Implantable microcoils for intracortical magnetic stimulation

Ultrasensitive fluorescent proteins for imaging neuronal activity

Chen, T.-W., Wardill, T. J., Sun, Y., Pulver, S. R., Renninger, S. L., Baohan, A., Schreiter, E. R., Kerr, R. A., Orger, M. B., Jayaraman, V., et al. (2013) · Nature · doi:10.1038/nature12354 · Cited by 6,474 · see citing works

Neurodegenerative Disorders: Parkinson's Disease and Huntington's Disease

Hague, S., Klaffke, S., & Bandmann, O. (2006) · IMPERIAL COLLEGE PRESS eBooks · doi:10.1142/9781860948961_0007 · Cited by 2,767 · see citing works

Neural Stimulation and Recording Electrodes

Cogan, S. F. (2008) · Annual Review of Biomedical Engineering · doi:10.1146/annurev.bioeng.10.061807.160518 · Cited by 2,243 · see citing works

Which elements are excited in electrical stimulation of mammalian central nervous system: A review

Ranck, J. B. (1975) · Brain Research · doi:10.1016/0006-8993(75)90364-9 · Cited by 2,024 · see citing works

Response of brain tissue to chronically implanted neural electrodes

Polikov, V. S., Tresco, P. A., & Reichert, W. M. (2005) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2005.08.015 · Cited by 1,896 · see citing works

Wireless magnetothermal deep brain stimulation

Chen, R., Romero, G., Christiansen, M. G., Mohr, A. C., & Anikeeva, P. (2015) · Science · doi:10.1126/science.1261821 · Cited by 690 · see citing works

Feasibility of a visual prosthesis for the blind based on intracortical micro stimulation of the visual cortex

Schmidt, E. M., Bak, M. J., Hambrecht, F. T., Kufta, C. V., O'Rourke, D. K., & Vallabhanath, P. (1996) · Brain · doi:10.1093/brain/119.2.507 · Cited by 672 · see citing works

Excitation of pyramidal tract cells by intracortical microstimulation: effective extent of stimulating current.

Stoney, S. D., Thompson, W., & Asanuma, H. (1968) · Journal of Neurophysiology · doi:10.1152/jn.1968.31.5.659 · Cited by 670 · see citing works

Multifunctional fibers for simultaneous optical, electrical and chemical interrogation of neural circuits in vivo

Canales, A., Jia, X., Froriep, U. P., Koppes, R. A., Tringides, C. M., Selvidge, J., Lu, C., Hou, C., Wei, L., Fink, Y., et al. (2015) · Nature Biotechnology · doi:10.1038/nbt.3093 · Cited by 668 · see citing works

Broadly tuned response properties of diverse inhibitory neuron subtypes in mouse visual cortex

Kerlin, A. M., Andermann, M. L., Berezovskii, V. K., & Reid, R. C. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.002 · Cited by 613 · see citing works

Direct activation of sparse, distributed populations of cortical neurons by electrical microstimulation

Histed, M. H., Bonin, V., & Reid, R. C. (2009) · Neuron · doi:10.1016/j.neuron.2009.07.016 · Cited by 604 · see citing works

The basic mechanism for the electrical stimulation of the nervous system

Rattay, F. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00330-3 · Cited by 572 · see citing works

Implanted Neural Interfaces: Biochallenges and Engineered Solutions

Grill, W. M., Norman, S. E., & Bellamkonda, R. V. (2009) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-061008-124927 · Cited by 488 · see citing works

Neural probe design for reduced tissue encapsulation in CNS

Seymour, J. P., & Kipke, D. R. (2007) · Biomaterials · doi:10.1016/j.biomaterials.2007.03.024 · Cited by 462 · see citing works

Selection of stimulus parameters for deep brain stimulation

Kuncel, A. M., & Grill, W. M. (2004) · Clinical Neurophysiology · doi:10.1016/j.clinph.2004.05.031 · Cited by 460 · see citing works

An optogenetic toolbox designed for primates

Diester, I., Kaufman, M. T., Mogri, M., Pashaie, R., Goo, W., Yizhar, O., Ramakrishnan, C., Deisseroth, K., & Shenoy, K. V. (2011) · Nature Neuroscience · doi:10.1038/nn.2749 · Cited by 443 · see citing works

Whisker movements evoked by stimulation of single pyramidal cells in rat motor cortex

Brecht, M., Schneider, M., Sakmann, B. J., & Margrie, T. W. (2004) · Nature · doi:10.1038/nature02266 · Cited by 429 · see citing works

Tissue damage thresholds during therapeutic electrical stimulation

Cogan, S. F., Ludwig, K. A., Welle, C. G., & Takmakov, P. (2016) · Journal of Neural Engineering · doi:10.1088/1741-2560/13/2/021001 · Cited by 386 · see citing works

Motor Control by Sensory Cortex

Mátyás, F., Sreenivasan, V., Marbach, F., Wacongne, C., Barsy, B., Matéo, C., Aronoff, R., & Petersen, C. (2010) · Science · doi:10.1126/science.1195797 · Cited by 377 · see citing works

Mechanisms and circuitry underlying directional selectivity in the retina

Fried, S. I., Münch, T. A., & Werblin, F. S. (2002) · Nature · doi:10.1038/nature01179 · Cited by 368 · see citing works

Restoring sensorimotor function through intracortical interfaces: progress and looming challenges

Bensmaia, S. J., & Miller, L. E. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3724 · Cited by 368 · see citing works

Photosensitivity of Neurons Enabled by Cell-Targeted Gold Nanoparticles

Carvalho-de-Souza, J. L., Treger, J. S., Dang, B., Kent, S. B. H., Pepperberg, D. R., & Bezanilla, F. (2015) · Neuron · doi:10.1016/j.neuron.2015.02.033 · Cited by 356 · see citing works

Direct and Indirect Activation of Cortical Neurons by Electrical Microstimulation

Tehovnik, E. J., Tolias, A. S., Sultan, F. R., Slocum, W. M., & Logothetis, N. K. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00126.2006 · Cited by 355 · see citing works

Magnetic coil stimulation of straight and bent amphibian and mammalian peripheral nerve in vitro: locus of excitation.

Maccabee, P. J., Amassian, V. E., Eberle, L., & Cracco, R. Q. (1993) · The Journal of Physiology · doi:10.1113/jphysiol.1993.sp019467 · Cited by 321 · see citing works

Dexamethasone-coated neural probes elicit attenuated inflammatory response and neuronal loss compared to uncoated neural probes

Zhong, Y., & Bellamkonda, R. V. (2007) · Brain Research · doi:10.1016/j.brainres.2007.02.024 · Cited by 321 · see citing works

Cell-attached voltage-clamp and current-clamp recording and stimulation techniques in brain slices

Perkins, K. L. (2006) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2006.02.010 · Cited by 312 · see citing works

Sensitivity of Neurons to Weak Electric Fields

Francis, J. T., Gluckman, B. J., & Schiff, S. J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-19-07255.2003 · Cited by 302 · see citing works

Direct and indirect activation of nerve cells by electrical pulses applied extracellularly.

Gustafsson, B., & Jankowska, E. (1976) · The Journal of Physiology · doi:10.1113/jphysiol.1976.sp011405 · Cited by 276 · see citing works

Modulation by applied electric fields of Purkinje and stellate cell activity in the isolated turtle cerebellum.

Chan, C., & Nicholson, C. (1986) · The Journal of Physiology · doi:10.1113/jphysiol.1986.sp015963 · Cited by 268 · see citing works

The impact of chronic blood–brain barrier breach on intracortical electrode function

Saxena, T. K., Karumbaiah, L., Gaupp, E. A., Patkar, R., Patil, K., Betancur, M. I., Stanley, G. B., & Bellamkonda, R. V. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.03.007 · Cited by 265 · see citing works

Cognitive Neural Prosthetics

Andersen, R. A., Hwang, E. J., & Mulliken, G. H. (2009) · Annual Review of Psychology · doi:10.1146/annurev.psych.093008.100503 · Cited by 238 · see citing works

A Method for Generating Precise Temporal Patterns of Retinal Spiking Using Prosthetic Stimulation

Fried, S. I., Hsueh, H.-A., & Werblin, F. S. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00849.2005 · Cited by 212 · see citing works

Axonal Sodium-Channel Bands Shape the Response to Electric Stimulation in Retinal Ganglion Cells

Fried, S. I., Lasker, A., Desai, N. J., Eddington, D. K., & Rizzo, J. F. (2009) · Journal of Neurophysiology · doi:10.1152/jn.91081.2008 · Cited by 206 · see citing works

Organization of rat vibrissa motor cortex and adjacent areas according to cytoarchitectonics, microstimulation, and intracellular stimulation of identified cells

Brecht, M., Krauß, A., Muhammad, S., Sinai‐Esfahani, L., Bellanca, S., & Margrie, T. W. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20306 · Cited by 180 · 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

Distribution of neurons in functional areas of the mouse cerebral cortex reveals quantitatively different cortical zones

Herculano‐Houzel, S., WATSON, C. R. R., & Paxinos, G. (2013) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2013.00035 · Cited by 159 · see citing works

Challenges and Opportunities for Next-Generation Intracortically Based Neural Prostheses

Gilja, V., Chestek, C. A., Diester, I., Henderson, J. M., Deisseroth, K. A., & Shenoy, K. V. (2011) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2011.2107553 · Cited by 157 · see citing works

Saccadic eye movements evoked by optogenetic activation of primate V1

Jazayeri, M., Lindbloom-Brown, Z., & Horwitz, G. D. (2012) · Nature Neuroscience · doi:10.1038/nn.3210 · Cited by 156 · see citing works

Improving the spatial resolution of epiretinal implants by increasing stimulus pulse duration

Weitz, A. C., Nanduri, D., Behrend, M. R., Gonzalez-Calle, A., Greenberg, R. J., Humayun, M. S., Chow, R. H., & Weiland, J. D. (2015) · Science Translational Medicine · doi:10.1126/scitranslmed.aac4877 · Cited by 154 · see citing works

Toward the development of a cortically based visual neuroprosthesis

Normann, R. A., Greger, B. A., House, P., Romero, S. F., Pelayo, F., & Fernandez, E. (2009) · Journal of Neural Engineering · doi:10.1088/1741-2560/6/3/035001 · Cited by 143 · see citing works

Neuronal loss due to prolonged controlled-current stimulation with chronically implanted microelectrodes in the cat cerebral cortex

McCreery, D. B., Pikov, V., & Troyk, P. R. (2010) · Journal of Neural Engineering · doi:10.1088/1741-2560/7/3/036005 · Cited by 137 · see citing works

Insights into cortical mechanisms of behavior from microstimulation experiments

Histed, M. H., Ni, A. M., & Maunsell, J. H. R. (2012) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.01.006 · Cited by 129 · 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

Resolution of the epiretinal prosthesis is not limited by electrode size

Behrend, M. R., Ahuja, A. K., Humayun, M. S., Chow, R. H., & Weiland, J. D. (2011) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2011.2140132 · Cited by 102 · 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

Spatial and temporal characteristics of V1 microstimulation during chronic implantation of a microelectrode array in a behaving macaque

Davis, T. S., Parker, R. A., House, P. A., Bagley, E. E., Wendelken, S., Normann, R. A., & Greger, B. E. (2012) · Journal of Neural Engineering · doi:10.1088/1741-2560/9/6/065003 · Cited by 91 · see citing works

Laminar Variation in Threshold for Detection of Electrical Excitation of Striate Cortex by Macaques

DeYoe, E. A., Lewine, J. D., & Doty, R. W. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00407.2005 · Cited by 85 · see citing works

Intrinsic dynamics and synaptic inputs control the activity patterns of subthalamic nucleus neurons in health and in Parkinson's disease

Wilson, C. J., & Bevan, M. D. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.06.049 · Cited by 75 · see citing works

Depth‐dependent detection of microampere currents delivered to monkey V1

Tehovnik, E. J., & Slocum, W. M. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06695.x · Cited by 54 · see citing works

Responses to pulsatile subretinal electric stimulation: effects of amplitude and duration

Lee, S. W., Eddington, D. K., & Fried, S. I. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00293.2012 · Cited by 47 · see citing works

Multimodal, longitudinal assessment of intracortical microstimulation

Koivuniemi, A. S., Wilks, S. J., Woolley, A. J., & Otto, K. J. (2011) · Progress in brain research · doi:10.1016/b978-0-444-53815-4.00011-x · Cited by 45 · see citing works

Autonomous initiation and propagation of action potentials in neurons of the subthalamic nucleus

Atherton, J. F., Wokosin, D. L., Ramanathan, S., & Bevan, M. D. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.155861 · Cited by 42 · see citing works

Electrical microstimulation thresholds for behavioral detection and saccades in monkey frontal eye fields

Murphey, D. K., & Maunsell, J. H. R. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0710820105 · Cited by 40 · see citing works

Mini-coil for magnetic stimulation in the behaving primate

Tischler, H., Wolfus, S., Friedman, A., Perel, E., Pashut, T., Michal Lavidor, B., Korngreen, A., Yeshurun, Y., & Bar‐Gad, I. (2010) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2010.10.015 · Cited by 39 · see citing works

The response of retinal neurons to high-frequency stimulation

Cai, C., Twyford, P., & Fried, S. (2013) · Journal of Neural Engineering · doi:10.1088/1741-2560/10/3/036009 · Cited by 38 · see citing works

Electrical induction of vision

Tehovnik, E. J., & Slocum, W. M. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.03.012 · Cited by 33 · see citing works

Suppression of Subthalamic Nucleus Activity by Micromagnetic Stimulation

Lee, S.-W., & Fried, S. (2014) · IEEE transactions on neural systems and rehabilitation engineering · doi:10.1109/tnsre.2014.2348415 · Cited by 31 · see citing works

Synergistic combination of near-infrared irradiation and targeted gold nanoheaters for enhanced photothermal neural stimulation

Eom, K., Im, C., Hwang, S., Eom, S., Kim, T.-S., Jeong, H. S., Kim, K. H., Byun, K. M., Jun, S. B., & Kim, S. J. (2016) · Biomedical Optics Express · doi:10.1364/boe.7.001614 · Cited by 29 · see citing works

The response of L5 pyramidal neurons of the PFC to magnetic stimulation from a micro-coil

Lee, S. W., & Fried, S. I. (2014) · doi:10.1109/embc.2014.6945027 · Cited by 19 · see citing works

Brain-Machine Interfaces: From Basic Science to Neuroprostheses and Neurorehabilitation

Lebedev, M., & Nicolelis, M. A. L. (2017) · Physiological Reviews · doi:10.1152/physrev.00027.2016 · Cited by 655 · 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

A model of ganglion axon pathways accounts for percepts elicited by retinal implants

Beyeler, M., Nanduri, D., Weiland, J. D., Rokem, A., Boynton, G. M., & Fine, I. (2019) · Scientific Reports · doi:10.1038/s41598-019-45416-4 · Cited by 143 · see citing works

Smart Contact Lenses as Wearable Ophthalmic Devices for Disease Monitoring and Health Management

Seo, H., Chung, W. G., Kwon, Y. W., Kim, S., Hong, Y., Park, W., Kim, E., Lee, J., Lee, S., Kim, M., et al. (2023) · Chemical Reviews · doi:10.1021/acs.chemrev.3c00290 · Cited by 152 · see citing works

The future of neuroscience: flexible and wireless implantable neural electronics

McGlynn, E., Nabaei, V., Ren, E., Galeote‐Checa, G., Das, R., Curia, G., & Heidari, H. (2021) · Advanced Science · doi:10.1002/advs.202002693 · Cited by 115 · see citing works

Development of visual Neuroprostheses: trends and challenges.

Fernandez, E. (2018) · Bioelectronic Medicine · doi:10.1186/s42234-018-0013-8 · Cited by 114 · see citing works

MEMS inductor fabrication and emerging applications in power electronics and neurotechnologies

Le, H. T., Haque, R. I., Ouyang, Z., Lee, S. W., Fried, S. I., Zhao, D., Qiu, M., & Han, A. (2021) · Microsystems & Nanoengineering · doi:10.1038/s41378-021-00275-w · Cited by 85 · see citing works

Magnetic Strategies for Nervous System Control

Christiansen, M. G., Senko, A. W., & Anikeeva, P. (2019) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070918-050241 · Cited by 76 · see citing works

Nanotechnology Enables Novel Modalities for Neuromodulation

Yang, X., McGlynn, E., Das, R., Pașca, S. P., Cui, B., & Heidari, H. (2021) · Advanced Materials · doi:10.1002/adma.202103208 · Cited by 76 · see citing works

Neuro‐Nano Interfaces: Utilizing Nano‐Coatings and Nanoparticles to Enable Next‐Generation Electrophysiological Recording, Neural Stimulation, and Biochemical Modulation

Young, A. T., Cornwell, N., & Daniele, M. A.-A. (2017) · Advanced Functional Materials · doi:10.1002/adfm.201700239 · Cited by 70 · see citing works

Challenges for Large-Scale Cortical Interfaces

Nurmikko, A. (2020) · Neuron · doi:10.1016/j.neuron.2020.10.015 · Cited by 68 · see citing works

Translational Neuroelectronics

Jastrzebska‐Perfect, P., Chowdhury, S., Spyropoulos, G. D., Zhao, Z., Cea, C., Gelinas, J. N., & Khodagholy, D. (2020) · Advanced Functional Materials · doi:10.1002/adfm.201909165 · Cited by 64 · see citing works

A software toolkit for TMS electric-field modeling with boundary element fast multipole method: an efficient MATLAB implementation

Makarov, S. N., Wartman, W. A., Daneshzand, M., Fujimoto, K., Raij, T., & Nummenmaa, A. R. (2020) · Journal of Neural Engineering · doi:10.1088/1741-2552/ab85b3 · Cited by 60 · see citing works

Emerging ultrasonic bioelectronics for personalized healthcare

Jiang, L., & Wu, J. (2023) · Progress in Materials Science · doi:10.1016/j.pmatsci.2023.101110 · Cited by 59 · see citing works

New Vision for Visual Prostheses

Farnum, A., & Pelled, G. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00036 · Cited by 58 · see citing works

Bidirectional brain-computer interfaces

Hughes, C. L., Herrera, A. J., Gaunt, R. A., & Collinger, J. L. (2020) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63934-9.00013-5 · Cited by 59 · see citing works

Recent progress on peripheral neural interface technology towards bioelectronic medicine

Cho, Y., Park, J., Lee, C., & Lee, S. (2020) · Bioelectronic Medicine · doi:10.1186/s42234-020-00059-z · Cited by 55 · see citing works

An Introductory Tutorial on Brain–Computer Interfaces and Their Applications

Bonci, A., Fiori, S., Higashi, H., Tanaka, T., & Verdini, F. (2021) · Electronics · doi:10.3390/electronics10050560 · Cited by 54 · see citing works

Thermal effects on neurons during stimulation of the brain

Kim, T., Kadji, H. G. E., Whalen, A. J., Ashourvan, A., Freeman, E. J., Fried, S. I., Tadigadapa, S. A., & Schiff, S. J. (2022) · Journal of Neural Engineering · doi:10.1088/1741-2552/ac9339 · Cited by 54 · see citing works

A self-powered brain multi-perception receptor for sensory-substitution application

Fu, Y., Zhang, M., Dai, Y., Zeng, H. J., Sun, C., Han, Y., Xing, L., Wang, S., Xue, X., Zhan, Y., et al. (2017) · Nano Energy · doi:10.1016/j.nanoen.2017.11.068 · Cited by 52 · see citing works

Toward advanced neural interfaces for the peripheral nervous system (PNS) and their future applications

Lee, S., & Lee, C. (2018) · Current Opinion in Biomedical Engineering · doi:10.1016/j.cobme.2018.05.004 · Cited by 48 · see citing works

Neuron matters: neuromodulation with electromagnetic stimulation must consider neurons as dynamic identities

Ye, H., Hendee, J., Ruan, J., Zhirova, A., Ye, J., & Dima, M. (2022) · Journal of NeuroEngineering and Rehabilitation · doi:10.1186/s12984-022-01094-4 · Cited by 46 · see citing works

Neurotechnological Approaches to the Diagnosis and Treatment of Alzheimer’s Disease

Ning, S., Jorfi, M., Patel, S. R., Kim, D. Y., & Tanzi, R. E. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.854992 · Cited by 41 · see citing works

Micromagnetic Stimulation of the Mouse Auditory Cortex In Vivo Using an Implantable Solenoid System

Minusa, S., Osanai, H., & Tateno, T. (2017) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2017.2748136 · Cited by 41 · see citing works

Toward Long-Term Communication With the Brain in the Blind by Intracortical Stimulation: Challenges and Future Prospects

Fernández, E., Alfaro, A., & González-López, P. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00681 · Cited by 35 · see citing works

Micro-Coil Design Influences the Spatial Extent of Responses to Intracortical Magnetic Stimulation

Lee, S. W., Thyagarajan, K., & Fried, S. I. (2018) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2018.2877713 · Cited by 37 · see citing works

Implantable Systems for Drug Delivery to the Brain

Kaurav, H., & Kapoor, D. N. (2017) · Therapeutic Delivery · doi:10.4155/tde-2017-0082 · Cited by 34 · see citing works

Retinal Prosthetic Approaches to Enhance Visual Perception for Blind Patients

Shim, S., Eom, K., Jeong, J., & Kim, S. J. (2020) · Micromachines · doi:10.3390/mi11050535 · Cited by 34 · see citing works

Neuromodulation with electromagnetic stimulation for seizure suppression: From electrode to magnetic coil

Ye, H., & Kaszuba, S. V. (2019) · IBRO Reports · doi:10.1016/j.ibror.2019.06.001 · Cited by 32 · see citing works

A self-powered brain-linked biosensing electronic-skin for actively tasting beverage and its potential application in artificial gustation

Zeng, H. J., He, H., Fu, Y., Zhao, T., Han, W., Xing, L., Zhang, Y., Zhan, Y., & Xue, X. (2018) · Nanoscale · doi:10.1039/c8nr06178e · Cited by 30 · see citing works

A multichannel magnetic stimulation system using submillimeter-sized coils: system development and experimental application to rodent brain in vivo

Minusa, S., Muramatsu, S., Osanai, H., & Tateno, T. (2019) · Journal of Neural Engineering · doi:10.1088/1741-2552/ab3187 · Cited by 30 · see citing works

Non-Invasive Brain Sensing Technologies for Modulation of Neurological Disorders

Alfihed, S., Majrashi, M. A., Ansary, M., Alshamrani, N., Albrahim, S. H., Alsolami, A., Alamari, H. A., Zaman, A., Almutairi, D., Kurdi, A., et al. (2024) · Biosensors · doi:10.3390/bios14070335 · Cited by 30 · see citing works

Preshaped 4D Photocurable Ultratough Organogel Microcoils for Personalized Endovascular Embolization

Wang, S., Qiu, M., Liu, J., Yin, T., Wu, C., Huang, C., Han, J., Cheng, S., Peng, Q., Li, Y., et al. (2023) · Advanced Materials · doi:10.1002/adma.202308130 · Cited by 25 · see citing works

Magnetic stimulation in the microscale: the development of a 6 × 6 array of micro-coils for stimulation of excitable cells in vitro

Rizou, M.-E., & Prodromakis, T. (2017) · Biomedical Physics & Engineering Express · doi:10.1088/2057-1976/aaa0dd · Cited by 24 · see citing works

The development of microfabricated solenoids with magnetic cores for micromagnetic neural stimulation

Khalifa, A., Zaeimbashi, M., Zhou, T. X., Abrishami, S. M. S., Sun, N., Park, S., Šumarac, T., Qu, J., Zohar, I., Yacoby, A., et al. (2021) · Microsystems & Nanoengineering · doi:10.1038/s41378-021-00320-8 · Cited by 23 · see citing works

Focal Suppression of Epileptiform Activity in the Hippocampus by a High-frequency Magnetic Field

Ye, H., Chen, V. C. ‐., Helon, J. W., & Apostolopoulos, N. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.02.018 · Cited by 22 · see citing works

Strength-frequency curve for micromagnetic neurostimulation through excitatory postsynaptic potentials (EPSPs) on rat hippocampal neurons and numerical modeling of magnetic microcoil ( μ coil)

Saha, R., Faramarzi, S., Bloom, R. P., Benally, O. J., Wu, K., di Girolamo, A., Tonini, D., Keirstead, S. A., Low, W. C., Netoff, T. I., et al. (2022) · Journal of Neural Engineering · doi:10.1088/1741-2552/ac4baf · Cited by 22 · see citing works

A review on magnetic and spintronic neurostimulation: challenges and prospects

Saha, R., Wu, K., Bloom, R. P., Liang, S. A., Tonini, D., & Wang, J. (2022) · Nanotechnology · doi:10.1088/1361-6528/ac49be · Cited by 20 · see citing works

Simulation-Based Optimization of Figure-of-Eight Coil Designs and Orientations for Magnetic Stimulation of Peripheral Nerve

Kosta, P., Mize, J. T., Warren, D. J., & Lazzi, G. (2020) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2020.3038406 · Cited by 21 · see citing works

Response of Mouse Visual Cortical Neurons to Electric Stimulation of the Retina

Ryu, S. B., Werginz, P., & Fried, S. I. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00324 · Cited by 20 · see citing works

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Dong, L., Li, G., Tian, C., Lin, L., Gao, Y., & Zheng, Y. (2021) · IEEE Transactions on Instrumentation and Measurement · doi:10.1109/tim.2021.3064805 · Cited by 19 · see citing works

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Zhou, Y., Ji, B., Wang, M., Zhang, K., Huangfu, S., Feng, H., Chang, H., & Yuan, X. (2021) · Coatings · doi:10.3390/coatings11020204 · Cited by 18 · see citing works

Somatic inhibition by microscopic magnetic stimulation

Ye, H., & Barrett, L. (2021) · Scientific Reports · doi:10.1038/s41598-021-93114-x · Cited by 17 · see citing works

Multiscale Modeling of Magnetoelectric Nanoparticles for the Analysis of Spatially Selective Neural Stimulation

Kumari, P., Wunderlich, H., Milojkovic, A., López, J. E., Fossati, A., Jahanshahi, A., & Kozielski, K. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202302871 · Cited by 17 · see citing works

Cellular mechanisms underlying carry-over effects after magnetic stimulation

Ye, H., Dima, M., Hall, V., & Hendee, J. (2024) · Scientific Reports · doi:10.1038/s41598-024-55915-8 · Cited by 17 · see citing works

Nanoparticle-based optical interfaces for retinal neuromodulation: a review

Stoddart, P. R., Begeng, J. M., Tong, W., Ibbotson, M. R., & Kameneva, T. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1360870 · Cited by 17 · see citing works

Spatially confined responses of mouse visual cortex to intracortical magnetic stimulation from micro-coils

Ryu, S. B., Paulk, A. C., Yang, J. C., Ganji, M., Dayeh, S. A., Cash, S. S., Fried, S. I., & Lee, S. W. (2020) · Journal of Neural Engineering · doi:10.1088/1741-2552/abbd22 · Cited by 18 · see citing works

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Grani, F., Soto-Sánchez, C., Fimia, A., & Fernández, E. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.1034270 · Cited by 16 · see citing works

Magnetic stimulation allows focal activation of the mouse cochlea

Lee, J.-I., Seist, R., McInturff, S., Lee, D. J., Brown, M. C., Stanković, K. M., & Fried, S. I. (2022) · eLife · doi:10.7554/elife.76682 · Cited by 15 · see citing works

MEMS micro-coils for magnetic neurostimulation

Liu, X., Whalen, A. J., Ryu, S. B., Lee, S. W., Fried, S. I., Kim, K., Cai, C., Lauritzen, M., Bertram, N., Chang, B., et al. (2023) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2023.115143 · Cited by 16 · see citing works

Implantable electrical stimulation bioreactor with liquid crystal polymer-based electrodes for enhanced bone regeneration at mandibular large defects in rabbit

Kim, C., Yang, H. J., Cho, T. H., Lee, B. S., Gwon, T. M., Shin, S., Kim, I. S., Kim, S. J., & Hwang, S. J. (2019) · Medical & Biological Engineering & Computing · doi:10.1007/s11517-019-02046-2 · Cited by 16 · see citing works

Neurophysiological considerations for visual implants

Meikle, S. J., & Wong, Y. T. (2022) · Brain Structure and Function · doi:10.1007/s00429-021-02417-2 · Cited by 15 · see citing works

Novel magnetic stimulation methodology for low-current implantable medical devices

Bernardo, R. M. C., Rodrigues, A., dos Santos, M. P. S., Carneiro, P. M. R., Lopes, A., Amaral, J. S., Amaral, V. S., & Morais, R. (2019) · Medical Engineering & Physics · doi:10.1016/j.medengphy.2019.07.015 · Cited by 15 · see citing works

Central nervous system microstimulation: Towards selective micro-neuromodulation

Urdaneta, M. E., Koivuniemi, A. S., & Otto, K. J. (2017) · Current Opinion in Biomedical Engineering · doi:10.1016/j.cobme.2017.09.012 · Cited by 16 · see citing works

Axonal blockage with microscopic magnetic stimulation

Skach, J., Conway, C. M., Barrett, L., & Ye, H. (2020) · Scientific Reports · doi:10.1038/s41598-020-74891-3 · Cited by 16 · see citing works

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Ge, C., Masalehdan, T., Baghini, M. S., Toro, V. D., Signorelli, L., Thomson, H. M., Gregureć, D., & Heidari, H. (2024) · Advanced Science · doi:10.1002/advs.202404254 · Cited by 14 · see citing works

Visual cortical prosthesis: an electrical perspective

Pio‐Lopez, L., Poulkouras, R., & Depannemaecker, D. (2021) · Journal of Medical Engineering & Technology · doi:10.1080/03091902.2021.1907468 · Cited by 14 · see citing works

Reduced Heat Generation During Magnetic Stimulation of Rat Sciatic Nerve Using Current Waveform Truncation

KAGAN, Z. B., Mize, J. T., Kosta, P., Lazzi, G., Normann, R. A., & Warren, D. J. (2019) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2019.2911054 · Cited by 14 · see citing works

A model of ganglion axon pathways accounts for percepts elicited by retinal implants

Beyeler, M., Nanduri, D., Weiland, J. D., Rokem, A., Boynton, G. M., & Fine, I. (2018) · doi:10.1101/453035 · Cited by 13 · see citing works

Cellular mechanisms underlying state-dependent neural inhibition with magnetic stimulation

Ye, H., Chen, V., & Hendee, J. (2022) · Scientific Reports · doi:10.1038/s41598-022-16494-8 · Cited by 13 · see citing works

The impact of synchronous versus asynchronous electrical stimulation in artificial vision

Moleirinho, S., Whalen, A. J., Fried, S. I., & Pezaris, J. S. (2021) · Journal of Neural Engineering · doi:10.1088/1741-2552/abecf1 · Cited by 14 · see citing works

Magneto‐Optogenetic Deep‐Brain Multimodal Neurostimulation

Walton, F., McGlynn, E., Das, R., Zhong, H., Heidari, H., & Degenaar, P. A. (2021) · Advanced Intelligent Systems · doi:10.1002/aisy.202100082 · Cited by 13 · see citing works

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Jeong, H., Cho, A., Ay, İ., & Bonmassar, G. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.938101 · Cited by 12 · see citing works

Planar coil-based contact-mode magnetic stimulation: synaptic responses in hippocampal slices and thermal considerations

Park, H.-J., Kang, H., Jo, J., Chung, E., & Kim, S. (2018) · Scientific Reports · doi:10.1038/s41598-018-31536-w · Cited by 10 · see citing works

Tunable magnetic skyrmions in spintronic nanostructures for cellular-level magnetic neurostimulation

Saha, R., Wu, K., Su, D., & Wang, J.-P. (2019) · Journal of Physics D Applied Physics · doi:10.1088/1361-6463/ab39a7 · Cited by 12 · see citing works

Ethics of Biohybrid Robotic Jellyfish Modification and Invertebrate ResearchPreprint

Xu, N. W., Lenczewska, O., Wieten, S., Federico, C., & Dabiri, J. (2020) · Preprints.org · doi:10.20944/preprints202010.0008.v1 · Cited by 16 · see citing works

Neural reflex control of vascular inflammation

Caravaca, A. S., Centa, M., Gallina, A. L., Tarnawski, L., & Olofsson, P. S. (2020) · Bioelectronic Medicine · doi:10.1186/s42234-020-0038-7 · Cited by 10 · see citing works

Development and Characterization of a Micromagnetic Alternative to Cochlear Implant Electrode Arrays

Sarreal, R. R. S., Blake, D. T., & Bhatti, P. T. (2022) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2022.3193342 · Cited by 10 · see citing works

Numerical Analysis of Microcoil‐Induced Electric Fields and Evaluation of In vivo Magnetic Stimulation of the Mouse Brain

Sugai, S., Higuchi, H., Nishikawa, J., Satoh, K., Murakami, S., & Tateno, T. (2020) · IEEJ Transactions on Electrical and Electronic Engineering · doi:10.1002/tee.23237 · Cited by 10 · see citing works

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Whalen, A. J., & Fried, S. I. (2023) · Journal of Neural Engineering · doi:10.1088/1741-2552/ace79a · Cited by 9 · see citing works

Multiphysics simulation of magnetoelectric micro core-shells for wireless cellular stimulation therapy via magnetic temporal interference

Narayanan, R., Khaleghi, A., Veletić, M., & Balasingham, I. (2024) · PLoS ONE · doi:10.1371/journal.pone.0297114 · Cited by 8 · see citing works

Ethics of biohybrid robotics and invertebrate research: biohybrid robotic jellyfish as a case study

Xu, N. W., Lenczewska, O., Wieten, S., Federico, C. A., & Dabiri, J. O. (2025) · Bioinspiration & Biomimetics · doi:10.1088/1748-3190/adc0d4 · Cited by 10 · see citing works

Micro‐Coil Neuromodulation at Single‐Cell and Circuit Levels for Inhibiting Natural Neuroactivity, Neutralizing Electric Neural Excitation, and Suppressing Seizures

Kim, K., Liu, X., Chang, B., Li, G., Anand, G. A. E., Genelioglu, S., Yonza, A. K. I., Whalen, A. J., Berg, R. W., Fried, S. I., et al. (2025) · Advanced Science · doi:10.1002/advs.202416771 · Cited by 9 · see citing works

Planar figure-8 coils for ultra-focal and directional micromagnetic brain stimulation

Jeong, H., Deng, J., & Bonmassar, G. (2021) · Journal of Vacuum Science & Technology B Nanotechnology and Microelectronics Materials Processing Measurement and Phenomena · doi:10.1116/6.0001281 · Cited by 9 · see citing works

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Koucheryavy, Y., Yastrebova, A., Martins, D. P., & Balasubramaniam, S. (2021) · arXiv.org · doi:10.48550/arxiv.2104.14944 · Cited by 9 · see citing works

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Tian, L., Song, L., Zheng, Y., Wang, J., & Chen, H. (2020) · IEEE Transactions on Magnetics · doi:10.1109/tmag.2020.2996955 · Cited by 8 · see citing works

Durable conducting polymer electrodes pursue low impedance, antifouling, and electrochemical stress tolerance

Bian, Y., Pan, Q., Zhu, Y., Liang, J., Zhang, Y., Zhang, Y., Zhang, S., Qian, S., Geng, Z. H., You, Z., et al. (2023) · Applied Surface Science · doi:10.1016/j.apsusc.2023.156902 · Cited by 8 · see citing works

Micromagnetic stimulation (µMS) dose-response of the rat sciatic nerve

Saha, R., Sanger, Z. T., Bloom, R. P., Benally, O. J., Wu, K., Tonini, D., Low, W. C., Keirstead, S. A., Netoff, T. I., & Wang, J. (2023) · Journal of Neural Engineering · doi:10.1088/1741-2552/acd582 · Cited by 8 · see citing works

Design and Optimization of Resonance-Based Wireless Power Transmission for Millimeter-Sized Planar Square Inductors Micro-Magnetic Stimulation

Tian, L., Liu, Q., Song, L., Jin, Z., Dong, L., & Zheng, Y. (2023) · IEEE Transactions on Instrumentation and Measurement · doi:10.1109/tim.2023.3292965 · Cited by 8 · see citing works

Toward Wireless Implantable Robotic Systems Driven by Magnetic Field for Personalized Therapy

Wang, Y., Ge, R., & Dong, X. (2025) · Advanced Robotics Research · doi:10.1002/adrr.202500077 · Cited by 7 · see citing works

Micro-magnetic stimulation of primary visual cortex induces focal and sustained activation of secondary visual cortex

Lee, S. W., & Fried, S. I. (2022) · Philosophical Transactions of the Royal Society A Mathematical Physical and Engineering Sciences · doi:10.1098/rsta.2021.0019 · Cited by 7 · see citing works

Finding the Location of Axonal Activation by a Miniature Magnetic Coil

Ye, H. (2022) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2022.932615 · Cited by 7 · see citing works

Improving focality and consistency in micromagnetic stimulation

Ye, H., Hall, V., & Hendee, J. (2023) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2023.1105505 · Cited by 7 · see citing works

Modelling, Linearity Analysis and Optimization of an Inductive Angular Displacement Sensor Based on Magnetic Focusing in Ships

Li, Z., Wang, B., Wang, X., Zhang, C., & Meng, X. (2023) · Journal of Marine Science and Engineering · doi:10.3390/jmse11051028 · Cited by 7 · see citing works

CMOS body dust — Towards drinkable diagnostics

Snoeijs, J., Georgiou, P., & Carrara, S. (2017) · IEEE Biomedical Circuits and Systems Conference (BioCAS) · doi:10.1109/biocas.2017.8325215 · Cited by 7 · see citing works

Micro-solenoid inductors with magnetic core for neural stimulation

Zaeimbashi, M., Wang, Z., Lee, S. W., Cash, S. S., Fried, S. I., & Sun, N. X. (2018) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc.2018.8512729 · Cited by 7 · see citing works

Tunable magnetic domain walls for therapeutic neuromodulation at cellular level: Stimulating neurons through magnetic domain walls

Su, D., Wu, K., Saha, R., & Wang, J.-P. (2019) · Journal of Applied Physics · doi:10.1063/1.5122753 · Cited by 7 · see citing works

Microelectrothermoforming (μETF): one-step versatile 3D shaping of flexible microelectronics for enhanced neural interfaces

Lee, D. H., Park, Y., Seo, Y., Noh, H., Jeong, H., Seo, J.-M., Seo, M., Eom, K., & Jeong, J. (2025) · npj Flexible Electronics · doi:10.1038/s41528-024-00378-0 · Cited by 6 · see citing works

MICROSIZE ENERGY SOURCES FOR IMPLANTABLE AND WEARABLE MEDICAL DEVICES

Plekhanova, Y. V., Tarasov, S. E., Somov, A., Bolshin, D. S., Vishnevskaya, M. V., Gotovtsev, P. M., & Reshetilov, A. N. (2019) · Nanotechnologies in Russia · doi:10.1134/s1995078019060144 · Cited by 6 · see citing works

A 4 × 4 array multichannel magnetic stimulation system using submillimeter sized planar square spiral coils: The spatial distribution of electromagnetic field

Tian, L., Song, L., Zheng, Y., & Wang, J. (2022) · International Journal of Applied Electromagnetics and Mechanics · doi:10.3233/jae-210139 · Cited by 6 · see citing works

Selective Activation of Cortical Columns Using Multichannel Magnetic Stimulation With a Bent Flat Microwire Array

Lee, S. W. (2020) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2020.3033491 · Cited by 6 · see citing works

Magnetic Temporal Interference For Noninvasive, High-resolution, and Localized Deep Brain Stimulation: Concept ValidationPreprint

Zaeimbashi, M., Khalifa, A., Dong, C., Wei, Y., Cash, S. S., & Sun, N. X. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.20.212845 · Cited by 6 · see citing works

From individual modalities to multi-physical synergy: Implantable electronic, photonic, magnetic platforms for the treatment of internal organ diseases

Tong, Y., Zhao, Z., Zhai, P., Zeng, Y., Wu, H., Shi, J., Wang, F., Wang, L., Zhong, X., Mu, W., et al. (2025) · Applied Physics Reviews · doi:10.1063/5.0233580 · Cited by 5 · see citing works

Fabrication of a Miniature Figure-of-Eight Coil for Micromagnetic Stimulation on Neuronal Tissue

(2021) · URSI Radio Science Letters · doi:10.46620/21-0008 · Cited by 5 · see citing works

Planar microcoil arrays for in vitro cellular-level micromagnetic activation of neurons

Saha, R., Benally, O. J., Faramarzi, S., Bloom, R. P., Wu, K., Tonini, D., Shiao, M. L., Keirstead, S. A., Low, W. C., Netoff, T. I., et al. (2024) · Journal of Vacuum Science & Technology B Nanotechnology and Microelectronics Materials Processing Measurement and Phenomena · doi:10.1116/6.0003362 · Cited by 5 · see citing works

Micro-coil probes for magnetic intracortical neural stimulation: Trade-offs in materials and design

Thyagarajan, K., Lujan, R. A., Wang, Q., Lu, J., Kor, S., Kakimoto, B., Chang, N., & Bert, J. A. (2021) · APL Materials · doi:10.1063/5.0023486 · Cited by 5 · see citing works

Impact of anesthesia on micromagnetic stimulation (μMS) of the vagus nerve

Saha, R., Helden, D. A. V., Hopper, M. S., Low, W. C., Netoff, T. I., Osborn, J. W., & Wang, J. (2024) · Biomedical Physics & Engineering Express · doi:10.1088/2057-1976/ad3968 · Cited by 4 · see citing works

Epidural magnetic stimulation of the motor cortex using an implantable coil

Lee, K. J., Jang, J., Kim, J. S., & Kim, S. (2024) · Brain stimulation · doi:10.1016/j.brs.2024.10.001 · Cited by 4 · see citing works

A pilot study of planar coil based magnetic stimulation using acute hippocampal slice in mice

Park, H. J., Kang, H. K., Wang, M., Jo, J., Chung, E., & Kim, S. (2017) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc.2017.8037025 · Cited by 4 · see citing works

Magnetic Stimulation of Dissociated Cortical Neurons on a Planar Mulitelectrode Array

Mukesh, S., Zeller-Townson, R., Butera, R. J., & Bhatti, P. T. (2019) · International IEEE/EMBS Conference on Neural Engineering · doi:10.1109/ner.2019.8717125 · Cited by 4 · see citing works

Towards a micro-coil based cortical visual prosthesis

Fried, S. I., & Lee, S. W. (2017) · German Medical Science (German Research Foundation) · doi:10.3205/17artvis37

Spatially confined responses of mouse visual cortex to intracortical magnetic stimulation from micro-coils

Ryu, S. B., Paulk, A. C., Yang, J. C., Ganji, M., Dayeh, S. A., Cash, S. S., Fried, S. I., & Lee, S. W. (2020) · Journal of Neural Engineering · doi:10.1088/1741-2552/abbd22 · Cited by 18 · see citing works

Abstract #39: Towards a microcoil-based cortical visual prosthesis

Fried, S. I., & Lee, S. W. (2019) · Brain stimulation · doi:10.1016/j.brs.2018.12.046 · Cited by 2 · see citing works

Micro-Coil Design Influences the Spatial Extent of Responses to Intracortical Magnetic Stimulation

Lee, S. W., Thyagarajan, K., & Fried, S. I. (2018) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2018.2877713 · Cited by 37 · see citing works

Enhanced Control of Cortical Pyramidal Neurons With Micromagnetic Stimulation

Lee, S. W., & Fried, S. I. (2016) · IEEE Transactions on Neural Systems and Rehabilitation Engineering · doi:10.1109/tnsre.2016.2631446 · Cited by 60 · see citing works