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Intrinsic functional architecture in the anaesthetized monkey brain
Abstract
The traditional approach to studying brain function is to measure physiological responses to controlled sensory, motor and cognitive paradigms. However, most of the brain's energy consumption is devoted to ongoing metabolic activity not clearly associated with any particular stimulus or behaviour. Functional magnetic resonance imaging studies in humans aimed at understanding this ongoing activity have shown that spontaneous fluctuations of the blood-oxygen-level-dependent signal occur continuously in the resting state. In humans, these fluctuations are temporally coherent within widely distributed cortical systems that recapitulate the functional architecture of responses evoked by experimentally administered tasks. Here, we show that the same phenomenon is present in anaesthetized monkeys even at anaesthetic levels known to induce profound loss of consciousness. We specifically demonstrate coherent spontaneous fluctuations within three well known systems (oculomotor, somatomotor and visual) and the 'default' system, a set of brain regions thought by some to support uniquely human capabilities. Our results indicate that coherent system fluctuations probably reflect an evolutionarily conserved aspect of brain functional organization that transcends levels of consciousness.
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“Functional architecture associated with sensory, motor, and cognitive tasks in humans are preserved during isoflurane anesthesia in nonhuman primates [149].”
From The Biology of General Anesthesia from Paramecium to Primate (2019) · cites this paper as [149]
In the citing paper
“there is ample evidence of robust functional connectivity between brain regions that lack direct structural connections28-29, 31.”
From Evolutionarily conserved prefrontal-amygdalar dysfunction in early-life anxiety (2014) · cites this paper as [28]
In the citing paper
“fMRI-derived measures of intrinsic functional connectivity are particularly useful because they are sensitive to functional networks spanning polysynaptic circuits27-29”
From Evolutionarily conserved prefrontal-amygdalar dysfunction in early-life anxiety (2014) · cites this paper as [28]
In the citing paper
“In addition, we report all injection sites by their stereotaxic coordinates in the F99 atlas space. This provides an even finer granularity for objectively comparing our connectivity data to alternative parcellation schemes and to other data modalities such as functional connectivity revealed by functional magnetic resonance imaging (fMRI) (Vincent et al. 2007) and structural connectivity revealed”
From A Weighted and Directed Interareal Connectivity Matrix for Macaque Cerebral Cortex (2014) · cites this paper as Vincent et al. 2007
Citations
Cites
Baltosser, W. H., & Zar, J. H. (1996) · Ecology · doi:10.2307/2265725 · Cited by 35,166
A default mode of brain function
Raichle, M. E., MacLeod, A. M., Snyder, A. Z., Powers, W. J., Gusnard, D. A., & Shulman, G. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.676 · Cited by 12,190
Self-citationCo-Planar Stereotaxic Atlas of the Human Brain
Talairach, J., & Tournoux, P. (1988) · Medical Entomology and Zoology · Cited by 11,798
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
The human brain is intrinsically organized into dynamic, anticorrelated functional networks
Fox, M. D., Snyder, A. Z., Vincent, J. L., Corbetta, M., Van Essen, D. C., & Raichle, M. E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504136102 · Cited by 8,553
Self-citationCo-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
Neuronal Oscillations in Cortical Networks
Buzsáki, G., & Draguhn, A. (2004) · Science · doi:10.1126/science.1099745 · Cited by 6,576
Functional connectivity in the resting brain: a network analysis of the default mode hypothesis
Greicius, M. D., Krasnow, B., Reiss, A. L., & Menon, V. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0135058100 · Cited by 6,358
(2023) · doi:10.1126/science · Cited by 6,063
Signals from Chloroplasts Converge to Regulate Nuclear Gene Expression
Koussevitzky, S., Nott, A., Mockler, T. C., Hong, F., Sachetto‐Martins, G., Surpin, M. A., Lim, J. C.-S., Mittler, R., & Chory, J. (2007) · Science · doi:10.1126/science.1140516 · Cited by 5,765
Research works printed but not linked: 2
- Brodmann, K. Localisation in the Cerebral Cortex (Smith-Gordon, London, 1994)
- Lewis, J. W. & Van Essen, D. C. Mapping of architectonic subdivisions in the macaque monkey, with emphasis on parieto-occipital cortex. J. Comp. Neurol. 428, 79–111 (2000) · DOI
Cited by
Sorted by citations
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Buckner, R. L., Andrews‐Hanna, J. R., & Schacter, D. L. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1440.011 · Cited by 9,761
The organization of the human cerebral cortex estimated by intrinsic functional connectivity
Thomas Yeo, B. T., Krienen, F. M., Sepulcre, J., Sabuncu, M. R., Lashkari, D., Hollinshead, M., Roffman, J. L., Smoller, J. W., Zöllei, L., Polimeni, J. R., et al. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00338.2011 · Cited by 9,182
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Self-citationHow do you feel — now? The anterior insula and human awareness
(Bud) Craig, A. D. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2555 · Cited by 6,657
Correspondence of the brain's functional architecture during activation and rest
Smith, S. M., Fox, P. T., Miller, K. L., Glahn, D. C., Fox, P. M., Mackay, C. E., Filippini, N., Watkins, K. E., Toro, R., Laird, A. R., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905267106 · Cited by 5,150
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Mapping the structural core of human cerebral cortex
Hagmann, P., Cammoun, L., Gigandet, X., Meuli, R., Honey, C. J., Wedeen, V. J., & Sporns, O. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060159 · Cited by 4,173
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Raichle, M. E. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071013-014030 · Cited by 3,904
Self-citationThe reorienting system of the human brain: from environment to theory of mind
Corbetta, M., Patel, G., & Shulman, G. L. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.017 · Cited by 3,889
Self-citationLocal-global parcellation of the human cerebral cortex from intrinsic functional connectivity MRI
Schaefer, A., Kong, R., Gordon, E. M., Laumann, T. O., Zuo, X.-N., Holmes, A. J., Eickhoff, S. B., & Yeo, B. T. T. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhx179 · Cited by 3,657
Predicting human resting-state functional connectivity from structural connectivity
Honey, C. J., Sporns, O., Cammoun, L., Gigandet, X., Thiran, J. P., Meuli, R., & Hagmann, P. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811168106 · Cited by 3,307
Toward discovery science of human brain function
Biswal, B. B., Mennes, M., Zuo, X.-N., Gohel, S., Kelly, C., Smith, S. M., Beckmann, C. F., Adelstein, J. S., Buckner, R. L., Colcombe, S., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911855107 · Cited by 2,970
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
Self-citationBuckner, R. L., Sepulcre, J., Talukdar, T., Krienen, F. M., Liu, H., Hedden, T., Andrews-Hanna, J. R., Sperling, R. A., & Johnson, K. A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5062-08.2009 · Cited by 2,862
Distinct brain networks for adaptive and stable task control in humans
Dosenbach, N. U. F., Fair, D. A., Miezin, F. M., Cohen, A. L., Wenger, K. K., Dosenbach, R. A. T., Fox, M. D., Snyder, A. Z., Vincent, J. L., Raichle, M. E., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704320104 · Cited by 2,632
Self-citationExperimental 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
Neurodegenerative Diseases Target Large-Scale Human Brain Networks
Seeley, W. W., Crawford, R. K., Zhou, J., Miller, B. L., & Greicius, M. D. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.024 · Cited by 2,350
The brain basis of emotion: a meta-analytic review
Lindquist, K. A., Wager, T. D., Kober, H., Bliss-Moreau, E., & Barrett, L. F. (2012) · Behavioral and Brain Sciences · doi:10.1017/s0140525x11000446 · Cited by 2,320
“These data reveal a number of large-scale distributed networks that are anatomically constrained and intrinsic to the human brain (Buckner 2010; Deco et al. 2011; Fox & Raichle 2007; Vincent et al. 2007).”
Resting-State Functional Connectivity Reflects Structural Connectivity in the Default Mode Network
Greicius, M. D., Supekar, K., Menon, V., & Dougherty, R. F. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn059 · Cited by 2,175
Evidence for a Frontoparietal Control System Revealed by Intrinsic Functional Connectivity
Vincent, J. L., Kahn, I., Snyder, A. Z., Raichle, M. E., & Buckner, R. L. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90355.2008 · Cited by 1,869
Self-citationVan Dijk, K. R. A., Hedden, T., Venkataraman, A., Evans, K. C., Lazar, S. W., & Buckner, R. L. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00783.2009 · Cited by 1,844
Emerging concepts for the dynamical organization of resting-state activity in the brain
Deco, G., Jirsa, V. K., & McIntosh, A. R. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn2961 · Cited by 1,798
Disruption of Large-Scale Brain Systems in Advanced Aging
Andrews-Hanna, J. R., Snyder, A. Z., Vincent, J. L., Lustig, C., Head, D., Raichle, M. E., & Buckner, R. L. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.038 · Cited by 1,592
Self-citationIntrinsic and task-evoked network architectures of the human brain
Cole, M. W., Bassett, D. S., Power, J. D., Braver, T. S., & Petersen, S. E. (2014) · Neuron · doi:10.1016/j.neuron.2014.05.014 · Cited by 1,564
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Whitfield-Gabrieli, S., & Ford, J. M. (2012) · Annual Review of Clinical Psychology · doi:10.1146/annurev-clinpsy-032511-143049 · Cited by 1,465
Generation and evaluation of a cortical area parcellation from resting-state correlations
Gordon, E. M., Laumann, T. O., Adeyemo, B., Huckins, J. F., Kelley, W. M., & Petersen, S. E. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhu239 · Cited by 1,463
Yan, C.-G., Cheung, B., Kelly, C., Colcombe, S., Craddock, R. C., Di Martino, A., Li, Q., Zuo, X.-N., Castellanos, F. X., & Milham, M. P. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.03.004 · Cited by 1,461
Competition between functional brain networks mediates behavioral variability
Kelly, A. M. C., Uddin, L. Q., Biswal, B. B., Castellanos, F. X., & Milham, M. P. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2007.08.008 · Cited by 1,287
Development of distinct control networks through segregation and integration
Fair, D. A., Dosenbach, N. U. F., Church, J. A., Cohen, A. L., Brahmbhatt, S., Miezin, F. M., Barch, D. M., Raichle, M. E., Petersen, S. E., & Schlaggar, B. L. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705843104 · Cited by 1,244
Self-citationFransson, P., & Marrelec, G. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.05.059 · Cited by 1,213
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Greicius, M. (2008) · Current Opinion in Neurology · doi:10.1097/wco.0b013e328306f2c5 · Cited by 1,180
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Zuo, X., Ehmke, R. C., Mennes, M., Imperati, D., Castellanos, F. X., Sporns, O., & Milham, M. P. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr269 · Cited by 1,190
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Individual Variability in Functional Connectivity Architecture of the Human Brain
Mueller, S., Wang, D., Fox, M., Yeo, B. T. T., Sepulcre, J., Sabuncu, M. R., Shafee, R., Lu, J., & Liu, H. (2013) · Neuron · doi:10.1016/j.neuron.2012.12.028 · Cited by 1,168
Self-citationDistinct cerebellar contributions to intrinsic connectivity networks
Habas, C., Kamdar, N., Nguyen, D., Prater, K., Beckmann, C. F., Menon, V., & Greicius, M. D. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1868-09.2009 · Cited by 1,115
The brain's default network and its adaptive role in internal mentation
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Raichle, M. E. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.01.008 · Cited by 1,111
Self-citationThe cognitive control network: Integrated cortical regions with dissociable functions
Cole, M. W., & Schneider, W. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.03.071 · Cited by 1,091
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
The brain’s default network: updated anatomy, physiology and evolving insights
Buckner, R. L., & DiNicola, L. M. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0212-7 · Cited by 1,058
Selective changes of resting-state networks in individuals at risk for Alzheimer’s disease
Sorg, C., Riedl, V., Mühlau, M., Calhoun, V. D., Eichele, T., Läer, L., Drzezga, A., Förstl, H., Kurz, A., Zimmer, C., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0708803104 · Cited by 1,036
Bridging animal and human models of exercise-induced brain plasticity
Voss, M. W., Vivar, C., Kramer, A. F., & van Praag, H. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.08.001 · Cited by 1,030
Zhou, J., Greicius, M. D., Gennatas, E. D., Growdon, M. E., Jang, J. Y., Rabinovici, G. D., Kramer, J. H., Weiner, M., Miller, B. L., & Seeley, W. W. (2010) · Brain · doi:10.1093/brain/awq075 · Cited by 1,016
Turken, A. U., & Dronkers, N. F. (2011) · Frontiers in System Neuroscience · doi:10.3389/fnsys.2011.00001 · Cited by 1,012
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Spreng, R. N., & Grady, C. L. (2010) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21282 · Cited by 985
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Precuneus shares intrinsic functional architecture in humans and monkeys
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Self-citationHe, Y., Chen, Z., & Evans, A. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.0141-08.2008 · Cited by 965
Advances and pitfalls in the analysis and interpretation of resting-state FMRI data
Cole, D. M. (2010) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2010.00008 · Cited by 1,011
Is the rostro-caudal axis of the frontal lobe hierarchical?
Badre, D., & D'Esposito, M. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2667 · Cited by 946
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Schölvinck, M. L., Maier, A., Ye, F. Q., Duyn, J. H., & Leopold, D. A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913110107 · Cited by 939
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Sporns, O. (2013) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2013.15.3/osporns · Cited by 964
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Shehzad, Z. E., Kelly, C. A. M., Reiss, P. T., Gee, D. G., Gotimer, K., Uddin, L. Q., Lee, S. H., Margulies, D. S., Roy, A. K., Biswal, B. B., et al. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn256 · Cited by 948
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Vanhaudenhuyse, A., Noirhomme, Q., Tshibanda, L. J.-F., Bruno, M.-A., Boveroux, P., Schnakers, C., Soddu, A., Perlbarg, V., Ledoux, D., Brichant, J.-F., et al. (2010) · Brain · doi:10.1093/brain/awp313 · Cited by 911
Disease and the brain's dark energy
Zhang, D., & Raichle, M. E. (2010) · Nature Reviews Neurology · doi:10.1038/nrneurol.2009.198 · Cited by 928
Self-citationBrain Imaging in Alzheimer Disease
Johnson, K. A., Fox, N. C., Sperling, R. A., & Klunk, W. E. (2012) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a006213 · Cited by 875
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Markov, N. T., Ercsey-Ravasz, M. M., Ribeiro Gomes, A. R., Lamy, C., Magrou, L., Vezoli, J., Misery, P., Falchier, A., Quilodran, R., Gariel, M. A., et al. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs270 · Cited by 857
Beyond Feeling: Chronic Pain Hurts the Brain, Disrupting the Default-Mode Network Dynamics
Baliki, M. N., Geha, P., Apkarian, A. V., & Chialvo, D. R. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4123-07.2008 · Cited by 881
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Uğurbil, K., Xu, J., Auerbach, E. J., Moeller, S., Vu, A. T., Duarte-Carvajalino, J. M., Lenglet, C., Wu, X., Schmitter, S., Van de Moortele, P. F., et al. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.012 · Cited by 812
Functional connectivity of the insula in the resting brain
Cauda, F., D'Agata, F., Sacco, K., Duca, S., Geminiani, G., & Vercelli, A. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.11.049 · Cited by 793
Longitudinal Analysis of Neural Network Development in Preterm Infants
Smyser, C. D., Inder, T. E., Shimony, J. S., Hill, J. E., Degnan, A. J., Snyder, A. Z., & Neil, J. J. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq035 · Cited by 791
Self-citationSegregated fronto-cerebellar circuits revealed by intrinsic functional connectivity
Krienen, F. M., & Buckner, R. L. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp135 · Cited by 782
Learning sculpts the spontaneous activity of the resting human brain
Lewis, C. M., Baldassarre, A., Committeri, G., Romani, G. L., & Corbetta, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0902455106 · Cited by 777
Self-citationOn the relationship between the “default mode network” and the “social brain
Mars, R. B., Neubert, F.-X., Noonan, M. P., Sallet, J., Toni, I., & Rushworth, M. F. S. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00189 · Cited by 766
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Deco, G., Jirsa, V., McIntosh, A. R., Sporns, O., & Kötter, R. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0901831106 · Cited by 777
Intrinsic Fluctuations within Cortical Systems Account for Intertrial Variability in Human Behavior
Fox, M., Snyder, A. Z., Vincent, J. L., & Raichle, M. E. (2007) · Neuron · doi:10.1016/j.neuron.2007.08.023 · Cited by 773
Self-citationThe development of human functional brain networks
Power, J. D., Fair, D. A., Schlaggar, B. L., & Petersen, S. E. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.017 · Cited by 751
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Sporns, O. (2014) · Nature Neuroscience · doi:10.1038/nn.3690 · Cited by 767
Zuo, X., Kelly, C. A. M., Martino, A. D., Mennes, M., Margulies, D. S., Bangaru, S. D., Grzadzinski, R., Evans, A. C., Zang, Y., Castellanos, F. X., et al. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2612-10.2010 · Cited by 755
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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
Self-citationResting-state networks in the infant brain
Fransson, P., Skiöld, B., Horsch, S., Nordell, A., Blennow, M., Lagercrantz, H., & Åden, U. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704380104 · Cited by 696
Spatiotemporal Dynamics of Cortical Sensorimotor Integration in Behaving Mice
Férézou, I., Haiss, F., Gentet, L. J., Aronoff, R., Weber, B., & Petersen, C. C. H. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.007 · Cited by 721
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
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Assaf, M., Jagannathan, K., Calhoun, V. D., Miller, L., Stevens, M. C., Sahl, R., O'Boyle, J. G., Schultz, R. T., & Pearlson, G. D. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.05.067 · Cited by 680
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Metadata
- Authors
- Vincent, J. L., Patel, G. H., Fox, M. D., Snyder, A. Z., Baker, J. T., Van Essen, D. C., Zempel, J. M., Snyder, L. H., Corbetta, M., & Raichle, M. E.
- Affiliations
- Washington University in St. Louis (US)
- Corresponding author
- Raichle, M. E.
- ORCID
- Venue
- Nature
- Published
- 2007-05
- Volume
- 447
- Issue
- 7140
- Pages
- 83-86
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2027781650
- Cited by
- 1,786
- References
- 46
- Citations by year
- 2026: 25 · 2025: 34 · 2024: 58 · 2023: 61 · 2022: 67 · 2021: 65 · 2020: 81 · 2019: 81 · 2018: 107 · 2017: 100 · 2016: 111 · 2015: 132 · 2014: 125 · 2013: 150 · 2012: 120
- FWCI
- 51.95
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Padua Research Archive (University of Padova) (submittedVersion)
- Funders
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke (F31NS051972)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Keywords
- spontaneous neural fluctuations, resting-state brain activity, default mode network, oculomotor system, visual system, functional architecture, primate brain evolution, cross-species conservation, BOLD signal
- MeSH terms
- Anesthesia, Animals, Brain, Brain Mapping, Consciousness, Humans, Isoflurane, Macaca fascicularis, Macaca mulatta, Magnetic Resonance Imaging, Visual Cortex, Anesthetics, Inhalation
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