Functional connectivity of default mode network components: correlation, anticorrelation, and causality
Open accessAbstract
The default mode network (DMN), based in ventromedial prefrontal cortex (vmPFC) and posterior cingulate cortex (PCC), exhibits higher metabolic activity at rest than during performance of externally oriented cognitive tasks. Recent studies have suggested that competitive relationships between the DMN and various task‐positive networks involved in task performance are intrinsically represented in the brain in the form of strong negative correlations (anticorrelations) between spontaneous fluctuations in these networks. Most neuroimaging studies characterize the DMN as a homogenous network, thus few have examined the differential contributions of DMN components to such competitive relationships. Here, we examined functional differentiation within the DMN, with an emphasis on understanding competitive relationships between this and other networks. We used a seed correlation approach on resting‐state data to assess differences in functional connectivity between these two regions and their anticorrelated networks. While the positively correlated networks for the vmPFC and PCC seeds largely overlapped, the anticorrelated networks for each showed striking differences. Activity in vmPFC negatively predicted activity in parietal visual spatial and temporal attention networks, whereas activity in PCC negatively predicted activity in prefrontal‐based motor control circuits. Granger causality analyses suggest that vmPFC and PCC exert greater influence on their anticorrelated networks than the other way around, suggesting that these two default mode nodes may directly modulate activity in task‐positive networks. Thus, the two major nodes comprising the DMN are differentiated with respect to the specific brain systems with which they interact, suggesting greater heterogeneity within this network than is commonly appreciated. Hum Brain Mapp 30:625–637, 2009. © 2008 Wiley‐Liss, Inc.
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
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.
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?
Dynamic causal modeling and intracranial EEG data point to a sustained causal influence of the DMN on other brain networks.
“Additionally, dynamic causal modeling applied to human fMRI and intracranial EEG data point to a sustained causal influence of the DMN on other brain networks.”
From 20 years of the default mode network: A review and synthesis. (2023) · cites this paper as [90]
The Results (Relationships between networks; page unavailable) say that Granger causality analyses of resting-state fMRI suggest DMN components may influence their respective anticorrelated networks. The Methods (Granger causality analysis; page unavailable) identify the method as Granger causality, not dynamic causal modeling, and describe fMRI rather than intracranial EEG data. The cited passages do not establish that the influence is sustained. (LLM, conf=0.88)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
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 · see citing works
Self-citationRizzolatti, G., & Craighero, L. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144230 · Cited by 7,433 · see citing works
Dissociable intrinsic connectivity networks for salience processing and executive control
Seeley, W. W., Menon, V., Schatzberg, A. F., Keller, J., Glover, G. H., Kenna, H., Reiss, A. L., & Greicius, M. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5587-06.2007 · Cited by 7,426 · see citing works
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 · see citing works
Empathy for Pain Involves the Affective but not Sensory Components of Pain
Singer, T., Seymour, B., O'Doherty, J., Kaube, H., Dolan, R. J., & Frith, C. D. (2004) · Science · doi:10.1126/science.1093535 · Cited by 3,929 · see citing works
Meeting of minds: the medial frontal cortex and social cognition
Amodio, D. M., & Frith, C. D. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1884 · Cited by 3,782 · see citing works
Cattaneo, L., & Rizzolatti, G. (2009) · Archives of Neurology · doi:10.1001/archneurol.2009.41 · Cited by 3,137 · see citing works
Buckner, R. L., & Carroll, D. C. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.11.004 · Cited by 2,691 · see citing works
Buckner, R. L., Snyder, A. Z., Shannon, B. J., LaRossa, G., Sachs, R., Fotenos, A. F., Sheline, Y. I., Klunk, W. E., Mathis, C. A., Morris, J. C., et al. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2177-05.2005 · Cited by 2,140 · see citing works
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 · see citing works
The neural bases of momentary lapses in attention
Weissman, D. H., Roberts, K. C., Visscher, K. M., & Woldorff, M. G. (2006) · Nature Neuroscience · doi:10.1038/nn1727 · Cited by 1,566 · see citing works
Competition between functional brain networks mediates behavioral variability
Kelly, A. M. C., Uddin, L. Q., Biswal, B. B., Castellanos, F. X., & Milham, M. P. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2007.08.008 · Cited by 1,287 · see citing works
Self-citationA Parametric Manipulation of Factors Affecting Task-induced Deactivation in Functional Neuroimaging
McKiernan, K. A., Kaufman, J. N., Kucera-Thompson, J., & Binder, J. R. (2003) · Journal of Cognitive Neuroscience · doi:10.1162/089892903321593117 · Cited by 1,080 · see citing works
Dissociable Medial Prefrontal Contributions to Judgments of Similar and Dissimilar Others
Mitchell, J. P., Macrae, C. N., & Banaji, M. R. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.040 · Cited by 1,023 · see citing works
Coherent spontaneous activity identifies a hippocampal-parietal memory network
Vincent, J. L., Snyder, A. Z., Fox, M. D., Shannon, B. J., Andrews, J. R., Raichle, M. E., & Buckner, R. L. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00048.2006 · Cited by 959 · cited 2× · see citing works
“, 2006], hippocampal memory systems [Vincent et al., 2006]).”
BackgroundGreicius, M. D., & Menon, V. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/0898929042568532 · Cited by 684 · see citing works
Medial prefrontal activity predicts memory for self
Macrae, C. N. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh025 · Cited by 581 · cited 2× · see citing works
“This region is also involved in representing self-knowledge [Macrae et al., 2004] or self-referential processing [D’Argembeau et al.”
BackgroundThe role of precuneus and left inferior frontal cortex during source memory episodic retrieval
Lundstrom, B. N., Ingvar, M., & Petersson, K. M. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.05.008 · Cited by 374 · see citing works
Distortion product otoacoustic emissions during the first year in term infants: A longitudinal study
Zang, Z., & Jiang, Z. D. (2007) · Brain and Development · doi:10.1016/j.braindev.2006.10.001 · Cited by 162 · see citing works
Flagged first, then by citations
Research works printed but not linked: 45
- Bellec P Perlbarg V Jbabdi S Pelegrini-Issac M Anton JL Doyon J Benali H 2006 Identification of large-scale networks in the brain using fMRI Neuroimage 29 4 1231 43 16246590
- Birn RM Diamond JB Smith MA Bandettini PA 2006 Separating respiratory-variation-related fluctuations from neuronal-activity-related fluctuations in fMRI Neuroimage 31 4 1536 48 16632379
- Carr L Iacoboni M Dubeau MC Mazziotta JC Lenzi GL 2003 Neural mechanisms of empathy in humans: a relay from neural systems for imitation to limbic areas Proc Natl Acad Sci U S A 100 9 5497 502 12682281 PMC154373
- Castellanos FX Margulies DS Kelly AMC Uddin LQ Ghaffari M Kirsch A Shaw D Shehzad Z Di Martino A Biswal B in press Cingulate-Precuneus Interactions: A New Locus of Dysfunction in Adult Attention-Deficit/Hyperactivity Disorder Biol Psychiatry PMC2745053 17888409
- Cavanna AE Trimble MR 2006 The precuneus: a review of its functional anatomy and behavioural correlates Brain 129 Pt 3 564 83 16399806
- Coull JT Nobre AC 1998 Where and when to pay attention: the neural systems for directing attention to spatial locations and to time intervals as revealed by both PET and fMRI J Neurosci 18 18 7426 35 9736662 PMC6793260
- D’Argembeau A Collette F Van der Linden M Laureys S Del Fiore G Degueldre C Luxen A Salmon E 2005 Self-referential reflective activity and its relationship with rest: a PET study Neuroimage 25 2 616 24 15784441
- Damoiseaux JS Rombouts SA Barkhof F Scheltens P Stam CJ Smith SM Beckmann CF 2006 Consistent resting-state networks across healthy subjects Proc Natl Acad Sci U S A PMC1564249 16945915
- De Luca M Beckmann CF De Stefano N Matthews PM Smith SM 2006 fMRI resting state networks define distinct modes of long-distance interactions in the human brain Neuroimage 29 4 1359 67 16260155
- Esposito F Bertolino A Scarabino T Latorre V Blasi G Popolizio T Tedeschi G Cirillo S Goebel R Di Salle F 2006 Independent component model of the default-mode brain function: Assessing the impact of active thinking Brain Res Bull 70 4–6 263 9 17027761
- Fox MD Snyder AZ Vincent JL Corbetta M Van Essen DC Raichle ME 2005 The human brain is intrinsically organized into dynamic, anticorrelated functional networks Proc Natl Acad Sci U S A 102 27 9673 8 15976020 PMC1157105
- Fransson P 2005 Spontaneous low-frequency BOLD signal fluctuations: an fMRI investigation of the resting-state default mode of brain function hypothesis Hum Brain Mapp 26 1 15 29 15852468 PMC6871700
- Fransson P 2006 How default is the default mode of brain function? Further evidence from intrinsic BOLD signal fluctuations Neuropsychologia 44 14 2836 45 16879844
- Gavrilescu M Shaw ME Stuart GW Eckersley P Svalbe ID Egan GF 2002 Simulation of the effects of global normalization procedures in functional MRI Neuroimage 17 2 532 42 12377132
- Gilbert SJ Spengler S Simons JS Steele JD Lawrie SM Frith CD Burgess PW 2006 Functional specialization within rostral prefrontal cortex (area 10): a meta-analysis J Cogn Neurosci 18 6 932 48 16839301
- Goebel R Roebroeck A Kim DS Formisano E 2003 Investigating directed cortical interactions in time-resolved fMRI data using vector autoregressive modeling and Granger causality mapping Magn Reson Imaging 21 10 1251 61 14725933
- Greicius MD Srivastava G Reiss AL Menon V 2004 Default-mode network activity distinguishes Alzheimer’s disease from healthy aging: evidence from functional MRI Proc Natl Acad Sci U S A 101 13 4637 42 15070770 PMC384799
- Gusnard DA Akbudak E Shulman GL Raichle ME 2001a Medial prefrontal cortex and self-referential mental activity: relation to a default mode of brain function Proc Natl Acad Sci U S A 98 7 4259 64 11259662 PMC31213
- Gusnard DA Raichle ME Raichle ME 2001b Searching for a baseline: functional imaging and the resting human brain Nat Rev Neurosci 2 10 685 94 11584306
- Hampson M Driesen NR Skudlarski P Gore JC Constable RT 2006 Brain connectivity related to working memory performance J Neurosci 26 51 13338 43 17182784 PMC2677699
- Honey CJ Kotter R Breakspear M Sporns O 2007 Network structure of cerebral cortex shapes functional connectivity on multiple time scales Proc Natl Acad Sci U S A 104 24 10240 5 17548818 PMC1891224
- Iacoboni M Lieberman MD Knowlton BJ Molnar-Szakacs I Moritz M Throop CJ Fiske AP 2004 Watching social interactions produces dorsomedial prefrontal and medial parietal BOLD fMRI signal increases compared to a resting baseline Neuroimage 21 3 1167 73 15006683
- Kennedy DP Redcay E Courchesne E 2006 Failing to deactivate: resting functional abnormalities in autism Proc Natl Acad Sci U S A 103 21 8275 80 16702548 PMC1472462
- Lee AT Glover GH Meyer CH 1995 Discrimination of large venous vessels in time-course spiral blood-oxygen-level-dependent magnetic-resonance functional neuroimaging Magn Reson Med 33 6 745 54 7651109
- Liang M Zhou Y Jiang T Liu Z Tian L Liu H Hao Y 2006 Widespread functional disconnectivity in schizophrenia with resting-state functional magnetic resonance imaging Neuroreport 17 2 209 13 16407773
- Liu H Liu Z Liang M Hao Y Tan L Kuang F Yi Y Xu L Jiang T 2006 Decreased regional homogeneity in schizophrenia: a resting state functional magnetic resonance imaging study Neuroreport 17 1 19 22 16361943
- Lou HC Luber B Crupain M Keenan JP Nowak M Kjaer TW Sackeim HA Lisanby SH 2004 Parietal cortex and representation of the mental Self Proc Natl Acad Sci U S A 101 17 6827 32 15096584 PMC404216
- Macey PM Macey KE Kumar R Harper RM 2004 A method for removal of global effects from fMRI time series Neuroimage 22 1 360 6 15110027
- Margulies DS Kelly AM Uddin LQ Biswal BB Castellanos FX Milham MP 2007 Mapping the functional connectivity of anterior cingulate cortex Neuroimage 37 2 579 88 17604651
- Mason MF Norton MI Van Horn JD Wegner DM Grafton ST Macrae CN 2007 Wandering minds: the default network and stimulus-independent thought Science 315 5810 393 5 17234951 PMC1821121
- McIntosh AR 2000 Towards a network theory of cognition Neural Netw 13 8–9 861 70 11156197
- McKiernan KA D’Angelo BR Kaufman JN Binder JR 2006 Interrupting the “stream of consciousness”: an fMRI investigation Neuroimage 29 4 1185 91 16269249 PMC1634934
- Miall RC Robertson EM 2006 Functional imaging: is the resting brain resting? Curr Biol 16 23 R998 1000 17141608 PMC6010146
- Mitchell JP Heatherton TF Macrae CN 2002 Distinct neural systems subserve person and object knowledge Proc Natl Acad Sci U S A 99 23 15238 43 12417766 PMC137574
- Nobre AC Sebestyen GN Gitelman DR Mesulam MM Frackowiak RS Frith CD 1997 Functional localization of the system for visuospatial attention using positron emission tomography Brain 120 Pt 3 515 33 9126062
- Nyberg L McIntosh AR Cabeza R Nilsson LG Houle S Habib R Tulving E 1996 Network analysis of positron emission tomography regional cerebral blood flow data: ensemble inhibition during episodic memory retrieval J Neurosci 16 11 3753 9 8642418 PMC6578843
- Raichle ME MacLeod AM Snyder AZ Powers WJ Gusnard DA Shulman GL 2001 A default mode of brain function Proc Natl Acad Sci U S A 98 2 676 82 11209064 PMC14647
- Roebroeck A Formisano E Goebel R 2005 Mapping directed influence over the brain using Granger causality and fMRI Neuroimage 25 1 230 42 15734358
- Saad ZS Ropella KM Cox RW DeYoe EA 2001 Analysis and use of FMRI response delays Hum Brain Mapp 13 2 74 93 11346887 PMC6872085
- Tian L Jiang T Wang Y Zang Y He Y Liang M Sui M Cao Q Hu S Peng M 2006 Altered resting-state functional connectivity patterns of anterior cingulate cortex in adolescents with attention deficit hyperactivity disorder Neurosci Lett 400 1–2 39 43 16510242
- Uddin LQ Iacoboni M Lange C Keenan JP 2007 The self and social cognition: the role of cortical midline structures and mirror neurons Trends Cogn Sci 17300981
- Uddin LQ Kaplan JT Molnar-Szakacs I Zaidel E Iacoboni M 2005 Self-face recognition activates a frontoparietal “mirror” network in the right hemisphere: an event-related fMRI study Neuroimage 25 3 926 35 15808992
- Wang L Zang Y He Y Liang M Zhang X Tian L Wu T Jiang T Li K 2006 Changes in hippocampal connectivity in the early stages of Alzheimer’s disease: evidence from resting state fMRI Neuroimage 31 2 496 504 16473024
- Wicker B Ruby P Royet JP Fonlupt P 2003 A relation between rest and the self in the brain? Brain Res Brain Res Rev 43 2 224 30 14572916
- Zang YF Yong H Chao-Zhe Z Qing-Jiu C Man-Qiu S Meng L Li-Xia T Tian-Zi J Yu-Feng W 2007 Altered baseline brain activity in children with ADHD revealed by resting-state functional MRI Brain Dev 29 2 83 91 16919409
Cited by
Sorted by citations
<i>Conn</i> : A Functional Connectivity Toolbox for Correlated and Anticorrelated Brain Networks
Whitfield-Gabrieli, S., & Nieto-Castanon, A. (2012) · Brain Connectivity · doi:10.1089/brain.2012.0073 · Cited by 4,885 · see citing works
The role of the posterior cingulate cortex in cognition and disease
Leech, R., & Sharp, D. J. (2014) · Brain · doi:10.1093/brain/awt162 · Cited by 2,247 · see citing works
Large-scale brain networks in cognition: emerging methods and principles
Bressler, S. L., & Menon, V. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.04.004 · Cited by 2,348 · see citing works
Andrews‐Hanna, J. R., Smallwood, J., & Spreng, R. N. (2014) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12360 · Cited by 2,102 · see citing works
The global signal and observed anticorrelated resting state brain networks
Fox, M. D., Zhang, D., Snyder, A. Z., & Raichle, M. E. (2009) · Journal of Neurophysiology · doi:10.1152/jn.90777.2008 · Cited by 1,877 · see citing works
Time–frequency dynamics of resting-state brain connectivity measured with fMRI
Chang, C., & Glover, G. H. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.12.011 · Cited by 1,808 · see citing works
Van Dijk, K. R. A., Hedden, T., Venkataraman, A., Evans, K. C., Lazar, S. W., & Buckner, R. L. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00783.2009 · Cited by 1,844 · see citing works
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 · see citing works
Default Mode Network Activity and Connectivity in Psychopathology
Whitfield-Gabrieli, S., & Ford, J. M. (2012) · Annual Review of Clinical Psychology · doi:10.1146/annurev-clinpsy-032511-143049 · Cited by 1,465 · see citing works
Brewer, J. A., Worhunsky, P. D., Gray, J. R., Tang, Y.-Y., Weber, J., & Kober, H. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1112029108 · Cited by 1,409 · see citing works
What does the retrosplenial cortex do?
Vann, S. D., Aggleton, J. P., & Maguire, E. A. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2733 · Cited by 1,409 · see citing works
Functional connectivity of human striatum: a resting state FMRI study
Di Martino, A., Scheres, A., Margulies, D. S., Kelly, A. M. C., Uddin, L. Q., Shehzad, Z., Biswal, B., Walters, J. R., Castellanos, F. X., & Milham, M. P. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn041 · Cited by 1,090 · see citing works
Self-citationBehavioral interpretations of intrinsic connectivity networks
Laird, A. R., Fox, P. M., Eickhoff, S. B., Turner, J. A., Ray, K. L., McKay, D. R., Glahn, D. C., Beckmann, C. F., Smith, S. M., & Fox, P. T. (2011) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00077 · Cited by 1,023 · see citing works
Depressive rumination, the default-mode network, and the dark matter of clinical neuroscience
Hamilton, J. P., Farmer, M., Fogelman, P., & Gotlib, I. H. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.02.020 · Cited by 952 · see citing works
20 years of the default mode network: A review and synthesis.
Menon, V. (2023) · Neuron · doi:10.1016/j.neuron.2023.04.023 · Cited by 934 · see citing works
“90 Building on this finding, information theoretic analysis of intracranial EEG signaling across widely distributed depth electrodes revealed that the DMN had signifi-cantly greater net causal outflow to other brain networks including sensory and motor networks than the reverse, during the resting…”
BackgroundFunctional connectivity of the human amygdala using resting state fMRI
Roy, A. K., Shehzad, Z., Margulies, D. S., Kelly, A. M. C., Uddin, L. Q., Gotimer, K., Biswal, B. B., Castellanos, F. X., & Milham, M. P. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.11.030 · Cited by 749 · see citing works
Self-citationZuo, X.-N., Kelly, C., Adelstein, J. S., Klein, D. F., Castellanos, F. X., & Milham, M. P. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.10.080 · Cited by 744 · see citing works
Self-citationAbnormal functional connectivity of default mode sub-networks in autism spectrum disorder patients
Assaf, M., Jagannathan, K., Calhoun, V. D., Miller, L., Stevens, M. C., Sahl, R., O'Boyle, J. G., Schultz, R. T., & Pearlson, G. D. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.05.067 · Cited by 680 · see citing works
Gao, W., Zhu, H., Giovanello, K. S., Smith, J. K., Shen, D., Gilmore, J. H., & Lin, W. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811221106 · Cited by 601 · see citing works
Sestieri, C., Corbetta, M., Romani, G. L., & Shulman, G. L. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.3335-10.2011 · Cited by 523 · see citing works
Genetic control over the resting brain
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 · see citing works
Palhano-Fontes, F., Andrade, K. C., Tofoli, L. F., Santos, A. C., Crippa, J. A. S., Hallak, J. E. C., Ribeiro, S., & de Araujo, D. B. (2015) · PLOS ONE · doi:10.1371/journal.pone.0118143 · Cited by 454 · see citing works
Network homogeneity reveals decreased integrity of default-mode network in ADHD
Uddin, L. Q., Kelly, A. M. C., Biswal, B. B., Margulies, D. S., Shehzad, Z., Shaw, D., Ghaffari, M., Rotrosen, J., Adler, L. A., Castellanos, F. X., et al. (2008) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2007.11.031 · Cited by 452 · see citing works
Self-citationNetwork-level structural covariance in the developing brain
Zielinski, B. A., Gennatas, E. D., Zhou, J., & Seeley, W. W. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1003109107 · Cited by 405 · see citing works
Psychedelics, meditation, and self-consciousness
Millière, R., Carhart-Harris, R. L., Roseman, L., Trautwein, F.-M., & Berkovich-Ohana, A. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.01475 · Cited by 390 · see citing works
Development of the Brain's Default Mode Network from Wakefulness to Slow Wave Sleep
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 · see citing works
Distinct parietal and temporal pathways to the homologues of Broca's area in the monkey
Petrides, M., & Pandya, D. N. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000170 · Cited by 396 · see citing works
A Treatment-Resistant Default Mode Subnetwork in Major Depression
Li, B., Liu, L., Friston, K. J., Shen, H., Wang, L., Zeng, L.-L., & Hu, D. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.11.007 · Cited by 333 · see citing works
A Review of the Functional and Anatomical Default Mode Network in Schizophrenia
Hu, M.-L., Zong, X.-F., Mann, J. J., Zheng, J.-J., Liao, Y.-H., Li, Z.-C., He, Y., Chen, X.-G., & Tang, J.-S. (2017) · Neuroscience Bulletin · doi:10.1007/s12264-016-0090-1 · Cited by 331 · see citing works
Resting Brain Connectivity: Changes during the Progress of Alzheimer Disease
Zhang, H.-Y., Wang, S.-J., Liu, B., Ma, Z.-L., Yang, M., Zhang, Z.-J., & Teng, G.-J. (2010) · Radiology · doi:10.1148/radiol.10091701 · Cited by 320 · see citing works
The default mode network and recurrent depression: A neurobiological model of cognitive risk factors
Marchetti, I., Koster, E. H. W., Sonuga-Barke, E. J., & De Raedt, R. (2012) · Neuropsychology Review · doi:10.1007/s11065-012-9199-9 · Cited by 287 · see citing works
fMRI reveals reciprocal inhibition between social and physical cognitive domains
Jack, A. I., Dawson, A. J., Begany, K. L., Leckie, R. L., Barry, K. P., Ciccia, A. H., & Snyder, A. Z. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.10.061 · Cited by 280 · see citing works
Horn (2010) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2010.00033 · Cited by 276 · see citing works
Stern, E. R., Fitzgerald, K. D., Welsh, R. C., Abelson, J. L., & Taylor, S. F. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036356 · Cited by 245 · see citing works
Functional connectivity of hippocampal networks in temporal lobe epilepsy
Haneef, Z., Lenartowicz, A., Yeh, H. J., Levin, H. S., Engel, J., & Stern, J. M. (2014) · Epilepsia · doi:10.1111/epi.12476 · Cited by 235 · see citing works
Sezer, I., Pizzagalli, D. A., & Sacchet, M. D. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104583 · Cited by 214 · see citing works
Kapogiannis, D., Reiter, D. A., Willette, A. A., & Mattson, M. P. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.09.029 · Cited by 211 · see citing works
Gao, W., Gilmore, J. H., Shen, D., Smith, J. K., Zhu, H., & Lin, W. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs043 · Cited by 194 · see citing works
Functional brain connectivity at rest changes after working memory training
Jolles, D. D., van Buchem, M. A., Crone, E. A., & Rombouts, S. A. R. B. (2013) · Human Brain Mapping · doi:10.1002/hbm.21444 · Cited by 183 · see citing works
Brain network dynamics in high-functioning individuals with autism
Watanabe, T., & Rees, G. (2017) · Nature Communications · doi:10.1038/ncomms16048 · Cited by 165 · see citing works
Noninvasive brain stimulation treatments for addiction and major depression
Dunlop, K., Hanlon, C. A., & Downar, J. (2017) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12985 · Cited by 171 · see citing works
Residual functional connectivity in the split-brain revealed with resting-state functional MRI
Uddin, L. Q., Mooshagian, E., Zaidel, E., Scheres, A., Margulies, D. S., Kelly, A. M. C., Shehzad, Z., Adelstein, J. S., Castellanos, F. X., Biswal, B. B., et al. (2008) · NeuroReport · doi:10.1097/wnr.0b013e3282fb8203 · Cited by 170 · see citing works
Self-citationPalva, J. M., & Palva, S. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.02.060 · Cited by 163 · see citing works
Autism As a Disorder of High Intelligence
Crespi, B. J. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00300 · Cited by 156 · see citing works
Sambataro, F., Wolf, N. D., Pennuto, M., Vasic, N., & Wolf, R. C. (2014) · Psychological Medicine · doi:10.1017/s0033291713002596 · Cited by 149 · see citing works
McIntyre, R. S., Xiao, H. X., Syeda, K., Vinberg, M., Carvalho, A. F., Mansur, R. B., Maruschak, N., & Cha, D. S. (2015) · CNS Drugs · doi:10.1007/s40263-015-0263-x · Cited by 145 · see citing works
Prefrontal connectomics: From anatomy to human imaging
Haber, S. N., Liu, H., Seidlitz, J., & Bullmore, E. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01156-6 · Cited by 129 · see citing works
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 · see citing works
The structural and functional brain networks that support human social networks
Noonan, M. P., Mars, R. B., Sallet, J., Dunbar, R. I. M., & Fellows, L. K. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.02.019 · Cited by 131 · see citing works
Kaunhoven, R. J., & Dorjee, D. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.01.007 · Cited by 130 · see citing works
Sun, Y.-W., Qin, L.-D., Zhou, Y., Xu, Q., Qian, L.-J., Tao, J., & Xu, J.-R. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.05.006 · Cited by 117 · see citing works
Schulz, K. P., Fan, J., Bédard, A.-C. V., Clerkin, S. M., Ivanov, I., Tang, C. Y., Halperin, J. M., & Newcorn, J. H. (2012) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2011.2053 · Cited by 114 · see citing works
Interoception primes emotional processing: multimodal evidence from neurodegeneration
Salamone, P. C., Legaz, A., Sedeño, L., Moguilner, S., Fraile-Vazquez, M., Campo, C. G., Fittipaldi, S., Yoris, A., Miranda, M., Birba, A., et al. (2021) · The Journal of Neuroscience · doi:10.1523/jneurosci.2578-20.2021 · Cited by 103 · see citing works
Kang, J., Wang, L., Yan, C., Wang, J., Liang, X., & He, Y. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.03.033 · Cited by 111 · see citing works
Lefebvre, S., Demeulemeester, M., Leroy, A., Delmaire, C., Lopes, R., Pins, D., Thomas, P., & Jardri, R. (2016) · Human Brain Mapping · doi:10.1002/hbm.23197 · Cited by 99 · see citing works
Daniels, J. (2011) · Journal of Psychiatry & Neuroscience · doi:10.1503/jpn.100050 · Cited by 93 · see citing works
Kluetsch, R. C., Schmahl, C., Niedtfeld, I., Densmore, M., Calhoun, V. D., Daniels, J., Kraus, A., Ludaescher, P., Bohus, M., & Lanius, R. A. (2012) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2012.476 · Cited by 91 · see citing works
Starck, T., Nikkinen, J., Rahko, J., Remes, J., Hurtig, T., Haapsamo, H., Jussila, K., Kuusikko-Gauffin, S., Mattila, M.-L., Jansson-Verkasalo, E., et al. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00802 · Cited by 75 · see citing works
From State-to-Trait Meditation: Reconfiguration of Central Executive and Default Mode Networks
Bauer, C. C. C., Whitfield-Gabrieli, S., Díaz, J. L., Pasaye, E. H., & Barrios, F. A. (2019) · eneuro · doi:10.1523/eneuro.0335-18.2019 · Cited by 81 · see citing works
Kumral, D., Schaare, H. L., Beyer, F., Reinelt, J., Uhlig, M., Liem, F., Lampe, L., Babayan, A., Reiter, A., Erbey, M., et al. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2018.10.027 · Cited by 64 · see citing works
Zhao, W., Yao, S., Li, Q., Geng, Y., Ma, X., Luo, L., Xu, L., & Kendrick, K. M. (2016) · Human Brain Mapping · doi:10.1002/hbm.23190 · Cited by 65 · see citing works
Palva, J. M., & Palva, S. (2011) · Progress in Brain Research · doi:10.1016/b978-0-444-53839-0.00022-3 · Cited by 63 · see citing works
Patterns of default mode network deactivation in obsessive compulsive disorder
Gonçalves, Ó. F., Soares, J. M., Carvalho, S., Leite, J., Ganho-Ávila, A., Fernandes-Gonçalves, A., Pocinho, F., Carracedo, A., & Sampaio, A. (2017) · Scientific Reports · doi:10.1038/srep44468 · Cited by 57 · see citing works
Farr, O. M., Zhang, S., Hu, S., Matuskey, D., Abdelghany, O., Malison, R. T., & Li, C.-S. R. (2014) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145714000674 · Cited by 57 · see citing works
Jamieson, A. J., Harrison, B. J., Razi, A., & Davey, C. G. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01214-z · Cited by 41 · see citing works
Feige, B., Biscaldi, M., Saville, C. W. N., Kluckert, C., Bender, S., Ebner-Priemer, U., Hennighausen, K., Rauh, R., Fleischhaker, C., & Klein, C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0069674 · Cited by 41 · see citing works
Liu, Q., Gao, F., Wang, X., Xia, J., Yuan, G., Zheng, S., Zhong, M., & Zhu, X. (2023) · Human Brain Mapping · doi:10.1002/hbm.26457 · Cited by 33 · see citing works
Keppler, J. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.01346 · Cited by 30 · see citing works
Nikolaidis, A., He, X., Pekar, J., Rosch, K., & Mostofsky, S. H. (2022) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2022.101101 · Cited by 28 · see citing works
Liu, Z., de Zwart, J. A., Chang, C., Duan, Q., van Gelderen, P., & Duyn, J. H. (2014) · Cerebral Cortex · doi:10.1093/cercor/bht164 · Cited by 22 · see citing works
Dynamic coupling of complex brain networks and dual-task behavior
Alavash, M., Thiel, C. M., & Gießing, C. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.01.028 · Cited by 25 · see citing works
Cha, D., Michele, F., Soczynska, J., Woldeyohannes, H., Kaidanovich-Beilin, O., Carvalho, A., Malhi, G., Patel, H., Sim, K., Brietzke, E., et al. (2015) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527313666141130205024 · Cited by 18 · see citing works
Biswas, A., & Ray, S. (2019) · eneuro · doi:10.1523/eneuro.0498-18.2019 · Cited by 12 · see citing works
Jin, H., Zhang, B., Cui, H., Li, W., Li, H., Hu, Q., Wang, J., & Li, C. (2020) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s248453 · Cited by 10 · see citing works
Bartholomeusz, E. J., Fong, A. K., Tervort, T. J., Gaufin, L. M., & Allen, M. D. (2025) · doi:10.1101/2025.10.08.25336734
- Authors
- Uddin, L. Q., Clare Kelly, A. M., Biswal, B. B., Xavier Castellanos, F., & Milham, M. P.
- Affiliations
- NYU Langone Health (US)
- Rutgers, The State University of New Jersey (US)
- New York University (US)
- Venue
- Human Brain Mapping
- Publisher
- Wiley
- Published
- 2009-01-19
- Volume
- 30
- Issue
- 2
- Pages
- 625-637
- ISSN
- 1065-9471 (ISSN-L)
- 1097-0193
- PMC
- PMC3654104
- OpenAlex
- W2144427015
- Cited by
- 1,135
- References
- 19
- Citations by year
- 2026: 24 · 2025: 52 · 2024: 64 · 2023: 58 · 2022: 58 · 2021: 75 · 2020: 84 · 2019: 84 · 2018: 78 · 2017: 82 · 2016: 68 · 2015: 77 · 2014: 75 · 2013: 69 · 2012: 59
- FWCI
- 21.60
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Human Brain Mapping (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r21mh066393-03, 5t32mh067763-10)
- National Institute of Mental Health (5T32MH067763, 5R21MH066393, R21-MH066393, T32MH-067763)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Mind wandering and attention
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- default mode network, ventromedial prefrontal cortex, posterior cingulate cortex, anticorrelation, functional connectivity, Granger causality, task-positive network, resting-state brain activity, network heterogeneity, visuospatial attention, temporal attention, motor control
- MeSH terms
- Adult, Attention, Brain Mapping, Female, Gyrus Cinguli, Humans, Image Processing, Computer-Assisted, Functional Laterality, Magnetic Resonance Imaging, Male, Nerve Net, Neural Pathways, Neuropsychological Tests, Psychomotor Performance, Space Perception, Causality, Prefrontal Cortex, Young Adult
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