Dynamic functional connectivity and brain metastability during altered states of consciousness
Open accessAbstract
The scientific study of human consciousness has greatly benefited from the development of non-invasive brain imaging methods. The quest to identify the neural correlates of consciousness combined psychophysical experimentation with neuroimaging tools such as functional magnetic resonance imaging (fMRI) to map the changes in neural activity associated with conscious vs. unconscious percepts. Different neuroimaging methods have also been applied to characterize spontaneous brain activity fluctuations during altered states of consciousness, and to develop quantitative metrics for the level of consciousness. Most of these studies, however, have not explored the dynamic nature of the whole-brain imaging data provided by fMRI. A series of empirical and computational studies strongly suggests that the temporal fluctuations observed in this data present a non-trivial structure, and that this structure is compatible with the exploration of a discrete repertoire of states. In this review we focus on how dynamic neuroimaging can be used to address theoretical accounts of consciousness based on the hypothesis of a dynamic core, i.e. a constantly evolving and transiently stable set of coordinated neurons that constitute an integrated and differentiated physical substrate for each conscious experience. We review work exploring the possibility that metastability in brain dynamics leads to a repertoire of dynamic core states, and discuss how it might be modified during altered states of consciousness. This discussion prompts us to review neuroimaging studies aimed to map the dynamic exploration of the repertoire of states as a function of consciousness. Complementary studies of the dynamic core hypothesis using perturbative methods are also discussed. Finally, we propose that a link between metastability in brain dynamics and the level of consciousness could pave the way towards a mechanistic understanding of altered states of consciousness using tools from dynamical systems theory and statistical physics.
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Cites
Functional connectivity in the motor cortex of resting human brain using echo‐planar mri
Biswal, B., Zerrin Yetkin, F., Haughton, V. M., & Hyde, J. S. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910340409 · Cited by 9,812 · see citing works
Ordering, metastability and phase transitions in two-dimensional systems
Kosterlitz, J. M., & Thouless, D. J. (1973) · Journal of Physics C Solid State Physics · doi:10.1088/0022-3719/6/7/010 · Cited by 9,566 · see citing works
Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging
Fox, M. D., & Raichle, M. E. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2201 · Cited by 6,700 · see citing works
Brain stem reticular formation and activation of the EEG
Moruzzi, G., & Magoun, H. W. (1949) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(49)90219-9 · Cited by 4,307 · see citing works
The brain's default mode network
Raichle, M. E. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071013-014030 · Cited by 3,904 · see citing works
Investigations into resting-state connectivity using independent component analysis
Beckmann, C. F., DeLuca, M., Devlin, J. T., & Smith, S. M. (2005) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2005.1634 · Cited by 3,398 · see citing works
Exploring the brain network: A review on resting-state fMRI functional connectivity
van den Heuvel, M. P., & Hulshoff Pol, H. E. (2010) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2010.03.008 · Cited by 3,326 · see citing works
Tracking whole-brain connectivity dynamics in the resting state
Allen, E. A., Damaraju, E., Plis, S. M., Erhardt, E. B., Eichele, T., & Calhoun, V. D. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs352 · Cited by 2,992 · see citing works
Dynamic functional connectivity: Promise, issues, and interpretations
Hutchison, R. M., Womelsdorf, T., Allen, E. A., Bandettini, P. A., Calhoun, V. D., Corbetta, M., Della Penna, S., Duyn, J. H., Glover, G. H., Gonzalez-Castillo, J., et al. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.079 · Cited by 2,962 · see citing works
Experimental and theoretical approaches to conscious processing
Dehaene, S., & Changeux, J.-P. (2011) · Neuron · doi:10.1016/j.neuron.2011.03.018 · Cited by 2,573 · see citing works
A theoretical model of phase transitions in human hand movements.
Haken, H., Kelso, J. A. S., & Bunz, H. (1985) · Biological Cybernetics · doi:10.1007/bf00336922 · Cited by 2,328 · see citing works
Neuronal Avalanches in Neocortical Circuits
Beggs, J. M., & Plenz, D. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-35-11167.2003 · Cited by 2,325 · see citing works
Conscious, preconscious, and subliminal processing: a testable taxonomy
Dehaene, S., Changeux, J.-P., Naccache, L., Sackur, J., & Sergent, C. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.03.007 · Cited by 2,067 · see citing works
Facing up to the problem of consciousness
Chalmers, D. J. (1996) · Toward a Science of Consciousness · doi:10.7551/mitpress/6860.003.0003 · Cited by 1,966 · see citing works
Principles of Biological Autonomy
Varela, F. J. (2025) · The MIT Press eBooks · doi:10.7551/mitpress/14875.001.0001 · Cited by 1,890 · see citing works
Deisseroth, K. A. (2010) · Nature Methods · doi:10.1038/nmeth.f.324 · Cited by 1,884 · see citing works
Time–frequency dynamics of resting-state brain connectivity measured with fMRI
Chang, C., & Glover, G. H. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.12.011 · Cited by 1,808 · see citing works
Nichols, D. E. (2016) · Pharmacological Reviews · doi:10.1124/pr.115.011478 · Cited by 1,762 · see citing works
An information integration theory of consciousness
Tononi, G. (2004) · BMC Neuroscience · doi:10.1186/1471-2202-5-42 · Cited by 1,757 · cited 15× · see citing works
“While a number of mechanistic models have been formulated, our focus is on those based on the phenomenology of consciousness that were pioneered by Tononi & Edelman (Tononi and Edelman, 1998; Edelman and Tononi, 2000; Tononi, 2004).”
BackgroundInfluentialMultimodal fast optical interrogation of neural circuitry
Zhang, F., Wang, L., Brauner, M., Liewald, J. F., Kay, K., Watzke, N., Wood, P. G., Bamberg, E., Nagel, G., GOTTSCHALK, A. R., et al. (2007) · Nature · doi:10.1038/nature05744 · Cited by 1,742 · see citing works
(1990) · CaltechAUTHORS (California Institute of Technology) · Cited by 1,661 · see citing works
Tononi, G., Sporns, O., & Edelman, G. M. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.11.5033 · Cited by 1,626 · see citing works
Neural correlates of consciousness: progress and problems
Koch, C., Massimini, M., Boly, M., & Tononi, G. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.22 · Cited by 1,600 · see citing works
Tononi, G. (1998) · Science · doi:10.1126/science.282.5395.1846 · Cited by 1,561 · see citing works
Breakdown of cortical effective connectivity during sleep
Massimini, M., Ferrarelli, F., Huber, R., Esser, S. K., Singh, H., & Tononi, G. (2005) · Science · doi:10.1126/science.1117256 · Cited by 1,534 · see citing works
Phase transitions and critical behavior in human bimanual coordination
Kelso, J. A. S. (1984) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1984.246.6.r1000 · Cited by 1,516 · see citing works
The Chronnectome: Time-Varying Connectivity Networks as the Next Frontier in fMRI Data Discovery
Calhoun, V. D., Miller, R. L., Pearlson, G. D., & Adalı, T. (2014) · Neuron · doi:10.1016/j.neuron.2014.10.015 · Cited by 1,388 · see citing works
(1996) · Journal of Consciousness Studies · Cited by 1,338 · see citing works
Facing Up to the Problem of Consciousness
Chalmers, D. J. (1998) · Routledge eBooks · doi:10.4324/9780203826430-11 · Cited by 1,334 · 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
Carhart-Harris, R. L., Leech, R., Hellyer, P. J., Shanahan, M., Feilding, A., Tagliazucchi, E., Chialvo, D. R., & Nutt, D. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00020 · Cited by 1,252 · see citing works
Self-citationA theoretically based index of consciousness independent of sensory processing and behavior
Casali, A. G., Gosseries, O., Rosanova, M., Boly, M., Sarasso, S., Casali, K. R., Casarotto, S., Bruno, M.-A., Laureys, S., Tononi, G., et al. (2013) · Science Translational Medicine · doi:10.1126/scitranslmed.3006294 · Cited by 1,246 · see citing works
Alkire, M. T., Hudetz, A. G., & Tononi, G. (2008) · Science · doi:10.1126/science.1149213 · Cited by 1,245 · see citing works
Emergent complex neural dynamics
Chialvo, D. R. (2010) · Nature Physics · doi:10.1038/nphys1803 · Cited by 1,165 · see citing works
Long-Range Temporal Correlations and Scaling Behavior in Human Brain Oscillations
Linkenkaer-Hansen, K., Nikouline, V. V., Palva, J. M., & Ilmoniemi, R. J. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-04-01370.2001 · Cited by 1,149 · see citing works
BOLD correlates of EEG topography reveal rapid resting-state network dynamics
Britz, J., Van De Ville, D., & Michel, C. M. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.02.052 · Cited by 1,070 · see citing works
Brain function in coma, vegetative state, and related disorders
Laureys, S., Owen, A. M., & Schiff, N. D. (2004) · The Lancet Neurology · doi:10.1016/s1474-4422(04)00852-x · Cited by 1,033 · see citing works
The conscious access hypothesis: origins and recent evidence
Baars, B. J. (2002) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01819-2 · Cited by 994 · see citing works
Spreng, R. N., & Grady, C. L. (2010) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21282 · Cited by 985 · see citing works
The AASM Manual for the Scoring of Sleep and Associated Events : Rules
Iber, C. (2007) · Medical Entomology and Zoology · Cited by 925 · see citing works
How is our self related to midline regions and the default-mode network?
Qin, P., & Northoff, G. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.05.028 · Cited by 909 · see citing works
Global workspace theory of consciousness: toward a cognitive neuroscience of human experience
Baars, B. J. (2005) · Progress in Brain Research · doi:10.1016/s0079-6123(05)50004-9 · Cited by 888 · see citing works
Shine, J. M., Bissett, P. G., Bell, P. T., Koyejo, O., Balsters, J. H., Gorgolewski, K. J., Moodie, C. A., & Poldrack, R. A. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.018 · Cited by 886 · see citing works
On spurious and real fluctuations of dynamic functional connectivity during rest
Leonardi, N., & Van De Ville, D. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2014.09.007 · Cited by 828 · see citing works
Díaz-Cruz, J. L., Hernández‐Sánchez, J., Moretti, S., & Rosado, A. (2008) · AIP conference proceedings · Cited by 800 · see citing works
Millisecond by Millisecond, Year by Year: Normative EEG Microstates and Developmental Stages
Koenig, T. W., Prichep, L. S., Lehmann, D., Valdes-Sosa, P. A., Bräker, E., Kleinlogel, H., Isenhart, R., & John, E. R. (2002) · NeuroImage · doi:10.1006/nimg.2002.1070 · Cited by 797 · see citing works
Dynamic reconfiguration of frontal brain networks during executive cognition in humans
Braun, U., Schäfer, A., Walter, H., Erk, S., Romanczuk-Seiferth, N., Haddad, L., Schweiger, J. I., Grimm, O., Heinz, A., Tost, H., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1422487112 · Cited by 791 · see citing works
Cortical coordination dynamics and cognition
Bressler, S. L., & Kelso, J. A. S. (2001) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01564-3 · Cited by 789 · see citing works
(2000) · Cited by 778 · see citing works
Brain Dynamics Underlying the Nonlinear Threshold for Access to Consciousness
Del Cul, A., Baillet, S., & Dehaene, S. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050260 · Cited by 753 · see citing works
Tognoli, E., & Kelso, J. A. S. (2014) · Neuron · doi:10.1016/j.neuron.2013.12.022 · Cited by 718 · see citing works
Criticality in Large-Scale Brain fMRI Dynamics Unveiled by a Novel Point Process Analysis
Tagliazucchi, E., Balenzuela, P., Fraiman, D., & Chialvo, D. R. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00015 · Cited by 716 · see citing works
Self-citationHutchison, R. M., Womelsdorf, T., Gati, J. S., Everling, S., & Menon, R. S. (2012) · Human Brain Mapping · doi:10.1002/hbm.22058 · Cited by 715 · see citing works
Temporal dynamics of spontaneous MEG activity in brain networks
de Pasquale, F., Della Penna, S., Snyder, A. Z., Lewis, C., Mantini, D., Marzetti, L., Belardinelli, P., Ciancetta, L., Pizzella, V., Romani, G. L., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913863107 · Cited by 698 · see citing works
Decoupling of the brain's default mode network during deep sleep
Horovitz, S. G., Braun, A. R., Carr, W. S., Picchioni, D., Balkin, T. J., Fukunaga, M., & Duyn, J. H. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0901435106 · Cited by 685 · see citing works
Signature of consciousness in the dynamics of resting-state brain activity
Barttfeld, P., Uhrig, L., Sitt, J. D., Sigman, M., Jarraya, B., & Dehaene, S. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1418031112 · Cited by 670 · see citing works
Rethinking segregation and integration: contributions of whole-brain modelling
Deco, G., Tononi, G., Boly, M., & Kringelbach, M. L. (2015) · Nature reviews. Neuroscience · doi:10.1038/nrn3963 · Cited by 658 · see citing works
Liu, X., & Duyn, J. H. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1216856110 · Cited by 647 · see citing works
Tagliazucchi, E., & Laufs, H. (2014) · Neuron · doi:10.1016/j.neuron.2014.03.020 · Cited by 637 · see citing works
Self-citationCan sliding-window correlations reveal dynamic functional connectivity in resting-state fMRI?
Hindriks, R., Adhikari, M. H., Murayama, Y., Ganzetti, M., Mantini, D., Logothetis, N. K., & Deco, G. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.11.055 · Cited by 632 · see citing works
<i>The Neural Correlates of Consciousness</i>: <i>An Update</i>
Tononi, G., & Koch, C. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1440.004 · Cited by 627 · see citing works
A Universe of Consciousness: How Matter Becomes Imagination
Brakel, L. (2001) · Neuropsychoanalysis · doi:10.1080/15294145.2001.10773360 · Cited by 617 · see citing works
EEG microstate sequences in healthy humans at rest reveal scale-free dynamics.
Van De Ville, D., Britz, J., & Michel, C. M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1007841107 · Cited by 606 · see citing works
Distilling the neural correlates of consciousness
Aru, J., Bachmann, T., Singer, W., & Melloni, L. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.12.003 · Cited by 589 · see citing works
Multistability and metastability: understanding dynamic coordination in the brain
Kelso, J. A. S. (2012) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2011.0351 · Cited by 565 · see citing works
Fast transient networks in spontaneous human brain activity
Baker, A. P., Brookes, M. J., Rezek, I. A., Smith, S. M., Behrens, T. E. J., Probert-Smith, P., & Woolrich, M. W. (2014) · eLife · doi:10.7554/elife.01867 · Cited by 555 · see citing works
No-Report Paradigms: Extracting the True Neural Correlates of Consciousness
Tsuchiya, N., Wilke, M., Frässle, S., & Lamme, V. A. F. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.10.002 · Cited by 551 · see citing works
On the stability of BOLD fMRI correlations
Laumann, T. O., Snyder, A. Z., Mitra, A., Gordon, E. M., Gratton, C., Adeyemo, B., Gilmore, A. W., Nelson, S. M., Berg, J. J., Greene, D. J., et al. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw265 · Cited by 516 · see citing works
Self-citationSpike-timing Dynamics of Neuronal Groups
Izhikevich, E. M. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh053 · Cited by 489 · see citing works
Stratification of unresponsive patients by an independently validated index of brain complexity
Casarotto, S., Comanducci, A., Rosanova, M., Sarasso, S., Fecchio, M., Napolitani, M., Pigorini, A., G. Casali, A., Trimarchi, P. D., Boly, M., et al. (2016) · Annals of Neurology · doi:10.1002/ana.24779 · Cited by 487 · see citing works
Transient Dynamics for Neural Processing
Rabinovich, M., Huerta, R., & Laurent, G. (2008) · Science · doi:10.1126/science.1155564 · Cited by 458 · see citing works
Haimovici, A., Tagliazucchi, E., Balenzuela, P., & Chialvo, D. R. (2013) · Physical Review Letters · doi:10.1103/physrevlett.110.178101 · Cited by 438 · see citing works
Self-citationAre there levels of consciousness?
Bayne, T., Hohwy, J., & Owen, A. M. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2016.03.009 · Cited by 438 · see citing works
Scale-Free Properties of the Functional Magnetic Resonance Imaging Signal during Rest and Task
He, B. J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2111-11.2011 · Cited by 437 · see citing works
Increased spontaneous MEG signal diversity for psychoactive doses of ketamine, LSD and psilocybin
Schartner, M. M., Carhart-Harris, R. L., Barrett, A. B., Seth, A. K., & Muthukumaraswamy, S. D. (2017) · Scientific Reports · doi:10.1038/srep46421 · Cited by 410 · see citing works
Development of the Brain's Default Mode Network from Wakefulness to Slow Wave Sleep
Sämann, P. G., Wehrle, R., Hoehn, D., Spoormaker, V. I., Peters, H., Tully, C., Holsboer, F., & Czisch, M. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq295 · Cited by 399 · see citing works
Enhanced repertoire of brain dynamical states during the psychedelic experience
Tagliazucchi, E., Carhart-Harris, R. L., Leech, R., Nutt, D., & Chialvo, D. R. (2014) · Human Brain Mapping · doi:10.1002/hbm.22562 · Cited by 399 · see citing works
Self-citationConsciousness and Complexity during Unresponsiveness Induced by Propofol, Xenon, and Ketamine
Sarasso, S., Boly, M., Napolitani, M., Gosseries, O., Charland-Verville, V., Casarotto, S., Rosanova, M., Casali, A. G., Brichant, J.-F., Boveroux, P., et al. (2015) · Current Biology · doi:10.1016/j.cub.2015.10.014 · Cited by 399 · see citing works
Intrinsic functional connectivity differentiates minimally conscious from unresponsive patients
Athena Demertzi, A., Antonopoulos, G., Heine, L., Voss, H. U., Crone, J. S., Angeles, C. D. L., Bahri, M. A., Perri, C. D., Vanhaudenhuyse, A., Charland‐Verville, V., et al. (2015) · Brain · doi:10.1093/brain/awv169 · Cited by 384 · see citing works
Sergent, C., & Dehaene, S. (2004) · Psychological Science · doi:10.1111/j.0956-7976.2004.00748.x · Cited by 384 · see citing works
Impaired consciousness in epilepsy
Blumenfeld, H. (2012) · The Lancet Neurology · doi:10.1016/s1474-4422(12)70188-6 · Cited by 368 · see citing works
Dynamic functional connectivity of the default mode network tracks daydreaming
Kucyi, A., & Davis, K. D. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.06.044 · Cited by 355 · see citing works
Tracking ongoing cognition in individuals using brief, whole-brain functional connectivity patterns
González-Castillo, J., Hoy, C. W., Handwerker, D. A., Robinson, M. E., Buchanan, L. C., Saad, Z. S., & Bandettini, P. A. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1501242112 · Cited by 344 · see citing works
EEG correlates of time-varying BOLD functional connectivity
Chang, C. E., Liu, Z., Chen, M. C., Liu, X., & Duyn, J. H. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.01.049 · Cited by 344 · see citing works
(1997) · Journal of Consciousness Studies · Cited by 340 · see citing works
Neuronal Avalanches in the Resting MEG of the Human Brain
Shriki, O., Alstott, J., Carver, F. W., Holroyd, T., Henson, R. N., Smith, M. L., Coppola, R., Bullmore, E. T., & Plenz, D. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4286-12.2013 · Cited by 335 · see citing works
The specious present: A neurophenomenology of time consciousness.
Varela, F. J. (1999) · Cited by 329 · see citing works
Metastable states in spin glasses
Bray, A. J., & Moore, M. A. (1980) · Journal of Physics C Solid State Physics · doi:10.1088/0022-3719/13/19/002 · Cited by 327 · see citing works
Karahanoğlu, F. I., & Ville, D. V. D. (2015) · Nature Communications · doi:10.1038/ncomms8751 · Cited by 320 · see citing works
The role of metastability in polymer phase transitions
Keller, A., & Cheng, S. Z. D. (1998) · Polymer · doi:10.1016/s0032-3861(97)10320-2 · Cited by 316 · see citing works
Tracking brain arousal fluctuations with fMRI
Chang, C. E., Leopold, D. A., Schölvinck, M. L., Mandelkow, H., Picchioni, D., Liu, X., Ye, F. Q., Turchi, J. N., & Duyn, J. H. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1520613113 · Cited by 308 · see citing works
Metastability of the folded states of globular proteins.
Honeycutt, J. D., & Thirumalai, D. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.9.3526 · Cited by 305 · 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
Dynamic BOLD functional connectivity in humans and its electrophysiological correlates
Tagliazucchi, E., von Wegner, F., Morzelewski, A., Brodbeck, V., & Laufs, H. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00339 · Cited by 285 · see citing works
Self-citationA role for the default mode network in the bases of disorders of consciousness
Fernández‐Espejo, D., Soddu, A., Cruse, D., Palacios, E. M., Junqué, C., Vanhaudenhuyse, A., Rivas, E., Newcombe, V., Menon, D. K., Pickard, J. D., et al. (2012) · Annals of Neurology · doi:10.1002/ana.23635 · Cited by 277 · see citing works
In Vivo Measurements of Neurotransmitters by Microdialysis Sampling
Watson, C. J., Venton, B. J., & Kennedy, R. T. (2006) · Analytical Chemistry · doi:10.1021/ac0693722 · Cited by 274 · see citing works
Metastable chimera states in community-structured oscillator networks
Shanahan, M. (2010) · Chaos An Interdisciplinary Journal of Nonlinear Science · doi:10.1063/1.3305451 · Cited by 274 · see citing works
Development of a large-scale functional brain network during human non-rapid eye movement sleep
Spoormaker, V. I., Schröter, M. S., Gleiser, P. M., Andrade, K. C., Dresler, M., Wehrle, R., Sämann, P. G., & Czisch, M. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.2015-10.2010 · Cited by 273 · see citing works
Fractional Gaussian noise, functional MRI and Alzheimer's disease
Maxim, V., Sendur, L., Fadili, J. M., John Suckling, A., Gould, R. L., Howard, R. J., & Bullmore, E. T. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2004.10.044 · Cited by 270 · see citing works
Transients, Metastability, and Neuronal Dynamics
Friston, K. J. (1997) · NeuroImage · doi:10.1006/nimg.1997.0259 · Cited by 269 · see citing works
Breakdown of long-range temporal dependence in default mode and attention networks during deep sleep
Tagliazucchi, E., von Wegner, F., Morzelewski, A., Brodbeck, V., Jahnke, K., & Laufs, H. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1312848110 · Cited by 251 · see citing works
Self-citationAre There Neural Correlates of Consciousness
Noë, A., & Thompson, E. T. (2004) · Journal of Consciousness Studies · Cited by 243 · see citing works
Deco, G., & Kringelbach, M. L. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.01.001 · Cited by 242 · see citing works
Dynamic Brain Network Correlates of Spontaneous Fluctuations in Attention
Kucyi, A., Hove, M. J., Esterman, M. S., Hutchison, R. M., & Valera, E. M. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw029 · Cited by 225 · see citing works
The Unity of ConsciousnessBinding, Integration, and Dissociation
Axel Cleeremans, B., & Frith, C. (2003) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198508571.001.0001 · Cited by 224 · see citing works
Priesemann, V., Valderrama, M. A., Wibral, M., & Quyen, M. L. V. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002985 · Cited by 220 · see citing works
General anesthesia and the neural correlates of consciousness
Alkire, M. T., & Miller, J. (2005) · Progress in brain research · doi:10.1016/s0079-6123(05)50017-7 · Cited by 219 · see citing works
Kaneko, K., & Tsuda, I. (2003) · Chaos An Interdisciplinary Journal of Nonlinear Science · doi:10.1063/1.1607783 · Cited by 209 · see citing works
Hellyer, P. J., Shanahan, M., Scott, G., Wise, R. J. S., Sharp, D. J., & Leech, R. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1853-13.2014 · Cited by 205 · see citing works
Metastability, mechanical strength, and the support of mountain belts
Jackson, J., Austrheim, H. O., McKenzie, D., & Priestley, K. F. (2004) · Geology · doi:10.1130/g20397.1 · Cited by 197 · see citing works
Hierarchical clustering of brain activity during human nonrapid eye movement sleep
Boly, M., Perlbarg, V., Marrelec, G., Schabus, M., Laureys, S., Doyon, J., Pélégrini‐Issac, M., Maquet, P., & Benali, H. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1111133109 · Cited by 190 · see citing works
Hellyer, P. J., Scott, G., Shanahan, M., Sharp, D. J., & Leech, R. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4648-14.2015 · Cited by 187 · see citing works
Spontaneous eyelid closures link vigilance fluctuation with fMRI dynamic connectivity states
Wang, C., Ong, J. L., Patanaik, A., Zhou, J. H., & Chee, M. W. L. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1523980113 · Cited by 187 · see citing works
Lumer, E. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.3.207 · Cited by 186 · see citing works
Large-scale signatures of unconsciousness are consistent with a departure from critical dynamics
Tagliazucchi, E., Chialvo, D. R., Siniatchkin, M., Amico, E., Brichant, J.-F., Bonhomme, V. L., Noirhomme, Q., Laufs, H., & Laureys, S. (2016) · Journal of The Royal Society Interface · doi:10.1098/rsif.2015.1027 · Cited by 186 · see citing works
Self-citationVoltage imaging of waking mouse cortex reveals emergence of critical neuronal dynamics
Scott, G., Fagerholm, E. D., Mutoh, H., Leech, R., Sharp, D. J., Shew, W. L., & Knöpfel, T. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.3474-14.2014 · Cited by 158 · see citing works
Metastability, criticality and phase transitions in brain and its models
Werner, G. (2006) · Biosystems · doi:10.1016/j.biosystems.2006.12.001 · Cited by 154 · see citing works
Neural correlates of consciousness
Mormann, F., & Koch, C. (2007) · Scholarpedia · doi:10.4249/scholarpedia.1740 · Cited by 153 · see citing works
Automatic sleep staging using fMRI functional connectivity data
Tagliazucchi, E., von Wegner, F., Morzelewski, A., Borisov, S. V., Jahnke, K., & Laufs, H. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.06.036 · Cited by 152 · see citing works
Self-citationHow can we construct a science of consciousness?
Chalmers, D. J. (2013) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12166 · Cited by 146 · see citing works
Bachmann, T. (1984) · Perception & Psychophysics · doi:10.3758/bf03205926 · Cited by 142 · see citing works
Dynamic Repertoire of Intrinsic Brain States Is Reduced in Propofol-Induced Unconsciousness
Hudetz, A. G., Liu, X., & Pillay, S. (2014) · Brain Connectivity · doi:10.1089/brain.2014.0230 · Cited by 142 · see citing works
Monti, M. M., Lutkenhoff, E. S., Rubinov, M., Boveroux, P., Vanhaudenhuyse, A., Gosseries, O., Bruno, M., Noirhomme, Q., Boly, M., & Laureys, S. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003271 · Cited by 136 · see citing works
Modulation of the brain’s functional network architecture in the transition from wake to sleep
Larson‐Prior, L. J., Power, J. D., Vincent, J. L., Nolan, T. S., Coalson, R. S., Zempel, J. M., Snyder, A. Z., Schlaggar, B. L., Raichle, M. E., & Petersen, S. E. (2011) · Progress in brain research · doi:10.1016/b978-0-444-53839-0.00018-1 · Cited by 135 · see citing works
Hutchison, R. M., Hutchison, M., Manning, K. Y., Menon, R. S., & Everling, S. (2014) · Human Brain Mapping · doi:10.1002/hbm.22583 · Cited by 135 · see citing works
Loss of Consciousness Is Associated with Stabilization of Cortical Activity
Solovey, G., Alonso, L. M., Yanagawa, T., Fujii, N., Magnasco, M. O., Cecchi, G., & Proekt, A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4895-14.2015 · Cited by 127 · see citing works
Prevalence of Unstable Attractors in Networks of Pulse-Coupled Oscillators
Timme, M., Wolf, F., & Geisel, T. (2002) · Physical Review Letters · doi:10.1103/physrevlett.89.154105 · Cited by 125 · see citing works
Dynamic resting state functional connectivity in awake and anesthetized rodents
Liang, Z., Liu, X., & Zhang, N. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.10.013 · Cited by 121 · see citing works
The Neural Basis of Time-Varying Resting-State Functional Connectivity
Keilholz, S. D. (2014) · Brain Connectivity · doi:10.1089/brain.2014.0250 · Cited by 119 · see citing works
Neural correlates of time-varying functional connectivity in the rat
Thompson, G. J., Merritt, M. D., Pan, W., Magnuson, M. E., Grooms, J. K., Jaeger, D., & Keilholz, S. D. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.07.036 · Cited by 116 · see citing works
Jobst, B., Hindriks, R., Laufs, H., Tagliazucchi, E., Hahn, G., Ponce‐Alvarez, A., Stevner, A. B. A., Kringelbach, M. L., & Deco, G. (2017) · Scientific Reports · doi:10.1038/s41598-017-04522-x · Cited by 114 · see citing works
Self-citationAmico, E., Gómez, F. A., Perri, C. D., Vanhaudenhuyse, A., Lesenfants, D., Boveroux, P., Bonhomme, V. L., Brichant, J.-F., Marinazzo, D., & Laureys, S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0100012 · Cited by 109 · see citing works
Fraiman, D., & Chialvo, D. R. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00307 · Cited by 108 · see citing works
Disentangling the dynamic core: a research program for a neurodynamics at the large-scale
Quyen, M. L. V. (2003) · Biological Research · doi:10.4067/s0716-97602003000100006 · Cited by 107 · see citing works
Tagliazucchi, E., von Wegner, F., Morzelewski, A., Brodbeck, V., Borisov, S. V., Jahnke, K., & Laufs, H. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.12.073 · Cited by 105 · see citing works
Self-citationA personalized history of EEG–fMRI integration
Laufs, H. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.039 · Cited by 103 · see citing works
Lehmann, D., Pascual-Marqui, R. D., & Michel, C. M. (2009) · Scholarpedia · doi:10.4249/scholarpedia.7632 · Cited by 98 · see citing works
Mooneyham, B. W., Mrazek, M. D., Mrazek, A. J., Mrazek, K. L., Phillips, D. T., & Schooler, J. W. (2017) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01066 · Cited by 86 · see citing works
Spoormaker, V. I., Gleiser, P. M., & Czisch, M. (2012) · Frontiers in Neurology · doi:10.3389/fneur.2012.00080 · Cited by 83 · see citing works
Seth, A. K. (2007) · Scholarpedia · doi:10.4249/scholarpedia.1328 · Cited by 80 · see citing works
Infraslow Electroencephalographic and Dynamic Resting State Network Activity
Grooms, J. K., Thompson, G. J., Pan, W.-J., Billings, J., Schumacher, E. H., Epstein, C. M., & Keilholz, S. D. (2017) · Brain Connectivity · doi:10.1089/brain.2017.0492 · Cited by 74 · see citing works
Tagliazucchi, E., Siniatchkin, M., Laufs, H., & Chialvo, D. R. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00381 · Cited by 70 · see citing works
Self-citationDynamic Connectivity Patterns in Conscious and Unconscious Brain
Ma, Y., Hamilton, C. M., & Zhang, N. (2016) · Brain Connectivity · doi:10.1089/brain.2016.0464 · Cited by 69 · see citing works
Boly, M., Sasai, S., Gosseries, O., Oizumi, M., Casali, A. G., Massimini, M., & Tononi, G. (2015) · PLoS ONE · doi:10.1371/journal.pone.0125337 · Cited by 64 · see citing works
Deco, G., Tagliazucchi, E., Laufs, H., Sanjuán, A., & Kringelbach, M. L. (2017) · eNeuro · doi:10.1523/eneuro.0106-17.2017 · Cited by 62 · see citing works
Self-citationDeep sleep divides the cortex into opposite modes of anatomical–functional coupling
Tagliazucchi, E., Crossley, N. A., Bullmore, E. T., & Laufs, H. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1162-0 · Cited by 55 · see citing works
Self-citationTagliazucchi, E. (2017) · Consciousness and Cognition · doi:10.1016/j.concog.2017.08.008 · Cited by 55 · see citing works
Self-citationWu, C. W., Liu, P.-Y., Tsai, P.-J., Wu, Y.-C., Hung, C.-S., Tsai, Y.-C., Cho, K.-H., Biswal, B. B., Chen, C.-J., & Lin, C.-P. (2012) · Brain Connectivity · doi:10.1089/brain.2012.0075 · Cited by 52 · see citing works
Multimodal Imaging of Dynamic Functional Connectivity
Tagliazucchi, E., & Laufs, H. (2015) · Frontiers in Neurology · doi:10.3389/fneur.2015.00010 · Cited by 52 · see citing works
Self-citationSleep Neuroimaging and Models of Consciousness
Tagliazucchi, E., Behrens, M., & Laufs, H. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00256 · Cited by 45 · see citing works
Self-citationSpin-glass model predicts metastable brain states that diminish in anesthesia
Hudetz, A. G., Humphries, C., & Binder, J. R. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00234 · Cited by 44 · see citing works
The Brain: What is Critical About It?
Chialvo, D. R., Balenzuela, P., Fraiman, D., Ricciardi, L. M., Buonocore, A., & Pirozzi, E. (2008) · AIP conference proceedings · doi:10.1063/1.2965095 · Cited by 41 · see citing works
Altmann, A., Schröter, M. S., Spoormaker, V. I., Kiem, S. A., Jordan, D., Ilg, R., Bullmore, E. T., Greicius, M. D., Czisch, M., & Sämann, P. G. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.09.072 · Cited by 39 · see citing works
Ott, E. (2006) · Scholarpedia · doi:10.4249/scholarpedia.1701 · Cited by 37 · see citing works
Different dynamic resting state fMRI patterns are linked to different frequencies of neural activity
Thompson, G. J., Pan, W., & Keilholz, S. D. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00235.2015 · Cited by 36 · see citing works
Werner, G. (2012) · Chaos Solitons & Fractals · doi:10.1016/j.chaos.2012.03.014 · Cited by 33 · see citing works
Neural correlates of consciousness
Rees, G. E. (2013) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12257 · Cited by 28 · see citing works
Bhowmik, D., & Shanahan, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0062234 · Cited by 25 · see citing works
Kafashan, M., Ching, S., & Palanca, B. J. A. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00107 · Cited by 24 · see citing works
Future directions for identifying the neural correlates of consciousness
Sandberg, K., Frässle, S., & Pitts, M. A. (2016) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.104 · Cited by 22 · see citing works
Repertoire of mesoscopic cortical activity is not reduced during anesthesia
Hudetz, A. G., Vizuete, J. A., Pillay, S., & Mashour, G. A. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.10.023 · Cited by 19 · see citing works
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Dynamical exploration of the repertoire of brain networks at rest is modulated by psilocybin
Lord, L.-D., Expert, P., Atasoy, S., Roseman, L., Rapuano, K. M., Lambiotte, R., Nutt, D., Deco, G., Carhart-Harris, R. L., Kringelbach, M. L., et al. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.05.060 · Cited by 210 · see citing works
Consciousness and complexity: a consilience of evidence
Sarasso, S., Casali, A. G., Casarotto, S., Rosanova, M., Sinigaglia, C., & Massimini, M. (2021) · Neuroscience of Consciousness · doi:10.1093/nc/niab023 · Cited by 171 · see citing works
Meditation Increases the Entropy of Brain Oscillatory Activity
Vivot, R. M., Pallavicini, C., Zamberlán, F., Vigo, D. E., & Tagliazucchi, E. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.01.033 · Cited by 107 · see citing works
Self-citationGeneral Anesthesia: A Probe to Explore Consciousness
Bonhomme, V. L., Staquet, C., Montupil, J., Defresne, A., Kirsch, M., Martial, C., Vanhaudenhuyse, A., Chatelle, C., Larroque, S. K., Raimondo, F., et al. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2019.00036 · Cited by 112 · see citing works
Battaglia, D. A., Boudou, T., Hansen, E. C. A., Lombardo, D., Chettouf, S., Daffertshofer, A., McIntosh, A. R., Zimmermann, J., Ritter, P., & Jirsa, V. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117156 · Cited by 98 · see citing works
Tapping into Multi-Faceted Human Behavior and Psychopathology Using fMRI Brain Dynamics
Bolton, T. A. W., Morgenroth, E., Preti, M. G., & Ville, D. V. D. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.06.005 · Cited by 89 · see citing works
Quantum effects in the brain: A review
Adams, B., & Petruccione, F. (2020) · AVS Quantum Science · doi:10.1116/1.5135170 · Cited by 80 · see citing works
Tewarie, P. K. B., Abeysuriya, R., Byrne, Á., O’Neill, G. C., Sotiropoulos, S. N., Brookes, M. J., & Coombes, S. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.10.079 · Cited by 76 · see citing works
Frequency‐dependent functional connectivity in resting state networks
Samogin, J., Marino, M., Porcaro, C., Wenderoth, N., Dupont, P. J., Swinnen, S. P., & Mantini, D. (2020) · Human Brain Mapping · doi:10.1002/hbm.25184 · Cited by 75 · see citing works
Yan, B., Xu, X., Liu, M., Zheng, K., Liu, J., Li, J., Lei, W., Zhang, B., Lu, H., & Baojuan Li, A. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00191 · Cited by 75 · see citing works
Neural and subjective effects of inhaled N,N-dimethyltryptamine in natural settings
Pallavicini, C., Cavanna, F., Zamberlán, F., de la Fuente, L. A., Ilksoy, Y. A., Perl, Y. S., Arias, M., Romero, C., Carhart-Harris, R. L., Timmermann, C., et al. (2021) · Journal of Psychopharmacology · doi:10.1177/0269881120981384 · Cited by 83 · see citing works
Self-citationDynamic cortical connectivity during general anesthesia in healthy volunteers
Li, D., Vlisides, P. E., Kelz, M. B., Avidan, M. S., Mashour, G. A., & for the ReCCognition Study Group (2019) · Anesthesiology · doi:10.1097/aln.0000000000002656 · Cited by 69 · see citing works
Panda, R., Thibaut, A., López‐González, A., Escrichs, A., Bahri, M. A., Hillebrand, A., Deco, G., Laureys, S., Gosseries, O., Annen, J., et al. (2022) · eLife · doi:10.7554/elife.77462 · Cited by 69 · see citing works
Open eyes and closed eyes elicit different temporal properties of brain functional networks
Weng, Y., Liu, X., Hu, H., Huang, H., Zheng, S., Chen, Q., Song, J., Cao, B., Wang, J., Wang, S., et al. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117230 · Cited by 58 · see citing works
Kotler, S., Mannino, M., Kelso, S., & Huskey, R. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104956 · Cited by 52 · see citing works
Brain flexibility associated with need for cognition contributes to creative achievement
He, L., Zhuang, K., Li, Y., Sun, J., Meng, J., Zhu, W., Mao, Y., Chen, Q., Chen, X., & Qiu, J. (2019) · Psychophysiology · doi:10.1111/psyp.13464 · Cited by 50 · see citing works
A synergistic workspace for human consciousness revealed by Integrated Information Decomposition
Luppi, A. I., Mediano, P. A. M., Rosas, F. E., Allanson, J. E., Pickard, J. D., Carhart-Harris, R. L., Williams, G. B., Craig, M. M., Finoia, P., Owen, A. M., et al. (2023) · eLife · doi:10.7554/elife.88173 · Cited by 111 · see citing works
Topological analysis of differential effects of ketamine and propofol anaesthesia on brain dynamics
Varley, T. F., Denny, V. C., Sporns, O., & Patania, A. (2021) · Royal Society Open Science · doi:10.1098/rsos.201971 · Cited by 46 · see citing works
Lombardo, D., Cassé‐Perrot, C., Ranjeva, J., Troter, A. L., Guye, M., Wirsich, J., Payoux, P., David Bartrés-faz, A., Bordet, R., Richardson, J. C., et al. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117155 · Cited by 41 · see citing works
Luppi, A. I., Mediano, P. A. M., Rosas, F. E., Harrison, D. J., Carhart-Harris, R. L., Bor, D., & Stamatakis, E. A. (2021) · Neuroscience of Consciousness · doi:10.1093/nc/niab027 · Cited by 45 · see citing works
A synergistic workspace for human consciousness revealed by Integrated Information Decomposition
Luppi, A. I., Mediano, P. A. M., Rosas, F. E., Allanson, J. E., Pickard, J. D., Carhart-Harris, R. L., Williams, G. B., Craig, M. M., Finoia, P., Owen, A. M., et al. (2024) · eLife · doi:10.7554/elife.88173.4 · Cited by 41 · see citing works
A Synergistic Workspace for Human Consciousness Revealed by Integrated Information DecompositionPreprint
Luppi, A. I., Mediano, P. A. M., Rosas, F. E., Allanson, J. E., Pickard, J. D., Carhart-Harris, R. L., Williams, G. B., Craig, M. M., Finoia, P., Owen, A. M., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.11.25.398081 · Cited by 43 · see citing works
Functional networks in prolonged disorders of consciousness
Li, H., Zhang, X., Sun, X., Dong, L., Lu, H., Yue, S., & Zhang, H. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1113695 · Cited by 38 · see citing works
Li, Y., Shi, W., Liu, Z., Li, J., Wang, Q., Yan, X., Cao, Z., & Wang, G. (2020) · IEEE Journal of Biomedical and Health Informatics · doi:10.1109/jbhi.2020.3008052 · Cited by 36 · see citing works
Long, Y., Liu, X., & Liu, Z. (2023) · Brain Sciences · doi:10.3390/brainsci13030429 · Cited by 36 · see citing works
Make the Unconscious Explicit to Boost the Science of Consciousness
Eriksson, J., Fontan, A., & Pedale, T. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2020.00260 · Cited by 38 · see citing works
Tracking the Main States of Dynamic Functional Connectivity in Resting State
Zhou, Q., Zhang, L., Feng, J., & Lo, C. Z. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00685 · Cited by 33 · see citing works
Shi, W., Li, Y., Liu, Z., Li, J., Wang, Q., Yan, X., & Wang, G. (2019) · International Journal of Neural Systems · doi:10.1142/s0129065720500057 · Cited by 32 · see citing works
Duclos, C., Maschke, C., Mahdid, Y., Berkun, K., Castanheira, J. D. S., Tarnal, V., Picton, P., Vanini, G., Golmirzaie, G., Janke, E., et al. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118171 · Cited by 32 · see citing works
Symmetry breaking organizes the brain’s resting state manifold
Fousek, J., Rabuffo, G., Gudibanda, K., Sheheitli, H., Petkoski, S., & Jirsa, V. (2024) · Scientific Reports · doi:10.1038/s41598-024-83542-w · Cited by 31 · see citing works
Conflicting emergences. Weak vs. strong emergence for the modelling of brain function
Turkheimer, F., Hellyer, P. J., Kehagia, A. A., Expert, P., Lord, L.-D., Vohryzek, J., Dafflon, J., Brammer, M. J., & Leech, R. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.01.023 · Cited by 30 · see citing works
The avalanche-like behaviour of large-scale haemodynamic activity from wakefulness to deep sleep
Bocaccio, H., Pallavicini, C., Castro, M. N., Sánchez, S. M., Pino, G. D., Laufs, H., Villarreal, M. F., & Tagliazucchi, E. (2019) · Journal of The Royal Society Interface · doi:10.1098/rsif.2019.0262 · Cited by 30 · see citing works
Self-citationDynamical properties and mechanisms of metastability: A perspective in neuroscience
Rossi, K. L., Budzinski, R. C., Medeiros, E. S., Boaretto, B. R. R., Muller, L., & Feudel, U. (2025) · Physical review. E · doi:10.1103/physreve.111.021001 · Cited by 29 · see citing works
Young, J. H., Arterberry, M. E., & Martin, J. P. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.628417 · Cited by 28 · see citing works
Piccinini, J., Ipiña, I. P., Laufs, H., Kringelbach, M. L., Deco, G., Perl, Y. S., & Tagliazucchi, E. (2021) · Chaos An Interdisciplinary Journal of Nonlinear Science · doi:10.1063/5.0025543 · Cited by 24 · see citing works
Self-citationLi, D., Vlisides, P. E., & Mashour, G. A. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.118891 · Cited by 24 · see citing works
Qin, L., Zhou, Q., Sun, Y., Pang, X., Chen, Z., & Zheng, J. (2024) · Journal of Translational Medicine · doi:10.1186/s12967-024-05580-2 · Cited by 23 · see citing works
A Review of the Methodology, Taxonomy, and Definitions in Recent fMRI Research on Meditation
Engström, M., Willander, J., & Simon, R. A. (2021) · Mindfulness · doi:10.1007/s12671-021-01782-7 · Cited by 21 · see citing works
Network dynamics scale with levels of awareness
Coppola, P., Spindler, L. R. B., Luppi, A. I., Adapa, R., Naçi, L., Allanson, J. E., Finoia, P., Williams, G. B., Pickard, J. D., Owen, A. M., et al. (2022) · NeuroImage · doi:10.1016/j.neuroimage.2022.119128 · Cited by 24 · see citing works
Temporal Mapper: Transition networks in simulated and real neural dynamics
Zhang, M., Chowdhury, S., & Saggar, M. (2022) · Network Neuroscience · doi:10.1162/netn_a_00301 · Cited by 23 · see citing works
Pei, L., Zhou, X., Leung, F., & Ouyang, G. (2023) · Psychophysiology · doi:10.1111/psyp.14259 · Cited by 22 · see citing works
The complexity of the stream of consciousness
Coppola, P., Allanson, J. E., Naçi, L., Adapa, R., Finoia, P., Williams, G. B., Pickard, J. D., Owen, A. M., Menon, D. K., & Stamatakis, E. A. (2022) · Communications Biology · doi:10.1038/s42003-022-04109-x · Cited by 22 · see citing works
Temporal flow of hubs and connectivity in the human brain
Fransson, P., & Thompson, W. H. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117348 · Cited by 20 · see citing works
Dynamic Changes of Amplitude of Low-Frequency Fluctuations in Patients With Diabetic Retinopathy
Huang, X., Wen, Z., Qi, C.-X., Tong, Y., & Shen, Y. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.611702 · Cited by 19 · see citing works
Xu, Z., Chang, Y., Guo, F., Wang, C., Chai, N., Zheng, M., Fang, P., & Zhu, Y. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14413 · Cited by 19 · see citing works
Standage, D., Areshenkoff, C. N., Nashed, J. Y., Hutchison, R. M., Hutchison, M., Heinke, D. G., Menon, R. S., Everling, S., & Gallivan, J. P. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa085 · Cited by 18 · see citing works
Noel, J.-P., Simon, D., Thelen, A., Maier, A., Blake, R., & Wallace, M. T. (2018) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01247 · Cited by 17 · see citing works
Neural and subjective effects of inhaled DMT in natural settingsPreprint
Pallavicini, C., Cavanna, F., Zamberlán, F., de la Fuente, L. A., Perl, Y. S., Arias, M., Romero, C., Carhart-Harris, R. L., Timmermann, C., & Tagliazucchi, E. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.19.258145 · Cited by 17 · see citing works
Self-citationZhang, L., Zhao, J., Zhou, Q., Liu, Z., Zhang, Y., Cheng, W., Gong, W., Hu, X., Lu, W., Bullmore, E. T., et al. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118188 · Cited by 18 · see citing works
Zheng, C.-Y., Cao, Y., Li, Y., Ye, Z., Jia, X., Li, M., Yu, Y., & Liu, W. (2024) · Brain Research · doi:10.1016/j.brainres.2024.148889 · Cited by 14 · see citing works
A systematic approach to brain dynamics: cognitive evolution theory of consciousness
Yurchenko, S. B. (2022) · Cognitive Neurodynamics · doi:10.1007/s11571-022-09863-6 · Cited by 14 · see citing works
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Coppola, P. (2023) · doi:10.31234/osf.io/2xvc4 · Cited by 14 · see citing works
Dynamic reconfiguration of human brain networks across altered states of consciousness
Liu, H., Hu, K., Peng, Y., Tian, X.-H., Wang, M., Ma, B., Wu, Y., Sun, W., Liu, B., Li, A., et al. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113685 · Cited by 13 · see citing works
Increased Entropy of Gamma Oscillations in the Frontal Region during Meditation
Kumar, G. P., Sharma, K., Ramakrishnan, A. G., & Adarsh, A. (2021) · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · doi:10.1109/embc46164.2021.9629633 · Cited by 12 · see citing works
Grecucci, A., Langerbeck, M., Bakiaj, R., Ghomroudi, P. A., Rivolta, D., Yi, X., & Messina, I. (2025) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2025.1589440 · Cited by 11 · see citing works
Yang, L., Xiao, A., Li, Q., Zhong, H.-F., Su, T., Shi, W., Ying, P., Liang, R., Xu, S., Shao, Y., et al. (2022) · Aging · doi:10.18632/aging.203877 · Cited by 12 · see citing works
Kim, M., Harris, R. E., DaSilva, A. F. M., & Lee, U. (2022) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2022.815099 · Cited by 10 · see citing works
Unconsciousness reconfigures modular brain network dynamics
del Pozo, S. M., Laufs, H., Bonhomme, V. L., Laureys, S., Balenzuela, P., & Tagliazucchi, E. (2021) · Chaos An Interdisciplinary Journal of Nonlinear Science · doi:10.1063/5.0046047 · Cited by 11 · see citing works
Self-citationBattaglia, D. A., Boudou, T., Hansen, E. C. A., Lombardo, D., Chettouf, S., Daffertshofer, A., McIntosh, A. R., Zimmermann, J., Ritter, P., & Jirsa, V. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/107243 · Cited by 13 · see citing works
Li, G., Zhang, Z., Chen, Y. S., Wang, W., Bi, J., Tang, X., & Li, C.-S. R. (2022) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.28336 · Cited by 10 · see citing works
Toscano, F. S., Galadí, J. A., Escrichs, A., Perl, Y. S., López‐González, A., Sitt, J. D., Annen, J., Gosseries, O., Thibaut, A., Panda, R., et al. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010412 · Cited by 10 · see citing works
Miskovic, V., Lynn, S. J., Bagg, J. O., Pouliot, J. J., Ríos, M., & Wackermann, J. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.01.014 · Cited by 11 · see citing works
Lessons From Astronomy and Biology for the Mind—Copernican Revolution in Neuroscience
Northoff, G. (2019) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2019.00319 · Cited by 10 · see citing works
Strindberg, M., Fransson, P., Cabral, J., & Ådén, U. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118287 · Cited by 10 · see citing works
Altered dynamical integration/segregation balance during anesthesia-induced loss of consciousness
Lord, L.-D., Carletti, T., Fernandes, H. M., Turkheimer, F., & Expert, P. (2023) · Frontiers in Network Physiology · doi:10.3389/fnetp.2023.1279646 · Cited by 8 · see citing works
Lu, L., Li, F., Li, H., Zhou, L., Wu, X., & Yuan, F. (2024) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14660 · Cited by 9 · see citing works
Metastable States of Multiscale Brain Networks Are Keys to Crack the Timing Problem
Gili, T., Ciullo, V., & Spalletta, G. (2018) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2018.00075 · Cited by 9 · see citing works
Bapat, R., Pathak, A., & Banerjee, A. (2024) · Frontiers in Neurorobotics · doi:10.3389/fnbot.2024.1336438 · Cited by 8 · see citing works
Review of Dynamic Resting‐State Methods in Neuroimaging: Applications to Depression and Rumination
Peterson, E. C., Smolker, H. R., Moser, A. D., & Kaiser, R. H. (2025) · Human Brain Mapping · doi:10.1002/hbm.70377 · Cited by 8 · see citing works
Dai, R., Huang, Z., Larkin, T. E., Tarnal, V., Picton, P., Vlisides, P. E., Janke, E., McKinney, A., Hudetz, A. G., Harris, R. E., et al. (2023) · Communications Biology · doi:10.1038/s42003-023-05678-1 · Cited by 8 · see citing works
Altered Temporal Dynamic Intrinsic Brain Activity in Late Blindness
Huang, X., Wen, Z., Qi, C.-X., Tong, Y., Dan, H., Xie, B., & Shen, Y. (2020) · BioMed Research International · doi:10.1155/2020/1913805 · Cited by 8 · see citing works
Dynamic Auditory Remapping Across the Sleep-Wake CyclePreprint
Arzi, A., Trentin, C., Laudini, A., Krugliak, A., Nikolla, D., & Bekinschtein, T. A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.16.431383 · Cited by 7 · see citing works
Whole-Brain Models to Explore Altered States of Consciousness from the Bottom Up
Cofré, R., Herzog, R. A., Mediano, P. A. M., Piccinini, J., Rosas, F. E., Perl, Y. S., & Tagliazucchi, E. (2020) · Brain Sciences · doi:10.3390/brainsci10090626 · Cited by 12 · see citing works
Self-citationChen, R.-B., Ye, S.-Y., Pei, C.-G., & Zhong, Y.-L. (2022) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2022.944100 · Cited by 7 · see citing works
Cui, Y., Li, M., Biswal, B. B., Jing, W., Zhou, C., Liu, H., Guo, D., Xia, Y., & Yao, D. (2021) · Brain Connectivity · doi:10.1089/brain.2020.0827 · Cited by 6 · see citing works
Altered trajectories in the dynamical repertoire of functional network states under psilocybinPreprint
Lord, L.-D., Expert, P., Atasoy, S., Roseman, L., Rapuano, K. M., Lambiotte, R., Nutt, D. J., Deco, G., Carhart-Harris, R. L., Kringelbach, M. L., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/376491 · Cited by 7 · see citing works
A Synergistic Workspace for Human Consciousness Revealed by Integrated Information DecompositionPreprint
Luppi, A. I., Mediano, P. A. M., Rosas, F. E., Allanson, J. E., Pickard, J. D., Carhart-Harris, R. L., Williams, G. B., Craig, M. M., Finoia, P., Owen, A. M., et al. (2023) · eLife · doi:10.7554/elife.88173.1 · Cited by 7 · see citing works
Grasso, V., Tennyson, J., Airan, R. D., & Ianni, T. D. (2025) · Neuropsychopharmacology · doi:10.1038/s41386-025-02108-0 · Cited by 6 · see citing works
A review of the sufficient conditions for consciousness
Coppola, P. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106333 · Cited by 6 · see citing works
Li, S., Chen, Y., Ren, P., Li, Z., Zhang, J., & Liang, X. (2022) · Human Brain Mapping · doi:10.1002/hbm.26103 · Cited by 6 · see citing works
de Alteriis, G., MacNicol, E., Hancock, F., Ciaramella, A., Cash, D., Expert, P., & Turkheimer, F. (2024) · Imaging Neuroscience · doi:10.1162/imag_a_00113 · Cited by 6 · see citing works
Wang, C., Lu, Y., Lin, Y., Wang, C., & Tian, P. (2023) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2022.922577 · Cited by 5 · see citing works
A Synergistic Workspace for Human Consciousness Revealed by Integrated Information DecompositionPreprint
Luppi, A. I., Mediano, P. A. M., Rosas, F. E., Allanson, J. E., Pickard, J. D., Carhart-Harris, R. L., Williams, G. B., Craig, M. M., Finoia, P., Owen, A. M., et al. (2024) · eLife · doi:10.7554/elife.88173.3 · Cited by 5 · see citing works
Altered periodic and aperiodic activities in patients with disorders of consciousness
Cai, L., Li, Y., Cheng, Z., & Dong, Y. (2025) · Frontiers in Neuroscience · doi:10.3389/fnins.2025.1657792 · Cited by 4 · see citing works
Apablaza-Yevenes, D. E., Corsi‐Cabrera, M., Martínez-Guerrero, A., Northoff, G., Romaniello, C., Farinelli, M., Bertoletti, E., Müller, M., & Muñoz‐Torres, Z. (2024) · PLoS ONE · doi:10.1371/journal.pone.0300075 · Cited by 4 · see citing works
Zhang, C., Bie, L., Han, S., Zhao, D., Li, P., Wang, X., Jiang, B., & Guo, Y. (2024) · Journal of Neurorestoratology · doi:10.1016/j.jnrt.2024.100095 · Cited by 4 · see citing works
Lehmann, M., Neumann, C., Wasserthal, S., Delis, A., Schultz, J., Hurlemann, R., & Ettinger, U. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.113925 · Cited by 4 · see citing works
A neurotheological perspective on altered states of consciousness
Newberg, A. B., & Yaden, D. B. (2018) · Journal of Consciousness Studies · Cited by 4 · see citing works
The role of connectivity for the degeneracy of the brain’s resting state dynamics
Gudibanda, K., Fousek, J., Petkoski, S., & Jirsa, V. (2026) · Journal of Computational Neuroscience · doi:10.1007/s10827-025-00919-0 · Cited by 3 · see citing works
Electroencephalogram-Based Metastability in Mild Cognitive Impairment Alzheimer's Disease
Das, S. S., & Puthankattil, S. D. (2023) · Brain Connectivity · doi:10.1089/brain.2023.0041 · Cited by 3 · see citing works
Development of brain metastable dynamics during the equivalent of the third gestational trimester
Champaud, J. L. Y., Asite, S., & Lorenzo Fabrizi, D. (2025) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2025.101556 · Cited by 3 · see citing works
Normal Sleep Compared to Altered Consciousness During Sedation
Beck, F., Gosseries, O., Weinhouse, G. L., & Bonhomme, V. L. (2022) · Springer eBooks · doi:10.1007/978-3-031-06447-0_4 · Cited by 3 · see citing works
Luppi, A. I., Mediano, P. A. M., Rosas, F. E., Harrison, D. J., Carhart-Harris, R. L., Bor, D., & Stamatakis, E. A. (2021) · doi:10.31234/osf.io/g9p3r · Cited by 5 · see citing works
de Alteriis, G., MacNicol, E., Hancock, F., Ciaramella, A., Cash, D., Expert, P., & Turkheimer, F. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.27.529688 · Cited by 3 · see citing works
Dynamic Cortical Connectivity During Propofol Sedation in Glioma Patients
Yang, W., Jian, M., Wang, X., Zhou, Y., Liang, Y., Chen, Y., Li, Y., Li, K., Ma, B., Liu, H., et al. (2024) · Journal of Neurosurgical Anesthesiology · doi:10.1097/ana.0000000000000964 · Cited by 2 · see citing works
Altered electrophysiological meta-state dynamics in disorders of consciousness
Nùñez, P., Tewarie, P. K. B., Rodríguez-González, V., Alnagger, N., van der Lande, G., Vitello, M. M., Cardone, P., Thibaut, A., Belloli, L. M. L., Laureys, S., et al. (2025) · NeuroImage · doi:10.1016/j.neuroimage.2025.121519 · Cited by 2 · see citing works
Self-reflection, sense of agency, and underlying neural correlates: A pilot study
Gupta, K. V., Beuria, J., Vijanapalli, L. K., Sethi, A., & Behera, L. (2025) · PLoS ONE · doi:10.1371/journal.pone.0335276 · Cited by 2 · see citing works
Exploring complex and integrated information during sleep
Onoda, K., & Akama, H. (2024) · Neuroscience of Consciousness · doi:10.1093/nc/niae029 · Cited by 2 · see citing works
Lagged Correlations among Physiological Variables as Indicators of Consciousness in Stroke Patients.
Yavuz, T. T., Claassen, J., & Kleinberg, S. (2019) · PubMed Central · Cited by 2 · see citing works
Skałbania, J., Polewik, K., Pietkiewicz, I. J., & Tomalski, R. (2021) · Psychiatria i Psychologia Kliniczna · doi:10.15557/pipk.2021.0003 · Cited by 1 · see citing works
- Authors
- Cavanna, F., Vilas, M. G., Palmucci, M., & Tagliazucchi, E.
- Affiliations
- Consejo Nacional de Investigaciones Científicas y Técnicas (AR)
- Institut du Cerveau (FR)
- Corresponding author
- Tagliazucchi, Enzo
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2018-10
- Volume
- 180
- Issue
- Pt B
- Pages
- 383-395
- ISSN
- 1053-8119 (ISSN-L)
- OpenAlex
- W2762088711
- Cited by
- 137
- References
- 162
- Citations by year
- 2026: 10 · 2025: 18 · 2024: 18 · 2023: 15 · 2022: 17 · 2021: 22 · 2020: 16 · 2019: 14 · 2018: 6 · 2017: 1
- FWCI
- 1.13
- Type
- journal article
- Language
- en
- Open access
- green
- americanae.aecid.es
- Licence
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- Americanae (AECID Library) (submittedVersion, cc-by-nc-nd)
- LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) (submittedVersion, cc-by-nc-nd)
- Funders
- Consejo Nacional de Investigaciones Científicas y Técnicas
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Philosophy and Theoretical Science
- Keywords
- dynamic functional connectivity, altered states of consciousness, neural correlates of consciousness, level of consciousness, dynamic brain states, perturbation method, dynamical systems theory
- MeSH terms
- Brain, Brain Mapping, Consciousness, Consciousness Disorders, Humans
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