Electrical brain stimulation for epilepsy

Safety, ethical considerations, and application guidelines for the use of transcranial magnetic stimulation in clinical practice and research

Rossi, S., Hallett, M., Rossini, P. M., & Pascual-Leone, A. (2009) · Clinical Neurophysiology · doi:10.1016/j.clinph.2009.08.016 · Cited by 5,367

Electrical stimulation of the anterior nucleus of thalamus for treatment of refractory epilepsy

Fisher, R. S., Salanova, V., Witt, T. C., Worth, R. M., Henry, T. R., Gross, R. E., Oommen, K. J., Osorio, I., Nazzaro, J. M., Labar, D., et al. (2010) · Epilepsia · doi:10.1111/j.1528-1167.2010.02536.x · Cited by 1,930

Effect on parkinsonian signs and symptoms of bilateral subthalamic nucleus stimulation

Limousin, P., Pollak, P., Benazzouz, A., Hoffmann, D., Bas, J. L., Perret, J., Benabid, A., & Broussolle, E. (1995) · The Lancet · doi:10.1016/s0140-6736(95)90062-4 · Cited by 1,480

Responsive cortical stimulation for the treatment of medically intractable partial epilepsy

Morrell, M. J. (2011) · Neurology · doi:10.1212/wnl.0b013e3182302056 · Cited by 1,282

Psychosomatic Disease and the "Visceral Brain": Recent Developments Bearing on the Papez Theory of Emotion

MACLEAN, P. D. (1949) · Psychosomatic Medicine · doi:10.1097/00006842-194911000-00003 · Cited by 1,203

Jasper's Basic Mechanisms of the Epilepsies

(2012) · Oxford University Press eBooks · doi:10.1093/med/9780199746545.001.0001 · Cited by 1,161

Vagus nerve stimulation therapy for partial-onset seizures

Handforth, A., DeGiorgio, C. M., Schachter, S. C., Uthman, B. M., Naritoku, D. K., Tecoma, E. S., Henry, T. R., Collins, S. D., Vaughn, B. V., Gilmartin, R. C., et al. (1998) · Neurology · doi:10.1212/wnl.51.1.48 · Cited by 1,107

Long-term treatment with vagus nerve stimulation in patients with refractory epilepsy

Morris, G. L., Mueller, W. M., & The Vagus Nerve Stimulation Study Group E–E (1999) · Neurology · doi:10.1212/wnl.53.8.1731 · Cited by 727

Chronic Anterior Thalamus Stimulation for Intractable Epilepsy

Hodaie, M., Wennberg, R. A., Dostrovsky, J. O., & Lozano, A. M. (2002) · Epilepsia · doi:10.1046/j.1528-1157.2002.26001.x · Cited by 605

Evidence-based guideline update: Vagus nerve stimulation for the treatment of epilepsy

Morris, G. L., Gloss, D. S., Buchhalter, J., Mack, K. J., Nickels, K. C., & Harden, C. L. (2013) · Neurology · doi:10.1212/wnl.0b013e3182a393d1 · Cited by 450

Thalamocortical hodology to personalize electrical stimulation for focal epilepsy

Damiani, A., Nouduri, S., Ho, J. C., Salazar, S., Jegou, A., Chen, J. J., Reedy, E. M., Ikegaya, N., Sarma, S. V., Aung, T., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-64922-w · Cited by 37

Neural mass modeling of slow-fast dynamics of seizure initiation and abortion

Ersöz, E. K., Modolo, J., Bartoloméi, F., & Wendling, F. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008430 · Cited by 33

A Molecular Approach to Epilepsy Management: from Current Therapeutic Methods to Preconditioning Efforts

Amini, E., Rezaei, M., Ibrahim, N. M., Golpich, M., Ghasemi, R., Mohamed, Z., Raymond, A. A., Dargahi, L., & Ahmadiani, A. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8876-5 · Cited by 32

Optogenetic Approaches for Controlling Seizure Activity

Tung, J. K., Berglund, K., & Gross, R. E. (2016) · Brain stimulation · doi:10.1016/j.brs.2016.06.055 · Cited by 32

Orally Ingested Self‐Powered Stimulators for Targeted Gut–Brain Axis Electrostimulation to Treat Obesity and Metabolic Disorders

Mac, C., Tai, H., Huang, S., Peng, H., Sharma, A. K., Nguyen, G. L. T., Chang, P., Wang, J., Chang, Y., Lin, Y., et al. (2024) · Advanced Materials · doi:10.1002/adma.202310351 · Cited by 31

Injectable 2D Material‐Based Sensor Array for Minimally Invasive Neural Implants

Kim, J., Hong, J., Park, K., Lee, S., Hoàng, A. T., Pak, S., Zhao, H., Ji, S., Yang, S., Chung, C. K., et al. (2024) · Advanced Materials · doi:10.1002/adma.202400261 · Cited by 34

Modulating limbic circuits in temporal lobe epilepsy: impacts on seizures, memory, mood and sleep

Křemen, V., Sladky, V., Mívalt, F., Gregg, N. M., Brinkmann, B. H., Balzekas, I., Marks, V. S., Kucewicz, M. T., Lundstrom, B. N., Cui, J., et al. (2025) · Brain Communications · doi:10.1093/braincomms/fcaf106 · Cited by 30

Cloud computing for seizure detection in implanted neural devices

Baldassano, S. N., Zhao, X., Brinkmann, B. H., Křemen, V., Bernabei, J. M., Cook, M. J., Denison, T., Worrell, G. A., & Litt, B. (2018) · Journal of Neural Engineering · doi:10.1088/1741-2552/aaf92e · Cited by 31

Low-frequency electrical stimulation reduces cortical excitability in the human brain

Manzouri, F., Meisel, C., Kunz, L., Dümpelmann, M., Stieglitz, T., & Schulze‐Bonhage, A. (2021) · NeuroImage Clinical · doi:10.1016/j.nicl.2021.102778 · Cited by 31

A Biohybrid Setup for Coupling Biological and Neuromorphic Neural Networks

Keren, H., Partzsch, J., Marom, S., & Mayr, C. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00432 · Cited by 30

Conformable Piezoelectric Devices and Systems for Advanced Wearable and Implantable Biomedical Applications

Kim, J., Yoon, H., Viswanath, S., & Dağdeviren, C. (2025) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-020524-121438 · Cited by 32

A universal model of electrochemical safety limits in vivo for electrophysiological stimulation

Vatsyayan, R., & Dayeh, S. A. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.972252 · Cited by 28

Single-pulse stimulation of cerebellar nuclei stops epileptic thalamic activity

Rooda, O. H. J. E., Kros, L., Faneyte, S. J., Holland, P. J., Gornati, S. V., Poelman, H. J., Jansen, N. A., Tolner, E. A., van den Maagdenberg, A. M. J. M., Zeeuw, C. I. D., et al. (2021) · Brain stimulation · doi:10.1016/j.brs.2021.05.002 · Cited by 28

Implantable electrodes

Jalili, R., Kanneganti, A., Romero‐Ortega, M. I., & Wallace, G. G. (2017) · Current Opinion in Electrochemistry · doi:10.1016/j.coelec.2017.07.003 · Cited by 28

Effects of radiation from a radiofrequency identification (RFID) microchip on human cancer cells

Lai, H. C., Chan, A. H. W., & Singh, N. P. (2016) · International Journal of Radiation Biology · doi:10.3109/09553002.2016.1135264 · Cited by 27

Utilization of temporal autoencoder for semi-supervised intracranial EEG clustering and classification

Nejedlý, P., Křemen, V., Lepkova, K., Mívalt, F., Sladky, V., Pridalova, T., Plešinger, F., Jurák, P., Pail, M., Brázdil, M., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-27978-6 · Cited by 28

Implant Site Infection and Bone Flap Osteomyelitis Associated with the NeuroPace Responsive Neurostimulation System

Wei, Z., Gordon, C. R., Bergey, G. K., Sacks, J. M., & Anderson, W. S. (2015) · World Neurosurgery · doi:10.1016/j.wneu.2015.11.106 · Cited by 26

In Search of Optimal DBS Paradigms to Treat Epilepsy: Bilateral Versus Unilateral Hippocampal Stimulation in a Rat Model for Temporal Lobe Epilepsy

Nieuwenhuyse, B. V., Raedt, R., Delbeke, J., Wadman, W. J., Boon, P., & Vonck, K. E. J. (2014) · Brain stimulation · doi:10.1016/j.brs.2014.11.016 · Cited by 26

Neurostimulation stabilizes spiking neural networks by disrupting seizure-like oscillatory transitions

Rich, S., Hutt, A., Skinner, F. K., Valiante, T. A., & Lefebvre, J. (2020) · Scientific Reports · doi:10.1038/s41598-020-72335-6 · Cited by 25

Multimodal Technologies for Closed‐Loop Neural Modulation and Sensing

Li, L., Zhang, B., Zhao, W., Sheng, D., Yin, L., Sheng, X., & Yao, D. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202303289 · Cited by 25

Medial pulvinar stimulation for focal drug-resistant epilepsy: interim 12-month results of the PULSE study

Pizzo, F., Carron, R., Laguitton, V., Clement, A., Giusiano, B., & Bartoloméi, F. (2024) · Frontiers in Neurology · doi:10.3389/fneur.2024.1480819 · Cited by 27

Control of Absence Seizures by the Thalamic Feed-Forward Inhibition

Chen, M., Guo, D., Xia, Y., & Yao, D. (2017) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2017.00031 · Cited by 25

Closed-Loop Control of Absence Seizures Inspired by Feedback Modulation of Basal Ganglia to the Corticothalamic Circuit

Fan, D., & Wang, Q. (2020) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2020.2969426 · Cited by 24

Personalized dynamic network models of the human brain as a future tool for planning and optimizing epilepsy therapy

Dallmer‐Zerbe, I., Jiruška, P., & Hlinka, J. (2023) · Epilepsia · doi:10.1111/epi.17690 · Cited by 24

Corticothalamic Responsive Neurostimulation for Focal Epilepsy: A Single-Center Experience

Burdette, D. E., Patra, S., & Johnson, L. A. (2024) · Journal of Clinical Neurophysiology · doi:10.1097/wnp.0000000000001060 · Cited by 24

Early Seizure Detection Using Neuronal Potential Similarity: A Generalized Low-Complexity and Robust Measure

Bandarabadi, M., Rasekhi, J., Teixeira, C., Netoff, T. I., Parhi, K. K., & Dourado, A. (2015) · International Journal of Neural Systems · doi:10.1142/s0129065715500197 · Cited by 24

Four-dimensional map of direct effective connectivity from posterior visual areas

Sugiura, A., Silverstein, B. H., Jeong, J., Nakai, Y., Sonoda, M., Motoi, H., & Asano, E. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.116548 · Cited by 23

Erratum to: Implantable neurotechnologies: bidirectional neural interfaces—applications and VLSI circuit implementations

Greenwald, E., Masters, M. R., & Thakor, N. V. (2016) · Medical & Biological Engineering & Computing · doi:10.1007/s11517-016-1452-6 · Cited by 23

Closing the loop for patients with epilepsy

Vonck, K., & Boon, P. (2015) · Nature Reviews Neurology · doi:10.1038/nrneurol.2015.56 · Cited by 23

Recent Development of Neural Microelectrodes with Dual-Mode Detection

Xu, M., Zhao, Y., Xu, G., Zhang, Y., Sun, S., Sun, Y., Wang, J., & Pei, R. (2022) · Biosensors · doi:10.3390/bios13010059 · Cited by 23

Potential of Photoelectric Stimulation with Ultrasmall Carbon Electrode on Neural Tissue: New Directions in Neurostimulation Technology Development

Chen, K., Wu, B., Krahe, D. D., Vazquez, A. L., Siegenthaler, J. R., Rechenberg, R., Li, W., Cui, X. T., & Kozai, T. D. Y. (2024) · Advanced Functional Materials · doi:10.1002/adfm.202403164 · Cited by 22

Optogenetic study of networks in epilepsy

Choy, M., Duffy, B. A., & Lee, J. H. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23767 · Cited by 22

Comparative analysis of energy transfer mechanisms for neural implants

Miziev, S., Pawlak, W. A., & Howard, N. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1320441 · Cited by 21

Nonperiodic stimulation for the treatment of refractory epilepsy: Applications, mechanisms, and novel insights

Cota, V. R., de Oliveira, J. C., Damázio, L. C. M., & Moraes, M. F. D. (2019) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2019.106609 · Cited by 21

Electrophysiological characteristics of CM-pf in diagnosis and outcome of patients with disorders of consciousness

He, J., Zhang, H., Dang, Y., Zhuang, Y., Ge, Q., Yang, Y., Xu, L., Xia, X., Laureys, S., Yu, S. P., et al. (2023) · Brain stimulation · doi:10.1016/j.brs.2023.09.021 · Cited by 21

A Proposed Mechanism for Spontaneous Transitions between Interictal and Ictal Activity

Jacob, T., Lillis, K. P., Wang, Z., Swiercz, W. B., Rahmati, N., & Staley, K. J. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0719-17.2018 · Cited by 20

Fine-grained brain tissue segmentation for brain modeling of stroke patient

Lee, J., Lee, M., Lee, J., Kim, R. E. Y., Lim, S. H., & Kim, D. (2022) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2022.106472 · Cited by 20

Noninvasive Electrical Stimulation Neuromodulation and Digital Brain Technology: A Review

Zhang, S., Qin, Y., Wang, J., Yu, Y., Wu, L., & Zhang, T. (2023) · Biomedicines · doi:10.3390/biomedicines11061513 · Cited by 20

Automated calibration of somatosensory stimulation using reinforcement learning

Borda, L., Gozzi, N., Preatoni, G., Valle, G., & Raspopović, S. (2023) · Journal of NeuroEngineering and Rehabilitation · doi:10.1186/s12984-023-01246-0 · Cited by 19

Deep Brain Stimulation for Children with Generalized Epilepsy

Piper, R. J., Ibrahim, G. M., & Tisdall, M. M. (2023) · Neurosurgery Clinics of North America · doi:10.1016/j.nec.2023.09.002 · Cited by 20

Automated epileptic seizure detection based on break of excitation/inhibition balance

Fan, X., Gaspard, N., Legros, B., Lucchetti, F., Ercek, R., & Nonclercq, A. (2019) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2019.02.005 · Cited by 20

Presynaptic GABAB receptors underlie the antiepileptic effect of low-frequency electrical stimulation in the 4-aminopyridine model of epilepsy in brain slices of young rats

Smirnova, E. Y., Chizhov, A. V., & Zaitsev, A. V. (2020) · Brain stimulation · doi:10.1016/j.brs.2020.07.013 · Cited by 20

Early experiences with tachycardia‐triggered vagus nerve stimulation using the AspireSR stimulator

Tahry, R. E., Hirsch, M., van Rijckevorsel, K., Santos, S. F., de Tourtchaninoff, M., Rooijakkers, H., Coenen, V. A., & Schulze‐Bonhage, A. (2016) · Epileptic Disorders · doi:10.1684/epd.2016.0831 · Cited by 20

Ligand-gated mechanisms leading to ictogenesis in focal epileptic disorders

Avoli, M., Chen, L., Cristo, G. D., Librizzi, L., Scalmani, P., Shiri, Z., Uva, L., de Curtis, M., & Lévesque, M. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106097 · Cited by 19

Transient targeting of hypothalamic orexin neurons alleviates seizures in a mouse model of epilepsy

Li, H., Viskaitis, P., Bracey, E. F., Peleg‐Raibstein, D., & Burdakov, D. (2024) · Nature Communications · doi:10.1038/s41467-024-45515-5 · Cited by 21

Arbitrary-Waveform Electro-Optical Intracranial Neurostimulator With Load-Adaptive High-Voltage Compliance

Kassiri, H., Chen, F., Salam, M. T., Chang, M., Vatankhahghadim, B., Carlen, P. L., Valiante, T. A., & Genov, R. (2019) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2019.2900455 · Cited by 20

Emerging treatments for progressive myoclonus epilepsies

Riva, A., Guglielmo, A., Balagura, G., Marchese, F., Amadori, E., Iacomino, M., Minassian, B. A., Zara, F., & Striano, P. (2020) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2020.1741350 · Cited by 18

Control and analysis of epilepsy waveforms in a disinhibition model of cortex network

Shen, Z., Deng, Z., Du, L., Zhang, H., Yan, L., & Xiao, P. (2021) · Nonlinear Dynamics · doi:10.1007/s11071-020-06131-2 · Cited by 18

Functional MRI during Hippocampal Deep Brain Stimulation in the Healthy Rat Brain

Berge, N. V. D., Vanhove, C., Descamps, B., Dauwe, I., van Mierlo, P., Vonck, K. E. J., Keereman, V., Raedt, R., Boon, P., & Holen, R. V. (2015) · PLoS ONE · doi:10.1371/journal.pone.0133245 · Cited by 17

Development and validation of a seizure initiated drug delivery system for the treatment of epilepsy

Muller, R., Yue, Z., Ahmadi, S., Ng, W., Grosse, W., Cook, M. J., Wallace, G. G., & Moulton, S. E. (2016) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2016.06.038 · Cited by 18

The Emerging Role of Biomarkers in Adaptive Modulation of Clinical Brain Stimulation

Hoang, K. B., & Turner, D. A. (2019) · Neurosurgery · doi:10.1093/neuros/nyz096 · Cited by 18

Synaptic reorganization of synchronized neuronal networks with synaptic weight and structural plasticity

Chauhan, K., NEIMAN, A. B., & Tass, P. A. (2024) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1012261 · Cited by 18

Low-frequency stimulation of the external globus palladium produces anti-epileptogenic and anti-ictogenic actions in rats

Cheng, H., Kuang, Y., Liu, Y., Wang, Y., Xu, Z., Gao, F., Zhang, S., Ding, M., & Chen, Z. (2015) · Acta Pharmacologica Sinica · doi:10.1038/aps.2015.45 · Cited by 17

Brain (Hyper)Excitability Revealed by Optimal Electrical Stimulation of GABAergic Interneurons

Wendling, F., Gerber, U. R., Cosandier‐Rimélé, D., Nica, A., de Montigny, J., Raineteau, O., Kalitzin, S., Lopes, F. H. D. S., & Benquet, P. (2016) · Brain stimulation · doi:10.1016/j.brs.2016.07.001 · Cited by 20

Long-term outcome of unilateral deep brain stimulation of the subthalamic nucleus for a patient with drug-resistant focal myoclonic seizure

Wang, X., Du, J., Wang, D., Xu, C., Ren, Z., Wang, Y., Li, Y., Yu, T., & Ren, L. (2020) · Annals of Translational Medicine · doi:10.21037/atm.2019.12.43 · Cited by 16

The Appearance Order of Varying Intervals Introduces Extra Modulation Effects on Neuronal Firing Through Non-linear Dynamics of Sodium Channels During High-Frequency Stimulations

Zheng, L., Feng, Z., Hu, H., Wang, Z., Yuan, Y., & Wei, X. F. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00397 · Cited by 17

Evidence for spreading seizure as a cause of theta-alpha activity electrographic pattern in stereo-EEG seizure recordings

Ší́p, V., Makhalova, J., Guye, M., Bartoloméi, F., & Jirsa, V. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008731 · Cited by 17

Optimal Vagus Nerve Stimulation Frequency for Suppression of Spike‐and‐Wave Seizures in Rats

Jiao, J., Harreby, K. R., Sevcencu, C., & Jensen, W. (2015) · Artificial Organs · doi:10.1111/aor.12669 · Cited by 17

A bimodal closed-loop neuromodulation implant integrated with ultraflexible probes to treat epilepsy

Li, G. L., Tian, Y., Jiang, L., Jin, S., Ye, Y., Lu, Y., Su, H., Yang, Y., Wei, X., Zhou, Z., et al. (2024) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2024.117071 · Cited by 15

Ultrasound Active Piezoelectric Nanostimulators for Long‐Acting Wireless Deep Brain Electric Stimulation to Inhibit Epileptic Seizures

Tang, Q., Li, D., Chen, J., Liu, M., Yuan, Q., Jia, J., Song, M., Yu, L., Wang, X., Sang, Y., et al. (2025) · Advanced Materials · doi:10.1002/adma.202420447 · Cited by 18

Nongenetic Precise Neuromodulation and Spatiotemporal Neuroprotection for Epilepsy Therapy via Rationally Designed Multifunctional Nanotransducer

Ren, Q., Wu, H., Zhang, Y., Dai, J., Chang, Z., Nie, J., Wang, B., & Fang, Y. (2024) · ACS Nano · doi:10.1021/acsnano.4c02546 · Cited by 16

Electrical stimulation and monitoring devices of the CNS: An imaging review.

Patel, S. H., Halpern, C., Shepherd, T., & Timpone, V. M. (2017) · Journal of neuroradiology. Journal de neuroradiologie · doi:10.1016/j.neurad.2016.12.005 · Cited by 13

Interictal waking and sleep electrophysiological properties of the thalamus in focal epilepsies

Biagioni, T., Fratello, M., Garnier, E. M., Lagarde, S., Carron, R., Villalon, S. M., Lambert, I., Marchi, A., Makhalova, J., Trébuchon, A., et al. (2025) · Brain Communications · doi:10.1093/braincomms/fcaf102 · Cited by 16

Preventive and Abortive Strategies for Stimulation Based Control of Epilepsy: A Computational Model Study

Koppert, M. M. J., Kalitzin, S., Velis, D. N., Lopes, F. H. D. S., & Viergever, M. A. (2016) · International Journal of Neural Systems · doi:10.1142/s0129065716500283 · Cited by 15

Pharmaco‐genetic inhibition of pyramidal neurons retards hippocampal kindling‐induced epileptogenesis

Chen, L., Liang, J., Fei, F., Ruan, Y., Cheng, H., Wang, Y., Chen, Z., & Xu, C. (2020) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13434 · Cited by 16

Delta oscillation underlies the interictal spike changes after repeated transcranial direct current stimulation in a rat model of chronic seizures

Wu, Y., Chien, M.-E., Chiang, C., Huang, Y., Durand, D. M., & Hsu, K. (2021) · Brain stimulation · doi:10.1016/j.brs.2021.04.025 · Cited by 15

Music in epilepsy: Predicting the effects of the unpredictable

Rafiee, M., Istasy, M. V., & Valiante, T. A. (2021) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2021.108164 · Cited by 17

Remote modulation of network excitability during deep brain stimulation for epilepsy

Li, D., & Yang, X. (2017) · Seizure · doi:10.1016/j.seizure.2017.02.016 · Cited by 15

Locally stable brain states predict suppression of epileptic activity by enhanced cognitive effort

Muldoon, S. F., Costantini, J. G., Webber, W. R., Lesser, R. P., & Bassett, D. S. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.02.027 · Cited by 16

Clinically indicated electrical stimulation strategies to treat patients with medically refractory epilepsy

Izadi, A., Ondek, K., Schedlbauer, A. M., Keselman, I., Shahlaie, K., & Gurkoff, G. G. (2018) · Epilepsia Open · doi:10.1002/epi4.12276 · Cited by 15

Chronic recording of the vagus nerve to analyze modulations by the light–dark cycle

Smets, H., Stumpp, L. I., Cerda, J. C., Cury, J., Perre, L. V., Doguet, P., Vanhoestenberghe, A., Delbeke, J., Tahry, R. E., & Nonclercq, A. (2022) · Journal of Neural Engineering · doi:10.1088/1741-2552/ac7c8f · Cited by 14

The Effect of Spinal Cord Stimulation on Epileptic Seizures

Jiao, J., Jensen, W., Harreby, K. R., & Sevcencu, C. (2015) · Neuromodulation Technology at the Neural Interface · doi:10.1111/ner.12362 · Cited by 14

Perturbations both trigger and delay seizures due to generic properties of slow-fast relaxation oscillators

Pérez-Cervera, A., & Hlinka, J. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008521 · Cited by 14

Comparison of fiber tract low frequency stimulation to focal and ANT stimulation in an acute rat model of focal cortical seizures

Couturier, N. H., & Durand, D. M. (2019) · Brain stimulation · doi:10.1016/j.brs.2019.12.026 · Cited by 14

Amygdala Low-Frequency Stimulation Reduces Pathological Phase-Amplitude Coupling in the Pilocarpine Model of Epilepsy

Mihály, I., Orbán-Kis, K., Gáll, Z., Berki, Á. J., Bod, R.-B., & Szilágyi, T. (2020) · Brain Sciences · doi:10.3390/brainsci10110856 · Cited by 14

A subgaleal electrode array for neurostimulation allows the recording of relevant information in closed loop applications

Dümpelmann, M., Reinacher, P. C., Kravalis, K., Jagschies, L., Tittelbach, M., Coenen, V. A., & Schulze‐Bonhage, A. (2021) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2021.109295 · Cited by 13

The safety of Micro-implants for the brain

Dabbour, A.-H., Tan, S., Kim, S. H., Guild, S.-J., Heppner, P., McCormick, D., Wright, B. E., Leung, D., Gallichan, R., Budgett, D., et al. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.796203 · Cited by 13

The anterior nucleus of the thalamus plays a role in the epileptic network

Yan, H., Wang, X., Yu, T., Ni, D., Qiao, L., Zhang, X., Xu, C., Shu, W., Wang, Y., & Ren, L. (2022) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.51693 · Cited by 13

Hippocampal closed-loop modeling and implications for seizure stimulation design

Sandler, R., Song, D. B., Hampson, R. E., Deadwyler, S. A., Berger, T. W., & Marmarelis, V. Z. (2015) · Journal of Neural Engineering · doi:10.1088/1741-2560/12/5/056017 · Cited by 13

Direct Electrical Stimulation of the Human Brain Has Inverse Effects on the Theta and Gamma Neural Activities

Lech, M., Berry, B. M., Topçu, Ç., Křemen, V., Nejedlý, P., Lega, B. C., Gross, R. E., Sperling, M. R., Jobst, B. C., Sheth, S. A., et al. (2021) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2021.3082320 · Cited by 15

50 Hz hippocampal stimulation in refractory epilepsy: Higher level of basal glutamate predicts greater release of glutamate

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