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Repetitive Transcranial Magnetic Stimulation of the Human Prefrontal Cortex Induces Dopamine Release in the Caudate Nucleus
Open accessAbstract
Dopamine is implicated in movement, learning, and motivation, and in illnesses such as Parkinson's disease, schizophrenia, and drug addiction. Little is known about the control of dopamine release in humans, but research in experimental animals suggests that the prefrontal cortex plays an important role in regulating the release of dopamine in subcortical structures. Here we used [(11)C]raclopride and positron emission tomography to measure changes in extracellular dopamine concentration in vivo after repetitive transcranial magnetic stimulation (rTMS) of the dorsolateral prefrontal cortex in healthy human subjects. Repetitive TMS of the left dorsolateral prefrontal cortex caused a reduction in [(11)C]raclopride binding in the left dorsal caudate nucleus compared with rTMS of the left occipital cortex. There were no changes in binding in the putamen, nucleus accumbens, or right caudate. This shows that rTMS of the prefrontal cortex induces the release of endogenous dopamine in the ipsilateral caudate nucleus. This finding has implications for the therapeutic and research use of rTMS in neurological and psychiatric disorders.
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“In the early 2000s, two influential studies demonstrated a causal relationship between the application of transcranial magnetic stimulation (TMS) on the prefrontal cortex and dopamine binding in the caudate nucleus, leading to an increase in extracellular dopamine and glutamate in the ventral striatum by TMS”
From A Narrative Review of Current and Emerging Trends in the Treatment of Alcohol Use Disorder (2024) · cites this paper as [106]
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“Another study by the same group, using the same tracer, demonstrated that rTMS of the left dlPFC induced dopamine release specifically in the head of the ipsilateral caudate nucleus, but not the NAcc, putamen or contralateral caudate nucleus (Strafella et al., 2001).”
From Cortico-striatal-thalamic loop circuits of the salience network: A central pathway in psychiatric disease and treatment (2016) · cites this paper as Strafella et al., 2001
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Cites
Talairach, J., Tournoux, P., & Rayport, M. (1988) · Thieme eBooks · Cited by 5,058
Automatic 3D intersubject registration of MR volumetric data in standardized Talairach space
Collins, D. L., Neelin, P., Peters, T. M., & Evans, A. C. (1994) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-199403000-00005 · Cited by 3,431 · cited 3×
“A high-resolution magnetic resonance image (MRI) of the subject’s brain was acquired and transformed into standardized stereotaxic space (Collins et al., 1994).”
MethodDepression of motor cortex excitability by low-frequency transcranial magnetic stimulation
Chen, R., Classen, J., Gerloff, C., Celnik, P., Wassermann, E. M., Hallett, M., & Cohen, L. G. (1997) · Neurology · doi:10.1212/wnl.48.5.1398 · Cited by 2,128 · cited 1×
“…of direct stimulation of the corticostriatal axons (Rothwell, 1997), indirect trans-synaptic activation of corticostriatal neurons caused by a reduction in GABA-mediated intracortical inhibition (Chen et al., 1997; Nakamura et al., 1997; Rothwell, 1997; Pascual-Leone et al., 1998), or both.”
BackgroundSimplified Reference Tissue Model for PET Receptor Studies
Lammertsma, A. A., & Hume, S. P. (1996) · NeuroImage · doi:10.1006/nimg.1996.0066 · Cited by 2,025
Uneven Pattern of Dopamine Loss in the Striatum of Patients with Idiopathic Parkinson's Disease
Kish, S. J., Shannak, K. S., & Hornykiewicz, O. (1988) · New England Journal of Medicine · doi:10.1056/nejm198804073181402 · Cited by 1,945
Grace, A. A. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90196-u · Cited by 1,831
MRI-PET Registration with Automated Algorithm
Woods, R. P., Mazziotta, J. C., & Cherry, A. S. R. (1993) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-199307000-00004 · Cited by 1,636
Evidence for striatal dopamine release during a video game
Koepp, M. J., Gunn, R. N., Lawrence, A. D., Cunningham, V. J., Dagher, A., Jones, T., Brooks, D. J., Bench, C. J., & Grasby, P. M. (1998) · Nature · doi:10.1038/30498 · Cited by 1,279
Self-citationParametric Imaging of Ligand-Receptor Binding in PET Using a Simplified Reference Region Model
Gunn, R. N., Lammertsma, A. A., Hume, S. P., & Cunningham, V. J. (1997) · NeuroImage · doi:10.1006/nimg.1997.0303 · Cited by 1,085
Longitudinal topography and interdigitation of corticostriatal projections in the rhesus monkey
Selemon, L. D., & Goldman-Rakic, P. S. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-03-00776.1985 · Cited by 1,074
Research works printed but not linked: 2
- Breier A, Su TP, Saunders R, Carson RE, Kolachana BS, De Bartolomeis A, Weinberger DR, Weisenfeld N, Malhotra AK, Eckelman WC, Pickar D (1998) Effects of NMDA antagonism on striatal dopamine release in healthy subjects: application of a novel PET approach. Syn- apse 29:142-147.
- Endres CJ, Kolachana BS, Saunders RC, Su T, Weinberger D, Breier A, Eckelman WC, Carson RE (1997) Kinetic modelling of [ 11 C]raclo- pride: combined PET-microdialysis studies. J Cereb Blood Flow Metab 9:932-942.
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Panidi, K., Vorobiova, A. N., Feurra, M., & Klucharev, V. A. (2022) · Scientific Reports · doi:10.1038/s41598-022-18529-6 · Cited by 18
Wang, Y., Tan, B., Shi, S., Yang, Y., & Che, X. (2023) · International Journal of Clinical and Health Psychology · doi:10.1016/j.ijchp.2023.100413 · Cited by 17
Chapter 4 Functional neuroimaging of cognition
Perani, D. (2008) · Handbook of clinical neurology · doi:10.1016/s0072-9752(07)88004-3 · Cited by 17
Edmond, E., Stagg, C. J., & Turner, M. R. (2019) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2018-320213 · Cited by 17
Ruiz, M. L., Sospedra, M., Arce, S. A., Tejeiro-Martínez, J., & Benito‐León, J. (2018) · Neurología · doi:10.1016/j.nrl.2018.03.023 · Cited by 17
Cordes, J., Arends, M., Mobascher, A., Brinkmeyer, J., Kornischka, J., Eichhammer, P., Klimke, A., Winterer, G., & Agelink, M. W. (2006) · Neuropsychobiology · doi:10.1159/000096990 · Cited by 17
Motor cortex stimulation: mild transient benefit in a primate model of Parkinson disease
Wu, A. K., McCairn, K. W., Zada, G., Wu, T. Z., & Turner, R. S. (2007) · Journal of neurosurgery · doi:10.3171/jns.2007.106.4.695 · Cited by 17
Zhang, Y., Ku, Y., Sun, J., Daskalakis, Z. J., & Yuan, T. (2021) · Psychological Medicine · doi:10.1017/s003329172100430x · Cited by 17
Amerio, A., Baccino, C., Breda, G. S., Cortesi, D., Spiezio, V., Magnani, L., Berardis, D. D., Conio, B., Costanza, A., Paola, G. D., et al. (2023) · Psychiatry Research · doi:10.1016/j.psychres.2023.115491 · Cited by 16
Ji, Y., Yang, C., Pang, X., Yan, Y., Wu, Y., Geng, Z., Hu, W., Hu, P., Wu, X., & Wang, K. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01201 · Cited by 19
Other therapeutic psychiatric uses of superficial brain stimulation
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Diminished appetitive startle modulation following targeted inhibition of prefrontal cortex
Hurlemann, R., Arndt, S. V., Schlaepfer, T. E., Reul, J., Maier, W., & Scheele, D. (2015) · Scientific Reports · doi:10.1038/srep08954 · Cited by 18
Gomis-Vicent, E., Thoma, V., Turner, J. J., Hill, K. P., & Pascual‐Leone, Á. (2019) · American Journal on Addictions · doi:10.1111/ajad.12945 · Cited by 16
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Ward, H. B., Mosquera, M. J., Suzuki, J., & Mariano, T. Y. (2020) · Neuromodulation Technology at the Neural Interface · doi:10.1111/ner.13108 · Cited by 16
Nitta, A., Izuo, N., Hamatani, K., Inagaki, R., Kusui, Y., Fu, K., Asano, T., Torii, Y., Habuchi, C., Sekiguchi, H., et al. (2021) · Journal of Personalized Medicine · doi:10.3390/jpm11070607 · Cited by 15
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Caballero‐Insaurriaga, J., Pineda‐Pardo, J. A., Obeso, I., Oliviero, A., & Foffani, G. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2219693120 · Cited by 16
Pharmacotherapy to enhance arousal: what is known and what is not
ZAFONTE, R. D., Hammond, F. M., Dennison, A. C., & Chew, E. (2009) · Progress in brain research · doi:10.1016/s0079-6123(09)17720-8 · Cited by 16
Sedláčková, S., Rektorová, I., Fanfrdlová, Z., & Rektor, I. (2008) · Journal of Psychophysiology · doi:10.1027/0269-8803.22.1.14 · Cited by 16
Repetitive transcranial magnetic stimulation: Re-wiring the alcoholic human brain
Diana, M., Bolloni, C., Antonelli, M., Giuda, D. D., Cocciolillo, F., Fattore, L., & Addolorato, G. (2018) · Alcohol · doi:10.1016/j.alcohol.2018.05.011 · Cited by 16
Spagnolo, P. A., Pérez, L. J. G., Terraneo, A., Gallimberti, L., & Bonci, A. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14313 · Cited by 19
rTMS as treatment strategy in psychiatric disorders--neurobiological concepts.
Keck, M. (2003) · Supplements to Clinical Neurophysiology · doi:10.1016/s1567-424x(09)70213-2 · Cited by 17
Centonze, D., Bernardi, G., & Koch, G. (2007) · Nature Clinical Practice Neurology · doi:10.1038/ncpneuro0617 · Cited by 18
Sahay, S., Reddy, M. V. S. R. R., Lennox, C., Wolinsky, E., McCullumsmith, R. E., & Singh, T. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03024-x · Cited by 17
Safiai, N. I. M., Mohamad, N. A., Basri, H., Mat, L. N. I., Hoo, F. K., Rashid, A. M. A., Khan, A. H. K. Y., Loh, W. C., Baharin, J., Fernandez, A., et al. (2022) · Cephalalgia · doi:10.1177/03331024221092423 · Cited by 15
Tang, Z., Zhu, Z. A., & Xu, J. (2022) · Biological Research For Nursing · doi:10.1177/10998004221122522 · Cited by 16
Invasive and Non-invasive Stimulation of the Obese Human Brain
Pleger, B. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00884 · Cited by 15
Impact of COMT val158met on tDCS-induced cognitive enhancement in older adults
Hayek, D., Antonenko, D., Witte, A. V., Lehnerer, S., Meinzer, M., Külzow, N., Prehn, K., Rujescu, D., Schneider, A., Grittner, U., et al. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.113081 · Cited by 17
Aloizou, A., Pateraki, G., Anargyros, K., Siokas, V., Bakirtzis, C., Sgantzos, M. N., Messinis, L., Nasios, G., Peristeri, E., Bogdanos, D. P., et al. (2021) · Healthcare · doi:10.3390/healthcare9080949 · Cited by 15
Cohen, O. S., Orlev, Y., Yahalom, G., Amiaz, R., Nitsan, Z., Ephraty, L., Rigbi, A., Shabat, C. S., Zangen, A., & Hassin‐Baer, S. (2015) · Clinical Neurology and Neurosurgery · doi:10.1016/j.clineuro.2015.11.017 · Cited by 15
Dockx, R., Baeken, C., Bundel, D. D., Saunders, J. H., Eeckhaut, A. V., & Peremans, K. Y. (2019) · Journal of Veterinary Behavior · doi:10.1016/j.jveb.2019.07.004 · Cited by 15
Liu, X., Zhao, X., Shen, Y., Liu, T., Liu, Q., Tang, L., Zhang, H., Luo, W., & Yuan, T. (2020) · Clinical and Translational Medicine · doi:10.1002/ctm2.48 · Cited by 15
Tremblay, C., Monetta, L., Langlois, M., & Schneider, C. (2015) · Archives of Physical Medicine and Rehabilitation · doi:10.1016/j.apmr.2015.09.002 · Cited by 15
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Potvin‐Desrochers, A., Moreno, A. M., Clouette, J., Parent‐L'Ecuyer, F., Lajeunesse, H., & Paquette, C. (2023) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2023.120770 · Cited by 14
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Natale, G., Colella, M., Carluccio, M. D., Lelli, D., Paffi, A., Carducci, F., Apollonio, F., Palacios, D., Viscomi, M. T., Liberti, M., et al. (2023) · Movement Disorders · doi:10.1002/mds.29599 · Cited by 15
Li, S., Ma, X., Chen, H., Wang, M., Zheng, Y., Yang, B., Ni, H., Potenza, M. N., & Dong, G. (2024) · Journal of Affective Disorders · doi:10.1016/j.jad.2024.01.048 · Cited by 13
Use of Transcranial Direct Stimulation in the Treatment of Negative Symptoms of Schizophrenia
Pontillo, M., Costanzo, F., Menghini, D., Averna, R., Santonastaso, O., Tata, M. C., & Vicari, S. (2017) · Clinical EEG and Neuroscience · doi:10.1177/1550059417746531 · Cited by 14
Luo, Y., Yang, J., Wang, H., Gan, Z., & Ran, D. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20184625 · Cited by 14
Differential functional dysconnectivity of caudate nucleus subdivisions in Parkinson’s disease
Jia, X., Pan, Z., Chen, H., Wang, Z., Li, K., Wang, X., Wang, Z., Ma, H., Feng, T., & Yang, Q. (2020) · Aging · doi:10.18632/aging.103628 · Cited by 14
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Steele, V. R. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.592343 · Cited by 14
Deng, Y., Hou, L., Chen, X., & Zhou, R. (2020) · Neuroscience Letters · doi:10.1016/j.neulet.2020.135513 · Cited by 16
Kearney-Ramos, T. E., & Haney, M. (2021) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2021.110290 · Cited by 12
Hsieh, T.-H., He, X., Liu, H.-H., Chen, J. J., Peng, C., Liu, H., Rotenberg, A., Chen, K., Chang, M., Chiang, Y. H., et al. (2021) · Neural Plasticity · doi:10.1155/2021/1763533 · Cited by 14
Caparelli, E. C., Schleyer, B., Zhai, T., Gu, H., Abulseoud, O. A., & Yang, Y. (2022) · Neuromodulation Technology at the Neural Interface · doi:10.1016/j.neurom.2022.03.002 · Cited by 14
Aggression, DRD1 polymorphism, and lesion location in penetrating traumatic brain injury
Pardini, M., Krüeger, F., Hodgkinson, C. A., Raymont, V., Strenziok, M., Amore, M., Wassermann, E. M., Goldman, D. A., & Grafman, J. H. (2014) · CNS Spectrums · doi:10.1017/s1092852914000108 · Cited by 14
Addiction: Informing drug abuse interventions with brain networks
Steele, V. R., Ding, X., & Ross, T. J. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-813838-0.00006-6 · Cited by 14
Brain Stimulation in Psychiatry
Rowny, S. B., & Lisanby, S. H. (2008) · Wiley eBooks · doi:10.1002/9780470515167.ch109 · Cited by 13
Brain Stimulation in Psychiatry: ECT, DBS, TMS and Other Modalities
Kellner, C. H. (2012) · Cited by 14
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Kahnt, T. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.08.028 · Cited by 16
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Muksuris, K., Scarisbrick, D. M., Mahoney, J. J., & Cherkasova, M. V. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12175448 · Cited by 14
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Cheng, W., Law, P. K., Kwan, H. C., & Cheng, R. S. S. (2014) · Open Journal of Regenerative Medicine · doi:10.4236/ojrm.2014.34009 · Cited by 13
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Arias-Carrión, Ó., Machado, S., Paes, F., Velasques, B., Teixeira, S., Cárdenas-Morales, L., Piedade, R., Ribeiro, P., & Nardi, A. (2011) · CNS and Neurological Disorders - Drug Targets · doi:10.2174/187152711797247821 · Cited by 12
Lacroix, A., Vergne‐Salle, P., Dumont, J.-C., Labrunie, A., Balestrat, P., Calvet, B., & Girard, M. F. (2022) · Neuromodulation Technology at the Neural Interface · doi:10.1016/j.neurom.2021.12.015 · Cited by 14
Henkin, R. I., Velicu, I., Potolicchio, S. J., Levy, L. M., Martin, B. M., & Moharram, R. (2010) · The American Journal of the Medical Sciences · doi:10.1097/maj.0b013e3181cda0e3 · Cited by 13
Parthoens, J., Verhaeghe, J. A. J., Stroobants, S. G., & Staelens, S. G. (2014) · Molecular Imaging and Biology · doi:10.1007/s11307-014-0757-9 · Cited by 13
A feasible repetitive transcranial magnetic stimulation clinical protocol in migraine prevention
Zardouz, S., Shi, L., & Leung, A. (2016) · SAGE Open Medical Case Reports · doi:10.1177/2050313x16675257 · Cited by 13
Bilateral theta-burst magnetic stimulation influence on event-related brain potentials
Pinto, N., Duarte, M., Gonçalves, H., Silva, R., Gama, J. M. R., & Pato, M. V. (2018) · PLoS ONE · doi:10.1371/journal.pone.0190693 · Cited by 14
High frequency deep transcranial magnetic stimulation acutely increases β-endorphins in obese humans
Ferrulli, A., Macrì, C., Terruzzi, I. M., Ambrogi, F., Milani, V., Adamo, M., & Luzi, L. (2018) · Endocrine · doi:10.1007/s12020-018-1791-1 · Cited by 13
Shen, Y., & Ward, H. B. (2020) · The American Journal of Drug and Alcohol Abuse · doi:10.1080/00952990.2020.1841784 · Cited by 13
Pallanti, S., Borgheresi, A., Pampaloni, I., Giovannelli, F., Bernardi, S., Cantisani, A., Zaccara, G., & Cincotta, M. (2010) · Journal of Neurology · doi:10.1007/s00415-010-5533-4 · Cited by 12
Zhang, F., & Iwaki, S. (2020) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2020.00279 · Cited by 12
Transcranial Stimulation for the Treatment of Stimulant Use Disorder
Edinoff, A. N., Sall, S., Roberts, T. D., Tomlinson, H., Soileau, L. G., Jackson, E. D., Murnane, K. S., Wenger, D. M., Cornett, E. M., Toms, J., et al. (2023) · Neurology International · doi:10.3390/neurolint15010021 · Cited by 12
Shaikh, U. J., Pellicano, A., Schüppen, A., Heinzel, A., Winz, O., Herzog, H. R., Mottaghy, F. M., & Binkofski, F. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1295151 · Cited by 13
Dong, K., Zhu, X., Xiao, W., Gan, C., Luo, Y., Jiang, M., Liu, H., & Chen, X. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1073310 · Cited by 12
Reduced Affective Biasing of Instrumental Action With tDCS Over the Prefrontal Cortex
Ly, V., Bergmann, T. O., Gladwin, T. E., Volman, I., Usberti, N., Cools, R., & Roelofs, K. (2016) · Brain stimulation · doi:10.1016/j.brs.2016.02.002 · Cited by 12
Henssen, D. J. H. A., Witkam, R. L., Dao, J. C. M. L., Comes, D. J., van Walsum, A. V. C., Kozicz, T., van Dongen, R. T. M., Vissers, K. C. P., Bartels, R., de Jong, G., et al. (2019) · Journal of Pain · doi:10.1016/j.jpain.2019.02.004 · Cited by 12
Zatorre, R. J. (2018) · Europe PMC (PubMed Central) · Cited by 12
Hemond, C. C., & Fregni, F. (2007) · Neuromodulation (Malden, Mass.) · doi:10.1111/j.1525-1403.2007.00120.x · Cited by 12
Bradberry, C. W. (2010) · Neurotoxicity Research · doi:10.1007/s12640-010-9156-4 · Cited by 12
Padberg, F., Goldstein-Müller, B., Zwanzger, P., & Möller, H. (2003) · Supplements to Clinical neurophysiology · doi:10.1016/s1567-424x(09)70245-4 · Cited by 12
Repetitive transcranial magnetic stimulation and treatment of negative symptoms of schizophrenia.
Přikryl, R. (2011) · PubMed · Cited by 12
Stimulation-induced plasticity in the human motor cortex
Claßen, J., & Ziemann, U. (2003) · Cambridge University Press eBooks · doi:10.1017/cbo9780511544903.007 · Cited by 12
Li, Y., Pang, J., Wang, J., Wang, W., Bo, Q., Lei, L., Wang, X., & Wang, M. (2023) · Frontiers in Psychology · doi:10.3389/fpsyg.2023.1144757 · Cited by 11
Harris, D. M., Latella, C., Tripodi, N., & O’Bryan, S. J. (2025) · Neurorehabilitation and neural repair · doi:10.1177/15459683241310984 · Cited by 11
Freitas, C., PEARLMAN, C. A., & Pascual‐Leone, Á. (2011) · Neurocase · doi:10.1080/13554794.2010.547864 · Cited by 11
Murgaš, M., Unterholzner, J., Stöhrmann, P., Philippe, C., Godbersen, G. M., Nics, L., Reed, M. B., Vraka, C., Vanicek, T., Wadsak, W., et al. (2023) · Translational Psychiatry · doi:10.1038/s41398-023-02319-3 · Cited by 12
Ramírez-Rodríguez, G. B., Juan, D. M.-S., Rico-Becerra, A. I., Gonzalez-Olvera, J. J., & Reyes‐Galindo, V. (2023) · Neuropharmacology · doi:10.1016/j.neuropharm.2023.109567 · Cited by 11
Kortekaas, R., van Nierop, L. E., Baas, V. G., Konopka, K.-H., Harbers, M., van der Hoeven, J. H., van Wijhe, M., Aleman, A., & Maurits, N. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061926 · Cited by 11
Deep magnetic stimulation in a progressive supranuclear palsy patient with speech involvement
Spagnolo, F., Coppi, E., Rosa, P. A. D., Fichera, M., Barbieri, A., Magnani, G., Falautano, M., Zangen, A., Comı, G., Perani, D., et al. (2012) · Journal of Neurology · doi:10.1007/s00415-012-6772-3 · Cited by 11
Mayer, J. T., Nicolier, M., Tio, G., Mouchabac, S., Haffen, É., & Bennabi, D. (2019) · Brain Sciences · doi:10.3390/brainsci9090230 · Cited by 11
Moretti, J., Poh, E. Z., Bolland, S. J., Harvey, A. R., Albrecht, M. A., & Rodger, J. (2020) · Behavioural Brain Research · doi:10.1016/j.bbr.2020.113011 · Cited by 9
Schecklmann, M., Landgrebe, M., Kleinjung, T., Frank, E., Sand, P. G., Rupprecht, R., Eichhammer, P., Hajak, G., & Langguth, B. (2014) · BMC Neuroscience · doi:10.1186/1471-2202-15-71 · Cited by 11
Combination of Transcranial Magnetic Stimulation and Brain Mapping
Paus, T. (2002) · Elsevier eBooks · doi:10.1016/b978-012693019-1/50027-7 · Cited by 11
Self-citationRewiring the Addicted Brain: Circuits-Based Treatment for AddictionPreprint
Madeo, G., & Bonci, A. (2018) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2018.83.038158 · Cited by 11
Kamp, D., Engelke, C., Wobrock, T., Wölwer, W., Winterer, G., Schmidt-Kraepelin, C., Gäebel, W., Langguth, B., Landgrebe, M., Eichhammer, P., et al. (2018) · Schizophrenia Research · doi:10.1016/j.schres.2018.09.017 · Cited by 10
Pan, J., Mi, T., Ma, J., Sun, H., & Chan, P. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2021.755352 · Cited by 12
Espiritu, A. I., Hara, T., Tolledo, J. K., Blair, M., & Burhan, A. M. (2023) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2023.1259481 · Cited by 10
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Self-citation
Metadata
- Authors
- Strafella, A. P., Paus, T., Barrett, J., & Dagher, A.
- Affiliations
- Montreal Neurological Institute and Hospital (CA)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2001-08-01
- Volume
- 21
- Issue
- 15
- Pages
- RC157-RC157
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6762641
- OpenAlex
- W2118266586
- Cited by
- 1,058
- References
- 39
- Citations by year
- 2026: 29 · 2025: 38 · 2024: 44 · 2023: 53 · 2022: 49 · 2021: 57 · 2020: 55 · 2019: 52 · 2018: 51 · 2017: 51 · 2016: 45 · 2015: 54 · 2014: 48 · 2013: 45 · 2012: 35
- FWCI
- 19.26
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Neurology › Transcranial Magnetic Stimulation Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Health Sciences › Medicine › Clinical Neurology › Deep Brain Stimulation and Movement Disorders
- Keywords
- repetitive transcranial magnetic stimulation, dopamine release, caudate nucleus, dorsolateral prefrontal cortex, dopamine transporter binding, extracellular dopamine, putamen, nucleus accumbens
- MeSH terms
- Adult, Autonomic Nervous System, Behavior, Carbon Isotopes, Caudate Nucleus, Dopamine, Electric Stimulation, Electromagnetic Fields, Female, Humans, Male, Nucleus Accumbens, Occipital Lobe, Putamen, Receptors, Dopamine, Reference Values, Tomography, Emission-Computed, Prefrontal Cortex, Dopamine Antagonists, Raclopride, Transcranial Magnetic Stimulation
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