Mechanisms of Gamma Oscillations

Neuronal Oscillations in Cortical Networks

Buzsáki, G., & Draguhn, A. (2004) · Science · doi:10.1126/science.1099745 · Cited by 6,576

Rhythms of the Brain

Buzsáki, G. (2006) · doi:10.1093/acprof:oso/9780195301069.001.0001 · Cited by 4,873

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

Über das Elektrenkephalogramm des Menschen

Berger, H. (1929) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/bf01797193 · Cited by 4,266

Oscillatory responses in cat visual cortex exhibit inter-columnar synchronization which reflects global stimulus properties

Gray, C. M., König, P., Engel, A. K., & Singer, W. (1989) · Nature · doi:10.1038/338334a0 · Cited by 4,183

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

Excitatory and Inhibitory Interactions in Localized Populations of Model Neurons

Wilson, H. R., & Cowan, J. D. (1972) · Biophysical Journal · doi:10.1016/s0006-3495(72)86068-5 · Cited by 3,579

Interneurons of the hippocampus

Freund, T. F., & Buzsáki, G. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:4 · Cited by 3,462

Dynamic predictions: Oscillations and synchrony in top–down processing

Engel, A. K., Fries, P., & Singer, W. (2001) · Nature Reviews Neuroscience · doi:10.1038/35094565 · Cited by 3,454

Pulvinar Modulates Synchrony across Visual Cortical Areas

Cortes, N., de Souza, B. O. F., & Casanova, C. (2020) · Vision · doi:10.3390/vision4020022 · Cited by 28

Generative modelling of the thalamo-cortical circuit mechanisms underlying the neurophysiological effects of ketamine

Shaw, A. D., Muthukumaraswamy, S. D., Saxena, N., Sumner, R. L., Adams, N., Moran, R., & Singh, K. D. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117189 · Cited by 28

The Logic of Developing Neocortical Circuits in Health and Disease

Hanganu‐Opatz, I. L., Butt, S. J. B., Hippenmeyer, S., García, N. V. D. M., Cardin, J. A., Voytek, B., & Muotri, A. R. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1655-20.2020 · Cited by 28

Ontogeny of kainate-induced gamma oscillations in the rat CA3 hippocampus in vitro

Tsintsadze, V., Minlebaev, M., Suchkov, D., Cunningham, M. O., & Khazipov, R. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00195 · Cited by 27

Laminar profile of visual response properties in ferret superior colliculus

Stitt, I., Galindo-Leon, E. E., Pieper, F., Engler, G., & Engel, A. K. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00957.2012 · Cited by 27

Ablation of neuropsin–neuregulin 1 signaling imbalances ErbB4 inhibitory networks and disrupts hippocampal gamma oscillation

Kawata, M., Morikawa, S., Shiosaka, S., & Tamura, H. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.20 · Cited by 27

Moderate prenatal alcohol exposure reduces parvalbumin expressing GABAergic interneurons in the dorsal hippocampus of adult male and female rat offspring

Madden, J. T., Thompson, S. M., Magcalas, C. M., Wagner, J. L., Hamilton, D. A., Savage, D. D., Clark, B. J., & Pentkowski, N. S. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2019.134700 · Cited by 27

The growth of cognition: Free energy minimization and the embryogenesis of cortical computation

Wright, J. J., & Bourke, P. D. (2020) · Physics of Life Reviews · doi:10.1016/j.plrev.2020.05.004 · Cited by 27

Theta, but Not Gamma Oscillations in Area V4 Depend on Input from Primary Visual Cortex

Kienitz, R., Cox, M. A., Dougherty, K., Saunders, R. C., Schmiedt, J. T., Leopold, D. A., Maier, A., & Schmid, M. C. (2020) · Current Biology · doi:10.1016/j.cub.2020.10.091 · Cited by 27

Cross-Frequency Power-Power Coupling Analysis: A Useful Cross-Frequency Measure to Classify ICA-Decomposed EEG

Thammasan, N., & Miyakoshi, M. (2020) · Sensors · doi:10.3390/s20247040 · Cited by 27

Normal and Abnormal Sharp Wave Ripples in the Hippocampal-Entorhinal Cortex System: Implications for Memory Consolidation, Alzheimer's Disease, and Temporal Lobe Epilepsy

Zhen, Z., Guo, M., Li, H.-M., Guo, O., Zhen, J., Fu, J., & Tan, G.-J. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.683483 · Cited by 27

Reduced readiness potential and post-movement beta synchronization reflect self-disorders in early course schizophrenia

Donati, F. L., Fecchio, M., Maestri, D., Cornali, M., Derchi, C., Casetta, C., Zalaffi, M., Sinigaglia, C., Sarasso, S., & D’Agostino, A. (2021) · Scientific Reports · doi:10.1038/s41598-021-94356-5 · Cited by 27

Criticality enhances the multilevel reliability of stimulus responses in cortical neural networks

Liang, J., & Zhou, C. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009848 · Cited by 27

Phase-Amplitude Coupling and Phase Synchronization Between Medial Temporal, Frontal and Posterior Brain Regions Support Episodic Autobiographical Memory Recall

Roehri, N., Bréchet, L., Seeber, M., Pascual‐Leone, Á., & Michel, C. M. (2022) · Brain Topography · doi:10.1007/s10548-022-00890-4 · Cited by 27

Cross-frequency phase-amplitude coupling in repetitive movements in patients with Parkinson’s disease

Gong, R., Mühlberg, C., Wegscheider, M., Fricke, C., Rumpf, J., Knösche, T. R., & Claßen, J. (2022) · Journal of Neurophysiology · doi:10.1152/jn.00541.2021 · Cited by 27

Cortical hyperexcitability in mouse models and patients with amyotrophic lateral sclerosis is linked to noradrenaline deficiency

Scekic‐Zahirovic, J., Benetton, C., Brunet, A., Ye, X., Logunov, E., Douchamps, V., Megat, S., Andry, V., Kan, V. W. Y., Stuart‐Lopez, G., et al. (2024) · Science Translational Medicine · doi:10.1126/scitranslmed.adg3665 · Cited by 27

Disrupted Gamma-Band Neural Oscillations During Coherent Motion Perception in Heavy Cannabis Users

Skosnik, P. D., Krishnan, G. P., D’Souza, D. C., Hetrick, W. P., & O’Donnell, B. F. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.166 · Cited by 27

Abnormal resting-state brain activity in headache-free migraine patients: A magnetoencephalography study

Li, F., Xiang, J., Wu, T., Zhu, D., & Shi, J. (2016) · Clinical Neurophysiology · doi:10.1016/j.clinph.2016.05.015 · Cited by 27

Hippocampal gamma‐band Synchrony and pupillary responses index memory during visual search

Montefusco‐Siegmund, R., Leonard, T. K., & Hoffman, K. L. (2016) · Hippocampus · doi:10.1002/hipo.22702 · Cited by 27

GABAergic effect on resting-state functional connectivity: Dynamics under pharmacological antagonism

Nasrallah, F. A., Singh, K. K. D. O. R., Yeow, L. Y., & Chuang, K. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.01.040 · Cited by 27

Novel Quantitative Analyses of Spontaneous Synaptic Events in Cortical Pyramidal Cells Reveal Subtle Parvalbumin-Expressing Interneuron Dysfunction in a Knock-In Mouse Model of Alzheimer’s Disease

Chen, L., Saito, T., Saido, T. C., & Módy, I. (2018) · eNeuro · doi:10.1523/eneuro.0059-18.2018 · Cited by 27

Synaptic entrainment of ectopic action potential generation in hippocampal pyramidal neurons

Thome, C., Roth, F. C., Obermayer, J., Yanez, A., Draguhn, A., & Egorov, A. V. (2018) · The Journal of Physiology · doi:10.1113/jp276720 · Cited by 27

Optogenetic Stimulation of the Basolateral Amygdala Increased Theta-Modulated Gamma Oscillations in the Hippocampus

Ahlgrim, N. S., & Manns, J. R. (2019) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2019.00087 · Cited by 27

Anxiety-like behavior induced by salicylate depends on age and can be prevented by a single dose of 5-MeO-DMT

Winne, J., Ciralli, B., Malfatti, T., Brisa, E., Doerl, J. G., Nogueira, I., Leão, K. E., & Leão, R. N. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113175 · Cited by 27

Power Modulations of ECoG Alpha/Beta and Gamma Bands Correlate With Time-Derivative of Force During Hand Grasp

Jiang, T., Pellizzer, G., Asman, P., Bastos, D. C. A., Bhavsar, S., Tummala, S., Prabhu, S. S., & Ince, N. F. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00100 · Cited by 27

Interictal scalp fast ripple occurrence and high frequency oscillation slow wave coupling in epileptic spasms

Bernardo, D., Nariai, H., Hussain, S. A., Sankar, R., & Wu, J. Y. (2020) · Clinical Neurophysiology · doi:10.1016/j.clinph.2020.03.025 · Cited by 27

Abnormal gamma phase-amplitude coupling in the parahippocampal cortex is associated with network hyperexcitability in Alzheimer’s disease

Prabhu, P., Morise, H., Kudo, K., Beagle, A. J., Mizuiri, D., Syed, F., Kotegar, K. A., Findlay, A. M., Miller, B. L., Kramer, J. H., et al. (2024) · Brain Communications · doi:10.1093/braincomms/fcae121 · Cited by 26

The role of parvalbumin interneuron dysfunction across neurodegenerative dementias

Smeralda, C. L., Pandit, S., Turrini, S., Reilly, J., Palmisano, A., Sprugnoli, G., Hampel, H. J., Benussi, A., Borroni, B., Press, D. Z., et al. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102509 · Cited by 26

Decorrelated Input Dissociates Narrow Band γ Power and BOLD in Human Visual Cortex

Butler, R., Bernier, P., Lefebvre, J., Gilbert, G., & Whittingstall, K. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.3938-16.2017 · Cited by 26

GABA metabolism and its role in gamma‐band oscillatory activity during auditory processing: An MRS and EEG study

Wyss, C., Tse, D. H. Y., Kometer, M., Dammers, J., Achermann, R., Shah, N. J., Kawohl, W., & Neuner, I. (2017) · Human Brain Mapping · doi:10.1002/hbm.23642 · Cited by 26

Modulation of Coordinated Activity across Cortical Layers by Plasticity of Inhibitory Synapses

Lourenço, J., Stasi, A. M. D., Deleuze, C., Bigot, M., Pazienti, A., Aguirre, A., Giugliano, M., Ostojic, S., & Bacci, A. (2020) · Cell Reports · doi:10.1016/j.celrep.2019.12.052 · Cited by 26

Mild traumatic brain injury is associated with dysregulated neural network functioning in children and adolescents

Safar, K., Zhang, J., Emami, Z., Gharehgazlou, A., Ibrahim, G. M., & Dunkley, B. T. (2021) · Brain Communications · doi:10.1093/braincomms/fcab044 · Cited by 26

Phase-locking patterns underlying effective communication in exact firing rate models of neural networks

Reyner-Parra, D., & Huguet, G. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009342 · Cited by 26

Spontaneous Spiking Is Governed by Broadband Fluctuations

Davis, Z. W., Muller, L., & Reynolds, J. H. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1899-21.2022 · Cited by 26

The role of brain oscillations in post-stroke motor recovery: An overview

Leonardi, G., Ciurleo, R., Cucinotta, F., Fonti, B., Borzelli, D., Costa, L., Tisano, A., Portaro, S., & Alito, A. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2022.947421 · Cited by 26

Aberrant protein S-nitrosylation contributes to hyperexcitability-induced synaptic damage in Alzheimer’s disease: Mechanistic insights and potential therapies

Ghatak, S., Nakamura, T., & Lipton, S. A. (2023) · Frontiers in Neural Circuits · doi:10.3389/fncir.2023.1099467 · Cited by 26

Daily rhythm in cortical chloride homeostasis underpins functional changes in visual cortex excitability

Pracucci, E., Graham, R., Alberio, L., Nardi, G., Cozzolino, O., Pillai, V., Pasquini, G., Saieva, L., Walsh, D. A., Landi, S., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-42711-7 · Cited by 26

Electrophysiological CNS-processes related to associative learning in humans

Christoffersen, G. R. J., & Schachtman, T. R. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.09.011 · Cited by 26

Acetylcholine, GABA and neuronal networks: A working hypothesis for compensations in the dystrophic brain

Cohen, E. J., Quarta, E., Fulgenzi, G., & Minciacchi, D. (2014) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2014.10.004 · Cited by 26

Low- and high-gamma oscillations deviate in opposite directions from zero-phase synchrony in the limbic corticostriatal loop

Catanese, J., Carmichael, J. E., & van der Meer, M. A. A. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00914.2015 · Cited by 26

Do Cortical Circuits Need Protecting from Themselves?

Trevelyan, A. J. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.06.002 · Cited by 26

Frequency mode excitations in two-dimensional Hindmarsh–Rose neural networks

Tabi, C. B., Etémé, A. S., & Mohamadou, A. (2017) · Physica A Statistical Mechanics and its Applications · doi:10.1016/j.physa.2017.01.075 · Cited by 26

An integrative model of the intrinsic hippocampal theta rhythm

Hummos, A., & Nair, S. S. (2017) · PLoS ONE · doi:10.1371/journal.pone.0182648 · Cited by 26

Cortical volume and sex influence visual gamma

van Pelt, S., Shumskaya, E., & Fries, P. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.06.005 · Cited by 26

How could N-Methyl-D-Aspartate Receptor Antagonists Lead to Excitation Instead of Inhibition?

Su, T., Lu, Y., Geng, Y., Lü, W., & Chen, Y. (2018) · Brain Science Advances · doi:10.26599/bsa.2018.2018.9050009 · Cited by 26

Dynamical state of the network determines the efficacy of single neuron properties in shaping the network activity

Sahasranamam, A., Vlachos, I., Aertsen, A., & Kumar, A. (2016) · Scientific Reports · doi:10.1038/srep26029 · Cited by 26

Putative Trace-Amine Associated Receptor 5 (TAAR5) Agonist α-NETA Increases Electrocorticogram Gamma-Rhythm in Freely Moving Rats

Belov, D., Efimova, E. V., Fesenko, Z. S., Antonova, K. A., Sf, K., Lakstygal, A. M., & Gainetdinov, R. R. (2019) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-019-00716-1 · Cited by 26

Cortical Glutamate/GABA Imbalance after Combined Radiation Exposure: Relevance to Human Deep-Space Missions

Kokhan, V. S., Anokhin, P. K., Belov, O., & Gulyaev, M. V. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.08.009 · Cited by 26

Morphine Differentially Alters the Synaptic and Intrinsic Properties of D1R- and D2R-Expressing Medium Spiny Neurons in the Nucleus Accumbens

McDevitt, D. S., Jonik, B., & Graziane, N. (2019) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2019.00035 · Cited by 26

Asynchronous and Coherent Dynamics in Balanced Excitatory-Inhibitory Spiking Networks

Bi, H., di Volo, M., & Torcini, A. (2021) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2021.752261 · Cited by 26

Phase Locking of Multiple Single Neurons to the Local Field Potential in Cat V1

Martin, K. A. C., & Schröder, S. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2547-14.2016 · Cited by 26

Voltage-gated potassium channels as a potential therapeutic target for the treatment of neurological and psychiatric disorders

Faulkner, I. E., Pajak, R. Z., Harte, M., Glazier, J. D., & Hager, R. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1449151 · Cited by 25

Unsupervised classification of neocortical activity patterns in neonatal and pre-juvenile rodents

Cichon, N., Denker, M., n, S. G. ⁄., & Hanganu‐Opatz, I. L. (2014) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00050 · Cited by 25

Transcranial photobiomodulation attenuates pentylenetetrazole‐induced status epilepticus in peripubertal rats

Tsai, C., Chang, S., & Chang, H. C. (2020) · Journal of Biophotonics · doi:10.1002/jbio.202000095 · Cited by 25

Synaptic inhibition in the neocortex: Orchestration and computation through canonical circuits and variations on the theme

Lourenço, J., Koukouli, F., & Bacci, A. (2020) · Cortex · doi:10.1016/j.cortex.2020.08.015 · Cited by 25

Gamma rhythms and visual information in mouse V1 specifically modulated by somatostatin+ neurons in reticular thalamus

Hoseini, M. S., Higashikubo, B. T., Cho, F. S., Chang, A. H., Clemente-Perez, A., Lew, I., Ciesielska, A., Stryker, M. P., & Paz, J. T. (2021) · eLife · doi:10.7554/elife.61437 · Cited by 25

Abnormal sleep physiology in children with 15q11.2-13.1 duplication (Dup15q) syndrome

Saravanapandian, V., Nadkarni, D., Hsu, S.-H., Hussain, S. A., Maski, K. P., Golshani, P., Colwell, C. S., Balasubramanian, S., Dixon, A., Geschwind, D. H., et al. (2021) · Molecular Autism · doi:10.1186/s13229-021-00460-8 · Cited by 25

Thalamocortical dysrhythmia in patients with schizophrenia spectrum disorder and individuals at clinical high risk for psychosis

Kim, M., Lee, T. H., Park, H., Moon, S., Lho, S. K., & Kwon, J. S. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01180-6 · Cited by 25

Soft, Thiol‐ene/Acrylate‐Based Electrode Array for Long‐Term Recording of Intracranial EEG Signals with Improved Biocompatibility in Mice

Fedor, F. Z., Madarász, M., Zátonyi, A., Szabó, Á., Lőrincz, T., Danda, V. R., Spurgin, L., Manz, C., Rózsa, B. J., & Fekete, Z. (2021) · Advanced Materials Technologies · doi:10.1002/admt.202100942 · Cited by 25

Net gain and loss: influence of natural rewards and drugs of abuse on perineuronal nets

Brown, T. E., & Sorg, B. A. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01337-x · Cited by 25

Multifunctional fibers enable modulation of cortical and deep brain activity during cognitive behavior in macaques

Garwood, I. C., Major, A. J., Antonini, M., Correa, J., Lee, Y., Sahasrabudhe, A., Mahnke, M. K., Miller, E. K., Brown, E. N., & Anikeeva, P. (2023) · Science Advances · doi:10.1126/sciadv.adh0974 · Cited by 25

Endogenous noise of neocortical neurons correlates with atypical sensory response variability in the Fmr1−/y mouse model of autism

Bhaskaran, A. A., Gauvrit, T., Vyas, Y., Bony, G., Ginger, M. R., & Frick, A. (2023) · Nature Communications · doi:10.1038/s41467-023-43777-z · Cited by 25

Clinical and Genetic Features of Dravet Syndrome: A Prime Example of the Role of Precision Medicine in Genetic Epilepsy

Fan, H., Yang, M., Lin, L., Chiang, K.-L., & Chen, C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms25010031 · Cited by 25

Transient demyelination causes long‐term cognitive impairment, myelin alteration and network synchrony defects

Mercier, O., Quilichini, P., Magalon, K., Gil, F., Ghestem, A., Richard, F., Boudier, T., Cayre, M., & Durbec, P. (2024) · Glia · doi:10.1002/glia.24513 · Cited by 25

Generators and Connectivity of the Early Auditory Evoked Gamma Band Response

Polomac, N., Leicht, G., Nolte, G., Andreou, C., Schneider, T. R., Steinmann, S., Engel, A. K., & Mulert, C. (2015) · Brain Topography · doi:10.1007/s10548-015-0434-6 · Cited by 25

40‐Hz oscillations underlying perceptual binding in young and older adults

Roß, B., & Fujioka, T. (2016) · Psychophysiology · doi:10.1111/psyp.12654 · Cited by 25

Hippocampal network dynamics in response to α7 nACh receptors activation in amyloid-β overproducing transgenic mice

Stoiljković, M., Kelley, C., Hajos, G. P., Nagy, D., Koenig, G., Leventhal, L., & Hajós, M. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.05.021 · Cited by 25

Methodological standards and functional correlates of depth in vivo electrophysiological recordings in control rodents. A TASK 1‐ WG 3 report of the AES / ILAE Translational Task Force of the ILAE

Hernan, A. E., Schevon, C. A., Worrell, G. A., Galanopoulou, A. S., Kahane, P., de Curtis, M., Ikeda, A., Quilichini, P., Williamson, A., Garcia‐Cairasco, N., et al. (2017) · Epilepsia · doi:10.1111/epi.13905 · Cited by 25

Basal forebrain somatostatin cells differentially regulate local gamma oscillations and functionally segregate motor and cognitive circuits

Espinosa, N., Alonso, A., Lara-Vásquez, A., & Fuentealba, P. (2019) · Scientific Reports · doi:10.1038/s41598-019-39203-4 · Cited by 25

Diversity of neuronal activity is provided by hybrid synapses

Xu, K., Maidana, J. P., & Orio, P. (2021) · Nonlinear Dynamics · doi:10.1007/s11071-021-06704-9 · Cited by 25

Subthalamic Nucleus Activity Influences Sensory and Motor Cortex during Force Transduction

Alhourani, A., Korzeniewska, A., Wozny, T. A., Lipski, W. J., Kondylis, E. D., Ghuman, A. S., Crone, N. E., Crammond, D. J., Turner, R. S., & Richardson, R. M. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz264 · Cited by 25

Adult trkB Signaling in Parvalbumin Interneurons is Essential to Prefrontal Network Dynamics

Guyon, N., Zacharias, L. R., van Lunteren, J. A., Immenschuh, J., Fuzik, J., Märtin, A., Xuan, Y., Zilberter, M. Y., Kim, H., Meletis, K., et al. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1848-20.2021 · Cited by 25

Causal functional maps of brain rhythms in working memory

Wischnewski, M., Berger, T. A., Opitz, A., & Alekseichuk, I. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2318528121 · Cited by 24

Multiple Stochastic Resonances and Oscillation Transitions in Cortical Networks With Time Delay

Yu, H., Guo, X., Wang, J., Li, K., Deng, B., Wei, X., & Liu, C. (2018) · IEEE Transactions on Fuzzy Systems · doi:10.1109/tfuzz.2018.2884229 · Cited by 24

Sleep, neuronal hyperexcitability, inflammation and neurodegeneration: Does early chronic short sleep trigger and is it the key to overcoming Alzheimer’s disease?

Ahnaou, A., & Drinkenburg, W. H. I. M. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.06.039 · Cited by 24

Gamma oscillations in primate primary visual cortex are severely attenuated by small stimulus discontinuities

Shirhatti, V., Ravishankar, P., & Ray, S. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001666 · Cited by 24

Enhancement of Motor Cortical Gamma Oscillations and Sniffing Activity by Medial Forebrain Bundle Stimulation Precedes Locomotion

Yoshimoto, A., Shibata, Y., Kudara, M., Ikegaya, Y., & Matsumoto, N. (2022) · eNeuro · doi:10.1523/eneuro.0521-21.2022 · Cited by 24

Hippocampal oscillatory dynamics in freely behaving rats during exploration of social and non-social stimuli

Zhu, N., Zhang, Y., Xiao, X., Wang, Y., Yang, J., Colgin, L. L., & Zheng, C. (2022) · Cognitive Neurodynamics · doi:10.1007/s11571-022-09829-8 · Cited by 24

Gamma Oscillations and Potassium Channel Modulation in Schizophrenia: Targeting GABAergic Dysfunction

Kaar, S. J., Nottage, J. F., Angelescu, I., Marques, T. R., & Howes, O. D. (2023) · Clinical EEG and Neuroscience · doi:10.1177/15500594221148643 · Cited by 24

Home-based transcranial alternating current stimulation (tACS) in Alzheimer’s disease: rationale and study design

Altomare, D., Benussi, A., Cantoni, V., Premi, E., Rivolta, J., Cupidi, C., Martorana, A., Santarnecchi, E., Padovani, A., Koch, G., et al. (2023) · Alzheimer s Research & Therapy · doi:10.1186/s13195-023-01297-4 · Cited by 24

Active dendrites mediate stratified gamma‐range coincidence detection in hippocampal model neurons

Das, A., & Narayanan, R. (2015) · The Journal of Physiology · doi:10.1113/jp270688 · Cited by 24

Dynamics of Gamma Bursts in Local Field Potentials

Greenwood, P. E., McDonnell, M. D., & Ward, L. M. (2014) · Neural Computation · doi:10.1162/neco_a_00688 · Cited by 24

Cell Type- and Layer-Specific Muscarinic Potentiation of Excitatory Synaptic Drive onto Parvalbumin Neurons in Mouse Prefrontal Cortex

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Modulating pathological oscillations by rhythmic non-invasive brain stimulation—a therapeutic concept?

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