The DOI matches its Crossref record; 33 of the 33 references it cites were found in a registry or an index.
Resting-state networks show dynamic functional connectivity in awake humans and anesthetized macaques
Open accessAbstract
Characterization of large-scale brain networks using blood-oxygenation-level-dependent functional magnetic resonance imaging is typically based on the assumption of network stationarity across the duration of scan. Recent studies in humans have questioned this assumption by showing that within-network functional connectivity fluctuates on the order of seconds to minutes. Time-varying profiles of resting-state networks (RSNs) may relate to spontaneously shifting, electrophysiological network states and are thus mechanistically of particular importance. However, because these studies acquired data from awake subjects, the fluctuating connectivity could reflect various forms of conscious brain processing such as passive mind wandering, active monitoring, memory formation, or changes in attention and arousal during image acquisition. Here, we characterize RSN dynamics of anesthetized macaques that control for these accounts, and compare them to awake human subjects. We find that functional connectivity among nodes comprising the "oculomotor (OCM) network" strongly fluctuated over time during awake as well as anaesthetized states. For time dependent analysis with short windows (<60 s), periods of positive functional correlations alternated with prominent anticorrelations that were missed when assessed with longer time windows. Similarly, the analysis identified network nodes that transiently link to the OCM network and did not emerge in average RSN analysis. Furthermore, time-dependent analysis reliably revealed transient states of large-scale synchronization that spanned all seeds. The results illustrate that resting-state functional connectivity is not static and that RSNs can exhibit nonstationary, spontaneous relationships irrespective of conscious, cognitive processing. The findings imply that mechanistically important network information can be missed when using average functional connectivity as the single network measure.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Functional connectivity in the motor cortex of resting human brain using echo‐planar mri
Biswal, B., Zerrin Yetkin, F., Haughton, V. M., & Hyde, J. S. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910340409 · Cited by 9,812
Distributed hierarchical processing in the primate cerebral cortex
Felleman, D. J., & Van Essen, D. C. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1 · Cited by 7,783
Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging
Fox, M. D., & Raichle, M. E. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2201 · Cited by 6,700
Neurophysiological investigation of the basis of the fMRI signal
Logothetis, N. K., Pauls, J., Augath, M., Trinath, T., & Oeltermann, A. (2001) · Nature · doi:10.1038/35084005 · Cited by 6,551
Consistent resting-state networks across healthy subjects
Damoiseaux, J. S., Rombouts, S. A. R. B., Barkhof, F., Scheltens, P., Stam, C. J., Smith, S. M., & Beckmann, C. F. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601417103 · Cited by 4,326
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
The Medial Temporal Lobe Memory System
Squire, L. R., & Zola-Morgan, S. (1991) · Science · doi:10.1126/science.1896849 · Cited by 3,282
Wandering minds: the default network and stimulus-independent thought
Mason, M. F., Norton, M. I., Van Horn, J. D., Wegner, D. M., Grafton, S. T., & Macrae, C. N. (2007) · Science · doi:10.1126/science.1131295 · Cited by 2,792
Murphy, K., Birn, R. M., Handwerker, D. A., Jones, T. B., & Bandettini, P. A. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.09.036 · Cited by 2,387
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
Cited by
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-citationTracking whole-brain connectivity dynamics in the resting state
Allen, E. A., Damaraju, E., Plis, S. M., Erhardt, E. B., Eichele, T., & Calhoun, V. D. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs352 · Cited by 2,992
Network attributes for segregation and integration in the human brain
Sporns, O. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.11.015 · Cited by 1,067
Shine, J. M., Bissett, P. G., Bell, P. T., Koyejo, O., Balsters, J. H., Gorgolewski, K. J., Moodie, C. A., & Poldrack, R. A. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.018 · Cited by 886
Opportunities and limitations of intrinsic functional connectivity MRI
Buckner, R. L., Krienen, F. M., & Yeo, B. T. T. (2013) · Nature Neuroscience · doi:10.1038/nn.3423 · Cited by 912
Time-resolved resting-state brain networks
Zalesky, A., Fornito, A., Cocchi, L., Gollo, L. L., & Breakspear, M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1400181111 · Cited by 753
On spurious and real fluctuations of dynamic functional connectivity during rest
Leonardi, N., & Van De Ville, D. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2014.09.007 · Cited by 828
Signature of consciousness in the dynamics of resting-state brain activity
Barttfeld, P., Uhrig, L., Sitt, J. D., Sigman, M., Jarraya, B., & Dehaene, S. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1418031112 · Cited by 670
Dynamic 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
Can sliding-window correlations reveal dynamic functional connectivity in resting-state fMRI?
Hindriks, R., Adhikari, M. H., Murayama, Y., Ganzetti, M., Mantini, D., Logothetis, N. K., & Deco, G. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.11.055 · Cited by 632
Questions and controversies in the study of time-varying functional connectivity in resting fMRI
Lurie, D. J., Kessler, D., Bassett, D. S., Betzel, R. F., Breakspear, M., Kheilholz, S., Kucyi, A., Liégeois, R., Lindquist, M. A., McIntosh, A. R., et al. (2020) · Network Neuroscience · doi:10.1162/netn_a_00116 · Cited by 648
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
Kucyi, A., & Davis, K. D. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2014.11.006 · Cited by 587
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
Cabral, J., Vidaurre, D., Marques, P., Magalhães, R., Silva Moreira, P., Miguel Soares, J., Deco, G., Sousa, N., & Kringelbach, M. L. (2017) · Scientific Reports · doi:10.1038/s41598-017-05425-7 · Cited by 386
Dynamic Resting-State Functional Connectivity in Major Depression
Kaiser, R. H., Whitfield-Gabrieli, S., Dillon, D. G., Goer, F., Beltzer, M., Minkel, J., Smoski, M., Dichter, G., & Pizzagalli, D. A. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2015.352 · Cited by 438
An anatomical substrate for integration among functional networks in human cortex
van den Heuvel, M. P., & Sporns, O. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.2128-13.2013 · Cited by 404
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
When the Brain Takes a Break: A Model-Based Analysis of Mind Wandering
Mittner, M., Boekel, W., Tucker, A. M., Turner, B. M., Heathcote, A., & Forstmann, B. U. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.2062-14.2014 · Cited by 228
Towards a new approach to reveal dynamical organization of the brain using topological data analysis
Saggar, M., Sporns, O., Gonzalez-Castillo, J., Bandettini, P. A., Carlsson, G., Glover, G., & Reiss, A. L. (2018) · Nature Communications · doi:10.1038/s41467-018-03664-4 · Cited by 253
Betzel, R. F., Fukushima, M., He, Y., Zuo, X.-N., & Sporns, O. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.12.001 · Cited by 249
“…applied widely to study dynamic connectivity of functional brain networks estimated from both fMRI BOLD (Allen et al., 2012; Bassett et al., 2013; Hutchison et al., 2013b; Gonzalez-Castillo et al., 2014; Zalesky et al., 2014; Shen et al., 2015b,a; Karahanoğlu and Van De Ville, 2015) and…”
BackgroundMethodInfluentialEstimation of dynamic functional connectivity using multiplication of temporal derivatives
Shine, J. M., Koyejo, O., Bell, P. T., Gorgolewski, K. J., Gilat, M., & Poldrack, R. A. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.07.064 · Cited by 166
Tasserie, J., Uhrig, L., Sitt, J. D., Manasova, D., Dupont, M., Dehaene, S., & Jarraya, B. (2022) · Science Advances · doi:10.1126/sciadv.abl5547 · Cited by 171
Network structure shapes spontaneous functional connectivity dynamics
Shen, K., Hutchison, R. M., Bezgin, G., Everling, S., & McIntosh, A. R. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.4903-14.2015 · Cited by 171
Self-citationIntrinsic functional connectivity variance and state‐specific under‐connectivity in autism
Chen, H., Nomi, J. S., Uddin, L. Q., Duan, X., & Chen, H. (2017) · Human Brain Mapping · doi:10.1002/hbm.23764 · Cited by 137
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
Chronnectomic patterns and neural flexibility underlie executive function
Nomi, J. S., Vij, S. G., Dajani, D. R., Steimke, R., Damaraju, E., Rachakonda, S., Calhoun, V. D., & Uddin, L. Q. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2016.10.026 · Cited by 131
Dynamic functional connectivity and brain metastability during altered states of consciousness
Cavanna, F., Vilas, M. G., Palmucci, M., & Tagliazucchi, E. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2017.09.065 · Cited by 137
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
Self-citationRashid, B., Blanken, L. M. E., Muetzel, R. L., Miller, R., Damaraju, E., Arbabshirani, M. R., Erhardt, E. B., Verhulst, F. C., van der Lugt, A., Jaddoe, V. W. V., et al. (2018) · Human Brain Mapping · doi:10.1002/hbm.24064 · Cited by 120
Predicting individual brain maturity using dynamic functional connectivity
Qin, J., Chen, S.-G., Hu, D., Zeng, L.-L., Fan, Y.-M., Chen, X.-P., & Shen, H. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00418 · Cited by 117
The spatial structure of resting state connectivity stability on the scale of minutes
Gonzalez-Castillo, J., Handwerker, D. A., Robinson, M. E., Hoy, C. W., Buchanan, L. C., Saad, Z. S., & Bandettini, P. A. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00138 · Cited by 116
Nguyen, T. T., Kovacevic, S., Dev, S. I., Lu, K., Liu, T. T., & Eyler, L. T. (2017) · Neuropsychology · doi:10.1037/neu0000317 · Cited by 109
Infraslow Electroencephalographic and Dynamic Resting State Network Activity
Grooms, J. K., Thompson, G. J., Pan, W.-J., Billings, J., Schumacher, E. H., Epstein, C. M., & Keilholz, S. D. (2017) · Brain Connectivity · doi:10.1089/brain.2017.0492 · Cited by 74
Origin of slow spontaneous resting-state neuronal fluctuations in brain networks
Krishnan, G. P., González, O. C., & Bazhenov, M. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1715841115 · Cited by 73
Bettinardi, R. G., Tort-Colet, N., Ruiz-Mejias, M., Sanchez-Vives, M. V., & Deco, G. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.03.037 · Cited by 68
Long-term alterations in brain and behavior after postnatal Zika virus infection in infant macaques
Raper, J., Kovacs-Balint, Z., Mavigner, M., Gumber, S., Burke, M. W., Habib, J., Mattingly, C., Fair, D., Earl, E., Feczko, E., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-16320-7 · Cited by 67
Altered topology of the functional speech production network in non-fluent/agrammatic variant of PPA
Mandelli, M. L., Welch, A. E., Vilaplana, E., Watson, C., Battistella, G., Brown, J. A., Possin, K. L., Hubbard, H. I., Miller, Z. A., Henry, M. L., et al. (2018) · Cortex · doi:10.1016/j.cortex.2018.08.002 · Cited by 67
Wens, V., Bourguignon, M., Vander Ghinst, M., Mary, A., Marty, B., Coquelet, N., Naeije, G., Peigneux, P., Goldman, S., & De Tiège, X. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.05.081 · Cited by 51
Yin, D., Liu, W., Zeljic, K., Wang, Z., Lv, Q., Fan, M., Cheng, W., & Wang, Z. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.1476-16.2016 · Cited by 43
Morin, E. L., Howell, B. R., Feczko, E., Earl, E., Pincus, M., Reding, K., Kovacs-Balint, Z. A., Meyer, J. S., Styner, M., Fair, D., et al. (2020) · Development and Psychopathology · doi:10.1017/s0954579420001133 · Cited by 37
Padilla, N., & Lagercrantz, H. (2020) · Acta Paediatrica · doi:10.1111/apa.15167 · Cited by 35
1024-channel electrophysiological recordings in macaque V1 and V4 during resting state
Chen, X., Morales-Gregorio, A., Sprenger, J., Kleinjohann, A., Sridhar, S., van Albada, S. J., Grün, S., & Roelfsema, P. R. (2022) · Scientific Data · doi:10.1038/s41597-022-01180-1 · Cited by 32
Salience network dynamics underlying successful resistance of temptation
Steimke, R., Nomi, J. S., Calhoun, V. D., Stelzel, C., Paschke, L. M., Gaschler, R., Goschke, T., Walter, H., & Uddin, L. Q. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsx123 · Cited by 30
Ainsworth, M., Sallet, J., Joly, O., Kyriazis, D., Kriegeskorte, N., Duncan, J., Schüffelgen, U., Rushworth, M. F. S., & Bell, A. H. (2021) · The Journal of Neuroscience · doi:10.1523/jneurosci.0870-20.2021 · Cited by 24
Metadata
- Authors
- Hutchison, R. M., Womelsdorf, T., Gati, J. S., Everling, S., & Menon, R. S.
- Venue
- Human Brain Mapping
- Publisher
- Wiley
- Published
- 2012-03-22
- Volume
- 34
- Issue
- 9
- Pages
- 2154-2177
- ISSN
- 1065-9471 (ISSN-L)
- OpenAlex
- W1552598564
- Cited by
- 721
- References
- 33
- FWCI
- 24.57
- Type
- journal article
- Language
- en
- Open access
- bronze
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
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.