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

The DOI matches its Crossref record; 45 of the 46 references it cites were found in a registry or an index.

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

Open this paper in CoChat — free account

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.

Integrity signals

Registry

Crossref · 10.1038/nature05758

Cites

45 of 45 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

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

Sorted by citations

Items 401–500 of 1,004

Disrupted intrinsic functional connectivity in the vegetative state
Cauda, F., Micon, B. M., Sacco, K., Duca, S., D’Agata, F., Geminiani, G. C., & Canavero, S. (2008) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2007.142349 · Cited by 145
Endless Fluctuations: Temporal Dynamics of the Amplitude of Low Frequency Fluctuations
Liao, W., Chen, H., Li, J., Ji, G., Wu, G., Long, Z., Xu, Q., Duan, X., Cui, Q., & Biswal, B. B. (2019) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2019.2904555 · Cited by 143
What can spontaneous fluctuations of the blood oxygenation-level-dependent signal tell us about psychiatric disorders?
Fornito, A., & Bullmore, E. T. (2010) · Current Opinion in Psychiatry · doi:10.1097/yco.0b013e328337d78d · Cited by 146
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 145
In vivo Large-Scale Cortical Mapping Using Channelrhodopsin-2 Stimulation in Transgenic Mice Reveals Asymmetric and Reciprocal Relationships between Cortical Areas
Lim, D. H., Mohajerani, M. H., LeDue, J. M., Boyd, J. D., Chen, S., & Murphy, T. H. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00011 · Cited by 142
Wandering tales: evolutionary origins of mental time travel and language
Corballis, M. C. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00485 · Cited by 141
Default‐mode network functional connectivity is closely related to metabolic activity
Passow, S., Specht, K., Adamsen, T. C. H., Biermann, M., Brekke, N., Craven, A. R., Ersland, L., Grüner, R., Kleven‐Madsen, N., Kvernenes, O. H., et al. (2015) · Human Brain Mapping · doi:10.1002/hbm.22753 · Cited by 146
Monkey in the middle: why non-human primates are needed to bridge the gap in resting-state investigations
Hutchison, R. M., & Everling, S. (2012) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2012.00029 · Cited by 143
How are different neural networks related to consciousness?
Qin, P., Wu, X., Huang, Z., Duncan, N. W., Tang, W., Wolff, A., Hu, J., Gao, L., Jin, Y., Wu, X., et al. (2015) · Annals of Neurology · doi:10.1002/ana.24479 · Cited by 146
Identifying the default‐mode component in spatial IC analyses of patients with disorders of consciousness
Soddu, A., Vanhaudenhuyse, A., Bahri, M. A., Bruno, M., Boly, M., Athena Demertzi, A., Tshibanda, J., Phillips, C. L. M., Stanziano, M., Ovadia‐Caro, S., et al. (2011) · Human Brain Mapping · doi:10.1002/hbm.21249 · Cited by 145
Functional MRI neurofeedback training on connectivity between two regions induces long-lasting changes in intrinsic functional network
Megumi, F., Yamashita, A., Kawato, M., & Imamizu, H. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00160 · Cited by 143
Anticorrelated resting-state functional connectivity in awake rat brain
Liang, Z., King, J. A., & Zhang, N. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.08.009 · Cited by 139
Large-Scale Brain Networks in the Awake, Truly Resting Marmoset Monkey
Belcher, A. M., Yen, C. C., Stepp, H., Gu, H., Lu, H., Yang, Y., Silva, A. C., & Stein, E. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3146-13.2013 · Cited by 142
Task-induced brain connectivity promotes the detection of individual differences in brain-behavior relationships
Jiang, R., Zuo, N., Ford, J. M., Qi, S., Zhi, D., Zhuo, C., Xu, Y., Fu, Z., Bustillo, J., Turner, J. A., et al. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116370 · Cited by 142
Individual-specific functional connectivity of the amygdala: A substrate for precision psychiatry
Sylvester, C. M., Yu, Q., Srivastava, A. B., Marek, S., Zheng, A., Alexopoulos, D., Smyser, C. D., Shimony, J. S., Ortega, M., Dierker, D. L., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1910842117 · Cited by 139
Self-citation
Resting-state networks in the macaque at 7T
Hutchison, R. M., Leung, L.-W. S., Mirsattari, S. M., Gati, J. S., Menon, R. S., & Everling, S. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.02.063 · Cited by 141
Development of the Brain’s Functional Network Architecture
Vogel, A. C., Power, J. D., Petersen, S. E., & Schlaggar, B. L. (2010) · Neuropsychology Review · doi:10.1007/s11065-010-9145-7 · Cited by 143
Cingulate cortex: Diverging data from humans and monkeys
Cole, M. W., Yeung, N., Freiwald, W. A., & Botvinick, M. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.07.001 · Cited by 143
Isoflurane induces dose-dependent alterations in the cortical connectivity profiles and dynamic properties of the brain's functional architecture
Hutchison, R. M., Hutchison, M., Manning, K. Y., Menon, R. S., & Everling, S. (2014) · Human Brain Mapping · doi:10.1002/hbm.22583 · Cited by 141
Functional connectivity and network analysis of midbrain and brainstem nuclei
Bär, K.-J., de la Cruz, F., Schumann, A., Koehler, S., Sauer, H., Critchley, H., & Wagner, G. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.03.071 · Cited by 134
A Novel Data-Driven Approach to Preoperative Mapping of Functional Cortex Using Resting-State Functional Magnetic Resonance Imaging
Mitchell, T. J., Hacker, C. D., Breshears, J. D., Szrama, N. P., Sharma, M., Bundy, D. T., Pahwa, M., Corbetta, M., Snyder, A. Z., Shimony, J. S., et al. (2013) · Neurosurgery · doi:10.1227/neu.0000000000000141 · Cited by 141
Self-citation
Default Mode Network Connectivity in Stroke Patients
Tuladhar, A. M., Snaphaan, L. J. A. E., Shumskaya, E., Rijpkema, M., Fernández, G., Norris, D. G., & de Leeuw, F. (2013) · PLoS ONE · doi:10.1371/journal.pone.0066556 · Cited by 143
Just a thought: How mind-wandering is represented in dynamic brain connectivity
Kucyi, A. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.07.001 · Cited by 142
The State of Resting State Networks
Seitzman, B. A., Snyder, A. Z., Leuthardt, E. C., & Shimony, J. S. (2019) · Topics in Magnetic Resonance Imaging · doi:10.1097/rmr.0000000000000214 · Cited by 153
Self-citation
Regional, Layer, and Cell-Type-Specific Connectivity of the Mouse Default Mode Network
Whitesell, J. D., Liska, A., Coletta, L., Hirokawa, K. E., Bohn, P., Williford, A., Groblewski, P. A., Graddis, N., Kuan, L., Knox, J. E., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.11.011 · Cited by 139
Self-similar correlation function in brain resting-state functional magnetic resonance imaging
Expert, P., Lambiotte, R., Chialvo, D. R., Christensen, K., Jensen, H. J., Sharp, D. J., & Turkheimer, F. (2010) · Journal of The Royal Society Interface · doi:10.1098/rsif.2010.0416 · Cited by 137
Recent advances in disorders of consciousness: Focus on the diagnosis
Gosseries, O., Zasler, N. D., & Laureys, S. (2014) · Brain Injury · doi:10.3109/02699052.2014.920522 · Cited by 133
Exploring the electrophysiological correlates of the default-mode network with intracerebral EEG
Jerbi (2010) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2010.00027 · Cited by 133
Cluster analysis of resting-state fMRI time series
Mezer, A., Yovel, Y., Pasternak, O., Gorfine, T., & Assaf, Y. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.12.015 · Cited by 135
Conceptual grounding of language in action and perception: a neurocomputational model of the emergence of category specificity and semantic hubs
Garagnani, M., & Friedemann Pulvermüller, A. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13145 · Cited by 142
Resting-state Dynamics as a Cortical Signature of Anesthesia in Monkeys
Uhrig, L., Sitt, J. D., Jacob, A., Tasserie, J., Barttfeld, P., Dupont, M., Dehaene, S., & Jarraya, B. (2018) · Anesthesiology · doi:10.1097/aln.0000000000002336 · Cited by 131
Intersubject Variability of and Genetic Effects on the Brain's Functional Connectivity during Infancy
Gao, W., Elton, A., Zhu, H., Alcauter, S., Smith, J. K., Gilmore, J. H., & Lin, W. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.5072-13.2014 · Cited by 131
Connectivity trajectory across lifespan differentiates the precuneus from the default network
Yang, Z., Chang, C., Xu, T., Jiang, L., Handwerker, D. A., Castellanos, F. X., Milham, M. P., Bandettini, P. A., & Zuo, X. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.10.039 · Cited by 133
Specific Substantial Dysconnectivity in Schizophrenia: A Transdiagnostic Multimodal Meta-analysis of Resting-State Functional and Structural Magnetic Resonance Imaging Studies
Brandl, F., Avram, M., Weise, B., Shang, J., Simões, B., Bertram, T., Ayala, D. H., Penzel, N., Gürsel, D. A., Bäuml, J., et al. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.12.003 · Cited by 142
Bridging the gap between the human and macaque connectome: a quantitative comparison of global interspecies structure–function relationships and network topology
Miranda-Dominguez, O., Mills, B. D., Grayson, D., Woodall, A., Grant, K. A., Kroenke, C. D., & Fair, D. A. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.4229-13.2014 · Cited by 130
Human neoteny revisited: The case of synaptic plasticity
Bufill, E., Agustí, J., & Blesa, R. (2011) · American Journal of Human Biology · doi:10.1002/ajhb.21225 · Cited by 130
Intrinsic Functional Brain Architecture Derived from Graph Theoretical Analysis in the Human Fetus
Thomason, M. E., Brown, J. A., Dassanayake, M. T., Shastri, R., Marusak, H. A., Hernandez-Andrade, E., Yeo, L., Mody, S., Berman, S., Hassan, S. S., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0094423 · Cited by 130
Intrinsic connectivity in the human brain does not reveal networks for ‘basic’ emotions
Touroutoglou, A., Lindquist, K. A., Dickerson, B. C., & Barrett, L. F. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv013 · Cited by 147
Intracranial Electrophysiology Reveals Reproducible Intrinsic Functional Connectivity within Human Brain Networks
Kucyi, A., Schrouff, J., Bickel, S., Foster, B. L., Shine, J. M., & Parvizi, J. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0217-18.2018 · Cited by 134
Task-free presurgical mapping using functional magnetic resonance imaging intrinsic activity
Liu, H., Buckner, R. L., Talukdar, T., Tanaka, N., Madsen, J. R., & Stufflebeam, S. M. (2009) · Journal of neurosurgery · doi:10.3171/2008.10.jns08846 · Cited by 129
Differential modulation of the default mode network via serotonin-1A receptors
Hahn, A., Wadsak, W., Windischberger, C., Baldinger, P., Höflich, A. S., Lošák, J., Nics, L., Philippe, C., Kranz, G. S., Kraus, C., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1117104109 · Cited by 133
Locomotion-dependent remapping of distributed cortical networks
Clancy, K. B., Oršolić, I., & Mrsic‐Flogel, T. D. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0357-8 · Cited by 134
Low-frequency BOLD fluctuations demonstrate altered thalamocortical connectivity in diabetic neuropathic pain
Cauda, F., Sacco, K., D’Agata, F., Duca, S., Cocito, D., Geminiani, G. C., Migliorati, F., & Isoardo, G. (2009) · BMC Neuroscience · doi:10.1186/1471-2202-10-138 · Cited by 131
Strengthening Connections: Functional Connectivity and Brain Plasticity
Kelly, C. A. M., & Castellanos, F. X. (2014) · Neuropsychology Review · doi:10.1007/s11065-014-9252-y · Cited by 132
Functional connectivity of left Heschl's gyrus in vulnerability to auditory hallucinations in schizophrenia
Shinn, A. K., Baker, J. T., Cohen, B. M., & Öngür, D. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.11.037 · Cited by 136
Self-citation
Structural Variability Across the Primate Brain: A Cross-Species Comparison
Croxson, P. L., Forkel, S. J., Cerliani, L., & de Schotten, M. T. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx244 · Cited by 133
Neural Basis of Motivational and Cognitive Control
Mars, R., Sallet, J., Mfs., R., & Yeung, N. (2011) · The MIT Press eBooks · doi:10.7551/mitpress/9780262016438.001.0001 · Cited by 128
Ongoing physiological processes in the cerebral cortex
Leopold, D. A., & Maier, A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.10.059 · Cited by 127
Functional MRI connectivity as a predictor of the surgical outcome of epilepsy
Negishi, M., Martuzzi, R., Novotny, E. J., Spencer, D. D., & Constable, R. T. (2011) · Epilepsia · doi:10.1111/j.1528-1167.2011.03191.x · Cited by 127
Resting-State Neural Activity across Face-Selective Cortical Regions Is Behaviorally Relevant
Zhu, Q., Zhang, J., Luo, Y., Dilks, D. D., & Liu, J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0873-11.2011 · Cited by 136
Stable and dynamic cortical electrophysiology of induction and emergence with propofol anesthesia
Breshears, J. D., Roland, J. L., Sharma, M., Gaona, C. M., Freudenburg, Z. V., Tempelhoff, R., Avidan, M. S., & Leuthardt, E. C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1011949107 · Cited by 129
Reduced Fractional Anisotropy of Corpus Callosum Modulates Inter-Hemispheric Resting State Functional Connectivity in Migraine Patients without Aura
Yuan, K., Qin, W., Liu, P., Zhao, L., Yu, D., Zhao, L., Dong, M., Liu, J., Yang, X., von Deneen, K. M., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0045476 · Cited by 130
Eigenmodes of brain activity: Neural field theory predictions and comparison with experiment
Robinson, P. A., Zhao, X., Aquino, K. M., Griffiths, J. D., Sarkar, S., & Mehta-Pandejee, G. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.04.050 · Cited by 129
Cortical network dynamics with time delays reveals functional connectivity in the resting brain
Ghosh, A., Rho, Y.-A., McIntosh, A. R., Kötter, R., & Jirsa, V. (2008) · Cognitive Neurodynamics · doi:10.1007/s11571-008-9044-2 · Cited by 130
The role of impaired neuronal communication in neurological disorders
He, B. J., Shulman, G. L., Snyder, A. Z., & Corbetta, M. (2007) · Current Opinion in Neurology · doi:10.1097/wco.0b013e3282f1c720 · Cited by 126
Self-citation
Mapping resting-state brain networks in conscious animals
Zhang, N., Rane, P., Huang, W., Liang, Z., Kennedy, D. N., Frazier, J. A., & King, J. A. (2010) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2010.04.001 · Cited by 128
Harmonic brain modes: a unifying framework for linking space and time in brain dynamics
Atasoy, S., Deco, G., Kringelbach, M. L., & Pearson, J. (2018) · The Neuroscientist · doi:10.1177/1073858417728032 · Cited by 124
Contrasting Activity Profile of Two Distributed Cortical Networks as a Function of Attentional Demands
Popa, D., Popescu, A. T., & Paré, D. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4867-08.2009 · Cited by 129
Characterization of Post-traumatic Stress Disorder Using Resting-State fMRI with a Multi-level Parametric Classification Approach
Liu, F., Xie, B., Wang, Y., Guo, W., Fouché, J., Long, Z., Wang, W., Chen, H., Li, M., Duan, X., et al. (2014) · Brain Topography · doi:10.1007/s10548-014-0386-2 · Cited by 126
Prefrontal and limbic resting state brain network functional connectivity differs between nicotine-dependent smokers and non-smoking controls
Janes, A. C., Nickerson, L. D. H., Frederick, B. B., & Kaufman, M. J. (2012) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2012.02.020 · Cited by 127
Replay, the default mode network and the cascaded memory systems model
Kaefer, K., Stella, F., McNaughton, B. L., & Battaglia, F. P. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-022-00620-6 · Cited by 132
Information processing architecture of functionally defined clusters in the macaque cortex
Shen, K., Bezgin, G., Hutchison, R. M., Gati, J. S., Menon, R. S., Everling, S., & McIntosh, A. R. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.2709-12.2012 · Cited by 123
Parcellating an Individual Subject's Cortical and Subcortical Brain Structures Using Snowball Sampling of Resting-State Correlations
Wig, G. S., Laumann, T. O., Cohen, A. L., Power, J. D., Nelson, S. M., Glasser, M. F., Miezin, F. M., Snyder, A. Z., Schlaggar, B. L., & Petersen, S. E. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht056 · Cited by 126
Self-citation
Functional connectivity in apathy of late-life depression: A preliminary study
Alexopoulos, G. S., Hoptman, M. J., Yuen, G. S., Kanellopoulos, D., Seirup, J. K., Lim, K. O., & Gunning, F. M. (2012) · Journal of Affective Disorders · doi:10.1016/j.jad.2012.11.023 · Cited by 122
Connectivity pattern changes in default-mode network with deep non-REM and REM sleep
Koike, T., Kan, S., Misaki, M., & Miyauchi, S. (2011) · Neuroscience Research · doi:10.1016/j.neures.2010.12.018 · Cited by 126
Emerging Roles of the Brain’s Default Network
Mantini, D., & Vanduffel, W. (2012) · The Neuroscientist · doi:10.1177/1073858412446202 · Cited by 129
Delineating functional segregations of the human middle temporal gyrus with resting‐state functional connectivity and coactivation patterns
Xu, J., Lyu, H., Li, T., Xu, Z., Fu, X., Jia, F., Wang, J., & Hu, Q. (2019) · Human Brain Mapping · doi:10.1002/hbm.24763 · Cited by 121
Asymmetry of Anticipatory Activity in Visual Cortex Predicts the Locus of Attention and Perception
Sylvester, C. M., Shulman, G. L., Jack, A. I., & Corbetta, M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3759-07.2007 · Cited by 124
Self-citation
Atypical network connectivity for imitation in autism spectrum disorder
Shih, P., Shen, M., Öttl, B., Keehn, B., Gaffrey, M. S., & Müller, R.-A. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.05.035 · Cited by 120
Mapping higher-order relations between brain structure and function with embedded vector representations of connectomes
Rosenthal, G., Váša, F., Griffa, A., Hagmann, P., Amico, E., Goñi, J., Avidan, G., & Sporns, O. (2018) · Nature Communications · doi:10.1038/s41467-018-04614-w · Cited by 127
Interspecies activity correlations reveal functional correspondence between monkey and human brain areas
Mantini, D., Hasson, U., Betti, V., Perrucci, M. G., Romani, G. L., Corbetta, M., Orban, G. A., & Vanduffel, W. (2012) · Nature Methods · doi:10.1038/nmeth.1868 · Cited by 120
Self-citation
Concurrent brain-stimulation and neuroimaging for studies of cognition
Driver, J., Blankenburg, F., Bestmann, S., Vanduffel, W., & Ruff, C. C. (2009) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2009.04.007 · Cited by 119
Functional connectivity of the frontal eye fields in humans and macaque monkeys investigated with resting-state fMRI
Hutchison, R. M., Gallivan, J. P., Culham, J. C., Gati, J. S., Menon, R. S., & Everling, S. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00891.2011 · Cited by 123
Focal Pontine Lesions Provide Evidence That Intrinsic Functional Connectivity Reflects Polysynaptic Anatomical Pathways
Lu, J., Liu, H., Zhang, M., Wang, D., Cao, Y., Ma, Q., Rong, D., Wang, X., Buckner, R. L., & Li, K. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2364-11.2011 · Cited by 118
Effects of Ketamine on Resting-State EEG Activity and Their Relationship to Perceptual/Dissociative Symptoms in Healthy Humans
de la Salle, S., Choueiry, J., Shah, D. K., Bowers, H., McIntosh, J. F., Ilivitsky, V., & Knott, V. (2016) · Frontiers in Pharmacology · doi:10.3389/fphar.2016.00348 · Cited by 118
Is the parietal lobe necessary for recollection in humans?
Simons, J. S., Peers, P. V., Hwang, D. Y., Ally, B. A., Fletcher, P. C., & Budson, A. E. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.07.024 · Cited by 118
Assessing neuronal networks: Understanding Alzheimer's disease
Bokde, A. L. W., Ewers, M., & Hampel, H. J. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.06.004 · Cited by 120
Organization of the human cerebral cortex estimated within individuals: networks, global topography, and function
Du, J., DiNicola, L. M., Angeli, P. A., Saadon‐Grosman, N., Sun, W., Kaiser, S., Ladopoulou, J., Xue, A., Yeo, B. T. T., Eldaief, M. C., et al. (2024) · Journal of Neurophysiology · doi:10.1152/jn.00308.2023 · Cited by 122
Attractors and noise: Twin drivers of decisions and multistability
Braun, J., & Mattia, M. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.12.126 · Cited by 124
Broadband Local Field Potentials Correlate with Spontaneous Fluctuations in Functional Magnetic Resonance Imaging Signals in the Rat Somatosensory Cortex Under Isoflurane Anesthesia
Pan, W., Thompson, G. J., Magnuson, M. E., Majeed, W., Jaeger, D., & Keilholz, S. D. (2011) · Brain Connectivity · doi:10.1089/brain.2011.0014 · Cited by 119
Slow EEG pattern predicts reduced intrinsic functional connectivity in the default mode network: An inter-subject analysis
Hlinka, J., Alexakis, C., Diukova, A., Liddle, P. F., & Auer, D. P. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.06.002 · Cited by 116
Sleep and the functional connectome
Picchioni, D., Duyn, J. H., & Horovitz, S. G. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.067 · Cited by 115
Deactivation of the Default Mode Network as a Marker of Impaired Consciousness: An fMRI Study
Crone, J. S., Ladurner, G., Höller, Y., Golaszewski, S. M., Trinka, E., & Kronbichler, M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026373 · Cited by 120
Measuring Cortical Connectivity in Alzheimer’s Disease as a Brain Neural Network Pathology: Toward Clinical Applications
Teipel, S. J., Grothe, M. J., Zhou, J. H., Sepulcre, J., Dyrba, M., Sorg, C., & Babiloni, C. (2016) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617715000995 · Cited by 117
Machine-learning to characterise neonatal functional connectivity in the preterm brain
Ball, G., Aljabar, P., Arichi, T., Tusor, N., Cox, D., Merchant, N., Nongena, P., Hajnal, J. V., Edwards, A. D., & Counsell, S. J. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.08.055 · Cited by 114
Effects of White Matter Injury on Resting State fMRI Measures in Prematurely Born Infants
Smyser, C. D., Snyder, A. Z., Shimony, J. S., Blazey, T., Inder, T. E., & Neil, J. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068098 · Cited by 120
Self-citation
Stable long-range interhemispheric coordination is supported by direct anatomical projections
Shen, K., Mišić, B., Cipollini, B., Bezgin, G., Buschkuehl, M., Hutchison, R. M., Jaeggi, S. M., Kross, E. F., Peltier, S., Everling, S., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1503436112 · Cited by 114
Watching my mind unfold versus yours: an fMRI study using a novel camera technology to examine neural differences in self-projection of self versus other perspectives
St. Jacques, P. L., Conway, M. A., Lowder, M. W., & Cabeza, R. (2011) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2010.21518 · Cited by 113
Human brain evolution writ large and small
Sherwood, C. C., Bauernfeind, A. L., Bianchi, S., Raghanti, M. A., & Hof, P. R. (2012) · Progress in Brain Research · doi:10.1016/b978-0-444-53860-4.00011-8 · Cited by 113
CRHR1 genotypes, neural circuits and the diathesis for anxiety and depression
Rogers, J., Raveendran, M., Fawcett, G., Fox, A. S., Shelton, S., Oler, J., Cheverud, J. M., Muzny, D., Gibbs, R. A., Davidson, R. J., et al. (2012) · Molecular Psychiatry · doi:10.1038/mp.2012.152 · Cited by 117
Interhemispheric neuroplasticity following limb deafferentation detected by resting-state functional connectivity magnetic resonance imaging (fcMRI) and functional magnetic resonance imaging (fMRI)
Pawela, C. P., Biswal, B. B., Hudetz, A. G., Li, R., Jones, S. R., Cho, Y. R., Matloub, H. S., & Hyde, J. S. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.09.054 · Cited by 112
Monkey Cortex through fMRI Glasses
Vanduffel, W., Zhu, Q., & Orban, G. A. (2014) · Neuron · doi:10.1016/j.neuron.2014.07.015 · Cited by 115
Hippocampal Sharp-Wave Ripples Influence Selective Activation of the Default Mode Network
Kaplan, R., Adhikari, M. H., Hindriks, R., Mantini, D., Murayama, Y., Logothetis, N. K., & Deco, G. (2016) · Current Biology · doi:10.1016/j.cub.2016.01.017 · Cited by 116
Animal Functional Magnetic Resonance Imaging: Trends and Path Toward Standardization
Mandino, F., Cerri, D. H., Garin, C. M., Straathof, M., van Tilborg, G. A. F., Chakravarty, M. M., Dhénain, M., Dijkhuizen, R. M., Gozzi, A., Heß, A., et al. (2020) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2019.00078 · Cited by 115
Evolution of working memory
Carruthers, P. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1301195110 · Cited by 110
Functional connectivity of the sensorimotor area in naturally sleeping infants
Liu, W.-C., Flax, J. F., Guise, K. G., Sukul, V., & Benasich, A. A. (2008) · Brain Research · doi:10.1016/j.brainres.2008.05.054 · Cited by 110
Detection of functional connectivity in the resting mouse brain
Nasrallah, F. A., Tay, H. C., & Chuang, K. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.10.025 · Cited by 110
Cross-species cortical alignment identifies different types of anatomical reorganization in the primate temporal lobe
Eichert, N., Robinson, E. C., Bryant, K., Jbabdi, S., Jenkinson, M., Li, L., Krug, K., Watkins, K. E., & Mars, R. B. (2020) · eLife · doi:10.7554/elife.53232 · Cited by 113
Characterizing individual differences in functional connectivity using dual-regression and seed-based approaches
Smith, D. V., Utevsky, A. V., Bland, A. R., Clement, N. J., Clithero, J. A., Harsch, A. E. W., Carter, R. M., & Huettel, S. A. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.03.042 · Cited by 116
Mapping putative hubs in human, chimpanzee and rhesus macaque connectomes via diffusion tractography
Li, L., Hu, X., Preuss, T. M., Glasser, M. F., Damen, F. W., Qiu, Y., & Rilling, J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.04.024 · Cited by 109

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

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Intrinsic functional architecture in the anaesthetized monkey brain

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks