The DOI matches its Crossref record; 98 of the 98 references it cites were found in a registry or an index.
The slow (<1 Hz) rhythm of non-REM sleep: a dialogue between three cardinal oscillators
Open accessAbstract
The slow (<1 Hz) rhythm, the most important electroencephalogram (EEG) signature of non–rapid eye movement (NREM) sleep, is generally viewed as originating exclusively from neocortical networks. Here we argue that the full manifestation of this fundamental sleep oscillation in a corticothalamic module requires the dynamic interaction of three cardinal oscillators: one predominantly synaptically based cortical oscillator and two intrinsic, conditional thalamic oscillators. The functional implications of this hypothesis are discussed in relation to other EEG features of NREM sleep, with respect to coordinating activities in local and distant neuronal assemblies and in the context of facilitating cellular and network plasticity during slow-wave sleep.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Apart from thalamic afferents and cortical astrocytes, somatostatin positive interneurons inhibiting pyramidal dendrites appear to be specifically implicated in the induction of downstates.161,172,173”
From Sleep—A brain-state serving systems memory consolidation (2023) · cites this paper as [173]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In vivo calcium imaging in naturally sleeping mice revealed that spindles, which nest into a SO upstate are characterized by a unique constellation of activity in cortical microcircuits, where inhibition (by somatostatin positive cells) is released from the dendrites of pyramidal cells that themselves display strongly increased calcium activity, whereas an effective somatic inhibition of the pyram”
From Sleep—A brain-state serving systems memory consolidation (2023) · cites this paper as [173]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“The slow oscillation is generated in cortical networks and can occur in isolated cortical slices (239, 1028, 1198).”
From About Sleep's Role in Memory (2013) · cites this paper as [239]
The cited source says what the claim attributes to it.
In the citing paper
“Nevertheless, the slow oscillation of the intact brain likely reflects an interaction between cortical and thalamic networks (239, 1196).”
From About Sleep's Role in Memory (2013) · cites this paper as [239]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Steriade, M., Nunez, A., & Amzica, F. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-08-03252.1993 · Cited by 1,903
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
McCormick, D. A. (1992) · Progress in Neurobiology · doi:10.1016/0301-0082(92)90012-4 · Cited by 1,117
Research works printed but not linked: 2
- Simon, N.R., Kemp, B., Manshanden, I. & Lopes da Silva, F.H. Whole-head measures of sleep from MEG signals and the ubiquitous “slow oscillation”. Sleep Res. Online 5, 105–113 (2003).
- Jones, E.G. The Thalamus (Plenum Press, New York, 2008).
Cited by
Sorted by citations
Rasch, B., & Born, J. (2013) · Physiological Reviews · doi:10.1152/physrev.00032.2012 · Cited by 2,783
Neurophysiological and Computational Principles of Cortical Rhythms in Cognition
Wang, X.-J. (2010) · Physiological Reviews · doi:10.1152/physrev.00035.2008 · Cited by 1,939
Control of sleep and wakefulness
Brown, R. E., Basheer, R., McKenna, J. T., Strecker, R. E., & McCarley, R. W. (2012) · Physiological Reviews · doi:10.1152/physrev.00032.2011 · Cited by 1,477
Regional Slow Waves and Spindles in Human Sleep
Nir, Y., Staba, R. J., Andrillon, T., Vyazovskiy, V. V., Cirelli, C., Fried, I., & Tononi, G. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.043 · Cited by 924
Hippocampal GABAergic Inhibitory Interneurons
Pelkey, K. A., Chittajallu, R., Craig, M. T., Tricoire, L., Wester, J. C., & McBain, C. J. (2017) · Physiological Reviews · doi:10.1152/physrev.00007.2017 · Cited by 889
Electroencephalogram signatures of loss and recovery of consciousness from propofol
Purdon, P. L., Pierce, E. T., Mukamel, E. A., Prerau, M. J., Walsh, J. L., Wong, K. F. K., Salazar-Gomez, A. F., Harrell, P. G., Sampson, A. L., Cimenser, A., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1221180110 · Cited by 854
Sleep promotes branch-specific formation of dendritic spines after learning
Yang, G., Lai, C. S. W., Cichon, J., Ma, L., Li, W., & Gan, W.-B. (2014) · Science · doi:10.1126/science.1249098 · Cited by 616
Mölle, M., Bergmann, T. O., Marshall, L., & Born, J. (2011) · Sleep · doi:10.5665/sleep.1290 · Cited by 557
Rapid fragmentation of neuronal networks at the onset of propofol-induced unconsciousness
Lewis, L. D., Weiner, V. S., Mukamel, E. A., Donoghue, J., Eskandar, E. N., Madsen, J. R., Anderson, W. S., Hochberg, L. R., Cash, S. S., Brown, E. N., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1210907109 · Cited by 387
Sleep and the single neuron: the role of global slow oscillations in individual cell rest
Vyazovskiy, V. V., & Harris, K. D. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3494 · Cited by 386
Impairments of neural circuit function in Alzheimer's disease
Busche, M. A., & Konnerth, A. (2016) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2015.0429 · Cited by 360
Sleep—A brain-state serving systems memory consolidation
Brodt, S., Inostroza, M., Niethard, N., & Born, J. (2023) · Neuron · doi:10.1016/j.neuron.2023.03.005 · Cited by 343
Sleep Neurophysiological Dynamics Through the Lens of Multitaper Spectral Analysis
Prerau, M. J., Brown, R. E., Bianchi, M. T., Ellenbogen, J. M., & Purdon, P. L. (2016) · Physiology · doi:10.1152/physiol.00062.2015 · Cited by 324
Bosch‐Bouju, C., Hyland, B. I., & Parr‐Brownlie, L. C. (2013) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2013.00163 · Cited by 316
EEG microstates of wakefulness and NREM sleep
Brodbeck, V., Kuhn, A., von Wegner, F., Morzelewski, A., Tagliazucchi, E., Borisov, S. V., Michel, C. M., & Laufs, H. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.05.060 · Cited by 301
Cortical circuit activity underlying sleep slow oscillations and spindles
Niethard, N., Ngo, H.-V. V., Ehrlich, I., & Born, J. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1805517115 · Cited by 245
Oscillating circuitries in the sleeping brain
Adamantidis, A. R., Gutierrez Herrera, C., & Gent, T. C. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0223-4 · Cited by 281
Senzai, Y., Fernández‐Ruiz, A., & Buzsáki, G. (2019) · Neuron · doi:10.1016/j.neuron.2018.12.009 · Cited by 274
The Slow Oscillation in Cortical and Thalamic Networks: Mechanisms and Functions
Neske, G. T. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00088 · Cited by 296
Sleep slow wave changes during the middle years of life: Changes in slow waves with age
Carrier, J., Viens, I., Poirier, G., Robillard, R., Lafortune, M., Vandewalle, G., Martin, N., Barakat, M., Paquet, J., & Filipini, D. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07543.x · Cited by 269
Origin of Active States in Local Neocortical Networks during Slow Sleep Oscillation
Chauvette, S., Volgushev, M., & Timofeev, I. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq009 · Cited by 266
Perri, C. D., Bahri, M. A., Amico, E., Thibaut, A., Heine, L., Antonopoulos, G., Charland‐Verville, V., Wannez, S., Gómez, F. A., Hustinx, R., et al. (2016) · The Lancet Neurology · doi:10.1016/s1474-4422(16)00111-3 · Cited by 277
Slow-wave sleep: From the cell to the clinic
Léger, D., Debellemanière, E., Rabat, A., Bayon, V., Benchenane, K., & Chennaoui, M. (2018) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2018.01.008 · Cited by 284
Making Waves: Initiation and Propagation of Corticothalamic Ca2+ Waves In Vivo
Stroh, A., Adelsberger, H., Groh, A., Rühlmann, C., Fischer, S., Schierloh, A., Deisseroth, K. A., & Konnerth, A. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.031 · Cited by 249
Facilitation of epileptic activity during sleep is mediated by high amplitude slow waves
Frauscher, B., von Ellenrieder, N., Ferrari-Marinho, T., Avoli, M., Dubeau, F., & Gotman, J. (2015) · Brain : a journal of neurology · doi:10.1093/brain/awv073 · Cited by 228
Laminar analysis of slow wave activity in humans
Csercsa, R., Dombovári, B., Fabó, D., Wittner, L., Erőss, L., Entz, L., Sólyom, A., Rásonyi, G., Szűcs, A., Kelemen, A., et al. (2010) · Brain · doi:10.1093/brain/awq169 · Cited by 239
Lüthi, A. (2013) · The Neuroscientist · doi:10.1177/1073858413500854 · Cited by 233
Essential Thalamic Contribution to Slow Waves of Natural Sleep
David, F., Schmiedt, J. T., Taylor, H. L., Orbán, G., Giovanni, G. D., Uebele, V. N., Renger, J. J., Lambert, R. C., Leresche, N., & Crunelli, V. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3169-13.2013 · Cited by 234
Self-citationAge-related changes in the cognitive function of sleep
Pace-Schott, E. F., & Spencer, R. M. C. (2011) · Progress in brain research · doi:10.1016/b978-0-444-53752-2.00012-6 · Cited by 235
Rescue of long-range circuit dysfunction in Alzheimer's disease models
Busche, M. A., Kekuš, M., Adelsberger, H., Noda, T., Förstl, H., Nelken, I., & Konnerth, A. (2015) · Nature Neuroscience · doi:10.1038/nn.4137 · Cited by 221
The Ca V 3.3 calcium channel is the major sleep spindle pacemaker in thalamus
Astori, S., Wimmer, R. D., Prosser, H. M., Corti, C., Corsi, M., Liaudet, N., Volterra, A., Franken, P., Adelman, J. P., & Lüthi, A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105115108 · Cited by 213
Thalamic reticular nucleus induces fast and local modulation of arousal state
Lewis, L. D., Voigts, J., Flores, F. J., Schmitt, L. I., Wilson, M. A., Halassa, M. M., & Brown, E. N. (2015) · eLife · doi:10.7554/elife.08760 · Cited by 215
The Neurobiology of Sleep and Wakefulness
Schwartz, M. D., & Kilduff, T. S. (2015) · Psychiatric Clinics of North America · doi:10.1016/j.psc.2015.07.002 · Cited by 207
Brain state dependent activity in the cortex and thalamus
McCormick, D. A., McGinley, M. J., & Salkoff, D. B. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.10.003 · Cited by 198
Siclari, F., Bernardi, G., Riedner, B. A., LaRocque, J. J., Benca, R. M., & Tononi, G. (2014) · Sleep · doi:10.5665/sleep.4070 · Cited by 181
The Impact of Cortical Deafferentation on the Neocortical Slow Oscillation
Lemieux, M., Chen, J., Lonjers, P., Bazhenov, M., & Timofeev, I. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1156-13.2014 · Cited by 182
Thalamocortical synchronization during induction and emergence from propofol-induced unconsciousness
Flores, F. J., Hartnack, K. E., Fath, A. B., Kim, S., Wilson, M. A., Brown, E. N., & Purdon, P. L. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1700148114 · Cited by 176
Shaping the Default Activity Pattern of the Cortical Network
Sanchez-Vives, M. V., Massimini, M., & Mattia, M. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.015 · Cited by 176
Time Multiplexed Active Neural Probe with 1356 Parallel Recording Sites
Raducanu, B. C., Yazıcıoğlu, R. F., López, C. M., Ballini, M., Putzeys, J., Wang, S., Andrei, A., Rochus, V., Welkenhuysen, M., Helleputte, N. V., et al. (2017) · Sensors · doi:10.3390/s17102388 · Cited by 166
NREM and REM Sleep: Complementary Roles in Recovery after Wakefulness
Vyazovskiy, V. V., & Delogu, A. (2014) · The Neuroscientist · doi:10.1177/1073858413518152 · Cited by 169
Rosanova, M., Fecchio, M., Casarotto, S., Sarasso, S., Casali, A. G., Pigorini, A., Comanducci, A., Seregni, F., Devalle, G., Citerio, G., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06871-1 · Cited by 167
Hays, S. A., Huber, K. M., & Gibson, J. R. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3157-11.2011 · Cited by 163
Local and Widespread Slow Waves in Stable NREM Sleep: Evidence for Distinct Regulation Mechanisms
Bernardi, G., Siclari, F., Handjaras, G., Riedner, B. A., & Tononi, G. (2018) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2018.00248 · Cited by 171
Parallel detection of theta and respiration-coupled oscillations throughout the mouse brain
Tort, A. B. L., Ponsel, S., Jessberger, J., Yanovsky, Y., Brankačk, J., & Draguhn, A. (2018) · Scientific Reports · doi:10.1038/s41598-018-24629-z · Cited by 169
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
Self-citationUP-DOWN cortical dynamics reflect state transitions in a bistable network
Jercog, D., Roxin, A., Barthó, P., Luczak, A., Compte, A., & de la Rocha, J. (2017) · eLife · doi:10.7554/elife.22425 · Cited by 166
Memory improvement via slow-oscillatory stimulation during sleep in older adults
Westerberg, C. E., Florczak, S. M., Weıntraub, S., Mesulam, M. M., Marshall, L., Zee, P. C., & Paller, K. A. (2015) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2015.05.014 · Cited by 171
Tapping the Brakes: Cellular and Synaptic Mechanisms that Regulate Thalamic Oscillations
Fogerson, P. M., & Huguenard, J. R. (2016) · Neuron · doi:10.1016/j.neuron.2016.10.024 · Cited by 155
An inhibitory gate for state transition in cortex
Zucca, S., D’Urso, G., Pasquale, V., Vecchia, D., Pica, G., Bovetti, S., Moretti, C., Varani, S., Molano‐Mazón, M., Chiappalone, M., et al. (2017) · eLife · doi:10.7554/elife.26177 · Cited by 160
Yüzgeç, Ö., Prsa, M., Zimmermann, R. A., & Huber, D. (2018) · Current Biology · doi:10.1016/j.cub.2017.12.049 · Cited by 163
Spinal Cord Injury Immediately Changes the State of the Brain
Aguilar, J., Humanes-Valera, D., Alonso‐Calviño, E., Yagüe, J. G., Moxon, K. A., Oliviero, A., & Foffani, G. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0379-10.2010 · Cited by 151
Sparsity enables estimation of both subcortical and cortical activity from MEG and EEG
Krishnaswamy, P., Obregon-Henao, G., Ahveninen, J., Khan, S., Babadi, B., Iglesias, J. E., Hämäläinen, M., & Purdon, P. L. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1705414114 · Cited by 149
A role for cortical nNOS/NK1 neurons in coupling homeostatic sleep drive to EEG slow wave activity
Morairty, S. R., Dittrich, L., Pasumarthi, R. K., Valladao, D., Heiss, J. E., Gerashchenko, D., & Kilduff, T. S. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1314762110 · Cited by 152
Molecular Mechanisms of Cancer-Induced Sleep Disruption
Walker, W. H., II, & Borniger, J. C. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20112780 · Cited by 149
Global Intracellular Slow-Wave Dynamics of the Thalamocortical System
Sheroziya, M., & Timofeev, I. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4460-13.2014 · Cited by 142
T-Type Ca2+Channels in Normal and Abnormal Brain Functions
Cheong, E., & Shin, H. (2013) · Physiological Reviews · doi:10.1152/physrev.00010.2012 · Cited by 139
Griemsmann, S., Höft, S. P., Bedner, P., Zhang, J., von Staden, E., Beinhauer, A., Degen, J., Dublin, P., Cope, D. W., Richter, N., et al. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu157 · Cited by 132
Self-citationDual function of thalamic low-vigilance state oscillations: rhythm-regulation and plasticity
Crunelli, V., Lörincz, M. L., Connelly, W. M., David, F., Hughes, S. W., Lambert, R. C., Leresche, N., & Errington, A. C. (2018) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.151 · Cited by 131
Self-citationTemporal dynamics of cortical sources underlying spontaneous and peripherally evoked slow waves
Riedner, B. A., Hulse, B. K., Murphy, M. J., Ferrarelli, F., & Tononi, G. (2011) · Progress in Brain Research · doi:10.1016/b978-0-444-53839-0.00013-2 · Cited by 130
McCafferty, C. P., David, F., Venzi, M., Lörincz, M. L., Delicata, F., Atherton, Z., Recchia, G. E., Orbán, G., Lambert, R. C., Giovanni, G. D., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0130-4 · Cited by 125
Self-citationPhillips, K. G., Bartsch, U., McCarthy, A. P., Edgar, D. M., Tricklebank, M. D., Wafford, K. A., & Jones, M. W. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.016 · Cited by 132
The Roles of GABAB Receptors in Cortical Network Activity
Kohl, M. M., & Paulsen, O. (2010) · Advances in pharmacology · doi:10.1016/s1054-3589(10)58009-8 · Cited by 126
Hippocampal memory consolidation during sleep: a comparison of mammals and birds
Rattenborg, N. C., Martínez-González, D., Roth, T. C., & Витальевич, П. В. (2010) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/j.1469-185x.2010.00165.x · Cited by 128
Rabiller, G., He, J.-W., Nishijima, Y., Wong, A. S. W., & Liu, J. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms161025605 · Cited by 124
Electrophysiological correlates of sleep homeostasis in freely behaving rats
Vyazovskiy, V. V., Cirelli, C., & Tononi, G. (2011) · Progress in brain research · doi:10.1016/b978-0-444-53839-0.00002-8 · Cited by 117
A Neocortical Delta Rhythm Facilitates Reciprocal Interlaminar Interactions via Nested Theta Rhythms
Carracedo, L. M., Kjeldsen, H., Cunnington, L. G., Jenkins, A., Schofield, I. S., Cunningham, M. O., Davies, C. H., Traub, R. D., & Whittington, M. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0735-13.2013 · Cited by 114
Sleep, oscillations, interictal discharges, and seizures in human focal epilepsy
Frauscher, B., & Gotman, J. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.04.007 · Cited by 113
Babaeeghazvini, P., Rueda‐Delgado, L. M., Gooijers, J., Swinnen, S. P., & Daffertshofer, A. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.721206 · Cited by 125
Longitudinal sleep EEG trajectories indicate complex patterns of adolescent brain maturation
Feinberg, I., & Campbell, I. G. (2012) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00422.2012 · Cited by 105
Infraslow (<0.1Hz) oscillations in thalamic relay nuclei
Hughes, S. W., Lőrincz, M. L., Parri, H. R., & Crunelli, V. (2011) · Progress in Brain Research · doi:10.1016/b978-0-444-53839-0.00010-7 · Cited by 104
Self-citationChan, R. W., Leong, A. T. L., Ho, L. C., Gao, P. P., Wong, E. C., Dong, C. M., Wang, X., He, J., Chan, Y., Lim, L. W., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1703309114 · Cited by 105
Nobili, L., De Gennaro, L., Proserpio, P., Moroni, F., Sarasso, S., Pigorini, A., De Carli, F., & Ferrara, M. (2012) · Progress in Brain Research · doi:10.1016/b978-0-444-59427-3.00013-7 · Cited by 100
Lehrer, P. M., & Eddie, D. (2013) · Applied Psychophysiology and Biofeedback · doi:10.1007/s10484-013-9217-6 · Cited by 106
Interneuron‐mediated inhibition synchronizes neuronal activity during slow oscillation
Chen, J., Chauvette, S., Skorheim, S. W., Timofeev, I., & Bazhenov, M. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.227462 · Cited by 99
D’Antoni, S., Spatuzza, M., Bonaccorso, C. M., Musumeci, S. A., Ciranna, L., Nicoletti, F., Huber, K. M., & Catania, M. V. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.02.003 · Cited by 97
Ayoub, A., Aumann, D., Hörschelmann, A., Kouchekmanesch, A., Paul, P., Born, J., & Marshall, L. (2013) · Sleep · doi:10.5665/sleep.2722 · Cited by 91
High-frequency oscillations in human and monkey neocortex during the wake–sleep cycle
Quyen, M. L. V., Muller, L., Teleńczuk, B., Halgren, E., Cash, S. S., Hatsopoulos, N. G., Dehghani, N., & Alain Destexhe, A. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1523583113 · Cited by 95
Thuault, S., Malleret, G., Constantinople, C. M., Nicholls, R. E., Chen, I., Zhu, J., Panteleyev, A. A., Vronskaya, S., Nolan, M. F., Bruno, R. M., et al. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2427-12.2013 · Cited by 96
Leresche, N., Lambert, R. C., Errington, A. C., & Crunelli, V. (2011) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-011-1009-3 · Cited by 90
Self-citationA mechanism for learning with sleep spindles
Peyrache, A., & Seibt, J. (2020) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2019.0230 · Cited by 89
Top-down control of arousal and sleep: Fundamentals and clinical implications
Krone, L. B., Frase, L., Piosczyk, H., Selhausen, P., Zittel, S., Jahn, F., Kühn, M., Feige, B., Mainberger, F., Klöppel, S., et al. (2016) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2015.12.005 · Cited by 96
Binder, S., Baier, P. C., Mölle, M., Inostroza, M., Jan Born, A., & Marshall, L. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.12.004 · Cited by 96
How the Human Brain Sleeps: Direct Cortical Recordings of Normal Brain Activity
von Ellenrieder, N., Gotman, J., Zelmann, R., Rogers, C., Nguyen, D. K., Kahane, P., Dubeau, F., & Frauscher, B. (2019) · Annals of Neurology · doi:10.1002/ana.25651 · Cited by 91
Hypocretin as a Hub for Arousal and Motivation
Tyree, S. M., Borniger, J. C., & de Lecea, L. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00413 · Cited by 83
Fiáth, R., Raducanu, B. C., Musa, S., Andrei, A., López, C. M., Hoof, C. A. V., Ruther, P., Aarts, A. A. A., Horváth, D., & Ulbert, I. (2018) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2018.01.060 · Cited by 81
Sustained Neuronal Activity Generated by Glial Plasticity
Pirttimäki, T., Hall, S. D., & Parri, H. R. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5783-10.2011 · Cited by 82
The human thalamus orchestrates neocortical oscillations during NREM sleep
Schreiner, T., Kaufmann, E., Noachtar, S., Mehrkens, J.-H., & Staudigl, T. (2022) · Nature Communications · doi:10.1038/s41467-022-32840-w · Cited by 77
Sleep Slow-Wave Activity Regulates Cerebral Glycolytic Metabolism
Wisor, J. P., Rempe, M. J., Schmidt, M. A., Moore, M. E., & Clegern, W. C. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs189 · Cited by 82
Pink noise: Effect on complexity synchronization of brain activity and sleep consolidation
Zhou, J., Liu, D., Li, X., Ma, J., Zhang, J., & Fang, J. (2012) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2012.04.006 · Cited by 79
Reimann, H. M., & Niendorf, T. (2020) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2020.00008 · Cited by 75
Slow Wave Sleep Induced by GABA Agonist Tiagabine Fails to Benefit Memory Consolidation
Feld, G. B., Wilhelm, I., Ma, Y., Groch, S., Binkofski, F., Mölle, M., & Jan Born, A. (2013) · SLEEP · doi:10.5665/sleep.2954 · Cited by 81
Inhibitory circuits for visual processing in thalamus
Wang, X., Sommer, F. T., & Hirsch, J. A. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.06.004 · Cited by 73
Development of Brain EEG Connectivity across Early Childhood: Does Sleep Play a Role?
Kurth, S., Achermann, P., Rusterholz, T., & LeBourgeois, M. K. (2013) · Brain Sciences · doi:10.3390/brainsci3041445 · Cited by 75
Temporal associations between sleep slow oscillations, spindles and ripples
Oyanedel, C. N., Durán, E., Niethard, N., Inostroza, M., & Born, J. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14906 · Cited by 71
Astroglial regulation of sleep homeostasis
Frank, M. G. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.02.009 · Cited by 72
Stasi, A. M. D., Farisello, P., Marcon, I., Cavallari, S., Forli, A., Vecchia, D., Losi, G., Mantegazza, M., Panzeri, S., Carmignoto, G., et al. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw002 · Cited by 69
Sleep Homeostasis and Models of Sleep Regulation
Achermann, P., & Borbély, A. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-24288-2.00036-2 · Cited by 97
Astroglial Connexin 43 Hemichannels Modulate Olfactory Bulb Slow Oscillations
Roux, L., Madar, A. D., Lacroix, M. M., Yi, C., Benchenane, K., & Giaume, C. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0861-15.2015 · Cited by 73
Focal lesions induce large-scale percolation of sleep-like intracerebral activity in awake humans
Russo, S., Pigorini, A., Mikulan, E., Sarasso, S., Rubino, A., Zauli, F. M., Parmigiani, S., d’Orio, P., Cattani, A., Francione, S., et al. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.117964 · Cited by 64
Lörincz, M. L., Gunner, D., Bao, Y., Connelly, W. M., Isaac, J. T. R., Hughes, S. W., & Crunelli, V. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3603-14.2015 · Cited by 67
Self-citation
Metadata
- Authors
- Crunelli, V., & Hughes, S. W.
- Affiliations
- Cardiff University (GB)
- Eli Lilly (United Kingdom) (GB)
- Corresponding author
- Crunelli, Vincenzo
- Venue
- Nature Neuroscience
- Published
- 2009-12-06
- Volume
- 13
- Issue
- 1
- Pages
- 9-17
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- PMC
- PMC2980822
- OpenAlex
- W2078049175
- Semantic Scholar
- 3ab0af75d4a753ac35afe4eed6a3db4f6dfe8853
- Cited by
- 435
- References
- 98
- Citations by year
- 2026: 7 · 2025: 12 · 2024: 14 · 2023: 15 · 2022: 24 · 2021: 22 · 2020: 23 · 2019: 27 · 2018: 30 · 2017: 28 · 2016: 26 · 2015: 40 · 2014: 39 · 2013: 44 · 2012: 32
- FWCI
- 2.11
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Wellcome Trust (078403, 078311, 78403, 78311, 071436, 71436)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroscience of respiration and sleep
- Keywords
- slow-wave sleep, NREM sleep, EEG oscillations, cell assemblies, network plasticity
- MeSH terms
- Action Potentials, Anesthetics, Animals, Biological Clocks, Brain Mapping, Cats, Cerebral Cortex, Delta Rhythm, Humans, Models, Biological, Nerve Net, Neurons, Sleep Stages, Thalamus, In Vitro Techniques
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
