S. A., Gaymard, B. M., Rivaud-Péchoux, S., Ploner, M., Villringer, A., & Pierrot‐Deseilligny, C. (2001) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2001.01397.x · Cited by 19

5-Fluoronicotine, noranhydroecgonine, and pyridyl-methylpyrrolidine release acetylcholine and biogenic amines in rat cortex in vivo

Summers, K. L., Lippiello, P. M., Verhulst, S. J., & Giacobini, E. (1995) · Neurochemical Research · doi:10.1007/bf00995564 · Cited by 19

Psychopharmacology -- in vivo neurochemistry and pharmacology

Grasby, P. M., Malizia, A. L., & Bench, C. J. (1996) · British Medical Bulletin · doi:10.1093/oxfordjournals.bmb.a011564 · Cited by 19

COMT val158met genotype and smooth pursuit eye movements in schizophrenia

Haraldsson, H. M., Ettinger, U., Magnúsdóttir, B. B., Sigmundsson, T., Sigurðsson, E., Ingason, A., & Pétursson, H. (2009) · Psychiatry Research · doi:10.1016/j.psychres.2008.10.003 · Cited by 18

Dopamine D2 receptor stimulation modulates the balance between ignoring and updating according to baseline working memory ability

Fallon, S. J., Kienast, A., Muhammed, K., Ang, Y., Manohar, S., & Husain, M. (2019) · Journal of Psychopharmacology · doi:10.1177/0269881119872190 · Cited by 18

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Hayley, A. C., Shiferaw, B. A., & Downey, L. A. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101929 · Cited by 18

D1, not D2, dopamine receptor activation dramatically improves MPTP-induced parkinsonism unresponsive to levodopa

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Executive control: balancing stability and flexibility via the duality of evolutionary neuroanatomical trends

Bilder, R. M. (2012) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2012.14.1/rbilder · Cited by 18

Similarities in the behavior and molecular deficits in the frontal cortex between the neurotensin receptor subtype 1 knockout mice and chronic phencyclidine-treated mice: Relevance to schizophrenia

Li, Z., Boules, M., Williams, K., Gordillo, A., Li, S., & Richelson, E. (2010) · Neurobiology of Disease · doi:10.1016/j.nbd.2010.07.011 · Cited by 18

Distinct prefrontal cortical regions negatively regulate evoked activity in nucleus accumbens subregions

Asher, A. M., & Lodge, D. J. (2011) · The International Journal of Neuropsychopharmacology · doi:10.1017/s146114571100143x · Cited by 18

An investigation into aripiprazole’s partial D2 agonist effects within the dorsolateral prefrontal cortex during working memory in healthy volunteers

Murphy, A., Dursun, S. M., McKie, S., Elliott, R., & Deakin, J. F. W. (2016) · Psychopharmacology · doi:10.1007/s00213-016-4234-9 · Cited by 18

Brain mechanisms of visual encoding and working memory in psychometrically identified schizotypal individuals and after acute administration of haloperidol

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Memory trace in prefrontal cortex: theory for the cognitive switch

Otani, S. (2002) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1017/s1464793102006012 · Cited by 18

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Proietti, R., Parr, T., Tessari, A., Friston, K. J., & Pezzulo, G. (2025) · Physics of Life Reviews · doi:10.1016/j.plrev.2025.05.008 · Cited by 17

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Singh, K. P., & Singh, M. K. (2017) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2016.12.006 · Cited by 17

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Sawaguchi, T., & Goldman‐Rakic, P. S. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.71.2.515 · Cited by 649

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Valentim, S. J. R. (2008) · riUfes (Universidade Federal do Espírito Santo)

Modulation of memory fields by dopamine Dl receptors in prefrontal cortex

Williams, G. V., & Goldman-Rakic, P. S. (1995) · Nature · doi:10.1038/376572a0 · Cited by 1,593

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Sawaguchi, T. (1995) · Springer eBooks · doi:10.1007/978-4-431-68547-0_11 · Cited by 4