Functional-anatomic fractionation of the brain’s default network
Open accessAbstract
One of the most consistent observations in human functional imaging is that a network of brain regions referred to as the "default network" increases its activity during passive states. Here we explored the anatomy and function of the default network across three studies to resolve divergent hypotheses about its contributions to spontaneous cognition and active forms of decision making. Analysis of intrinsic activity revealed the network comprises multiple, dissociated components. A midline core (posterior cingulate and anterior medial prefrontal cortex) is active when people make self-relevant, affective decisions. In contrast, a medial temporal lobe subsystem becomes engaged when decisions involve constructing a mental scene based on memory. During certain experimentally directed and spontaneous acts of future-oriented thought, these dissociated components are simultaneously engaged, presumably to facilitate construction of mental models of personally significant events.
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Nodes of the medial temporal lobe subsystem of the core network implicated in detailed event and scene processing, such as the hippocampus, parahippocampal gyrus, and inferior parietal lobule, exhibit greater activity during divergent thinking tasks compared with various controls.
“In particular, nodes of the medial temporal lobe subsystem of the core network implicated in detailed event and scene processing (Andrews-Hanna et al. 2010), such as the hippocampus, parahippocampal gyrus, and inferior parietal lobule, have been found to exhibit greater activity during these tasks compared with various controls”
From Neural Mechanisms of Episodic Retrieval Support Divergent Creative Thinking (2019) · cites this paper as Andrews-Hanna et al. 2010
Retrieval orientation effects via ESI could be observed not just during formal tasks that recruit episodic mechanisms but during subsequent rest where default or core network activity is also often exhibited.
“An extension of this logic is that retrieval orientation effects via ESI could be observed not just during formal tasks that recruit episodic mechanisms but during subsequent rest where default or core network activity is also often exhibited (Andrews-Hanna et al. 2010).”
From Neural Mechanisms of Episodic Retrieval Support Divergent Creative Thinking (2019) · cites this paper as Andrews-Hanna et al. 2010
Hierarchical clustering of resting-state and task fMRI data from default network regions identified two separable components, each highly correlated with a midline core.
“Initial evidence for subsystems within the DN was provided by Andrews-Hanna et al.,50 who used hierarchical clustering analyses to partition RSFC and task-related fMRI data from eleven left-lateralized and midline DN regions into two separable components, each of which were highly correlated with a midline core (Fig. 3A).”
From The default network and self-generated thought: component processes, dynamic control, and clinical relevance (2014) · cites this paper as [50]
Areas within VMPFC are densely interconnected and strongly positively correlated.
“areas within VMPFC are densely interconnected and strongly positively correlated (38, 59)”
From Hyperactive error responses and altered connectivity in ventromedial and frontoinsular cortices in obsessive-compulsive disorder (2011) · cites this paper as [59]
Greater precuneus/PCC activation corresponds to a stronger tendency to attach to, ruminate on, and personalize pain appraisals.
“Thus, in the context of the present data, we propose that greater precuneus/PCC–related activation uniquely corresponds to greater propensity to attach to [32], ruminate on [34] and personalize [3] pain appraisals.”
From Neural mechanisms supporting the relationship between dispositional mindfulness and pain (2018) · cites this paper as [3]
ICA components 12 and 15 include several parts of the default mode network and support the hypothesis that this network includes functionally distinct subregions.
“ICA components 12 and 15 include several parts of the default mode network, and support the hypothesis that this network includes functionally distinct subregions (Andrews-Hanna et al., 2010).”
From The WU-Minn Human Connectome Project: An overview (2013) · cites this paper as Andrews-Hanna et al., 2010
The default mode network comprises the posterior medial cortex, medial prefrontal cortex, and temporoparietal junction.
“The DMN, which includes the posterior medial cortex, medial prefrontal cortex and temporoparietal junction1–3”
From The default mode network: where the idiosyncratic self meets the shared social world (2021) · cites this paper as [3]
The regions co-activating with cVMPFC and aVMPFC seeds are remarkably similar to some subnetworks of the canonical default mode network.
“Interestingly, the regions co-activating with the cVMPFC and aVMPFC seeds are remarkably similar to some of the subnetworks of the canonical default mode network, a result found across a wide variety of tasks (Smith et al., 2009;Andrews-Hanna et al., 2010).”
From Informatic parcellation of the network involved in the computation of subjective value (2014) · cites this paper as Andrews-Hanna et al., 2010
The two networks involving VMPFC are remarkably similar to some subnetworks of the default mode network found across a wide variety of tasks.
“Furthermore, these two networks involving VMPFC are remarkably similar to some of the subnetworks of the default mode network found across a wide variety of tasks (Smith et al., 2009;Andrews-Hanna et al., 2010).”
From Informatic parcellation of the network involved in the computation of subjective value (2014) · cites this paper as Andrews-Hanna et al., 2010
Many of the regions in the results mirror components of established functional networks.
“Many of the regions in our results mirror components of established functional networks (Smith et al., 2009;Andrews-Hanna et al., 2010;Bressler and Menon, 2010).”
From Informatic parcellation of the network involved in the computation of subjective value (2014) · cites this paper as Andrews-Hanna et al., 2010
In a recent study in healthy individuals, activity in the medial prefrontal cortex and posterior cingulate correlated significantly with participants' ratings of personal significance and affect.
“This idea is further qualified by a recent study in healthy individuals, in which activity in the medial prefrontal cortex and posterior cingulate correlated significantly with participants' ratings of personal significance and affect (Andrews-Hanna et al., 2010).”
From Considering the role of semantic memory in episodic future thinking: evidence from semantic dementia (2012) · cites this paper as Andrews-Hanna et al., 2010
Subsequent hits were associated with posterior cingulate cortex and rostral medial PFC, which are core midline regions of the default network that support self-referential processes and successful encoding of self-relevant information.
“Compared with subsequent false alarms, we found that subsequent hits were associated with posterior cingulate cortex and rostral medial PFC, which are core midline regions of the default network (74) that support self-referential processes (82, 83) and successful encoding of self-relevant information (84–86).”
From Neural mechanisms of reactivation-induced updating that enhance and distort memory (2013) · cites this paper as [74]
Hippocampus and vmPFC are part of a MTL subsystem of the default network that supports the formation of mental models based on mnemonic content during both memory retrieval and the simulation and encoding of future events.
“Hippocampus and vmPFC are part of a MTL subsystem of the default network (74) that supports the formation of mental models based on mnemonic content during both memory retrieval and the simulation and encoding of future events (36, 75, 76).”
From Neural mechanisms of reactivation-induced updating that enhance and distort memory (2013) · cites this paper as [74]
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Cites
James, W. (1891) · Henry Holt and Company eBooks · doi:10.1037/11059-000 · Cited by 25,799 · see citing works
Brainard, D. H. (1997) · Spatial Vision · doi:10.1163/156856897x00357 · Cited by 19,308 · see citing works
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 · see citing works
A set of measures of centrality based upon betweenness
Freeman, L. (1977) · Sociometry · doi:10.2307/3033543 · Cited by 10,557 · see citing works
<i>The Brain's Default Network</i>: <i>Anatomy, Function, and Relevance to Disease</i>
Buckner, R. L., Andrews‐Hanna, J. R., & Schacter, D. L. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1440.011 · Cited by 9,761 · see citing works
Self-citationSpontaneous 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 · see citing works
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 · see citing works
Binder, J. R., Desai, R. H., Graves, W. W., & Conant, L. L. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp055 · Cited by 4,060 · 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
Greicius, M. D., Srivastava, G., Reiss, A. L., & Menon, V. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308627101 · Cited by 3,684 · see citing works
Frith, C., & Frith, U. (2005) · Current Biology · doi:10.1016/j.cub.2005.08.041 · Cited by 3,494 · see citing works
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 · see citing works
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 · see citing works
Buckner, R. L., Sepulcre, J., Talukdar, T., Krienen, F. M., Liu, H., Hedden, T., Andrews-Hanna, J. R., Sperling, R. A., & Johnson, K. A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5062-08.2009 · Cited by 2,862 · see citing works
Self-citationWandering 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 · see citing works
An algorithm for drawing general undirected graphs
Kamada, T., & Kawai, S. (1989) · Information Processing Letters · doi:10.1016/0020-0190(89)90102-6 · Cited by 2,670 · see citing works
Remembering the past to imagine the future: the prospective brain
Schacter, D. L., Addis, D. R., & Buckner, R. L. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2213 · Cited by 2,394 · cited 2× · see citing works
“They further argued that mental simulation based on memory is a core process of future-oriented cognition (Schacter et al., 2007).”
Self-citationPeople thinking about thinking peopleThe role of the temporo-parietal junction in “theory of mind”
Saxe, R., & Kanwisher, N. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00230-1 · Cited by 2,316 · cited 2× · see citing works
“…regions within the dMPFC subsystem are also activated when participants infer the mental states of other people (e.g., Gallagher et al., 2000; Saxe and Kanwisher, 2003; Saxe et al., 2006; Ochsner et al., 2005; Lombardo et al., 2009; reviewed in Frith and Frith, 2003; Ochsner et al., 2004;…”
Development and neurophysiology of mentalizing
Frith, U., & Frith, C. D. (2003) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.2002.1218 · Cited by 2,306 · see citing works
Spreng, R. N., Mar, R. A., & Kim, A. S. N. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.21029 · Cited by 2,143 · see citing works
Common blood flow changes across visual tasks: II. Decreases in cerebral cortex
Shulman, G. L., Fiez, J. A., Corbetta, M., Buckner, R. L., Miezin, F. M., Raichle, M. E., & Petersen, S. E. (1997) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.1997.9.5.648 · Cited by 1,890 · see citing works
Self-citationVan 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
Self-citationThe cognitive neuroscience of constructive memory: remembering the past and imagining the future
Schacter, D. L., & Addis, D. R. (2007) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2007.2087 · Cited by 1,836 · see citing works
VISUAL IMAGERY DIFFERENCES IN THE RECALL OF PICTURES
MARKS, D. F. (1973) · British Journal of Psychology · doi:10.1111/j.2044-8295.1973.tb01322.x · Cited by 1,778 · see citing works
Christoff, K., Gordon, A. M., Smallwood, J., Smith, R., & Schooler, J. W. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900234106 · Cited by 1,769 · 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
Finding the self? An event-related fMRI study
Kelley, W. M., Macrae, C. N., Wyland, C. L., Caglar, S., Inati, S., & Heatherton, T. F. (2002) · Journal of Cognitive Neuroscience · doi:10.1162/08989290260138672 · Cited by 1,606 · cited 1× · see citing works
“…the aMPFC (and often PCC) activates when participants make judgments or remember trait adjectives about themselves compared to other people (e.g., Kelley et al., 2002; Lou et al., 2004; Heatherton et al., 2006; Mitchell et al., 2006; D’Argembeau et al., 2005) and the regions correlate with…”
Disruption of Large-Scale Brain Systems in Advanced Aging
Andrews-Hanna, J. R., Snyder, A. Z., Vincent, J. L., Lustig, C., Head, D., Raichle, M. E., & Buckner, R. L. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.038 · Cited by 1,592 · see citing works
Self-citationPatients with hippocampal amnesia cannot imagine new experiences
Hassabis, D., Kumaran, D., Vann, S. D., & Maguire, E. A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610561104 · Cited by 1,414 · see citing works
Gallagher, H. L., Happé, F., Brunswick, N., Fletcher, P. C., Frith, U., & Frith, C. D. (2000) · Neuropsychologia · doi:10.1016/s0028-3932(99)00053-6 · Cited by 1,394 · see citing works
Implementation intentions and effective goal pursuit.
Gollwitzer, P. M., & Brandstätter, V. (1997) · Journal of Personality and Social Psychology · doi:10.1037/0022-3514.73.1.186 · Cited by 1,343 · see citing works
Deconstructing episodic memory with construction
Hassabis, D., & Maguire, E. A. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.05.001 · Cited by 1,229 · see citing works
Fransson, P., & Marrelec, G. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.05.059 · Cited by 1,213 · cited 1× · see citing works
“The PCC, in particular, correlates with all regions that fall within the default network, even after taking the correlation between other default network regions into account (Fransson and Marrelec, 2008).”
A Population-Average, Landmark- and Surface-based (PALS) atlas of human cerebral cortex
Van Essen, D. C. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.06.058 · Cited by 1,151 · see citing works
The proactive brain: using analogies and associations to generate predictions
Bar, M. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.05.005 · Cited by 1,144 · see citing works
Perirhinal and parahippocampal cortices of the macaque monkey: Cortical afferents
Suzuki, W., & Amaral, D. G. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903500402 · Cited by 1,134 · see citing works
A 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
Conceptual Processing during the Conscious Resting State: A Functional MRI Study
Binder, J. R., Frost, J. A., Hammeke, T. A., Bellgowan, P. S. F., Rao, S. M., & Cox, R. W. (1999) · Journal of Cognitive Neuroscience · doi:10.1162/089892999563265 · Cited by 1,066 · 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
Precuneus shares intrinsic functional architecture in humans and monkeys
Margulies, D. S., Vincent, J. L., Kelly, C., Lohmann, G., Uddin, L. Q., Biswal, B. B., Villringer, A., Castellanos, F. X., Milham, M. P., & Petrides, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905314106 · Cited by 965 · cited 13× · see citing works
“This observation provides an important clue about why constructed thoughts about one’s future may activate such a widely distributed set of Neuron 65, 550–562, February 25, 2010 ª2010 Elsevier Inc. 551 B D PHC Rsp pIPL vMPFC TempP TPJ HF+ dMPFC pIPL Rsp PHC HF+ vMPFC TempP LTC dMPFC TPJ C PCC 0.000 - 0.249 0.250 - 0.4…”
InfluentialCoherent 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
“Using fcMRI in humans, we previously demonstrated that the HF is intrinsically correlated with a similar set of regions, including pIPL, Rsp, and vMPFC (Vincent et al., 2006; Kahn et al., 2008; see also Greicius et al., 2004) and similar patterns of connectivity have been found when examining intrinsic correlations wi…”
Self-citationNeural correlates of self-reflection
Johnson, S. C. (2002) · Brain · doi:10.1093/brain/awf181 · Cited by 930 · see citing works
Mazoyer, B., Zago, L., Mellet, E., Bricogne, S., Etard, O., Houdé, O., Crivello, F., Joliot, M., Petit, L., & Tzourio-Mazoyer, N. (2001) · Brain Research Bulletin · doi:10.1016/s0361-9230(00)00437-8 · Cited by 906 · see citing works
Ochsner, K. N., Knierim, K., Ludlow, D. H., Hanelin, J., Ramachandran, T., Glover, G., & Mackey, S. C. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/0898929042947829 · Cited by 850 · see citing works
Mapping the functional connectivity of anterior cingulate cortex
Margulies, D. S., Kelly, C. A. M., Uddin, L. Q., Biswal, B. B., Castellanos, F. X., & Milham, M. P. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.05.019 · Cited by 751 · see citing works
Using Imagination to Understand the Neural Basis of Episodic Memory
Hassabis, D., Kumaran, D., & Maguire, E. A. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4549-07.2007 · Cited by 744 · cited 3× · see citing works
“Consistent with this finding, patients with hippocampal amnesia lack the ability to imagine a coherent scene presumably void of a temporal context (Hassabis et al., 2007b; see also Hassabis et al., 2007a; Addis et al., 2009).”
Parietal cortex and representation of the mental Self
Lou, H. C., Luber, B., Crupain, M., Keenan, J. P., Nowak, M., Kjaer, T. W., Sackeim, H. A., & Lisanby, S. H. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0400049101 · Cited by 631 · see citing works
Schilbach, L., Eickhoff, S. B., Rotarska-Jagiela, A., Fink, G. R., & Vogeley, K. (2008) · Consciousness and Cognition · doi:10.1016/j.concog.2008.03.013 · Cited by 615 · see citing works
Addis, D. R., Pan, L., Vu, M.-A. T., Laiser, N., & Schacter, D. L. (2008) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2008.10.026 · Cited by 600 · see citing works
Remembering the past: two facets of episodic memory explored with positron emission tomography
(1995) · American Journal of Psychiatry · doi:10.1176/ajp.152.11.1576 · Cited by 593 · see citing works
The neural correlates of direct and reflected self-knowledge
Ochsner, K. N., Beer, J. S., Robertson, E. R., Cooper, J. C., Gabrieli, J. D. E., Kihsltrom, J. F., & D'Esposito, M. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.06.069 · Cited by 562 · see citing works
Neural activation during selective attention to subjective emotional responses
Lane, R. D., Fink, G. R., Chau, P. M.-L., & Dolan, R. J. (1997) · Neuroreport · doi:10.1097/00001756-199712220-00024 · Cited by 558 · see citing works
In defense of the simulation theory.
GOLDMAN, A. I. (1992) · Mind & Language · doi:10.1111/j.1468-0017.1992.tb00200.x · Cited by 516 · see citing works
Kahn, I., Andrews‐Hanna, J. R., Vincent, J. L., Snyder, A. Z., & Buckner, R. L. (2008) · Journal of Neurophysiology · doi:10.1152/jn.00077.2008 · Cited by 490 · see citing works
Self-citationSelf-referential reflective activity and its relationship with rest: a PET study
D’Argembeau, A., Collette, F., der Linden, M. V., Laureys, S., Fiore, G. D., Degueldre, C., Luxen, A., & Salmon, É. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2004.11.048 · Cited by 489 · see citing works
Macaque monkey retrosplenial cortex: III. Cortical efferents
Kobayashi, Y., & Amaral, D. G. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21346 · Cited by 487 · see citing works
Interrupting the “stream of consciousness”: An fMRI investigation
McKiernan, K. A., D'Angelo, B. R., Kaufman, J. N., & Binder, J. R. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.09.030 · Cited by 443 · see citing works
Structure and Functions of Fantasy
Dissanayake, E., & Klinger, E. (1974) · Leonardo · doi:10.2307/1573079 · Cited by 425 · see citing works
Evidence from intrinsic activity that asymmetry of the human brain is controlled by multiple factors
Liu, H., Stufflebeam, S. M., Sepulcre, J., Hedden, T., & Buckner, R. L. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0908073106 · Cited by 410 · see citing works
Self-citationPRICE, J. L. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1401.008 · Cited by 395 · see citing works
Medial prefrontal activity differentiates self from close others
Heatherton, T. F., Wyland, C. L., Macrae, C. N., Demos, K. E., Denny, B. T., & Kelley, W. M. (2006) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsl001 · Cited by 380 · see citing works
Macaque monkey retrosplenial cortex: II. Cortical afferents
Kobayashi, Y., & Amaral, D. G. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10883 · Cited by 378 · see citing works
Does the brain have a baseline? Why we should be resisting a rest
Morcom, A. M., & Fletcher, P. C. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.09.013 · Cited by 369 · see citing works
Shared Neural Circuits for Mentalizing about the Self and Others
Lombardo, M. V., Chakrabarti, B., Bullmore, E. T., Wheelwright, S. J., Sadek, S. A., John Suckling, A., & Baron‐Cohen, S. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21287 · Cited by 355 · see citing works
Daydreaming : an introduction to the experimental study of inner experience
Singer, J. L. (1966) · Random House eBooks · Cited by 340 · see citing works
Perirhinal and parahippocampal cortices of the macaque monkey: Projections to the neocortex
Lavenex, P., SUZUKI, W. A., & Amaral, D. G. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10243 · Cited by 317 · see citing works
Dimensions of Thought Flow in Everyday Life
Klinger, E., & Cox, W. M. (1987) · Imagination, Cognition and Personality · doi:10.2190/7k24-g343-mtqw-115v · Cited by 313 · see citing works
Saxe, R. R., Moran, J. M., Scholz, J., & Gabrieli, J. D. E. (2006) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsl034 · Cited by 306 · see citing works
The role of social cognition in emotion
Olsson, A., & Ochsner, K. N. (2008) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.11.010 · Cited by 289 · see citing works
Small, D., & White, T. (1998) · doi:10.1145/281388.281499 · Cited by 262 · see citing works
Morecraft, R. J., Cipolloni, P. B., Stilwell‐Morecraft, K. S., Gedney, M., & Pandya, D. Ν. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10980 · Cited by 238 · see citing works
Kondo, H., Saleem, K. S., & Price, J. L. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20796 · Cited by 236 · see citing works
Comment on "Wandering Minds: The Default Network and Stimulus-Independent Thought"
Gilbert, S. J., Dumontheil, I., Simons, J. S., Frith, C., & Burgess, P. W. (2007) · Science · doi:10.1126/science.1140801 · Cited by 207 · see citing works
A relation between rest and the self in the brain?
Wicker, B., Ruby, P. M., Royet, J., & Fonlupt, P. (2003) · Brain Research Reviews · doi:10.1016/j.brainresrev.2003.08.003 · Cited by 195 · see citing works
The Neural Basis of Personal Goal Processing When Envisioning Future Events
D'Argembeau, A., Stawarczyk, D., Majerus, S., Collette, F., Van der Linden, M., Feyers, D., Maquet, P., & Salmon, E. (2010) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21314 · Cited by 194 · see citing works
Self, mother and abstract other: an fMRI study of reflective social processing
Vanderwal, T., Hunyadi, E., Grupe, D. W., Connors, C. M., & Schultz, R. T. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.03.058 · Cited by 134 · see citing works
Contextual Processing in Episodic Future Thought
Szpunar, K. K., Chan, J. C. K., & McDermott, K. B. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn191 · Cited by 132 · see citing works
Mentalizing and Marr: An information processing approach to the study of social cognition
Mitchell, J. P. (2006) · Brain Research · doi:10.1016/j.brainres.2005.12.113 · Cited by 122 · see citing works
Fitzgibbon, T., Bittar, R. G., & Dreher, B. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19990802)410:3 · Cited by 18 · see citing works
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The organization of the human cerebral cortex estimated by intrinsic functional connectivity
Thomas Yeo, B. T., Krienen, F. M., Sepulcre, J., Sabuncu, M. R., Lashkari, D., Hollinshead, M., Roffman, J. L., Smoller, J. W., Zöllei, L., Polimeni, J. R., et al. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00338.2011 · Cited by 9,182 · see citing works
Self-citationThe organization of the human cerebellum estimated by intrinsic functional connectivity
Buckner, R. L., Krienen, F. M., Castellanos, A., Diaz, J. C., & Yeo, B. T. T. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00339.2011 · Cited by 7,304 · see citing works
Self-citationThe WU-Minn Human Connectome Project: An overview
Van Essen, D. C., Smith, S. M., Barch, D. M., Behrens, T. E. J., Yacoub, E., & Ugurbil, K. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.041 · Cited by 5,651 · see citing works
The brain's default mode network
Raichle, M. E. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071013-014030 · Cited by 3,904 · see citing works
Di Martino, A., Yan, C.-G., Li, Q., Denio, E., Castellanos, F. X., Alaerts, K., Anderson, J. S., Assaf, M., Bookheimer, S. Y., Dapretto, M., et al. (2014) · Molecular Psychiatry · doi:10.1038/mp.2013.78 · Cited by 2,780 · see citing works
Kaiser, R. H., Andrews-Hanna, J. R., Wager, T. D., & Pizzagalli, D. A. (2015) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2015.0071 · Cited by 2,281 · see citing works
Self-citationSpreng, R. N., Mar, R. A., & Kim, A. S. N. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.21029 · Cited by 2,143 · 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
Self-citationThe Angular Gyrus: Multiple Functions and Multiple Subdivisions
Seghier, M. L. (2013) · The Neuroscientist · doi:10.1177/1073858412440596 · Cited by 1,585 · see citing works
Control of sleep and wakefulness
Brown, R. E., Basheer, R., McKenna, J. T., Strecker, R. E., & McCarley, R. W. (2012) · Physiological Reviews · doi:10.1152/physrev.00032.2011 · Cited by 1,477 · 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
The human connectome: a complex network
Sporns, O. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05888.x · Cited by 1,399 · see citing works
The future of memory: remembering, imagining, and the brain
Schacter, D. L., Addis, D. R., Hassabis, D., Martin, V. C., Spreng, R. N., & Szpunar, K. K. (2012) · Neuron · doi:10.1016/j.neuron.2012.11.001 · Cited by 1,398 · see citing works
Two cortical systems for memory-guided behaviour
Ranganath, C., & Ritchey, M. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3338 · Cited by 1,377 · see citing works
Mind-wandering as spontaneous thought: a dynamic framework
Christoff, K., Irving, Z. C., Fox, K. C. R., Spreng, R. N., & Andrews-Hanna, J. R. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.113 · Cited by 1,376 · see citing works
Self-citationMichel, C. M., & Koenig, T. W. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.11.062 · Cited by 1,370 · see citing works
The cognitive neuroscience of ageing
Grady, C. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3256 · Cited by 1,286 · see citing works
Spreng, R. N., Stevens, W. D., Chamberlain, J. P., Gilmore, A. W., & Schacter, D. L. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.06.016 · Cited by 1,256 · see citing works
The brain's default network and its adaptive role in internal mentation
Andrews-Hanna, J. R. (2012) · The Neuroscientist · doi:10.1177/1073858411403316 · Cited by 1,114 · see citing works
Self-citationNetwork 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 · see citing works
The brain’s default network: updated anatomy, physiology and evolving insights
Buckner, R. L., & DiNicola, L. M. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0212-7 · Cited by 1,058 · see citing works
Self-citationNeural network of cognitive emotion regulation—an ALE meta-analysis and MACM analysis
Kohn, N., Eickhoff, S. B., Scheller, M., Laird, A. R., Fox, P. T., & Habel, U. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.11.001 · Cited by 956 · see citing works
Frontocingulate Dysfunction in Depression: Toward Biomarkers of Treatment Response
Pizzagalli, D. A. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2010.166 · Cited by 945 · see citing works
The default mode network in cognition: a topographical perspective
Smallwood, J., Bernhardt, B. C., Leech, R., Bzdok, D., Jefferies, E., & Margulies, D. S. (2021) · Nature Reviews Neuroscience · doi:10.1038/s41583-021-00474-4 · Cited by 935 · 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
Yan, C.-G., Chen, X., Li, L., Castellanos, F. X., Bai, T.-J., Bo, Q.-J., Cao, J., Chen, G.-M., Chen, N.-X., Chen, W., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1900390116 · Cited by 895 · see citing works
Resting-state functional connectivity in major depressive disorder: A review
Mulders, P. C., van Eijndhoven, P. F., Schene, A. H., Beckmann, C. F., & Tendolkar, I. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.07.014 · Cited by 884 · see citing works
The cingulate cortex and limbic systems for emotion, action, and memory
Rolls, E. T. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01945-2 · Cited by 859 · see citing works
Large-scale brain systems in ADHD: beyond the prefrontal–striatal model
Castellanos, F. X., & Proal, E. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.11.007 · Cited by 831 · see citing works
The human imagination: the cognitive neuroscience of visual mental imagery
Pearson, J. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0202-9 · Cited by 820 · see citing works
Fjell, A. M., McEvoy, L., Holland, D., Dale, A. M., & Walhovd, K. B. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2014.02.004 · Cited by 799 · see citing works
The social brain in psychiatric and neurological disorders
Kennedy, D. P., & Adolphs, R. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.09.006 · Cited by 798 · see citing works
Neural Networks of the Mouse Neocortex
Zingg, B., Hintiryan, H., Gou, L., Song, M. Y., Bay, M., Bienkowski, M. S., Foster, N. N., Yamashita, S., Bowman, I., Toga, A. W., et al. (2014) · Cell · doi:10.1016/j.cell.2014.02.023 · Cited by 797 · see citing works
On the relationship between the “default mode network” and the “social brain
Mars, R. B., Neubert, F.-X., Noonan, M. P., Sallet, J., Toni, I., & Rushworth, M. F. S. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00189 · Cited by 766 · see citing works
Brain networks underlying episodic memory retrieval
Rugg, M. D., & Vilberg, K. L. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.11.005 · Cited by 751 · see citing works
Emotion and the prefrontal cortex: an integrative review
Dixon, M. L., Thiruchselvam, R., Todd, R., & Christoff, K. (2017) · Psychological Bulletin · doi:10.1037/bul0000096 · Cited by 745 · see citing works
Informatic parcellation of the network involved in the computation of subjective value
Clithero, J. A., & Rangel, A. (2014) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nst106 · Cited by 706 · see citing works
Lutz, A., Jha, A. P., Dunne, J. D., & Saron, C. D. (2015) · American Psychologist · doi:10.1037/a0039585 · Cited by 697 · see citing works
“In the Attention Network Test (ANT, Fan, McCandliss, Sommer, Raz, & Posner, 2002), for example, the orienting subsystem of attention is characterized by faster target detection reaction times for those targets appearing at locations at which attention was directed prior to the target onset versus targets appearing at…”
BackgroundInfluentialFox, K. C. R., Spreng, R. N., Ellamil, M., Andrews-Hanna, J. R., & Christoff, K. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.02.039 · Cited by 690 · see citing works
Self-citationEvidence for the Default Network's Role in Spontaneous Cognition
Andrews-Hanna, J. R., Reidler, J. S., Huang, C., & Buckner, R. L. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00830.2009 · Cited by 685 · see citing works
Self-citationTowards a universal taxonomy of macro-scale functional human brain networks
Uddin, L. Q., Yeo, B. T. T., & Spreng, R. N. (2019) · Brain Topography · doi:10.1007/s10548-019-00744-6 · Cited by 683 · see citing works
The default mode network: where the idiosyncratic self meets the shared social world
Yeshurun, Y., Nguyen, M., & Hasson, U. (2021) · Nature Reviews Neuroscience · doi:10.1038/s41583-020-00420-w · Cited by 682 · see citing works
Zhou, H.-X., Chen, X., Shen, Y.-Q., Li, L., Chen, N.-X., Zhu, Z.-C., Castellanos, F. X., & Yan, C.-G. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2019.116287 · Cited by 656 · see citing works
Barrett, L. F., & Satpute, A. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.12.012 · Cited by 58 · see citing works
Shared memories reveal shared structure in neural activity across individuals
Chen, J., Leong, Y. C., Honey, C. J., Yong, C. H., Norman, K. A., & Hasson, U. (2017) · Nature Neuroscience · doi:10.1038/nn.4450 · Cited by 645 · see citing works
Zhu, X., Wang, X., Xiao, J., Liao, J., Zhong, M., Wang, W., & Yao, S. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.10.035 · Cited by 638 · see citing works
Targeted enhancement of cortical-hippocampal brain networks and associative memory
Wang, J. X., Rogers, L. M., Gross, E. Z., Ryals, A. J., Dokucu, M. E., Brandstatt, K. L., Hermiller, M. S., & Voss, J. L. (2014) · Science · doi:10.1126/science.1252900 · Cited by 615 · see citing works
Dixon, M. L., De La Vega, A., Mills, C., Andrews-Hanna, J., Spreng, R. N., Cole, M. W., & Christoff, K. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1715766115 · Cited by 595 · see citing works
Self-citationRat brains also have a default mode network
Lu, H., Zou, Q., Gu, H., Raichle, M. E., Stein, E. A., & Yang, Y. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1200506109 · Cited by 595 · see citing works
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 · see citing works
Braga, R. M., & Buckner, R. L. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.038 · Cited by 588 · see citing works
Self-citationFunctional brain connectivity using fMRI in aging and Alzheimer’s disease
Dennis, E. L., & Thompson, P. M. (2014) · Neuropsychology Review · doi:10.1007/s11065-014-9249-6 · Cited by 583 · see citing works
Electroencephalographic Resting-State Networks: Source Localization of Microstates
Custo, A., Ville, D. V. D., Wells, W. M., Tomescu, M. I., Brunet, D., & Michel, C. M. (2017) · Brain Connectivity · doi:10.1089/brain.2016.0476 · Cited by 547 · see citing works
Fornito, A., Harrison, B. J., Zalesky, A., & Simons, J. S. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1204185109 · Cited by 538 · see citing works
Cascading network failure across the Alzheimer’s disease spectrum
Jones, D. T., Knopman, D. S., Gunter, J. L., Graff‐Radford, J., Vemuri, P., Boeve, B. F., Petersen, R. C., Weiner, M. W., & Jack, C. R. (2015) · Brain · doi:10.1093/brain/awv338 · Cited by 532 · 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
Zeithamová, D., Dominick, A. L., & Preston, A. R. (2012) · Neuron · doi:10.1016/j.neuron.2012.05.010 · Cited by 521 · see citing works
Functional connectivity tracks clinical deterioration in Alzheimer's disease
Damoiseaux, J. S., Prater, K. E., Miller, B. L., & Greicius, M. D. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.06.024 · Cited by 504 · see citing works
Resting state functional connectivity in addiction: Lessons learned and a road ahead
Sutherland, M. T., McHugh, M. J., Pariyadath, V., & Stein, E. A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.117 · Cited by 495 · see citing works
Dong, D., Wang, Y., Chang, X., Luo, C., & Yao, D. (2018) · Schizophrenia Bulletin · doi:10.1093/schbul/sbx034 · Cited by 486 · see citing works
Posterior cingulate cortex: adapting behavior to a changing world
Pearson, J. M., Heilbronner, S. R., Barack, D. L., Hayden, B. Y., & Platt, M. L. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.02.002 · Cited by 482 · see citing works
Functional network disruption in the degenerative dementias
Pievani, M., de Haan, W., Wu, T., Seeley, W. W., & Frisoni, G. B. (2011) · The Lancet Neurology · doi:10.1016/s1474-4422(11)70158-2 · Cited by 481 · see citing works
Understanding brain networks and brain organization
Pessoa, L. (2014) · Physics of Life Reviews · doi:10.1016/j.plrev.2014.03.005 · Cited by 464 · see citing works
“Along these lines, recent work has suggested that task-negative networks can be subdivided in a number of ways [165].”
BackgroundLi, W., Mai, X., & Liu, C. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00074 · Cited by 459 · see citing works
Witte, A. V., Kerti, L., Margulies, D. S., & Floel, A. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0385-14.2014 · Cited by 455 · see citing works
Default mode network functional and structural connectivity after traumatic brain injury
Sharp, D. J., Beckmann, C. F., Greenwood, R., Kinnunen, K. M., Bonnelle, V., Boissezon, X. D., Powell, J. H., Counsell, S. J., Patel, M. C., & Leech, R. (2011) · Brain · doi:10.1093/brain/awr175 · Cited by 442 · see citing works
An open science resource for establishing reliability and reproducibility in functional connectomics
Zuo, X., Anderson, J. S., Bellec, P., Birn, R. M., Biswal, B. B., Blautzik, J., Breitner, J. C. S., Buckner, R. L., Calhoun, V. D., Castellanos, F. X., et al. (2014) · Scientific Data · doi:10.1038/sdata.2014.49 · Cited by 441 · see citing works
Self-citationDynamic 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 · see citing works
Association between Functional Connectivity Hubs and Brain Networks
Tomasi, D. G., & Volkow, N. D. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq268 · Cited by 434 · see citing works
Bzdok, D., Laird, A. R., Zilles, K., Fox, P. T., & Eickhoff, S. B. (2012) · Human Brain Mapping · doi:10.1002/hbm.22138 · Cited by 430 · see citing works
Dynamic cooperation and competition between brain systems during cognitive control
Cocchi, L., Zalesky, A., Fornito, A., & Mattingley, J. B. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.08.006 · Cited by 429 · see citing works
Adaptive constructive processes and the future of memory
Schacter, D. L. (2012) · American Psychologist · doi:10.1037/a0029869 · Cited by 417 · see citing works
Transcutaneous Vagus Nerve Stimulation Modulates Default Mode Network in Major Depressive Disorder
Fang, J., Rong, P., Yang, H., Fan, Y., Liu, J. H., Wang, H., Zhang, G., Chen, X., Shi, S. R., Wang, L., et al. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.03.025 · Cited by 416 · see citing works
Using Dual Regression to Investigate Network Shape and Amplitude in Functional Connectivity Analyses
Nickerson, L. D. H., Smith, S. M., Öngür, D., & Beckmann, C. F. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00115 · Cited by 409 · see citing works
Network-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
Considering the role of semantic memory in episodic future thinking: evidence from semantic dementia
Irish, M., Addis, D. R., Hodges, J. R., & Piguet, O. (2012) · Brain · doi:10.1093/brain/aws119 · Cited by 405 · see citing works
Mind wandering away from pain dynamically engages antinociceptive and default mode brain networks
Kucyi, A., Salomons, T. V., & Davis, K. D. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1312902110 · Cited by 402 · 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
Social brain, social dysfunction and social withdrawal
Porcelli, S., van der Wee, N. J. A., van der Werff, S. J., Aghajani, M., Glennon, J. C., van Heukelum, S., Mogavero, F., Lobo, A., Olivera, F. J. N., Lobo, E., et al. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.09.012 · Cited by 397 · see citing works
Kucyi, A., Moayedi, M., Weissman-Fogel, I., Goldberg, M. B., Freeman, B. V., Tenenbaum, H. C., & Davis, K. D. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.5055-13.2014 · Cited by 396 · see citing works
The hippocampus: a manifesto for change
Maguire, E. A., & Mullally, S. L. (2013) · Journal of Experimental Psychology: General · doi:10.1037/a0033650 · Cited by 393 · see citing works
The brain on art: intense aesthetic experience activates the default mode network
Vessel, E. A., Starr, G. G., & Rubin, N. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00066 · Cited by 392 · see citing works
The Default Mode Network in Autism
Padmanabhan, A., Lynch, C. J., Schaer, M., & Menon, V. (2017) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2017.04.004 · Cited by 381 · see citing works
Physical Activity and Cognitive Vitality
Prakash, R. S., Voss, M. W., Erickson, K. I., & Kramer, A. F. (2015) · Annual Review of Psychology · doi:10.1146/annurev-psych-010814-015249 · Cited by 376 · see citing works
Fractionation of social brain circuits in autism spectrum disorders
Gotts, S. J., Simmons, W. K., Milbury, L. A., Wallace, G. L., Cox, R. W., & Martin, A. (2012) · Brain · doi:10.1093/brain/aws160 · Cited by 369 · see citing works
The inferior parietal lobule and temporoparietal junction: A network perspective
Igelström, K. M., & Graziano, M. S. A. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2017.01.001 · Cited by 367 · see citing works
Benoit, R. G., & Schacter, D. L. (2015) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2015.06.034 · Cited by 366 · see citing works
Akiki, T. J., Averill, C. L., & Abdallah, C. G. (2017) · Current Psychiatry Reports · doi:10.1007/s11920-017-0840-4 · Cited by 365 · see citing works
Brain default-mode network dysfunction in addiction
Zhang, R., & Volkow, N. D. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.06.036 · Cited by 365 · see citing works
Lynch, C. J., Uddin, L. Q., Supekar, K., Khouzam, A., Phillips, J. M., & Menon, V. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.12.013 · Cited by 357 · see citing works
Alves, P. N., Foulon, C., Karolis, V., Bzdok, D., Margulies, D. S., Volle, E., & Thiebaut de Schotten, M. (2019) · Communications Biology · doi:10.1038/s42003-019-0611-3 · Cited by 357 · see citing works
Dynamic functional connectivity of the default mode network tracks daydreaming
Kucyi, A., & Davis, K. D. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.06.044 · Cited by 355 · see citing works
Spontaneous fluctuations in neural responses to heartbeats predict visual detection
Park, H.-D., Correia, S., Ducorps, A., & Tallon-Baudry, C. (2014) · Nature Neuroscience · doi:10.1038/nn.3671 · Cited by 349 · see citing works
The amygdala as a hub in brain networks that support social life
Bickart, K. C., Dickerson, B. C., & Feldman Barrett, L. (2014) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2014.08.013 · Cited by 344 · see citing works
Nielsen, J. A., Zielinski, B. A., Ferguson, M. A., Lainhart, J. E., & Anderson, J. S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071275 · Cited by 339 · see citing works
Default Mode of Brain Function in Monkeys
Mantini, D., Gerits, A., Nelissen, K., Durand, J., Joly, O., Simone, L., Sawamura, H., Wardak, C., Orban, G. A., Buckner, R. L., et al. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2318-11.2011 · Cited by 337 · see citing works
Self-citationCapturing the spatiotemporal dynamics of self-generated, task-initiated thoughts with EEG and fMRI
Bréchet, L., Brunet, D., Birot, G., Rolf Gruetter, A., Michel, C. M., & Jorge, J. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.03.029 · Cited by 333 · see citing works
Mormino, E. C., Smiljic, A., Hayenga, A. O., Onami, S. H., Greicius, M. D., Rabinovici, G. D., Janabi, M., Baker, S. L., Yen, I. V., Madison, C. M., et al. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr025 · Cited by 332 · 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
- Authors
- Andrews-Hanna, J. R., Reidler, J. S., Sepulcre, J., Poulin, R., & Buckner, R. L.
- Affiliations
- Harvard University (US)
- Howard Hughes Medical Institute (US)
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2010-02
- Volume
- 65
- Issue
- 4
- Pages
- 550-562
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC2848443
- OpenAlex
- W1991771535
- Cited by
- 2,767
- References
- 79
- Citations by year
- 2026: 170 · 2025: 174 · 2024: 207 · 2023: 184 · 2022: 190 · 2021: 242 · 2020: 225 · 2019: 196 · 2018: 186 · 2017: 169 · 2016: 154 · 2015: 170 · 2014: 145 · 2013: 145 · 2012: 101
- FWCI
- 67.89
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1262 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health
- National Institute on Aging (AG021910, R01AG021910, R01AG034556)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Mind wandering and attention
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Keywords
- default mode network, intrinsic brain activity, spontaneous cognition, decision-making, posterior cingulate cortex, anterior medial prefrontal cortex, medial temporal lobe, memory-based decision making, emotional decision-making, mental models
- MeSH terms
- Adolescent, Adult, Analysis of Variance, Brain, Brain Mapping, Cognition, Emotions, Female, Humans, Image Processing, Computer-Assisted, Imagination, Magnetic Resonance Imaging, Male, Memory, Nerve Net, Neuropsychological Tests, Cluster Analysis
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.
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