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Saliency, switching, attention and control: a network model of insula function
Open accessAbstract
The insula is a brain structure implicated in disparate cognitive, affective, and regulatory functions, including interoceptive awareness, emotional responses, and empathic processes. While classically considered a limbic region, recent evidence from network analysis suggests a critical role for the insula, particularly the anterior division, in high-level cognitive control and attentional processes. The crucial insight and view we present here is of the anterior insula as an integral hub in mediating dynamic interactions between other large-scale brain networks involved in externally oriented attention and internally oriented or self-related cognition. The model we present postulates that the insula is sensitive to salient events, and that its core function is to mark such events for additional processing and initiate appropriate control signals. The anterior insula and the anterior cingulate cortex form a “salience network” that functions to segregate the most relevant among internal and extrapersonal stimuli in order to guide behavior. Within the framework of our network model, the disparate functions ascribed to the insula can be conceptualized by a few basic mechanisms: (1) bottom–up detection of salient events, (2) switching between other large-scale networks to facilitate access to attention and working memory resources when a salient event is detected, (3) interaction of the anterior and posterior insula to modulate autonomic reactivity to salient stimuli, and (4) strong functional coupling with the anterior cingulate cortex that facilitates rapid access to the motor system. In this manner, with the insula as its integral hub, the salience network assists target brain regions in the generation of appropriate behavioral responses to salient stimuli. We suggest that this framework provides a parsimonious account of insula function in neurotypical adults, and may provide novel insights into the neural basis of disorders of affective and social cognition.
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“As part of the viscerosensory cortex, the anterior insula plays a pivotal role in appraising an interoceptive inference based on incoming raw interoceptive and exteroceptive input (Seeley et al., 2007; Menon and Uddin, 2010; Zaki et al., 2012; Wager et al., 2015).”
From How Processing of Sensory Information From the Internal and External Worlds Shape the Perception and Engagement With the World in the Aftermath of Trauma: Implications for PTSD (2021) · cites this paper as Menon and Uddin, 2010
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.
In the citing paper
“Here, the insula helps direct information to lateralized frontoparietal networks in the brain that involve the dorsolateral prefrontal cortex and the posterior parietal cortex in order to facilitate multisensory integration (Menon and Uddin, 2010; Figure 4).”
From How Processing of Sensory Information From the Internal and External Worlds Shape the Perception and Engagement With the World in the Aftermath of Trauma: Implications for PTSD (2021) · cites this paper as Menon and Uddin, 2010
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.
In the citing paper
“Developing an awareness of an emotional feeling underlying a sensory experience may aid in its translation to the central executive network, which plays a role in identifying the contextual meaning of an emotional feeling (Seeley et al., 2007; Menon and Uddin, 2010; Wager et al., 2015).”
From How Processing of Sensory Information From the Internal and External Worlds Shape the Perception and Engagement With the World in the Aftermath of Trauma: Implications for PTSD (2021) · cites this paper as Menon and Uddin, 2010
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.
In the citing paper
“However, while both insula and dACC are components of the SN, they subserve different functions, with insula more related to internal somatic function and monitoring task performance (Eckert et al. 2009;Menon and Uddin 2010;Cai et al. 2014), while the dACC is”
From Brain Activity and Functional Connectivity Associated with Hypnosis (2016) · cites this paper as Menon and Uddin 2010
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.
In the citing paper
“the insula is involved in the processing of body control and experience, emotion, empathy, and time through its extensive connections to cortical and subcortical limbic structures (Menon and Uddin 2010;Cai et al. 2014).”
From Brain Activity and Functional Connectivity Associated with Hypnosis (2016) · cites this paper as Menon and Uddin 2010
Experimental — accuracy not yet measured
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Salience Network (SN): Crucial for detecting relevant internal and external stimuli and switching between the DMN and CCN/CEN, dysfunction in the SN (often involving the dorsal anterior cingulate cortex (dACC) and insula) has been linked to fatigue, aPective symptoms, and cognitive diPiculties post-concussion 12 13 .”
From Functional MRI Guided Accelerated Intermittent Theta Burst Stimulation for Chronic Post-Concussive Syndrome: A Feasibility and Efficacy Study (2025) · cites this paper as [12]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Here, the insula plays a putative role in engaging large-scale neural systems by translating incoming sensory information to intrinsic cortical connectivity networks that assist in modulating and contextualizing incoming salient sensory information to guide behavioral responses (Menon and Uddin, 2010; Seeley et al., 2007).”
From How Processing of Sensory Information From the Internal and External Worlds Shape the Perception and Engagement With the World in the Aftermath of Trauma: Implications for PTSD (2021) · cites this paper as Menon and Uddin, 2010
The cited source says what the claim attributes to it.
In the citing paper
“The insular cortex has reciprocal connections to the ACC and can facilitate cognitive control by acting as the switch between the central-executive network and the default mode network DMN (Cole and Schneider, 2007; Sridharan et al., 2008; Menon and Uddin, 2010).”
From Mindfulness, Interoception, and the Body: A Contemporary Perspective (2019) · cites this paper as Menon and Uddin, 2010
The cited source says what the claim attributes to it.
In the citing paper
“The anterior insula node of the salience network, in particular, is crucial for bottom-up detection of salient events and switching between other large-scale networks to facilitate access to attention and working memory resources. 25”
From 20 years of the default mode network: A review and synthesis. (2023) · cites this paper as [25]
The cited source says what the claim attributes to it.
In the citing paper
“The SN governs our attention to the external and internal world (Menon and Uddin, 2010), and as such, integrates sensory, emotional and cognitive information to facilitate optimal communication, social behavior and self-awareness (Menon, 2015).”
From Distinct functional connectivities predict clinical response with emotion regulation therapy (2017) · cites this paper as Menon and Uddin, 2010
The cited source says what the claim attributes to it.
In the citing paper
“The anterior insula is associated with the integration of interoception and cognition (Menon and Uddin, 2010), and the right anterior VLPFC with reflexive reorienting and response inhibition (Levy and Wagner, 2011).”
From Neural correlates of emotion acceptance vs worry or suppression in generalized anxiety disorder (2017) · cites this paper as Menon and Uddin, 2010
The cited source says what the claim attributes to it.
In the citing paper
“Notably, suppression of the DMN and engagement of cognitive control networks during task performance are thought to be controlled by a common mechanism, with the salience network playing a crucial role.”
From 20 years of the default mode network: A review and synthesis. (2023) · cites this paper as [25]
The cited source says what the claim attributes to it.
In the citing paper
“as well as empathic perception of pain in others, (Menon and Uddin 2010;Gu et al. 2012)”
From Brain Activity and Functional Connectivity Associated with Hypnosis (2016) · cites this paper as Menon and Uddin 2010
The check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“While decreases have been for MPFC and ACC in depression [74], but also social anxiety [75] or Alzheimer disease [76], a recent study in bipolar depression rather indicated an increase in MPFC ReHo [74].”
From State and training effects of mindfulness meditation on brain networks reflect neuronal mechanisms of its antidepressant effect (2016) · cites this paper as [74]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“The rationale for applying TMS, and specifically iTBS, to PCS stems from converging evidence suggesting that persistent post-concussive symptoms are associated with disruptions in largescale functional brain networks.”
From Functional MRI Guided Accelerated Intermittent Theta Burst Stimulation for Chronic Post-Concussive Syndrome: A Feasibility and Efficacy Study (2025) · cites this paper as [12]
Experimental — accuracy not yet measuredIn the citing paper
“The right aINS has previously been identified as a critical node for suppressing DN activity and reallocating attentional resources to salient events.244,245”
From The default network and self-generated thought: component processes, dynamic control, and clinical relevance (2014) · cites this paper as [244]
In the citing paper
“Detected hub nodes were located within the CON (i.e., the left dACC), the salience network (53) (i.e., the right anterior insula, right intraparietal sulcus, and bilateral dACC), and the motor network (i.e., bilateral pre- and post-central gyri).”
From Impact of Childhood Trauma on Executive Function in Adolescence—Mediating Functional Brain Networks and Prediction of High-Risk Drinking (2020) · cites this paper as [53]
In the citing paper
“Together these distributed brain networks integrate bottom-up attention with top-down control and generate appropriate behavioral responses to salient stimuli, thereby contributing to behavioral regulation and sound executive function (51–57).”
From Impact of Childhood Trauma on Executive Function in Adolescence—Mediating Functional Brain Networks and Prediction of High-Risk Drinking (2020) · cites this paper as [53]
In the citing paper
“As such, the SN has been proposed to play a key role in cognitive control (Ham et al., 2013), i.e., switching brain activity between introspective, ruminative functions of the default-mode network and externally focused, task-based functions of the central executive network (Menon and Uddin, 2010).”
From Cortico-striatal-thalamic loop circuits of the salience network: A central pathway in psychiatric disease and treatment (2016) · cites this paper as Menon and Uddin, 2010
In the citing paper
“It is activated in a wide variety of cognitive and emotional tasks (Dosenbach et al., 2006) and forms the important salience network in resting state literature (Menon and Uddin, 2010).”
From Cognitive flexibility in adolescence: Neural and behavioral mechanisms of reward prediction error processing in adaptive decision making during development (2015) · cites this paper as Menon and Uddin, 2010
In the citing paper
“Indeed, activity in the AIC is a common feature in studies of cognitive control and inhibitory processing [7, 46–50] and reward sensitivity [8, 9].”
From The role of the anterior insula in adolescent decision making (2014) · cites this paper as [8]
In the citing paper
“The SN dynamically switches between the ECN and DMN, which are generally anticorrelated, following detection of relevant stimulation or condition”
From The Insula: A Brain Stimulation Target for the Treatment of Addiction (2019) · cites this paper as Menon and Uddin, 2010
In the citing paper
“These include automatic salience evaluation, [ 4 9 8 _ T D $ D I F F ] inhibition/interruption of ongoing activity[ 4 9 9 _ T D $ D I F F ] , alerting, salience-driven switching, and reflexive orienting [40,43,47,48].”
From Anxiety and Threat-Related Attention: Cognitive-Motivational Framework and Treatment (2018) · cites this paper as [48]
In the citing paper
“In addition, over-reactive threat salience-driven switching may cause excessive threat-prioritisation in cognitive system functioning (attention, working memory), and resultant anxiety [48].”
From Anxiety and Threat-Related Attention: Cognitive-Motivational Framework and Treatment (2018) · cites this paper as [48]
In the citing paper
“The adaptive value of this inhibitory mechanism in salient, emotional situations may be to prepare for immediate action in the external world [39].”
From On the interaction of social affect and cognition: empathy, compassion and theory of mind (2018) · cites this paper as [39]
In the citing paper
“These regions are interconnected with the ventral striatum and form core components of the brain's incentive salience system (Menon and Uddin, 2010).”
From Neural networks involved in adolescent reward processing: an activation likelihood estimation meta-analysis of functional neuroimaging studies (2015) · cites this paper as Menon and Uddin, 2010
In the citing paper
“The insula is a critical component of the brain's salience network (Craig, 2009; Menon and Uddin, 2010) and participates in interoceptive awareness, the representation of physiological states associated with risk (Xue et al., 2010), and integration of such states with behavior during risky contexts that are characterized by uncertainty (Singer et al., 2009).”
From Neural networks involved in adolescent reward processing: an activation likelihood estimation meta-analysis of functional neuroimaging studies (2015) · cites this paper as Menon and Uddin, 2010
In the citing paper
“The anterior cingulate, frequently co-activated with the anterior insula (Menon and Uddin, 2010) may play a role in integrating emotion and motivational signals pertaining to contextual salience with executive control systems (Pessoa, 2009) so that adaptive behavioral responses can be formulated and executed.”
From Neural networks involved in adolescent reward processing: an activation likelihood estimation meta-analysis of functional neuroimaging studies (2015) · cites this paper as Menon and Uddin, 2010
In the citing paper
“The SORT not only activates brain regions involved in semantic memory recall, which include bilateral inferior frontal gyrus (including Broca's area), left DLPFC, left middle temporal gyrus, bilateral angular gyrus, and PCC [Assaf et al., 2006;Binder et al., 2009], but also activates salience-related regions, including dorsal anterior cingulate cortex (dACC), pre-SMA [Assaf et al., 2006] and”
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 Menon and Uddin, 2010
In the citing paper
“SN also plays a role in adaptive switching between the central executive network (CEN), involved in focused attentional states, and the default mode network (DMN), active during introspective self-referential thought and social emotional processes ( Amodio and Frith, 2006 ; Sridharan et al., 2008 ; Menon and Uddin, 2010 ; Spreng and Grady, 2010 ; Menon, 2015 ).”
From The brain-body disconnect: A somatic sensory basis for trauma-related disorders (2022) · cites this paper as Menon and Uddin, 2010
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Cites
An Integrative Theory of Prefrontal Cortex Function
Miller, E. K., & Cohen, J. D. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.167 · Cited by 12,803
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 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
Dissociable intrinsic connectivity networks for salience processing and executive control
Seeley, W. W., Menon, V., Schatzberg, A. F., Keller, J., Glover, G. H., Kenna, H., Reiss, A. L., & Greicius, M. D. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5587-06.2007 · Cited by 7,426
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
How do you feel — now? The anterior insula and human awareness
(Bud) Craig, A. D. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2555 · Cited by 6,657 · cited 6×
“Descending pathways from the dorsal posterior insula have been described which terminate in the brainstem parabrachial nuclei, constituting a mechanism for cortical control of brainstem homeostatic systems (Craig 2002).”
InfluentialFunctional 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
Self-citationHow do you feel? Interoception: The sense of the physiological condition of the body
Craig, A. D. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn894 · Cited by 6,006
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
Binder, J. R., Desai, R. H., Graves, W. W., & Conant, L. L. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp055 · Cited by 4,060
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Park, C., Rosenblat, J. D., Lee, Y. L., Pan, Z., Cao, B., Iacobucci, M., & McIntyre, R. S. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.04.002 · Cited by 142
Nicholson, A. A., Sapru, I., Densmore, M., Frewen, P. A., Neufeld, R. W. J., Théberge, J., McKinnon, M. C., & Lanius, R. A. (2016) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2016.02.002 · Cited by 128
Altered Spontaneous Brain Activity in Schizophrenia: A Meta-Analysis and a Large-Sample Study
Xu, Y., Zhuo, C., Qin, W., Zhu, J., & Yu, C. (2015) · BioMed Research International · doi:10.1155/2015/204628 · Cited by 128
Surprise disrupts cognition via a fronto-basal ganglia suppressive mechanism
Wessel, J. R., Jenkinson, N., Brittain, J., Voets, S. H. E. M., Aziz, T. Z., & Aron, A. R. (2016) · Nature Communications · doi:10.1038/ncomms11195 · Cited by 131
Effects of Aging and Adult-Onset Hearing Loss on Cortical Auditory Regions
Cardin, V. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00199 · Cited by 136
Torta, D. M. E., Legrain, V., Mouraux, A., & Valentini, E. (2017) · Cortex · doi:10.1016/j.cortex.2017.01.010 · Cited by 143
Sex differences in fear extinction
Velasco, E. R., Florido, A., Milad, M. R., & Andero, R. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.05.020 · Cited by 132
Neuroimaging-based biomarkers for treatment selection in major depressive disorder
Dunlop, B. W., & Mayberg, H. S. (2014) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2014.16.4/bdunlop · Cited by 127
Divergent task-dependent functional connectivity of executive control and salience networks
Elton, A., & Gao, W. (2014) · Cortex · doi:10.1016/j.cortex.2013.10.012 · Cited by 127
Jamadar, S. D., Fielding, J., & Egan, G. F. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2013.00749 · Cited by 137
Bastin, J., Deman, P., David, O., Gueguen, M., Benis, D., Minotti, L., Hoffman, D., Combrisson, E., Kujala, J., Perrone-Bertolotti, M., et al. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv352 · Cited by 127
Transdiagnostic Associations Between Functional Brain Network Integrity and Cognition
Sheffield, J. M., Kandala, S., Tamminga, C. A., Pearlson, G. D., Keshavan, M. S., Sweeney, J. A., Clementz, B. A., Lerman-Sinkoff, D. B., Hill, S. K., & Barch, D. M. (2017) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2017.0669 · Cited by 129
Dysconnectivity of Large-Scale Functional Networks in Early Psychosis: A Meta-analysis
O’Neill, A., Mechelli, A., & Bhattacharyya, S. (2018) · Schizophrenia Bulletin · doi:10.1093/schbul/sby094 · Cited by 127
Kilroy, E., Aziz‐Zadeh, L., & Cermak, S. A. (2019) · Brain Sciences · doi:10.3390/brainsci9030068 · Cited by 171
Mindfulness-based training attenuates insula response to an aversive interoceptive challenge.
Haase, L., Thom, N. J., Shukla, A., Davenport, P. W., Simmons, A. N., Stanley, E. A., Paulus, M. P., & Johnson, D. C. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsu042 · Cited by 124
“insula and the ACC facilitate cognitive control by switching between the central-executive control network and default-mode network (Sridharan et al., 2008; Menon and Uddin, 2010).”
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Husain, F. T. (2015) · Hearing Research · doi:10.1016/j.heares.2015.09.010 · Cited by 128
Cognitive, affective, and conative theory of mind (ToM) in children with traumatic brain injury
Dennis, M., Simić, N., Bigler, E. D., Abildskov, T. J., Agostino, A., Taylor, H. G., Rubin, K. H., Vannatta, K. A., Gerhardt, C. A., Stancin, T., et al. (2012) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2012.11.006 · Cited by 139
Guo, C. C., Sturm, V. E., Zhou, J. H., Gennatas, E. D., Trujillo, A. J., Hua, A. Y., Crawford, R. K., Stables, L. A., Kramer, J. H., Rankin, K. P., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1509184113 · Cited by 130
Insular and anterior cingulate cortex deep stimulation for central neuropathic pain
Galhardoni, R., da Silva, V. A., Garcı́a-Larrea, L., Dale, C. S., Baptista, A. F., Barbosa, L. M., Menezes, L. M. B., de Siqueira, S. R. D. T., Valério, F., Rosí, J., et al. (2019) · Neurology · doi:10.1212/wnl.0000000000007396 · Cited by 125
To wake or not to wake? The two-sided nature of the human K-complex
Jahnke, K., von Wegner, F., Morzelewski, A., Borisov, S. V., Maischein, M., Steinmetz, H., & Laufs, H. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.09.013 · Cited by 126
Kalmady, S. V., Greiner, R., Agrawal, R., Shivakumar, V., Narayanaswamy, J. C., Brown, M. R. G., Greenshaw, A. J., Dursun, S. M., & Venkatasubramanian, G. (2019) · Schizophrenia · doi:10.1038/s41537-018-0070-8 · Cited by 131
McNaughton, N., DeYoung, C. G., & Corr, P. J. (2016) · Neuroimaging Personality, Social Cognition, and Character · doi:10.1016/b978-0-12-800935-2.00002-6 · Cited by 123
Alonso-Solís, A., Vives‐Gilabert, Y., Grasa, E., Portella, M. J., Rabella, M., Sauras-Quetcuti, R. B., Roldán, A., Núñez-Marín, F., Gómez‐Ansón, B., Pérez, V., et al. (2014) · Schizophrenia Research · doi:10.1016/j.schres.2014.10.047 · Cited by 124
Metabolic connectivity mapping reveals effective connectivity in the resting human brain
Riedl, V., Utz, L., Castrillón, G., Grimmer, T., Rauschecker, J. P., Ploner, M., Friston, K. J., Drzezga, A. E., & Sorg, C. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1513752113 · Cited by 121
Electrophysiological dynamics of antagonistic brain networks reflect attentional fluctuations
Kucyi, A., Daitch, A. L., Raccah, O., Zhao, B., Zhang, C., Esterman, M. S., Zeineh, M., Halpern, C. H., Zhang, K., Zhang, J., et al. (2020) · Nature Communications · doi:10.1038/s41467-019-14166-2 · Cited by 128
Evidence for neural encoding of Bayesian surprise in human somatosensation
Ostwald, D., Spitzer, B., Guggenmos, M., Schmidt, T. T., Kiebel, S. J., & Blankenburg, F. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.04.050 · Cited by 126
The neural underpinnings of cognitive flexibility and their disruption in psychotic illness
Waltz, J. A. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2016.06.005 · Cited by 122
“…of both activating executive control network (ECN) structures, in the service of goal-directed behavior, and suppressing activity in default mode network (DMN) structures that are most active when the brain is “idling” (Seeley et al., 2007, Sridharan et al., 2008, Menon and Uddin, 2010).”
Backgroundvan Rooij, S. J. H., Kennis, M., Vink, M., & Geuze, E. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2015.257 · Cited by 122
Chong, J. S. X., Ng, G. J. P., Lee, S. C., & Zhou, J. (2017) · Brain Structure and Function · doi:10.1007/s00429-016-1297-7 · Cited by 122
Waltz, J. A., Kasanova, Z., Ross, T. J., Salmeron, B. J., McMahon, R. P., Gold, J. M., & Stein, E. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0057257 · Cited by 127
Bast, N., Poustka, L., & Freitag, C. M. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.13795 · Cited by 121
Neuronal network disintegration: common pathways linking neurodegenerative diseases
Ahmed, R. M., Devenney, E. M., Irish, M., Ittner, A., Naismith, S., Ittner, L. M., Rohrer, J. D., Halliday, G. M., Eisen, A., Hodges, J. R., et al. (2016) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp-2014-308350 · Cited by 128
Changes in resting connectivity during recovery from severe traumatic brain injury
Hillary, F. G., Slocomb, J. E., Hills, E. C., Fitzpatrick, N. M., Medaglia, J. D., Wang, J. C., Good, D. C., & Wylie, G. R. (2011) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2011.03.011 · Cited by 119
Neurobehavioral Mechanisms of Temporal Processing Deficits in Parkinson's Disease
Harrington, D. L., Castillo, G. N., Greenberg, P. A., Song, D. D., Lessig, S. L., Lee, R. R., & Rao, S. M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017461 · Cited by 122
Ainley, V., Maister, L., Brokfeld, J., Farmer, H., & Manos Tsakiris, A. (2013) · Consciousness and Cognition · doi:10.1016/j.concog.2013.08.004 · Cited by 121
The Acute Effects of Aerobic Exercise on the Functional Connectivity of Human Brain Networks
Weng, T. B., Pierce, G. L., Darling, W. G., Falk, D. M., Magnotta, V. A., & Voss, M. W. (2016) · Brain Plasticity · doi:10.3233/bpl-160039 · Cited by 122
Wang, H., He, W., Wu, J., Zhang, J., Jin, Z., & Li, L. (2019) · Brain and Cognition · doi:10.1016/j.bandc.2019.01.002 · Cited by 125
Grace, S. A., Rossell, S. L., Heinrichs, M., Kordsachia, C., & Labuschagne, I. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2018.05.031 · Cited by 120
Pain and temperature processing in dementia: a clinical and neuroanatomical analysis
Fletcher, P. D., Downey, L. E., Golden, H. L., Clark, C. N., Slattery, C. F., Paterson, R. W., Rohrer, J. D., Schott, J. M., Rossor, M. N., & Warren, J. D. (2015) · Brain · doi:10.1093/brain/awv276 · Cited by 120
Metzler‐Baddeley, C., Caeyenberghs, K., Foley, S. F., & Jones, D. K. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.01.007 · Cited by 123
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Wonch, K. E., de Medeiros, C. B., Barrett, J. A., Dudin, A., Cunningham, W. A., Hall, G. B., Steiner, M. S., & Fleming, A. S. (2015) · Social Neuroscience · doi:10.1080/17470919.2015.1131193 · Cited by 120
Connectivity patterns during music listening: Evidence for action‐based processing in musicians
Alluri, V., Toiviainen, P., Burunat, I., Kliuchko, M., Vuust, P., & Brattico, E. (2017) · Human Brain Mapping · doi:10.1002/hbm.23565 · Cited by 129
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Kogler, L., Müller, V. I., Werminghausen, E., Eickhoff, S. B., & Derntl, B. (2020) · Cortex · doi:10.1016/j.cortex.2020.04.031 · Cited by 134
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Nani, A., Manuello, J., Mancuso, L., Liloia, D., Costa, T., & Cauda, F. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01169 · Cited by 119
Krause-Utz, A., Frost, R., Winter, D., & Elzinga, B. M. (2017) · Current Psychiatry Reports · doi:10.1007/s11920-017-0757-y · Cited by 116
Martins, D., Rademacher, L., Gabay, A. S., Taylor, R., Richey, J. A., Smith, D. V., Goerlich, K. S., Nawijn, L., Cremers, H. R., Wilson, R., et al. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.12.034 · Cited by 119
Elman, J. A., Madison, C. M., Baker, S. L., Vogel, J. W., Marks, S. M., Crowley, S., O’Neil, J. P., & Jagust, W. J. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu259 · Cited by 122
Guldenmund, P., Athena Demertzi, A., Boveroux, P., Boly, M., Vanhaudenhuyse, A., Bruno, M., Gosseries, O., Noirhomme, Q., Brichant, J.-F., Bonhomme, V. L., et al. (2013) · Brain Connectivity · doi:10.1089/brain.2012.0117 · Cited by 122
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Pasquini, L., Palhano-Fontes, F., & de Araújo, D. B. (2020) · Journal of Psychopharmacology · doi:10.1177/0269881120909409 · Cited by 120
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Arns, M., Batail, J.-M., Bioulac, S., Congedo, M., Daudet, C., Drapier, D., Fovet, T., Jardri, R., Le-Van-Quyen, M., Lotte, F., et al. (2017) · L'Encéphale · doi:10.1016/j.encep.2016.11.003 · Cited by 117
Dai, L., Zhou, H., Xu, X., & Zuo, Z. (2019) · PeerJ · doi:10.7717/peerj.8170 · Cited by 118
van Duijvenvoorde, A. C. K., Op de Macks, Z. A., Overgaauw, S., Gunther Moor, B., Dahl, R. E., & Crone, E. A. (2014) · Brain and Cognition · doi:10.1016/j.bandc.2013.10.005 · Cited by 118
Ho, T. C., Walker, J. C., Teresi, G. I., Kulla, A., Kirshenbaum, J. S., Gifuni, A. J., Singh, M. K., & Gotlib, I. H. (2021) · Translational Psychiatry · doi:10.1038/s41398-020-01103-x · Cited by 121
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Palmer, S. M., Crewther, S. G., Carey, L. M., & The START Project Team (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.01045 · Cited by 116
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Contreras-Huerta, L. S., Baker, K. S., Reynolds, K. J., Batalha, L., & Cunnington, R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0084001 · Cited by 116
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Jia, H., Hu, X. P., & Deshpande, G. (2014) · Brain Connectivity · doi:10.1089/brain.2014.0300 · Cited by 125
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Allen, M., Fardo, F., Dietz, M. J., Hillebrandt, H. F., Friston, K. J., Rees, G. E., & Roepstorff, A. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.11.030 · Cited by 125
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Huang, Z., Tarnal, V., Vlisides, P. E., Janke, E., McKinney, A., Picton, P., Mashour, G. A., & Hudetz, A. G. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109081 · Cited by 122
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Centanni, S. W., Janes, A. C., Haggerty, D. L., Atwood, B. K., & Hopf, F. W. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2021.108765 · Cited by 116
Couto, B., Sedeño, L., Sposato, L. A., Sigman, M., Riccio, P. M., Salles, A., López, V., Schröeder, J., Manes, F. F., & Ibáñez, A. M. (2012) · Cortex · doi:10.1016/j.cortex.2012.08.006 · Cited by 122
Sex‐based differences in brain alterations across chronic pain conditions
Gupta, A., Mayer, E. A., Fling, C., Labus, J. S., Naliboff, B. D., Hong, J., & Kilpatrick, L. A. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23856 · Cited by 116
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Shany, O., Singer, N., Gold, B. P., Jacoby, N., Tarrasch, R., Hendler, T., & Granot, R. (2019) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsz019 · Cited by 114
Teipel, S. J., Grothe, M. J., Zhou, J. H., Sepulcre, J., Dyrba, M., Sorg, C., & Babiloni, C. (2016) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617715000995 · Cited by 117
Gao, X., Yu, H., Sáez, I., Blue, P. R., Zhu, L., Hsu, M., & Zhou, X. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1802523115 · Cited by 119
Emergence of abstract rules in the primate brain
Mansouri, F. A., Freedman, D. J., & Buckley, M. J. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-0364-5 · Cited by 115
Plitt, M., Barnes, K. A., Wallace, G. L., Kenworthy, L., & Martin, A. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1510098112 · Cited by 114
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Coxon, J. P., Goble, D. J., Leunissen, I., Impe, A. V., Wenderoth, N., & Swinnen, S. P. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu165 · Cited by 122
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Boehme, R., Hauser, S. C., Gerling, G. J., Heilig, M. A., & Olausson, H. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1816278116 · Cited by 118
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Putcha, D., Ross, R. S., Cronin‐Golomb, A., Janes, A. C., & Stern, C. E. (2015) · NeuroImage Clinical · doi:10.1016/j.nicl.2015.01.012 · Cited by 117
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Sours, C., Zhuo, J., Janowich, J. R., Aarabi, B., Shanmuganathan, K., & Gullapalli, R. P. (2013) · Brain Research · doi:10.1016/j.brainres.2013.08.034 · Cited by 117
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Legget, K. T., Tregellas, J. R., Shott, M. E., & Frank, G. (2014) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.130046 · Cited by 119
Wang, J., Wei, Q., Wang, L., Zhang, H., Bai, T., Li, C., Tian, Y., & Wang, K. (2017) · Human Brain Mapping · doi:10.1002/hbm.23928 · Cited by 111
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Avram, M., Brandl, F., Bäuml, J., & Sorg, C. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0059-z · Cited by 107
Harel, M., Perini, I., Kämpe, R., Alyagon, U., Shalev, H., Besser, I., Sommer, W. H., Heilig, M., & Zangen, A. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2021.11.020 · Cited by 115
Jennings, J. R., Sheu, L. K., Kuan, D. C.-H., Manuck, S. B., & Gianaros, P. J. (2015) · Psychophysiology · doi:10.1111/psyp.12586 · Cited by 116
Hilger, K., Ekman, M., Fiebach, C. J., & Basten, U. (2016) · Intelligence · doi:10.1016/j.intell.2016.11.001 · Cited by 113
Kaiser, R. H., Kang, M. S., Lew, Y., Feen, J. V. D., Aguirre, B. A., Clegg, R. A., Goer, F., Esposito, E. C., Auerbach, R. P., Hutchison, R. M., et al. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0399-3 · Cited by 112
Du, J., DiNicola, L. M., Angeli, P. A., Saadon‐Grosman, N., Sun, W., Kaiser, S., Ladopoulou, J., Xue, A., Yeo, B. T. T., Eldaief, M. C., et al. (2024) · Journal of Neurophysiology · doi:10.1152/jn.00308.2023 · Cited by 122
Harricharan, S., McKinnon, M. C., & Lanius, R. A. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.625490 · Cited by 110
“As part of the viscerosensory cortex, the anterior insula plays a pivotal role in appraising an interoceptive inference based on incoming raw interoceptive and exteroceptive input (Seeley et al., 2007; Menon and Uddin, 2010; Zaki et al., 2012; Wager et al., 2015).”
BackgroundInfluentialDambacher, F., Sack, A. T., Lobbestael, J., Arntz, A. R., Brugman, S., & Schuhmann, T. (2014) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsu077 · Cited by 122
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Zhang, Y., Zhou, W., Wang, S., Zhou, Q., Wang, H., Zhang, B., Huang, J., Hong, B., & Wang, X. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhx334 · Cited by 112
Xu, A., Larsen, B., Baller, E. B., Scott, J. C., Sharma, V., Adebimpe, A., Basbaum, A. I., Dworkin, R. H., Edwards, R. R., Woolf, C. J., et al. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.01.004 · Cited by 116
van Balkom, T. D., van den Heuvel, O. A., Berendse, H. W., van der Werf, Y. D., & Vriend, C. (2020) · Neuropsychology Review · doi:10.1007/s11065-020-09440-w · Cited by 122
Cottam, W. J., Iwabuchi, S. J., Drabek, M. M., Reckziegel, D., & Auer, D. P. (2018) · Pain · doi:10.1097/j.pain.0000000000001209 · Cited by 110
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Smith, A. R., Steinberg, L., & Chein, J. (2014) · Developmental Neuroscience · doi:10.1159/000358918 · Cited by 110
Heni, M., Kullmann, S., Ketterer, C., Guthoff, M., Linder, K., Wagner, R. J., Stingl, K. T., Veit, R., Staiger, H., Häring, H., et al. (2012) · Diabetologia · doi:10.1007/s00125-012-2528-y · Cited by 113
Impaired integration in psychopathy: A unified theory of psychopathic dysfunction.
Hamilton, R. K. B., Racer, K. H., & Newman, J. P. (2015) · Psychological Review · doi:10.1037/a0039703 · Cited by 116
Pang, Y., Chen, H., Wang, Y., Long, Z., He, Z., Zhang, H., Liao, W., Cui, Q., & Chen, H. (2018) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2018.03.020 · Cited by 113
Lips, M. A., Wijngaarden, M. A., van der Grond, J., van Buchem, M. A., de Groot, G. H., Rombouts, S. A. R. B., Pijl, H., & Veer, I. M. (2014) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.113.080671 · Cited by 110
Cortical thickness predicts the first onset of major depression in adolescence
Foland‐Ross, L. C., Sacchet, M. D., Prasad, G., Gilbert, B., Thompson, P. M., & Gotlib, I. H. (2015) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2015.07.007 · Cited by 109
van Tol, M.-J., Demenescu, L. R., van der Wee, N. J. A., Kortekaas, R., Marjan M.A., N., Boer, J. A. D., Renken, R. J., van Buchem, M. A., Zitman, F. G., Aleman, A., et al. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.11.016 · Cited by 105
Mapping putative hubs in human, chimpanzee and rhesus macaque connectomes via diffusion tractography
Li, L., Hu, X., Preuss, T. M., Glasser, M. F., Damen, F. W., Qiu, Y., & Rilling, J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.04.024 · Cited by 109
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Alfini, A. J., Weiss, L. R., Nielson, K. A., Verber, M., & Smith, J. C. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-180728 · Cited by 120
Doucet, G. E., Lee, W. H., & Frangou, S. (2019) · Human Brain Mapping · doi:10.1002/hbm.24722 · Cited by 112
Zeng, J., Yu, S., Cao, H., Su, Y., Dong, Z., & Yang, X. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.06.031 · Cited by 110
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Kok, A. (2022) · Brain and Cognition · doi:10.1016/j.bandc.2022.105880 · Cited by 128
Jankowski, K. F., & Takahashi, H. (2014) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.12182 · Cited by 115
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Joos, K., Gilles, A., de Heyning, P. V., Ridder, D. D., & Vanneste, S. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.02.009 · Cited by 112
Metadata
- Authors
- Menon, V., & Uddin, L. Q.
- Affiliations
- Stanford Medicine (US)
- Corresponding author
- Menon, Vinod
- Uddin, Lucina Q.
- Venue
- Brain Structure and Function
- Published
- 2010-05-29
- Volume
- 214
- Issue
- 5-6
- Pages
- 655-667
- ISSN
- 1863-2653 (ISSN-L)
- 1863-2661
- PMC
- PMC2899886
- OpenAlex
- W2129624700
- Semantic Scholar
- 7fd8bee2d3a38b29ae2228466d3431a34c7ae240
- Cited by
- 5,592
- References
- 93
- Citations by year
- 2026: 429 · 2025: 445 · 2024: 429 · 2023: 398 · 2022: 428 · 2021: 568 · 2020: 437 · 2019: 397 · 2018: 389 · 2017: 368 · 2016: 356 · 2015: 334 · 2014: 225 · 2013: 200 · 2012: 118
- FWCI
- 8.97
- 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)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute of Mental Health (K01MH092288)
- National Institute of Neurological Disorders and Stroke (NS058899, R21NS058899)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD057610, HD047520, HD057610, R01HD047520, R01HD059205)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- anterior insula, salience network, cognitive control, attention, network switching, anterior cingulate cortex, saliency detection, bottom-up processing, interoception, autonomic reactivity, working memory, large-scale brain networks
- MeSH terms
- Animals, Cerebral Cortex, Humans, Nerve Net, Neural Networks, Computer, Executive Function
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