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

Inhibition of the norepinephrine transporter improves behavioral flexibility in rats and monkeys

Seu, E., Lang, A., Rivera, R. J., & Jentsch, J. D. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1250-4 · Cited by 128

Adrenergic targets for the treatment of cognitive deficits in schizophrenia

Arnsten, A. F. T. (2003) · Psychopharmacology · doi:10.1007/s00213-003-1724-3 · Cited by 128

Pramipexole in Psychiatry

Aiken, C. (2007) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.v68n0810 · Cited by 128

What the rodent prefrontal cortex can teach us about attention-deficit/hyperactivity disorder: the critical role of early developmental events on prefrontal function

Sullivan, R. M., & Brake, W. G. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.09.015 · Cited by 128

Molecular mechanisms of stress-induced prefrontal cortical impairment: Implications for mental illness

Hains, A. B., & Arnsten, A. F. T. (2008) · Learning & Memory · doi:10.1101/lm.921708 · Cited by 127

Molecular modulation of prefrontal cortex: Rational development of treatments for psychiatric disorders.

Gamo, N. J., & Arnsten, A. F. T. (2011) · Behavioral Neuroscience · doi:10.1037/a0023165 · Cited by 128

Muscarinic and nicotinic receptor modulation of object and spatial -back working memory in humans

GREEN, A., Ellis, K. A., Ellis, J. R., Bartholomeusz, C., ILIC, S., Croft, R. J., LUANPHAN, K., & NATHAN, P. (2005) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2005.04.010 · Cited by 127

Selective blockade of dopamine D3versus D2receptors enhances frontocortical cholinergic transmission and social memory in rats: a parallel neurochemical and behavioural analysis

Millan, M. J., Cara, B. D., Dekeyne, A., Panayi, F., de Groote, L., Sicard, D., Cistarelli, L., Billiras, R., & Gobert, A. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04262.x · Cited by 126

Ovarian hormones differentially influence immunoreactivity for dopamine ?- hydroxylase, choline acetyltransferase, and serotonin in the dorsolateral prefrontal cortex of adult rhesus monkeys

Kritzer, M. F., & Kohama, S. G. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990705)409:3 · Cited by 126

Modulation of neocortical interneurons: extrinsic influences and exercises in self-control

Bacci, A., Huguenard, J. R., & Prince, D. A. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.08.007 · Cited by 126

Psychopharmacological approaches to modulating attention in the five-choice serial reaction time task: implications for schizophrenia

Chudasama, Y., & Robbins, T. W. (2004) · Psychopharmacology · doi:10.1007/s00213-004-1805-y · Cited by 125

Dopamine D1 receptors and age differences in brain activation during working memory

Bäckman, L., Karlsson, S., Fischer, H., Karlsson, P., Brehmer, Y., Rieckmann, A., MacDonald, S. W. S., Farde, L., & Nyberg, L. H. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.10.018 · Cited by 125

Neural Correlates of Executive Control in the Avian Brain

Rose, J., & Colombo, M. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030190 · Cited by 125

Modeling functions of striatal dopamine modulation in learning and planning

Suri, R. E., Bargas, J., & Arbib, M. A. (2001) · Neuroscience · doi:10.1016/s0306-4522(00)00554-6 · Cited by 124

Presynaptic D1Dopamine Receptors in Primate Prefrontal Cortex: Target-Specific Expression in the Glutamatergic Synapse

Paspalas, C. D., & Goldman-Rakic, P. S. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3436-04.2005 · Cited by 94

Dopaminergic Modulation of Visual-Spatial Working Memory in Parkinson’s Disease

da Costa, A. L. C., Peppe, A., Dell’Agnello, G., Carlesimo, G. A., Murri, L., Bonuccelli, U., & Caltagirone, C. (2003) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000067968 · Cited by 124

Studies of Brain and Cognitive Maturation Through Childhood and Adolescence: A Strategy for Testing Neurodevelopmental Hypotheses

Luna, B., & Sweeney, J. A. (2001) · Schizophrenia Bulletin · doi:10.1093/oxfordjournals.schbul.a006886 · Cited by 124

Mechanisms of Working Memory Impairment in Schizophrenia

Van Snellenberg, J. X., Girgis, R. R., Horga, G., van de Giessen, E., Slifstein, M., Ojeil, N., Weinstein, J. J., Moore, H., Lieberman, J. A., Shohamy, D., et al. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.02.017 · Cited by 123

Planning ability in Parkinson's disease is influenced by the COMT val 158 met polymorphism

Foltynie, T., Goldberg, T. E., Lewis, S. J. G., Blackwell, A. D., Kolachana, B. S., Weinberger, D. R., Robbins, T. W., & Barker, R. A. (2004) · Movement Disorders · doi:10.1002/mds.20118 · Cited by 122

The convergent evolution of neural substrates for cognition

Güntürkün, O. (2011) · Psychological Research · doi:10.1007/s00426-011-0377-9 · Cited by 122

Double dissociation of serotonergic and dopaminergic mechanisms on attentional performance using a rodent five-choice reaction time task

Passetti, F., Dalley, J. W., & Robbins, T. W. (2003) · Psychopharmacology · doi:10.1007/s00213-002-1227-7 · Cited by 121

The Presence of Background Dopamine Signal Converts Long-Term Synaptic Depression to Potentiation in Rat Prefrontal Cortex

Matsuda, Y., Marzo, A., & Otani, S. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5312-05.2006 · Cited by 121

Subpopulations of cortical GABAergic interneurons differ by their expression of D1 and D2 dopamine receptor subtypes

Moine, C. L., & Gaspar, P. (1998) · Molecular Brain Research · doi:10.1016/s0169-328x(98)00118-1 · Cited by 121

Distinct Representations of Cognitive and Motivational Signals in Midbrain Dopamine Neurons

Matsumoto, M., & Takada, M. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.002 · Cited by 120

Dopamine Receptor D1/D5 Gene Expression in the Medial Prefrontal Cortex Predicts Impulsive Choice in Rats

Loos, M., Pattij, T., Janssen, M. C. W., Counotte, D. S., Schoffelmeer, A. N. M., Smit, A. B., Spijker, S., & van Gaalen, M. M. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp167 · Cited by 120

Exploring a Neuroplasticity Model of Music Therapy

Stegemöller, E. L. (2014) · Journal of Music Therapy · doi:10.1093/jmt/thu023 · Cited by 118

Dopaminergic Modulation of Cognitive Control: Distinct Roles for the Prefrontal Cortex and the Basal Ganglia

van Schouwenburg, M. R., Aarts, E., & Cools, R. (2010) · Current Pharmaceutical Design · doi:10.2174/138161210791293097 · Cited by 118

Locomotion and conditioned place preference produced by acute intravenous amphetamine: role of dopamine receptors and individual differences in amphetamine self-administration

Bardo, M. T., Valone, J. M., & Bevins, R. A. (1999) · Psychopharmacology · doi:10.1007/s002130050917 · Cited by 118

Neuroendocrine Mechanisms Regulating Reproductive Cycles and Reproductive Behavior in Birds

Ball, G. F., & Balthazart, J. (2002) · Elsevier eBooks · doi:10.1016/b978-012532104-4/50034-2 · Cited by 117

Levodopa ameliorates learning and memory deficits in a murine model of Alzheimer’s disease

Ambrée, O., Richter, H., Sachser, N., Lewejohann, L., Dere, E., de Souza Silva, M. A., Herring, A., Keyvani, K., Paulus, W., & Schäbitz, W.-R. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.11.010 · Cited by 115

Cortical dopaminergic innervation among humans, chimpanzees, and macaque monkeys: A comparative study

Raghanti, M. A., Stimpson, C. D., Marcinkiewicz, J. L., Erwin, J. M., Hof, P. R., & Sherwood, C. C. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.05.008 · Cited by 115

Traumatic brain injury and cognition

Cristofori, I., & Levin, H. S. (2015) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63521-1.00037-6 · Cited by 115

Impaired spatial working memory and decreased frontal cortex BDNF protein level in dopamine transporter knockout mice

Li, B., Arime, Y., Hall, F. S., Uhl, G. R., & Sora, I. (2009) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2009.11.036 · Cited by 115

Verbal working memory dysfunction in schizophrenia: use of a Brown-Peterson paradigm

Fleming, K., Goldberg, T. E., Gold, J. M., & Weinberger, D. R. (1995) · Psychiatry Research · doi:10.1016/0165-1781(95)02589-3 · Cited by 114

Molecular activity underlying working memoryPreprint

Dash, P. K., Moore, A. N., Kobori, N., & Runyan, J. D. (2007) · Learning & Memory · doi:10.1101/lm.558707 · Cited by 114

The role of prefrontal catecholamines in attention and working memory

Clark, K., & Noudoost, B. (2014) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00033 · Cited by 113

Increased dopamine release in the human amygdala during performance of cognitive tasks

Fried, I., Wilson, C. L., Morrow, J. W., Cameron, K. A., Behnke, E., Ackerson, L. C., & Maidment, N. T. (2001) · Nature Neuroscience · doi:10.1038/84041 · Cited by 112

Dopamine D1-Class Receptors Selectively Modulate a Slowly Inactivating Potassium Current in Rat Medial Prefrontal Cortex Pyramidal Neurons

Dong, Y., & White, F. J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-07-02686.2003 · Cited by 112

Selective Effects of Acute Serotonin and Catecholamine Depletion on Memory in Healthy Women

Harrison, B. J., Olver, J. S., Norman, T. R., Burrows, G. D., Wesnes, K. A., & Nathan, P. J. (2004) · Journal of Psychopharmacology · doi:10.1177/0269881104040225 · Cited by 111

Brain-derived neurotrophic factor transiently stabilizes silent synapses on developing neuromuscular junctions

Kwon, Y. W., & Gurney, M. E. (1996) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(199604)29:4 · Cited by 44

Haloperidol Differentially Modulates Prepulse Inhibition and P50 Suppression in Healthy Humans Stratified for Low and High Gating Levels

Csomor, P., Stadler, R. R., Feldon, J., Yee, B. K., Geyer, M. A., & Vollenweider, F. X. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301421 · Cited by 110

Noradrenaline and Dopamine Elevations in the Rat Prefrontal Cortex in Spatial Working Memory

Rossetti, Z. L., & Carboni, S. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3038-04.2005 · Cited by 110

Dopamine Increases the Gain of the Input-Output Response of Rat Prefrontal Pyramidal Neurons

Thurley, K., Senn, W., & Lüscher, H. (2008) · Journal of Neurophysiology · doi:10.1152/jn.01098.2007 · Cited by 110

Distribution of mGluR1α and mGluR5 immunolabeling in primate prefrontal cortex

Muly, E. C., Maddox, M., & Smith, Y. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10937 · Cited by 110

Working memory after traumatic brain injury in children

Levin, H. S., Hanten, G. R., Chang, C., Zhang, L., Schachar, R. J., Ewing‐Cobbs, L., & Max, J. E. (2002) · Annals of Neurology · doi:10.1002/ana.10252 · Cited by 110

Unifying cognitive aging: From neuromodulation to representation to cognition

Li, S., Lindenberger, U., & Frensch, P. A. (2000) · Neurocomputing · doi:10.1016/s0925-2312(00)00256-3 · Cited by 110

Dissociation of Haloperidol, Clozapine, and Olanzapine Effects on Electrical Activity of Mesocortical Dopamine Neurons and Dopamine Release in the Prefrontal Cortex

Gessa, G. L. (2000) · Neuropsychopharmacology · doi:10.1016/s0893-133x(00)00087-7 · Cited by 110

Normal Genetic Variation, Cognition, and Aging

Greenwood, P. M., & Parasuraman, R. (2003) · Behavioral and Cognitive Neuroscience Reviews · doi:10.1177/1534582303260641 · Cited by 110

MGluR-Mediated Calcium Waves that Invade the Soma Regulate Firing in Layer V Medial Prefrontal Cortical Pyramidal Neurons

Hagenston, A. M., Fitzpatrick, J. S., & Yeckel, M. F. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm075 · Cited by 109

Argument for a non‐linear relationship between severity of human obesity and dopaminergic tone

Horstmann, A., Fenske, W. K., & Hankir, M. K. (2015) · Obesity Reviews · doi:10.1111/obr.12303 · Cited by 109

Variability in Dopamine Genes Dissociates Model-Based and Model-Free Reinforcement Learning

Doll, B. B., Bath, K. G., Daw, N. D., & Frank, M. J. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1901-15.2016 · Cited by 110

Linkage of the dopamine receptor D1 gene to attention-deficit/hyperactivity disorder

Misener, V. L., Luca, P., Azeke, O., Crosbie, J., Waldman, I. D., Tannock, R., Roberts, W., MALONE, M. A., Schachar, R. J., Ickowicz, A., et al. (2003) · Molecular Psychiatry · doi:10.1038/sj.mp.4001440 · Cited by 109

Altered function of ventral striatum during reward-based decision making in old age

Mell, T. (2009) · Frontiers in Human Neuroscience · doi:10.3389/neuro.09.034.2009 · Cited by 109

Venlafaxine: Discrepancy between in vivo 5-HT and NE reuptake blockade and affinity for reuptake sites

B��que, J.-C., de Montigny, C., Blier, P., & Debonnel, G. (1999) · Synapse · doi:10.1002/(sici)1098-2396(19990601)32:3 · Cited by 69

COMT val158met moderation of dopaminergic drug effects on cognitive function: a critical review

Schacht, J. P. (2016) · The Pharmacogenomics Journal · doi:10.1038/tpj.2016.43 · Cited by 108

Persistent neural activity during the maintenance of spatial position in working memory

Srimal, R., & Curtis, C. E. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.08.040 · Cited by 108

Adolescent Maturation of Cortical Dopamine

O’Donnell, P. (2010) · Neurotoxicity Research · doi:10.1007/s12640-010-9157-3 · Cited by 107

The effects of dopamine and its antagonists on directional delay-period activity of prefrontal neurons in monkeys during an oculomotor delayed-response task

Sawaguchi, T. (2001) · Neuroscience Research · doi:10.1016/s0168-0102(01)00270-x · Cited by 107

Differential effects of clozapine and haloperidol on interval timing in the supraseconds range

MacDonald, C. J., & Meck, W. H. (2005) · Psychopharmacology · doi:10.1007/s00213-005-0074-8 · Cited by 106

Unique and shared roles of the posterior parietal and dorsolateral prefrontal cortex in cognitive functions

Katsuki, F. (2012) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2012.00017 · Cited by 107

Effects of tryptophan loading on verbal, spatial and affective working memory functions in healthy adults

Luciana, M. M., Burgund, E. D., Berman, M. I., & Hanson, K. L. (2001) · Journal of Psychopharmacology · doi:10.1177/026988110101500410 · Cited by 105

Sleep Deprivation During Early-Adult Development Results in Long-Lasting Learning Deficits in Adult Drosophila

Seugnet, L., Suzuki, Y., Donlea, J. M., Gottschalk, L., & Shaw, P. J. (2011) · SLEEP · doi:10.1093/sleep/34.2.137 · Cited by 104

Prefrontal Cortical Representation of Visuospatial Working Memory in Monkeys Examined by Local Inactivation With Muscimol

Sawaguchi, T., & Iba, M. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.4.2041 · Cited by 104

Buspirone modulates basal and fluoxetine-stimulated dialysate levels of dopamine, noradrenaline and serotonin in the frontal cortex of freely moving rats: activation of serotonin1A receptors and blockade of α2-adrenergic receptors underlie its actions

Gobert, A., Rivet, J., Cistarelli, L., Melon, C., & Millan, M. J. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00211-0 · Cited by 103

D1 Receptor Modulation of Action Potential Firing in a Subpopulation of Layer 5 Pyramidal Neurons in the Prefrontal Cortex

Seong, H. J., & Carter, A. G. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1367-12.2012 · Cited by 103

Memory and frontal lobe functions; possible relations with dopamine D2 receptors in the hippocampus

Takahashi, H., Kato, M., Hayashi, M., Okubo, Y., Takano, A., Ito, H., & Suhara, T. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.11.008 · Cited by 102

Catecholamines and cognition after traumatic brain injury

Jenkins, P. O., Mehta, M. A., & Sharp, D. J. (2016) · Brain · doi:10.1093/brain/aww128 · Cited by 102

Sequence skill learning in persons who stutter: Implications for cortico-striato-thalamo-cortical dysfunction

Smits‐Bandstra, S., & Nil, L. F. D. (2007) · Journal of Fluency Disorders · doi:10.1016/j.jfludis.2007.06.001 · Cited by 101

Vulnerability in early life to changes in the rearing environment plays a crucial role in the aetiopathology of psychiatric disorders

Niwa, M., Matsumoto, Y., Mouri, A., Ozaki, N., & Nabeshima, T. (2010) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145710001239 · Cited by 101

Cortical effects of bromocriptine, a D-2 dopamine receptor agonist, in human subjects, revealed by fMRI

Kimberg, D. Y., Aguirre, G. K., Lease, J., & D’Esposito, M. (2001) · Human Brain Mapping · doi:10.1002/1097-0193(200104)12:4 · Cited by 102

Antipsychotic Medications and the Elderly

Byerly, M., Weber, M., Brooks, D. L., Snow, L. R., Worley, M. A., & Lescouflair, E. (2001) · Drugs & Aging · doi:10.2165/00002512-200118010-00004 · Cited by 101

Impaired β-arrestin recruitment and reduced desensitization by non-catechol agonists of the D1 dopamine receptor

Gray, D. L., Allen, J., Mente, S., O’Connor, R. E., DeMarco, G. J., Efremov, I. V., Tierney, P. L., Volfson, D., Davoren, J. E., Guilmette, E. R., et al. (2018) · Nature Communications · doi:10.1038/s41467-017-02776-7 · Cited by 100

LSD and structural analogs: pharmacological evaluation at D1 dopamine receptors

Watts, V. J., Mailman, R. B., Lawler, C. P., Neve, K. A., & Nichols, D. E. (1995) · Psychopharmacology · doi:10.1007/bf02245940 · Cited by 100

Effects of morphine and naltrexone on impulsive decision making in rats

Kieres, A. K., Hausknecht, K. A., Farrar, A. M., Acheson, A., de Wit, H., & Richards, J. B. (2004) · Psychopharmacology · doi:10.1007/s00213-003-1697-2 · Cited by 100

Effects of normal aging on prefrontal area 46 in the rhesus monkey

Luebke, J. I., Barbas, H., & Peters, A. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.12.002 · Cited by 99

Gonadectomy in adult life increases tyrosine hydroxylase immunoreactivity in the prefrontal cortex and decreases open field activity in male rats

Adler, A., Vescovo, P., Robinson, J. K., & Kritzer, M. F. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00341-8 · Cited by 100

Dopamine and the motivation of cognitive control

Cools, R., Froböse, M. I., Aarts, E., & Hofmans, L. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-12-804281-6.00007-0 · Cited by 99

Differential Contributions of Dopamine and Serotonin to Orbitofrontal Cortex Function in the Marmoset

Walker, S. C., Robbins, T. W., & Roberts, A. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn136 · Cited by 99

Reversal of phencyclidine-induced effects by glycine and glycine transport inhibitors

Javitt, D. C., Balla, A., Sershen, H. W., & Lajtha, Á. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(98)00237-6 · Cited by 99

Role for dopamine in the behavioral functions of the prefrontal corticostriatal system: implications for mental disorders and psychotropic drug action

Jentsch, J. D., Roth, R. H., & Taylor, J. R. (2000) · Progress in Brain Research · doi:10.1016/s0079-6123(00)26028-7 · Cited by 99

An animal model of early-treated PKU

Diamond, A. D., Ciaramitaro, V. M., Donner, E. J., Djali, S., & Robinson, M. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-05-03072.1994 · Cited by 99

NEUROPSYCHOLOGY OF SUBCORTICAL DEMENTIAS

Savage, C. R. (1997) · Psychiatric Clinics of North America · doi:10.1016/s0193-953x(05)70352-x · Cited by 99

Dopamine tunes prefrontal outputs to orchestrate aversive processing

Weele, C. M. V., Siciliano, C. A., & Tye, K. M. (2018) · Brain Research · doi:10.1016/j.brainres.2018.11.044 · Cited by 98

Khat Use Is Associated with Impaired Working Memory and Cognitive Flexibility

Colzato, L. S., Ruiz, M. J., van den Wildenberg, W. P. M., & Hommel, B. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020602 · Cited by 98

Deficits in selective and sustained attention processes in early treated children with phenylketonuria — result of impaired frontal lobe functions?

Weglage, J., Pietsch, M., Fünders, B., Koch, H. G., & Ullrich, K. (1996) · European Journal of Pediatrics · doi:10.1007/bf01953938 · Cited by 98

The Signaling and Pharmacology of the Dopamine D1 Receptor

Jones-Tabah, J., Mohammad, H., Paulus, E., Clarke, P. B. S., & Hébert, T. E. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.806618 · Cited by 97

Age-related spatial working memory impairment is caused by prefrontal cortical dopaminergic dysfunction in rats

Mizoguchi, K., Shoji, H., Tanaka, Y., Maruyama, W., & Tabira, T. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.05.023 · Cited by 97

Recreational cocaine polydrug use impairs cognitive flexibility but not working memory

Colzato, L. S., Huizinga, M., & Hommel, B. (2009) · Psychopharmacology · doi:10.1007/s00213-009-1650-0 · Cited by 95

Saccadic abnormalities in psychotic patients. II. The role of neuroleptic treatment

Crawford, T. J., Haeger, B., Kennard, C., Reveley, M. A., & Henderson, L. (1995) · Psychological Medicine · doi:10.1017/s0033291700033390 · Cited by 95

The Neurobiology of Thought: The Groundbreaking Discoveries of Patricia Goldman-Rakic 1937-2003

Arnsten, A. F. T. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht195 · Cited by 94

Performance of patients with schizophrenia on a pen and paper visuospatial working memory task with short delay

Keefe, R. S. E., Roitman, S. E. L., & Dupre, R. L. (1997) · Schizophrenia Research · doi:10.1016/s0920-9964(97)00037-6 · Cited by 94

Neural Substrates of Dopamine D2 Receptor Modulated Executive Functions in the Monkey Prefrontal Cortex

Puig, M. V., & Miller, E. K. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu096 · Cited by 94

Dopamine Receptors Differentially Enhance Rule Coding in Primate Prefrontal Cortex Neurons

Ott, T., Jacob, S. N., & Nieder, A. (2014) · Neuron · doi:10.1016/j.neuron.2014.11.012 · Cited by 93

Ovarian Cycle Effects on Immediate Reward Selection Bias in Humans: A Role for Estradiol

Smith, C. T., Sierra, Y., Oppler, S. H., & Boettiger, C. A. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0014-14.2014 · Cited by 93

Opposite effects of dopamine D2 and D3 receptors on learning and memory in the rat

Sigala, S., Missale, C., & Spano, P. (1997) · European Journal of Pharmacology · doi:10.1016/s0014-2999(97)01235-1 · Cited by 93

Chronic NMDA Antagonism Impairs Working Memory, Decreases Extracellular Dopamine, and Increases D1 Receptor Binding in Prefrontal Cortex of Conscious Monkeys

Tsukada, H., Nishiyama, S., Fukumoto, D., Sato, K., Kakiuchi, T., & Domino, E. F. (2005) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300732 · Cited by 93

Decreased density of tyrosine hydroxylase–immunoreactive axons in the entorhinal cortex of schizophrenic subjects

Akil, M., Edgar, C. L., Pierri, J. N., Casali, S., & Lewis, D. A. (2000) · Biological Psychiatry · doi:10.1016/s0006-3223(99)00282-6 · Cited by 93

Stimulus Load and Oscillatory Activity in Higher Cortex

Kornblith, S., Buschman, T. J., & Miller, E. K. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv182 · Cited by 92

Instructed Delay Activity in the Human Prefrontal Cortex is Modulated by Monetary Reward Expectation

Ramnani, N. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.3.318 · Cited by 92

The role of D1-dopamine receptor in working memory: local injections of dopamine antagonists into the prefrontal cortex of rhesus monkeys performing an oculomotor delayed-response task

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

The role of D1-dopamine receptors in working memory-guided movements mediated by frontal cortical areas

Sawaguchi, T. (2000) · Parkinsonism & Related Disorders · doi:10.1016/s1353-8020(00)00044-4 · Cited by 39

Modulação dopaminérgica da memória operacional espacial no córtex pré-frontal medial em ratos: envolvimento de receptores dos tipos D1 e D4

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

The Role of Dopamine in Frontal Motor Cortical Functions of Monkeys

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