Mechanisms of action of deep brain stimulation (DBS)

The Concept of Mind

Ryle, G. (2006) · Rowman & Littlefield Publishers eBooks · doi:10.5040/9798216413257.ch-2 · Cited by 6,804 · see citing works

The functional anatomy of basal ganglia disorders

Albin, R. L., Young, A. B., & Penney, J. B. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90074-x · Cited by 5,353 · see citing works

Primate models of movement disorders of basal ganglia origin

DeLong, M. R. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90110-v · Cited by 3,824 · see citing works

A double‐blind controlled trial of bilateral fetal nigral transplantation in Parkinson's disease

Olanow, C. W., Goetz, C. G., Kordower, J. H., Stoessl, A. J., Sossi, V., Brin, M. F., Shannon, K. M., Nauert, G. M., Perl, D. P., Godbold, J., et al. (2003) · Annals of Neurology · doi:10.1002/ana.10720 · Cited by 1,600 · see citing works

Deep-brain stimulation of the subthalamic nucleus or the pars interna of the globus pallidus in Parkinson's disease.

Obeso, J., Olanow, C., Rodríguez-Oroz, M., Krack, P., Kumar, R., & Lang, A. E. (2001) · New England Journal of Medicine · doi:10.1056/nejmoa000827 · Cited by 1,494 · see citing works

The primate subthalamic nucleus. II. Neuronal activity in the MPTP model of parkinsonism

Bergman, H., Wichmann, T., Karmon, B., & DeLong, M. R. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.72.2.507 · Cited by 1,366 · see citing works

Weakly Connected Neural Networks

Hoppensteadt, F. C., & Izhikevich, E. M. (1997) · Applied mathematical sciences · doi:10.1007/978-1-4612-1828-9 · Cited by 1,264 · see citing works

Dopamine Dependency of Oscillations between Subthalamic Nucleus and Pallidum in Parkinson's Disease

Brown, P., Oliviero, A., Mazzone, P. A. M., Insola, A., Tonali, P. A., & Lazzaro, V. D. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-03-01033.2001 · Cited by 1,168 · see citing works

Stochastic resonance and sensory information processing: A tutorial and review of application

Moss, F., Ward, L. M., & Sannita, W. G. (2004) · Clinical Neurophysiology · doi:10.1016/j.clinph.2003.09.014 · Cited by 994 · see citing works

Stimulation of the Subthalamic Nucleus Changes the Firing Pattern of Pallidal Neurons

Hashimoto, T., Elder, C. M., Okun, M., Patrick, S. K., & Vitek, J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-05-01916.2003 · Cited by 925 · see citing works

Reduction in subthalamic 8–35 Hz oscillatory activity correlates with clinical improvement in Parkinson's disease

Kühn, A. A., Kupsch, A. R., Schneider, G., & Brown, P. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04717.x · Cited by 895 · see citing works

Cellular Effects of Deep Brain Stimulation: Model-Based Analysis of Activation and Inhibition

McIntyre, C. C., Grill, W. M., Sherman, D. L., & Thakor, N. V. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00989.2003 · Cited by 817 · see citing works

Bilateral deep brain stimulation of the pedunculopontine and subthalamic nuclei in severe Parkinson's disease

Stefani, A., Lozano, A. M., Peppe, A., Stanzione, P., Galati, S., Tropepi, D., Pierantozzi, M., Brusa, L., Scarnati, E., & Mazzone, P. (2007) · Brain · doi:10.1093/brain/awl346 · Cited by 805 · see citing works

A basal ganglia pacemaker formed by the subthalamic nucleus and external globus pallidus

Plenz, D., & Kital, S. T. (1999) · Nature · doi:10.1038/23281 · Cited by 715 · see citing works

Activity Patterns in a Model for the Subthalamopallidal Network of the Basal Ganglia

Terman, D. H., Rubin, J. E., Yew, A. C., & Wilson, C. J. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-07-02963.2002 · Cited by 690 · see citing works

Neurons in the globus pallidus do not show correlated activity in the normal monkey, but phase-locked oscillations appear in the MPTP model of parkinsonism

Nini, A., Feingold, A., Slovin, H., & Bergman, H. (1995) · Journal of Neurophysiology · doi:10.1152/jn.1995.74.4.1800 · Cited by 653 · see citing works

Move to the rhythm: oscillations in the subthalamic nucleus–external globus pallidus network

Bevan, M. D. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02235-x · Cited by 633 · see citing works

High-frequency Synchronization of Neuronal Activity in the Subthalamic Nucleus of Parkinsonian Patients with Limb Tremor

Levy, R., Hutchison, W. D., Lozano, A. M., & Dostrovsky, J. O. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-20-07766.2000 · Cited by 610 · see citing works

High Frequency Stimulation of the Subthalamic Nucleus Eliminates Pathological Thalamic Rhythmicity in a Computational Model

Rubin, J. E., & Terman, D. H. (2004) · Journal of Computational Neuroscience · doi:10.1023/b:jcns.0000025686.47117.67 · Cited by 598 · see citing works

High-Frequency Stimulation Produces a Transient Blockade of Voltage-Gated Currents in Subthalamic Neurons

Beurrier, C., Bioulac, B. H., Audin, J., & Hammond, C. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.4.1351 · Cited by 532 · see citing works

Basal ganglia local field potential activity: Character and functional significance in the human

Brown, P., & Williams, D. R. (2005) · Clinical Neurophysiology · doi:10.1016/j.clinph.2005.05.009 · Cited by 529 · see citing works

Deep brain stimulation for refractory obsessive-compulsive disorder

Abelson, J. L., Curtis, G. C., Sagher, O., Albucher, R. C., Harrigan, M., Taylor, S. F., Martis, B., & Giordani, B. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.11.042 · Cited by 522 · see citing works

High‐frequency unilateral thalamic stimulation in the treatment of essential and parkinsonian tremor

Koller, W., Pahwa, R., Busenbark, K., Hubble, J., Wilkinson, S., Lang, A., Tuite, P., Sime, E., Lazano, A., Hauser, R., et al. (1997) · Annals of Neurology · doi:10.1002/ana.410420304 · Cited by 516 · see citing works

Dopamine-dependent changes in the functional connectivity between basal ganglia and cerebral cortex in humans

Williams, D. (2002) · Brain · doi:10.1093/brain/awf156 · Cited by 511 · see citing works

Microstimulation-Induced Inhibition of Neuronal Firing in Human Globus Pallidus

Dostrovsky, J. O., Levy, R., Wu, J. P., Hutchison, W. D., Tasker, R. R., & Lozano, A. M. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.1.570 · Cited by 470 · see citing works

Bilateral deep brain stimulation of the pedunculopontine nucleus for Parkinson's disease

Plaha, P., & Gill, S. S. (2005) · Neuroreport · doi:10.1097/01.wnr.0000187637.20771.a0 · Cited by 463 · see citing works

Patterning of globus pallidus local field potentials differs between Parkinson's disease and dystonia

Silberstein, P. (2003) · Brain · doi:10.1093/brain/awg267 · Cited by 435 · see citing works

The interpretation of spike potentials of motoneurones

Coombs, J. S., Curtis, D., & Eccles, J. C. (1957) · The Journal of Physiology · doi:10.1113/jphysiol.1957.sp005887 · Cited by 382 · see citing works

Subthalamic high frequency stimulation resets subthalamic firing and reduces abnormal oscillations

Meissner, W. G., Leblois, A., Hansel, D., Bioulac, B. H., Gross, C. E., Benazzouz, A., & Boraud, T. (2005) · Brain · doi:10.1093/brain/awh616 · Cited by 348 · see citing works

Effect of high-frequency stimulation of the subthalamic nucleus on the neuronal activities of the substantia nigra pars reticulata and ventrolateral nucleus of the thalamus in the rat

Benazzouz, A., Gao, D. M., Ni, Z., Piallat, B., Bouali‐Benazzouz, R., & Benabid, A. (2000) · Neuroscience · doi:10.1016/s0306-4522(00)00199-8 · Cited by 338 · see citing works

Effects of high frequency stimulation of subthalamic nucleus on extracellular glutamate and GABA in substantia nigra and globus pallidus in the normal rat

Windels, F., Bruet, N., Poupard, A., Urbain, N., Chouvet, G., Feuerstein, C., & Savasta, M. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00296.x · Cited by 334 · see citing works

Excitation of Central Nervous System Neurons by Nonuniform Electric Fields

McIntyre, C. C., & Grill, W. M. (1999) · Biophysical Journal · doi:10.1016/s0006-3495(99)77251-6 · Cited by 319 · see citing works

Neuronal Oscillations in the Basal Ganglia and Movement Disorders: Evidence from Whole Animal and Human Recordings: Figure 1.

Hutchison, W. D., Dostrovsky, J. O., Walters, J. R., Courtemanche, R., Boraud, T., Goldberg, J. A., & Brown, P. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3366-04.2004 · Cited by 305 · see citing works

Bilateral high-frequency stimulation in the subthalamic nucleus for the treatment of Parkinson disease: correlation of therapeutic effect with anatomical electrode position

Voges, J., Volkmann, J., Allert, N., Lehrke, R., Koulousakis, A., Freund, H., & Sturm, V. (2002) · Journal of neurosurgery · doi:10.3171/jns.2002.96.2.0269 · Cited by 301 · see citing works

Stimulation-induced inhibition of neuronal firing in human subthalamic nucleus

Filali, M., Hutchison, W. D., Palter, V. N., Lozano, A. M., & Dostrovsky, J. O. (2004) · Experimental Brain Research · doi:10.1007/s00221-003-1784-y · Cited by 300 · see citing works

Synchronized Neuronal Discharge in the Basal Ganglia of Parkinsonian Patients Is Limited to Oscillatory Activity

Levy, R., Hutchison, W. D., Lozano, A. M., & Dostrovsky, J. O. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-07-02855.2002 · Cited by 290 · see citing works

Effects of High-Frequency Stimulation in the Internal Globus Pallidus on the Activity of Thalamic Neurons in the Awake Monkey

Anderson, M. E., Postupna, N. O., & Ruffo, M. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00475.2002 · Cited by 280 · see citing works

Handbook of Parkinson's Disease

Pahwa, R., & Lyons, K. (2013) · CRC Press eBooks · doi:10.1201/b14361 · Cited by 272 · see citing works

Mechanisms of deep brain stimulation and future technical developments

Erwin, B., Montgomery, M., Jr., & Baker, K. K. (2000) · Neurological Research · doi:10.1080/01616412.2000.11740668 · Cited by 265 · see citing works

Basal ganglia motor control. II. Late pallidal timing relative to movement onset and inconsistent pallidal coding of movement parameters

Mink, J. W., & Thach, W. T. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.65.2.301 · Cited by 264 · see citing works

Electrophysiological and metabolic evidence that high‐frequency stimulation of the subthalamic nucleus bridles neuronal activity in the subthalamic nucleus and the substantia nigra reticulata

Tai, C., Boraud, T., Bézard, E., Bioulac, B. H., Gross, C. E., & Benazzouz, A. (2003) · The FASEB Journal · doi:10.1096/fj.03-0163com · Cited by 261 · see citing works

Deep brain stimulation of the subthalamic nucleus: anatomical, neurophysiological, and outcome correlations with the effects of stimulation

Lanotte, M. (2002) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.72.1.53 · Cited by 256 · see citing works

Deep brain stimulation of the subthalamic nucleus in Parkinson's disease: effects of variation in stimulation parameters

Rizzone, M. G. (2001) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.71.2.215 · Cited by 248 · see citing works

Dynamics of tremor-related oscillations in the human globus pallidus: a single case study

Hurtado, J. M., Gray, C. M., Tamas, L. B., & Sigvardt, K. A. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.4.1674 · Cited by 246 · see citing works

Dual Effect of High-Frequency Stimulation on Subthalamic Neuron Activity

García, L., Audin, J., D’Alessandro, G., Bioulac, B. H., & Hammond, C. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-25-08743.2003 · Cited by 245 · see citing works

Bad oscillations in Parkinson’s disease

Brown, P. (2006) · Springer eBooks · doi:10.1007/978-3-211-45295-0_6 · Cited by 218 · see citing works

Deep Brain Stimulation in Epilepsy

Loddenkemper, T., Pan, A., Neme-Mercante, S., Baker, K. B., Rezai, A. R., Dinner, D. S., Montgomery, E. B., & Lüders, H. O. (2001) · Journal of Clinical Neurophysiology · doi:10.1097/00004691-200111000-00002 · Cited by 217 · see citing works

Spontaneous and Evoked Activity of Substantia Nigra Pars Reticulata Neurons during High-Frequency Stimulation of the Subthalamic Nucleus

Maurice, N., Thierry, A. M., Glowinski, J., & Deniau, J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-30-09929.2003 · Cited by 216 · see citing works

Deep brain stimulation for Parkinson’s disease dissociates mood and motor circuits: a functional MRI case study

Stefurak, T., Mikulis, D., Mayberg, H., Lang, A. E., Hevenor, S., Pahapill, P., Saint‐Cyr, J., & Lozano, A. (2003) · Movement Disorders · doi:10.1002/mds.10593 · Cited by 215 · see citing works

Globus pallidus internus deep brain stimulation for dystonic conditions: A prospective audit

Yianni, J., Bain, P. G., Giladi, N., Auca, M., Gregory, R. P., Joint, C., Nandi, D., Stein, J. F., Scott, R., & Aziz, T. Z. (2003) · Movement Disorders · doi:10.1002/mds.10380 · Cited by 194 · see citing works

Does stimulation of the GPi control dyskinesia by activating inhibitory axons?

Wu, Y.-Y., Levy, R., Ashby, P., Tasker, R. R., & Dostrovsky, J. O. (2001) · Movement Disorders · doi:10.1002/mds.1046 · Cited by 181 · see citing works

Deep Brain Stimulation for Epilepsy

Koch, P., & Baltuch, G. H. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-805353-9.00083-8 · Cited by 181 · see citing works

Blood flow responses to deep brain stimulation of thalamus

Perlmutter, J. S., Mink, J. W., Bastian, A. J., Zackowski, K. M., Hershey, T. G., Miyawaki, E. K., Koller, W. C., & Videen, T. O. (2002) · Neurology · doi:10.1212/wnl.58.9.1388 · Cited by 175 · see citing works

High-frequency stimulation of the subthalamic nucleus silences subthalamic neurons: a possible cellular mechanism in Parkinson’s disease

Magariños-Ascone, C. M., Pazo, J. H., Macadar, O., & Buño, W. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00538-9 · Cited by 169 · see citing works

Balance of Monosynaptic Excitatory and Disynaptic Inhibitory Responses of the Globus Pallidus Induced after Stimulation of the Subthalamic Nucleus in the Monkey

Kita, H., Tachibana, Y., Nambu, A., & Chiken, S. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1719-05.2005 · Cited by 161 · see citing works

Inhibitory processes and interneuronal apparatus in motor cortex during sleep and waking. I. Background firing and responsiveness of pyramidal tract neurons and interneurons.

Steriade, M., Deschênes, M., & Oakson, G. (1974) · Journal of Neurophysiology · doi:10.1152/jn.1974.37.5.1065 · Cited by 161 · see citing works

Complex Locking Rather Than Complete Cessation of Neuronal Activity in the Globus Pallidus of a 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine-Treated Primate in Response to Pallidal Microstimulation

Bar‐Gad, I., Elias, S., Vaadia, E., & Bergman, H. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1691-04.2004 · Cited by 160 · see citing works

Neurophysiological effects of stimulation through electrodes in the human subthalamic nucleus

Ashby, P., Kim, Y. J., Kumar, R., Lang, A. E., & Lozano, A. M. (1999) · Brain · doi:10.1093/brain/122.10.1919 · Cited by 159 · see citing works

Neurotransmitter release from high-frequency stimulation of the subthalamic nucleus

Lee, K. H., Chang, S.-Y., Roberts, D. W., & Kim, U. (2004) · Journal of neurosurgery · doi:10.3171/jns.2004.101.3.0511 · Cited by 159 · see citing works

MECHANISMS OF SUPRASPINAL ACTIONS UPON SPINAL CORD ACTIVITIES. RETICULAR INHIBITORY MECHANISMS UPON FLEXOR MOTONEURONS

Llinas, R. H., & Terzuolo, C. A. (1965) · Journal of Neurophysiology · doi:10.1152/jn.1965.28.2.413 · Cited by 158 · see citing works

Subthalamic nucleus deep brain stimulus evoked potentials: Physiological and therapeutic implications

Baker, K. B., Montgomery, E. B., Rezai, A. R., Burgess, R. C., & Lüders, H. O. (2002) · Movement Disorders · doi:10.1002/mds.10206 · Cited by 155 · see citing works

Multisecond Oscillations in Firing Rate in the Basal Ganglia: Robust Modulation by Dopamine Receptor Activation and Anesthesia

Ruskin, D. N., Bergstrom, D. A., Kaneoke, Y., Patel, B. N., Twery, M. J., & Walters, J. R. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.81.5.2046 · Cited by 149 · see citing works

Effects of GPi stimulation on human thalamic neuronal activity

Montgomery, E. B. (2006) · Clinical Neurophysiology · doi:10.1016/j.clinph.2006.08.011 · Cited by 145 · see citing works

MECHANISMS OF SUPRASPINAL ACTIONS UPON SPINAL CORD ACTIVITIES. RETICULAR INHIBITORY MECHANISMS ON ALPHA-EXTENSOR MOTONEURONS

Llinas, R. H., & Terzuolo, C. A. (1964) · Journal of Neurophysiology · doi:10.1152/jn.1964.27.4.579 · Cited by 143 · see citing works

Frequency-Dependent Reciprocal Modulation of Verbal Fluency and Motor Functions in Subthalamic Deep Brain Stimulation

Wojtecki, L., Timmermann, L., Jörgens, S., Südmeyer, M., Maarouf, M., Treuer, H., Groß, J., Lehrke, R., Koulousakis, A., Voges, J., et al. (2006) · Archives of Neurology · doi:10.1001/archneur.63.9.1273 · Cited by 141 · see citing works

Neuronal activity in the striatum and pallidum of primates related to the execution of externally cued reaching movements

Jaeger, D., Gilman, S., & Aldridge, J. W. (1995) · Brain Research · doi:10.1016/0006-8993(95)00780-t · Cited by 134 · see citing works

Disturbances of Rhythm Formation in Patients with Parkinson's Disease: Part I. Characteristics of Tapping Response to the Periodic Signals

Nakamura, R., Nagasaki, H., & Narabayashi, H. (1978) · Perceptual and Motor Skills · doi:10.2466/pms.1978.46.1.63 · Cited by 130 · see citing works

Subthalamic stimulation activates internal pallidus: Evidence from cGMP microdialysis in PD patients

Stefani, A., Fedele, E., Galati, S., Pepicelli, O., Frasca, S., Pierantozzi, M., Peppe, A., Brusa, L., Orlacchio, A., Hainsworth, A. H., et al. (2005) · Annals of Neurology · doi:10.1002/ana.20402 · Cited by 129 · see citing works

Acute stimulation in the external segment of the globus pallidus improves parkinsonian motor signs

Vitek, J. L., Hashimoto, T., Peoples, J., DeLong, M. R., & Bakay, R. A. E. (2004) · Movement Disorders · doi:10.1002/mds.20137 · Cited by 127 · see citing works

Frequency dependent effects of subthalamic nucleus stimulation in Parkinson's disease

Fogelson, N., Kühn, A. A., Silberstein, P., Limousin, P. D., Hariz, M. I., Trottenberg, T., Kupsch, A. R., & Brown, P. (2005) · Neuroscience Letters · doi:10.1016/j.neulet.2005.02.050 · Cited by 124 · see citing works

Selective Attenuation of Afferent Synaptic Transmission as a Mechanism of Thalamic Deep Brain Stimulation-Induced Tremor Arrest

Anderson, T. R., Hu, B., Iremonger, K. J., & Kiss, Z. H. T. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3523-05.2006 · Cited by 113 · see citing works

Subthalamic nucleus stimulation modulates motor cortex oscillatory activity in Parkinson's disease

Devos, D. (2004) · Brain · doi:10.1093/brain/awh053 · Cited by 111 · see citing works

Organization of thalamostriatal terminals from the ventral motor nuclei in the macaque

McFarland, N. R., & Haber, S. N. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20000108)429:2 · Cited by 109 · see citing works

Visually Guided Movements Suppress Subthalamic Oscillations in Parkinson's Disease Patients

Amirnovin, R., Williams, Z. M., Cosgrove, G. R., & Eskandar, E. N. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3242-04.2004 · Cited by 106 · see citing works

Modifications of precentral cortex discharge and EMG activity in monkeys with MPTP-induced lesions of DA nigral neurons

Doudet, D. J., Gross, C. E., Arluison, M., & Bioulac, B. H. (1990) · Experimental Brain Research · doi:10.1007/bf00228859 · Cited by 102 · see citing works

Extradural motor cortex stimulation for advanced Parkinson disease

Canavero, S., Paolotti, R., Bonicalzi, V., Castellano, G., Crasto, S. G., Rizzo, L. B., Davini, O., Zenga, F., & Ragazzi, P. (2002) · Journal of neurosurgery · doi:10.3171/jns.2002.97.5.1208 · Cited by 97 · see citing works

Reciprocal interactions between oscillatory activities of different frequencies in the subthalamic region of patients with Parkinson's disease

Fogelson, N., Pogosyan, A. H., Kühn, A. A., Kupsch, A. R., Bruggen, G. V., Speelman, H. D., Tijssen, M. A. J., Quartarone, A., Insola, A., Mazzone, P. A. M., et al. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04179.x · Cited by 97 · see citing works

Chronic thalamic stimulation for the tremor of multiple sclerosis

Montgomery, E. B., Baker, K. B., Kinkel, R. P., & Barnett, G. H. (1999) · Neurology · doi:10.1212/wnl.53.3.625 · Cited by 94 · see citing works

Cellular Mechanisms Preventing Sustained Activation of Cortex During Subcortical High-Frequency Stimulation

Iremonger, K. J., Anderson, T. R., Hu, B., & Kiss, Z. H. T. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00105.2006 · Cited by 93 · see citing works

The oscillatory activity in the Parkinsonian subthalamic nucleus investigated using the macro-electrodes for deep brain stimulation

Liu, X., Ford-Dunn, H. L., Hayward, G., Nandi, D., Miall, R. C., Aziz, T. Z., & Stein, J. F. (2002) · Clinical Neurophysiology · doi:10.1016/s1388-2457(02)00256-0 · Cited by 92 · see citing works

Analysis of the electrical excitation of CNS neurons

Rattay, F. (1998) · IEEE Transactions on Biomedical Engineering · doi:10.1109/10.678611 · Cited by 89 · see citing works

Bradykinesia in early Huntington’s disease

Sánchez‐Pernaute, R., Künig, G., Alba, A. D. B., de Yébenes, J. G., Vontobel, P., & Leenders, K. L. (2000) · Neurology · doi:10.1212/wnl.54.1.119 · Cited by 85 · see citing works

Neuronal response to local electrical stimulation in rat thalamus: physiological implications for mechanisms of deep brain stimulation

Kiss, Z. H. T., Mooney, D., Renaud, L. P., & Hu, B. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00122-7 · Cited by 82 · see citing works

DBS therapy for the vegetative state and minimally conscious state

Yamamoto, T., Kobayashi, K., Kasai, M., Oshima, H., Fukaya, C., & Katayama, Y. (2005) · Acta neurochirurgica. Supplementum · doi:10.1007/3-211-27577-0_17 · Cited by 77 · see citing works

Handbook of Parkinson's Disease

(2003) · CRC Press eBooks · doi:10.1201/9780203912164 · Cited by 77 · see citing works

Inhibition of voluntary activity by thalamic stimulation in humans: Relevance for the control of tremor

Strafella, A. P., Ashby, P., Munz, M., Dostrovsky, J. O., Lozano, A. M., & Lang, A. E. (1997) · Movement Disorders · doi:10.1002/mds.870120517 · Cited by 72 · see citing works

Chapter 78 How does DBS work?

Lozano, A. M., & Eltahawy, H. A. (2004) · Supplements to Clinical neurophysiology · doi:10.1016/s1567-424x(09)70414-3 · Cited by 71 · see citing works

Brain Dynamics and the Striatal Complex

Miller, R. J., & Wickens, J. (2000) · CRC Press eBooks · doi:10.1201/9781482283556 · Cited by 66 · see citing works

Somatosensory evoked high-frequency oscillation in Parkinson's disease and myoclonus epilepsy

Mochizuki, H., Ugawa, Y., Machii, K., Terao, Y., Hanajima, R., Furubayashi, T., Uesugi, H., & Kanazawa, I. (1999) · Clinical Neurophysiology · doi:10.1016/s0168-5597(98)00057-4 · Cited by 65 · see citing works

The periodogram and its optical analogy

Schuster, A. (1906) · Proceedings of the Royal Society of London Series A Containing Papers of a Mathematical and Physical Character · doi:10.1098/rspa.1906.0011 · Cited by 64 · see citing works

Muscle sounds in Parkinson's disease

Brown, P. (1997) · The Lancet · doi:10.1016/s0140-6736(97)80086-4 · Cited by 60 · see citing works

The striatum and motor cortex in motor initiation and execution

Montgomery, E. B., & Buchholz, S. R. (1991) · Brain Research · doi:10.1016/0006-8993(91)90461-4 · Cited by 58 · see citing works

Therapeutic extradural cortical stimulation for movement disorders: A review

Canavero, S., Bonicalzi, V., Paolotti, R., Castellano, G., Crasto, S. G., Rizzo, L. B., Davini, O., & Maina, R. (2003) · Neurological Research · doi:10.1179/016164103101201238 · Cited by 55 · see citing works

Effect of deep brain stimulation on amplitude and frequency characteristics of rest tremor in Parkinson's disease

Beuter, A. C. (2001) · Thalamus & Related Systems · doi:10.1016/s1472-9288(01)00020-6 · Cited by 53 · see citing works

Methods for isolating extracellular action potentials and removing stimulus artifacts from microelectrode recordings of neurons requiring minimal operator intervention

Montgomery, E. B., Gale, J. T., & He, H. (2004) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2004.10.017 · Cited by 48 · see citing works

Effect of subthalamic nucleus stimulation patterns on motor performance in Parkinson's disease

Montgomery, E. B. (2005) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2004.12.002 · Cited by 44 · see citing works

Dynamically Coupled, High-Frequency Reentrant, Non-linear Oscillators Embedded in Scale-Free Basal Ganglia-Thalamic-Cortical Networks Mediating Function and Deep Brain Stimulation Effects

Montgomery, E. B. (2004) · Nonlinear studies · Cited by 39 · see citing works

Elevations in local gamma activity are accompanied by changes in the firing rate and information coding capacity of neurons in the region of the subthalamic nucleus in Parkinson's disease

Pogosyan, A. H., Kühn, A. A., Trottenberg, T., Schneider, G., Kupsch, A. R., & Brown, P. (2006) · Experimental Neurology · doi:10.1016/j.expneurol.2006.06.014 · Cited by 39 · see citing works

Deep brain stimulation for hyperkinetic disorders

Montgomery, E. B. (2004) · Neurosurgical FOCUS · doi:10.3171/foc.2004.17.1.1 · Cited by 37 · see citing works

Intermuscular coherence in Parkinson's disease: relationship to bradykinesia

Brown, P., Marsden, J. F., Defebvre, L., Cassim, F., Mazzone, P. A. M., Oliviero, A., Altibrandi, M. G., Lazzaro, V. D., Limousin, P. D., Fraix, V., et al. (2001) · Neuroreport · doi:10.1097/00001756-200108080-00057 · Cited by 36 · see citing works

Disturbances of Rhythm Formation in Patients with Parkinson's Disease: Part II. A Forced Oscillation Model

Nagasaki, H., Nakamura, R., & Taniguchi, R. (1978) · Perceptual and Motor Skills · doi:10.2466/pms.1978.46.1.79 · Cited by 33 · see citing works

The Optimal Stimulation Site for Chronic Stimulation of the Subthalamic Nucleus in Parkinson’s Disease

Yokoyama, T., Sugiyama, K., Nishizawa, S., Yokota, N., Ohta, S., Akamine, S., & Namba, H. (2001) · Stereotactic and Functional Neurosurgery · doi:10.1159/000064598 · Cited by 31 · see citing works

Involvement of Human Thalamic Neurons in Internally and Externally Generated Movements

MacMillan, M., Dostrovsky, J. O., Lozano, A. M., & Hutchison, W. D. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00835.2003 · Cited by 30 · see citing works

Detection of neuronal periodic oscillations in the basal ganglia of normal and parkinsonian monkeys.

Karmon, B., & Bergman, H. (1993) · PubMed · Cited by 24 · see citing works

Levodopa reversible loss of the Piper frequency oscillation component in Parkinson's disease

McAuley, J. (2001) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.70.4.471 · Cited by 22 · see citing works

Brain Dynamics and the Striatal Complex

Wickens, J. R. (2000) · Taylor & Francis eBooks · doi:10.4324/9780203304914 · Cited by 19 · see citing works

Neurophysiology/circuitry

Montgomery, E. B. (2003) · Neurological disease and therapy · doi:10.1201/9780203912164.ch11 · Cited by 3 · see citing works

Axonal loss in multiple sclerosis lesions: magnetic resonance imaging insights substrates of disability

Sperfeld (1999) · Pure Amsterdam UMC · doi:10.1002/1531-8249(199911)46:5 · Cited by 2 · see citing works

Untitled work

Waldvogel (1999) · doi:10.1002/1531-8249(199907)46:1

Hydrogel bioelectronics

Yuk, H., Lu, B., & Zhao, X. (2018) · Chemical Society Reviews · doi:10.1039/c8cs00595h · Cited by 2,124 · see citing works

The neural basis of the speed–accuracy tradeoff

Bogacz, R., Wagenmakers, E., Forstmann, B. U., & Nieuwenhuis, S. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.09.002 · Cited by 721 · see citing works

Revealing neuronal function through microelectrode array recordings

Obien, M. E. J., Deligkaris, K., Bullmann, T., Bakkum, D. J., & Frey, U. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00423 · Cited by 705 · see citing works

Probing and regulating dysfunctional circuits using deep brain stimulation

Lozano, A. M., & Lipsman, N. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.020 · Cited by 665 · see citing works

Linking Molecules to Mood: New Insight Into the Biology of Depression

Krishnan, V., & Nestler, E. J. (2010) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2009.10030434 · Cited by 643 · see citing works

Network perspectives on the mechanisms of deep brain stimulation

McIntyre, C. C., & Hahn, P. J. (2010) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.09.022 · Cited by 439 · see citing works

Deep brain stimulation can suppress pathological synchronisation in parkinsonian patients

Eusébio, A., Thevathasan, W., Gaynor, L. D., Pogosyan, A. H., Bye, E., Foltynie, T., Zrinzo, L. U., Ashkan, K., Aziz, T. Z., & Brown, P. (2010) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2010.217489 · Cited by 412 · see citing works

Insights into the mechanisms of deep brain stimulation

Ashkan, K., Rogers, P., Bergman, H., & Ughratdar, I. (2017) · Nature Reviews Neurology · doi:10.1038/nrneurol.2017.105 · Cited by 365 · see citing works

Therapeutic Deep Brain Stimulation in Parkinsonian Rats Directly Influences Motor Cortex

Li, Q., Ke, Y., Chan, D. C. W., Qian, Z., Yung, K. K. L., Ko, H., Arbuthnott, G. W., & Yung, W. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.032 · Cited by 313 · see citing works

Review: Deep brain stimulation in Parkinson’s disease

Groiss, S. J., Wojtecki, L., Südmeyer, M., & Schnitzler, A. (2009) · Therapeutic Advances in Neurological Disorders · doi:10.1177/1756285609339382 · Cited by 287 · see citing works

Real-Time Functional Magnetic Resonance Imaging Neurofeedback for Treatment of Parkinson's Disease

Subramanian, L., Hindle, J. V., Johnston, S. J., Roberts, M. V., Masud Husain, B., Goebel, R., & Linden, D. E. J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3498-11.2011 · Cited by 266 · see citing works

A history of deep brain stimulation: Technological innovation and the role of clinical assessment tools

Gardner, J. (2013) · Social Studies of Science · doi:10.1177/0306312713483678 · Cited by 243 · see citing works

Cellular, molecular, and clinical mechanisms of action of deep brain stimulation—a systematic review on established indications and outlook on future developments

Jakobs, M., Fomenko, A., Lozano, A. M., & Kiening, K. L. (2019) · EMBO Molecular Medicine · doi:10.15252/emmm.201809575 · Cited by 229 · see citing works

Latest view on the mechanism of action of deep brain stimulation

Hammond, C., Ammari, R., Bioulac, B. H., & García, L. (2008) · Movement Disorders · doi:10.1002/mds.22120 · Cited by 216 · see citing works

Direct electrical stimulation as an input gate into brain functional networks: principles, advantages and limitations

Mandonnet, E., Winkler, P., & Duffau, H. (2009) · Acta Neurochirurgica · doi:10.1007/s00701-009-0469-0 · Cited by 217 · see citing works

Deep brain stimulation mechanisms: beyond the concept of local functional inhibition

Deniau, J., Degos, B., Bosch‐Bouju, C., & Maurice, N. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07413.x · Cited by 203 · see citing works

Closed-Loop Control of Deep Brain Stimulation: A Simulation Study

Santaniello, S., Fiengo, G., Glielmo, L., & Grill, W. M. (2010) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2010.2081377 · Cited by 203 · see citing works

Opportunities of connectomic neuromodulation

Horn, A., & Fox, M. D. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117180 · Cited by 187 · see citing works

Nonresonant powering of injectable nanoelectrodes enables wireless deep brain stimulation in freely moving mice

Kozielski, K., Jahanshahi, A., Gilbert, H. B., Yu, Y., Erin, Ö., Francisco, D., Alosaimi, F., Temel, Y., & Sitti, M. (2021) · Science Advances · doi:10.1126/sciadv.abc4189 · Cited by 183 · see citing works

Microscopic magnetic stimulation of neural tissue

Bonmassar, G., Lee, S. W., Freeman, D. K., Polášek, M., Fried, S. I., & Gale, J. T. (2012) · Nature Communications · doi:10.1038/ncomms1914 · Cited by 180 · see citing works

Deep Brain Stimulation Reduces Neuronal Entropy in the MPTP-Primate Model of Parkinson's Disease

Dorval, A. D., Russo, G. S., Hashimoto, T., Xu, W., Grill, W. M., & Vitek, J. L. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90763.2008 · Cited by 172 · see citing works

Subthalamic nucleus stimulation influences expression and suppression of impulsive behaviour in Parkinson’s disease

Wylie, S. A., Ridderinkhof, K. R., Elias, W. J., Frysinger, R. C., Bashore, T. R., Downs, K. E., van Wouwe, N. C., & van den Wildenberg, W. P. M. (2010) · Brain · doi:10.1093/brain/awq239 · Cited by 171 · see citing works

Effects of Deep Brain Stimulation on the Lived Experience of Obsessive-Compulsive Disorder Patients: In-Depth Interviews with 18 Patients

de Haan, S., Rietveld, E., Stokhof, M., & Denys, D. A. J. P. (2015) · PLoS ONE · doi:10.1371/journal.pone.0135524 · Cited by 166 · see citing works

From flexible electronics technology in the era of IoT and artificial intelligence toward future implanted body sensor networks

Lee, S., Shi, Q., & Lee, C. (2019) · APL Materials · doi:10.1063/1.5063498 · Cited by 164 · see citing works

Short latency activation of cortex during clinically effective subthalamic deep brain stimulation for Parkinson's disease

Walker, H. C., Huang, H., Gonzalez, C. L., Bryant, J. E., Killen, J. F., Cutter, G., Knowlton, R. C., Montgomery, E. B., Guthrie, B. L., & Watts, R. L. (2012) · Movement Disorders · doi:10.1002/mds.25025 · Cited by 136 · see citing works

Deep brain stimulation for treatment-resistant depression: Efficacy, safety and mechanisms of action

Anderson, R. J., Frye, M. A., Abulseoud, O. A., Lee, K. H., McGillivray, J., Berk, M., & Tye, S. J. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.06.001 · Cited by 137 · see citing works

Deep Brain Stimulation of the Globus Pallidus Internus in the Parkinsonian Primate: Local Entrainment and Suppression of Low-Frequency Oscillations

McCairn, K. W., & Turner, R. S. (2009) · Journal of Neurophysiology · doi:10.1152/jn.91092.2008 · Cited by 127 · see citing works

Creating the Feedback Loop

Hebb, A. O., Zhang, J. J., Mahoor, M. H., Tsiokos, C., Matlack, C., Chizeck, H. J., & Pouratian, N. (2013) · Neurosurgery Clinics of North America · doi:10.1016/j.nec.2013.08.006 · Cited by 118 · see citing works

Deep Brain Stimulation of the Nucleus Accumbens Shell Attenuates Cocaine Reinstatement through Local and Antidromic Activation

Vassoler, F. M., White, S., Hopkins, T. J., Guercio, L. A., Espallergues, J., Berton, O., Schmidt, H. D., & Pierce, R. C. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4804-12.2013 · Cited by 115 · see citing works

Electrical stimulation of retinal neurons in epiretinal and subretinal configuration using a multicapacitor array

Eickenscheidt, M., Jenkner, M., Thewes, R., Fromherz, P., & Zeck, G. M. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00909.2011 · Cited by 118 · see citing works

Resonance in subthalamo-cortical circuits in Parkinson's disease

Eusébio, A., Pogosyan, A. H., Wang, S., Averbeck, B. B., Gaynor, L. D., Cantiniaux, S., Witjas, T., Limousin, P. D., Azulay, J., & Brown, P. (2009) · Brain · doi:10.1093/brain/awp079 · Cited by 116 · see citing works

“Connectomic surgery”: diffusion tensor imaging (DTI) tractography as a targeting modality for surgical modulation of neural networks

Henderson, J. M. (2012) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2012.00015 · Cited by 111 · see citing works

Does suppression of oscillatory synchronisation mediate some of the therapeutic effects of DBS in patients with Parkinson's disease?

Eusébio, A., Cagnan, H., & Brown, P. (2012) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2012.00047 · Cited by 104 · see citing works

Closed-loop cortical neuromodulation in Parkinson’s disease: An alternative to deep brain stimulation?

Beuter, A., Lefaucheur, J.-P., & Modolo, J. (2014) · Clinical Neurophysiology · doi:10.1016/j.clinph.2014.01.006 · Cited by 107 · see citing works

Deep brain stimulation induces BOLD activation in motor and non-motor networks: An fMRI comparison study of STN and EN/GPi DBS in large animals

Min, H.-K. P., Hwang, S.-C., Marsh, M. P., Kim, I., Knight, E. J., Striemer, B. L., Felmlee, J. P., Welker, K. M., Blaha, C. D., Chang, S.-Y., et al. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.08.006 · Cited by 107 · see citing works

Effects of cerebellar neuromodulation in movement disorders: A systematic review

França, C., de Andrade, D. C., Teixeira, M. J., Galhardoni, R., da Silva, V. A., Barbosa, E. R., & Cury, R. G. (2017) · Brain stimulation · doi:10.1016/j.brs.2017.11.015 · Cited by 106 · see citing works

The thalamus and language revisited

Hebb, A. O., & Ojemann, G. A. (2012) · Brain and Language · doi:10.1016/j.bandl.2012.06.010 · Cited by 102 · see citing works

Robust modulation of arousal regulation, performance, and frontostriatal activity through central thalamic deep brain stimulation in healthy nonhuman primates

Baker, J., Ryou, J.-W., Wei, X. F., Butson, C. R., Schiff, N. D., & Purpura, K. P. (2016) · Journal of Neurophysiology · doi:10.1152/jn.01129.2015 · Cited by 98 · see citing works

A brain network for deep brain stimulation induced cognitive decline in Parkinson’s disease

Reich, M. M., Hsu, J., Ferguson, M., Schaper, F. L. W. V. J., Joutsa, J., Roothans, J., Nickl, R. C., Frankemolle-Gilbert, A., Alberts, J., Volkmann, J., et al. (2022) · Brain · doi:10.1093/brain/awac012 · Cited by 104 · see citing works

Antidepressant-like Effects of Cortical Deep Brain Stimulation Coincide With Pro-neuroplastic Adaptations of Serotonin Systems

Veerakumar, A., Challis, C., Gupta, P., Da, J., Upadhyay, A., Beck, S. G., & Berton, O. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.12.009 · Cited by 102 · see citing works

Electronic and Ionic Materials for Neurointerfaces

Ferro, M. D., & Melosh, N. A. (2017) · Advanced Functional Materials · doi:10.1002/adfm.201704335 · Cited by 95 · see citing works

Subthalamic Local Field Beta Oscillations during Ongoing Deep Brain Stimulation in Parkinson’s Disease in Hyperacute and Chronic Phases

Rosa, M., Giannicola, G., Servello, D., Marceglia, S. R. F., Pacchetti, C., Porta, M., Sassi, M., Scelzo, E., Barbieri, S., & Priori, A. (2011) · Neurosignals · doi:10.1159/000328508 · Cited by 95 · see citing works

Magnetic seizure therapy in treatment-resistant depression: clinical, neuropsychological and metabolic effects

Kayser, S., Bewernick, B. H., Matusch, A., Hurlemann, R., Soehle, M., & Schlaepfer, T. E. (2015) · Psychological Medicine · doi:10.1017/s0033291714002244 · Cited by 94 · see citing works

Activation of the central nervous system induced by micro-magnetic stimulation

Park, H.-J., Bonmassar, G., Kaltenbach, J. A., Machado, A. G., Manzoor, N. F., & Gale, J. T. (2013) · Nature Communications · doi:10.1038/ncomms3463 · Cited by 93 · see citing works

Reduction of Influence of Task Difficulty on Perceptual Decision Making by STN Deep Brain Stimulation

Green, N., Bogacz, R., Huebl, J., Beyer, A.-K., Kühn, A. A., & Heekeren, H. R. (2013) · Current Biology · doi:10.1016/j.cub.2013.07.001 · Cited by 93 · see citing works

Multifunctional Conductive Hydrogel Interface for Bioelectronic Recording and Stimulation

Tang, H., Li, Y., Liao, S., Liu, H., Qiao, Y., & Zhou, J. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202400562 · Cited by 91 · see citing works

Selective Activation of Resting-State Networks following Focal Stimulation in a Connectome-Based Network Model of the Human Brain

Spiegler, A., Hansen, E. C. A., Bernard, C., McIntosh, A. R., & Jirsa, V. (2016) · eNeuro · doi:10.1523/eneuro.0068-16.2016 · Cited by 92 · see citing works

Therapeutic mechanisms of high-frequency stimulation in Parkinson’s disease and neural restoration via loop-based reinforcement

Santaniello, S., McCarthy, M. M., Montgomery, E. B., Gale, J. T., Kopell, N., & Sarma, S. V. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1406549111 · Cited by 89 · see citing works

The temporal pattern of stimulation may be important to the mechanism of deep brain stimulation

Hess, C. W., Vaillancourt, D. E., & Okun, M. S. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.02.001 · Cited by 87 · see citing works

Diffusion Tractography in Deep Brain Stimulation Surgery: A Review

Calabrese, E. (2016) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2016.00045 · Cited by 88 · see citing works

Machine learning for adaptive deep brain stimulation in Parkinson’s disease: closing the loop

de Oliveira, A. M. R., Coelho, L. P., de Carvalho, E. A., Ferreira‐Pinto, M. J., Vaz, R. M., & Aguiar, P. (2023) · Journal of Neurology · doi:10.1007/s00415-023-11873-1 · Cited by 85 · see citing works

Design, simulation and experimental validation of a novel flexible neural probe for deep brain stimulation and multichannel recording

Lai, H., Liao, L., Lin, C., Hsu, J.-H., He, X., Chen, Y., Chang, J.-Y., Chen, H.-F., Tsang, S., & Shih, Y. I. (2012) · Journal of Neural Engineering · doi:10.1088/1741-2560/9/3/036001 · Cited by 83 · see citing works

Activation of AMPA Receptors Mediates the Antidepressant Action of Deep Brain Stimulation of the Infralimbic Prefrontal Cortex

Jiménez-Sánchez, L., Castañé, A., Pérez-Caballero, L., Grifoll, M., López-Gil, X., Campa, L., Galofré, M., Berrocoso, E., & Adell, A. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv133 · Cited by 83 · see citing works

Deep Brain Stimulation Does Not Silence Neurons in Subthalamic Nucleus in Parkinson's Patients

Carlson, J. D., Cleary, D. R., Cetas, J. S., Heinricher, M. M., & Burchiel, K. J. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00363.2009 · Cited by 82 · see citing works

Direct Electrical Stimulation in Electrocorticographic Brain–Computer Interfaces: Enabling Technologies for Input to Cortex

Caldwell, D. J., Ojemann, J. G., & Rao, R. P. N. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00804 · Cited by 81 · see citing works

High frequency stimulation and pharmacological inactivation of the subthalamic nucleus reduces ‘compulsive’ lever-pressing in rats

Klavir, O., Flash, S., Winter, C., & Joel, D. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2008.09.017 · Cited by 80 · see citing works

Anxiety: An ignored aspect of Parkinson's disease lacking attention.

Khatri, D., Choudhary, M., Sood, A., & Singh, S. B. (2020) · Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · doi:10.1016/j.biopha.2020.110776 · Cited by 65 · see citing works

Optogenetic Inactivation of the Subthalamic Nucleus Improves Forelimb Akinesia in a Rat Model of Parkinson Disease

Yoon, H. H., Park, J. H., Kim, Y. H., Min, J., Hwang, E., Lee, C. J., Suh, J. F., Hwang, O., & Jeon, S. R. (2014) · Neurosurgery · doi:10.1227/neu.0000000000000297 · Cited by 77 · see citing works

Gene Therapy in Parkinsonʼs Disease

Feng, L., & Maguire‐Zeiss, K. A. (2010) · CNS Drugs · doi:10.2165/11533740-000000000-00000 · Cited by 78 · see citing works

Basal ganglia physiology and pathophysiology: A reappraisal

Montgomery, E. B. (2007) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2007.07.020 · Cited by 77 · see citing works

Deep brain stimulation for the treatment of addiction: basic and clinical studies and potential mechanisms of action

Pierce, R. C., & Vassoler, F. M. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3214-6 · Cited by 75 · see citing works

Coordinated reset stimulation in a large-scale model of the STN-GPe circuit

Ebert, M., Hauptmann, C., & Tass, P. A. (2014) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2014.00154 · Cited by 74 · see citing works

Deep brain stimulation for Parkinson's disease modulates high-frequency evoked and spontaneous neural activity

Sinclair, N. C., McDermott, H. J., Fallon, J. B., Perera, T., Brown, P., Bulluss, K. J., & Thevathasan, W. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.104522 · Cited by 70 · see citing works

Deep Brain Stimulation Treating Dystonia: A Systematic Review of Targets, Body Distributions and Etiology Classifications

Fan, H., Zheng, Z., Yin, Z., Zhang, J., & Lu, G. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.757579 · Cited by 69 · see citing works

DBS of nucleus accumbens on heroin seeking behaviors in self-administering rats

Guo, L., Zhou, H., Wang, R., Xu, J., Zhou, W., Zhang, F., Tang, S., Liu, H., & Jiang, J. (2012) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2012.09.012 · Cited by 67 · see citing works

Sustained cortical and subcortical neuromodulation induced by electrical tongue stimulation

Wildenberg, J. C., Tyler, M. E., Danilov, Y. P., Kaczmarek, K. A., & Meyerand, M. E. (2010) · Brain Imaging and Behavior · doi:10.1007/s11682-010-9099-7 · Cited by 66 · see citing works

Effects of DBS on auditory and somatosensory processing in Parkinson's disease

Airaksinen, K., Mäkelä, J. P., Taulu, S., Ahonen, A. I., Nurminen, J., Schnitzler, A., & Pekkonen, E. (2010) · Human Brain Mapping · doi:10.1002/hbm.21096 · Cited by 66 · see citing works

Astroglial Control of the Antidepressant-Like Effects of Prefrontal Cortex Deep Brain Stimulation

Etiévant, A., Oosterhof, C., Bétry, C., Abrial, E., Novo-Perez, M., Rovera, R., Scarna, H., Devader, C., Mazella, J., Wegener, G., et al. (2015) · EBioMedicine · doi:10.1016/j.ebiom.2015.06.023 · Cited by 65 · see citing works

Suppression of deep brain stimulation artifacts from the electroencephalogram by frequency-domain Hampel filtering

Allen, D. P., Stegemöller, E. L., Zadikoff, C., Rosenow, J. M., & MacKinnon, C. D. (2010) · Clinical Neurophysiology · doi:10.1016/j.clinph.2010.02.156 · Cited by 62 · see citing works

Temporal pattern of electrical stimulation is a new dimension of therapeutic innovation

Grill, W. M. (2018) · Current Opinion in Biomedical Engineering · doi:10.1016/j.cobme.2018.08.007 · Cited by 61 · see citing works

Clinical outcome and mechanisms of deep brain stimulation for obsessive-compulsive disorder

van Westen, M., Rietveld, E., Figee, M., & Denys, D. (2015) · Current Behavioral Neuroscience Reports · doi:10.1007/s40473-015-0036-3 · Cited by 60 · see citing works

Sing the mind electric – principles of deep brain stimulation

Kringelbach, M. L., Green, A. L., Owen, S. L. F., Schweder, P. M., & Aziz, T. Z. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07419.x · Cited by 60 · see citing works

Optimizing a Rodent Model of Parkinson's Disease for Exploring the Effects and Mechanisms of Deep Brain Stimulation

Nowak, K., Mix, E., Gimsa, J., Strauß, U., Sriperumbudur, K. K., Benecke, R., & Gimsa, U. (2011) · Parkinson s Disease · doi:10.4061/2011/414682 · Cited by 59 · see citing works

Activation of subthalamic neurons by contralateral subthalamic deep brain stimulation in Parkinson disease

Walker, H. C., Watts, R. L., Schrandt, C. J., Huang, H., Guthrie, S. L., Guthrie, B. L., & Montgomery, E. B. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00266.2010 · Cited by 58 · see citing works

Thalamic stimulation in absence epilepsy

Lüttjohann, A., & van Luijtelaar, G. (2013) · Epilepsy Research · doi:10.1016/j.eplepsyres.2013.03.009 · Cited by 56 · see citing works

Effects of DBS in parkinsonian patients depend on the structural integrity of frontal cortex

Muthuraman, M., Deuschl, G., Koirala, N., Riedel, C. H., Volkmann, J., & Groppa, S. (2017) · Scientific Reports · doi:10.1038/srep43571 · Cited by 56 · see citing works

Effects of deep brain stimulation frequency on bradykinesia of Parkinson's disease

Huang, H., Watts, R. L., & Montgomery, E. B. (2014) · Movement Disorders · doi:10.1002/mds.25773 · Cited by 54 · see citing works

Neurosurgical targets for compulsivity: What can we learn from acquired brain lesions?

Figee, M., Wielaard, I., Mazaheri, A., & Denys, D. A. J. P. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.01.005 · Cited by 53 · see citing works

Saccadic latency during electrical stimulation of the human subthalamic nucleus

Temel, Y., Visser-Vandewalle, V. E. R. M., & Carpenter, R. H. S. (2008) · Current Biology · doi:10.1016/j.cub.2008.03.008 · Cited by 51 · see citing works

Investigating the depth electrode–brain interface in deep brain stimulation using finite element models with graded complexity in structure and solution

Yousif, N., & Liu, X. (2009) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2009.07.005 · Cited by 48 · see citing works

Advances in the Application of Technology to Epilepsy: The CIMIT/NIO Epilepsy Innovation Summit

Schachter, S., Guttag, J., Schiff, S., & Schomer, D. (2009) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2009.06.028 · Cited by 47 · see citing works

Functional disconnection of axonal fibers generated by high frequency stimulation in the hippocampal CA1 region in-vivo

Feng, Z., Zheng, X., Yu, Y., & Durand, D. M. (2013) · Brain Research · doi:10.1016/j.brainres.2013.02.048 · Cited by 47 · see citing works

Fidelity of frequency and phase entrainment of circuit-level spike activity during DBS

Agnesi, F., Muralidharan, A., Baker, K. B., Vitek, J. L., & Johnson, M. D. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00259.2015 · Cited by 46 · see citing works

Neurophysiology of Deep Brain Stimulation

Rosa, M., Giannicola, G., Marceglia, S. R. F., Fumagalli, M., Barbieri, S., & Priori, A. (2012) · International review of neurobiology · doi:10.1016/b978-0-12-404706-8.00004-8 · Cited by 44 · see citing works

Deep brain stimulation in tinnitus: Current and future perspectives

Smit, J. V., Janssen, M. L. F., Schulze, H., Jahanshahi, A., van Overbeeke, J. J., Temel, Y., & Stokroos, R. J. (2015) · Brain Research · doi:10.1016/j.brainres.2015.02.050 · Cited by 43 · see citing works

Neural Hijacking

Cheney, P. D., Griffin, D. M., & Acker, G. M. V. (2012) · The Neuroscientist · doi:10.1177/1073858412458368 · Cited by 43 · see citing works

Moving toward a generalizable application of central thalamic deep brain stimulation for support of forebrain arousal regulation in the severely injured brain

Schiff, N. D. (2012) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2012.06712.x · Cited by 43 · see citing works

A Computational Model of Loss of Dopaminergic Cells in Parkinson's Disease Due to Glutamate-Induced Excitotoxicity

Muddapu, V. R., Mandali, A., Chakravarthy, S. V., & Ramaswamy, S. (2019) · Frontiers in Neural Circuits · doi:10.3389/fncir.2019.00011 · Cited by 42 · see citing works

α-Synuclein: A therapeutic target for Parkinson’s disease?

Maguire‐Zeiss, K. A. (2008) · Pharmacological Research · doi:10.1016/j.phrs.2008.09.006 · Cited by 44 · see citing works

Invasive and Non-invasive Neurostimulation for OCD

Bergfeld, I. O., Dijkstra, E., Graat, I., de Koning, P. P., van den Boom, B. J. G., Arbab, T., Vulink, N. C. C., Denys, D. A. J. P., Willuhn, I., & Mocking, R. J. T. (2021) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_206 · Cited by 43 · see citing works

Reciprocal interactions between the human thalamus and periaqueductal gray may be important for pain perception

Wu, D., Wang, S., Stein, J. F., Aziz, T. Z., & Green, A. L. (2013) · Experimental Brain Research · doi:10.1007/s00221-013-3761-4 · Cited by 42 · see citing works

Deep Brain Stimulation for Arm Tremor: A Randomized Trial Comparing Two Targets

Kvernmo, N., Konglund, A. E., Reich, M. M., Roothans, J., Pripp, A. H., Dietrichs, E., Volkmann, J., & Skogseid, I. M. (2022) · Annals of Neurology · doi:10.1002/ana.26317 · Cited by 40 · see citing works

Automatic removal of high-amplitude stimulus artefact from neuronal signal recorded in the subthalamic nucleus

Al-ani, T., Cazettes, F., Palfi, S., & Lefaucheur, J. (2011) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2011.03.022 · 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

Analysis of Deep Brain Stimulation Lead Targeting in the Stimulation of Anterior Nucleus of the Thalamus for Epilepsy Clinical Trial

Gross, R. E., Fisher, R. S., Sperling, M. R., Giftakis, J. E., Stypulkowski, P. H., & on behalf of the SANTÉ Study Group (2021) · Neurosurgery · doi:10.1093/neuros/nyab186 · Cited by 40 · see citing works

Effect of high-frequency stimulation on nerve pulse propagation in the FitzHugh–Nagumo model

Ratas, I., & Pyragas, K. (2011) · Nonlinear Dynamics · doi:10.1007/s11071-011-0197-x · Cited by 40 · see citing works

Long-Term Measurement of Therapeutic Electrode Impedance in Deep Brain Stimulation

Sillay, K. A., Chen, J. C., & Montgomery, E. B. (2010) · Neuromodulation Technology at the Neural Interface · doi:10.1111/j.1525-1403.2010.00275.x · Cited by 39 · see citing works

Closed-Loop Control of Tremor-Predominant Parkinsonian State Based on Parameter Estimation

Liu, C., Wang, J., Deng, B., Wei, X., Yu, H., Li, H., Fietkiewicz, C., & Loparo, K. A. (2016) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2016.2535358 · Cited by 38 · see citing works

Deep brain stimulation for essential tremor

(2013) · Handbook of Clinical Neurology · doi:10.1016/b978-0-444-53497-2.00013-9 · Cited by 38 · see citing works

Electroceutically induced subthalamic high-frequency oscillations and evoked compound activity may explain the mechanism of therapeutic stimulation in Parkinson’s disease

Öztürk, M., Viswanathan, A., Sheth, S. A., & Ince, N. F. (2021) · Communications Biology · doi:10.1038/s42003-021-01915-7 · Cited by 37 · see citing works

Mechanism of DBS: Inhibition, Excitation, or Disruption?

Nambu, A., & Chiken, S. (2014) · Springer eBooks · doi:10.1007/978-3-319-08476-3_2 · Cited by 10 · see citing works

Mechanisms of Action of Deep Brain Stimulation

Lee, K. H., Mosier, E. M., & Blaha, C. D. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-805353-9.00017-6 · Cited by 9 · see citing works

Mechanism of Deep Brain Stimulation

Chiken, S., & Nambu, A. (2015) · The Neuroscientist · doi:10.1177/1073858415581986 · Cited by 375 · see citing works

Mechanisms of deep brain stimulation: Excitation or inhibition

Vitek, J. L. (2002) · Movement Disorders · doi:10.1002/mds.10144 · Cited by 412 · see citing works

Mechanisms of Deep Brain Stimulation

Miocinovic, S., McIntyre, C. C., Savasta, M., & Vitek, J. L. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-360-8_8 · Cited by 6 · see citing works