Ephaptic coupling to endogenous electric field activity: Why bother?

The dielectric properties of biological tissues: II. Measurements in the frequency range 10 Hz to 20 GHz.

Gabriel, S., Lau, R.-W.-M., & Gabriel, C. (1996) · Physics in Medicine and Biology · doi:10.1088/0031-9155/41/11/002 · Cited by 4,487 · see citing works

The origin of extracellular fields and currents — EEG, ECoG, LFP and spikes

Buzsáki, G., Anastassiou, C. A., & Koch, C. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3241 · Cited by 4,225 · see citing works

EPILEPSY AND THE FUNCTIONAL ANATOMY OF THE HUMAN BRAIN

Penfield, W., & Jasper, H. (1954) · Southern Medical Journal · doi:10.1097/00007611-195407000-00024 · Cited by 4,092 · see citing works

Deep Brain Stimulation for Treatment-Resistant Depression

Mayberg, H. S., Lozano, A. M., Voon, V., McNeely, H. E., Seminowicz, D., Hamani, C., Schwalb, J. M., & Kennedy, S. H. (2005) · Neuron · doi:10.1016/j.neuron.2005.02.014 · Cited by 4,059 · see citing works

Regulation of Synaptic Efficacy by Coincidence of Postsynaptic APs and EPSPs

Markram, H., Lübke, J., Frotscher, M., & Sakmann, B. (1997) · Science · doi:10.1126/science.275.5297.213 · Cited by 3,832 · see citing works

Biophysics of Computation

Koch, C. (1998) · Oxford University Press eBooks · doi:10.1093/oso/9780195104912.001.0001 · Cited by 2,306 · see citing works

Boosting slow oscillations during sleep potentiates memory

Marshall, L., Helgadóttir, H., Mölle, M., & Born, J. (2006) · Nature · doi:10.1038/nature05278 · Cited by 1,792 · see citing works

Optical Deconstruction of Parkinsonian Neural Circuitry

Gradinaru, V., Mogri, M., Thompson, K. R., Henderson, J. M., & Deisseroth, K. A. (2009) · Science · doi:10.1126/science.1167093 · Cited by 1,536 · see citing works

Transcranial magnetic stimulation in neurology

Kobayashi, M., & Pascual‐Leone, Á. (2003) · The Lancet Neurology · doi:10.1016/s1474-4422(03)00321-1 · Cited by 1,299 · see citing works

Neural syntax: cell assemblies, synapsembles, and readers

Buzsáki, G. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.023 · Cited by 1,289 · see citing works

Sharp wave-associated high-frequency oscillation (200 Hz) in the intact hippocampus: network and intracellular mechanisms

Ylinen, A., Bragin, A., Nadasdy, Z., Jando, G., Szabo, I., Sik, A., & Buzsaki, G. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00030.1995 · Cited by 1,092 · see citing works

Subcallosal cingulate gyrus deep brain stimulation for treatment-resistant depression

Lozano, A. M., Mayberg, H. S., Giacobbe, P., Hamani, C., Craddock, R. C., & Kennedy, S. H. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.05.034 · Cited by 1,024 · see citing works

Biophysics of computation: information processing in single neurons

(1999) · Choice Reviews Online · doi:10.5860/choice.36-5662 · Cited by 999 · see citing works

Intracellular Features Predicted by Extracellular Recordings in the Hippocampus In Vivo

Henze, D. A., Borhegyi, Z., Csicsvari, J., Mamiya, A., Harris, K. D., & Buzsáki, G. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.1.390 · Cited by 942 · see citing works

Endogenous electric fields may guide neocortical network activity

Fröhlich, F., & McCormick, D. A. (2010) · Neuron · doi:10.1016/j.neuron.2010.06.005 · Cited by 913 · see citing works

Epilepsy and the functional anatomy of the human brain

Gastaut, H. (1954) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(54)90103-0 · Cited by 781 · see citing works

Effects of uniform extracellular DC electric fields on excitability in rat hippocampal slices in vitro

Bikson, M., Inoue, M., Akiyama, H., Deans, J. K., Fox, J. E., Miyakawa, H., & Jefferys, J. G. R. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2003.055772 · Cited by 744 · see citing works

Gamma-band synchronization in visual cortex predicts speed of change detection

Womelsdorf, T., Fries, P., Mitra, P. P., & Desimone, R. (2005) · Nature · doi:10.1038/nature04258 · Cited by 741 · see citing works

Role of cortical cell type and morphology in subthreshold and suprathreshold uniform electric field stimulation in vitro

Radman, T., Ramos, R. L., Brumberg, J. C., & Bikson, M. (2009) · Brain stimulation · doi:10.1016/j.brs.2009.03.007 · Cited by 704 · see citing works

Nonsynaptic modulation of neuronal activity in the brain: electric currents and extracellular ions

Jefferys, J. G. R. (1995) · Physiological Reviews · doi:10.1152/physrev.1995.75.4.689 · Cited by 686 · see citing works

Boosting Cortical Activity at Beta-Band Frequencies Slows Movement in Humans

Pogosyan, A. H., Gaynor, L. D., Eusébio, A., & Brown, P. (2009) · Current Biology · doi:10.1016/j.cub.2009.07.074 · Cited by 644 · see citing works

Ephaptic coupling of cortical neurons

Anastassiou, C. A., Perin, R., Markram, H., & Koch, C. (2011) · Nature Neuroscience · doi:10.1038/nn.2727 · Cited by 628 · 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

On the Origin of the Extracellular Action Potential Waveform: A Modeling Study

Gold, C., Henze, D. A., Christof Koch, A., & Buzsáki, G. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00979.2005 · Cited by 587 · see citing works

Low-Intensity Electrical Stimulation Affects Network Dynamics by Modulating Population Rate and Spike Timing

Reato, D., Rahman, A., Bikson, M., & Parra, L. C. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2059-10.2010 · Cited by 576 · see citing works

Cellular effects of acute direct current stimulation: somatic and synaptic terminal effects

Rahman, A., Reato, D., Arlotti, M., Gasca, F., Datta, A., Parra, L. C., & Bikson, M. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.247171 · Cited by 560 · see citing works

Synchronization of oscillatory responses in visual cortex correlates with perception in interocular rivalry

Fries, P., Roelfsema, P. R., Engel, A. K., Peter König, B., & Singer, W. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.23.12699 · Cited by 505 · see citing works

Long-term potentiation in the dentate gyrus is induced preferentially on the positive phase of θ-rhythm

Pavlides, C., Greenstein, Y. J., Grudman, M., & Winson, J. (1988) · Brain Research · doi:10.1016/0006-8993(88)91499-0 · Cited by 485 · see citing works

In Vivo Measurement of Cortical Impedance Spectrum in Monkeys: Implications for Signal Propagation

Logothetis, N. K., Kayser, C., & Oeltermann, A. (2007) · Neuron · doi:10.1016/j.neuron.2007.07.027 · Cited by 447 · see citing works

Synchronized bursting of CA1 hippocampal pyramidal cells in the absence of synaptic transmission

Jefferys, J. G. R., & Haas, H. L. (1982) · Nature · doi:10.1038/300448a0 · Cited by 436 · see citing works

Transcranial Electric Stimulation Entrains Cortical Neuronal Populations in Rats

Irmak, S. O., Sirota, A., Belluscio, M., Anastassiou, C. A., Stark, E., Christof Koch, A., & Buzsáki, G. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5252-09.2010 · Cited by 414 · see citing works

Stimulation on the Positive Phase of Hippocampal Theta Rhythm Induces Long-Term Potentiation That Can Be Depotentiated by Stimulation on the Negative Phase in Area CA1<i>In Vivo</i>

Hölscher, C., Anwyl, R., & Rowan, M. J. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-16-06470.1997 · Cited by 411 · see citing works

Effects of weak transcranial alternating current stimulation on brain activity—a review of known mechanisms from animal studies

Reato, D., Rahman, A., Bikson, M., & Parra, L. C. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00687 · Cited by 363 · see citing works

Electrical Interactions via the Extracellular Potential Near Cell Bodies

Holt, G. R., & Koch, C. (1999) · Journal of Computational Neuroscience · doi:10.1023/a:1008832702585 · Cited by 360 · see citing works

Hemichannel-Mediated Inhibition in the Outer Retina

Kamermans, M., Fahrenfort, I., Schultz, K., Janssen‐Bienhold, U., Sjoerdsma, T., & Weiler, R. (2001) · Science · doi:10.1126/science.1060101 · Cited by 359 · 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

EFFECTS EVOKED IN AN AXON BY THE ACTIVITY OF A CONTIGUOUS ONE

Arvanitaki, A. (1942) · Journal of Neurophysiology · doi:10.1152/jn.1942.5.2.89 · Cited by 331 · see citing works

Long-Term Enhancement of Brain Function and Cognition Using Cognitive Training and Brain Stimulation

Snowball, A., Tachtsidis, I., Popescu, T., Thompson, J., Delazer, M., Zamarian, L., Zhu, T., & Kadosh, R. C. (2013) · Current Biology · doi:10.1016/j.cub.2013.04.045 · Cited by 323 · see citing works

Modeling Extracellular Field Potentials and the Frequency-Filtering Properties of Extracellular Space

Bédard, C., Kröger, H., & Alain Destexhe, A. (2004) · Biophysical Journal · doi:10.1016/s0006-3495(04)74250-2 · Cited by 301 · see citing works

Sensitivity of coherent oscillations in rat hippocampus to AC electric fields

Deans, J. K., Powell, A. D., & Jefferys, J. G. R. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.137711 · Cited by 294 · see citing works

Spike Timing Amplifies the Effect of Electric Fields on Neurons: Implications for Endogenous Field Effects

Radman, T., Su, Y., An, J. H., Parra, L. C., & Bikson, M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0095-07.2007 · Cited by 293 · see citing works

A Biophysically Detailed Model of Neocortical Local Field Potentials Predicts the Critical Role of Active Membrane Currents

Reimann, M., Anastassiou, C. A., Perin, R., Hill, S., Markram, H., & Koch, C. (2013) · Neuron · doi:10.1016/j.neuron.2013.05.023 · Cited by 270 · see citing works

Effects of stimulation of the subthalamic area on oscillatory pallidal activity in Parkinson's disease

Brown, P., Mazzone, P. A. M., Oliviero, A., Altibrandi, M. G., Pilato, F., Tonali, P. A., & Lazzaro, V. D. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.05.009 · Cited by 269 · 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

Specific impedance of rabbit cerebral cortex

Ranck, J. B. (1963) · Experimental Neurology · doi:10.1016/s0014-4886(63)80005-9 · Cited by 256 · see citing works

Modeling extracellular field potentials and the frequency-filtering properties of extracellular space

Bédard, C., Kröger, H., Alain Destexhe, A., & Alain Destexhe, A. (2004) · Cited by 249 · see citing works

Electrical stimulation of the human brain: perceptual and behavioral phenomena reported in the old and new literature

Selimbeyoglu, A. (2010) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2010.00046 · Cited by 239 · see citing works

Surge of neurophysiological coherence and connectivity in the dying brain

Borjigin, J., Lee, U., Liu, T., Pal, D., Huff, S., Klarr, D., Sloboda, J., Hernandez, J., Wang, M. M., & Mashour, G. A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1308285110 · Cited by 219 · see citing works

The Effect of Spatially Inhomogeneous Extracellular Electric Fields on Neurons

Anastassiou, C. A., Montgomery, S. M., Barahona, M., Buzsáki, G., & Koch, C. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3635-09.2010 · Cited by 217 · see citing works

Modulation of LTP at rat hippocampal CA3-CA1 synapses by direct current stimulation

Ranieri, F., Podda, M. V., Riccardi, E., Frisullo, G., Dileone, M., Profice, P., Pilato, F., Lazzaro, V. D., & Grassi, C. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00319.2011 · Cited by 208 · see citing works

Effects of electric fields on transmembrane potential and excitability of turtle cerebellar Purkinje cells in vitro.

Chan, C., Hounsgaard, J., & Nicholson, C. (1988) · The Journal of Physiology · doi:10.1113/jphysiol.1988.sp017232 · Cited by 177 · see citing works

Electrical field effects: their relevance in central neural networks

Faber, D. S., & Korn, H. (1989) · Physiological Reviews · doi:10.1152/physrev.1989.69.3.821 · Cited by 144 · see citing works

Subthreshold voltage noise of rat neocortical pyramidal neurones

Jacobson, G. A., Diba, K., Yaron‐Jakoubovitch, A., Oz, Y., Christof Koch, A., Segev, I., & Yarom, Y. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2004.080903 · Cited by 140 · see citing works

Ultra-rapid axon-axon ephaptic inhibition of cerebellar Purkinje cells by the pinceau

Blot, A., & Barbour, B. (2014) · Nature Neuroscience · doi:10.1038/nn.3624 · Cited by 131 · see citing works

Electrical inhibition of Purkinje cells in the cerebellum of the rat.

Korn, H., & Axelrad, H. (1980) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.77.10.6244 · Cited by 124 · see citing works

Analysis of specific impedance of rabbit cerebral cortex

Ranck, J. B. (1963) · Experimental Neurology · doi:10.1016/s0014-4886(63)80006-0 · Cited by 117 · see citing works

Computer simulations indicate that electrical field effects contribute to the shape of the epileptiform field potential

Traub, R. D., Dudek, F. E., Snow, R. W., et al. (1985) · Neuroscience · doi:10.1016/0306-4522(85)90245-3 · Cited by 96 · see citing works

A Model of the Effects of Applied Electric Fields on Neuronal Synchronization

Park, E.-H., Barreto, E., Gluckman, B. J., Schiff, S. J., & So, P. (2005) · Journal of Computational Neuroscience · doi:10.1007/s10827-005-0214-5 · Cited by 95 · see citing works

Field effects in the CNS play functional roles

Weiss, S. A. (2010) · Frontiers in Neural Circuits · doi:10.3389/fncir.2010.00015 · Cited by 94 · see citing works

Simulation of hippocampal afterdischarges synchronized by electrical interactions

Traub, R. D., Dudek, F. E., Taylor, C. P., & Knowles, W. D. (1985) · Neuroscience · doi:10.1016/0306-4522(85)90274-x · Cited by 87 · see citing works

Evidence for frequency-dependent extracellular impedance from the transfer function between extracellular and intracellular potentials

Bédard, C., Rodrigues, S., Roy, N. C., Contreras, D., & Alain Destexhe, A. (2010) · Journal of Computational Neuroscience · doi:10.1007/s10827-010-0250-7 · Cited by 62 · see citing works

Modulation of hippocampal rhythms by subthreshold electric fields and network topology

Berzhanskaya, J., Chernyy, N., Gluckman, B. J., Schiff, S. J., & Ascoli, G. A. (2012) · Journal of Computational Neuroscience · doi:10.1007/s10827-012-0426-4 · Cited by 53 · see citing works

Single-Shot Channel Activation Accounts for Duration of Inhibitory Postsynaptic Potentials in a Central Neuron

Faber, D. S., & Korn, H. (1980) · Science · doi:10.1126/science.6245449 · Cited by 50 · see citing works

Deep brain stimulation for parkinsonian gait disorders

Lozano, A. M., & Snyder, B. (2008) · Journal of Neurology · doi:10.1007/s00415-008-4005-6 · Cited by 47 · see citing works

Chronometric readout from a memory trace: Gamma-frequency field stimulation recruits timed recurrent activity in the rat CA3 network

Fujisawa, S., Matsuki, N., & Ikegaya, Y. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.066639 · Cited by 36 · see citing works

Postsynaptic hyperpolarization increases the strength of AMPA-mediated synaptic transmission at large synapses between mossy fibers and CA3 pyramidal cells

Berretta, N., Rossokhin, A. V., Kasyanov, A. M., Sokolov, M., Cherubini, E., & Voronin, L. L. (2000) · Neuropharmacology · doi:10.1016/s0028-3908(00)00076-9 · Cited by 22 · see citing works

Evidence for an ephaptic feedback in cortical synapses: postsynaptic hyperpolarization alters the number of response failures and quantal content

Voronin, L. L., Volgushev, M., Sokolov, M., et al. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00150-5 · Cited by 19 · see citing works

Dynamic Network Communication as a Unifying Neural Basis for Cognition, Development, Aging, and Disease

Voytek, B., & Knight, R. T. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.04.016 · Cited by 556 · see citing works

Integrating information in the brain's EM field: the cemi field theory of consciousness

McFadden, J. (2020) · Neuroscience of Consciousness · doi:10.1093/nc/niaa016 · Cited by 148 · see citing works

Ephaptic coupling promotes synchronous firing of cerebellar purkinje cells

Han, K.-S., Guo, C., Chen, C. H., Witter, L., Osorno, T., & Regehr, W. G. (2018) · Neuron · doi:10.1016/j.neuron.2018.09.018 · Cited by 144 · see citing works

Revisiting the Quantum Brain Hypothesis: Toward Quantum (Neuro)biology?

Jedlicka, P. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00366 · Cited by 97 · see citing works

In vivo ephaptic coupling allows memory network formation

Pinotsis, D. A., & Miller, E. K. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad251 · Cited by 62 · see citing works

Induced neural phase precession through exogenous electric fields

Wischnewski, M., Tran, H., Zhao, Z., Shirinpour, S., Haigh, Z. J., Rotteveel, J., Perera, N. D., Alekseichuk, I., Zimmermann, J., & Opitz, A. (2024) · Nature Communications · doi:10.1038/s41467-024-45898-5 · Cited by 46 · see citing works

The electromagnetic will

McFadden, J. (2021) · NeuroSci · doi:10.3390/neurosci2030021 · Cited by 13 · see citing works

Consciousness and its hard problems: Separating the ontological from the evolutionary.

Lacalli, T. (2023) · Frontiers in Psychology · doi:10.3389/fpsyg.2023.1196576 · Cited by 4 · see citing works

Analog Cognition and Consciousness

Miller, E. K., Brincat, S. L., & Roy, J. E. (2026) · The Journal of Neuroscience · doi:10.1523/jneurosci.0711-26.2026 · Cited by 4 · see citing works

Scaling up from sentience: Modularity, conscious broadcast, and a constitutive solution to the combination problem.

Lacalli, T. (2025) · Frontiers in Psychology · doi:10.3389/fpsyg.2025.1648930 · Cited by 1 · see citing works

Cyclic AMP and prostaglandins in periodontal disease.

ElAttar, T. M. A., & Lin, H. S. (1980) · PubMed · Cited by 8 · see citing works

Two pools for amines in neoplastic mast cells

Green, J. P., & Furano, A. V. (1962) · Biochemical Pharmacology · doi:10.1016/0006-2952(62)90164-8 · Cited by 35 · see citing works

Effects of Nitrogen-Free Diet Method and Fasting Method on Endogenous Amino Acid Losses of Yangzhou Geese

Haiming, Y. (2013) · Dongwu yingyang xuebao

Are the kidneys involved in the removal of endogenous pyrogens in the rabbit?

Turnbull, A. J., Kluger, M. J., Cranston, W. I., et al. (1982) · Journal of Thermal Biology · doi:10.1016/0306-4565(82)90038-9 · Cited by 3 · see citing works

Bioluminescent probe for detecting endogenous hypochlorite in living mice

Tang, C., Gao, Y., Liu, T., Lin, Y., Zhang, X., Zhang, C., Li, X., Zhang, T., Du, L., & Li, M. (2017) · Organic & Biomolecular Chemistry · doi:10.1039/c7ob02842c · Cited by 31 · see citing works