Cited by 1,028Functional Brain Connectivity StudiesNeural dynamics and brain functionMind wandering and attention

The DOI matches its Crossref record; 38 of the 38 references it cites were found in a registry or an index.

Electroencephalographic signatures of attentional and cognitive default modes in spontaneous brain activity fluctuations at rest

Open access

Laufs, H., Krakow, K., Sterzer, P., Eger, E., Beyerle, A., Salek-Haddadi, A., Kleinschmidt, A.·2003·Proceedings of the National Academy of Sciences

DOI 10.1073/pnas.1831638100PMC PMC196925

Open this paper in CoChat — free account

Abstract

We assessed the relation between hemodynamic and electrical indices of brain function by performing simultaneous functional MRI (fMRI) and electroencephalography (EEG) in awake subjects at rest with eyes closed. Spontaneous power fluctuations of electrical rhythms were determined for multiple discrete frequency bands, and associated fMRI signal modulations were mapped on a voxel-by-voxel basis. There was little positive correlation of localized brain activity with alpha power (8–12 Hz), but strong and widespread negative correlation in lateral frontal and parietal cortices that are known to support attentional processes. Power in a 17–23 Hz range of beta activity was positively correlated with activity in retrosplenial, temporo-parietal, and dorsomedial prefrontal cortices. This set of areas has previously been characterized by high but coupled metabolism and blood flow at rest that decrease whenever subjects engage in explicit perception or action. The distributed patterns of fMRI activity that were correlated with power in different EEG bands overlapped strongly with those of functional connectivity, i.e., intrinsic covariations of regional activity at rest. This result indicates that, during resting wakefulness, and hence the absence of a task, these areas constitute separable and dynamic functional networks, and that activity in these networks is associated with distinct EEG signatures. Taken together with studies that have explicitly characterized the response properties of these distributed cortical systems, our findings may suggest that alpha oscillations signal a neural baseline with “inattention” whereas beta rhythms index spontaneous cognitive operations during conscious rest.

Integrity signals

Registry

Crossref · 10.1073/pnas.1831638100

Cites

38 of 38 references verified0 citation errors · 0 not checkable

Statistics

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

Claims the paper makes

We couldn’t retrieve this paper’s full text, 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?

Control of goal-directed and stimulus-driven attention in the brain
Corbetta, M., & Shulman, G. L. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn755 · Cited by 12,881
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
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
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
Brain magnetic resonance imaging with contrast dependent on blood oxygenation.
Ogawa, S., Lee, T. M., Kay, A. R., & Tank, D. W. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.24.9868 · Cited by 6,483
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
Über das Elektrenkephalogramm des Menschen
Berger, H. (1929) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/bf01797193 · Cited by 4,266
Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation.
Kwong, K. K., Belliveau, J. W., Chesler, D. A., Goldberg, I. E., Weisskoff, R. M., Poncelet, B. P., Kennedy, D. N., Hoppel, B. E., Cohen, M. S., & Turner, R. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.12.5675 · Cited by 4,212
Searching for a baseline: Functional imaging and the resting human brain
Gusnard, D. A., & Raichle, M. E. (2001) · Nature Reviews Neuroscience · doi:10.1038/35094500 · Cited by 3,371
Medial prefrontal cortex and self-referential mental activity: Relation to a default mode of brain function
Gusnard, D. A., Akbudak, E., Shulman, G. L., & Raichle, M. E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.071043098 · Cited by 2,997

Show all 37 references

Research works printed but not linked: 5

Vogel, F. (1962) Dtsch. Z. Nervenheilkd. 184, 137–173.13997623
Cordes, D., Haughton, V. M., Arfanakis, K., Carew, J. D., Turski, P. A., Moritz, C. H., Quigley, M. A. & Meyerand, M. E. (2001) AJNR Am. J. Neuroradiol. 22, 1326–1333.11498421
McGuire, P. K., Paulesu, E., Frackowiak, R. S. & Frith, C. D. (1996) NeuroReport 7, 2095–2099.8930966
Adrian, E. D. & Matthews, B. H. C. (1934) Brain 57, 356.
Jung, R. (1953) in Handbuch der Inneren Medizin, eds. von Bergmann, G., Frey, W. & Schwiegk, H. (Springer, Berlin), Vol. 1, pp. 1216–1325.

Sorted by citations

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
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
EEG alpha oscillations: The inhibition–timing hypothesis
Klimesch, W., Sauseng, P., & Hanslmayr, S. (2006) · Brain Research Reviews · doi:10.1016/j.brainresrev.2006.06.003 · Cited by 3,890
Spontaneous neuronal activity distinguishes human dorsal and ventral attention systems
Fox, M. D., Corbetta, M., Snyder, A. Z., Vincent, J. L., & Raichle, M. E. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604187103 · Cited by 2,101
Evidence for a Frontoparietal Control System Revealed by Intrinsic Functional Connectivity
Vincent, J. L., Kahn, I., Snyder, A. Z., Raichle, M. E., & Buckner, R. L. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90355.2008 · Cited by 1,869
Electrophysiological signatures of resting state networks in the human brain
Mantini, D., Perrucci, M. G., Del Gratta, C., Romani, G. L., & Corbetta, M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700668104 · Cited by 1,938
Default-mode brain dysfunction in mental disorders: A systematic review
Broyd, S. J., Demanuele, C., Debener, S., Helps, S. K., James, C. J., & Sonuga-Barke, E. J. S. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.09.002 · Cited by 1,675
Spontaneous low‐frequency BOLD signal fluctuations: An fMRI investigation of the resting‐state default mode of brain function hypothesis
Fransson, P. (2005) · Human Brain Mapping · doi:10.1002/hbm.20113 · Cited by 1,388
The dynamic functional connectome: State-of-the-art and perspectives
Preti, M. G., Bolton, T. A. W., & Ville, D. V. D. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.12.061 · Cited by 1,454
EEG microstates as a tool for studying the temporal dynamics of whole-brain neuronal networks: A review
Michel, C. M., & Koenig, T. W. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.11.062 · Cited by 1,418
Large-scale cortical correlation structure of spontaneous oscillatory activity
Hipp, J. F., Hawellek, D. J., Corbetta, M., Siegel, M., & Engel, A. K. (2012) · Nature Neuroscience · doi:10.1038/nn.3101 · Cited by 1,113
REBUS and the anarchic brain: Toward a unified model of the brain action of psychedelics
Carhart-Harris, R. L., & Friston, K. J. (2019) · Pharmacological Reviews · doi:10.1124/pr.118.017160 · Cited by 1,180
Clinical applications of resting state functional connectivity
Fox, M. (2010) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2010.00019 · Cited by 1,219
Distinct cerebellar contributions to intrinsic connectivity networks
Habas, C., Kamdar, N., Nguyen, D., Prater, K., Beckmann, C. F., Menon, V., & Greicius, M. D. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1868-09.2009 · Cited by 1,115
BOLD correlates of EEG topography reveal rapid resting-state network dynamics
Britz, J., Van De Ville, D., & Michel, C. M. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.02.052 · Cited by 1,070
Trial-by-Trial Coupling of Concurrent Electroencephalogram and Functional Magnetic Resonance Imaging Identifies the Dynamics of Performance Monitoring
Debener, S., Ullsperger, M., Siegel, M., Fiehler, K., von Cramon, D. Y., & Engel, A. K. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3286-05.2005 · Cited by 1,096
Coupling Between Neuronal Firing, Field Potentials, and fMRI in Human Auditory Cortex
Mukamel, R., Gelbard, H., Arieli, A., Hasson, U., Fried, I., & Malach, R. (2005) · Science · doi:10.1126/science.1110913 · Cited by 1,023
Neural Activity When People Solve Verbal Problems with Insight
Beeman, M. J., Bowden, E. M., Haberman, J. M., Frymiare, J. L., Arambel-Liu, S., Greenblatt, R. E., Reber, P. J., & Kounios, J. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020097 · Cited by 1,059
Motivation, emotion, and their inhibitory control mirrored in brain oscillations
Knyazev, G. G. (2006) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2006.10.004 · Cited by 1,034
Advances and pitfalls in the analysis and interpretation of resting-state FMRI data
Cole, D. M. (2010) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2010.00008 · Cited by 1,011
Breakdown of Functional Connectivity in Frontoparietal Networks Underlies Behavioral Deficits in Spatial Neglect
He, B. J., Snyder, A. Z., Vincent, J. L., Epstein, A. A., Shulman, G. L., & Corbetta, M. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.013 · Cited by 945
Graph theoretical analysis of magnetoencephalographic functional connectivity in Alzheimer's disease
Stam, C. J., de Haan, W., Daffertshofer, A., Jones, B. F., Manshanden, I., van Walsum, A. M. V. C., Montez, T., Verbunt, J. P. A., de Munck, J. C., van Dijk, B. W., et al. (2008) · Brain · doi:10.1093/brain/awn262 · Cited by 922
Brain connectivity related to working memory performance
Hampson, M., Driesen, N. R., Skudlarski, P., Gore, J. C., & Constable, R. T. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.3408-06.2006 · Cited by 853
Intrinsic Fluctuations within Cortical Systems Account for Intertrial Variability in Human Behavior
Fox, M., Snyder, A. Z., Vincent, J. L., & Raichle, M. E. (2007) · Neuron · doi:10.1016/j.neuron.2007.08.023 · Cited by 773
Temporal dynamics of spontaneous MEG activity in brain networks
de Pasquale, F., Della Penna, S., Snyder, A. Z., Lewis, C., Mantini, D., Marzetti, L., Belardinelli, P., Ciancetta, L., Pizzella, V., Romani, G. L., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913863107 · Cited by 698
Resting-state networks show dynamic functional connectivity in awake humans and anesthetized macaques
Hutchison, R. M., Womelsdorf, T., Gati, J. S., Everling, S., & Menon, R. S. (2012) · Human Brain Mapping · doi:10.1002/hbm.22058 · Cited by 732
Natural Frequencies of Human Corticothalamic Circuits
Rosanova, M., Casali, A. G., Bellina, V., Resta, F., Mariotti, M., & Massimini, M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0445-09.2009 · Cited by 689
Default-Mode Activity during a Passive Sensory Task: Uncoupled from Deactivation but Impacting Activation
Greicius, M. D., & Menon, V. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/0898929042568532 · Cited by 684
Spontaneous Fluctuations in Posterior -Band EEG Activity Reflect Variability in Excitability of Human Visual Areas
Romei, V., Brodbeck, V., Michel, C. M., Amedi, A., Pascual‐Leone, Á., & Thut, G. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm229 · Cited by 717
Resting-state fMRI confounds and cleanup
Murphy, K., Birn, R. M., & Bandettini, P. A. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.04.001 · Cited by 666
Decoding Wakefulness Levels from Typical fMRI Resting-State Data Reveals Reliable Drifts between Wakefulness and Sleep
Tagliazucchi, E., & Laufs, H. (2014) · Neuron · doi:10.1016/j.neuron.2014.03.020 · Cited by 656
Self-citation
How default is the default mode of brain function?
Fransson, P. (2006) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.06.017 · Cited by 611
Robustly Estimating the Flow Direction of Information in Complex Physical Systems
Nolte, G., Ziehe, A., Nikulin, V. V., Schlögl, A., Krämer, N., Brismar, T., & Müller, K. (2008) · Physical Review Letters · doi:10.1103/physrevlett.100.234101 · Cited by 595
Prefrontal Transcranial Direct Current Stimulation Changes Connectivity of Resting-State Networks during fMRI
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
Fast transient networks in spontaneous human brain activity
Baker, A. P., Brookes, M. J., Rezek, I. A., Smith, S. M., Behrens, T. E. J., Probert-Smith, P., & Woolrich, M. W. (2014) · eLife · doi:10.7554/elife.01867 · Cited by 569
Intrinsic Connectivity Networks, Alpha Oscillations, and Tonic Alertness: A Simultaneous Electroencephalography/Functional Magnetic Resonance Imaging Study
Sadaghiani, S., Scheeringa, R., Lehongre, K., Morillon, B., Giraud, A.-L., & Kleinschmidt, A. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.1004-10.2010 · Cited by 504
Self-citation
Persistent default‐mode network connectivity during light sedation
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
From emotion perception to emotion experience: Emotions evoked by pictures and classical music
Baumgärtner, T., Esslen, M., & Jäncke, L. (2005) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2005.04.007 · Cited by 546
Oscillatory power decreases and long-term memory: the information via desynchronization hypothesis
Hanslmayr, S., Staudigl, T., & Fellner, M.-C. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00074 · Cited by 543
Interhemispheric correlations of slow spontaneous neuronal fluctuations revealed in human sensory cortex
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
Fronto-parietal cortex controls spatial attention through modulation of anticipatory alpha rhythmsPreprint
Capotosto, P., Babiloni, C., Romani, G., & Corbetta, M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0539-09.2009 · Cited by 530
Intrinsic Coupling Modes: Multiscale Interactions in Ongoing Brain Activity
Engel, A. K., Gerloff, C., Hilgetag, C. C., & Nolte, G. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.038 · Cited by 471
Functional Roles of Alpha-Band Phase Synchronization in Local and Large-Scale Cortical Networks
Palva, S., & Palva, J. M. (2011) · Frontiers in Psychology · doi:10.3389/fpsyg.2011.00204 · Cited by 503
Prediction of human errors by maladaptive changes in event-related brain networks
Eichele, T., Debener, S., Calhoun, V. D., Specht, K., Engel, A. K., Hugdahl, K., von Cramon, D. Y., & Ullsperger, M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0708965105 · Cited by 472
Neuronal Dynamics Underlying High- and Low-Frequency EEG Oscillations Contribute Independently to the Human BOLD Signal
Scheeringa, R., Fries, P., Petersson, K. M., Oostenveld, R., Grothe, I., Norris, D. G., Peter Hagoort, A., & BASTIAANSEN, M. C. M. (2011) · Neuron · doi:10.1016/j.neuron.2010.11.044 · Cited by 479
Brain Networks and α-Oscillations: Structural and Functional Foundations of Cognitive Control
Sadaghiani, S., & Kleinschmidt, A. K. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2016.09.004 · Cited by 447
Self-citation
Resting oscillatory cortico-subthalamic connectivity in patients with Parkinson’s disease
Vladimir Litvak, A., Jha, A., Eusébio, A., Oostenveld, R., Foltynie, T., Limousin, P. D., Zrinzo, L. U., Hariz, M. I., Friston, K. J., & Brown, P. (2010) · Brain · doi:10.1093/brain/awq332 · Cited by 447
Unrest at rest: Default activity and spontaneous network correlations
Buckner, R. L., & Vincent, J. L. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.01.010 · Cited by 523
Endogenous Cortical Rhythms Determine Cerebral Specialization for Speech Perception and Production
Giraud, A., Kleinschmidt, A. K., Poeppel, D., Lund, T. E., Frackowiak, R. S. J., & Laufs, H. (2007) · Neuron · doi:10.1016/j.neuron.2007.09.038 · Cited by 442
Self-citation
Single-trial EEG–fMRI reveals the dynamics of cognitive function
Debener, S., Ullsperger, M., Siegel, M., & Engel, A. K. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.09.010 · Cited by 428
Functional disintegration in paranoid schizophrenia using resting-state fMRI
Zhou, Y., Liang, M., Tian, L., Wang, K., Hao, Y., Liu, H., Liu, Z., & Jiang, T. (2007) · Schizophrenia Research · doi:10.1016/j.schres.2007.05.029 · Cited by 444
Rolandic alpha and beta EEG rhythms' strengths are inversely related to fMRI‐BOLD signal in primary somatosensory and motor cortex
Ritter, P., Moosmann, M., & Villringer, A. (2009) · Human Brain Mapping · doi:10.1002/hbm.20585 · Cited by 400
A Cortical Core for Dynamic Integration of Functional Networks in the Resting Human Brain
de Pasquale, F., Penna, S. D., Snyder, A. Z., Marzetti, L., Pizzella, V., Romani, G. L., & Corbetta, M. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.031 · Cited by 422
Hippocampal and Neocortical Gamma Oscillations Predict Memory Formation in Humans
Sederberg, P. B., Schulze‐Bonhage, A., Madsen, J. R., Bromfield, E. B., McCarthy, D. C., Brandt, A., Tully, M., & Kahana, M. J. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhl030 · Cited by 426
Estimating workload using EEG spectral power and ERPs in the n-back task
Brouwer, A.-M., Hogervorst, M. A., van Erp, J. B. F., Heffelaar, T., Zimmerman, P. H., & Oostenveld, R. (2012) · Journal of Neural Engineering · doi:10.1088/1741-2560/9/4/045008 · Cited by 407
Spontaneous brain activity and EEG microstates. A novel EEG/fMRI analysis approach to explore resting-state networks
Musso, F., Brinkmeyer, J., Mobascher, A., Warbrick, T., & Winterer, G. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.01.093 · Cited by 387
Frontal theta EEG activity correlates negatively with the default mode network in resting state
Scheeringa, R., Bastiaansen, M. C. M., Petersson, K. M., Oostenveld, R., Norris, D. G., & Hagoort, P. (2008) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2007.05.017 · Cited by 400
Enhanced repertoire of brain dynamical states during the psychedelic experience
Tagliazucchi, E., Carhart-Harris, R. L., Leech, R., Nutt, D., & Chialvo, D. R. (2014) · Human Brain Mapping · doi:10.1002/hbm.22562 · Cited by 412
Where the BOLD signal goes when alpha EEG leaves
Laufs, H., Holt, J. L., Elfont, R. M., Krams, M., Paul, J. S., Krakow, K., & Kleinschmidt, A. K. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.02.002 · Cited by 394
Self-citation
Intrinsic Brain Activity in Altered States of Consciousness
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
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
Abnormal intrinsic brain functional network dynamics in Parkinson’s disease
Kim, J., Criaud, M., Cho, S. S., Díez‐Cirarda, M., Mihaescu, A. S., Coakeley, S., Ghadery, C., Valli, M., Jacobs, M. F., Houle, S., et al. (2017) · Brain · doi:10.1093/brain/awx233 · Cited by 373
Spatiotemporal dynamics of the brain at rest — Exploring EEG microstates as electrophysiological signatures of BOLD resting state networks
Yuan, H., Zotev, V., Phillips, R., Drevets, W. C., & Bodurka, J. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.02.031 · Cited by 352
The Prepared Mind
Kounios, J., Frymiare, J. L., Bowden, E. M., Fleck, J. I., Subramaniam, K., Parrish, T. B., & Beeman, M. J. (2006) · Psychological Science · doi:10.1111/j.1467-9280.2006.01798.x · Cited by 363
Short-term Effects of Antipsychotic Treatment on Cerebral Function in Drug-Naive First-Episode Schizophrenia Revealed by “Resting State” Functional Magnetic Resonance Imaging
Lui, S., Li, T., Deng, W., Jiang, L., Wu, Q., Tang, H., Yue, Q., Huang, X., Chan, R. C. K., Collier, D. A., et al. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.84 · Cited by 365
Consistency and functional specialization in the default mode brain network
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
Brain neural synchronization and functional coupling in Alzheimer's disease as revealed by resting state EEG rhythms
Babiloni, C., Lizio, R., Marzano, N., Capotosto, P., Soricelli, A., Triggiani, A. I., Cordone, S., Gesualdo, L., & Percio, C. D. (2015) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2015.02.008 · Cited by 388
The role of physiological noise in resting-state functional connectivity
Birn, R. M. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.016 · Cited by 379
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
Correlating the alpha rhythm to BOLD using simultaneous EEG/fMRI: Inter-subject variability
Goncalves, S. I., de Munck, J. C., Pouwels, P. J. W., Schoonhoven, R., Kuijer, J. P. A., Maurits, N. M., Hoogduin, J. M., Someren, E. J. W. V., Heethaar, R. M., & Lopes, F. H. D. S. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.09.062 · Cited by 355
Trial-by-trial coupling between EEG and BOLD identifies networks related to alpha and theta EEG power increases during working memory maintenance
Scheeringa, R., Petersson, K. M., Oostenveld, R., Norris, D. G., Peter Hagoort, A., & BASTIAANSEN, M. C. M. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.08.041 · Cited by 393
Spontaneous cortical activity transiently organises into frequency specific phase-coupling networks
Vidaurre, D., Hunt, L. T., Quinn, A. J., Hunt, B. A. E., Brookes, M. J., Nobre, A. C., & Woolrich, M. W. (2018) · Nature Communications · doi:10.1038/s41467-018-05316-z · Cited by 384
The origins of insight in resting-state brain activity
Kounios, J., Fleck, J. I., Green, D. L., Payne, L., Stevenson, J. L., Bowden, E. M., & Beeman, M. J. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.07.013 · Cited by 358
Recovery of Sensorimotor Function after Experimental Stroke Correlates with Restoration of Resting-State Interhemispheric Functional Connectivity
van Meer, M. P. A., van der Marel, K., Wang, K., Otte, W. M., el Bouazati, S., Roeling, T. A. P., Viergever, M. A., van der Sprenkel, J. W. B., & Dijkhuizen, R. M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5709-09.2010 · Cited by 352
Multi-level bootstrap analysis of stable clusters in resting-state fMRI
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
How and when the fMRI BOLD signal relates to underlying neural activity: The danger in dissociation
Ekstrom, A. D. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.12.004 · Cited by 349
Temporal lobe interictal epileptic discharges affect cerebral activity in “default mode” brain regions
Laufs, H., Hamandi, K., Salek‐Haddadi, A., Kleinschmidt, A. K., Duncan, J. S., & Lemieux, L. (2006) · Human Brain Mapping · doi:10.1002/hbm.20323 · Cited by 326
Self-citation
Ongoing spontaneous activity controls access to consciousness: a neuronal model for inattentional blindness
Dehaene, S., & Changeux, J.-P. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030141 · Cited by 329
Magnetoencephalographic evaluation of resting-state functional connectivity in Alzheimer's disease
Stam, C. J., Jones, B. F., Manshanden, I., van Walsum, A. M. V. C., Montez, T., Verbunt, J. P. A., de Munck, J. C., van Dijk, B. W., Berendse, H. W., & Scheltens, P. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.05.033 · Cited by 333
Exploring mechanisms of spontaneous functional connectivity in MEG: How delayed network interactions lead to structured amplitude envelopes of band-pass filtered oscillations
Cabral, J., Luckhoo, H., Woolrich, M. W., Joensson, M., Mohseni, H., Baker, A. P., Kringelbach, M. L., & Deco, G. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.11.047 · Cited by 320
The status of spectral EEG abnormality as a diagnostic test for schizophrenia
Boutros, N. N., Arfken, C. L., Galderisi, S., Warrick, J. I., Pratt, G., & Iacono, W. G. (2007) · Schizophrenia Research · doi:10.1016/j.schres.2007.11.020 · Cited by 324
Functional connectivity in the default network during resting state is preserved in a vegetative but not in a brain dead patient
Boly, 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
Spontaneous locally restricted EEG alpha activity determines cortical excitability in the motor cortex
Sauseng, P., Klimesch, W., Gerloff, C. P., & Hummel, F. C. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2008.07.021 · Cited by 315
Interpolated memory tests reduce mind wandering and improve learning of online lectures
Szpunar, K. K., Khan, N. Y., & Schacter, D. L. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1221764110 · Cited by 415
Mindfulness-induced changes in gamma band activity – Implications for the default mode network, self-reference and attention
Berkovich-Ohana, A., Glicksohn, J., & Goldstein, A. (2012) · Clinical Neurophysiology · doi:10.1016/j.clinph.2011.07.048 · Cited by 298
The Dynamical Balance of the Brain at Rest
Deco, G., & Corbetta, M. (2010) · The Neuroscientist · doi:10.1177/1073858409354384 · Cited by 323
Assessing the spatiotemporal evolution of neuronal activation with single-trial event-related potentials and functional MRI
Eichele, T., Specht, K., Moosmann, M., Jongsma, M. L. A., Quiroga, R. Q., Nordby, H., & Hugdahl, K. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505508102 · Cited by 308
Methods for Simultaneous EEG-fMRI: An Introductory Review
Huster, R. J., Debener, S., Eichele, T., & Herrmann, C. S. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0447-12.2012 · Cited by 328
Simultaneous EEG–fMRI
Ritter, P., & Villringer, A. (2006) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2006.06.008 · Cited by 294
Combining and comparing EEG, peripheral physiology and eye-related measures for the assessment of mental workload
Hogervorst, M. A., Brouwer, A.-M., & van Erp, J. B. F. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00322 · Cited by 292
BOLD correlates of EEG alpha phase-locking and the fMRI default mode network
Jann, K., Dierks, T., Boesch, C., Kottlow, M., Strik, W., & Koenig, T. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.01.001 · Cited by 286
Dynamic BOLD functional connectivity in humans and its electrophysiological correlates
Tagliazucchi, E., von Wegner, F., Morzelewski, A., Brodbeck, V., & Laufs, H. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00339 · Cited by 300
Self-citation
Where smart brains are different: A quantitative meta-analysis of functional and structural brain imaging studies on intelligence
Basten, U., Hilger, K., & Fiebach, C. J. (2015) · Intelligence · doi:10.1016/j.intell.2015.04.009 · Cited by 324
The effect of respiration variations on independent component analysis results of resting state functional connectivity.
Birn, R. M., Murphy, K., & Bandettini, P. A. (2008) · Human Brain Mapping · doi:10.1002/hbm.20577 · Cited by 283
Combining EEG and fMRI: A multimodal tool for epilepsy research
Gotman, J., Kobayashi, E., Bagshaw, A. P., Bénar, C., & Dubeau, F. (2006) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.20577 · Cited by 278
Slowing of oscillatory brain activity is a stable characteristic of Parkinson's disease without dementia
Stoffers, D., Bosboom, J. L. W., Deijen, J. B., Wolters, E. C., Berendse, H. W., & Stam, C. J. (2007) · Brain · doi:10.1093/brain/awm034 · Cited by 277
Human oscillatory activity associated to reward processing in a gambling task
Marco‐Pallarés, J., Cucurell, D., Toni Cunillera, B., García, R., Pueyo, A. A., Münte, T. F., & Rodríguez‐Fornells, A. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.07.016 · Cited by 277
Breathing as a fundamental rhythm of brain function.
Heck, D. H., McAfee, S. S., Liu, Y., Babajani-Feremi, A., Rezaie, R., Freeman, W. J., Wheless, J. W., Papanicolaou, A. C., Ruszinkó, M., Sokolov, Y., et al. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00115 · Cited by 272
Annotation: What electrical brain activity tells us about brain function that other techniques cannot tell us – a child psychiatric perspective
Banaschewski, T., & Brandeis, D. (2006) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2006.01681.x · Cited by 275
Twenty years of functional MRI: The science and the stories
Bandettini, P. A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.04.026 · Cited by 293

Authors: Laufs, H., Krakow, K., Sterzer, P., Eger, E., Beyerle, A., Salek-Haddadi, A., & Kleinschmidt, A.
Affiliations: Goethe University Frankfurt (DE)
Cognitive Neurology Unit, Department of Neurology, J. W. Goethe University, Theodor-Stern-Kai 7, D-60590 Frankfurt am Main, Germany; and Department of Clinical and Experimental Epilepsy, Institute of Neurology, University College London, London WC1N 3BG, United Kingdom
ORCID: Laufs, H.
Krakow, K.
Sterzer, P.
Eger, E.
Kleinschmidt, A.
Venue: Proceedings of the National Academy of Sciences
Publisher: National Academy of Sciences
Published: 2003-09-04
Volume: 100
Issue: 19
Pages: 11053-11058
ISSN: 0027-8424 (ISSN-L)
1091-6490
DOI: 10.1073/pnas.1831638100
PMC: PMC196925
OpenAlex: W2153394220
Cited by: 1,028
References: 37
Citations by year: 2026: 27 · 2025: 28 · 2024: 33 · 2023: 28 · 2022: 39 · 2021: 67 · 2020: 44 · 2019: 43 · 2018: 42 · 2017: 44 · 2016: 51 · 2015: 45 · 2014: 60 · 2013: 67 · 2012: 67
FWCI: 11.89
Type: journal article
Language: en
Open access: green
europepmc.org
Locations: Proceedings of the National Academy of Sciences (publishedVersion)
Europe PMC (PubMed Central) (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
UCL Discovery (University College London) (submittedVersion)
Funders: Volkswagen Foundation
Bundesministerium für Bildung und Forschung
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Life Sciences › Neuroscience › Cognitive Neuroscience › Mind wandering and attention
Keywords: resting state, spontaneous brain activity, alpha oscillations, beta oscillations, functional connectivity, default mode network, attention, frontal and parietal cortex, dorsomedial prefrontal cortex, temporoparietal cortex, retrosplenial cortex, inattention
MeSH terms: Attention, Brain, Cognition, Electroencephalography, Humans, Magnetic Resonance Imaging

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

Electroencephalographic signatures of attentional and cognitive default modes in spontaneous brain activity fluctuations at rest

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