Functional Neuroimaging Insights into the Physiology of Human Sleep.
Open accessAbstract
Functional brain imaging has been used in humans to noninvasively investigate the neural mechanisms underlying the generation of sleep stages. On the one hand, REM sleep has been associated with the activation of the pons, thalamus, limbic areas, and temporo-occipital cortices, and the deactivation of prefrontal areas, in line with theories of REM sleep generation and dreaming properties. On the other hand, during non-REM (NREM) sleep, decreases in brain activity have been consistently found in the brainstem, thalamus, and in several cortical areas including the medial prefrontal cortex (MPFC), in agreement with a homeostatic need for brain energy recovery. Benefiting from a better temporal resolution, more recent studies have characterized the brain activations related to phasic events within specific sleep stages. In particular, they have demonstrated that NREM sleep oscillations (spindles and slow waves) are indeed associated with increases in brain activity in specific subcortical and cortical areas involved in the generation or modulation of these waves. These data highlight that, even during NREM sleep, brain activity is increased, yet regionally specific and transient. Besides refining the understanding of sleep mechanisms, functional brain imaging has also advanced the description of the functional properties of sleep. For instance, it has been shown that the sleeping brain is still able to process external information and even detect the pertinence of its content. The relationship between sleep and memory has also been refined using neuroimaging, demonstrating post-learning reactivation during sleep, as well as the reorganization of memory representation on the systems level, sometimes with long-lasting effects on subsequent memory performance. Further imaging studies should focus on clarifying the role of specific sleep patterns for the processing of external stimuli, as well as the consolidation of freshly encoded information during sleep.
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Some brain regions supporting episodic future simulation in wake are conspicuously deactivated during sleep, including dorsolateral prefrontal cortex and regions of the posterior parietal lobes.
“Prospective cognition during sleep also differs from that during wake in that some brain regions supporting episodic future stimulation in wake are conspicuously deactivated during sleep, including dorsolateral prefrontal cortex and regions of the posterior parietal lobes [64–66].”
From Constructive episodic simulation in dreams (2022) · cites this paper as [65]
The REM Sleep passage (indexed as Abstract; page unavailable) reports that activity in the dorsolateral prefrontal cortex and inferior parietal cortex decreases during REM sleep compared with wakefulness. It does not identify these regions as supporting episodic future simulation, and its finding is specific to REM sleep rather than sleep generally. (LLM, conf=0.86)
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Cites
Co-Planar Stereotaxic Atlas of the Human Brain
Talairach, J., & Tournoux, P. (1988) · Medical Entomology and Zoology · Cited by 11,798 · see citing works
Rechtschaffen, A. (1968) · Medical Entomology and Zoology · Cited by 11,772 · see citing works
Wolpert, E. (1969) · Archives of General Psychiatry · doi:10.1001/archpsyc.1969.01740140118016 · Cited by 9,814 · see citing works
Co-planar stereotaxic atlas of the human brain
Laitinen, L. (1989) · Clinical Neurology and Neurosurgery · doi:10.1016/0303-8467(89)90128-5 · Cited by 7,565 · see citing works
Diekelmann, S., & Born, J. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2762 · Cited by 3,760 · see citing works
Reactivation of hippocampal ensemble memories during sleep
Wilson, M. A., & McNaughton, B. L. (1994) · Science · doi:10.1126/science.8036517 · Cited by 3,118 · see citing works
Sleep function and synaptic homeostasis
Tononi, G., & Cirelli, C. (2006) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2005.05.002 · Cited by 2,151 · see citing works
Huber, R., Felice Ghilardi, M., Massimini, M., & Tononi, G. (2004) · Nature · doi:10.1038/nature02663 · Cited by 1,854 · see citing works
Boosting slow oscillations during sleep potentiates memory
Marshall, L., Helgadóttir, H., Mölle, M., & Born, J. (2006) · Nature · doi:10.1038/nature05278 · Cited by 1,792 · see citing works
A Method for Removing Imaging Artifact from Continuous EEG Recorded during Functional MRI
Allen, P. J., Josephs, O., & Turner, R. (2000) · NeuroImage · doi:10.1006/nimg.2000.0599 · Cited by 1,301 · see citing works
Heart rate variability: measurement and clinical utility.
Kleiger, R. E., Stein, P. K., & Bigger, J. T. (2005) · Annals of Noninvasive Electrocardiology · doi:10.1111/j.1542-474x.2005.10101.x · Cited by 1,290 · see citing works
Regional cerebral blood flow throughout the sleep-wake cycle. An H2(15)O PET study
Braun, A. (1997) · Brain · doi:10.1093/brain/120.7.1173 · Cited by 1,268 · see citing works
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 · see citing works
Brainstem Control of Wakefulness and Sleep
Steriade, M., & McCarley, R. W. (1990) · doi:10.1007/978-1-4757-4669-3 · Cited by 1,188 · see citing works
Odor cues during slow-wave sleep prompt declarative memory consolidation
Rasch, B., Büchel, C., Gais, S., & Born, J. (2007) · Science · doi:10.1126/science.1138581 · Cited by 1,181 · see citing works
The role of sleep in learning and memory
Maquet, P. (2001) · Science · doi:10.1126/science.1062856 · Cited by 1,177 · see citing works
Functional neuroanatomy of human rapid-eye-movement sleep and dreaming
Maquet, P., Péters, J.-M., Aerts, J., Delfiore, G., Degueldre, C., Luxen, A., & Franck, G. (1996) · Nature · doi:10.1038/383163a0 · Cited by 1,168 · see citing works
Temporally structured replay of awake hippocampal ensemble activity during rapid eye movement sleep
Louie, K., & Wilson, M. A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00186-6 · Cited by 1,148 · see citing works
Overnight therapy? The role of sleep in emotional brain processing
Walker, M. P., & van der Helm, E. (2009) · Psychological Bulletin · doi:10.1037/a0016570 · Cited by 1,087 · see citing works
Coordinated interactions between hippocampal Ripples and Cortical Spindles during Slow-Wave Sleep
Siapas, A. G., & Wilson, M. A. (1998) · Neuron · doi:10.1016/s0896-6273(00)80629-7 · Cited by 1,052 · see citing works
Effects of early and late nocturnal sleep on declarative and procedural memory
Plihal, W., & Born, J. (1997) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1997.9.4.534 · Cited by 1,026 · see citing works
Gennaro, L. D., & Ferrara, M. (2003) · Sleep Medicine Reviews · doi:10.1053/smrv.2002.0252 · Cited by 925 · see citing works
The thalamus as a neuronal oscillator
Steriade, M., & Deschênes, M. (1984) · Brain Research Reviews · doi:10.1016/0165-0173(84)90017-1 · Cited by 916 · see citing works
Allen, P. J., Polizzi, G., Krakow, K., Fish, D. R., & Lemieux, L. (1998) · NeuroImage · doi:10.1006/nimg.1998.0361 · Cited by 914 · see citing works
Steriade, M., Nunez, A., & Amzica, F. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-08-03266.1993 · Cited by 894 · see citing works
Amygdaloid projections to the mesencephalon, pons and medulla oblongata in the cat
Hopkins, D. A., & Holstege, G. (1978) · Experimental Brain Research · doi:10.1007/bf00239551 · Cited by 866 · see citing works
Learning-dependent increases in sleep spindle density
Gais, S., Mölle, M., Helms, K., & Born, J. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06830.2002 · Cited by 859 · see citing works
Are spatial memories strengthened in the human hippocampus during slow wave sleep?
Peigneux, P., Laureys, S., Fuchs, S., Collette, F., Perrin, F., Reggers, J., Phillips, C., Degueldre, C., Del Fiore, G., Aerts, J., et al. (2004) · Neuron · doi:10.1016/j.neuron.2004.10.007 · Cited by 766 · see citing works
Critchley, H. D., Corfield, D. R., Chandler, M. P., Mathias, C. J., & Dolan, R. J. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.t01-1-00259.x · Cited by 757 · see citing works
Experience-dependent changes in cerebral activation during human REM sleep
Maquet, P., Laureys, S., Peigneux, P., Fuchs, S., Petiau, C., Phillips, C., Aerts, J., Del Fiore, G., Degueldre, C., Meulemans, T., et al. (2000) · Nature Neuroscience · doi:10.1038/77744 · Cited by 747 · see citing works
Llinás, R. R., & Paré, D. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90075-y · Cited by 641 · see citing works
The deafferented reticular thalamic nucleus generates spindle rhythmicity
Steriade, M., Domich, L., Oakson, G., & Deschenes, M. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.57.1.260 · Cited by 640 · see citing works
Neuronal Plasticity in Thalamocortical Networks during Sleep and Waking Oscillations
Steriade, M., & Timofeev, I. (2003) · Neuron · doi:10.1016/s0896-6273(03)00065-5 · Cited by 638 · see citing works
Grouping of spindle activity during slow oscillations in human non-rapid eye movement sleep
Mölle, M., Marshall, L., Gais, S., & Born, J. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-24-10941.2002 · Cited by 617 · see citing works
Functional neuroimaging of normal human sleep by positron emission tomography
Maquet (2000) · Journal of Sleep Research · doi:10.1046/j.1365-2869.2000.00214.x · Cited by 581 · see citing works
Arm immobilization causes cortical plastic changes and locally decreases sleep slow wave activity
Huber, R., Ghilardi, M. F., Massimini, M., Ferrarelli, F., Riedner, B. A., Peterson, M. J., & Tononi, G. (2006) · Nature Neuroscience · doi:10.1038/nn1758 · Cited by 579 · see citing works
The whats and whens of sleep-dependent memory consolidation
Diekelmann, S., Wilhelm, I., & Born, J. (2009) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2008.08.002 · Cited by 566 · see citing works
Sleep Spindles and Their Significance for Declarative Memory Consolidation
Schabus, M., Gruber, G., Parapatics, S., Sauter, C., Klösch, G., Anderer, P., Klimesch, W., Saletu, B., & Zeitlhofer, J. (2004) · Sleep · doi:10.1093/sleep/27.7.1479 · Cited by 560 · see citing works
Early sleep triggers memory for early visual discrimination skills
Gais, S., Plihal, W., Wagner, U., & Born, J. (2000) · Nature Neuroscience · doi:10.1038/81881 · Cited by 558 · see citing works
Altered brain response to verbal learning following sleep deprivation
Drummond, S. P. A., Brown, G. G., Gillin, J. C., Stricker, J. L., Wong, E. C., & Buxton, R. B. (2000) · Nature · doi:10.1038/35001068 · Cited by 557 · see citing works
Takashima, A., Petersson, K. M., Rutters, F., Tendolkar, I., Jensen, O., Zwarts, M. J., McNaughton, B. L., & Fernández, G. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507774103 · Cited by 557 · see citing works
Functional Neuroanatomy of Human Slow Wave Sleep
Maquet, P., Degueldre, C., Delfiore, G., Aerts, J. J., Peters, J., Luxen, A., & Franck, G. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-08-02807.1997 · Cited by 514 · see citing works
Forebrain activation in REM sleep: an FDG PET study
Nofzinger, E. A., Mintun, M. A., Wiseman, M., Kupfer, D. J., & Moore, R. Y. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00807-x · Cited by 501 · see citing works
Functional neuroimaging of normal human sleep by positron emission tomography
Aquet, P. I. M. (2000) · Cited by 496 · see citing works
Hemodynamic cerebral correlates of sleep spindles during human non-rapid eye movement sleep
Schabus, M., Dang-Vu, T. T., Albouy, G., Balteau, E., Boly, M., Carrier, J., Darsaud, A., Degueldre, C., Desseilles, M., Gais, S., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0703084104 · Cited by 488 · see citing works
Self-citationBoth the Hippocampus and Striatum Are Involved in Consolidation of Motor Sequence Memory
Albouy, G., Sterpenich, V., Balteau, E., Vandewalle, G., Desseilles, M., Dang-Vu, T., Darsaud, A., Ruby, P., Luppi, P.-H., Degueldre, C., et al. (2008) · Neuron · doi:10.1016/j.neuron.2008.02.008 · Cited by 463 · see citing works
Self-citationSpontaneous neural activity during human slow wave sleep
Dang‐Vu, T. T., Schabus, M., Desseilles, M., Albouy, G., Boly, M., Darsaud, A., Gais, S., Rauchs, G., Virginie Sterpenich, A., Vandewalle, G., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0801819105 · Cited by 436 · see citing works
Self-citationSleep transforms the cerebral trace of declarative memories
Gais, S., Albouy, G., Boly, M., Dang-Vu, T. T., Darsaud, A., Desseilles, M., Rauchs, G., Schabus, M., Sterpenich, V., Vandewalle, G., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705454104 · Cited by 412 · see citing works
Self-citationDaytime sleep condenses the time course of motor memory consolidation
Korman, M., Doyon, J., Doljansky, J., Carrier, J., Dagan, Y., & Karni, A. (2007) · Nature Neuroscience · doi:10.1038/nn1959 · Cited by 408 · see citing works
Overnight verbal memory retention correlates with the number of sleep spindles
Clemens, Z., Fabó, D., & Halász, P. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.01.011 · Cited by 405 · see citing works
Auditory Processing across the Sleep-Wake Cycle
Portas, C. M., Krakow, K., Allen, P., Josephs, O., Armony, J. L., & Frith, C. D. (2000) · Neuron · doi:10.1016/s0896-6273(00)00169-0 · Cited by 392 · see citing works
The sequential hypothesis of the function of sleep
Giuditta, A., Ambrosini, M. V., Montagnese, P., Mandile, P., Cotugno, M., Zucconi, G. G., & Vescia, S. (1995) · Behavioural Brain Research · doi:10.1016/0166-4328(95)00012-i · Cited by 382 · see citing works
Ellenbogen, J. M., Hulbert, J. C., Stickgold, R., Dinges, D. F., & Thompson-Schill, S. L. (2006) · Current Biology · doi:10.1016/j.cub.2006.05.024 · Cited by 377 · see citing works
Effects of early and late nocturnal sleep on priming and spatial memory
Plihal, W., & Born, J. (1999) · Psychophysiology · doi:10.1111/1469-8986.3650571 · Cited by 364 · see citing works
Hofle, N., Paus, T., Reutens, D. C., Fiset, P., Gotman, J., Evans, A. C., & Jones, B. E. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-12-04800.1997 · Cited by 360 · see citing works
Sleep facilitates consolidation of emotional declarative memory
Hu, P., Stylos-Allan, M., & Walker, M. P. (2006) · Psychological Science · doi:10.1111/j.1467-9280.2006.01799.x · Cited by 355 · see citing works
Are corticothalamic ‘up’ states fragments of wakefulness?
Destexhe, A., Hughes, S. W., Rudolph, M., & Crunelli, V. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.04.006 · Cited by 355 · see citing works
Low-frequency rhythms in the thalamus of intact-cortex and decorticated cats
Timofeev, I., & Steriade, M. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.76.6.4152 · Cited by 353 · see citing works
Functional topography of the human nonREM sleep electroencephalogram
Finelli, L. A., Borbély, A. A., & Achermann, P. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01597.x · Cited by 351 · see citing works
Sleep-dependent learning and motor-skill complexity
Kuriyama, K., Stickgold, R., & Walker, M. P. (2004) · Learning & Memory · doi:10.1101/lm.76304 · Cited by 334 · see citing works
Peigneux, P., Laureys, S., Fuchs, S., Destrebecqz, A., Collette, F., Delbeuck, X., Phillips, C. L. M., Aerts, J. J., Fiore, G. D., Degueldre, C., et al. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00278-7 · Cited by 309 · see citing works
Sleep-dependent motor memory plasticity in the human brain
Walker, M. P., Stickgold, R., Alsop, D., Gaab, N., & Schlaug, G. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.04.007 · Cited by 308 · see citing works
Left-insular cortex lesions perturb cardiac autonomic tone in humans
Oppenheimer, S. M., Kedem, G., & Martin, W. M. (1996) · Clinical Autonomic Research · doi:10.1007/bf02281899 · Cited by 308 · see citing works
Brief sleep after learning keeps emotional memories alive for years
Wagner, U., Hallschmid, M., Rasch, B., & Born, J. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.03.061 · Cited by 296 · see citing works
Human regional cerebral glucose metabolism during non-rapid eye movement sleep in relation to waking
Nofzinger, E. A., Buysse, D. J., Miewald, J. M., Meltzer, C. C., Price, J. C., Sembrat, R. C., Ombao, H., Reynolds, C. F., Monk, T. H., Hall, M., et al. (2002) · Brain · doi:10.1093/brain/awf103 · Cited by 295 · see citing works
Maquet, P., Dive, D., Salmon, E., Sadzot, B., Franco, G., Poirrier, R., von Frenckell, R., & Franck, G. (1990) · Brain Research · doi:10.1016/0006-8993(90)91099-3 · Cited by 292 · see citing works
State-dependent spike-timing relationships between hippocampal and prefrontal circuits during sleep
Wierzynski, C. M., Lubenov, E. V., Gu, M., & Siapas, A. G. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.011 · Cited by 289 · see citing works
The relationships between memory systems and sleep stages
Rauchs, G., Desgranges, B., Foret, J., & Eustache, F. (2005) · Journal of Sleep Research · doi:10.1111/j.1365-2869.2005.00450.x · Cited by 279 · see citing works
An ultra short episode of sleep is sufficient to promote declarative memory performance
Lahl, O., WISPEL, C., WILLIGENS, B., & Pietrowsky, R. (2008) · Journal of Sleep Research · doi:10.1111/j.1365-2869.2008.00622.x · Cited by 279 · see citing works
Shift from hippocampal to neocortical centered retrieval network with consolidation
Takashima, A., Nieuwenhuis, I. L. C., Jensen, O., Talamini, L. M., Rijpkema, M., & Fernández, G. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.0799-09.2009 · Cited by 276 · see citing works
Fronto‐occipital EEG power gradients in human sleep
Werth, E., Achermann, P., & Borbély, A. A. (1997) · Journal of Sleep Research · doi:10.1046/j.1365-2869.1997.d01-36.x · Cited by 276 · see citing works
Datta, S. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-22-08607.2000 · Cited by 273 · see citing works
Ribeiro, S., Gervasoni, D., Soares, E. S., Zhou, Y., Lin, S.-C., Pantoja, J., Lavine, M., & Nicolelis, M. A. L. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020024 · Cited by 272 · see citing works
Kaufmann, C., Wehrle, R., Wetter, T. C., Holsboer, F., Auer, D. P., Pollmächer, T., & Czisch, M. (2005) · Brain · doi:10.1093/brain/awh686 · Cited by 269 · see citing works
Sleep-related hippocampo-cortical interplay during emotional memory recollection
Sterpenich, V., Albouy, G., Boly, M., Vandewalle, G., Darsaud, A., Balteau, E., Dang-Vu, T. T., Desseilles, M., D'Argembeau, A., Gais, S., et al. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050282 · Cited by 265 · see citing works
Self-citationSrivastava, G., Crottaz‐Herbette, S., Lau, K. M., Glover, G. H., & Menon, V. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.09.041 · Cited by 264 · see citing works
Schabus, M., Hödlmoser, K., Gruber, G., Sauter, C., Anderer, P., Klösch, G., Parapatics, S., Saletu, B., Klimesch, W., & Zeitlhofer, J. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04694.x · Cited by 261 · see citing works
Self-citationFunctional neuroimaging insights into how sleep and sleep deprivation affect memory and cognition
Chee, M. W. L., & Chuah, L. Y. M. (2008) · Current Opinion in Neurology · doi:10.1097/wco.0b013e3283052cf7 · Cited by 261 · see citing works
Motor Memory Consolidation in Sleep Shapes More Effective Neuronal Representations
Fischer, S., Nitschke, M. F., Melchert, U. H., Erdmann, C., & Born, J. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1743-05.2005 · Cited by 255 · see citing works
Doyon, J., Korman, M., Morin, A., Dostie, V., Tahar, A. H., Benali, H., Karni, A., Ungerleider, L. G., & Carrier, J. (2009) · Experimental Brain Research · doi:10.1007/s00221-009-1748-y · Cited by 247 · see citing works
Maquet, P., Smith, C. T., & Stickgold, R. (2003) · doi:10.1093/acprof:oso/9780198574002.001.0001 · Cited by 240 · see citing works
Maintaining memories by reactivation
Rasch, B., & Born, J. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.11.007 · Cited by 240 · see citing works
Maquet, P., Ruby, P., Maudoux, A., Albouy, G., Sterpenich, V., Dang-Vu, T., Desseilles, M., Boly, M., Perrin, F., Peigneux, P., et al. (2005) · Progress in Brain Research · doi:10.1016/s0079-6123(05)50016-5 · Cited by 239 · see citing works
Self-citationEncoding Difficulty Promotes Postlearning Changes in Sleep Spindle Activity during Napping
Schmidt, C., Peigneux, P., Muto, V., Schenkel, M., Knoblauch, V., Münch, M. Y., de Quervain, D. J. ‐., Wirz‐Justice, A., & Cajochen, C. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2464-06.2006 · Cited by 230 · see citing works
Sleep's function in the spontaneous recovery and consolidation of memories.
Drosopoulos, S., Schulze, C., Fischer, S., & Born, J. (2007) · Journal of Experimental Psychology: General · doi:10.1037/0096-3445.136.2.169 · Cited by 230 · see citing works
Wehrle, R., Kaufmann, C., Wetter, T. C., Holsboer, F., Auer, D. P., Pollmächer, T., & Czisch, M. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05314.x · Cited by 224 · see citing works
Topographic distribution of sleep spindles in young healthy subjects
ZEITLHOFER, J., GRUBER, G., ANDERER, P., ASENBAUM, S., SCHIMICEK, P., & SALETU, B. (1997) · Journal of Sleep Research · doi:10.1046/j.1365-2869.1997.00046.x · Cited by 222 · see citing works
Brain Control of Wakefulness and Sleep
Steriade, M. 1.-2., & McCarley, R. W. (2005) · Springer eBooks · doi:10.1007/b102230 · Cited by 219 · see citing works
Sleep imaging and the neuro-psychological assessment of dreams
Schwartz, S., & Maquet, P. (2002) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01818-0 · Cited by 218 · see citing works
Sleep promotes the neural reorganization of remote emotional memory
Sterpenich, V., Albouy, G., Darsaud, A., Schmidt, C., Vandewalle, G., Dang Vu, T. T., Desseilles, M., Phillips, C., Degueldre, C., Balteau, E., et al. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.0561-09.2009 · Cited by 217 · see citing works
Self-citationMotor Sequence Learning Increases Sleep Spindles and Fast Frequencies in Post-Training Sleep
(2008) · Sleep · doi:10.5665/sleep/31.8.1149 · Cited by 213 · see citing works
Czisch, M., Wetter, T. C., Kaufmann, C., Pollmächer, T., Holsboer, F., & Auer, D. P. (2002) · NeuroImage · doi:10.1006/nimg.2002.1071 · Cited by 207 · see citing works
Activation of the Insular Cortex During Dynamic Exercise in Humans
WILLIAMSON, J. W., da Nóbrega, A. C. L., McColl, R. W., Mathews, D., Winchester, P., Friberg, L., & Mitchell, J. H. (1997) · The Journal of Physiology · doi:10.1111/j.1469-7793.1997.277bh.x · Cited by 200 · see citing works
Maquet, P., Schwartz, S., Passingham, R. E., & Frith, C. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-04-01432.2003 · Cited by 199 · see citing works
Activation of the insular cortex is affected by the intensity of exercise
WILLIAMSON, J. W., McColl, R. W., Mathews, D., Ginsburg, M., & Mitchell, J. H. (1999) · Journal of Applied Physiology · doi:10.1152/jappl.1999.87.3.1213 · Cited by 191 · see citing works
Functional MRI during sleep: BOLD signal decreases and their electrophysiological correlates
Czisch, M., Wehrle, R., Kaufmann, C., Wetter, T. C., Holsboer, F., Pollmächer, T., & Auer, D. P. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03518.x · Cited by 188 · see citing works
Destrebecqz, A., Peigneux, P., Laureys, S., Degueldre, C., Fiore, G. D., Aerts, J. J., Luxen, A., der Linden, M. V., Cleeremans, A., & Maquet, P. (2005) · Learning & Memory · doi:10.1101/lm.95605 · Cited by 187 · see citing works
Kajimura, N., Uchiyama, M., Takayama, Y., Uchida, S., Uema, T., Kato, M., Sekimoto, M., Watanabe, T., Nakajima, T., Horikoshi, S., et al. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-22-10065.1999 · Cited by 186 · see citing works
Nielsen (2000) · doi:10.1007/s00221-008-1579-2 · Cited by 185 · see citing works
Cerebral correlates of delta waves during non-REM sleep revisited
Dang‐Vu, T. T., Desseilles, M., Laureys, S., Degueldre, C., Perrin, F., Phillips, C. L. M., Maquet, P., & Peigneux, P. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.05.028 · Cited by 183 · see citing works
Self-citationClemens, Z., Fabó, D., & Halász, P. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2006.04.035 · Cited by 179 · see citing works
Interindividual sleep spindle differences and their relation to learning-related enhancements
Schabus, M., Hoedlmoser, K., Pecherstorfer, T., Anderer, P., Gruber, G., Parapatics, S., Sauter, C., Kloesch, G., Klimesch, W., Saletu, B., et al. (2008) · Brain Research · doi:10.1016/j.brainres.2007.10.106 · Cited by 174 · see citing works
Self-citationHoedlmoser, K., Pecherstorfer, T., Gruber, G., Anderer, P., Doppelmayr, M. M., Klimesch, W., & Schabus, M. (2008) · SLEEP · doi:10.5665/sleep/31.10.1401 · Cited by 172 · see citing works
Tamaki, M., Matsuoka, T., Nittono, H., & Hori, T. (2008) · SLEEP · doi:10.1093/sleep/31.2.204 · Cited by 171 · see citing works
Tucker, M. A., & Fishbein, W. (2008) · Sleep · doi:10.1093/sleep/31.2.197 · Cited by 171 · see citing works
Sleep after spatial learning promotes covert reorganization of brain activity
Orban, P., Rauchs, G., Balteau, E., Degueldre, C., Luxen, A., Maquet, P., & Peigneux, P. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510198103 · Cited by 167 · see citing works
Jankel, W. R., & Niedermeyer, E. (1985) · Journal of Clinical Neurophysiology · doi:10.1097/00004691-198501000-00001 · Cited by 166 · see citing works
Datta, S., Mavanji, V., Ulloor, J., & Patterson, E. H. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4111-03.2004 · Cited by 162 · see citing works
Generation of rapid eye movements during paradoxical sleep in humans
Peigneux, P., Laureys, S., Fuchs, S., Delbeuck, X., Degueldre, C., Aerts, J., Delfiore, G., Luxen, A., & Maquet, P. (2001) · NeuroImage · doi:10.1006/nimg.2001.0874 · Cited by 162 · see citing works
Smith, C. T., Nixon, M. R., & Nader, R. S. (2004) · Learning & Memory · doi:10.1101/lm.74904 · Cited by 159 · see citing works
Cellular Basis of Pontine Ponto-geniculo-occipital Wave Generation and Modulation
Datta, S. (1997) · Cellular and Molecular Neurobiology · doi:10.1023/a:1026398402985 · Cited by 156 · see citing works
Laureys, S., Peigneux, P., Phillips, C. L. M., Fuchs, S., Degueldre, C., Aerts, J. J., Fiore, G. D., Petiau, C., Luxen, A., der Linden, M. V., et al. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00269-x · Cited by 155 · see citing works
Pontogeniculooccipital waves: spontaneous visual system activity during rapid eye movement sleep
Callaway, C. W., Lydic, R., Baghdoyan, H. A., & Hobson, J. A. (1987) · Cellular and Molecular Neurobiology · doi:10.1007/bf00711551 · Cited by 153 · see citing works
Topographical Analysis of Sleep Spindle Activity
Jobert, M., Poiseau, É., Jähnig, P., Schulz, H., & Kubicki, S. (2008) · Neuropsychobiology · doi:10.1159/000118923 · Cited by 153 · see citing works
Sleep directly following learning benefits consolidation of spatial associative memory
Talamini, L. M., Nieuwenhuis, I. L. C., Takashima, A., & Jensen, O. (2008) · Learning & Memory · doi:10.1101/lm.771608 · Cited by 151 · see citing works
Sleep, dreams, and sudden death: the case for sleep as an autonomic stress test for the heart
Verrier, R. L., Muller, J. E., & Hobson, J. A. (1996) · Cardiovascular Research · doi:10.1016/s0008-6363(95)00211-1 · Cited by 137 · see citing works
Neuronal Basis of the Slow (<1 Hz) Oscillation in Neurons of the Nucleus Reticularis ThalamiIn Vitro
Blethyn, K. L., Hughes, S. W., Toth, T. I., Cope, D. W., & Crunelli, V. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3607-05.2006 · Cited by 135 · see citing works
Location-Specific Cortical Activation Changes during Sleep after Training for Perceptual Learning
Yotsumoto, Y., Sasaki, Y., Chan, P., Vasios, C. E., Bonmassar, G., Ito, N., Náñez, J. E., Shimojo, S., & Watanabe, T. (2009) · Current Biology · doi:10.1016/j.cub.2009.06.011 · Cited by 129 · see citing works
A role for sleep in brain plasticity
Dang‐Vu, T. T., Desseilles, M., Peigneux, P., & Maquet, P. (2006) · Developmental Neurorehabilitation · doi:10.1080/13638490500138702 · Cited by 129 · see citing works
Self-citationThe Sleeping Brain's Influence on Verbal Memory: Boosting Resistance to Interference
Ellenbogen, J. M., Hulbert, J. C., Jiang, Y., & Stickgold, R. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004117 · Cited by 128 · see citing works
Sleep enhances explicit recollection in recognition memory
Drosopoulos, S., Wagner, U., & Born, J. (2005) · Learning & Memory · doi:10.1101/lm.83805 · Cited by 128 · see citing works
Massimini, M., Rosanova, M., & Mariotti, M. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00373.2002 · Cited by 124 · see citing works
McCarley, R. W., Winkelman, J. W., & Duffy, F. H. (1983) · Brain Research · doi:10.1016/0006-8993(83)90719-9 · Cited by 117 · see citing works
Wehrle, R., Czisch, M., Kaufmann, C., Wetter, T. C., Holsboer, F., Auer, D. P., & Pollm??cher, T. (2005) · NeuroReport · doi:10.1097/00001756-200505310-00015 · Cited by 116 · see citing works
Neuronal activity in the peribrachial area: Relationship to behavioral state control
Datta, S. (1995) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(94)00043-z · Cited by 115 · see citing works
Brain Networks Affected by Synchronized Sleep Visualized by Positron Emission Tomography
Andersson, J., Onoe, H., Hetta, J. E., Lidström, K., Valind, S., Lilja, A., Sundin, A., Fasth, K., Westerberg, G., Broman, J., et al. (1998) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-199807000-00001 · Cited by 115 · see citing works
Paré, D., Steriade, M., Deschênes, M., & Oakson, G. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.57.6.1669 · Cited by 114 · see citing works
Habitual napping moderates motor performance improvements following a short daytime nap
Milner, C. E., Fogel, S. M., & Cote, K. A. (2006) · Biological Psychology · doi:10.1016/j.biopsycho.2006.01.015 · Cited by 113 · see citing works
EEG slow waves and sleep spindles: windows on the sleeping brain
Dijk, D. (1995) · Behavioural Brain Research · doi:10.1016/0166-4328(95)00007-g · Cited by 111 · see citing works
Henderson, L. A., Macey, P. M., Macey, K. E., Frysinger, R. C., Woo, M. A., Harper, R. K., Alger, J. R., Yan-Go, F. L., & Harper, R. M. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00107.2002 · Cited by 109 · see citing works
Slow Wave Sleep and REM Sleep Awakenings Do Not Affect Sleep Dependent Memory Consolidation
Genzel, L., Dresler, M., Wehrle, R., Grözinger, M., & Steiger, A. (2009) · Sleep · doi:10.1093/sleep/32.3.302 · Cited by 107 · see citing works
Cortical Deactivation Induced by Visual Stimulation in Human Slow-Wave Sleep
Born, A. P., Law, I. G., Lund, T. E., Rostrup, E., Hanson, L. G., Wildschiødtz, G., Lou, H. C., & Paulson, O. B. (2002) · NeuroImage · doi:10.1006/nimg.2002.1249 · Cited by 107 · see citing works
The role of the spindle in human information processing of high‐intensity stimuli during sleep
Côté, K. A., Epps, T. M., & Campbell, K. B. (2000) · Journal of Sleep Research · doi:10.1046/j.1365-2869.2000.00188.x · Cited by 100 · see citing works
Cyclic and circadian variations in cardiovascular events*1
Elliott, W. J. (2001) · American Journal of Hypertension · doi:10.1016/s0895-7061(01)02174-4 · Cited by 99 · see citing works
[Electromyographic correlations of sleep in the chronic decorticate & mesencephalic cat].
Jouvet, M., & MICHEL, F. (1959) · PubMed · Cited by 98 · see citing works
Sleep and rest facilitate auditory learning
Gottselig, J. M., Hofer-Tinguely, G., Borbély, A. A., Regel, S. J., Landolt, H., Rétey, J., & Achermann, P. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.05.053 · Cited by 97 · see citing works
Event‐related potentials to tones in the absence and presence of sleep spindles
ELTON, M., Winter, O., Heslenfeld, D. J., Loewy, D. H., Campbell, K. B., & Kok, A. (1997) · Journal of Sleep Research · doi:10.1046/j.1365-2869.1997.00033.x · Cited by 90 · see citing works
Ficca, G. (2004) · Sleep Medicine · doi:10.1016/j.sleep.2004.01.018 · Cited by 90 · see citing works
Acoustic Oddball during NREM Sleep: A Combined EEG/fMRI Study
Czisch, M., Wehrle, R., Stiegler, A., Peters, H., Andrade, K. C., Holsboer, F., & Sämann, P. G. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006749 · Cited by 81 · see citing works
Neuroimaging and sleep medicine
Nofzinger, E. A. (2005) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2004.07.003 · Cited by 80 · see citing works
Mavanji, V., & Datta, S. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02460.x · Cited by 76 · see citing works
Different Roles for REM and Stage 2 Sleep in Motor Learning: A Proposed Model
Smith, C. T., Aubrey, J. B., & Peters, K. R. (2004) · Psychologica Belgica · doi:10.5334/pb.1018 · Cited by 76 · see citing works
Sleep and rest facilitate implicit memory in a visual search task
Mednick, S. C., Makovski, T., Cai, D. J., & Jiang, Y. V. (2009) · Vision Research · doi:10.1016/j.visres.2009.04.011 · Cited by 72 · see citing works
Shaffery, J. P., Roffwarg, H. P., Speciale, S. G., & Marks, G. A. (1999) · Developmental Brain Research · doi:10.1016/s0165-3806(99)00027-9 · Cited by 71 · see citing works
Sleep Processes Exert a Predominant Influence on the 24-h Profile of Heart Rate Variability
Viola, A., Simon, C., Ehrhart, J., Gény, B., Piquard, F., Muzet, A. G., & BRANDENBERGER, G. (2002) · Journal of Biological Rhythms · doi:10.1177/0748730402238236 · Cited by 68 · see citing works
Sleep Modulates the Neural Substrates of Both Spatial and Contextual Memory Consolidation
Rauchs, G., Orban, P., Schmidt, C., Albouy, G., Balteau, E., Degueldre, C., Schnackers, C., Virginie Sterpenich, A., Tinguely, G., Luxen, A., et al. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002949 · Cited by 62 · see citing works
Scalp Topography of the Spontaneous K-Complex and of Delta-Waves in Human Sleep
Happe, S., Anderer, P., Gruber, G., Klösch, G., Saletu, B., & Zeitlhofer, J. (2002) · Brain Topography · doi:10.1023/a:1019992523246 · Cited by 54 · see citing works
Yamashita, K.-I., Hirose, S., Kunimatsu, A., Aoki, S., Chikazoe, J., Jimura, K., Masutani, Y., Abe, O., Ohtomo, K., Miyashita, Y., et al. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.1328-09.2009 · Cited by 51 · see citing works
Schabus, M., Hoedlmoser, K., Pecherstorfer, T., & Klösch, G. (2005) · Somnologie - Schlafforschung und Schlafmedizin · doi:10.1111/j.1439-054x.2005.00054.x · Cited by 49 · see citing works
Desseilles, M., Dang‐Vu, T. T., Laureys, S., Peigneux, P., Degueldre, C., Phillips, C. L. M., & Maquet, P. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.06.008 · Cited by 47 · see citing works
Self-citationSuppression of PGO waves in the kitten: Anatomical effects on the lateral geniculate nucleus
Davenne, D., & Adrien, J. (1984) · Neuroscience Letters · doi:10.1016/0304-3940(84)90325-2 · Cited by 44 · see citing works
Slow wave sleep and recollection in recognition memory
Daurat, A., Terrier, P., Foret, J., & Tiberge, M. (2007) · Consciousness and Cognition · doi:10.1016/j.concog.2006.06.011 · Cited by 38 · see citing works
Leclercq, Y., Balteau, E., Dang‐Vu, T. T., Schabus, M., Luxen, A., Maquet, P., & Phillips, C. L. M. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.10.017 · Cited by 38 · see citing works
Self-citationXia, Y., & Krukoff, T. L. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00290-2 · Cited by 34 · see citing works
Davenne, D., Frégnac, Y., Imbert, M., & Adrien, J. (1989) · Brain Research · doi:10.1016/0006-8993(89)90570-2 · Cited by 28 · see citing works
Davenne, D., & Adrien, J. (1987) · Brain Research · doi:10.1016/0006-8993(87)90735-9 · Cited by 24 · see citing works
Marini, G., Gritti, I., & Mancia, M. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90276-8 · Cited by 21 · see citing works
Still Missing Some Significant Ingredients
Schabus, M. (2009) · SLEEP · doi:10.1093/sleep/32.3.291 · Cited by 17 · see citing works
Regulation of circulation and breathing during sleep: experimental aspects.
Parmeggiani, P. L. (1985) · PubMed · Cited by 14 · see citing works
[THE PHASIC ELECTRICAL ACTIVITY OF THE CORTEX AND THALAMUS DURING DESYCHONIZED SLEEP IN CATS].
Hobson, J. A. (1964) · PubMed · Cited by 14 · see citing works
Neuroimaging of REM sleep and dreaming
Dang‐Vu, T. T., Schabus, M., Desseilles, M., Schwartz, S., & Maquet, P. (2007) · Repository of the University of Namur · Cited by 13 · see citing works
Self-citationPossible Mechanisms Contributing to Memory Consolidation During Sleep
(2006) · Journal of Sleep Research · doi:10.1111/j.1365-2869.2006.00540_6.x · Cited by 10 · see citing works
Sleep and Sleep States: PET Activation Patterns
Dang‐Vu, T. T., Desseilles, M., Peigneux, P., Laureys, S., & Maquet, P. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00056-5 · Cited by 8 · see citing works
Self-citationSleep: Implications for Theories of Dreaming and Consciousness
Dang‐Vu, T. T., Schabus, M., Cologan, V., & Maquet, P. (2009) · Elsevier eBooks · doi:10.1016/b978-012373873-8.00072-4 · Cited by 4 · see citing works
Self-citation
Flagged first, then by citations
2 of the 166 references couldn’t be matched to a known paper.
Research works printed but not linked: 9
- [3]Mouret J, Jeannerod M, Jouvet M. L'activite éelectrique du systeme visuel au cours de la phase paradoxale du sommeil chez le chat. J Physiol (Paris) 1963;55:305–6. [Google Scholar]
- [59]Datta S. PGO wave generation: mechanism and functional significance. In: Mallick BN, Inoue S, editors. Rapid eye movement sleep. New Delhi: Narosa Publishing House; 1999. pp. 91–106. [Google Scholar]
- [61]Hobson JA. L'activitée éelectrique du cortex et du thalamus au cours du sommeil déesynchronisée chez le chat. C R Soc Biol (Paris) 1964;158:2131–5. [PubMed] [Google Scholar]
- [62]Jouvet M, Michel F. Corréelations éelectromyographiques du sommeil chez le Chat déecortiquée et méesencéephalique chronique. C R Soc Biol (Paris) 1959;153:422–5. [PubMed] [Google Scholar]
- [63]Mikiten TH, Niebyl PH, Hendley CD. EEG desynchronization during behavioral sleep associated with spike discharges from the thalamus of the cat. Fed Proc. 1961;20:327. [Google Scholar]
- [100]Yeshenko O, Moelle M, Marshall L, Born J, Sara SJ. Locus coeruleus firing during SWS is time locked to slow oscillations: possible contribution of the noradrenergic system to off-line information processing in rats. J Sleep Res. 2006;15:11. [Google Scholar]
- [104]Portas CM, Krakow K, Allen P, Josephs O, Armony JL, Frith CD. Auditory processing across the sleep-wake cycle: simultaneous EEG and fMRI monitoring in humans. Neuron. 2000;28:991–9. doi: 10.1016/s0896-6273(00)00169-0. [DOI] [PubMed] [Google Scholar] · DOI · Paper page
- [137]Gais S, Albouy G, Boly M, et al. Sleep transforms the cerebral trace of declarative memories. Proc Natl Acad Sci U S A. 2007;104:18778–83. doi: 10.1073/pnas.0705454104. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI · Paper page
- [141]Schabus M, Höodlmoser K, Pecherstorfer T, Klöosch G. Influence of midday naps on declarative memory performance and motivation. Somnology. 2005;9:148–53. [Google Scholar]
Cited by
Sorted by citations
Rasch, B., & Born, J. (2013) · Physiological Reviews · doi:10.1152/physrev.00032.2012 · Cited by 2,783 · see citing works
“, parietal and prefrontal cortices) (189, 253, 764, 769, 1335).”
The role of sleep in emotional brain function
Goldstein, A. N., & Walker, M. P. (2014) · Annual Review of Clinical Psychology · doi:10.1146/annurev-clinpsy-032813-153716 · Cited by 1,052 · see citing works
“…the brain areas recognized to support fear acquisition and extinction (mPFC, amygdala, hippocampus) are all reactivated during REM sleep (Dang-Vu et al 2010, Miyauchi et al 2009, Nofzinger 2005, Phelps et al 2004), and through such REM sleep brain network restoration, may aide the…”
BackgroundSleep and Alzheimer disease pathology--a bidirectional relationship
Ju, Y.-E. S., Lucey, B. P., & Holtzman, D. M. (2014) · Nature Reviews Neurology · doi:10.1038/nrneurol.2013.269 · Cited by 996 · see citing works
Vyazovskiy, V. V., Olcese, U., Hanlon, E. C., Nir, Y., Cirelli, C., & Tononi, G. (2011) · Nature · doi:10.1038/nature10009 · Cited by 865 · see citing works
Sleep and anxiety: From mechanisms to interventions
Chellappa, S. L., & Aeschbach, D. (2022) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2021.101583 · Cited by 509 · see citing works
Sleep and emotional processing
Tempesta, D., Socci, V., De Gennaro, L., & Ferrara, M. (2018) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2017.12.005 · Cited by 443 · see citing works
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 294 · see citing works
“PET studies of N3 sleep confirm a frontal predominance of slow waves in human NREMsleep (Dang-Vu et al., 2010).”
BackgroundMonoaminergic neuropathology in Alzheimer’s disease
Šimić, G., Leko, M. B., Wray, S., Harrington, C. R., Delalle, I., Milošević, N. J., Bažadona, D., Buée, L., de Silva, R., Giovanni, G. D., et al. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.04.001 · Cited by 289 · see citing works
“A uthor M anuscript A uthor M anuscript A uthor M anuscript A uthor M anuscript et al., 2009; Dang-Vu et al., 2010).”
Discovery of key whole-brain transitions and dynamics during human wakefulness and non-REM sleep
Stevner, A. B. A., Vidaurre, D., Cabral, J., Rapuano, K. M., Nielsen, S. F. V., Tagliazucchi, E., Laufs, H., Vuust, P., Deco, G., Woolrich, M. W., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-08934-3 · Cited by 268 · see citing works
The role of REM sleep theta activity in emotional memory
Hutchison, I. C., & Rathore, S. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01439 · Cited by 245 · see citing works
“Functional neuroimaging studies reveal significantly increased activation in the amygdala, striatum, hippocampus, medial prefrontal cortex and insula, which are areas strongly associated with emotional processing in wake (Nofzinger, 2005; Miyauchi et al., 2009; Dang-Vu et al., 2010).”
BackgroundSleep deprivation, oxidative stress and inflammation
Atrooz, F., & Salim, S. (2019) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2019.03.001 · Cited by 258 · see citing works
Effects of sleep on memory for conditioned fear and fear extinction.
Pace-Schott, E. F., Germain, A., & Milad, M. R. (2015) · Psychological Bulletin · doi:10.1037/bul0000014 · Cited by 218 · see citing works
“, 2002) that decreases further with the deepening of NREM sleep (Dang-Vu et al., 2010; Kaufmann et al., 2006).”
BackgroundInfluentialEmotion, Emotion Regulation and Sleep: An Intimate Relationship
Vandekerckhove, M. M. P., & Wang, Y. (2017) · AIMS neuroscience · doi:10.3934/neuroscience.2018.5.1 · Cited by 225 · see citing works
Slow-wave activity saturation and thalamocortical isolation during propofol anesthesia in humans
Ní Mhuircheartaigh, R., Warnaby, C., Rogers, R., Jbabdi, S., & Tracey, I. (2013) · Science Translational Medicine · doi:10.1126/scitranslmed.3006007 · Cited by 202 · see citing works
Sleeping on the motor engram: The multifaceted nature of sleep-related motor memory consolidation
King, B. R., Hoedlmoser, K., Hirschauer, F., Dolfen, N., & Albouy, G. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.04.026 · Cited by 202 · see citing works
“Oscillatory properties within REM sleep resemble those of wakefulness and oxygen consumption in extrastriate cortical areas is even higher than during waking [see (Dang-Vu et al., 2010) for a review].”
Emotion, emotion regulation and sleep: An intimate relationship
Vandekerckhove, M. M. P., & Wang, Y. (2017) · AIMS neuroscience · doi:10.3934/neuroscience.2018.1.1 · Cited by 190 · see citing works
“More interestingly, the extent of the fear extinction was found to be correlated with the amount of REM-sleep [51,52].”
BackgroundIt's complicated: The relationship between sleep and Alzheimer's disease in humans
Lucey, B. P. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.105031 · Cited by 165 · see citing works
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 · see citing works
Individual Differences in White Matter Diffusion Affect Sleep Oscillations
Piantoni, G., Poil, S., Linkenkaer‐Hansen, K., Verweij, I. M., Ramautar, J. R., Someren, E. J. W. V., & van der Werf, Y. D. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2030-12.2013 · Cited by 152 · see citing works
Measuring consciousness in dreams: The lucidity and consciousness in dreams scale
Voss, U., Schermelleh-Engel, K., Windt, J., Frenzel, C., & Hobson, A. J. (2012) · Consciousness and Cognition · doi:10.1016/j.concog.2012.11.001 · Cited by 150 · see citing works
Heart rate variability: a tool to explore the sleeping brain?
Chouchou, F., & Desseilles, M. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00402 · Cited by 145 · see citing works
“…to wakefulness; whereas REMS is characterized by low-amplitude, high-frequency EEG rhythms, rapid eye movements (REM), and muscular atonia despite global brain activity similar to wakefulness (called “paradoxical” sleep) (Desseilles et al., 2008, 2011b; Dang-Vu et al., 2010; Dang-Vu, 2012).”
Sleep and the functional connectome
Picchioni, D., Duyn, J. H., & Horovitz, S. G. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.067 · Cited by 115 · see citing works
Losing the struggle to stay awake: Divergent thalamic and cortical activity during microsleeps
Poudel, G. R., Innes, C., Bones, P. J., Watts, R., & Jones, R. D. (2012) · Human Brain Mapping · doi:10.1002/hbm.22178 · Cited by 119 · see citing works
“Simultaneous fMRI/ EEG studies of transition from wakefulness to sleep provide evidence for deactivation of both cortical and subcortical activity during NREM sleep compared with wakefulness [reviewed by Dang-Vu et al., 2010].”
Sprenger, T., & Borsook, D. (2012) · Current Opinion in Neurology · doi:10.1097/wco.0b013e3283532ca3 · Cited by 119 · see citing works
What is the link between hallucinations, dreams, and hypnagogic–hypnopompic experiences?
Waters, F., Blom, J. D., Dang-Vu, T. T., Cheyne, A. J., Alderson-Day, B., Woodruff, P., & Collerton, D. (2016) · Schizophrenia Bulletin · doi:10.1093/schbul/sbw076 · Cited by 119 · see citing works
Self-citationSleep habits, academic performance, and the adolescent brain structure
Urrila, A. S., Eric Artiges, A., Massicotte, J., Miranda, R., Vulser, H., Frère, P., Lapidaire, W., Lemaître, H., Penttilä, J., Conrod, P., et al. (2017) · Scientific Reports · doi:10.1038/srep41678 · Cited by 115 · see citing works
Adenosine, Caffeine, and Performance: From Cognitive Neuroscience of Sleep to Sleep Pharmacogenetics
Urry, E., & Landolt, H. (2014) · Current topics in behavioral neurosciences · doi:10.1007/7854_2014_274 · Cited by 108 · see citing works
“non-rapid-eye-movement (NREM) sleep (Dang-Vu et al. 2010), which represents the primary”
BackgroundElectroencephalographic Variation during End Maintenance and Emergence from Surgical Anesthesia
Chander, D., García, P. S., MacColl, J. N., Illing, S., & SLEIGH, J. W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0106291 · Cited by 105 · see citing works
“Although the different sleep stages were arbitrarily and heuristically defined, based on EEG patterns described above [5,47], they have been successfully used by clinicians and researchers to relate sleep physiology to functional neuroanatomy [48], consolidation of memory [49–51], and sleep disorders [52,53].”
MethodSleep: a synchrony of cell activity‐driven small network states
Krueger, J. M., Huang, Y. H., Rector, D. M., & Buysse, D. J. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12238 · Cited by 95 · see citing works
“Several sleepregulatory circuits, such as the hypothalamic ventrolateral preoptic area, are well characterized and reviewed extensively elsewhere (Jones, 2003; Saper et al., 2005; Datta & Maclean, 2007; Szymusiak & McGinty, 2008).”
BackgroundStructural brain correlates of human sleep oscillations
Saletin, J. M., van der Helm, E., & Walker, M. P. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.06.021 · Cited by 93 · see citing works
“Interestingly, and further compatible with a sleep protection hypothesis (Dang-Vu et al., 2010a; De Gennaro and Ferrara, 2003; Landis et al., 2004), this same sleep spindle metric explained inter-individual differences in both sleep efficiency (R 2 = 0.22, p = 0.027; those with slower frequency…”
InfluentialHefti, K., Holst, S. C., Sóvágó, J., Bachmann, V., Buck, A., Ametamey, S. M., Scheidegger, M., Berthold, T., Gomez‐Mancilla, B., Seifritz, E., et al. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.07.030 · Cited by 93 · see citing works
The REM sleep circuit and how its impairment leads to REM sleep behavior disorder
Iranzo, Á. (2018) · Cell and Tissue Research · doi:10.1007/s00441-018-2852-8 · Cited by 92 · see citing works
Heterogeneity of arousals in human sleep: A stereo-electroencephalographic study
Peter‐Derex, L., Magnin, M., & Bastuji, H. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.07.057 · Cited by 90 · see citing works
Functional connectivity of paired default mode network subregions in primary insomnia
Dai, X., Nie, X., Shao, Y., Liu, S., Li, H., Wan, A.-L., Nie, S., & Peng, D.-C. (2015) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s95224 · Cited by 90 · see citing works
Frontal beta-theta network during REM sleep
Vijayan, S., Lepage, K., Kopell, N., & Cash, S. (2017) · eLife · doi:10.7554/elife.18894 · Cited by 72 · see citing works
“DOI: 10.7554/eLife.18894 1 of 19 Ribary, 1993; Steriade et al., 1996), and pontine-geniculate-occipital (PGO) waves (Calvo and Fer- nández-Guardiola, 1984; Datta, 1997; Datta and Hobson, 1994; Steriade et al., 1989).”
InfluentialSleep and dreaming are for important matters
Perogamvros, L., Dang-Vu, T. T., Desseilles, M., & Schwartz, S. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00474 · Cited by 77 · see citing works
“More specifically, decreases of brain perfusion and brain glucose metabolism in the brainstem, thalamus, basal ganglia, basal forebrain and across several cortical areas including the medial prefrontal cortex (mPFC) and precuneus have been demonstrated (Dang-Vu et al., 2010).”
BackgroundSelf-citationOffline memory consolidation during waking rest
Wamsley, E. J. (2022) · Nature Reviews Psychology · doi:10.1038/s44159-022-00072-w · Cited by 76 · see citing works
Holst, S. C., & Landolt, H. (2018) · Sleep Medicine Clinics · doi:10.1016/j.jsmc.2018.03.002 · Cited by 75 · see citing works
Early Failure of the Default‐Mode Network and the Pathogenesis of Alzheimer's Disease
Šimić, G., Leko, M. B., Borovečki, F., & Hof, P. R. (2014) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.12260 · Cited by 73 · see citing works
Alzheimer's disease and sleep disturbances: a review
Borges, C. R., Poyares, D. R., Piovezan, R. D., Nitríni, R., & Brucki, S. M. D. (2019) · Arquivos de Neuro-Psiquiatria · doi:10.1590/0004-282x20190149 · Cited by 76 · see citing works
Miano, S., Parisi, P., & Villa, M. P. (2012) · Medical Hypotheses · doi:10.1016/j.mehy.2012.04.020 · Cited by 74 · see citing works
Cipolli, C., Ferrara, M., De Gennaro, L., & Plazzi, G. (2017) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2016.07.005 · Cited by 67 · see citing works
Scalp spindles are associated with widespread intracranial activity with unexpectedly low synchrony
Frauscher, B., von Ellenrieder, N., Dubeau, F., & Gotman, J. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.10.048 · Cited by 68 · see citing works
“Recent research points to the importance of spindles formemory consolidation, cortical development, and sleep stability (Khazipov et al., 2004; Schabus et al., 2004; Dang-Vu et al., 2010a; Fogel and Smith, 2011).”
Bassetti, C. L., Ferini‐Strambi, L., Brown, S. A., Adamantidis, A., Benedetti, F., Bruni, O., Cajochen, C., Dolenc‐Grošelj, L., Ferri, R., Gais, S., et al. (2015) · European Journal of Neurology · doi:10.1111/ene.12781 · Cited by 68 · see citing works
“independent component analysis), source reconstruction and multivariate pattern classification to provide better insights about the spatiotemporal characteristics of sleep, including its underlying neuronal networks and their oscillations in spindles and slow wave frequencies [92–94].”
BackgroundCooper, D. C., Ziegler, M. G., Milic, M. S., Ancoli‐Israel, S., Mills, P. J., Loredo, J. S., von Känel, R., & Dimsdale, J. E. (2013) · Journal of Sleep Research · doi:10.1111/jsr.12083 · Cited by 60 · see citing works
Role of Sleep Disturbance in the Trajectory of Alzheimer’s Disease
Kang, D. W., Lee, C. U., & Lim, H. K. (2017) · Clinical Psychopharmacology and Neuroscience · doi:10.9758/cpn.2017.15.2.89 · Cited by 60 · see citing works
Sleep Spindles as an Electrographic Element: Description and Automatic Detection Methods
Wallant, D. C. ’., Maquet, P., & Phillips, C. L. M. (2016) · Neural Plasticity · doi:10.1155/2016/6783812 · Cited by 59 · see citing works
Why REM sleep? Clues beyond the laboratory in a more challenging world
Horne, J. (2012) · Biological Psychology · doi:10.1016/j.biopsycho.2012.10.010 · Cited by 58 · see citing works
Chylinski, D., Egroo, M. V., Narbutas, J., Muto, V., Bahri, M. A., Berthomier, C., Salmon, É., Bastin, C., Phillips, C. L. M., Collette, F., et al. (2022) · eLife · doi:10.7554/elife.78191 · Cited by 56 · see citing works
“=3) over the medial prefrontal areas, known to be an early site for A β deposits and the most important generator of SWs during sleep ( Mander et al., 2015 ; Dang-Vu et al., 2005 ; Dang-Vu et al., 2010 ; Saletin et al., 2013 ).”
Olcese, U., Lohuis, M. N. O., & Pennartz, C. M. A. (2018) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00049 · Cited by 49 · see citing works
Guldenmund, P., Gantner, I. S., Baquero, K., Das, T. K., Athena Demertzi, A., Boveroux, P., Bonhomme, V. L., Vanhaudenhuyse, A., Bruno, M., Gosseries, O., et al. (2015) · Brain Connectivity · doi:10.1089/brain.2015.0369 · Cited by 51 · see citing works
“Possible frontal cortex deactivation is also seen during nonrapid eye movement (non-REM) sleep, where increased slow delta waves are associated with decreased frontal cortex metabolism as measured with FDG-PET (Dang-Vu et al., 2010; Muzur et al., 2002).”
The Role of Sleep and the Effects of Sleep Loss on Cognitive, Affective, and Behavioral Processes
Hyndych, A., El-Abassi, R. N., & Mader, E. C. (2025) · Cureus · doi:10.7759/cureus.84232 · Cited by 74 · see citing works
“Dang-Vu et al. highlighted that during normal sleep, functional neuroimaging consistently shows reduced prefrontal cortex activity in slow-wave sleep and increased activation in limbic and paralimbic structures during REM sleep, reflecting the complex role of sleep in regulating brain function [13].”
How amyloid, sleep and memory connect
Lucey, B. P., & Holtzman, D. M. (2015) · Nature Neuroscience · doi:10.1038/nn.4048 · Cited by 49 · see citing works
Gilson, M., Tagliazucchi, E., & Cofré, R. (2023) · Physical review. E · doi:10.1103/physreve.107.024121 · Cited by 48 · see citing works
Holst, S. C., & Landolt, H. (2022) · Sleep Medicine Clinics · doi:10.1016/j.jsmc.2022.03.002 · Cited by 51 · see citing works
“Furthermore, human and animal studies employing different methodologies suggested diverse additional brain regions, neuronal structures and receptors as important regulators of wakefulness and sleep (Maquet et al., 1997; Dang‐Vu et al., 2008; Murphy et al., 2009; Dang‐Vu et al., 2010; Dittrich et al., 2015; Holst et a…”
BackgroundLocal awakening: Regional reorganizations of brain oscillations after sleep
Tsai, P.-J., Chen, S. C.-J., Hsu, C.-Y., Wu, C. W., Wu, Y., Hung, C., Yang, A. C., Liu, P., Biswal, B. B., & Lin, C. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.07.032 · Cited by 44 · see citing works
“However, studies have shown that the simple dichotomy between sleep and wakefulness is invalid (Edgar et al., 1993; Steriade et al., 2001).”
Ang, G., McKillop, L. E., Purple, R. J., Blanco‐Duque, C., Peirson, S. N., Foster, F., Harrison, P. J., Sprengel, R., Davies, K. E., Oliver, P. L., et al. (2018) · Translational Psychiatry · doi:10.1038/s41398-018-0199-2 · Cited by 45 · see citing works
Weigend, S., Holst, S. C., Treyer, V., Tuura, R., Meier, J., Ametamey, S. M., Buck, A., & Landolt, H. (2019) · SLEEP · doi:10.1093/sleep/zsz161 · Cited by 43 · see citing works
“Fourteen VOIs previously associated with sleep–wake regulation [16, 17, 49] were selected for secondary PET image analyses.”
MethodExploring the Effect of Sleep and Reduced Interference on Different Forms of Declarative Memory
Schönauer, M., Pawlizki, A., Köck, C., & Gais, S. (2014) · SLEEP · doi:10.5665/sleep.4258 · Cited by 46 · see citing works
Näsi, T., Virtanen, J., Noponen, T., Toppila, J. P., Salmi, T. K., & Ilmoniemi, R. J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025415 · Cited by 41 · see citing works
Plailly, J., Villalba, M., Vallat, R., Nicolas, A., & Ruby, P. (2019) · Scientific Reports · doi:10.1038/s41598-019-51497-y · Cited by 40 · see citing works
Wide-spread brain activation and reduced CSF flow during avian REM sleep
Ungurean, G., Behroozi, M., Böger, L., Helluy, X., Libourel, P., Güntürkün, O., & Rattenborg, N. C. (2023) · Nature Communications · doi:10.1038/s41467-023-38669-1 · Cited by 44 · see citing works
Specific EEG Sleep Pattern in the Prefrontal Cortex in Primary Insomnia
Perrier, J., Clochon, P., Bertran, F., Couque, C., Bulla, J., Denise, P., & Bocca, M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0116864 · Cited by 40 · see citing works
“The increased sigma power spectrum during stage 3+4 in insomnia patients compared to good sleepers found in the other areas can be view as an increased sleep stability [25].”
BackgroundSleep spindles provide indirect support to the consolidation of emotional encoding contexts
Cairney, S. A., Durrant, S. J., Jackson, R. L., & Lewis, P. A. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.09.016 · Cited by 39 · see citing works
Nocturnal sleep enhances working memory training in Parkinson's disease but not Lewy body dementia
Scullin, M. K., Trotti, L. M., Wilson, A. G., Greer, S. A., & Bliwise, D. L. (2012) · Brain · doi:10.1093/brain/aws192 · Cited by 39 · see citing works
“In addition to offline memory reactivation, slow-wave sleep has generally been linked to synaptic plasticity and cortical reorganization (Tononi and Cirelli, 2003; Takashima et al., 2006; Dang-Vu et al., 2010), thereby making it a candidate for facilitating working memory training.”
BackgroundResultIntegrating sleep, neuroimaging, and computational approaches for precision psychiatry
Goldstein‐Piekarski, A. N., Holt-Gosselin, B., O’Hora, K., & Williams, L. M. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0483-8 · Cited by 38 · see citing works
Rothenberger, S. D., Krafty, R. T., Taylor, B. J., Cribbet, M. R., Thayer, J. F., Buysse, D. J., Kravitz, H. M., Buysse, E. D., & Hall, M. H. (2014) · Psychophysiology · doi:10.1111/psyp.12383 · Cited by 36 · see citing works
“For instance, the ventromedial prefrontal cortex is involved in regulation of both vagal activity and delta EEG power (Dang-Vu et al., 2010; Thayer & Lane, 2000).”
BackgroundDauvilliers, Y. A., Evangelista, E., de Verbizier, D., Barateau, L., & Peigneux, P. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00350 · Cited by 34 · see citing works
Havekes, R., Heckman, P. R. A., Wams, E. J., Stasiukonytė, N., Meerlo, P., & Eisel, U. L. M. (2019) · Cellular Signalling · doi:10.1016/j.cellsig.2019.109420 · Cited by 34 · see citing works
Human REM sleep: influence on feeding behaviour, with clinical implications
Horne, J. A. (2015) · Sleep Medicine · doi:10.1016/j.sleep.2015.04.002 · Cited by 33 · see citing works
McAvoy, M. P., Larson‐Prior, L. J., Ludwikow, M., Zhang, D., Snyder, A. Z., Gusnard, D. L., Raichle, M. E., & d’Avossa, G. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00900.2011 · Cited by 31 · see citing works
Role of sleep in neurodegeneration: the consensus report of the 5th Think Tank World Sleep Forum
Ferini‐Strambi, L., Liguori, C., Lucey, B. P., Mander, B. A., Spira, A. P., Videnović, A., Baumann, C. R., Franco, O. H., Fernandes, M., Gnarra, O., et al. (2023) · Neurological Sciences · doi:10.1007/s10072-023-07232-7 · Cited by 32 · see citing works
“Neuronal metabolic activity measured by 18F-fluorode-oxyglucose PET decreases during NREM sleep [26, 27].”
Perogamvros, L., & Schwartz, S. (2013) · Current topics in behavioral neurosciences · doi:10.1007/7854_2013_271 · Cited by 28 · see citing works
“More specifically, activity decreases in the brainstem, thalamus, basal ganglia, basal forebrain and in several cortical areas including the medial prefrontal cortex (PFC) and precuneus (Dang-Vu et al. 2010).”
BackgroundMishra, A., Yang, P., Manuel, T. J., Newton, A. T., Phipps, M. A., Luo, H., Sigona, M. K., Reed, J. L., Gore, J. C., Grissom, W. A., et al. (2023) · Brain stimulation · doi:10.1016/j.brs.2023.09.013 · Cited by 28 · see citing works
“Alternatively, cingulotomy is performed for pain relief in late-stage cancer pain patients.”
The Influence of EEG References on the Analysis of Spatio-Temporal Interrelation Patterns
Ríos-Herrera, W. A., Olguín-Rodríguez, P. V., Arzate-Mena, J. D., Corsi‐Cabrera, M., Escalona, J., Marín-García, A., Ramos‐Loyo, J., Rivera, A. L., Rivera, D., Berruecos, J. F. Z., et al. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00941 · Cited by 27 · see citing works
“For instance, dominant sources alter drastically during the transition from wake state to sleep (Steriade, 2003) and during sleep cycles (Pace-Schott and Hobson, 2002; Steriade, 2003; Dang-Vu et al., 2010; Brown et al., 2012; Jones, 2019).”
BackgroundCorrelations between adolescent processing speed and specific spindle frequencies
Nader, R. S., & Smith, C. T. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00030 · Cited by 26 · see citing works
“Dang-Vu et al. (2010) observed that the faster spindle activity was associated with more extensive cortical activation; the results from our adolescents suggest that it is the faster (or higher frequency) brain activity that is associated with some forms of intelligence.”
BackgroundThe occurrence of individual slow waves in sleep is predicted by heart rate
Mensen, A., Zhang, Z., Qi, M., & Khatami, R. (2016) · Scientific Reports · doi:10.1038/srep29671 · Cited by 25 · see citing works
Lassmann, Ł., Pollis, M., Żółtowska, A., & Manfredini, D. (2022) · Biomedicines · doi:10.3390/biomedicines10071528 · Cited by 25 · see citing works
Kong, S. D., Gordon, C. J., Hoyos, C. M., Wassing, R., D'Rozario, A. L., Mowszowski, L., Ireland, C., Palmer, J. R., Grunstein, R. R., Shine, J. M., et al. (2023) · Brain Communications · doi:10.1093/braincomms/fcad129 · Cited by 23 · see citing works
“prefrontal cortex, anterior cingulate cortex, and precuneus) regions.(75)”
BackgroundJakobson, A., Fitzgerald, P. B., & Conduit, R. (2012) · Journal of Sleep Research · doi:10.1111/j.1365-2869.2011.00994.x · Cited by 23 · see citing works
“The general consensus from neuroimaging research is that posterior temporo–occipital association regions are activated consistently during REM sleep (Dang-Vu et al., 2010).”
Constructive episodic simulation in dreams
Wamsley, E. J. (2022) · PLOS ONE · doi:10.1371/journal.pone.0264574 · Cited by 22 · see citing works
Autonomic/central coupling benefits working memory in healthy young adults
Chen, P., Whitehurst, L. N., Naji, M., & Mednick, S. C. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107267 · Cited by 26 · see citing works
Shi, Y., Zhang, L., He, C., Yin, Y., Song, R., Chen, S., Fan, D., Zhou, D., Yuan, Y., Xie, C., et al. (2021) · Journal of Affective Disorders · doi:10.1016/j.jad.2021.08.027 · Cited by 22 · see citing works
Horne, J. (2013) · Sleep Medicine · doi:10.1016/j.sleep.2013.05.019 · Cited by 21 · see citing works
Investigating the effect of a nap following experimental trauma on analogue PTSD symptoms
Wilhelm, I., Azza, Y., Brennwald, K., Ehrt‐Schäfer, Y., Seifritz, E., & Kleim, B. (2021) · Scientific Reports · doi:10.1038/s41598-021-83838-1 · Cited by 20 · see citing works
Motor imagery practice benefits during arm immobilization
Debarnot, U., Perrault, A. A., Virginie Sterpenich, A., Legendre, G., Huber, C., Guillot, A., & Schwartz, S. (2021) · Scientific Reports · doi:10.1038/s41598-021-88142-6 · Cited by 21 · see citing works
Building your best day for healthy brain aging—The neuroprotective effects of optimal time use
Mellow, M. L., Dumuid, D., Thacker, J. S., Dorrian, J., & Smith, A. E. (2019) · Maturitas · doi:10.1016/j.maturitas.2019.04.204 · Cited by 19 · see citing works
Akkol, E. K., Bardakçı, H., Yücel, Ç., Karatoprak, G. Ş., Karpuz, B., & Khan, H. Z. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/6168199 · Cited by 20 · see citing works
“This impairment was claimed to be located in subcortical and cortical regions and might be due to the neurons ’ overpolarized silent state during slow-wave sleep [53].”
Belinda, C. D., & Christian, M. S. (2022) · Academy of Management Journal · doi:10.5465/amj.2021.0377 · Cited by 20 · see citing works
Frank, E., Benabou, M., Bentzley, B. S., Bianchi, M. T., Goldstein, T. R., Konopka, G., Maywood, E. S., Pritchett, D., Sheaves, B., & Thomas, J. (2014) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12600 · Cited by 20 · see citing works
Memory traces of long-range coordinated oscillations in the sleeping human brain
Piantoni, G., van der Werf, Y. D., Jensen, O. B., & Someren, E. J. W. V. (2014) · Human Brain Mapping · doi:10.1002/hbm.22613 · Cited by 21 · see citing works
“Reactivation of distributed neuronal networks is thought to be of key importance in memory consolidation, in particular for tasks that require the integration of information from separate systems [Dang-Vu et al., 2010], such as the MT task used in this experiment [Fogel et al., 2007].”
MethodAutonomic Activity during a Daytime Nap Facilitates Working Memory Improvement
Chen, P., Whitehurst, L. N., Naji, M., & Mednick, S. C. (2020) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01588 · Cited by 19 · see citing works
“In addition, SWS has been linked to synaptic plasticity and cortical reorganization (Tononi and Cirelli, 2003; Takashima et al., 2006; Dang-Vu et al., 2010).”
BackgroundZempel, J. M., Politte, D. G., Kelsey, M., Verner, R., Nolan, T. S., Abbas Babajani-feremi, A., Prior, F., & Larson‐Prior, L. J. (2012) · Frontiers in Neurology · doi:10.3389/fneur.2012.00076 · Cited by 21 · see citing works
Altered brain perfusion patterns in wakefulness and slow-wave sleep in sleepwalkers
Desjardins, M.-È., Baril, A., Soucy, J., Dang‐Vu, T. T., Désautels, A., Petit, D., Montplaisir, J. Y., & Zadra, A. L. (2018) · SLEEP · doi:10.1093/sleep/zsy039 · Cited by 20 · see citing works
Self-citationEdwards, C. L., Malinowski, J., Rohner, S. L., Bennett, P. D., Ruby, P. M., & Blagrove, M. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.00831 · Cited by 21 · see citing works
“…eye movement (REM) sleep, is involved in functional reorganization of the brain that subserves emotional memory consolidation (Nishida et al., 2009; Dang-Vu et al., 2010; Wamsley and Stickgold, 2011; Groch et al., 2013, 2015), emotion regulation (Walker and Van der Helm, 2009), and cognitive…”
BackgroundThe Neuroscience of Sleep and Dreams
McNamara, P. (2019) · Cambridge University Press eBooks · doi:10.1017/9781316817094 · Cited by 19 · see citing works
Llewellyn, S. (2016) · Consciousness and Cognition · doi:10.1016/j.concog.2016.09.018 · Cited by 17 · see citing works
Sleep-Dependent Consolidation of Value-Based Learning
Baran, B., Daniels, D., & Spencer, R. M. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075326 · Cited by 17 · see citing works
Stickgold, R., & Wamsley, E. J. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-24288-2.00048-9 · Cited by 17 · see citing works
Zhang, F., Zhong, R., Li, S., Chang, R. C., & Le, W. (2017) · Journal of Neural Transmission · doi:10.1007/s00702-017-1696-9 · Cited by 17 · see citing works
- Authors
- Dang-Vu, T. T., Schabus, M., Desseilles, M., Sterpenich, V., Bonjean, M., & Maquet, P.
- Affiliations
- University of Liège (BE)
- University of Geneva (CH)
- Howard Hughes Medical Institute (US)
- Venue
- SLEEP
- Publisher
- Oxford University Press (OUP)
- Published
- 2010-12
- Volume
- 33
- Issue
- 12
- Pages
- 1589-1603
- ISSN
- 0161-8105 (ISSN-L)
- 1550-9109
- PMC
- PMC2982729
- OpenAlex
- W2101059856
- Cited by
- 284
- References
- 166
- Citations by year
- 2026: 17 · 2025: 27 · 2024: 15 · 2023: 14 · 2022: 20 · 2021: 10 · 2020: 13 · 2019: 38 · 2018: 15 · 2017: 13 · 2016: 12 · 2015: 19 · 2014: 21 · 2013: 26 · 2012: 19
- FWCI
- 1.17
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- SLEEP (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Open Repository and Bibliography (University of Liège) (submittedVersion)
- Repository of the University of Namur (submittedVersion)
- Funders
- National Institute of Biomedical Imaging and Bioengineering (R01EB009282)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and related disorders
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Keywords
- sleep physiology, REM sleep, NREM sleep, sleep stages, dreams, sleep spindles, slow waves, sleep oscillations, brain energy homeostasis, medial prefrontal cortex, sleep and memory, memory consolidation
- MeSH terms
- Brain, Electroencephalography, Humans, Learning, Magnetic Resonance Imaging, Memory, Sleep, Wakefulness, Positron-Emission Tomography
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 ›
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