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The Common Neural Basis of Autobiographical Memory, Prospection, Navigation, Theory of Mind, and the Default Mode: A Quantitative Meta-analysis
Open accessAbstract
A core brain network has been proposed to underlie a number of different processes, including remembering, prospection, navigation, and theory of mind [Buckner, R. L., & Carroll, D. C. Self-projection and the brain. Trends in Cognitive Sciences, 11, 49–57, 2007]. This purported network—medial prefrontal, medial-temporal, and medial and lateral parietal regions—is similar to that observed during default-mode processing and has been argued to represent self-projection [Buckner, R. L., & Carroll, D. C. Self-projection and the brain. Trends in Cognitive Sciences, 11, 49–57, 2007] or scene-construction [Hassabis, D., & Maguire, E. A. Deconstructing episodic memory with construction. Trends in Cognitive Sciences, 11, 299–306, 2007]. To date, no systematic and quantitative demonstration of evidence for this common network has been presented. Using the activation likelihood estimation (ALE) approach, we conducted four separate quantitative meta-analyses of neuroimaging studies on: (a) autobiographical memory, (b) navigation, (c) theory of mind, and (d) default mode. A conjunction analysis between these domains demonstrated a high degree of correspondence. We compared these findings to a separate ALE analysis of prospection studies and found additional correspondence. Across all domains, and consistent with the proposed network, correspondence was found within the medial-temporal lobe, precuneus, posterior cingulate, retrosplenial cortex, and the temporo-parietal junction. Additionally, this study revealed that the core network extends to lateral prefrontal and occipital cortices. Autobiographical memory, prospection, theory of mind, and default mode demonstrated further reliable involvement of the medial prefrontal cortex and lateral temporal cortices. Autobiographical memory and theory of mind, previously studied as distinct, exhibited extensive functional overlap. These findings represent quantitative evidence for a core network underlying a variety of cognitive domains.
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“Consistent with this perspective, the DMN is implicated in a broad range of tasks probing social cognition and communication, with consistent activation patterns reported in the PCC, mPFC, AG, and adjoining temporal parietal junction. 42,43”
From 20 years of the default mode network: A review and synthesis. (2023) · cites this paper as [43]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
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“The DMN includes medial cortical structures, such as the ventromedial prefrontal cortex and the posterior cingulate cortex, and it is critical to negative self-referential processing such as rumination and worrying known to go awry in depression (35–38).”
From Feasibility and preliminary efficacy of a novel RDoC-based treatment program for adolescent depression: "Training for Awareness Resilience and Action" (TARA)-A pilot study (2017) · cites this paper as [35]
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“The DMN plays a crucial role in episodic memory operations, particularly those related to personally relevant details of remembered experiences.”
From 20 years of the default mode network: A review and synthesis. (2023) · cites this paper as [43]
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“ToM, autobiographical memory and resting-state cognition have been proposed to draw on a shared ‘core’ network including mPFC, precuneus, posterior cingulate and TPJ (Spreng et al., 2009).”
From The brain's conversation with itself: neural substrates of dialogic inner speech (2016) · cites this paper as Spreng et al., 2009
In the citing paper
“The profound deficits in simulating future events exhibited by patients with semantic dementia, despite a relative preservation of past episodic memory, suggest that other forms of self-projection, such as theory of mind, empathy and moral reasoning (Spreng et al., 2009), may also be compromised.”
From Considering the role of semantic memory in episodic future thinking: evidence from semantic dementia (2012) · cites this paper as Spreng et al., 2009
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“Recent studies suggest that the DMN consists of several subnetworks with diverse and specialized roles, including subnetworks specific for self-referential or social cognitive processing [Menon, 2011;Spreng et al., 2009], or differentiating between the self and others [van Veluw and Chance, 2014].”
From Specific default mode subnetworks support mentalizing as revealed through opposing network recruitment by social and semantic FMRI tasks: Mentalizing and Default-Mode Subnetworks (2015) · cites this paper as Spreng et al., 2009
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“The results of the meta-analysis of ToM were consistent with earlier quantitative analyses”
From Parsing the neural correlates of moral cognition: ALE meta-analysis on morality, theory of mind, and empathy (2012) · cites this paper as Spreng et al. 2009
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“Similar brain mechanisms in remembering past episodes and envisioning future circumstances is supported by their engagement of identical brain areas, as evidenced by a quantitative meta-analysis (Spreng et al. 2009).”
From Parsing the neural correlates of moral cognition: ALE meta-analysis on morality, theory of mind, and empathy (2012) · cites this paper as Spreng et al. 2009
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Cites
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
Co-Planar Stereotaxic Atlas of the Human Brain
Talairach, J., & Tournoux, P. (1988) · Medical Entomology and Zoology · Cited by 11,798
AFNI: Software for analysis and visualization of functional magnetic resonance neuroimages
Cox, R. W. (1996) · Computers and Biomedical Research · doi:10.1006/cbmr.1996.0014 · Cited by 10,913
The Brain's Default Network: Anatomy, Function, and Relevance to Disease
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
Bruner, J. (1986) · doi:10.4159/9780674029019 · Cited by 8,657
Co-planar stereotaxic atlas of the human brain
Laitinen, L. (1989) · Clinical Neurology and Neurosurgery · doi:10.1016/0303-8467(89)90128-5 · Cited by 7,565
Actual Minds, Possible Worlds.
Mergler, N. L., Schleifer, R., & Bruner, J. S. (1986) · MLN · doi:10.2307/2905728 · Cited by 6,626
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
Saliency, switching, attention and control: a network model of insula function
Menon, V., & Uddin, L. Q. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0262-0 · Cited by 5,592
Tulving, E. (1985) · Canadian Psychology / Psychologie canadienne · doi:10.1037/h0080017 · Cited by 4,638
Cited by
Sorted by citations
Saliency, switching, attention and control: a network model of insula function
Menon, V., & Uddin, L. Q. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0262-0 · Cited by 5,592
Large-scale brain networks and psychopathology: a unifying triple network model
Menon, V. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.08.003 · Cited by 4,168
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
Functional-anatomic fractionation of the brain’s default network
Andrews-Hanna, J. R., Reidler, J. S., Sepulcre, J., Poulin, R., & Buckner, R. L. (2010) · Neuron · doi:10.1016/j.neuron.2010.02.005 · Cited by 2,767
The brain basis of emotion: a meta-analytic review
Lindquist, K. A., Wager, T. D., Kober, H., Bliss-Moreau, E., & Barrett, L. F. (2012) · Behavioral and Brain Sciences · doi:10.1017/s0140525x11000446 · Cited by 2,320
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
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
Self-citationThe neurobiology of semantic memory
Binder, J. R., & Desai, R. H. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.10.001 · Cited by 2,114
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
Fractionating theory of mind: a meta-analysis of functional brain imaging studies
Schurz, M., Radua, J., Aichhorn, M., Richlan, F., & Perner, J. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.01.009 · Cited by 1,656
The Angular Gyrus: Multiple Functions and Multiple Subdivisions
Seghier, M. L. (2013) · The Neuroscientist · doi:10.1177/1073858412440596 · Cited by 1,585
Toward a second-person neuroscience
Schilbach, L., Timmermans, B., Reddy, V., Costall, A., Bente, G., Schlicht, T., & Vogeley, K. (2013) · Behavioral and Brain Sciences · doi:10.1017/s0140525x12000660 · Cited by 1,510
Two cortical systems for memory-guided behaviour
Ranganath, C., & Ritchey, M. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3338 · Cited by 1,377
An opportunity cost model of subjective effort and task performance
Kurzban, R., Duckworth, A., Kable, J. W., & Myers, J. (2013) · Behavioral and Brain Sciences · doi:10.1017/s0140525x12003196 · Cited by 1,381
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
Self-citationThe 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
Self-citationWhat 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
Vago, D. R., & Silbersweig, D. A. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00296 · Cited by 1,310
The Function of Fiction is the Abstraction and Simulation of Social Experience
Mar, R. A., & Oatley, K. (2008) · Perspectives on Psychological Science · doi:10.1111/j.1745-6924.2008.00073.x · Cited by 1,345
Self-citationSpreng, 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
Self-citationThe cognitive neuroscience of ageing
Grady, C. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3256 · Cited by 1,286
The neuroscience of empathy: Progress, pitfalls and promise
Zaki, J., & Ochsner, K. N. (2012) · Nature Neuroscience · doi:10.1038/nn.3085 · Cited by 1,231
Social cognition in schizophrenia
Green, M. F., Horan, W. P., & Lee, J. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn4005 · Cited by 1,159
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
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
Episodic memory and beyond: the hippocampus and neocortex in transformation
Moscovitch, M., Cabeza, R., Winocur, G., & Nadel, L. (2016) · Annual Review of Psychology · doi:10.1146/annurev-psych-113011-143733 · Cited by 1,062
Spreng, R. N., & Grady, C. L. (2010) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21282 · Cited by 985
Self-citationThe 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
Opportunities and limitations of intrinsic functional connectivity MRI
Buckner, R. L., Krienen, F. M., & Yeo, B. T. T. (2013) · Nature Neuroscience · doi:10.1038/nn.3423 · Cited by 912
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
The evolution of distributed association networks in the human brain
Buckner, R. L., & Krienen, F. M. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.09.017 · Cited by 836
The Neural Bases of Social Cognition and Story Comprehension
Mar, R. A. (2011) · Annual Review of Psychology · doi:10.1146/annurev-psych-120709-145406 · Cited by 950
Self-citationHow is our self related to midline regions and the default-mode network?
Qin, P., & Northoff, G. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.05.028 · Cited by 909
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
“43 The DMN’s role in autobiographical memory has been well articulated in previous reviews.”
BackgroundThe Unengaged Mind: Defining Boredom in Terms of Attention
Eastwood, J. D., Frischen, A., Fenske, M. J., & Smilek, D. (2012) · Perspectives on Psychological Science · doi:10.1177/1745691612456044 · Cited by 909
Ventromedial prefrontal–subcortical systems and the generation of affective meaning
Roy, M., Shohamy, D., & Wager, T. D. (2012) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2012.01.005 · Cited by 856
Hamilton, J. P., Furman, D. J., Chang, C., Thomason, M. E., Dennis, E., & Gotlib, I. H. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.02.003 · Cited by 823
Segregated fronto-cerebellar circuits revealed by intrinsic functional connectivity
Krienen, F. M., & Buckner, R. L. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp135 · Cited by 782
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
Dynamic reconfiguration of frontal brain networks during executive cognition in humans
Braun, U., Schäfer, A., Walter, H., Erk, S., Romanczuk-Seiferth, N., Haddad, L., Schweiger, J. I., Grimm, O., Heinz, A., Tost, H., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1422487112 · Cited by 791
Signature of consciousness in the dynamics of resting-state brain activity
Barttfeld, P., Uhrig, L., Sitt, J. D., Sigman, M., Jarraya, B., & Dehaene, S. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1418031112 · Cited by 670
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
Functional neuroimaging of autobiographical memory
Cabeza, R., & St Jacques, P. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.02.005 · Cited by 736
Fox, 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
Self-citationThe 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
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
Towards 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
Self-citationShared 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
A conceptual framework for the neurobiological study of resilience
Kalisch, R., Müller, M. B., & Tüscher, O. (2015) · Behavioral and Brain Sciences · doi:10.1017/s0140525x1400082x · Cited by 669
Evaluation of the evidence for the trauma and fantasy models of dissociation.
Dalenberg, C. J., Brand, B. L., Gleaves, D. H., Dorahy, M. J., Loewenstein, R. J., Cardeña, E., Frewen, P. A., Carlson, E. B., & Spiegel, D. (2012) · Psychological Bulletin · doi:10.1037/a0027447 · Cited by 667
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
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
The role of PFC networks in cognitive control and executive function
Menon, V., & D’Esposito, M. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01152-w · Cited by 654
Bzdok, D., Schilbach, L., Vogeley, K., Schneider, K., Laird, A. R., Langner, R., & Eickhoff, S. B. (2012) · Brain Structure and Function · doi:10.1007/s00429-012-0380-y · Cited by 653
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
Self-citationAnterior hippocampus: the anatomy of perception, imagination and episodic memory
Zeidman, P., & Maguire, E. A. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2015.24 · Cited by 542
Making sense by making sentient: Effectance motivation increases anthropomorphism.
Waytz, A., Morewedge, C. K., Epley, N., Monteleone, G., Gao, J.-H., & Cacioppo, J. T. (2010) · Journal of Personality and Social Psychology · doi:10.1037/a0020240 · Cited by 587
Patel, R., Spreng, R. N., Shin, L. M., & Girard, T. A. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.06.003 · Cited by 546
Self-citationMar, R. A., Oatley, K., & Peterson, J. B. (2009) · COMM · doi:10.1515/comm.2009.025 · Cited by 552
Self-citationThe construction system of the brain
Hassabis, D., & Maguire, E. A. (2009) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2008.0296 · Cited by 483
Emotion regulation: quantitative meta-analysis of functional activation and deactivation
Frank, D. W., Dewitt, M., Hudgens-Haney, M., Schaeffer, D. J., Ball, B. H., Schwarz, N. F., Hussein, A. A., Smart, L. M., & Sabatinelli, D. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.06.010 · Cited by 454
A neural mechanism mediating the impact of episodic prospection on farsighted decisions
Benoit, R. G., Gilbert, S. J., & Burgess, P. W. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.6559-10.2011 · Cited by 422
Boyd, J. E., Lanius, R. A., & McKinnon, M. C. (2018) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.170021 · Cited by 407
The Role of the Hippocampus in Prediction and Imagination
Buckner, R. L. (2010) · Annual Review of Psychology · doi:10.1146/annurev.psych.60.110707.163508 · Cited by 419
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
Sripada, R. K., King, A. P., Welsh, R. C., Garfinkel, S. N., Wang, X., Sripada, C. S., & Liberzon, I. (2012) · Psychosomatic Medicine · doi:10.1097/psy.0b013e318273bf33 · Cited by 412
Smallwood, J., Brown, K., Baird, B., & Schooler, J. W. (2012) · Brain Research · doi:10.1016/j.brainres.2011.03.072 · Cited by 379
Benoit, R. G., & Schacter, D. L. (2015) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2015.06.034 · Cited by 366
Inferences about mental states
Mitchell, J. P. (2009) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2008.0318 · Cited by 387
Event memory: A theory of memory for laboratory, autobiographical, and fictional events.
Rubin, D. C., & Umanath, S. (2015) · Psychological Review · doi:10.1037/a0037907 · Cited by 379
Imaging suicidal thoughts and behaviors: a comprehensive review of 2 decades of neuroimaging studies
Schmaal, L., van Harmelen, A.-L., Chatzi, V., Lippard, E. T. C., Toenders, Y. J., Averill, L. A., Mazure, C. M., & Blumberg, H. P. (2020) · Molecular Psychiatry · doi:10.1038/s41380-019-0587-x · Cited by 373
Laird, A. R. (2009) · Frontiers in Neuroinformatics · doi:10.3389/neuro.11.023.2009 · Cited by 372
Model-based and model-free Pavlovian reward learning: Revaluation, revision, and revelation
Dayan, P., & Berridge, K. C. (2014) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/s13415-014-0277-8 · Cited by 357
The Pivotal Role of Semantic Memory in Remembering the Past and Imagining the Future
Irish, M., & Piguet, O. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00027 · Cited by 345
Connolly, C. G., Wu, J., Ho, T. C., Hoeft, F., Wolkowitz, O., Eisendrath, S., Frank, G., Hendren, R., Max, J. E., Paulus, M. P., et al. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.05.036 · Cited by 356
Uddin, L. Q. (2010) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2010.00021 · Cited by 343
Shared understanding of narratives is correlated with shared neural responses
Nguyen, M., Vanderwal, T., & Hasson, U. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2018.09.010 · Cited by 304
Baird, B., Smallwood, J., Gorgolewski, K. J., & Margulies, D. S. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.0786-13.2013 · Cited by 315
The fallacy of a “task‐negative” network
Spreng, R. N. (2012) · Frontiers in Psychology · doi:10.3389/fpsyg.2012.00145 · Cited by 320
Self-citationHow the Opinion of Others Affects Our Valuation of Objects
Campbell-Meiklejohn, D. K., Bach, D. R., Roepstorff, A., Dolan, R. J., & Frith, C. D. (2010) · Current Biology · doi:10.1016/j.cub.2010.04.055 · Cited by 339
Mapping the information flow from one brain to another during gestural communication
Schippers, M. B., Roebroeck, A., Renken, R., Nanetti, L., & Keysers, C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1001791107 · Cited by 323
Concept representation reflects multimodal abstraction: A framework for embodied semantics
Fernandino, L., Binder, J. R., Desai, R. H., Pendl, S. L., Humphries, C. J., Gross, W. L., Conant, L. L., & Seidenberg, M. S. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv020 · Cited by 305
Stawarczyk, D., Majerus, S., Maquet, P., & D'Argembeau, A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016997 · Cited by 305
The Default Mode Network in Healthy Aging and Alzheimer′s Disease
Mevel, K., Chételat, G., Eustache, F., & Desgranges, B. (2011) · International Journal of Alzheimer’s Disease · doi:10.4061/2011/535816 · Cited by 302
Developmental changes in large-scale network connectivity in autism
Nomi, J. S., & Uddin, L. Q. (2015) · NeuroImage: Clinical · doi:10.1016/j.nicl.2015.02.024 · Cited by 274
The Modulation of BOLD Variability between Cognitive States Varies by Age and Processing Speed
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Metadata
- Authors
- Spreng, R. N., Mar, R. A., & Kim, A. S. N.
- Affiliations
- University of Toronto (CA)
- York University (CA)
- Venue
- Journal of Cognitive Neuroscience
- Publisher
- MIT Press
- Published
- 2009-03-01
- Volume
- 21
- Issue
- 3
- Pages
- 489-510
- ISSN
- 0898-929X (ISSN-L)
- 1530-8898
- OpenAlex
- W2144421443
- Semantic Scholar
- 65ab3415072bded398074af8ecc57f410ed75b07
- Cited by
- 2,143
- References
- 241
- Citations by year
- 2026: 83 · 2025: 93 · 2024: 107 · 2023: 101 · 2022: 112 · 2021: 158 · 2020: 139 · 2019: 148 · 2018: 131 · 2017: 174 · 2016: 143 · 2015: 141 · 2014: 137 · 2013: 156 · 2012: 131
- FWCI
- 31.52
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Cognitive Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- eScholarship@McGill (McGill) (submittedVersion, cc-by)
- Funders
- Social Sciences and Humanities Research Council of Canada
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Cognitive Functions and Memory
- Keywords
- autobiographical memory, prospection, navigation, theory of mind, default mode network, self-projection, scene construction, medial prefrontal cortex, medial temporal lobe, precuneus, posterior cingulate cortex, retrosplenial cortex, temporoparietal junction, activation likelihood estimation
- MeSH terms
- Autobiographies as Topic, Brain, Brain Mapping, Diagnostic Imaging, Humans, Memory, Models, Psychological, Meta-Analysis as Topic
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.
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