The slow (<1 Hz) rhythm of non-REM sleep: a dialogue between three cardinal oscillators

A novel slow (< 1 Hz) oscillation of neocortical neurons in vivo: depolarizing and hyperpolarizing components

Steriade, M., Nunez, A., & Amzica, F. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-08-03252.1993 · Cited by 1,903

Local sleep and learning

Huber, R., Felice Ghilardi, M., Massimini, M., & Tononi, G. (2004) · Nature · doi:10.1038/nature02663 · Cited by 1,854

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

Coordinated memory replay in the visual cortex and hippocampus during sleep

Ji, D., & Wilson, M. A. (2007) · Nature Neuroscience · doi:10.1038/nn1825 · Cited by 1,669

Cellular and network mechanisms of rhythmic recurrent activity in neocortex

Sanchez-Vives, M. V., & McCormick, D. A. (2000) · Nature Neuroscience · doi:10.1038/79848 · Cited by 1,539

Natural waking and sleep states: a view from inside neocortical neurons

Steriade, M., Timofeev, I., & Grenier, F. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.5.1969 · Cited by 1,296

Grouping of brain rhythms in corticothalamic systems

Steriade, M. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.10.029 · Cited by 1,296

Memory of sequential experience in the hippocampus during slow wave sleep

Lee, A. K., & Wilson, M. A. (2002) · Neuron · doi:10.1016/s0896-6273(02)01096-6 · Cited by 1,296

The sleep slow oscillation as a traveling wave

Massimini, M., Huber, R., Ferrarelli, F., Hill, S., & Tononi, G. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1318-04.2004 · Cited by 1,221

Neurotransmitter actions in the thalamus and cerebral cortex and their role in neuromodulation of thalamocortical activity

McCormick, D. A. (1992) · Progress in Neurobiology · doi:10.1016/0301-0082(92)90012-4 · Cited by 1,117

Impact of sex steroids and reproductive stage on sleep-dependent memory consolidation in women

Baker, F. C., Sattari, N. S., de Zambotti, M., Goldstone, A., Alaynick, W. A., & Mednick, S. C. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.03.017 · Cited by 28

Sleep’s contribution to memory formation

Lutz, N. D., Harkotte, M., & Jan Born, A. (2025) · Physiological Reviews · doi:10.1152/physrev.00054.2024 · Cited by 51

Fragments of wake-like activity frame down-states of sleep slow oscillations in humans: New vistas for studying homeostatic processes during sleep

Menicucci, D., Piarulli, A., Allegrini, P., Laurino, M., Mastorci, F., Sebastiani, L., Bedini, R., & Gemignani, A. (2013) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2013.01.014 · Cited by 26

Corticothalamic Synaptic Noise as a Mechanism for Selective Attention in Thalamic Neurons

Béhuret, S., Deleuze, C., & Bal, T. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00080 · Cited by 25

Acoustic Stimulation Following Sleep Spindle Activity May Enhance Procedural Memory Consolidation During a Nap

Choi, J., Won, K., & Jun, S. C. (2019) · IEEE Access · doi:10.1109/access.2019.2913457 · Cited by 27

Functional reorganization of the forepaw cortical representation immediately after thoracic spinal cord hemisection in rats

Yagüe, J. G., Humanes-Valera, D., Aguilar, J., & Foffani, G. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.03.015 · Cited by 25

Robustness of intrinsic connectivity networks in the human brain to the presence of acoustic scanner noise

Langers, D. R. M., & van Dijk, P. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.01.019 · Cited by 25

Sleep architecture in children with spinal muscular atrophy type 2

Verrillo, E., Pavone, M., Bruni, O., Paglietti, M. G., Ferri, R., Petreschi, F., Testa, M. B. C., & Cutrera, R. (2016) · Sleep Medicine · doi:10.1016/j.sleep.2015.12.015 · Cited by 25

Cholinergic and Adenosinergic Modulation of Synaptic Release

Yang, D., Ding, C., Qi, G., & Feldmeyer, D. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2020.06.006 · Cited by 24

An intra-K-complex oscillation with independent and labile frequency and topography in NREM sleep

Kokkinos, V., Koupparis, A. M., & Kostopoulos, G. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00163 · Cited by 24

Interdependent Conductances Drive Infraslow Intrinsic Rhythmogenesis in a Subset of Accessory Olfactory Bulb Projection Neurons

Gorin, M., Tsitoura, C., Kahan, A., Watznauer, K., Drose, D. R., Arts, M., Mathar, R., O'Connor, S., Hanganu‐Opatz, I. L., Ben‐Shaul, Y., et al. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2520-15.2016 · Cited by 25

Can REM Sleep Localize the Epileptogenic Zone? A Systematic Review and Analysis

McLeod, G. A., Ghassemi, A., & Ng, M. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.00584 · Cited by 24

From Physiology to Pathology of Cortico-Thalamo-Cortical Oscillations: Astroglia as a Target for Further Research

Gobbo, D., Scheller, A., & Kirchhoff, F. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.661408 · Cited by 25

Emergence of Sensory Patterns during Sleep Highlights Differential Dynamics of REM and Non-REM Sleep Stages

Ramot, M., Fisch, L., Davidesco, I., Harel, M., Kipervasser, S., Andelman, F., Neufeld, M. Y., Kramer, U., Fried, I., & Malach, R. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0232-13.2013 · Cited by 25

Corticothalamic network dysfunction and Alzheimer’s disease

Jagirdar, R., & Chin, J. (2017) · Brain Research · doi:10.1016/j.brainres.2017.09.014 · Cited by 24

Cortically-Controlled Population Stochastic Facilitation as a Plausible Substrate for Guiding Sensory Transfer across the Thalamic Gateway

Béhuret, S., Deleuze, C., Gómez‐Sena, L., Frégnac, Y., & Bal, T. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003401 · Cited by 24

Balancing Prediction and Surprise: A Role for Active Sleep at the Dawn of Consciousness?

Poll, M. N. V. D., & van Swinderen, B. (2021) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2021.768762 · Cited by 21

Pathological changes of brain oscillations following ischemic stroke

Satō, Y., Schmitt, O., Ip, Z., Rabiller, G., Omodaka, S., Tominaga, T., Yazdan-Shahmorad, A., & Liu, J. (2022) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x221105677 · Cited by 23

Alterations to parvalbumin-expressing interneuron function and associated network oscillations in the hippocampal – medial prefrontal cortex circuit during natural sleep in AppNL-G-F/NL-G-F mice

Brady, E. S., Griffiths, J., Andrianova, L., Bielska, M. H., Saito, T., Saido, T. C., Randall, A. D., Tamagnini, F., Witton, J., & Craig, M. T. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106151 · Cited by 20

The design and discovery of T-type calcium channel inhibitors for the treatment of central nervous system disorders

Choi, K.-H. (2013) · Expert Opinion on Drug Discovery · doi:10.1517/17460441.2013.796926 · Cited by 22

Cortical nNOS/NK1 Receptor Neurons are Regulated by Cholinergic Projections From the Basal Forebrain

Williams, R. H., Vazquez-DeRose, J., Thomas, A. M., Piquet, J., Cauli, B., & Kilduff, T. S. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx102 · Cited by 26

Transition dynamics and adaptive synchronization of time-delay interconnected corticothalamic systems via nonlinear control

Fan, D., Zhang, L., & Wang, Q. (2018) · Nonlinear Dynamics · doi:10.1007/s11071-018-4526-1 · Cited by 22

Inhibition and oscillations in the human brain tissue in vitro

de la Prida, L. M., & Huberfeld, G. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.02.006 · Cited by 21

Local Gamma Activity During Non-REM Sleep in the Context of Sensory Evoked K-Complexes

Laurino, M., Piarulli, A., Menicucci, D., & Gemignani, A. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01094 · Cited by 18

An iterative search algorithm to identify oscillatory dynamics in neurophysiological time seriesPreprint

Beck, A. M., He, M., Gutiérrez, R. G., Hotan, G. C., & Purdon, P. L. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.30.514422 · Cited by 22

Treatment effects on event-related EEG potentials and oscillations in Alzheimer's disease

Yener, G., Gündüz, D. H., Yıldırım, E., Aktürk, T., Başar‐Eroğlu, C., Bonanni, L., Percio, C. D., Farina, F. R., Ferri, R., Güntekin, B., et al. (2022) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2022.05.008 · Cited by 21

General anaesthesia and electroencephalographic spindles

Sleigh, J. W., Scheib, C. M., & Sanders, R. D. (2011) · Trends in Anaesthesia and Critical Care · doi:10.1016/j.tacc.2011.10.001 · Cited by 22

Fine-scale mapping of cortical laminar activity during sleep slow oscillations using high-density linear silicon probes

Fiáth, R., Raducanu, B. C., Musa, S., Andrei, A., López, C. M., Welkenhuysen, M., Ruther, P., Aarts, A. A. A., & Ulbert, I. (2018) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2018.08.020 · Cited by 19

Sleep slow oscillations favour local cortical plasticity underlying the consolidation of reinforced procedural learning in human sleep

Menicucci, D., Piarulli, A., Laurino, M., Zaccaro, A., Agrimi, J., & Gemignani, A. (2020) · Journal of Sleep Research · doi:10.1111/jsr.13117 · Cited by 23

Infra-slow Fluctuation Training in Clinical Practice: A Technical History

Smith, M. L., Collura, T. F., Ferrera, J., & Vries, J. D. (2014) · NeuroRegulation · doi:10.15540/nr.1.2.187 · Cited by 21

Dataset of cortical activity recorded with high spatial resolution from anesthetized rats

Horváth, C., Tóth, L. F., Ulbert, I., & Fiáth, R. (2021) · Scientific Data · doi:10.1038/s41597-021-00970-3 · Cited by 20

Effects of Anti-Seizure Medication on Sleep Spindles and Slow Waves in Drug-Resistant Epilepsy

Roebber, J. K., Lewis, P. A., Crunelli, V., Navarrete, M., & Hamandi, K. (2022) · Brain Sciences · doi:10.3390/brainsci12101288 · Cited by 23

Unbalanced Peptidergic Inhibition in Superficial Neocortex Underlies Spike and Wave Seizure Activity

Hall, S., Hunt, M. J., Simon, A., Cunnington, L. G., Carracedo, L. M., Schofield, I. S., Forsyth, R. J., Traub, R. D., & Whittington, M. A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4245-14.2015 · Cited by 20

The thalamic low-threshold Ca 2+ potential: a key determinant of the local and global dynamics of the slow (<1 Hz) sleep oscillation in thalamocortical networks

Crunelli, V., Errington, A. C., Hughes, S. W., & Toth, T. I. (2011) · Philosophical Transactions of the Royal Society A Mathematical Physical and Engineering Sciences · doi:10.1098/rsta.2011.0126 · Cited by 20

Sleep is neither a passive nor an active phenomenon

Kumar, V. M. (2010) · Sleep and Biological Rhythms · doi:10.1111/j.1479-8425.2010.00445.x · Cited by 19

Neuromodulation by means of phase-locked auditory stimulation affects key marker of excitability and connectivity during sleep

Sousouri, G., Krugliakova, E., Skoručak, J., Leach, S., Snipes, S., Ferster, M. L., Poian, G. D., Karlen, W., & Huber, R. (2021) · SLEEP · doi:10.1093/sleep/zsab204 · Cited by 21

Mutual interaction between visual homeostatic plasticity and sleep in adult humans

Menicucci, D., Lunghi, C., Zaccaro, A., Morrone, M. C., & Gemignani, A. (2022) · eLife · doi:10.7554/elife.70633 · Cited by 21

Stereotypical spatiotemporal activity patterns during slow-wave activity in the neocortex

Fucke, T., Suchanek, D., Nawrot, M. P., Seamari, Y., Heck, D. H., Aertsen, A., & Boucsein, C. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00811.2010 · Cited by 19

Neural Plasticity Is Involved in Physiological Sleep, Depressive Sleep Disturbances, and Antidepressant Treatments

Zhang, M., Li, R., Wang, Y., & Huang, Z. (2017) · Neural Plasticity · doi:10.1155/2017/5870735 · Cited by 19

On the Hierarchical Organization of Oscillatory Assemblies: Layered Superimposition and a Global Bioelectric Framework

Jerath, R., Beveridge, C., & Jensen, M. A. (2019) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2019.00426 · Cited by 22

Neural Networks and Neurofeedback in Parkinson’s Disease

Esmail, S., & Linden, D. E. J. (2014) · NeuroRegulation · doi:10.15540/nr.1.3-4.240 · Cited by 19

Partial sleep in the context of augmentation of brain function

Pigarev, I. N., & Pigareva, M. L. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00075 · Cited by 20

Thalamic activity during scalp slow waves in humans

Ujma, P. P., Szalárdy, O., Fabó, D., Erőss, L., & Bódizs, R. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119325 · Cited by 18

Alterations in TRN-anterodorsal thalamocortical circuits affect sleep architecture and homeostatic processes in oxidative stress vulnerable Gclm−/− mice

Czekus, C., Steullet, P., López, A. O., Bozic, I., Rusterholz, T., Bandarabadi, M., Kim, Q., & Herrera, C. G. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01700-w · Cited by 18

Cannabis, psychosis and the thalamus: A theoretical review

Vukadinovic, Z., Herman, M., & Rosenzweig, I. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.02.013 · Cited by 18

Detecting cell assemblies by NMF-based clustering from calcium imaging data

Nagayama, M., Aritake, T., Hino, H., Kanda, T., Miyazaki, T., Yanagisawa, M., Akaho, S., & Murata, N. (2022) · Neural Networks · doi:10.1016/j.neunet.2022.01.023 · Cited by 17

A circuit from the locus coeruleus to the anterior cingulate cortex modulates offspring interactions in mice

Corona, A., Choe, J., Muñoz-Castañeda, R., Osten, P., & Shea, S. D. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112771 · Cited by 19

Analysis of the role of the low threshold currents IT and Ih in intrinsic delta oscillations of thalamocortical neurons

Amarillo, Y., Mato, G., & Nadal, M. S. (2015) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2015.00052 · Cited by 19

Spontaneous Up states in vitro: a single-metric index of the functional maturation and regional differentiation of the cerebral cortex

Rigas, P., Adamos, D. A., Sigalas, C., Tsakanikas, P., Laskaris, N., & Skaliora, I. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00059 · Cited by 17

Prefrontal Cortical GABAergic Dysfunction Contributes to Aberrant UP-State Duration in APP Knockout Mice

Huo, Q., Chen, M., He, Q., Zhang, J., Li, B., Jin, K., Chen, X., Long, C., & Yang, L. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw218 · Cited by 17

The neurophysiological basis of excessive daytime sleepiness: suggestions of an altered state of consciousness

Hitchcott, P. K., Menicucci, D., Frumento, S., Zaccaro, A., & Gemignani, A. (2019) · Sleep And Breathing · doi:10.1007/s11325-019-01865-9 · Cited by 18

Slow Oscillation–Spindle Coupling Predicts Sequence-Based Language Learning

Cross, Z. R., Helfrich, R. F., Corcoran, A. W., Dede, A. J. O., Kohler, M. J., Coussens, S. W., Zou-Williams, L., Schlesewsky, M., Gaskell, M. G., Knight, R. T., et al. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.2193-23.2024 · Cited by 21

Spontaneous and electrically modulated spatiotemporal dynamics of the neocortical slow oscillation and associated local fast activity

Greenberg, A., & Dickson, C. T. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.07.034 · Cited by 18

Effects of Hallucinogens on Neuronal Activity

Lladó-Pelfort, L., Celada, P., Riga, M. S., Troyano‐Rodriguez, E., Santana, N., & Artigas, F. (2017) · Current topics in behavioral neurosciences · doi:10.1007/7854_2017_473 · Cited by 17

TRPM4 Conductances in Thalamic Reticular Nucleus Neurons Generate Persistent Firing during Slow Oscillations

O’Malley, J. J., Seibt, F., Chin, J., & Beierlein, M. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0324-20.2020 · Cited by 16

Wave propagation of cortical population activity under urethane anesthesia is state dependent

Wanger, T., Takagaki, K., Lippert, M., Goldschmidt, J., & Ohl, F. W. (2013) · BMC Neuroscience · doi:10.1186/1471-2202-14-78 · Cited by 15

Do Brain Oscillations Orchestrate Memory?

Luo, W., & Guan, J. (2018) · Brain Science Advances · doi:10.26599/bsa.2018.9050008 · Cited by 22

Spontaneous neural activity during human non-rapid eye movement sleep

Mascetti, L., Foret, A., Bourdiec, A. S.-L., Muto, V., Kussé, C., Jaspar, M., Matarazzo, L., Dang‐Vu, T. T., Schabus, M., & Maquet, P. (2011) · Progress in brain research · doi:10.1016/b978-0-444-53839-0.00008-9 · Cited by 16

Neuroimaging Of Dreaming: State Of The Art And Limitations

Kussé, C., Muto, V., Mascetti, L., Matarazzo, L., Foret, A., Bourdiec, A. S.-L., & Maquet, P. (2010) · International review of neurobiology · doi:10.1016/s0074-7742(10)92005-9 · Cited by 18

Reduction in cortical gamma synchrony during depolarized state of slow wave activity in mice

Hwang, E., McNally, J. M., & Choi, J. H. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00107 · Cited by 16

Individual slow wave events give rise to macroscopic fMRI signatures and drive the strength of the BOLD signal in human resting-state EEG-fMRI recordings

Ilhan-Bayrakcı, M., Cabral‐Calderín, Y., Bergmann, T. O., Tüscher, O., & Stroh, A. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhab516 · Cited by 17

Thalamic T-Type Calcium Channels as Targets for Hypnotics and General Anesthetics

Stamenić, T. T., & Todorovic, S. M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23042349 · Cited by 16

Chronic Stability of Local Field Potentials Using Amorphous Silicon Carbide Microelectrode Arrays Implanted in the Rat Motor Cortex

Jeakle, E. N., Abbott, J., Usoro, J. O., Wu, Y., Haghighi, P., Radhakrishna, R., Sturgill, B. S., Nakajima, S., Thai, T. T. D., Pancrazio, J. J., et al. (2023) · Micromachines · doi:10.3390/mi14030680 · Cited by 15

Rapid thalamocortical network switching mediated by cortical synchronization underlies propofol-induced EEG signatures: a biophysical model

Soplata, A. E., Adam, E. M., Brown, E. N., Purdon, P. L., McCarthy, M. M., & Kopell, N. (2023) · Journal of Neurophysiology · doi:10.1152/jn.00068.2022 · Cited by 15

Infragranular layers lead information flow during slow oscillations according to information directionality indicators

Amigó, J. M., Monetti, R., Tort‐Colet, N., & Sanchez-Vives, M. V. (2015) · Journal of Computational Neuroscience · doi:10.1007/s10827-015-0563-7 · Cited by 15

Ionotropic glutamate receptor GluA4 and T‐type calcium channel Ca v 3.1 subunits control key aspects of synaptic transmission at the mouse L5B‐POm giant synapse

Seol, M., & Kuner, T. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13084 · Cited by 15

Early recovery of frontal EEG slow wave activity during propofol sedation predicts outcome after cardiac arrest

Kortelainen, J., Ala‐Kokko, T., Tiainen, M., Strbian, D., Rantanen, K. K., Laurila, J. J., Koskenkari, J. K., Kallio, M., Toppila, J. P., Väyrynen, E., et al. (2021) · Resuscitation · doi:10.1016/j.resuscitation.2021.05.032 · Cited by 14

Broadband macroscopic cortical oscillations emerge from intrinsic neuronal response failures

Goldental, A., Vardi, R., Sardi, S., Sabo, P., & Kanter, I. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00065 · Cited by 14

Brain oscillatory activity during sleep shows unknown dysfunctions in early encephalopathy

Martino, M. E., Fernández-Lorente, J., Romero-Vives, M., Bárcena, R., & Gaztelu, J. M. (2014) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-014-0351-2 · Cited by 14

Neuronal Oscillations and Reactivation Subserving Memory Consolidation

Bergmann, T. O., & Staresina, B. P. (2017) · Studies in neuroscience, psychology and behavioral economics · doi:10.1007/978-3-319-45066-7_12 · Cited by 14

Thalamic Influence on Slow Wave Slope Renormalization During Sleep

Jaramillo, V., Jendoubi, J., Maric, A., Mensen, A., Heyse, N. C., Eberhard‐Moscicka, A. K., Wiest, R., Bassetti, C. L., & Huber, R. (2021) · Annals of Neurology · doi:10.1002/ana.26217 · Cited by 14

The Role of Sleep Spindles in Sleep-Dependent Memory Consolidation

McDevitt, E. A., Krishnan, G. P., Bazhenov, M., & Mednick, S. C. (2017) · Studies in neuroscience, psychology and behavioral economics · doi:10.1007/978-3-319-45066-7_13 · Cited by 16

Modelling Sleep and General Anaesthesia

SLEIGH, J. W., Voss, L. J., Steyn‐Ross, M. L., Steyn‐Ross, D. A., & Wilson, M. T. (2011) · Springer eBooks · doi:10.1007/978-1-4614-0173-5_2 · Cited by 15

Intrinsic coupling modes reveal the functional architecture of cortico-tectal networks

Stitt, I., Galindo-Leon, E. E., Pieper, F., Engler, G., Fiedler, E., Stieglitz, T., & Engel, A. K. (2015) · Science Advances · doi:10.1126/sciadv.1500229 · Cited by 13

Large-scale functional brain networks in human non-rapid eye movement sleep: insights from combined electroencephalographic/functional magnetic resonance imaging studies

Ictor, B. Y. V., Poormaker, I. S., Zisch, M. I. C., Aquet, P. I. M., & Äncke, L. U. J. (2015) · Cited by 13

Emergence of a 600-Hz buzz UP state Purkinje cell firing in alert mice

Cheron, G. A., Prigogine, C., Chéron, J., Márquez‐Ruiz, J., Traub, R. D., & Dan, B. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.01.007 · Cited by 13

Pilot Study of Propofol-induced Slow Waves as a Pharmacologic Test for Brain Dysfunction after Brain Injury

Kortelainen, J., Väyrynen, E., Huuskonen, U., Laurila, J., Koskenkari, J. K., Backman, J. T., Alahuhta, S., Seppänen, T., & Ala-Kokko, T. I. (2016) · Anesthesiology · doi:10.1097/aln.0000000000001385 · Cited by 13

Dynamics of Cortical Local Connectivity during Sleep–Wake States and the Homeostatic Process

Miyazaki, T., Kanda, T., Tsujino, N., Ishii, R., Nakatsuka, D., Mariko, K., Kasagi, Y., Hino, H., & Yanagisawa, M. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa012 · Cited by 13

From macro to micro: slow-wave sleep and its pivotal health implications

Ishii, T., Taweesedt, P. T., Chick, C. F., O'Hara, R. M., & Kawai, M. (2024) · Frontiers in Sleep · doi:10.3389/frsle.2024.1322995 · Cited by 15

NMDA receptors are the basis for persistent network activity in neocortex slices

Castro‐Alamancos, M. A., & Favero, M. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00090.2015 · Cited by 12

Beyond the Neuron: Astroglial Regulation of Mammalian Sleep

Frank, M. G. (2011) · Current Topics in Medicinal Chemistry · doi:10.2174/156802611797470321 · Cited by 12

Relationship between cortical state and spiking activity in the lateral geniculate nucleus of marmosets

Pietersen, A. N. J., Cheong, S. K., Munn, B., Gong, P., Martin, P. R., & Solomon, S. G. (2017) · The Journal of Physiology · doi:10.1113/jp273569 · Cited by 13

Delayed in vitro Development of Up States but Normal Network Plasticity in Fragile X Circuits

Motanis, H., & Buonomano, D. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13010 · Cited by 13

Spatiotemporal Coordination of Slow-Wave Ongoing Activity across Auditory Cortical Areas

Farley, B. J., & Noreña, A. J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5079-12.2013 · Cited by 12

Local Origin of Slow EEG Waves during Sleep

Timofeev, I. (2013) · Журнал высшей нервной деятельности им И П Павлова · doi:10.7868/s0044467713010139 · Cited by 13

The Memory, Cognitive and PsychologicalFunctions of Sleep: Update from Electroencephalographic and Neuroimaging Studies

Kirov, R., & Br, S. (2012) · InTech eBooks · doi:10.5772/22929 · Cited by 12

Polymorphisms in ion channel genes: emerging roles in pain

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Non-rapid eye movement sleep slow-wave activity features are associated with amyloid accumulation in older adults with obstructive sleep apnoea

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UP states rise from the depths

Hughes, S. W., & Crunelli, V. (2013) · Nature Neuroscience · doi:10.1038/nn.3313 · Cited by 11

Response of sleep slow oscillations to acoustic stimulation is evidenced by distinctive synchronization processes

Navarrete, M., Osorio-Forero, A., Gómez, A., Henao, D., Segura-Quijano, F. E., Quyen, M. L. V., & Valderrama, M. (2023) · SLEEP · doi:10.1093/sleep/zsad110 · Cited by 13

Modeling the role of the thalamus in resting-state functional connectivity: Nature or structure

Cabrera-Álvarez, J., Doorn, N., Maestú, F., & Susi, G. (2023) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011007 · Cited by 11

Sleep is Essential for Mental Health: Potential Role of Slow Oscillations

Aquino, G., Alfì, G., Riemann, D. W., Laurino, M., Menicucci, D., Piarulli, A., Palagini, L., & Gemignani, A. (2024) · Current Sleep Medicine Reports · doi:10.1007/s40675-024-00277-w · Cited by 15

Rhythmic dendritic Ca2+ oscillations in thalamocortical neurons during slow non‐REM sleep‐related activity in vitro

Errington, A. C., Hughes, S. W., & Crunelli, V. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.232132 · Cited by 11

Slow‐wave activity preceding the onset of 10–15‐Hz sleep spindles and 5–9‐Hz oscillations in electroencephalograms in rats with and without absence seizures

Sitnikova, E., Grubov, V., & Hramov, A. E. (2019) · Journal of Sleep Research · doi:10.1111/jsr.12927 · Cited by 11

Brain-wide neural co-activations in resting human

Ding, L., Shou, G., Cha, Y., Sweeney, J. A., & Yuan, H. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119461 · Cited by 13

Propagating population activity patterns during spontaneous slow waves in the thalamus of rodents

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Dynamism in Activity of the Neural Networks in Brain is the Basis of Sleep-Wakefulness Oscillations

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Assessing EEG slow wave activity during anesthesia using Hilbert-Huang Transform

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Forehead electrodes sufficiently detect propofol-induced slow waves for the assessment of brain function after cardiac arrest

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Neocortical Focus

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Corticothalamic Rhythms during States of Reduced Vigilance

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Sleep and Neuronal Plasticity: Cellular Mechanisms of Corticothalamic Oscillations

Luppi, P. (2004) · CRC Press eBooks · doi:10.1201/9780203496732-7 · Cited by 1

Essential Thalamic Contribution to Slow Waves of Natural Sleep

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The thalamocortical network as a single slow wave-generating unit

Crunelli, V., David, F., Lörincz, M. L., & Hughes, S. W. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.09.001 · Cited by 171

The Slow (4 Hz) Oscillation in Reticular Thalamic and Thalamocortical Neurons: Scenario of Sleep Rhythm Generation in Interacting Thalamic and Neocortical Networks

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