The DOI matches its Crossref record; 143 of the 143 references it cites were found in a registry or an index.
The Neuropsychopharmacology of Fronto-Executive Function: Monoaminergic Modulation
Open accessAbstract
We review the modulatory effects of the catecholamine neurotransmitters noradrenaline and dopamine on prefrontal cortical function. The effects of pharmacologic manipulations of these systems, sometimes in comparison with the indoleamine serotonin (5-HT), on performance on a variety of tasks that tap working memory, attentional-set formation and shifting, reversal learning, and response inhibition are compared in rodents, nonhuman primates, and humans using, in a behavioral context, several techniques ranging from microiontophoresis and single-cell electrophysiological recording to pharmacologic functional magnetic resonance imaging. Dissociable effects of drugs and neurotoxins affecting these monoamine systems suggest new ways of conceptualizing state-dependent fronto-executive functions, with implications for understanding the molecular genetic basis of mental illness and its treatment.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Dopamine modulates motivation and reinforcement learning; norepinephrine regulates arousal and vigilance; serotonin contributes to impulse control and mood stabilization; acetylcholine enhances attention and memory encoding (Robbins and Arnsten, 2009).”
From Enhancement of modern defense capabilities by convergence of cognitive neuroscience and artificial intelligence (2026) · cites this paper as Robbins and Arnsten, 2009
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Neurobiological mechanisms and neurotransmitter systems ranging from neurotransmitter regulation, like, dopamine, norepinephrine, serotonin, and acetylcholine to stress physiology related to hypothalamic-pituarity-adrenal axis or HPA axis and neural oscillations—provide the substrates for adaptability and resilience (Buzsáki, 2006; McEwen, 2007; Robbins and Arnsten, 2009).”
From Enhancement of modern defense capabilities by convergence of cognitive neuroscience and artificial intelligence (2026) · cites this paper as Robbins and Arnsten, 2009
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Dopamine modulates motivation and reinforcement learning; norepinephrine regulates arousal and vigilance; serotonin contributes to impulse control and mood stabilization; acetylcholine enhances attention and memory encoding (Robbins and Arnsten, 2009).”
From Enhancement of modern defense capabilities by convergence of cognitive neuroscience and artificial intelligence (2026) · cites this paper as Robbins and Arnsten, 2009
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Dopamine modulates motivation and reinforcement learning; norepinephrine regulates arousal and vigilance; serotonin contributes to impulse control and mood stabilization; acetylcholine enhances attention and memory encoding (Robbins and Arnsten, 2009).”
From Enhancement of modern defense capabilities by convergence of cognitive neuroscience and artificial intelligence (2026) · cites this paper as Robbins and Arnsten, 2009
The cited source says what the claim attributes to it.
In the citing paper
“In general, optimal levels of dopamine in PFC are essential for WM performance”
From Systematic reviews of the acute effects of amphetamine on working memory and other cognitive performances in healthy individuals, with a focus on the potential influence of personality traits (2023) · cites this paper as Robbins & Arnsten, 2009
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Dopamine modulates motivation and reinforcement learning; norepinephrine regulates arousal and vigilance; serotonin contributes to impulse control and mood stabilization; acetylcholine enhances attention and memory encoding (Robbins and Arnsten, 2009).”
From Enhancement of modern defense capabilities by convergence of cognitive neuroscience and artificial intelligence (2026) · cites this paper as Robbins and Arnsten, 2009
Experimental — accuracy not yet measuredIn the citing paper
“monoaminergic modulation of the efficacy of synaptic connections in PFC circuits has profound effects on PFC-mediated executive function, including working memory, regulation of attention, inhibition of inappropriate behaviors, and impulsivity control 45.”
From Mechanisms of synaptic transmission dysregulation in the prefrontal cortex: pathophysiological implications (2022) · cites this paper as [45]
In the citing paper
“On the basis of animal models (Berridge et al, 2006;Robbins and Arnsten, 2009), the optimum alert state (see Figure 4) appears to be related to more moderate levels of activation of NE a-2A and DA D1 receptors in the PFC, but that stress-related increases of release of NE and DA and results in the activation of NE a-1 and b-1 receptor and excessive activation of D1 receptors (Arnsten, 2009).”
From Understanding the Effects of Stimulant Medications on Cognition in Individuals with Attention-Deficit Hyperactivity Disorder: A Decade of Progress (2011) · cites this paper as Robbins and Arnsten, 2009
In the citing paper
“Research in adult human and animal models has suggested that intermediate levels of DA signaling in both PFC and striatum are necessary for optimal performance, following a Yerkes-Dodson inverted U-shaped dose response curve of DA signaling and behavior (Robbins and Arnsten 2009; Cools and D'Esposito 2011).”
From Developmental imaging genetics: Linking dopamine function to adolescent behavior (2014) · cites this paper as Robbins and Arnsten 2009
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
An Integrative Theory of Prefrontal Cortex Function
Miller, E. K., & Cohen, J. D. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.167 · Cited by 12,803
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
The Wellcome Trust Case Control Consortium, Management Committee, Burton, P. R., Clayton, D. G., Cardon, L. R., Craddock, N., Deloukas, P., Duncanson, A., Kwiatkowski, D. P., McCarthy, M. I., et al. (2007) · Nature · doi:10.1038/nature05911 · Cited by 9,442
Aston-Jones, G., & Cohen, J. D. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135709 · Cited by 4,472
Inhibition and the right inferior frontal cortex
Aron, A. R., Robbins, T. W., & Poldrack, R. A. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.02.010 · Cited by 3,197
Self-citationBerridge, C. W., & Waterhouse, B. D. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(03)00143-7 · Cited by 2,529
Effect of COMT Val 108/158 Met genotype on frontal lobe function and risk for schizophrenia
Egan, M. F., Goldberg, T. E., Kolachana, B. S., Callicott, J. H., Mazzanti, C. M., Straub, R. E., Goldman, D. A., & Weinberger, D. R. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.111134598 · Cited by 2,416
Circuitry of Primate Prefrontal Cortex and Regulation of Behavior by Representational Memory
Goldman‐Rakic, P. S. (1987) · Comprehensive Physiology · doi:10.1002/cphy.cp010509 · Cited by 1,960
Neuroscience of attention-deficit/hyperactivity disorder: the search for endophenotypes
Castellanos, F. X., & Tannock, R. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn896 · Cited by 1,827 · cited 1×
“ADHD is often associated with genetic alterations in catecholamine signaling (Castellanos & Tannock 2002).”
BackgroundThe sleep switch: hypothalamic control of sleep and wakefulness
Saper, C. B., Chou, T. C., & Scammell, T. E. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)02002-6 · Cited by 1,656
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
Research works printed but not linked: 11
- Arnsten AFT, 2008, Fut. Neurol., 3
- Baddeley AD, 1986, Working memory
- 10.1176/appi.ajp.163.7.1282 · DOI · Paper page
- Durstewictz D, 2000, J. Neurophysiology, 19, 2807
- Goldman-Rakic PS, 1987, Handbook of Physiology, 373
- Hess C, 2008, J. Neural. Transm.
- Kieling C, 2007, Am. J. Med. Genet. B Neuropsychiatr. Genet.
- Manji HK, 1999, J. Clin. Psychiatry, 60, 27
- Moore RY, 2001, Arch. Ital. Biol., 139, 195
- Robbins TW, 1995, Psychopharmacology—4th Generation of Progress, 363
- Seamans JK, 2009, Dopamine Receptors
Cited by
Sorted by citations
Items 301–400 of 955
Gasbarri, A., Tavares, M. C. H., Rodrigues, R. C., Tomaz, C. A. B., & Pompili, A. (2012) · Reviews in the Neurosciences · doi:10.1515/revneuro-2012-0051 · Cited by 51
Noradrenergic modulation of risk/reward decision making
Montes, D. R., Stopper, C. M., & Floresco, S. (2015) · Psychopharmacology · doi:10.1007/s00213-015-3904-3 · Cited by 50
Fardell, J. E., Vardy, J. L., Logge, W., & Johnston, I. (2010) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2010.08.019 · Cited by 50
Barak, S., & Weiner, I. (2011) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2011.03.011 · Cited by 51
Cognitive Abilities on Transitive Inference Using a Novel Touchscreen Technology for Mice
Silverman, J. L., Gastrell, P. T., Karras, M. N., Solomon, M., & Crawley, J. N. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht293 · Cited by 51
Nimitvilai, S., Lopez, M. F., Mulholland, P. J., & Woodward, J. J. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.22 · Cited by 50
Estrogens, Aging, and Working Memory
Hampson, E. (2018) · Current Psychiatry Reports · doi:10.1007/s11920-018-0972-1 · Cited by 54
Apical amplification—a cellular mechanism of conscious perception?
Marvan, T., Polák, M., Bachmann, T., & Phillips, W. A. (2021) · Neuroscience of Consciousness · doi:10.1093/nc/niab036 · Cited by 45
Modulation of Social Influence by Methylphenidate
Campbell-Meiklejohn, D. K., Simonsen, A., Jensen, M., Wohlert, V., Gjerløff, T., Scheel‐Krüger, J., Møller, A., Frith, C., & Roepstorff, A. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2011.337 · Cited by 54
Burke, A. R., Forster, G. L., Novick, A. M., Roberts, C. L., & Watt, M. J. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.11.013 · Cited by 49
Sárvári, M., Kalló, I., Hrabovszky, E., Solymosi, N., Tóth, K., Likó, I., Molnar, B. A., Tihanyi, K., & Liposits, Z. (2010) · Endocrinology · doi:10.1210/en.2010-0375 · Cited by 50
Boosting Norepinephrine Transmission Triggers Flexible Reconfiguration of Brain Networks at Rest
Guedj, C., Monfardini, E., Reynaud, A. J., Farnè, A., Meunier, M., & Hadj‐Bouziane, F. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw262 · Cited by 55
The Lateral Habenula as a Relay of Cortical Information to Process Working Memory
Mathis, V., Barbelivien, A., Majchrzak, M. J., Mathis, C., Cassel, J., & Lecourtier, L. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw316 · Cited by 54
Jacob, S. N., Stalter, M., & Nieder, A. (2016) · Nature Communications · doi:10.1038/ncomms13218 · Cited by 52
Stokholm, M. G., Iranzo, Á., Østergaard, K., Serradell, M., Otto, M., Svendsen, K. B., Garrido, A., Vilas, D., Parbo, P., Borghammer, P., et al. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.02.017 · Cited by 49
Adolescent social defeat decreases spatial working memory performance in adulthood
Novick, A. M., Miiller, L. C., Forster, G. L., & Watt, M. J. (2013) · Behavioral and Brain Functions · doi:10.1186/1744-9081-9-39 · Cited by 47
Exploring intermediate phenotypes with EEG: Working memory dysfunction in schizophrenia
Haenschel, C., & Linden, D. E. J. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.08.045 · Cited by 54
Neurotransmitter Systems in a Mild Blast Traumatic Brain Injury Model: Catecholamines and Serotonin
Kawa, L., Arborelius, U. P., Yoshitake, T., Kehr, J., Hökfelt, T. G. M., Risling, M., & Agoston, D. V. (2014) · Journal of Neurotrauma · doi:10.1089/neu.2014.3669 · Cited by 48
The influence of emotions on cognitive control: feelings and beliefs—where do they meet?
Harlé, K. M., Shenoy, P., & Paulus, M. P. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00508 · Cited by 56
Xiang, L., Harel, A., Gao, H., Pickering, A. E., Sara, S. J., & Wiener, S. I. (2019) · Scientific Reports · doi:10.1038/s41598-018-37227-w · Cited by 46
Lohani, S., Martig, A. K., Underhill, S. M., Oranburg, T. D., Roberts, M. J., Rinaman, L., Amara, S., & Moghaddam, B. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0088-7 · Cited by 48
Janssens, A., Noortgate, W. V. D., Goossens, L., Verschueren, K., Colpin, H., Laet, S. D., Claes, S. J., & Leeuwen, K. G. V. (2015) · Journal of Youth and Adolescence · doi:10.1007/s10964-015-0304-2 · Cited by 54
Effects of α-2A adrenergic receptor agonist on time and risk preference in primates
Kim, S., Bobeica, I., Gamo, N. J., Arnsten, A. F. T., & Lee, D. (2012) · Psychopharmacology · doi:10.1007/s00213-011-2520-0 · Cited by 47
Self-citationvan Heesch, F., Prins, J., Konsman, J. P., Korte-Bouws, G. A. H., Westphal, K. G. C., Rybka, J., Olivier, B., Kraneveld, A. D., & Korte, S. M. (2014) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2014.01.014 · Cited by 47
Linley, S. B., Gallo, M. M., & Vertes, R. P. (2016) · Brain Research · doi:10.1016/j.brainres.2016.08.022 · Cited by 51
Disruption of Timing: NeuroHIV Progression in the Post-cART Era
McLaurin, K. A., Li, H., Booze, R. M., & Mactutus, C. F. (2019) · Scientific Reports · doi:10.1038/s41598-018-36822-1 · Cited by 47
Baker, P. M., Raynor, S. A., Francis, N.-M., & Mizumori, S. J. Y. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.02.010 · Cited by 49
Piccolo genotype modulates neural correlates of emotion processing but not executive functioning
Woudstra, S., Bochdanovits, Z., van Tol, M.-J., Veltman, D. J., Zitman, F. G., van Buchem, M. A., van der Wee, N. J., Opmeer, E. M., Demenescu, L. R., Aleman, A., et al. (2012) · Translational Psychiatry · doi:10.1038/tp.2012.29 · Cited by 45
Noradrenergic α2A-receptor stimulation in the ventral hippocampus reduces impulsive decision-making
Abela, A. R., & Chudasama, Y. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3262-y · Cited by 47
Millan, M. J., Rivet, J., & Gobert, A. (2016) · Journal of Psychopharmacology · doi:10.1177/0269881116672342 · Cited by 44
Executive (dys)function after stroke: special considerations for behavioral pharmacology
Povroznik, J. M., Ozga, J. E., Haar, C. V., & Engler-Chiurazzi, E. B. (2018) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000432 · Cited by 48
Mäki-Marttunen, V., Hagen, T., & Espeseth, T. (2019) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-019-00691-6 · Cited by 53
Bangasser, D. A., & Kawasumi, Y. (2015) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.04.003 · Cited by 46
Beck, S. M., Ruge, H., Schindler, C., Burkart, M., Miller, R. E., Kirschbaum, C., & Goschke, T. (2016) · Human Psychopharmacology Clinical and Experimental · doi:10.1002/hup.2534 · Cited by 44
Nonkes, L. J. P., Tomson, K., Märtin, A., Dederen, J., Maes, J. H. R., & Homberg, J. R. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2010.04.002 · Cited by 42
Potential Moderators of Physical Activity on Brain Health
Leckie, R. L., Weinstein, A. M., Hodzic, J. C., & Erickson, K. I. (2012) · Journal of Aging Research · doi:10.1155/2012/948981 · Cited by 47
Dopamine D2 Receptors Enhance Population Dynamics in Primate Prefrontal Working Memory Circuits
Ott, T., & Nieder, A. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw244 · Cited by 46
Xu, H., Zhang, Y., Zhang, F., Yuan, S., Shao, F., & Wang, W. (2016) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2016.00095 · Cited by 42
Neurocognitive Function in Dopamine-β-Hydroxylase Deficiency
Jepma, M., Deinum, J., Asplund, C. L., Rombouts, S. A. R. B., Tamsma, J. T., Tjeerdema, N., Spapé, M., Garland, E. M., Robertson, D., Lenders, J. W. M., et al. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.42 · Cited by 41
Tomlinson, A., Grayson, B., Marsh, S., Hayward, A., Marshall, K. M., & Neill, J. C. (2014) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2014.11.016 · Cited by 42
Impulsivity is related to striatal dopamine transporter availability in healthy males
Costa, A. C. L., la Fougère, C. J., Pogarell, O. M., Möller, H., Riedel, M. J., & Ettinger, U. (2012) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2012.07.011 · Cited by 41
Drowsiness or mind-wandering? Fluctuations in ocular parameters during attentional lapses
Stawarczyk, D., François, C., Wertz, J., & D’Argembeau, A. (2020) · Biological Psychology · doi:10.1016/j.biopsycho.2020.107950 · Cited by 41
Alsene, K. M., & Bakshi, V. P. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.47 · Cited by 38
Schmeichel, B. E., Zemlan, F. P., & Berridge, C. W. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.07.005 · Cited by 40
Costanzi, M., Cianfanelli, B., Santirocchi, A., Lasaponara, S., Spataro, P., Rossi-Arnaud, C., & Cestari, V. (2021) · Journal of Personalized Medicine · doi:10.3390/jpm11040241 · Cited by 39
Trent, S., Cassano, T., Bedse, G., Ojarikre, O. A., Humby, T., & Davies, W. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.314 · Cited by 39
Beste, C., Domschke, K., Radenz, B., Falkenstein, M., & Konrad, C. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2011.05.014 · Cited by 40
Women are more sensitive than men to prior trial events on the S top‐signal task
Thakkar, K. N., Congdon, E. L., Poldrack, R. A., Sabb, F. W., London, E. D., Cannon, T. D., & Bilder, R. M. (2013) · British Journal of Psychology · doi:10.1111/bjop.12034 · Cited by 43
Imaging dopamine neurotransmission in live human brain
Badgaiyan, R. D. (2014) · Progress in brain research · doi:10.1016/b978-0-444-63425-2.00007-6 · Cited by 40
Effect of Smoking on Cognitive Functioning in Young Saudi Adults
Bashir, S., Alghamd, F., Alhussien, A., Alohali, M., Alatawi, A., Almusned, T., & Habib, S. S. (2017) · Medical science monitor basic research/Medical science monitor. Basic research · doi:10.12659/msmbr.902385 · Cited by 41
Wolff, N., Mückschel, M., Ziemssen, T., & Beste, C. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1531-y · Cited by 42
Opinion on monoaminergic contributions to traits and temperament
Robbins, T. W. (2018) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2017.0153 · Cited by 37
Self-citationAlterations in white matter network topology contribute to freezing of gait in Parkinson’s disease
Hall, J. M., Shine, J. M., Martens, K. A. E., Gilat, M., Broadhouse, K. M., Szeto, J. Y. Y., Walton, C. C., Moustafa, A. A., & Lewis, S. J. G. (2018) · Journal of Neurology · doi:10.1007/s00415-018-8846-3 · Cited by 42
Kennedy, D. O., Bonnländer, B., Lang, S. C., Pischel, I., Forster, J. S., Khan, J., Jackson, P. A., & Wightman, E. L. (2020) · Nutrients · doi:10.3390/nu12061598 · Cited by 38
Andersen, S. L., & Navalta, C. P. (2011) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2011.02376.x · Cited by 40
Dopamine Gene Profiling to Predict Impulse Control and Effects of Dopamine Agonist Ropinirole
MacDonald, H. J., Stinear, C. M., Ren, A., Coxon, J. P., Kao, J., Macdonald, L., Snow, B. J., Cramer, S. C., & Byblow, W. D. (2016) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00946 · Cited by 38
De Bundel, D., Femenía, T., DuPont, C. M., Konradsson-Geuken, Å., Feltmann, K., Schilström, B., & Lindskog, M. (2013) · International Journal of Neuropsychopharmacology · doi:10.1017/s1461145713000370 · Cited by 37
Cerebrospinal fluid norepinephrine and cognition in subjects across the adult age span
Wang, L. Y., Murphy, R. R., Hanscom, B. S., Li, G., Millard, S. P., Petrie, E. C., Galasko, D. R., Sikkema, C. L., Raskind, M. A., Wilkinson, C. W., et al. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2013.04.007 · Cited by 35
Impact of estrogen receptor alpha and beta agonists on delayed alternation in middle-aged rats
Neese, S. L., Korol, D. L., Katzenellenbogen, J. A., & Schantz, S. L. (2010) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.08.017 · Cited by 37
Dopamine D2-Receptor Blockade Enhances Decoding of Prefrontal Signals in Humans
Kahnt, T., Weber, S. C., Haker, H., Robbins, T. W., & Tobler, P. N. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4182-14.2015 · Cited by 35
Self-citationLevy‐Gigi, E., Kelemen, O., Gluck, M. A., & Kéri, S. (2011) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2011.08.005 · Cited by 37
Plaßmann, H., & Karmarkar, U. R. (2015) · Cambridge University Press eBooks · doi:10.1017/cbo9781107706552.006 · Cited by 40
Pinto, A., Almeida, M., Ramos, P. C., Rocha, S. M., Guimas, A., Ribeiro, R., Martins, E., Bandeira, A., MacDonald, A., & Rocha, J. C. (2017) · European Journal of Clinical Nutrition · doi:10.1038/ejcn.2017.38 · Cited by 37
de Bartolomeis, A., Barone, A., Buonaguro, E. F., Tomasetti, C., Vellucci, L., & Iasevoli, F. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104596 · Cited by 40
Konjusha, A., Yu, S., Mückschel, M., Colzato, L. S., Ziemssen, T., & Beste, C. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.2004-22.2023 · Cited by 39
Xiao, H., Li, N., Meng, Q., Shao, F., & Wang, W. (2011) · Neuropsychobiology · doi:10.1159/000322455 · Cited by 39
Knapman, A., Heinzmann, J.-M., Holsboer, F., Landgraf, R., & Touma, C. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2010.04.010 · Cited by 39
Anshu, K., Nair, A. K., Kumaresan, U. D., Kutty, B. M., Srinath, S., & Laxmi, T. R. (2017) · Autism Research · doi:10.1002/aur.1852 · Cited by 38
Harlé, K. M., Guo, D., Zhang, S., Paulus, M. P., & Yu, A. J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0186473 · Cited by 36
Zhang, Y., Xu, H., Zhang, F., Shao, F., Ellenbroek, B. A., Wang, J., & Wang, W. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.02.010 · Cited by 34
Zhukovsky, P., Puaud, M., Jupp, B., Sala‐Bayo, J., Alsiö, J., Xia, J., Searle, L., Morris, Z. S., Sabir, A., Giuliano, C., et al. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0381-0 · Cited by 33
Self-citationUnderstanding and Managing Cognition in the Depressed Patient
Papakostas, G. I., & Culpepper, L. (2015) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.13086ah1c · Cited by 35
Endocannabinoids and the Processing of Value-Related Signals
Melis, M., Muntoni, A. L., & Pistis, M. (2012) · Frontiers in Pharmacology · doi:10.3389/fphar.2012.00007 · Cited by 36
Chronic methamphetamine self-administration alters cognitive flexibility in male rats
Cox, B. M., Cope, Z. A., Parsegian, A., Floresco, S., Aston‐Jones, G., & See, R. E. (2016) · Psychopharmacology · doi:10.1007/s00213-016-4283-0 · Cited by 35
A Neuroeconomic Framework for Creative Cognition
Lin, H., & Vartanian, O. A. (2018) · Perspectives on Psychological Science · doi:10.1177/1745691618794945 · Cited by 43
Campbell-Meiklejohn, D. K., Simonsen, A., Scheel‐Krüger, J., Wohlert, V., Gjerløff, T., Frith, C., Rogers, R. D., Roepstorff, A., & Møller, A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0151-12.2012 · Cited by 35
Laet, S. D., Colpin, H., Leeuwen, K. G. V., Noortgate, W. V. D., Claes, S. J., Janssens, A., Goossens, L., & Verschueren, K. (2016) · Journal of Youth and Adolescence · doi:10.1007/s10964-016-0466-6 · Cited by 43
Central Noradrenergic Interactions with Alcohol and Regulation of Alcohol-Related Behaviors
Vazey, E. M., den Hartog, C. R., & Moorman, D. E. (2018) · Handbook of experimental pharmacology · doi:10.1007/164_2018_108 · Cited by 33
Callahan, P. M., Plagenhoef, M. R., Blake, D. T., & Terry, A. V. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.05.016 · Cited by 39
Weber, M. A., Conlon, M. M., Stutt, H. R., Wendt, L. H., Eyck, P. T., & Narayanan, N. S. (2022) · Behavioral Neuroscience · doi:10.1037/bne0000512 · Cited by 38
Alsene, K. M., Fallace, K., & Bakshi, V. P. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.106 · Cited by 34
CANTAB delayed matching to sample task performance in juvenile baboons
Rodriguez, J. S., Zürcher, N. R., Bartlett, T. Q., Nathanielsz, P. W., & Nijland, M. J. (2011) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2011.01.012 · Cited by 34
Takahashi, K., Nakagawasai, O., Nemoto, W., Odaira, T., Arai, Y., Hisamitsu, T., & Tan–No, K. (2017) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2017.08.071 · Cited by 34
Tei, S., Fujino, J., Hashimoto, R.-I., Itahashi, T., Ohta, H., Kanai, C., Kubota, M., Nakamura, M., Kato, N., & Takahashi, H. (2018) · Scientific Reports · doi:10.1038/s41598-018-26465-7 · Cited by 37
Tůma, J., Kolinko, Y., Vožeh, F., & Cendelín, J. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00116 · Cited by 34
Further evidence for executive dysfunction in subjects with RLS from a non-clinical sample
Fulda, S., Szesny, N., Ising, M., Heck, A., Grübl, A., Lieb, R., & Reppermund, S. (2011) · Sleep Medicine · doi:10.1016/j.sleep.2011.04.013 · Cited by 33
COMT genotype, gambling activity, and cognition
Grant, J. E., Leppink, E. W., Redden, S. A., Odlaug, B. L., & Chamberlain, S. R. (2015) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2015.04.029 · Cited by 32
van Holst, R. J., van der Meer, J. N., McLaren, D. G., van den Brink, W., Veltman, D. J., & Goudriaan, A. E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049923 · Cited by 35
Novick, A. M., Mears, M., Forster, G. L., Lei, Y., Tejani‐Butt, S. M., & Watt, M. J. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.02.013 · Cited by 33
Mar, A. C., Nilsson, S. R. O., Gamallo‐Lana, B., Lei, M., Dourado, T., Alsiö, J., Saksida, L. M., Bussey, T. J., & Robbins, T. W. (2017) · Psychopharmacology · doi:10.1007/s00213-017-4679-5 · Cited by 31
Self-citationVijayraghavan, S., Major, A. J., & Everling, S. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00091 · Cited by 34
Steding, J., Boehm, I., King, J. A., Geisler, D., Ritschel, F., Seidel, M., Doose, A., Jaite, C., Roessner, V., Smolka, M. N., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-49884-6 · Cited by 37
Xu, T., Ma, Q., Spealman, R. D., & Yao, W. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.07073.x · Cited by 33
COMT Val 158 Met and Cognitive and Functional Outcomes after Traumatic Brain Injury
Willmott, C., Withiel, T., Ponsford, J. L., & Burke, R. (2014) · Journal of Neurotrauma · doi:10.1089/neu.2013.3308 · Cited by 33
Social brains on drugs: tools for neuromodulation in social neuroscience
Crockett, M. J., & Fehr, E. (2013) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nst113 · Cited by 32
Lee, M. L., Mueller, A. L., & Moore, T. (2020) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2020.574130 · Cited by 32
Impact of Serotonin (5-HT)2C Receptors On Executive Control Processes
Pennanen, L., van der Hart, M., Yu, L., & Tecott, L. H. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2012.258 · Cited by 33
Shehzad, Z. E., DeYoung, C. G., Kang, Y., Grigorenko, E. L., & Gray, J. R. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.097 · Cited by 32
COMT and ANKK1 Genetics Interact With Depression to Influence Behavior Following Severe TBI
Myrga, J. M., Juengst, S. B., Failla, M. D., Conley, Y. P., Arenth, P. M., Grace, A. A., & Wagner, A. K. (2016) · Neurorehabilitation and neural repair · doi:10.1177/1545968316648409 · Cited by 33
Effects of dopamine D2/D3 receptor antagonism on human planning and spatial working memory
Naef, M., Müller, U., Linssen, A. M. W., Clark, L., Robbins, T. W., & Eisenegger, C. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.56 · Cited by 31
Self-citation
Metadata
- Authors
- Robbins, T. W., & Arnsten, A. F. T.
- Affiliations
- University of Cambridge (GB)
- Yale University (US)
- Venue
- Annual Review of Neuroscience
- Publisher
- Annual Reviews
- Published
- 2009-06-01
- Volume
- 32
- Issue
- 1
- Pages
- 267-287
- ISSN
- 0147-006X (ISSN-L)
- 1545-4126
- PMC
- PMC2863127
- OpenAlex
- W2160985876
- Cited by
- 957
- References
- 143
- Citations by year
- 2026: 37 · 2025: 45 · 2024: 38 · 2023: 66 · 2022: 41 · 2021: 41 · 2020: 47 · 2019: 48 · 2018: 58 · 2017: 64 · 2016: 64 · 2015: 70 · 2014: 53 · 2013: 90 · 2012: 72
- FWCI
- 5.61
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Annual Review of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Yale University
- National Alliance for Research on Schizophrenia and Depression
- Wellcome Trust
- Medical Research Council
- National Institute on Alcohol Abuse and Alcoholism (RL1AA017536)
- National Institute on Aging (R37AG006036, P01AG030004, R01AG006036, AG06036)
- National Institute of Mental Health (P50MH068789)
- National Center for Research Resources (U54RR024350)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- norepinephrine, dopamine, serotonin, prefrontal cortex, working memory, set-shifting, reversal learning, response inhibition, neuropsychopharmacology, neurotoxins, mental illness
- MeSH terms
- Animals, Catecholamines, Cognition, Humans, Mental Processes, Synaptic Transmission, Neuropharmacology, Psychomotor Performance, Serotonin, Prefrontal Cortex, Neurocognitive Disorders
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review