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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
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Hasson, U., Malach, R., & Heeger, D. J. (2009) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2009.10.011 · Cited by 597
Rat brains also have a default mode network
Lu, H., Zou, Q., Gu, H., Raichle, M. E., Stein, E. A., & Yang, Y. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1200506109 · Cited by 622
Self-citationDynamic reconfiguration of the default mode network during narrative comprehension
Simony, E., Honey, C. J., Chen, J., Lositsky, O., Yeshurun, Y., Wiesel, A., & Hasson, U. (2016) · Nature Communications · doi:10.1038/ncomms12141 · Cited by 588
Braga, R. M., & Buckner, R. L. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.038 · Cited by 602
Functional Alterations in Memory Networks in Early Alzheimer’s Disease
Sperling, R. A., Dickerson, B. C., Pihlajamaki, M. M., Vannini, P., LaViolette, P. S., Vitolo, O. V., Hedden, T., Becker, J. A., Rentz, D. M., Selkoe, D. J., et al. (2010) · NeuroMolecular Medicine · doi:10.1007/s12017-009-8109-7 · Cited by 617
Keeser, D., Meindl, T., Bor, J., Palm, U., Pogarell, O. M., Mulert, C., Brunelin, J., Möller, H., Reiser, M. F., & Padberg, F. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0542-11.2011 · Cited by 615
Shmuel, A., & Leopold, D. A. (2008) · Human Brain Mapping · doi:10.1002/hbm.20580 · Cited by 584
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Cohen, A. L., Fair, D. A., Dosenbach, N. U. F., Miezin, F. M., Dierker, D., Van Essen, D. C., Schlaggar, B. L., & Petersen, S. E. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.01.066 · Cited by 582
Functional network dysfunction in anxiety and anxiety disorders
Sylvester, C. M., Corbetta, M., Raichle, M. E., Rodebaugh, T. L., Schlaggar, B. L., Sheline, Y. I., Zorumski, C. F., & Lenze, E. J. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.04.012 · Cited by 579
Self-citationAbnormalities of intrinsic functional connectivity in autism spectrum disorders
Monk, C. S., Peltier, S. J., Wiggins, J. L., Weng, S.-J., Carrasco, M., Risi, S., & Lord, C. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.04.069 · Cited by 578
Deco, G., Ponce-Alvarez, A., Mantini, D., Romani, G. L., Hagmann, P., & Corbetta, M. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1091-13.2013 · Cited by 576
Self-citationEmergence of resting state networks in the preterm human brain
Doria, V., Beckmann, C. F., Arichi, T., Merchant, N., Groppo, M., Turkheimer, F. E., Counsell, S. J., Murgasova, M., Aljabar, P., Nunes, R. G., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1007921107 · Cited by 574
Development of Anterior Cingulate Functional Connectivity from Late Childhood to Early Adulthood
Kelly, A. M. C., Di Martino, A., Uddin, L. Q., Shehzad, Z., Gee, D. G., Reiss, P. T., Margulies, D. S., Castellanos, F. X., & Milham, M. P. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn117 · Cited by 572
Altered corticostriatal functional connectivity in obsessive-compulsive disorder
Harrison, B. J., Soriano-Mas, C., Pujol, J., Ortiz, H., López-Solà, M., Hernández-Ribas, R., Deus, J., Alonso, P., Yücel, M., Pantelis, C., et al. (2009) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2009.152 · Cited by 571
Identifying the brain's most globally connected regions
Cole, M. W., Pathak, S., & Schneider, W. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.11.001 · Cited by 572
Resting-brain functional connectivity predicted by analytic measures of network communication
Goñi, J., van den Heuvel, M. P., Avena‐Koenigsberger, A., de Mendizábal, N. V., Betzel, R. F., Griffa, A., Hagmann, P., Corominas‐Murtra, B., Thiran, J., & Sporns, O. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1315529111 · Cited by 570
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Petersen, S. E., & Sporns, O. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.027 · Cited by 553
The modular and integrative functional architecture of the human brain
Bertolero, M. A., Yeo, B. T. T., & D’Esposito, M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1510619112 · Cited by 572
Noise during Rest Enables the Exploration of the Brain's Dynamic Repertoire
Ghosh, A., Rho, Y.-A., McIntosh, A. R., Kötter, R., & Jirsa, V. (2008) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000196 · Cited by 576
Biophysical and Physiological Origins of Blood Oxygenation Level-Dependent fMRI Signals
Kim, S.-G., & Ogawa, S. (2012) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2012.23 · Cited by 547
Dreier, J. P., Major, S., Manning, A. P., Woitzik, J., Drenckhahn, C., Steinbrink, J. M., Tolias, C. M., Oliveira-Ferreira, A. I., Fabricius, M. E., Hartings, J. A., et al. (2009) · Brain · doi:10.1093/brain/awp102 · Cited by 556
Surface-Based and Probabilistic Atlases of Primate Cerebral Cortex
Essen, D. C. V., & Dierker, D. L. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.015 · Cited by 540
Baseline brain activity fluctuations predict somatosensory perception in humans
Boly, M., Balteau, E., Schnakers, C., Degueldre, C., Moonen, G., Luxen, A., Phillips, C., Peigneux, P., Maquet, P., & Laureys, S. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611404104 · Cited by 529
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
Self-citationRole of local network oscillations in resting-state functional connectivity
Cabral, J., Hugues, E., Sporns, O., & Deco, G. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.04.010 · Cited by 531
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Greicius, M. D., Kiviniemi, V. J., Tervonen, O. A., Vainionpää, V., Alahuhta, S., Reiss, A. L., & Menon, V. (2008) · Human Brain Mapping · doi:10.1002/hbm.20537 · Cited by 514
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van den Heuvel, M. P., & Fornito, A. (2014) · Neuropsychology Review · doi:10.1007/s11065-014-9248-7 · Cited by 531
Resting-state brain networks: literature review and clinical applications
Rosazza, C., & Minati, L. (2011) · Neurological Sciences · doi:10.1007/s10072-011-0636-y · Cited by 535
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Sheline, Y. I., & Raichle, M. E. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.11.028 · Cited by 509
Self-citationThalamocortical Dysconnectivity in Schizophrenia
Woodward, N. D., Karbasforoushan, H., & Heckers, S. (2012) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2012.12010056 · Cited by 512
Resting state fMRI: A personal history
Biswal, B. B. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.090 · Cited by 522
The intrinsic functional organization of the brain is altered in autism
Kennedy, D. P., & Courchesne, E. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.10.052 · Cited by 515
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Kahn, I., Andrews‐Hanna, J. R., Vincent, J. L., Snyder, A. Z., & Buckner, R. L. (2008) · Journal of Neurophysiology · doi:10.1152/jn.00077.2008 · Cited by 509
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Nir, Y., Mukamel, R., Dinstein, I., Privman, E., Harel, M., Fisch, L., Gelbard-Sagiv, H., Kipervasser, S., Andelman, F., Neufeld, M. Y., et al. (2008) · Nature Neuroscience · doi:10.1038/nn.2177 · Cited by 492
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Mars, R. B., Jbabdi, S., Sallet, J., O’Reilly, J. X., Croxson, P. L., Olivier, E., Noonan, M. P., Bergmann, C., Mitchell, A. S., Baxter, M. G., et al. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5102-10.2011 · Cited by 486
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Engel, A. K., Gerloff, C., Hilgetag, C. C., & Nolte, G. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.038 · Cited by 471
Fair, D. A., Nigg, J. T., Iyer, S., Bathula, D., Mills, K. L., Dosenbach, N. U. F., Schlaggar, B. L., Mennes, M., Gutman, D., Bangaru, S., et al. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2012.00080 · Cited by 463
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Glahn, D. C., Winkler, A. M., Kochunov, P., Almasy, L., Duggirala, R., Carless, M. A., Curran, J. C., Olvera, R. L., Laird, A. R., Smith, S. M., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909969107 · Cited by 450
Two Distinct Neuronal Networks Mediate the Awareness of Environment and of Self
Vanhaudenhuyse, A., Athena Demertzi, A., Schabus, M., Noirhomme, Q., Brédart, S., Boly, M., Phillips, C. L. M., Soddu, A., Luxen, A., Moonen, G., et al. (2010) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2010.21488 · Cited by 476
Alexopoulos, G. S., Hoptman, M. J., Kanellopoulos, D., Murphy, C. F., Lim, K. O., & Gunning, F. M. (2012) · Journal of Affective Disorders · doi:10.1016/j.jad.2011.12.002 · Cited by 437
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Zhang, D., Snyder, A. Z., Fox, M. D., Sansbury, M. W., Shimony, J. S., & Raichle, M. E. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90463.2008 · Cited by 437
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Cortical network functional connectivity in the descent to sleep
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Self-citationWeng, S.-J., Wiggins, J. L., Peltier, S., Carrasco, M., Risi, S., Lord, C., & Monk, C. S. (2009) · Brain Research · doi:10.1016/j.brainres.2009.11.057 · Cited by 441
Imaging human connectomes at the macroscale
Craddock, R. C., Jbabdi, S., Yan, C.-G., Vogelstein, J. T., Castellanos, F. X., Di Martino, A., Kelly, C., Heberlein, K., Colcombe, S., & Milham, M. P. (2013) · Nature Methods · doi:10.1038/nmeth.2482 · Cited by 419
Neubert, F.-X., Mars, R. B., Thomas, A. G., Sallet, J., & Rushworth, M. F. S. (2014) · Neuron · doi:10.1016/j.neuron.2013.11.012 · Cited by 416
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Sallet, J., Mars, R. B., Noonan, M. P., Neubert, F.-X., Jbabdi, S., O'Reilly, J. X., Filippini, N., Thomas, A. G., & Rushworth, M. F. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5108-12.2013 · Cited by 416
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Lu, H., Zuo, Y., Gu, H., Waltz, J. A., Wang, Z., Scholl, C. A., Rea, W. P., Yang, Y., & Stein, E. A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705791104 · Cited by 424
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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
Fox, M. D., Halko, M. A., Eldaief, M. C., & Pascual-Leone, A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.035 · Cited by 395
Self-citationFolloni, D., Verhagen, L., Mars, R. B., Fouragnan, E. F., Constans, C., Aubry, J., Rushworth, M. F. S., & Sallet, J. (2019) · Neuron · doi:10.1016/j.neuron.2019.01.019 · Cited by 405
Leonardi, N., Richiardi, J., Gschwind, M., Simioni, S., Annoni, J., Schluep, M., Vuilleumier, P. O., & Ville, D. V. D. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.07.019 · Cited by 401
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Boly, M., Phillips, C. L. M., Tshibanda, L., Vanhaudenhuyse, A., Schabus, M., Dang‐Vu, T. T., Moonen, G., Hustinx, R., Maquet, P., & Laureys, S. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1417.015 · Cited by 401
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Mohajerani, M. H., Chan, A. W., Mohsenvand, M. ‘., LeDue, J. M., Liu, R., McVea, D. A., Boyd, J. D., Wang, Y. T., Reimers, M., & Murphy, T. H. (2013) · Nature Neuroscience · doi:10.1038/nn.3499 · Cited by 375
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Kelly, C., Toro, R., Di Martino, A., Cox, C. L., Bellec, P., Castellanos, F. X., & Milham, M. P. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.021 · Cited by 374
Okon-Singer, H., Hendler, T., Pessoa, L., & Shackman, A. J. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00058 · Cited by 371
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Ment, L. R., Hirtz, D., & Hüppi, P. S. (2009) · The Lancet Neurology · doi:10.1016/s1474-4422(09)70257-1 · Cited by 383
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Gotts, S. J., Simmons, W. K., Milbury, L. A., Wallace, G. L., Cox, R. W., & Martin, A. (2012) · Brain · doi:10.1093/brain/aws160 · Cited by 369
Resting brains never rest: computational insights into potential cognitive architectures
Deco, G., Jirsa, V., & McIntosh, A. R. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.03.001 · Cited by 388
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Kiviniemi, V. J., Starck, T., Remes, J. J., Long, X., Nikkinen, J., Haapea, M., Veijola, J. M., Moilanen, I. K., Isohanni, M. K., Zang, Y., et al. (2009) · Human Brain Mapping · doi:10.1002/hbm.20813 · Cited by 376
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VALKENBURG, C. T. V. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374168-4.x0001-9 · Cited by 366
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Harrison, B. J., Pujol, J., López-Solà, M., Hernández-Ribas, R., Deus, J., Ortiz, H., Soriano-Mas, C., Yücel, M., Pantelis, C., & Cardoner, N. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711791105 · Cited by 363
Alves, P. N., Foulon, C., Karolis, V., Bzdok, D., Margulies, D. S., Volle, E., & Thiebaut de Schotten, M. (2019) · Communications Biology · doi:10.1038/s42003-019-0611-3 · Cited by 357
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Mennes, M., Kelly, C. A. M., Zuo, X., Martino, A. D., Biswal, B. B., Castellanos, F. X., & Milham, M. P. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.01.002 · Cited by 368
Atypical default network connectivity in youth with attention-deficit/hyperactivity disorder
Fair, D. A., Posner, J., Nagel, B. J., Bathula, D., Dias, T. G. C., Mills, K. L., Blythe, M. S., Giwa, A., Schmitt, C. F., & Nigg, J. T. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.07.003 · Cited by 354
Petrides, M., Tomaiuolo, F., Yeterian, E. H., & Pandya, D. Ν. (2011) · Cortex · doi:10.1016/j.cortex.2011.07.002 · Cited by 353
Yuan, H., Zotev, V., Phillips, R., Drevets, W. C., & Bodurka, J. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.02.031 · Cited by 352
Exploring the network dynamics underlying brain activity during rest
Cabral, J., Kringelbach, M. L., & Deco, G. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.12.005 · Cited by 351
Unraveling the Miswired Connectome: A Developmental Perspective
Martino, A. D., Fair, D. A., Kelly, C. A. M., Satterthwaite, T. D., Castellanos, F. X., Thomason, M. E., Craddock, R. C., Luna, B., LEVENTHAL, B. L., Zuo, X., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.050 · Cited by 357
High-resolution photoacoustic tomography of resting-state functional connectivity in the mouse brain
Avanaki, K., Xia, J., Wan, H., Bauer, A. Q., Culver, J. P., & Wang, L. V. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1311868111 · Cited by 350
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Zhang, D., Snyder, A. Z., Shimony, J. S., Fox, M., & Raichle, M. E. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp182 · Cited by 351
Self-citationGrandjean, J., Schroeter, A., Batata, I., & Rudin, M. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.08.043 · Cited by 339
Brain spontaneous functional connectivity and intelligence
Song, M., Zhou, Y., Li, J., Liu, Y., Tian, L., Yu, C., & Jiang, T. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.02.036 · Cited by 353
The contribution of network organization and integration to the development of cognitive control
Marek, S., Hwang, K., Foran, W., Hallquist, M. N., & Luna, B. (2015) · PLOS Biology · doi:10.1371/journal.pbio.1002328 · Cited by 337
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Bellec, P., Rosa‐Neto, P., Lyttelton, O. C., Benali, H., & Evans, A. C. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.02.082 · Cited by 343
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He, B. J., & Raichle, M. E. (2009) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2009.04.004 · Cited by 332
Self-citationBoly, M., Tshibanda, L., Vanhaudenhuyse, A., Noirhomme, Q., Schnakers, C., Ledoux, D., Boveroux, P., Garweg, C., Lambermont, B. C., Phillips, C. L. M., et al. (2009) · Human Brain Mapping · doi:10.1002/hbm.20672 · Cited by 333
Offline impact of transcranial focused ultrasound on cortical activation in primates
Verhagen, L., Galléa, C., Folloni, D., Constans, C., Jensen, D. E. A., Ahnine, H., Roumazeilles, L., Santin, M. D., Ahmed, B., Lehéricy, S., et al. (2019) · eLife · doi:10.7554/elife.40541 · Cited by 319
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Self-citationSpontaneous local variations in ongoing neural activity bias perceptual decisions
Hesselmann, G., Kell, C. A., Eger, E., & Kleinschmidt, A. K. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0712043105 · Cited by 333
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Deco, G., & Corbetta, M. (2010) · The Neuroscientist · doi:10.1177/1073858409354384 · Cited by 323
Self-citationBrain connectivity in neurodegenerative diseases—from phenotype to proteinopathy
Pievani, M., Filippini, N., van den Heuvel, M. P., Cappa, S. F., & Frisoni, G. B. (2014) · Nature Reviews Neurology · doi:10.1038/nrneurol.2014.178 · Cited by 320
Propagation of Protein Aggregation in Neurodegenerative Diseases
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Gu, H., Salmeron, B. J., Ross, T. J., Geng, X., Wang, Z., Stein, E. A., & Yang, Y. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.06.066 · Cited by 306
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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