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Definition and characterization of an extended social-affective default network
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Recent evidence suggests considerable overlap between the default mode network (DMN) and regions involved in social, affective and introspective processes. We considered these overlapping regions as the social-affective part of the DMN. In this study, we established a robust mapping of the underlying brain network formed by these regions and those strongly connected to them (the extended social-affective default network). We first seeded meta-analytic connectivity modeling and resting-state analyses in the meta-analytically defined DMN regions that showed statistical overlap with regions associated with social and affective processing. Consensus connectivity of each seed was subsequently delineated by a conjunction across both connectivity analyses. We then functionally characterized the ensuing regions and performed several cluster analyses. Among the identified regions, the amygdala/hippocampus formed a cluster associated with emotional processes and memory functions. The ventral striatum, anterior cingulum, subgenual cingulum and ventromedial prefrontal cortex formed a heterogeneous subgroup associated with motivation, reward and cognitive modulation of affect. Posterior cingulum/precuneus and dorsomedial prefrontal cortex were associated with mentalizing, self-reference and autobiographic information. The cluster formed by the temporo-parietal junction and anterior middle temporal sulcus/gyrus was associated with language and social cognition. Taken together, the current work highlights a robustly interconnected network that may be central to introspective, socio-affective, that is, self- and other-related mental processes.
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“Second, the location of the DMN as equidistant from all sensory/motor systems is aligned with its broad range of functions that require integration between multiple sensory systems, including episodic [51] and semantic memory [52-54], social cognition [55, 56], goal-directed working memory tasks [26, 32, 33, 35] and reward-guided decision making [57, 58].”
From Situating the default-mode network along a principal gradient of macroscale cortical organization (2016) · cites this paper as [56]
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Cites
Algorithm AS 136: A K-Means Clustering Algorithm
Hartigan, J. A., & Wong, M. A. (1979) · Applied Statistics · doi:10.2307/2346830 · Cited by 14,523
Control of goal-directed and stimulus-driven attention in the brain
Corbetta, M., & Shulman, G. L. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn755 · Cited by 12,881
A default mode of brain function
Raichle, M. E., MacLeod, A. M., Snyder, A. Z., Powers, W. J., Gusnard, D. A., & Shulman, G. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.676 · Cited by 12,190
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
The human brain is intrinsically organized into dynamic, anticorrelated functional networks
Fox, M. D., Snyder, A. Z., Vincent, J. L., Corbetta, M., Van Essen, D. C., & Raichle, M. E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504136102 · Cited by 8,553
Ashburner, J., & Friston, K. J. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.02.018 · Cited by 7,507
The precuneus: a review of its functional anatomy and behavioural correlates
Cavanna, A. E., & Trimble, M. R. (2006) · Brain · doi:10.1093/brain/awl004 · Cited by 5,128
Consistent resting-state networks across healthy subjects
Damoiseaux, J. S., Rombouts, S. A. R. B., Barkhof, F., Scheltens, P., Stam, C. J., Smith, S. M., & Beckmann, C. F. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601417103 · Cited by 4,326
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
Binder, J. R., Desai, R. H., Graves, W. W., & Conant, L. L. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp055 · Cited by 4,060
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 · cited 4×
“Moreover, Amodio and Frith (2006) highlighted the role of the medial prefrontal cortex in social cognition and self-other referencing.”
InfluentialGreicius, 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
Frith, C., & Frith, U. (2005) · Current Biology · doi:10.1016/j.cub.2005.08.041 · Cited by 3,561
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
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
Sridharan, D., Levitin, D. J., & Menon, V. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800005105 · Cited by 2,892
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
Self-referential processing in our brain—A meta-analysis of imaging studies on the self
Northoff, G., Heinzel, A., de Greck, M., Bermpohl, F., Dobrowolny, H., & Panksepp, J. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.12.002 · Cited by 2,792
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
Buckner, R. L., & Carroll, D. C. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.11.004 · Cited by 2,691
Pain Affect Encoded in Human Anterior Cingulate But Not Somatosensory Cortex
Rainville, P., Duncan, G. H., Price, D. D., Carrier, B., & Bushnell, M. C. (1997) · Science · doi:10.1126/science.277.5328.968 · Cited by 2,629 · cited 1×
“Rainville et al. (1997) further found the anterior cingulate cortex to be involved in pain affect.”
Mayberg, H. S., Liotti, M., Brannan, S. K., McGinnis, S., Mahurin, R. K., Jerabek, P. A., Silva, J. A., Tekell, J. L., Martin, C. C., Lancaster, J. L., et al. (1999) · American Journal of Psychiatry · doi:10.1176/ajp.156.5.675 · Cited by 2,416
Self-citationThe human hippocampus and spatial and episodic memory
Burgess, N., Maguire, E. A., & O'Keefe, J. (2002) · Neuron · doi:10.1016/s0896-6273(02)00830-9 · Cited by 2,401
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×
“Schacter et al. (2007) consider parts of the DMN including PCC/PrC to be related to memory functions as well as thinking about the future (for further discussion see below).”
Murphy, K., Birn, R. M., Handwerker, D. A., Jones, T. B., & Bandettini, P. A. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.09.036 · Cited by 2,387
People 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 4×
“Taken together, literature indicates that a lot of default mode regions are routinely involved in social cognition and affective processing (Adams et al. 2010; Mars et al. 2012a; Saxe and Kanwisher 2003).”
InfluentialDrevets, W. C., Price, J. L., & Furey, M. L. (2008) · Brain Structure and Function · doi:10.1007/s00429-008-0189-x · Cited by 2,241 · cited 1×
“Drevets et al. (2008) further stress the role of SGC in the regulation of mood and emotional behavior and furthermore assume a network involved in emotional regulation including other brain regions such as amygdala.”
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
Cluster analysis of multivariate data : efficiency versus interpretability of classifications
Forgy, E. W. (1965) · Biometrics · Cited by 2,124
Satterthwaite, T. D., Elliott, M. A., Gerraty, R. T., Ruparel, K., Loughead, J., Calkins, M. E., Eickhoff, S. B., Hakonarson, H. H., Gur, R. C., Gur, R. E., et al. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.08.052 · Cited by 1,982
Self-citationKRINGELBACH, M. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.03.006 · Cited by 1,977
Eickhoff, S. B., Laird, A. R., Grefkes, C., Wang, L. E., Zilles, K., & Fox, P. T. (2009) · Human Brain Mapping · doi:10.1002/hbm.20718 · Cited by 1,924
Self-citationPrimate anterior cingulate cortex: Where motor control, drive and cognition interface
Paus, T. (2001) · Nature Reviews Neuroscience · doi:10.1038/35077500 · Cited by 1,722 · cited 1×
“Paus (2001) emphasized the role of ACC in translations to actions as well as the involvement in reward.”
Behavioral Theories and the Neurophysiology of Reward
Schultz, W. (2006) · Annual Review of Psychology · doi:10.1146/annurev.psych.56.091103.070229 · Cited by 1,637
Human emotion and memory: Interactions of the amygdala and hippocampal complex
Phelps, E. A. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.03.015 · Cited by 1,577
Activation Likelihood Estimation meta-analysis revisited
Eickhoff, S., Bzdok, D., Laird, A., Kurth, F., & Fox, P. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.09.017 · Cited by 1,448
Self-citationFransson, P. (2005) · Human Brain Mapping · doi:10.1002/hbm.20113 · Cited by 1,388
How do emotion and motivation direct executive control?
Pessoa, L. (2009) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2009.01.006 · Cited by 1,286
Fransson, P., & Marrelec, G. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.05.059 · Cited by 1,213 · cited 2×
“Indeed, there are also several studies indicating the critical role of the PCC/PrC in the DMN (Buckner et al. 2008, 2009; Fransson and Marrelec 2008; Laird et al. 2009).”
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
Turkeltaub, P., Eickhoff, S., Laird, A. R., Fox, M., Wiener, M., & Fox, P. (2011) · Human Brain Mapping · doi:10.1002/hbm.21186 · Cited by 1,114
Self-citationDecety, J., & Lamm, C. (2007) · The Neuroscientist · doi:10.1177/1073858407304654 · Cited by 1,044
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
Speaker-listener neural coupling underlies successful communication
Stephens, G. J., Silbert, L. J., & Hasson, U. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1008662107 · Cited by 970
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 2×
“2012) and its diverse functional connectivity, this region is discussed as ‘‘core node’’(Andrews-Hanna et al. 2010b; Margulies et al. 2009) within the DMN.”
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
The Human Amygdala: An Evolved System for Relevance Detection
Sander, D., Grafman, J., & Zalla, T. (2003) · Reviews in the Neurosciences · doi:10.1515/revneuro.2003.14.4.303 · Cited by 944 · cited 2×
“Some of the functions identified indicate that this group of regions is important for the processing of biologically relevant information from the environment (Sander et al. 2003; Sergerie et al. 2008).”
Neural correlates of self-reflection
Johnson, S. C. (2002) · Brain · doi:10.1093/brain/awf181 · Cited by 930
Allman, J. M., Hakeem, A. Y., Erwin, J. M., Nimchinsky, E. A., & Hof, P. R. (2001) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2001.tb03476.x · Cited by 922
Sergerie, K., Chochol, C., & Armony, J. L. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2007.12.002 · Cited by 917
How 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
Denny, B. T., Kober, H., Wager, T. D., & Ochsner, K. N. (2012) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00233 · Cited by 830
It's the Thought That Counts: Specific Brain Regions for One Component of Theory of Mind
Saxe, R., & Powell, L. J. (2006) · Psychological Science · doi:10.1111/j.1467-9280.2006.01768.x · Cited by 815
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
Langner, R., & Eickhoff, S. B. (2013) · Psychological Bulletin · doi:10.1037/a0030694 · Cited by 746
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
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
Self-citationSchilbach, 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
Self-citationLaird, A. R., Eickhoff, S. B., Li, K., Robin, D. A., Glahn, D. C., & Fox, P. T. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4004-09.2009 · Cited by 561
Self-citationLateralization of amygdala activation: a systematic review of functional neuroimaging studies
Baas, D., Aleman, A., & Kahn, R. S. (2004) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.02.004 · Cited by 531
Mars, R. B., Sallet, J., Schuffelgen, U., Jbabdi, S., Toni, I., & Rushworth, M. F. S. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr268 · Cited by 520
The subcallosal cingulate gyrus in the context of major depression
Hamani, C., Mayberg, H., Stone, S., Laxton, A., Haber, S., & Lozano, A. M. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.09.034 · Cited by 508
Vogt, B. A., & Laureys, S. (2005) · Progress in brain research · doi:10.1016/s0079-6123(05)50015-3 · Cited by 497
Eickhoff, S. B., Bzdok, D., Laird, A. R., Roski, C., Caspers, S., Zilles, K., & Fox, P. T. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.05.021 · Cited by 484 · cited 1×
“Second, hierarchical clustering is an approach in which clusters are formed by first linking the seeds that were more similar to each other and then performing a complete linkage of the clusters (Eickhoff et al. 2011).”
Self-citationThe Out-of-Body Experience: Disturbed Self-Processing at the Temporo-Parietal Junction
Blanke, O., & Arzy, S. (2005) · The Neuroscientist · doi:10.1177/1073858404270885 · Cited by 469 · cited 1×
“Blanke and Arzy (2005), for example, analyzed TPJ activation during out-of-body-experiences and came to the conclusion that TPJ is an important node of self-processing and spatial unity of self and body.”
Activity in Right Temporo-Parietal Junction is Not Selective for Theory-of-Mind
Mitchell, J. P. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm051 · Cited by 469 · cited 1×
“In a non-social context, the importance of right TPJ for attention and reorientation has likewise been emphasized (Corbetta and Shulman 1998; Langner and Eickhoff 2012; Mitchell 2008).”
Iacoboni, M., Lieberman, M. D., Knowlton, B. J., Molnar-Szakacs, I., Moritz, M., Throop, C. J., & Fiske, A. P. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.11.013 · Cited by 459
Meta-analytical definition and functional connectivity of the human vestibular cortex
zu Eulenburg, P., Caspers, S., Roski, C., & Eickhoff, S. B. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.12.032 · Cited by 453
Self-citationCross-cultural Reading the Mind in the Eyes: An fMRI Investigation
Adams, R. B., Rule, N. O., Franklin, R. G., Wang, E. J., Stevenson, M. T., Yoshikawa, S., Nomura, M., Sato, W., Kveraga, K., & Ambady, N. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21187 · Cited by 452
Bzdok, D., Laird, A. R., Zilles, K., Fox, P. T., & Eickhoff, S. B. (2012) · Human Brain Mapping · doi:10.1002/hbm.22138 · Cited by 450
Self-citationMinds made for sharing: initiating joint attention recruits reward-related neurocircuitry
Schilbach, L., Wilms, M., Eickhoff, S. B., Romanzetti, S., Tepest, R., Bente, G., Shah, N. J., Fink, G. R., & Vogeley, K. (2010) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21401 · Cited by 415
Self-citationCieslik, E. C., Zilles, K., Caspers, S., Roski, C., Kellermann, T. S., Jakobs, O., Langner, R., Laird, A. R., Fox, P. T., & Eickhoff, S. B. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs256 · Cited by 391
Self-citationImpaired declarative memory for emotional material following bilateral amygdala damage in humans.
Adolphs, R., Cahill, L., Schul, R., & Babinsky, R. (1997) · Learning & Memory · doi:10.1101/lm.4.3.291 · Cited by 389
Shared Neural Circuits for Mentalizing about the Self and Others
Lombardo, M. V., Chakrabarti, B., Bullmore, E. T., Wheelwright, S. J., Sadek, S. A., Suckling, J., & Baron‐Cohen, S. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2009.21287 · Cited by 373
The Role of the Human Prefrontal Cortex in Social Cognition and Moral Judgment
Forbes, C. E., & Grafman, J. H. (2010) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-153230 · Cited by 331
Chase, H. W., Eickhoff, S. B., Laird, A. R., & Hogarth, L. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.05.025 · Cited by 316
Self-citationBzdok, D., Langner, R., Schilbach, L., Jakobs, O., Roski, C., Caspers, S., Laird, A. R., Fox, P. T., Zilles, K., & Eickhoff, S. B. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.046 · Cited by 262
Self-citationCaspers, S., Eickhoff, S. B., Rick, T., von Kapri, A., Kuhlen, T., Huang, R., Shah, N. J., & Zilles, K. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.06.027 · Cited by 254
Self-citationLiu, X., Powell, D. K., Wang, H., Gold, B. T., Corbly, C. R., & Joseph, J. E. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.5227-06.2007 · Cited by 242
Schilbach, L., Bzdok, D., Timmermans, B., Fox, P. T., Laird, A. R., Vogeley, K. T., & Eickhoff, S. B. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030920 · Cited by 234
Self-citationDimaggio, G., Lysaker, P. H., Carcione, A., Nicolò, G., & Semerari, A. (2008) · Consciousness and Cognition · doi:10.1016/j.concog.2008.02.005 · Cited by 232
Segregation of the human medial prefrontal cortex in social cognition
Bzdok, D., Langner, R., Schilbach, L., Engemann, D. A., Laird, A. R., Fox, P. T., & Eickhoff, S. B. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00232 · Cited by 229
Self-citationHuman cortical mechanisms of visual attention during orienting and search
Corbetta, M., & Shulman, G. L. (1998) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1998.0289 · Cited by 220
Schnell, K., Bluschke, S., Konradt, B., & Walter, H. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.08.024 · Cited by 217
Cortical activation during delay discounting in abstinent methamphetamine dependent individuals
Hoffman, W. F., Schwartz, D. L., Huckans, M. S., McFarland, B. H., Meiri, G., Stevens, A. A., & Mitchell, S. H. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1261-1 · Cited by 210
How the Brain Represents the Reward Value of Fat in the Mouth
Fabian Grabenhorst, B., Rolls, E. T., Parris, B. A., & D’Souza, A. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp169 · Cited by 210
Functional Dissociations of Risk and Reward Processing in the Medial Prefrontal Cortex
Xue, G., Lu, Z., Levin, I. P., Weller, J. A., Li, X., & Bechara, A. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn147 · Cited by 209
The BrainMap strategy for standardization, sharing, and meta-analysis of neuroimaging data
Laird, A. R., Eickhoff, S. B., Fox, P. M., Uecker, A. M., Ray, K. L., Saenz, J. J., McKay, D., Bzdok, D., Laird, R. W., Robinson, J. L., et al. (2011) · BMC Research Notes · doi:10.1186/1756-0500-4-349 · Cited by 207
Self-citationThe Primate Ventral Pallidum Encodes Expected Reward Value and Regulates Motor Action
Tachibana, Y., & Hikosaka, O. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.030 · Cited by 175
The neural dynamics of updating person impressions
Mende‐Siedlecki, P., Cai, Y., & Todorov, A. T. (2012) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nss040 · Cited by 148
Müller, J. (2009) · doi:10.1037/11919-047 · Cited by 144
Functional Heterogeneity within the Default Network during Semantic Processing and Speech Production
Seghier, M. L., & Price, C. J. (2012) · Frontiers in Psychology · doi:10.3389/fpsyg.2012.00281 · Cited by 111
Jakobs, O., Langner, R., Caspers, S., Roski, C., Cieslik, E. C., Zilles, K., Laird, A. R., Fox, P. T., & Eickhoff, S. B. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.02.037 · Cited by 105
Self-citationResting State Functional Connectivity in Patients with Chronic Hallucinations
Sommer, I. E., Clos, M., Meijering, A. L., Diederen, K. M. J., & Eickhoff, S. B. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043516 · Cited by 103
Self-citationHigher order thoughts in action: consciousness as an unconscious re-description process
Timmermans, B., Schilbach, L., Pasquali, A., & Axel Cleeremans, B. (2012) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2011.0421 · Cited by 91
Self-citationLost in localization: The need for a universal coordinate database
Derrfuss, J., & Mar, R. A. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.01.053 · Cited by 83
Reetz, K., Dogan, I., Rolfs, A., Binkofski, F., Schulz, J. B., Laird, A. R., Fox, P. T., & Eickhoff, S. B. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.05.058 · Cited by 72
Self-citationCostandi, M. (2015) · Springer eBooks · doi:10.1007/978-3-662-44191-6_41 · Cited by 53
Orosz, A., Jann, K., Federspiel, A., Horn, H., Höfle, O., Dierks, T., Wiest, R., Strik, W. K., Müller, T., & Walther, S. (2012) · Brain Connectivity · doi:10.1089/brain.2012.0101 · Cited by 53
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- Bzdok D, Langner R, Schilbach L, Jakobs O, Roski C, Caspers S, Eickhoff SB (2013c) Characterization of the temporo-parietal junction by combining data-driven parcellation, complementary connectivity analyses, and functional decoding. Neuroimage 81:381–392. doi: 10.1016/j.neuroimage.2013.05.046 · DOI
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Metadata
- Authors
- Amft, M., Bzdok, D., Laird, A. R., Fox, P. T., Schilbach, L., & Eickhoff, S. B.
- Affiliations
- Heinrich Heine University Düsseldorf (DE)
- Forschungszentrum Jülich (DE)
- The University of Texas at San Antonio Health Science Center (US)
- University of Cologne (DE)
- Corresponding author
- Eickhoff, Simon B.
- Venue
- Brain Structure and Function
- Published
- 2014-01-08
- Volume
- 220
- Issue
- 2
- Pages
- 1031-1049
- ISSN
- 1863-2653 (ISSN-L)
- 1863-2661
- PMC
- PMC4087104
- OpenAlex
- W2054233890
- Cited by
- 208
- References
- 100
- Citations by year
- 2026: 6 · 2025: 16 · 2024: 10 · 2023: 17 · 2022: 19 · 2021: 24 · 2020: 16 · 2019: 13 · 2018: 21 · 2017: 15 · 2016: 26 · 2015: 16 · 2014: 8
- FWCI
- 2.10
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Brain Structure and Function (publishedVersion)
- PubMed (publishedVersion)
- Kölner Universitäts PublikationsServer (Universität zu Köln) (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Mental Health (R01MH074457)
- 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 and Behavioral Psychology Studies
- Keywords
- default mode network, social cognition, emotional processing, self-reflection, meta-analytic connectivity modeling, resting-state functional connectivity, amygdala, hippocampus, ventral striatum, anterior cingulate cortex, subgenual anterior cingulate cortex, ventromedial prefrontal cortex, posterior cingulate cortex, precuneus, dorsomedial prefrontal cortex, temporoparietal junction, middle temporal gyrus, mentalization, self-reference, autobiographical memory, reward processing
- MeSH terms
- Adult, Affect, Brain, Brain Mapping, Cognition, Female, Humans, Magnetic Resonance Imaging, Male, Memory, Middle Aged, Models, Neurological, Motivation, Nerve Net, Retrospective Studies, Self Concept, Social Behavior, Cluster Analysis, Databases, Factual, Young Adult, Theory of Mind
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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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