Cited by 1,786Functional Brain Connectivity StudiesNeural dynamics and brain functionAdvanced Neuroimaging Techniques and Applications

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Intrinsic functional architecture in the anaesthetized monkey brain

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.·2007·Nature

DOI 10.1038/nature05758

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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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Biostatistical Analysis
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-citation
Co-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-citation
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
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
Science
(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

Show all 46 references

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

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White matter microstructure underlying default mode network connectivity in the human brain
Teipel, S. J., Bokde, A. L. W., Meindl, T., Amaro, E., Soldner, J., Reiser, M. F., Herpertz, S. C., Möller, H., & Hampel, H. J. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.10.067 · Cited by 208
Resting‐state functional connectivity of the rat brain
Pawela, C. P., Biswal, B. B., Cho, Y. R., Kao, D. S., Li, R., Jones, S. R., Schulte, M. L., Matloub, H. S., Hudetz, A. G., & Hyde, J. S. (2008) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21524 · Cited by 200
The Relationship of Anatomical and Functional Connectivity to Resting-State Connectivity in Primate Somatosensory Cortex
Wang, Z., Chen, L. M., Négyessy, L., Friedman, R. M., Mishra, A., Gore, J. C., & Roe, A. W. (2013) · Neuron · doi:10.1016/j.neuron.2013.04.023 · Cited by 210
Graph-theory based parcellation of functional subunits in the brain from resting-state fMRI data
Shen, X., Papademetris, X., & Constable, R. T. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.12.119 · Cited by 202
Distributed BOLD and CBV-weighted resting-state networks in the mouse brain
Sforazzini, F., Schwarz, A. J., Galbusera, A., Bifone, A., & Gozzi, A. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.09.050 · Cited by 207
Ising-like dynamics in large-scale functional brain networks
Fraiman, D., Balenzuela, P., Foss, J., & Chialvo, D. R. (2009) · Physical Review E · doi:10.1103/physreve.79.061922 · Cited by 205
Brain resting state is disrupted in chronic back pain patients
Tagliazucchi, E., Balenzuela, P., Fraiman, D., & Chialvo, D. R. (2010) · Neuroscience Letters · doi:10.1016/j.neulet.2010.08.053 · Cited by 203
Intrinsic functional architecture predicts electrically evoked responses in the human brain
Keller, C. J., Bickel, S., Entz, L., Ulbert, I., Milham, M. P., Kelly, C. A. M., & Mehta, A. D. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1019750108 · Cited by 206
Cerebral cortical folding, parcellation, and connectivity in humans, nonhuman primates, and mice
Essen, D. C. V., Donahue, C. J., Coalson, T. S., Kennedy, H., Hayashi, T., & Glasser, M. F. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1902299116 · Cited by 198
Annual research review: growth connectomics--the organization and reorganization of brain networks during normal and abnormal development
Vértes, P. E., & Bullmore, E. T. (2015) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.12365 · Cited by 197
A comparison of resting-state brain activity in humans and chimpanzees
Rilling, J. K., Barks, S. K., Parr, L. A., Preuss, T. M., Faber, T. L., Pagnoni, G., Bremner, J. D., & Votaw, J. R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705132104 · Cited by 197
Decreased functional connectivity in an executive control network is related to impaired executive function in Internet gaming disorder
Dong, G., Lin, X., & Potenza, M. N. (2014) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2014.10.012 · Cited by 201
The Synchronization within and Interaction between the Default and Dorsal Attention Networks in Early Infancy
Gao, W., Gilmore, J. H., Shen, D., Smith, J. K., Zhu, H., & Lin, W. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs043 · Cited by 194
Functional connectivity of visual cortex in the blind follows retinotopic organization principles
Striem-Amit, E., Ovadia-Caro, S., Caramazza, A., Margulies, D. S., Villringer, A., & Amedi, A. (2015) · Brain · doi:10.1093/brain/awv083 · Cited by 194
PREOPERATIVE SENSORIMOTOR MAPPING IN BRAIN TUMOR PATIENTS USING SPONTANEOUS FLUCTUATIONS IN NEURONAL ACTIVITY IMAGED WITH FUNCTIONAL MAGNETIC RESONANCE IMAGING
Zhang, D., Johnston, J. M., Fox, M., Leuthardt, E. C., Grubb, R. L., Chicoine, M. R., Smyth, M. D., Snyder, A. Z., Raichle, M. E., & Shimony, J. S. (2009) · Operative Neurosurgery · doi:10.1227/01.neu.0000350868.95634.ca · Cited by 198
Self-citation
Inferring multi-scale neural mechanisms with brain network modelling
Schirner, M., McIntosh, A. R., Jirsa, V., Deco, G., & Ritter, P. (2018) · eLife · doi:10.7554/elife.28927 · Cited by 204
Control networks and hubs
Gratton, C., Sun, H., & Petersen, S. E. (2017) · Psychophysiology · doi:10.1111/psyp.13032 · Cited by 218
Defining Individual-Specific Functional Neuroanatomy for Precision Psychiatry
Gratton, C., Kraus, B. T., Greene, D. J., Gordon, E. M., Laumann, T. O., Nelson, S. M., Dosenbach, N. U. F., & Petersen, S. E. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.10.026 · Cited by 202
The future of the human connectome
Essen, D. C. V., & Uǧurbil, K. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.032 · Cited by 197
Challenges and Opportunities in Mining Neuroscience Data
Akil, H., Martone, M. E., & Essen, D. C. V. (2011) · Science · doi:10.1126/science.1199305 · Cited by 200
Transcriptional profiles of supragranular-enriched genes associate with corticocortical network architecture in the human brain
Krienen, F. M., Yeo, B. T. T., Ge, T., Buckner, R. L., & Sherwood, C. C. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1510903113 · Cited by 190
Elevated hippocampal resting-state connectivity underlies deficient neurocognitive function in aging
Salami, A., Pudas, S., & Nyberg, L. H. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1410233111 · Cited by 198
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Sperling, R. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.09.009 · Cited by 187
Structural and functional rich club organization of the brain in children and adults
Grayson, D. S., Ray, S., Carpenter, S., Iyer, S., Dias, T. G. C., Stevens, C., Nigg, J. T., & Fair, D. A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0088297 · Cited by 187
Age-related increases in long-range connectivity in fetal functional neural connectivity networks in utero
Thomason, M. E., Grove, L. E., Lozon, T. A., Vila, A. M., Ye, Y., Nye, M. J., Manning, J. H., Pappas, A., Hernandez‐Andrade, E. A., Yeo, L., et al. (2014) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2014.09.001 · Cited by 198
Resting state functional connectivity of the whole head with near-infrared spectroscopy
Mesquita, R. C., Franceschini, M. A., & Boas, D. A. (2010) · Biomedical Optics Express · doi:10.1364/boe.1.000324 · Cited by 195
Functional connectivity and alterations in baseline brain state in humans
Martuzzi, R., Ramani, R., Qiu, M., Rajeevan, N., & Constable, R. T. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.07.028 · Cited by 199
Lag structure in resting-state fMRI
Mitra, A., Snyder, A. Z., Hacker, C. D., & Raichle, M. E. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00804.2013 · Cited by 188
Self-citation
Intrinsic Functional Connectivity in Attention-Deficit/Hyperactivity Disorder: A Science in Development
Castellanos, F. X., & Aoki, Y. Y. (2016) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2016.03.004 · Cited by 196
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Kwak, Y., Peltier, S., Bohnen, N. I., Müller, M. L. T. M., Dayalu, P., & Seidler, R. D. (2010) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2010.00143 · Cited by 189
Correlated Low-Frequency BOLD Fluctuations in the Resting Human Brain Are Modulated by Recent Experience in Category-Preferential Visual Regions
Stevens, W. D., Buckner, R. L., & Schacter, D. L. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp270 · Cited by 195
Natural Scenes Viewing Alters the Dynamics of Functional Connectivity in the Human Brain
Betti, V., Penna, S. D., de Pasquale, F., Mantini, D., Marzetti, L., Romani, G. L., & Corbetta, M. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.022 · Cited by 191
Self-citation
Dynamic reorganization of human resting-state networks during visuospatial attention
Spadone, S., Penna, S. D., Sestieri, C., Betti, V., Tosoni, A., Perrucci, M. G., Romani, G. L., & Corbetta, M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1415439112 · Cited by 182
Self-citation
An approach for parcellating human cortical areas using resting-state correlations
Wig, G. S., Laumann, T. O., & Petersen, S. E. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.07.035 · Cited by 188
Cortical parcellations of the macaque monkey analyzed on surface-based atlases.
van Essen, D., Glasser, M., Dierker, D. L., & Harwell, J. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr290 · Cited by 198
Low-frequency BOLD fluctuations demonstrate altered thalamocortical connectivity in schizophrenia
Welsh, R. C., Chen, A. C., & Taylor, S. F. (2010) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn145 · Cited by 181
A comprehensive study of whole-brain functional connectivity in children and young adults
Jolles, D. D., van Buchem, M. A., Crone, E. A., & Rombouts, S. A. R. B. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq104 · Cited by 181
Transient neuronal coactivations embedded in globally propagating waves underlie resting-state functional connectivity
Matsui, T., Murakami, T., & Ohki, K. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1521299113 · Cited by 194
Simultaneous electroencephalographic and functional magnetic resonance imaging indicate impaired cortical top-down processing in association with anesthetic-induced unconsciousness
Jordan, D., Ilg, R., Riedl, V., Schorer, A., Grimberg, S., Neufang, S., Omerovic, A., Berger, S., Untergehrer, G., Preibisch, C., et al. (2013) · Anesthesiology · doi:10.1097/aln.0b013e3182a7ca92 · Cited by 180
Uncovering Intrinsic Connectional Architecture of Functional Networks in Awake Rat Brain
Liang, Z., King, J. A., & Zhang, N. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4557-10.2011 · Cited by 185
A pairwise maximum entropy model accurately describes resting-state human brain networks
Watanabe, T., Hirose, S., Wada, H., Imai, Y., Machida, T., Shirouzu, I., Konishi, S., Miyashita, Y., & Masuda, N. (2013) · Nature Communications · doi:10.1038/ncomms2388 · Cited by 186
Common data elements in radiologic imaging of traumatic brain injury
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Creativityâ€”the unconscious foundations of the incubation period
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Local structure-function relationships in human brain networks across the lifespan
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Functional connectivity hubs of the mouse brain
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On the existence of a generalized non-specific task-dependent network
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Self-citation
Electrophysiological correlates of default-mode processing in macaque posterior cingulate cortex
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Intrinsic organization of the anesthetized brain
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Spontaneous default network activity reflects behavioral variability independent of mind-wandering
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Resting-state activity in development and maintenance of normal brain function
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Self-citation
Neural Origin of Spontaneous Hemodynamic Fluctuations in Rats under Burst-Suppression Anesthesia Condition
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LABORATORY PRIMATE NEWSLETTER
Schrier, J. E., Harper, J. S., Hankinson, G. J., Hulsebos, L., Povar, M. L., Mathiesen, E., & Schrier, A. M. (2009) · Cited by 166
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Self-citation
Quasi-periodic patterns (QPP): Large-scale dynamics in resting state fMRI that correlate with local infraslow electrical activity
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Dubovik, S., Pignat, J., Ptak, R., Brakha, T. A., Allet, L., Gillabert, N., Magnin, C., Albert, F., Momjian‐Mayor, I., NAHUM, L. H., et al. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.024 · Cited by 166
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Resting functional connectivity in patients with brain tumors in eloquent areas
Martino, J., Honma, S. M., Findlay, A. M., Guggisberg, A. G., Owen, J. P., Kirsch, H. E., Berger, M. S., & Nagarajan, S. S. (2011) · Annals of Neurology · doi:10.1002/ana.22167 · Cited by 155
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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: Patel, G. H.
Fox, M. D.
Snyder, A. Z.
Baker, J. T.
Zempel, J. M.
Snyder, L. H.
Corbetta, M.
Raichle, M. E.
Venue: Nature
Publisher: Springer Science and Business Media LLC
Published: 2007-05
Volume: 447
Issue: 7140
Pages: 83-86
ISSN: 0028-0836 (ISSN-L)
1476-4687
DOI: 10.1038/nature05758
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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Intrinsic functional architecture in the anaesthetized monkey brain

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