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Attention-deficit/hyperactive disorder updates

Kessi, M., Duan, H., Xiong, J., Chen, B., He, F., Yang, L., Ma, Y., Bamgbade, O. A., Peng, J., & Yin, F. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.925049 · Cited by 82 · see citing works

Molecular Imaging of Opioid and Dopamine Systems: Insights Into the Pharmacogenetics of Opioid Use Disorders

Burns, J. A., Kroll, D. S., Feldman, D. E., Liu, C. K., Manza, P., Wiers, C. E., Volkow, N. D., & Wang, G. (2019) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.00626 · Cited by 72 · see citing works

Motivating inhibition – reward prospect speeds up response cancellation

Boehler, C. N., Hopf, J., Stoppel, C. M., & Krebs, R. M. (2012) · Cognition · doi:10.1016/j.cognition.2012.07.018 · Cited by 72 · see citing works

Recent insights into the neurobiology of impulsivity

Mitchell, M. R., & Potenza, M. N. (2014) · Current Addiction Reports · doi:10.1007/s40429-014-0037-4 · Cited by 70 · see citing works

Using mice to model Obsessive Compulsive Disorder: From genes to circuits

Ahmari, S. E. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.11.009 · Cited by 68 · see citing works

When Too Much Is Not Enough: Obsessive-Compulsive Disorder as a Pathology of Stopping, Rather than Starting

Hinds, A. L., Woody, E. Z., Ameringen, M. V., Schmidt, L. A., & Szechtman, H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030586 · Cited by 64 · see citing works

Highly impulsive rats: modelling an endophenotype to determine the neurobiological, genetic and environmental mechanisms of addiction

Jupp, B., Caprioli, D., & Dalley, J. W. (2013) · Disease Models & Mechanisms · doi:10.1242/dmm.010934 · Cited by 65 · see citing works

Dopamine and executive function: Increased spontaneous eye blink rates correlate with better set-shifting and inhibition, but poorer updating

Zhang, T., Mou, D., Wang, C., Tan, F., Jiang, Y., Lijun, Z., & Li, H. (2015) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2015.04.010 · Cited by 57 · see citing works

Convergent pharmacological mechanisms in impulsivity and addiction: insights from rodent models

Jupp, B., & Dalley, J. W. (2014) · British Journal of Pharmacology · doi:10.1111/bph.12787 · Cited by 56 · see citing works

Chronic Corticosterone Exposure during Adolescence Reduces Impulsive Action but Increases Impulsive Choice and Sensitivity to Yohimbine in Male Sprague-Dawley Rats

Torregrossa, M. M., Xie, M., & Taylor, J. R. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2012.11 · Cited by 55 · see citing works

Proficient motor impulse control in Parkinson disease patients with impulsive and compulsive behaviors

Claassen, D. O., van den Wildenberg, W. P. M., Harrison, M. B., van Wouwe, N. C., Kanoff, K. E., Neimat, J. S., & Wylie, S. A. (2014) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2014.11.017 · Cited by 55 · see citing works

Dorsal and ventral striatal dopamine D1 and D2 receptors differentially modulate distinct phases of serial visual reversal learning

Sala‐Bayo, J., Fiddian, L., Nilsson, S. R. O., Hervig, M. E.-S., McKenzie, C., Mareschi, A., Boulos, M., Zhukovsky, P., Nicholson, J. R., Dalley, J. W., et al. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-0612-4 · Cited by 48 · see citing works

Deep Brain Stimulation of the Subthalamic Nucleus, but not Dopaminergic Medication, Improves Proactive Inhibitory Control of Movement Initiation in Parkinson's Disease

Favre, É., Ballanger, B., Thobois, S., Broussolle, E., & Boulinguez, P. (2012) · Neurotherapeutics · doi:10.1007/s13311-012-0166-1 · Cited by 52 · see citing works

Dopamine D2 Receptor Modulation of Human Response Inhibition and Error Awareness

Nandam, L. S., Hester, R., Wagner, J., Dean, A. J., Messer, C., Honeysett, A., Nathan, P. J., & Bellgrove, M. A. (2013) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00327 · Cited by 50 · see citing works

Dopamine receptors D1 and D2 are related to observed maternal behavior

Mileva‐Seitz, V. R., Fleming, A. S., Meaney, M. J., Mastroianni, A., Sinnwell, J. P., Steiner, M. S., Atkinson, L. R., Levitan, R. D., Matthews, S. G., Kennedy, J. L., et al. (2012) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2012.00804.x · Cited by 48 · see citing works

Segregating domain-general from emotional context-specific inhibitory control systems - ventral striatum and orbitofrontal cortex serve as emotion-cognition integration hubs

Zhuang, Q., Xu, L., Zhou, F., Yao, S., Zheng, X., Zhou, X., Li, J., Xu, X., Fu, M., Li, K., et al. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118269 · Cited by 44 · see citing works

Selective Effects of PDE10A Inhibitors on Striatopallidal Neurons Require Phosphatase Inhibition by DARPP-32

Polito, M., Guiot, E., Gangarossa, G., Longueville, S., Doulazmi, M., Valjent, E., Hervé, D., Girault, J., Paupardin‐Tritsch, D., Castro, L. R., et al. (2015) · eNeuro · doi:10.1523/eneuro.0060-15.2015 · Cited by 45 · see citing works

Differences in response initiation and behavioral flexibility between adolescent and adult rats.

Simon, N. W., Gregory, T. A., Wood, J. T., & Moghaddam, B. (2013) · Behavioral Neuroscience · doi:10.1037/a0031328 · Cited by 42 · see citing works

Toxoplasma gondii, Suicidal Behavior, and Intermediate Phenotypes for Suicidal Behavior

Postolache, T. T., Wadhawan, A., Rujescu, D., Hoisington, A. J., Dagdag, A., Baca‐García, E., Lowry, C. A., Okusaga, O. O., & Brenner, L. A. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.665682 · Cited by 44 · see citing works

Swimming exercise alleviates the symptoms of attention-deficit hyperactivity disorder in spontaneous hypertensive rats

Ko, I., Kim, S., Kim, T.-W., Ji, E., Shin, M., Kim, C., Hong, M., & Bahn, G. H. (2013) · Molecular Medicine Reports · doi:10.3892/mmr.2013.1531 · Cited by 41 · see citing works

Inhibition of 5α-reductase attenuates behavioral effects of D1-, but not D2-like receptor agonists in C57BL/6 mice

Frau, R., Pillolla, G., Bini, V., Tambaro, S., Devoto, P., & Bortolato, M. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.07.014 · Cited by 42 · see citing works

Cortical dopamine release during a behavioral response inhibition task

Albrecht, D., Kareken, D. A., Christian, B. T., Džemidžić, M., & Yoder, K. K. (2014) · Synapse · doi:10.1002/syn.21736 · Cited by 41 · see citing works

Impulsivity, Stimulant Abuse, and Dopamine Receptor Signaling

London, E. D. (2016) · Advances in pharmacology · doi:10.1016/bs.apha.2016.01.002 · Cited by 40 · see citing works

The Psychopharmacology of Obsessive-Compulsive Disorder: A Preclinical Roadmap

Szechtman, H., Harvey, B. H., Woody, E. Z., & Hoffman, K. L. (2019) · Pharmacological Reviews · doi:10.1124/pr.119.017772 · Cited by 40 · see citing works

Drugs currently in Phase II clinical trials for cocaine addiction

Kim, J. H., & Lawrence, A. J. (2014) · Expert Opinion on Investigational Drugs · doi:10.1517/13543784.2014.915312 · Cited by 40 · see citing works

A comparative study on the neurophysiological mechanisms underlying effects of methylphenidate and neurofeedback on inhibitory control in attention deficit hyperactivity disorder

Bluschke, A., Friedrich, J., Schreiter, M. L., Roessner, V., & Beste, C. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.10.027 · Cited by 58 · see citing works

Response inhibition signals and miscoding of direction in dorsomedial striatum

Bryden, D. W., Burton, A. C., Kashtelyan, V., Barnett, B. R., & Roesch, M. R. (2012) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2012.00069 · Cited by 38 · see citing works

Dissociable electrophysiological subprocesses during response inhibition are differentially modulated by dopamine D1 and D2 receptors

Beste, C., Stock, A., Epplen, J. T., & Arning, L. (2016) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2016.03.002 · Cited by 37 · see citing works

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 38 · see citing works

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 · see citing works

A Single 30 Minutes Bout of Combination Physical Exercises Improved Inhibition and Vigor-Mood in Middle-Aged and Older Females: Evidence From a Randomized Controlled Trial

Nouchi, R., Nouchi, H., & Kawashima, R. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.00179 · Cited by 35 · see citing works

Cognitive control of gaze in bipolar disorder and schizophrenia

Thakkar, K. N., Schall, J. D., Logan, G. D., & Park, S. (2015) · Psychiatry Research · doi:10.1016/j.psychres.2014.12.033 · Cited by 34 · see citing works

Dysfunctional inhibitory control in Parkinson’s disease patients with levodopa-induced dyskinesias

Picazio, S., Ponzo, V., Caltagirone, C., Brusa, L., & Koch, G. (2018) · Journal of Neurology · doi:10.1007/s00415-018-8945-1 · Cited by 33 · see citing works

Reinstatement of synaptic plasticity in the aging brain through specific dopamine transporter inhibition

Lubec, J., Kalaba, P., Hussein, A. M., Feyissa, D. D., Kotob, M. H., Mahmmoud, R. R., Wieder, O., Garon, A., Sagheddu, C., Ilic, M., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01214-x · Cited by 31 · see citing works

Dissecting Impulsivity: Brain Mechanisms and Neuropsychiatric Implications

Robbins, T. W., & Dalley, J. W. (2017) · Nebraska Symposium on Motivation/The Nebraska symposium on motivation · doi:10.1007/978-3-319-51721-6_7 · Cited by 30 · see citing works

Neurobiological mechanisms of control in alcohol use disorder – Moving towards mechanism-based non-invasive brain stimulation treatments

Ghin, F., Beste, C., & Stock, A. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.12.031 · Cited by 29 · see citing works

A cross-species genetic analysis identifies candidate genes for mouse anxiety and human bipolar disorder

Ashbrook, D. G., Williams, R. W., Lu, L., & Hager, R. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00171 · Cited by 24 · see citing works

MR imaging central thalamic deep brain stimulation restored autistic-like social deficits in the rat

Lin, T.-C., Lo, Y., Lin, H., Li, S., Lin, S.-H., Wu, H.-F., Chu, M.-C., Lee, C. J., Lin, I., Chang, C.-W., et al. (2019) · Brain stimulation · doi:10.1016/j.brs.2019.07.004 · Cited by 25 · see citing works

The role of dopamine in action control: Insights from medication effects in Parkinson’s disease

Ruitenberg, M. F. L., van Wouwe, N. C., Wylie, S. A., & Abrahamse, E. L. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.04.023 · Cited by 25 · see citing works

The Human Basal Ganglia Mediate the Interplay between Reactive and Proactive Control of Response through Both Motor Inhibition and Sensory Modulation

Criaud, M., Anton, J., Nazarian, B., Longcamp, M., Météreau, É., Boulinguez, P., & Ballanger, B. (2021) · Brain Sciences · doi:10.3390/brainsci11050560 · Cited by 25 · see citing works

Quetiapine improves response inhibition in alcohol dependent patients: A placebo-controlled pilot study

Moallem, N. R., & Ray, L. A. (2011) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2011.10.012 · Cited by 23 · see citing works

The effects of methylphenidate on cerebral activations to salient stimuli in healthy adults.

Farr, O. M., Hu, S., Matuskey, D., Zhang, S., Abdelghany, O., & Li, C. R. (2013) · Experimental and Clinical Psychopharmacology · doi:10.1037/a0034465 · Cited by 23 · see citing works

Ropinirole, a dopamine agonist with high D3 affinity, reduces proactive inhibition: A double-blind, placebo-controlled study in healthy adults

Rawji, V., Rocchi, L., Foltynie, T., Rothwell, J. C., & Jahanshahi, M. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.108278 · Cited by 21 · see citing works

The right inferior frontal gyrus as pivotal node and effective regulator of the basal ganglia-thalamocortical response inhibition circuit

Zhuang, Q., Qiao, L., Xu, L., Yao, S., Chen, S., Zheng, X., Li, J., Fu, M., Li, K., Vatansever, D., et al. (2023) · Psychoradiology · doi:10.1093/psyrad/kkad016 · Cited by 21 · see citing works

Low Cognitive Impulsivity Is Associated with Better Gain and Loss Learning in a Probabilistic Decision-Making Task

Cáceres, P., & Martín, R. S. (2017) · Frontiers in Psychology · doi:10.3389/fpsyg.2017.00204 · Cited by 22 · see citing works

Human Brain Imaging Links Dopaminergic Systems to Impulsivity

London, E. D. (2020) · Current topics in behavioral neurosciences · doi:10.1007/7854_2019_125 · Cited by 22 · see citing works

Neurochemical substrates linked to impulsive and compulsive phenotypes in addiction: A preclinical perspective

Jones, J. A., Zühlsdorff, K., & Dalley, J. W. (2021) · Journal of Neurochemistry · doi:10.1111/jnc.15380 · Cited by 22 · see citing works

Marr's Levels Revisited: Understanding How Brains Break

Hardcastle, V. G., & Hardcastle, K. (2015) · Topics in Cognitive Science · doi:10.1111/tops.12130 · Cited by 21 · see citing works

Systemic Administration of 8-OH-DPAT and Eticlopride, but not SCH23390, Alters Loss-Chasing Behavior in the Rat

Rogers, R. D., Wong, A. C., McKinnon, C., & Winstanley, C. A. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.8 · Cited by 21 · see citing works

Haloperidol 2 mg impairs inhibition but not visuospatial attention

Logemann, H. N. A., Böcker, K. B. E., Deschamps, P. K. H., van Harten, P. N., Koning, J., Kemner, C., Logemann-Molnár, Z., & Kenemans, J. L. (2016) · Psychopharmacology · doi:10.1007/s00213-016-4454-z · Cited by 21 · see citing works

The 5-HT1A/1B-receptor agonist eltoprazine increases both catecholamine release in the prefrontal cortex and dopamine release in the nucleus accumbens and decreases motivation for reward and “waiting” impulsivity, but increases “stopping” impulsivity

Korte, S. M., Prins, J., van den Bergh, F. S., Oosting, R. S., Dupree, R., Korte-Bouws, G. A. H., Westphal, K. G. C., Olivier, B., Denys, D. A. J. P., Garland, A., et al. (2016) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2016.11.024 · Cited by 19 · see citing works

Controllability affects endocrine response of adolescent male rats to stress as well as impulsivity and behavioral flexibility during adulthood

Sanchís-Ollé, M., Fuentes, S., Úbeda-Contreras, J., Lalanza, J. F., Ramos-Prats, A., Armario, A., & Nadal, R. A. (2019) · Scientific Reports · doi:10.1038/s41598-019-40061-3 · Cited by 19 · see citing works

An insulin resistance associated neural correlate of impulsivity in type 2 diabetes mellitus

Eckstrand, K., Mummareddy, N., Kang, H., Cowan, R. L., Zhou, M., Zald, D. H., Silver, H. J., Niswender, K. D., & Avison, M. J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0189113 · Cited by 18 · see citing works

Neural correlates and role of medication in reactive motor impulsivity in Tourette disorder

Atkinson-Clément, C., Porte, C.-A., de Liege, A., Wattiez, N., Klein-Koerkamp, Y., Béranger, B., Valabrègue, R., Sofia, F., Hartmann, A., Pouget, P., et al. (2019) · Cortex · doi:10.1016/j.cortex.2019.12.007 · Cited by 15 · see citing works

Neural evidence for automatic value-modulated approach behaviour

Kim, H., & Anderson, B. A. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.12.050 · Cited by 18 · see citing works

A Single-Blind Study of ‘As-Needed’ Ecopipam for Gambling Disorder

Grant, J. E., Odlaug, B. L., Black, D. W., FONG, T. W., Davtian, M., Chipkin, R. E., & Kim, S. W. (2014) · Annals of Clinical Psychiatry · doi:10.1177/104012371402600304 · Cited by 17 · see citing works

Does Response Inhibition Have Pre- and Postdiagnostic Utility in Parkinson's Disease?

MacDonald, H. J., & Byblow, W. D. (2015) · Journal of Motor Behavior · doi:10.1080/00222895.2014.941784 · Cited by 16 · see citing works

Moderation of the relationship between Toxoplasma gondii seropositivity and trait impulsivity in younger men by the phenylalanine-tyrosine ratio

Peng, X., Brenner, L. A., Mathai, A. J., Cook, T. B., Fuchs, D., Postolache, N., Groer, M. W., Pandey, J. P., Mohyuddin, F., Giegling, I., et al. (2018) · Psychiatry Research · doi:10.1016/j.psychres.2018.03.045 · Cited by 16 · see citing works

The Fyn kinase inhibitor, AZD0530 , suppresses mouse alcohol self‐administration and seeking

Morisot, N., Berger, A. L., Phamluong, K., Cross, A. J., & Dorit Ron, A. (2018) · Addiction Biology · doi:10.1111/adb.12699 · Cited by 16 · see citing works

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., & Masud Husain, B. (2019) · Journal of Psychopharmacology · doi:10.1177/0269881119872190 · Cited by 17 · see citing works

Ghrelin modulates dopaminergic neuron formation and attention deficit hyperactivity disorder-like behaviors: From animals to human models

Shi, X., Guan, K., Peng, X., Xu, B., Zhou, X.-Y., Wang, S., Xu, S., Zheng, M., Huang, J. Y., Wan, X., et al. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.12.029 · Cited by 16 · see citing works

Impulsivity, Risky Choice, and Impulse Control Disorders

Robbins, T. W., & Dalley, J. W. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-805308-9.00007-5 · Cited by 16 · see citing works

Mapping functional gradients of the striatal circuit using simultaneous microelectric stimulation and ultrahigh-field fMRI in non-human primates

Han, M., Park, C.-U., Kang, S., Kim, B., Nikolaidis, A., Milham, M. P., Hong, S., Kim, S., & Baeg, E. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118077 · Cited by 15 · see citing works

Impulsivity is affected by cognitive enrichment and links to brain gene expression in red junglefowl chicks

Ryding, S., Garnham, L. C., Abbey‐Lee, R. N., Petkova, I., Kreshchenko, A., & Løvlie, H. (2021) · Animal Behaviour · doi:10.1016/j.anbehav.2021.06.007 · Cited by 15 · see citing works

Striatal D1- and D2-type Dopamine Receptors Are Linked to Motor Response Inhibition in Human Subjects

Robertson, C. L., Ishibashi, K., Mandelkern, M. A., Brown, A. K., Ghahremani, D. G., Sabb, F. W., Bilder, R. M., Cannon, T. D., Borg, J., & London, E. D. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4850-14.2015 · Cited by 85 · see citing works

Examination of the effects of SCH23390 and raclopride infused in the dorsal striatum on amphetamine-induced timing impulsivity measured on a differential reinforcement of low-rate responding (DRL) task in rats

Cheng, R., & Liao, R. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112364 · Cited by 9 · see citing works

Involvement of dopamine D1 and D2 receptors in the nucleus accumbens core and shell in inhibitory response control

Pattij, T., Janssen, M. C. W., Vanderschuren, L. J. M. J., Schoffelmeer, A. N. M., & van Gaalen, M. M. (2006) · Psychopharmacology · doi:10.1007/s00213-006-0533-x · Cited by 208 · see citing works

Early childhood adversity and serum lipid profiles in major depression: Correlations with cognitive functions

Péterfalvi, Á., Németh, N., Herczeg, R., Tényi, T., Miseta, A., Simon, M., & Czéh, B. (2019) · Clinica Chimica Acta · doi:10.1016/j.cca.2019.03.1269

Lesions of the medial prefrontal cortex or nucleus accumbens core do not impair inhibitory control in rats performing a stop-signal reaction time task

Eagle, D. M., & Robbins, T. W. (2003) · Behavioural Brain Research · doi:10.1016/j.bbr.2003.09.022 · Cited by 129 · see citing works