Salience processing and insular cortical function and dysfunction

The Autism Diagnostic Observation Schedule—Generic: A Standard Measure of Social and Communication Deficits Associated with the Spectrum of Autism

Lord, C., Risi, S., Lambrecht, L., Cook, E. H., Leventhal, B. L., DiLavore, P. C., Pickles, A., & Rutter, M. (2000) · Journal of Autism and Developmental Disorders · doi:10.1023/a:1005592401947 · Cited by 7,520

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

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

How 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

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

Functional Network Organization of the Human Brain

Power, J. D., Cohen, A. L., Nelson, S. M., Wig, G. S., Barnes, K. A., Church, J. A., Vogel, A. C., Laumann, T. O., Miezin, F. M., Schlaggar, B. L., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.006 · Cited by 4,124

The reorienting system of the human brain: from environment to theory of mind

Corbetta, M., Patel, G., & Shulman, G. L. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.017 · Cited by 3,889

Large-scale automated synthesis of human functional neuroimaging data.

Yarkoni, T., Poldrack, R. A., Nichols, T. E., Van Essen, D. C., & Wager, T. D. (2011) · Nature Methods · doi:10.1038/nmeth.1635 · Cited by 3,686

Neural systems supporting interoceptive awareness

Critchley, H. D., Wiens, S., Rotshtein, P., Öhman, A., & Dolan, R. J. (2004) · Nature Neuroscience · doi:10.1038/nn1176 · Cited by 3,406

A critical role for the right fronto-insular cortex in switching between central-executive and default-mode networks

Sridharan, D., Levitin, D. J., & Menon, V. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800005105 · Cited by 2,892

Neuroanatomical Abnormalities in Older Depressed Adults With Apathy: A Systematic Review

Pimontel, M. A., Kanellopoulos, D., & Gunning, F. M. (2019) · Journal of Geriatric Psychiatry and Neurology · doi:10.1177/0891988719882100 · Cited by 23

Transcranial Direct Current Stimulation Applied to the Dorsolateral and Ventromedial Prefrontal Cortices in Smokers Modifies Cognitive Circuits Implicated in the Nicotine Withdrawal Syndrome

Fischell, S. A., Ross, T. J., Deng, Z., Salmeron, B. J., & Stein, E. A. (2020) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2019.12.020 · Cited by 26

High γ‐Aminobutyric Acid Content Within the Medial Prefrontal Cortex Is a Functional Signature of Somatic Symptoms Disorder in Patients With Parkinson's Disease

Pizzi, S. D., Franciotti, R., Ferretti, A., Edden, R. A. E., Zöllner, H. J., Esposito, R., Bubbico, G., Aiello, C., Calvanese, F., Sensi, S. L., et al. (2020) · Movement Disorders · doi:10.1002/mds.28221 · Cited by 22

A cortical network that marks the moment when conscious representations are updated

Stöttinger, E., Filipowicz, A., Valadao, D. F., Culham, J. C., Goodale, M. A., Anderson, B., & Danckert, J. A. (2015) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2015.10.037 · Cited by 22

Intrinsic Insular-Frontal Networks Predict Future Nicotine Dependence Severity

Hsu, L., Keeley, R. J., Liang, X., Brynildsen, J. K., Lu, H., Yang, Y., & Stein, E. A. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.0140-19.2019 · Cited by 22

Interoceptive awareness mitigates deficits in emotional prosody recognition in Autism

Mulcahy, J. S., Davies, M., Quadt, L., Critchley, H. D., & Garfinkel, S. N. (2019) · Biological Psychology · doi:10.1016/j.biopsycho.2019.05.011 · Cited by 21

Beyond NMDA Receptors: A Narrative Review of Ketamine’s Rapid and Multifaceted Mechanisms in Depression Treatment

Antos, Z., Żukow, X., Bursztynowicz, L., & Jakubów, P. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252413658 · Cited by 21

Towards a Real-Life Understanding of the Altered Functional Behaviour of the Default Mode and Salience Network in Chronic Pain: Are People with Chronic Pain Overthinking the Meaning of Their Pain?

Johansson, E., Xiong, H.-Y., Polli, A., Coppieters, I., & Nijs, J. (2024) · Journal of Clinical Medicine · doi:10.3390/jcm13061645 · Cited by 23

The ‘reading’ brain: Meta-analytic insight into functional activation during reading in adults

Turker, S., Fumagalli, B., Kuhnke, P., & Hartwigsen, G. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106166 · Cited by 24

Association of quality of life with structural, functional and molecular brain imaging in community-dwelling older adults

Ourry, V., Gonneaud, J., Landeau, B., Moulinet, I., Touron, E., Dautricourt, S., Du, G. L., Mézenge, F., André, C., Bejanin, A., et al. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.117819 · Cited by 21

Disrupted Functional Connectivity Within and Between Resting-State Networks in the Subacute Stage of Post-stroke Aphasia

Zhang, C., Xia, Y., Feng, T., Yu, K., Zhang, H., Sami, M. U., Xiang, J., & Xu, K. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.746264 · Cited by 21

Temporal fluctuations in vigilance and neural networks after sleep deprivation

Mai, Z., Li, M., Pan, L., & Ma, N. (2022) · European Journal of Neuroscience · doi:10.1111/ejn.15663 · Cited by 21

Neural connectome features of procrastination: Current progress and future direction

Chen, Z., & Feng, T. (2022) · Brain and Cognition · doi:10.1016/j.bandc.2022.105882 · Cited by 22

Comparison of Functional and Structural Neural Network Features in Older Adults With Depression With vs Without Apathy and Association With Response to Escitalopram

Oberlin, L. E., Victoria, L. W., Ilieva, I. P., Dunlop, K., Hoptman, M. J., Avari, J., Alexopoulos, G. S., & Gunning, F. M. (2022) · JAMA Network Open · doi:10.1001/jamanetworkopen.2022.24142 · Cited by 24

Anterior Insula–Associated Social Novelty Recognition: Pivotal Roles of a Local Retinoic Acid Cascade and Oxytocin Signaling

Kim, S.-H., An, K., Namkung, H., Saito, A., Rannals, M. D., Moore, J. R., Mihaljevic, M. M., Saha, S., Oh, S., Kondo, M., et al. (2022) · American Journal of Psychiatry · doi:10.1176/appi.ajp.21010053 · Cited by 23

Singing training predicts increased insula connectivity with speech and respiratory sensorimotor areas at rest

Zamorano, A. M., Zatorre, R. J., Vuust, P., Friberg, A., Birbaumer, N., & Kleber, B. (2023) · Brain Research · doi:10.1016/j.brainres.2023.148418 · Cited by 23

Subjective states induced by intracranial electrical stimulation matches the cytoarchitectonic organization of the human insula

Duong, A., Quabs, J., Kucyi, A., Lusk, Z., Buch, V., Caspers, S., & Parvizi, J. (2023) · Brain stimulation · doi:10.1016/j.brs.2023.11.001 · Cited by 21

Interactions of Insula Subdivisions-Based Networks with Default-Mode and Central-Executive Networks in Mild Cognitive Impairment

Chand, G. B., Wu, J., Hajjar, I. M., & Qiu, D. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00367 · Cited by 21

Feelings of shame and guilt are associated with distinct neural activation in youth

Bastin, C., Rakesh, D., Harrison, B. J., Davey, C. G., Allen, N. B., Muller, S., & Whittle, S. (2021) · Biological Psychology · doi:10.1016/j.biopsycho.2021.108025 · Cited by 23

Amygdala hyperconnectivity in the paranoid state: A transdiagnostic study

Fan, L., Klein, H., Bass, E., Springfield, C., & Pinkham, A. (2021) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2021.03.049 · Cited by 21

Trait self-control mediates the association between resting-state neural correlates and emotional well-being in late adolescence

Li, Q., Xiang, G., Song, S., Xiao, M., & Chen, H. (2021) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsab046 · Cited by 21

Response control networks are selectively modulated by attention to rare events and memory load regardless of the need for inhibition

Wijeakumar, S., Magnotta, V. A., Buss, A. T., Ambrose, J., Wifall, T., Hazeltine, E., & Spencer, J. P. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.07.026 · Cited by 25

Listening to music in a risk-reward context: The roles of the temporoparietal junction and the orbitofrontal/insular cortices in reward-anticipation, reward-gain, and reward-loss

Li, C., Chen, J., & Tsai, C. (2015) · Brain Research · doi:10.1016/j.brainres.2015.10.024 · Cited by 22

Attention-Deficit Hyperactivity Disorder and the Dysregulation of Emotion Generation and Emotional Expression

Blader, J. C. (2021) · Child and Adolescent Psychiatric Clinics of North America · doi:10.1016/j.chc.2020.10.005 · Cited by 20

Altered Hippocampal Resting-state Functional Connectivity in Highly Superior Autobiographical Memory

Daviddi, S., Pedale, T., Serra, L., Macrı̀, S., Campolongo, P., & Santangelo, V. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.11.004 · Cited by 20

Learning induces coordinated neuronal plasticity of metabolic demands and functional brain networks

Klug, S., Godbersen, G. M., Rischka, L., Wadsak, W., Pichler, V., Klöbl, M., Hacker, M., Lanzenberger, R. R., & Hahn, A. (2022) · Communications Biology · doi:10.1038/s42003-022-03362-4 · Cited by 21

Lifespan associations of resting-state brain functional networks with ADHD symptoms

Wang, R., Fan, Y., Wu, Y., Zang, Y., & Zhou, C. (2022) · iScience · doi:10.1016/j.isci.2022.104673 · Cited by 21

Sex-related differences in violence exposure, neural reactivity to threat, and mental health

Dark, H. E., Harnett, N. G., Hurst, D. R., Wheelock, M. D., Wood, K. H., Goodman, A. M., Mrug, S., Elliott, M. N., Emery, S. T., Schuster, M. A., et al. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01430-1 · Cited by 21

Updating Contextual Sensory Expectations for Adaptive Behavior

Ferrari, A., Richter, D., & de Lange, F. P. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1107-22.2022 · Cited by 23

Borderline Personality Disorder: Updates in a Postpandemic World

Choi-Kain, L. W., Şahin, Z., & Traynor, J. M. (2022) · FOCUS The Journal of Lifelong Learning in Psychiatry · doi:10.1176/appi.focus.20220057 · Cited by 24

Exploring the behavioral and neural correlates of semantic distance in creative writing

Li, F., Zhuang, K., Wang, X., Zhang, J., Liu, C., Gu, J., & Qiu, J. (2022) · Psychophysiology · doi:10.1111/psyp.14239 · Cited by 20

Dynamics of Internal Attention and Internally-Directed Cognition: The Attention-to-Thoughts (A2T) Model

Amir, I., & Bernstein, A. (2022) · Psychological Inquiry · doi:10.1080/1047840x.2022.2141000 · Cited by 25

Associations between thalamocortical functional connectivity and sensory over-responsivity in infants at high likelihood for ASD

Wagner, L., Banchik, M., Okada, N. J., McDonald, N. M., Jeste, S., Bookheimer, S. Y., Green, S. A., & Dapretto, M. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad100 · Cited by 24

Gradient Organization of Space, Time, and Numbers in the Brain: A Meta-analysis of Neuroimaging Studies

Cona, G., Wiener, M., Allegrini, F., & Scarpazza, C. (2023) · Neuropsychology Review · doi:10.1007/s11065-023-09609-z · Cited by 20

The extended neural architecture of human attachment: An fMRI coordinate-based meta-analysis of affiliative studies

Bortolini, T., Laport, M. C., Latgé-Tovar, S., Fischer, R. D., Zahn, R., de Oliveira‐Souza, R., & Moll, J. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105584 · Cited by 22

Structural and functional brain alterations in subthreshold depression: A multimodal coordinate‐based meta‐analysis

Li, J., Kuang, S., Liu, Y., Wu, Y., & Li, H. (2024) · Human Brain Mapping · doi:10.1002/hbm.26702 · Cited by 21

Small Changes, But Huge Impact? The Right Anterior Insula's Loss of Connection Strength during the Transition of Old to Very Old Age

Muller, A. M., Mérillat, S., & Jäncke, L. (2016) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2016.00086 · Cited by 20

Causal Contributions of the SMA to Alertness and Consciousness Interactions

Martín-Signes, M., Pérez-Serrano, C., & Chica, A. B. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx346 · Cited by 20

Inter-subject phase synchronization for exploratory analysis of task-fMRI

Bolt, T., Nomi, J. S., Vij, S. G., Chang, C., & Uddin, L. Q. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.04.015 · Cited by 20

Pain management decisions in emergency hospitals are predicted by brain activity during empathy and error monitoring

Corradi‐Dell’Acqua, C., Foerster, M., Sharvit, G., Trueb, L., Foucault, É., Fournier, Y., Vuilleumier, P. O., & Hügli, O. (2019) · British Journal of Anaesthesia · doi:10.1016/j.bja.2019.01.039 · Cited by 20

Beyond consensus: Embracing heterogeneity in curated neuroimaging meta-analysis

Ngo, G. H., Eickhoff, S. B., Nguyen, M., Sevinc, G., Fox, P. T., Spreng, R. N., & Yeo, B. T. T. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.06.037 · Cited by 20

Experience-dependent neuroplasticity in trained musicians modulates the effects of chronic pain on insula-based networks – A resting-state fMRI study

Zamorano, A. M., Montoya, P., Cifré, I., Vuust, P., Riquelme, I., & Kleber, B. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116103 · Cited by 20

Network convergence zones in the anterior midcingulate cortex

Margulies, D. S., & Uddin, L. Q. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64196-0.00007-8 · Cited by 20

Network Mapping of Connectivity Alterations in Disorder of Consciousness: Towards Targeted Neuromodulation

Mencarelli, L., Biagi, M. C., Salvador, R., Romanella, S. M., Ruffini, G., Rossi, S., & Santarnecchi, E. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9030828 · Cited by 22

Brain function associated with reaction time after sport-related concussion

Churchill, N. W., Hutchison, M. G., Graham, S. J., & Schweizer, T. A. (2020) · Brain Imaging and Behavior · doi:10.1007/s11682-020-00349-9 · Cited by 22

The “when” and “where” of the interplay between attentional capture and response inhibition during a Go/NoGo variant

Happer, J. P., Wagner, L. C., Beaton, L. E., Rosen, B. Q., & Marinković, K. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.117837 · Cited by 20

Extracting brain disease‐related connectome subgraphs by adaptive dense subgraph discovery

Wu, Q., Huang, X., Culbreth, A. J., Waltz, J. A., Hong, L. E., & Chen, S. (2021) · Biometrics · doi:10.1111/biom.13537 · Cited by 20

Brain Network Activity During Face Perception: The Impact of Perceptual Familiarity and Individual Differences in Childhood Experience

Cloutier, J., Li, T., Mišić, B., Correll, J., & Berman, M. G. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw232 · Cited by 20

State and trait characteristics of anterior insula time-varying functional connectivity

Pasquini, L., Toller, G., Staffaroni, A. M., Brown, J. A., Deng, J., Lee, A. J., Kurcyus, K., Shdo, S. M., Allen, I. E., Sturm, V. E., et al. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.116425 · Cited by 20

Dynamic lag analysis reveals atypical brain information flow in autism spectrum disorder

Raatikainen, V., Korhonen, V., Borchardt, V., Huotari, N., Helakari, H., Kananen, J., Raitamaa, L., Joskitt, L., Loukusa, S., Hurtig, T., et al. (2020) · Autism Research · doi:10.1002/aur.2218 · Cited by 19

Differential structure-function network coupling in the inattentive and combined types of attention deficit hyperactivity disorder

Lee, D., Knight, E. Q., Song, H., Lee, S., Pae, C., Yoo, S., & Park, H. (2021) · PLoS ONE · doi:10.1371/journal.pone.0260295 · Cited by 20

Intrinsic connectivity of left ventrolateral prefrontal cortex predicts individual differences in controlled semantic retrieval

Zhang, M., Nathaniel, U., Savill, N. J., Smallwood, J., & Jefferies, E. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118760 · Cited by 20

Salience network anatomical and molecular markers are linked with cognitive dysfunction in mild cognitive impairment

Chand, G. B., Thakuri, D. S., & Soni, B. (2022) · Journal of Neuroimaging · doi:10.1111/jon.12980 · Cited by 19

Early alterations in cortical morphology after neoadjuvant chemotherapy in breast cancer patients: A longitudinal magnetic resonance imaging study

Zhou, X., Tan, Y., Yu, H. L., Liu, J., Lan, X., Deng, Y., Yu, F., Wang, C., Chen, J., Zeng, X., et al. (2022) · Human Brain Mapping · doi:10.1002/hbm.25969 · Cited by 19

Pain modalities in the body and brain: Current knowledge and future perspectives

Chae, Y., Park, H., & Lee, I. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104744 · Cited by 20

Altered effective connectivity among core brain networks in patients with bipolar disorder

Zhang, Z., Bo, Q., Li, F., Zhao, L., Wang, Y., Liu, R., Chen, X., Wang, C., & Zhou, Y. (2022) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2022.06.031 · Cited by 21

Pain avoidance and functional connectivity between insula and amygdala identifies suicidal attempters in patients with major depressive disorder using machine learning

Hao, Z., Li, H., Ouyang, L., Sun, F., Wen, X., & Wang, X. (2022) · Psychophysiology · doi:10.1111/psyp.14136 · Cited by 19

Dissecting structural connectivity of the left and right inferior frontal cortex in children who stutter

Neef, N. E., Angstadt, M., Koenraads, S. P. C., & Chang, S. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac328 · Cited by 21

Clinical neuroscience and neurotechnology: An amazing symbiosis

Cometa, A., Falasconi, A., Biasizzo, M., Carpaneto, J., Horn, A., Mazzoni, A., & Micera, S. (2022) · iScience · doi:10.1016/j.isci.2022.105124 · Cited by 21

The salience network is activated during self‐recognition from both first‐person and third‐person perspectives

Asakage, S., & Nakano, T. (2022) · Human Brain Mapping · doi:10.1002/hbm.26084 · Cited by 19

Cortical thickness and intrinsic activity changes in middle-aged men with alcohol use disorder

Dai, X., Yu, J., Gao, L., Zhang, J., Li, Y., Du, B., Huang, X., & Zhang, H. (2022) · Alcohol · doi:10.1016/j.alcohol.2022.10.001 · Cited by 19

The structure of anticorrelated networks in the human brain

Martínez, E., Jiménez-Marín, A., Stramaglia, S., & Cortés, J. M. (2022) · Frontiers in Network Physiology · doi:10.3389/fnetp.2022.946380 · Cited by 20

The Angiotensin Antagonist Losartan Modulates Social Reward Motivation and Punishment Sensitivity via Modulating Midbrain-Striato-Frontal Circuits

Zhou, X., Xu, T., Zeng, Y., Zhang, R., Qi, Z., Zhao, W., Kendrick, K. M., & Becker, B. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1114-22.2022 · Cited by 19

Semantic knowledge of social interactions is mediated by the hedonic evaluation system in the brain

Rijpma, M. G., Montembeault, M., Shdo, S. M., Kramer, J. H., Miller, B. L., & Rankin, K. P. (2023) · Cortex · doi:10.1016/j.cortex.2022.12.015 · Cited by 19

Resting-State EEG Reveals Abnormal Microstate Characteristics of Depression with Insomnia

Cao, Q., Wang, Y., Ji, Y., He, Z., & Lei, X. (2023) · Brain Topography · doi:10.1007/s10548-023-00949-w · Cited by 19

Highly Superior Autobiographical Memory (HSAM): A Systematic Review

Talbot, J., Convertino, G., Marco, M. D., Venneri, A., & Mazzoni, G. A. L. (2024) · Neuropsychology Review · doi:10.1007/s11065-024-09632-8 · Cited by 19

Low-intensity focused ultrasound to the human insular cortex differentially modulates the heartbeat-evoked potential: a proof-of-concept study

Strohman, A., Isaac, G., Payne, B., Verdonk, C., Khalsa, S. S., & Legon, W. (2024) · Clinical Neurophysiology · doi:10.1016/j.clinph.2024.09.006 · Cited by 20

UMBRAE: Unified Multimodal Brain Decoding

Xia, W., de Charette, R., Öztireli, C., & Xue, J. (2024) · Lecture notes in computer science · doi:10.1007/978-3-031-72667-5_14 · Cited by 31

Looming Threats and Animacy: Reduced Responsiveness in Youth with Disrupted Behavior Disorders

White, S. F., Thornton, L. C., Leshin, J. C., Clanton, R. L., Sinclair, S., Coker-Appiah, D. S., Meffert, H., Hwang, S., & Blair, J. (2017) · Research on Child and Adolescent Psychopathology · doi:10.1007/s10802-017-0335-0 · Cited by 19

Functional segregation loss over time is moderated by APOE genotype in healthy elderly

Ng, K. K., Qiu, Y., Lo, J. C.-Y., Koay, E. S.-C., Koh, W., Chee, M. W. L., & Zhou, J. H. (2018) · Human Brain Mapping · doi:10.1002/hbm.24036 · Cited by 19

The Motivation-Based Promotion of Proactive Control: The Role of Salience Network

Qiao, L., Xu, L., Che, X., Zhang, L., Li, Y., Xue, G., Li, H., & Chen, A. (2018) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2018.00328 · Cited by 21

Role of the insula in top–down processing: an intracranial EEG study using a visual oddball detection paradigm

Citherlet, D., Boucher, O., Tremblay, J., Robert, M., Gallagher, A., Bouthillier, A., Leporé, F., & Nguyen, D. K. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01892-y · Cited by 19

Enhanced insular/prefrontal connectivity when resisting from emotional distraction during visual search

Pedale, T., Macaluso, E., & Santangelo, V. (2019) · Brain Structure and Function · doi:10.1007/s00429-019-01873-1 · Cited by 20

Information Theoretic Characterization of Uncertainty Distinguishes Surprise From Accuracy Signals in the Brain

Loued‐Khenissi, L., & Preuschoff, K. (2020) · Frontiers in Artificial Intelligence · doi:10.3389/frai.2020.00005 · Cited by 19

Inter-subject phase synchronization differentiates neural networks underlying physical pain empathy

Xu, L., Bolt, T., Nomi, J. S., Li, J., Zheng, X., Fu, M., Kendrick, K. M., Becker, B., & Uddin, L. Q. (2020) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsaa025 · Cited by 19

Reconfiguration of Directed Functional Connectivity Among Neurocognitive Networks with Aging: Considering the Role of Thalamo-Cortical Interactions

Das, M., Singh, V., Uddin, L. Q., Banerjee, A., & Roy, D. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa334 · Cited by 19

Structural covariance pattern abnormalities of insula in major depressive disorder: A CAN-BIND study report

Ge, R., Hassel, S., Arnott, S. R., Davis, A. D., Harris, J. K., Zamyadi, M., Milev, R. V., Frey, B. N., Strother, S. C., Müller, D. J., et al. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.110194 · Cited by 19

A lateralized model of the pain-depression dyad

Maallo, A. M. S., Moulton, E. A., Sieberg, C. B., Giddon, D. B., Borsook, D., & Holmes, S. A. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.06.003 · Cited by 19

Spacetime in the brain: rapid brain network reorganization in visual processing and recovery

Wu, Z., & Sabel, B. A. (2021) · Scientific Reports · doi:10.1038/s41598-021-96971-8 · Cited by 19

Fetal programming of human energy homeostasis brain networks: Issues and considerations

Rasmussen, J. M., Thompson, P. M., Entringer, S., Buß, C., & Wadhwa, P. D. (2021) · Obesity Reviews · doi:10.1111/obr.13392 · Cited by 20

Functions of the Salience Network

Uddin, L. Q. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-804593-0.00003-5 · Cited by 22

Parsing Heterogeneity in Autism Spectrum Disorder and Attention-Deficit/Hyperactivity Disorder with Individual Connectome Mapping

Dajani, D. R., Burrows, C. A., Nebel, M. B., Mostofsky, S. H., Gates, K. M., & Uddin, L. Q. (2019) · Brain Connectivity · doi:10.1089/brain.2019.0669 · Cited by 23

Common neural responses to romantic rejection and acceptance in healthy adults

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