The Theta-Gamma Neural Code

The magical number seven, plus or minus two: Some limits on our capacity for processing information.

Miller, G. A. (1956) · Psychological Review · doi:10.1037/h0043158 · Cited by 17,812

The magical number seven, plus or minus two: Some limits on our capacity for processing information.

Miller, G. A. (1994) · Psychological Review · doi:10.1037/0033-295x.101.2.343 · Cited by 17,559

A feature-integration theory of attention.

Treisman, A. M., & Gelade, G. (1980) · Cognitive Psychology · doi:10.1016/0010-0285(80)90005-5 · Cited by 12,366

The magical number 4 in short-term memory: A reconsideration of mental storage capacity

Cowan, N. (2001) · Behavioral and Brain Sciences · doi:10.1017/s0140525x01003922 · Cited by 6,779

The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat

O'Keefe, J., & Dostrovsky, J. (1971) · Brain Research · doi:10.1016/0006-8993(71)90358-1 · Cited by 6,151

The brainweb: phase synchronization and large-scale integration

Varela, F., Lachaux, J.-P., Rodriguez, E., & Martinerie, J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35067550 · Cited by 4,761

A mechanism for cognitive dynamics: neuronal communication through neuronal coherence.

Fries, P. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.08.011 · Cited by 4,284

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

High-speed scanning in human memory

Sternberg, S. (1966) · Science · doi:10.1126/science.153.3736.652 · Cited by 3,576

Mechanisms of Gamma Oscillations

Buzsáki, G., & Wang, X.-J. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150444 · Cited by 2,796

Dynamic functional connectivity: Promise, issues, and interpretations

Hutchison, R. M., Womelsdorf, T., Allen, E. A., Bandettini, P. A., Calhoun, V. D., Corbetta, M., Della Penna, S., Duyn, J. H., Glover, G. H., Gonzalez-Castillo, J., et al. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.079 · Cited by 2,962

Working memory and neural oscillations: alpha–gamma versus theta–gamma codes for distinct WM information?

Roux, F., & Uhlhaas, P. J. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.10.010 · Cited by 906

Where Does EEG Come From and What Does It Mean?

Cohen, M. X. (2017) · Trends in Neurosciences · doi:10.1016/j.tins.2017.02.004 · Cited by 722

Beyond the Status Quo: A Role for Beta Oscillations in Endogenous Content (Re)Activation

Spitzer, B., & Haegens, S. (2017) · eNeuro · doi:10.1523/eneuro.0170-17.2017 · Cited by 667

Untangling cross-frequency coupling in neuroscience

Aru, J., Aru, J., Priesemann, V., Wibral, M., Lana, L., Pipa, G., Singer, W., & Vicente, R. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.08.002 · Cited by 628

Nasal Respiration Entrains Human Limbic Oscillations and Modulates Cognitive Function

Zelano, C., Jiang, H., Zhou, G., Arora, N., Schuele, S., Rosenow, J., & Gottfried, J. A. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.2586-16.2016 · Cited by 599

Theta Oscillations in Human Memory

Herweg, N. A., Solomon, E. A., & Kahana, M. J. (2020) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.12.006 · Cited by 605

Frontal midline theta oscillations during working memory maintenance and episodic encoding and retrieval

Hsieh, L.-T., & Ranganath, C. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.08.003 · Cited by 525

Neural Cross-Frequency Coupling: Connecting Architectures, Mechanisms, and Functions

Hyafil, A., Giraud, A., Fontolan, L., & Gutkin, B. S. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.09.001 · Cited by 527

A Rhythmic Theory of Attention

Fiebelkorn, I. C., & Kästner, S. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.11.009 · Cited by 514

Theta Phase Segregation of Input-Specific Gamma Patterns in Entorhinal-Hippocampal Networks

Schomburg, E. W., Fernández-Ruiz, A., Mizuseki, K., Berényi, A., Anastassiou, C. A., Koch, C., & Buzsáki, G. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.051 · Cited by 465

Temporal coding organized by coupled alpha and gamma oscillations prioritize visual processing

Jensen, O., Gips, B., Bergmann, T. O., & Bonnefond, M. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.04.001 · Cited by 389

Theta and Alpha Oscillations Are Traveling Waves in the Human Neocortex

Zhang, H., Watrous, A. J., Patel, A., & Jacobs, J. (2018) · Neuron · doi:10.1016/j.neuron.2018.05.019 · Cited by 396

Spatial Working Memory in Humans Depends on Theta and High Gamma Synchronization in the Prefrontal Cortex

Alekseichuk, I., Turi, Z., de Lara, G., Antal, A., & Paulus, W. (2016) · Current Biology · doi:10.1016/j.cub.2016.04.035 · Cited by 389

Oscillations and Episodic Memory: Addressing the Synchronization/Desynchronization Conundrum

Hanslmayr, S., Staresina, B. P., & Bowman, H. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2015.11.004 · Cited by 394

Hippocampal theta sequences reflect current goals

Wikenheiser, A. M., & Redish, A. D. (2015) · Nature Neuroscience · doi:10.1038/nn.3909 · Cited by 367

A Dynamic Interplay within the Frontoparietal Network Underlies Rhythmic Spatial Attention

Fiebelkorn, I. C., Pinsk, M. A., & Kastner, S. (2018) · Neuron · doi:10.1016/j.neuron.2018.07.038 · Cited by 356

Entorhinal-CA3 Dual-Input Control of Spike Timing in the Hippocampus by Theta-Gamma Coupling

Fernández‐Ruiz, A., Oliva, A., Nagy, G. A., Maurer, A. P., Berényi, A., & Buzsáki, G. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.017 · Cited by 344

Local Entrainment of Alpha Oscillations by Visual Stimuli Causes Cyclic Modulation of Perception

Spaak, E., de Lange, F. P., & Jensen, O. B. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4385-13.2014 · Cited by 333

Distinct inhibitory circuits orchestrate cortical beta and gamma band oscillations

Chen, G., Zhang, Y., Li, X., Zhao, X., Ye, Q., Lin, Y., Tao, H. W., Rasch, M. J., & Zhang, X. (2017) · Neuron · doi:10.1016/j.neuron.2017.11.033 · Cited by 345

The neural oscillations of speech processing and language comprehension: state of the art and emerging mechanisms

Meyer, L. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13748 · Cited by 326

Oscillatory multiplexing of population codes for selective communication in the mammalian brain

Akam, T., & Kullmann, D. M. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3668 · Cited by 327

What does gamma coherence tell us about inter-regional neural communication?

Buzsáki, G., & Schomburg, E. W. (2015) · Nature Neuroscience · doi:10.1038/nn.3952 · Cited by 333

Neuromodulatory Influences on Integration and Segregation in the Brain

Shine, J. M. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.04.002 · Cited by 328

Oscillatory Dynamics of Prefrontal Cognitive Control

Helfrich, R. F., & Knight, R. T. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2016.09.007 · Cited by 322

The rate of transient beta frequency events predicts behavior across tasks and species

Shin, H., Law, R., Tsutsui, S., Moore, C. I., & Jones, S. R. (2017) · eLife · doi:10.7554/elife.29086 · Cited by 325

Fear and safety engage competing patterns of theta-gamma coupling in the basolateral amygdala

Stujenske, J. M., Likhtik, E., Topiwala, M. A., & Gordon, J. A. (2014) · Neuron · doi:10.1016/j.neuron.2014.07.026 · Cited by 303

When brain rhythms aren't ‘rhythmic’: implication for their mechanisms and meaning

Jones, S. R. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.06.010 · Cited by 316

Frontosubthalamic Circuits for Control of Action and Cognition

Aron, A. R., Herz, D. M., Brown, P., Forstmann, B. U., & Zaghloul, K. A. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2348-16.2016 · Cited by 299

Episodic sequence memory is supported by a theta-gamma phase code

Heusser, A. C., Poeppel, D., Ezzyat, Y., & Davachi, L. (2016) · Nature Neuroscience · doi:10.1038/nn.4374 · Cited by 290

Thalamocortical Dysrhythmia: A Theoretical Update in Tinnitus

Ridder, D. D., Vanneste, S., Langguth, B., & Llinás, R. (2015) · Frontiers in Neurology · doi:10.3389/fneur.2015.00124 · Cited by 290

Communication between Brain Areas Based on Nested Oscillations

Bonnefond, M., Kästner, S., & Jensen, O. B. (2017) · eNeuro · doi:10.1523/eneuro.0153-16.2017 · Cited by 302

Synaptic Plasticity, Engrams, and Network Oscillations in Amygdala Circuits for Storage and Retrieval of Emotional Memories

Bocchio, M., Nabavi, S., & Capogna, M. (2017) · Neuron · doi:10.1016/j.neuron.2017.03.022 · Cited by 265

Inferring Causality from Noninvasive Brain Stimulation in Cognitive Neuroscience

Bergmann, T. O., & Hartwigsen, G. (2020) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01591 · Cited by 271

Thalamocortical dysrhythmia detected by machine learning

Vanneste, S., Song, J., & Ridder, D. D. (2018) · Nature Communications · doi:10.1038/s41467-018-02820-0 · Cited by 263

Neuroplastic Changes Following Brain Ischemia and their Contribution to Stroke Recovery: Novel Approaches in Neurorehabilitation

Alia, C., Spalletti, C., Lai, S., Panarese, A., Lamola, G., Bertolucci, F., Vallone, F., Garbo, A. D., Chisari, C., Micera, S., et al. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00076 · Cited by 272

Modulating Human Memory via Entrainment of Brain Oscillations

Hanslmayr, S., Axmacher, N., & Inman, C. S. (2019) · Trends in Neurosciences · doi:10.1016/j.tins.2019.04.004 · Cited by 264

Hippocampal-prefrontal theta-gamma coupling during performance of a spatial working memory task

Tamura, M., Spellman, T., Rosen, A. M., Gogos, J. A., & Gordon, J. A. (2017) · Nature Communications · doi:10.1038/s41467-017-02108-9 · Cited by 261

Nonsinusoidal Beta Oscillations Reflect Cortical Pathophysiology in Parkinson's Disease

Cole, S. R., Peterson, E. J., van der Meij, R., de Hemptinne, C., Starr, P. A., & Voytek, B. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2208-16.2017 · Cited by 245

Electrophysiological Brain Connectivity: Theory and Implementation

He, B., Astolfi, L., Valdes-Sosa, P. A., Marinazzo, D., Palva, S., Bénar, C., Michel, C. M., & Koenig, T. W. (2019) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2019.2913928 · Cited by 242

Speech encoding by coupled cortical theta and gamma oscillations

Hyafil, A., Fontolan, L., Kabdebon, C., Gutkin, B. S., & Giraud, A. (2015) · eLife · doi:10.7554/elife.06213 · Cited by 227

Gamma rhythm communication between entorhinal cortex and dentate gyrus neuronal assemblies

Fernández‐Ruiz, A., Oliva, A., Soula, M., Rocha-Almeida, F., Nagy, G. A., Martín-Vázquez, G., & Buzsáki, G. (2021) · Science · doi:10.1126/science.abf3119 · Cited by 238

Theta–gamma coupling in the entorhinal–hippocampal system

Colgin, L. L. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.08.001 · Cited by 226

The frequency architecture of brain and brain body oscillations: an analysis

Klimesch, W. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14192 · Cited by 250

Functions of gamma‐band synchronization in cognition: from single circuits to functional diversity across cortical and subcortical systems

Bosman, C. A., Lansink, C. S., & Pennartz, C. M. A. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12606 · Cited by 239

Geometry of sequence working memory in macaque prefrontal cortex

Xie, Y., Hu, P., Li, J., Chen, J., Song, W., Wang, X., Yang, T., Dehaene, S., Tang, S., Min, B., et al. (2022) · Science · doi:10.1126/science.abm0204 · Cited by 222

Working Memory Maturation: Can We Get at the Essence of Cognitive Growth?

Cowan, N. (2016) · Perspectives on Psychological Science · doi:10.1177/1745691615621279 · Cited by 225

Oscillatory dynamics coordinating human frontal networks in support of goal maintenance

Voytek, B., Kayser, A. S., Badre, D., Fegen, D., Chang, E. F., Crone, N. E., Parvizi, J., Knight, R. T., & D’Esposito, M. (2015) · Nature Neuroscience · doi:10.1038/nn.4071 · Cited by 229

How brain oscillations form memories — A processing based perspective on oscillatory subsequent memory effects

Hanslmayr, S., & Staudigl, T. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.121 · Cited by 231

Theta-Gamma-Modulated Synaptic Currents in Hippocampal Granule Cells In Vivo Define a Mechanism for Network Oscillations

Pernía‐Andrade, A. J., & Jónás, P. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.046 · Cited by 227

Widespread theta synchrony and high-frequency desynchronization underlies enhanced cognition

Solomon, E. A., Kragel, J. E., Sperling, M. R., Sharan, A., Worrell, G., Kucewicz, M., Inman, C. S., Lega, B., Davis, K. A., Stein, J. M., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-01763-2 · Cited by 221

A predictive coding framework for rapid neural dynamics during sentence-level language comprehension

Lewis, A., & BASTIAANSEN, M. C. M. (2015) · Cortex · doi:10.1016/j.cortex.2015.02.014 · Cited by 226

Basic and functional effects of transcranial Electrical Stimulation (tES)—An introduction

Yavari, F., Jamil, A., Mosayebi-Samani, M., Vidor, L. P., & Nitsche, M. A. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.06.015 · Cited by 242

Supervised learning in spiking neural networks with FORCE training

Nicola, W., & Clopath, C. (2017) · Nature Communications · doi:10.1038/s41467-017-01827-3 · Cited by 214

Physical principles of brain–computer interfaces and their applications for rehabilitation, robotics and control of human brain states

Hramov, A. E., Александрович, М. В., & Pisarchik, A. N. (2021) · Physics Reports · doi:10.1016/j.physrep.2021.03.002 · Cited by 228

Quantification of Phase-Amplitude Coupling in Neuronal Oscillations: Comparison of Phase-Locking Value, Mean Vector Length, Modulation Index, and Generalized-Linear-Modeling-Cross-Frequency-Coupling

Hülsemann, M., nat, D. R., Naumann, E., nat, D. R., & Rasch, B. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00573 · Cited by 205

Boosting vocabulary learning by verbal cueing during sleep

Schreiner, T., & Rasch, B. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu139 · Cited by 202

Independent control of gamma and theta activity by distinct interneuron networks in the olfactory bulb

Fukunaga, I., Herb, J. T., Köllő, M., Boyden, E. S., & Schaefer, A. T. (2014) · Nature Neuroscience · doi:10.1038/nn.3760 · Cited by 200

Interneuronal mechanisms of hippocampal theta oscillations in a full-scale model of the rodent CA1 circuit

Bezaire, M. J., Raikov, I., Burk, K., Vyas, D., & Soltesz, I. (2016) · eLife · doi:10.7554/elife.18566 · Cited by 198

Theta-Gamma Coupling and Working Memory in Alzheimer’s Dementia and Mild Cognitive Impairment

Goodman, M. S., Kumar, S., Zomorrodi, R., Ghazala, Z., Cheam, A., Barr, M. S., Daskalakis, Z. J., Blumberger, D. M., Fischer, C. E., Flint, A. J., et al. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00101 · Cited by 216

Organization of prefrontal network activity by respiration-related oscillations

Biskamp, J., Bartos, M., & Sauer, J.-F. (2017) · Scientific Reports · doi:10.1038/srep45508 · Cited by 197

Impaired Tuning of Neural Ensembles and the Pathophysiology of Schizophrenia: A Translational and Computational Neuroscience Perspective

Krystal, J. H., Anticevic, A., Yang, G., Dragoi, G., Driesen, N. R., Wang, X., & Murray, J. D. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.01.004 · Cited by 201

Activity-dependent switch of GABAergic inhibition into glutamatergic excitation in astrocyte-neuron networks

Perea, G., Gómez, R., Mederos, S., Covelo, A., Ballesteros, J. J., Schlosser, L., Hernández-Vivanco, A., Martín-Fernández, M., Quintana, R., Rayan, A., et al. (2016) · eLife · doi:10.7554/elife.20362 · Cited by 194

Entrainment of Prefrontal Beta Oscillations Induces an Endogenous Echo and Impairs Memory Formation

Hanslmayr, S., Matuschek, J., & Fellner, M.-C. (2014) · Current Biology · doi:10.1016/j.cub.2014.03.007 · Cited by 193

Amygdala–prefrontal interactions in (mal)adaptive learning

Likhtik, E., & Paz, R. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2014.12.007 · Cited by 198

Increase in short-term memory capacity induced by down-regulating individual theta frequency via transcranial alternating current stimulation

Vosskuhl, J., Huster, R. J., & Herrmann, C. S. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00257 · Cited by 204

The Functional Role of Dreaming in Emotional Processes

Scarpelli, S., Bartolacci, C., D'Atri, A., Gorgoni, M., & De Gennaro, L. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.00459 · Cited by 190

Long-lasting, dissociable improvements in working memory and long-term memory in older adults with repetitive neuromodulation

Grover, S., Wen, W., Viswanathan, V., Gill, C. T., & Reinhart, R. M. G. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01132-3 · Cited by 187

Subsequent memory effect in intracranial and scalp EEG

Long, N. M., Burke, J. F., & Kahana, M. J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.08.052 · Cited by 179

Dynamic Changes in Phase-Amplitude Coupling Facilitate Spatial Attention Control in Fronto-Parietal Cortex

Szczepanski, S. M., Crone, N. E., Kuperman, R. A., Auguste, K. I., Parvizi, J., & Knight, R. T. (2014) · PLoS Biology · doi:10.1371/journal.pbio.1001936 · Cited by 183

The modulation of neural gain facilitates a transition between functional segregation and integration in the brain

Shine, J. M., Aburn, M. J., Breakspear, M. J., & Poldrack, R. A. (2018) · eLife · doi:10.7554/elife.31130 · Cited by 183

Slow Oscillations in the Mouse Hippocampus Entrained by Nasal Respiration

Yanovsky, Y., Ciatipis, M., Draguhn, A., Tort, A. B. L., & Brankačk, J. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.5287-13.2014 · Cited by 175

A review of theta oscillation and its functional correlates

Karakaş, S. (2020) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2020.04.008 · Cited by 196

Decay Theory of Immediate Memory: From Brown (1958) to Today (2014)

Ricker, T. J., Vergauwe, E., & Cowan, N. (2014) · Quarterly Journal of Experimental Psychology · doi:10.1080/17470218.2014.914546 · Cited by 165

A Neural Chronometry of Memory Recall

Staresina, B. P., & Wimber, M. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.09.011 · Cited by 177

Oscillatory Control over Representational States in Working Memory

de Vries, I. E. J., Slagter, H. A., & Olivers, C. N. L. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.11.006 · Cited by 168

The Theta Rhythm of the Hippocampus: From Neuronal and Circuit Mechanisms to Behavior

Núñez, Á., & Buño, W. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.649262 · Cited by 183

Control of working memory by phase–amplitude coupling of human hippocampal neurons

Daume, J., Kamiński, J., Gómez-Palacio-Schjetnan, A., Salimpour, Y., Khan, U., Kyzar, M., Reed, C. M., Anderson, W. S., Valiante, T. A., Mamelak, A. N., et al. (2024) · Nature · doi:10.1038/s41586-024-07309-z · Cited by 187

NMDA receptor antagonist rodent models for cognition in schizophrenia and identification of novel drug treatments, an update

Cadinu, D., Grayson, B., Podda, G., Harte, M., Doostdar, N., & Neill, J. C. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.11.045 · Cited by 169

Layer-Specific GABAergic Control of Distinct Gamma Oscillations in the CA1 Hippocampus

Lasztóczi, B., & Klausberger, T. (2014) · Neuron · doi:10.1016/j.neuron.2014.01.021 · Cited by 176

Long-Range Neural Synchrony in Behavior

Harris, A. Z., & Gordon, J. A. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-034111 · Cited by 168

Self-Organized Criticality in the Brain

Plenz, D., Ribeiro, T. L., Miller, S. R., Kells, P. A., Vakili, A., & Capek, E. L. (2021) · Frontiers in Physics · doi:10.3389/fphy.2021.639389 · Cited by 185

The applied principles of EEG analysis methods in neuroscience and clinical neurology

Zhang, H., Zhou, Q.-Q., Chen, H., Hu, X., Li, W., Bai, Y., Han, J., Wang, Y., Liang, Z., Chen, D., et al. (2023) · Military Medical Research · doi:10.1186/s40779-023-00502-7 · Cited by 197

The what, where and how of delay activity

Sreenivasan, K. K., & D’Esposito, M. (2019) · Nature reviews. Neuroscience · doi:10.1038/s41583-019-0176-7 · Cited by 168

Spatial Sequence Coding Differs during Slow and Fast Gamma Rhythms in the Hippocampus

Zheng, C., Bieri, K. W., Hsiao, Y., & Colgin, L. L. (2016) · Neuron · doi:10.1016/j.neuron.2015.12.005 · Cited by 171

GABAergic signaling to astrocytes in the prefrontal cortex sustains goal-directed behaviors

Mederos, S., Sánchez‐Puelles, C., Esparza, J., Valero, M., Ponomarenko, A. A., & Perea, G. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-00752-x · Cited by 169

Propagating Neocortical Gamma Bursts Are Coordinated by Traveling Alpha Waves

Bahramisharif, A., van Gerven, M. A. J., Aarnoutse, E. J., Mercier, M. R., Schwartz, T. H., Foxe, J. J., Ramsey, N. F., & Jensen, O. B. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2455-13.2013 · Cited by 158

Theta-gamma coordination between anterior cingulate and prefrontal cortex indexes correct attention shifts

Voloh, B., Valiante, T. A., Everling, S., & Womelsdorf, T. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1500438112 · Cited by 157

Theta activity and cognitive functioning: Integrating evidence from resting-state and task-related developmental electroencephalography (EEG) research

Tan, E., Troller‐Renfree, S. V., Morales, S., Buzzell, G. A., McSweeney, M., Antúnez, M., & Fox, N. A. (2024) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2024.101404 · Cited by 193

Low-Frequency Neural Oscillations Support Dynamic Attending in Temporal Context

Henry, M. J., & Herrmann, B. (2013) · Timing & Time Perception · doi:10.1163/22134468-00002011 · Cited by 168

Directional coupling of slow and fast hippocampal gamma with neocortical alpha/beta oscillations in human episodic memory

Griffiths, B., Parish, G., Roux, F., Michelmann, S., van der Plas, M., Kolibius, L. D., Chelvarajah, R., Rollings, D. T., Sawlani, V., Hamer, H. M., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1914180116 · Cited by 166

Over and above frequency: Gamma oscillations as units of neural circuit operations

Fernández‐Ruiz, A., Sirota, A., Lopes‐dos‐Santos, V., & Dupret, D. (2023) · Neuron · doi:10.1016/j.neuron.2023.02.026 · Cited by 178

The hippocampus, time, and memory across scales.

Howard, M. W., & Eichenbaum, H. (2013) · Journal of Experimental Psychology General · doi:10.1037/a0033621 · Cited by 163

Hippocampal theta codes for distances in semantic and temporal spaces

Solomon, E. A., Lega, B. C., Sperling, M. R., & Kahana, M. J. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1906729116 · Cited by 149

Rethinking retrosplenial cortex: Perspectives and predictions

Alexander, A. S., Place, R., Starrett, M. J., Chrastil, E. R., & Nitz, D. A. (2022) · Neuron · doi:10.1016/j.neuron.2022.11.006 · Cited by 176

Embodying Others in Immersive Virtual Reality: Electro-Cortical Signatures of Monitoring the Errors in the Actions of an Avatar Seen from a First-Person Perspective

Pavone, E. F., Tieri, G., Rizza, G., Tidoni, E., Grisoni, L., & Aglioti, S. M. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0494-15.2016 · Cited by 146

On cross-frequency phase-phase coupling between theta and gamma oscillations in the hippocampus

Scheffer-Teixeira, R., & Tort, A. B. L. (2016) · eLife · doi:10.7554/elife.20515 · Cited by 155

Impact of different intensities of intermittent theta burst stimulation on the cortical properties during TMS‐EEG and working memory performance

Chung, S. W., Rogasch, N. C., Hoy, K. E., Sullivan, C. M., Cash, R. F. H., & Fitzgerald, P. B. (2017) · Human Brain Mapping · doi:10.1002/hbm.23882 · Cited by 155

Finding the answer in space: the mental whiteboard hypothesis on serial order in working memory

Abrahamse, E. L., van Dijck, J., Majerus, S., & Fias, W. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00932 · Cited by 153

From mechanisms to markers: novel noninvasive EEG proxy markers of the neural excitation and inhibition system in humans

Ahmad, J., Ellis, C. L., Leech, R., Voytek, B., Garcés, P., Jones, E. J. H., Buitelaar, J. K., Loth, E., dos Santos, F. P., Amil, A. F., et al. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-02218-z · Cited by 181

A Neural Coding Scheme Formed by the Combined Function of Gamma and Theta Oscillations

Lisman, J. E., & Buzsáki, G. (2008) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn060 · Cited by 468

Theta–gamma coupling as a ubiquitous brain mechanism: implications for memory, attention, dreaming, imagination, and consciousness

Ursino, M., & Pirazzini, G. (2024) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2024.101433 · Cited by 40

The theta/gamma discrete phase code occuring during the hippocampal phase precession may be a more general brain coding scheme

Lisman, J. (2005) · Hippocampus · doi:10.1002/hipo.20121 · Cited by 435

Mathematical analysis of multiple spike time series synchronized in phase with collective theta wave using neural cell model

Noyama, H., Yoshikai, Y., Kotani, K., & Jimbo, Y. (2020) · Electronics and Communications in Japan · doi:10.1002/ecj.12294 · Cited by 1

Theta-Gamma Coding Meets Communication-through-Coherence: Neuronal Oscillatory Multiplexing Theories Reconciled

McLelland, D., & VanRullen, R. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005162 · Cited by 54