Functional connectivity of the insula in the resting brain

“Mini-mental state”

Folstein, M. F., Folstein, S. E., & McHugh, P. R. (1975) · Journal of Psychiatric Research · doi:10.1016/0022-3956(75)90026-6 · Cited by 88,282 · see citing works

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 · see citing works

Functional connectivity in the motor cortex of resting human brain using echo‐planar mri

Biswal, B., Zerrin Yetkin, F., Haughton, V. M., & Hyde, J. S. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910340409 · Cited by 9,812 · see citing works

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 · see citing works

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 · see citing works

A New Clinical Scale for the Staging of Dementia

Hughes, C. P., Berg, L., Danziger, W., Coben, L. A., & Martin, R. L. (1982) · British Journal of Psychiatry · doi:10.1192/bjp.140.6.566 · Cited by 7,056 · see citing works

FCM: The fuzzy c-means clustering algorithm

Bezdek, J. C., Ehrlich, R., & Full, W. E. (1984) · Computers & Geosciences · doi:10.1016/0098-3004(84)90020-7 · Cited by 6,706 · see citing works

Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging

Fox, M. D., & Raichle, M. E. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2201 · Cited by 6,700 · see citing works

Functional connectivity in the resting brain: a network analysis of the default mode hypothesis

Greicius, M. D., Krasnow, B., Reiss, A. L., & Menon, V. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0135058100 · Cited by 6,358 · see citing works

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 · see citing works

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 · see citing works

Co-planar stereotaxic atlas of the human brain : 3-dimensional proportional system : an approach to cerebral imaging

Talairach, J., Tournoux, P., & Rayport, M. (1988) · Thieme eBooks · Cited by 5,058 · see citing works

Thresholding of statistical maps in functional neuroimaging using the false discovery rate

Genovese, C. R., Lazar, N. A., & Nichols, T. (2002) · NeuroImage · doi:10.1006/nimg.2001.1037 · Cited by 4,923 · see citing works

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 · see citing works

Mapping the structural core of human cerebral cortex

Hagmann, P., Cammoun, L., Gigandet, X., Meuli, R., Honey, C. J., Wedeen, V. J., & Sporns, O. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060159 · Cited by 4,173 · see citing works

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 · cited 2× · see citing works

Investigations into resting-state connectivity using independent component analysis

Beckmann, C. F., DeLuca, M., Devlin, J. T., & Smith, S. M. (2005) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2005.1634 · Cited by 3,398 · see citing works

Contributions of anterior cingulate cortex to behaviour

Devinsky, O., Morrell, M. J., & Vogt, B. A. (1995) · Brain · doi:10.1093/brain/118.1.279 · Cited by 3,377 · see citing works

L’examen Clinique en Psychologie

Rubé, P. (1959) · American Journal of Psychotherapy · doi:10.1176/appi.psychotherapy.1959.13.4.989 · Cited by 3,343 · see citing works

Statistical Parametric Mapping: The Analysis of Functional Brain Images

Penny, W. D., Friston, K. J., Ashburner, J., Kiebel, S. J., & Thomas, N. (2007) · UCL Discovery (University College London) · Cited by 3,339 · see citing works

Handbook of Emotions

Lewis, M., & Haviland, J. M. (1993) · Cited by 3,308 · see citing works

Improved assessment of significant activation in functional magnetic resonance imaging (fMRI): use of a cluster-size threshold

Forman, S. D., Cohen, J. D., Fitzgerald, M., Eddy, W. F., Mintun, M. A., & Noll, D. C. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910330508 · Cited by 3,202 · see citing works

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 · see citing works

Temporal Autocorrelation in Univariate Linear Modeling of FMRI Data

Woolrich, M. W., Ripley, B. D., Brady, M., & Smith, S. M. (2001) · NeuroImage · doi:10.1006/nimg.2001.0931 · Cited by 2,859 · see citing works

Distinct brain networks for adaptive and stable task control in humans

Dosenbach, N. U. F., Fair, D. A., Miezin, F. M., Cohen, A. L., Wenger, K. K., Dosenbach, R. A. T., Fox, M. D., Snyder, A. Z., Vincent, J. L., Raichle, M. E., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704320104 · Cited by 2,632 · see citing works

The Organization of Networks within the Orbital and Medial Prefrontal Cortex of Rats, Monkeys and Humans

Ongur, D. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.3.206 · Cited by 2,627 · see citing works

Interoception: the sense of the physiological condition of the body

(Bud) Craig, A. (2003) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(03)00090-4 · Cited by 2,556 · see citing works

A Resilient, Low-Frequency, Small-World Human Brain Functional Network with Highly Connected Association Cortical Hubs

Achard, S., Salvador, R., Whitcher, B., Suckling, J., & Bullmore, E. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.3874-05.2006 · Cited by 2,393 · see citing works

Resting-State Functional Connectivity Reflects Structural Connectivity in the Default Mode Network

Greicius, M. D., Supekar, K., Menon, V., & Dougherty, R. F. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn059 · Cited by 2,175 · see citing works

Spontaneous neuronal activity distinguishes human dorsal and ventral attention systems

Fox, M. D., Corbetta, M., Snyder, A. Z., Vincent, J. L., & Raichle, M. E. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0604187103 · Cited by 2,101 · see citing works

Functional Connectivity: The Principal-Component Analysis of Large (PET) Data Sets

Friston, K. J., Frith, C., Liddle, P., & Frackowiak, R. (1993) · Journal of Cerebral Blood Flow and Metabolism · doi:10.1038/jcbfm.1993.4 · Cited by 2,094 · see citing works

The global signal and observed anticorrelated resting state brain networks

Fox, M. D., Zhang, D., Snyder, A. Z., & Raichle, M. E. (2009) · Journal of Neurophysiology · doi:10.1152/jn.90777.2008 · Cited by 1,877 · see citing works

Intrinsic functional connectivity as a tool for human connectomics: theory, properties, and optimization

Van Dijk, K. R. A., Hedden, T., Venkataraman, A., Evans, K. C., Lazar, S. W., & Buckner, R. L. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00783.2009 · Cited by 1,844 · see citing works

The relation of the Trail Making Test to organic brain damage.

Reitan, R. M. (1955) · Journal of Consulting Psychology · doi:10.1037/h0044509 · Cited by 1,817 · see citing works

Intrinsic functional architecture in the anaesthetized monkey brain

Vincent, J. L., Patel, G. H., Fox, M. D., Snyder, A. Z., Baker, J. T., Van Essen, D. C., Zempel, J. M., Snyder, L. H., Corbetta, M., & Raichle, M. E. (2007) · Nature · doi:10.1038/nature05758 · Cited by 1,786 · see citing works

Circuitry and functional aspects of the insular lobe in primates including humans

AUGUSTINE, J. (1996) · Brain Research Reviews · doi:10.1016/s0165-0173(96)00011-2 · Cited by 1,776 · see citing works

A Core System for the Implementation of Task Sets

Dosenbach, N. U. F., Visscher, K. M., Palmer, E. D., Miezin, F. M., Wenger, K. K., Kang, H. C., Burgund, E. D., Grimes, A. L., Schlaggar, B. L., & Petersen, S. E. (2006) · Neuron · doi:10.1016/j.neuron.2006.04.031 · Cited by 1,772 · see citing works

The human nervous system

Paxinos, G., & Jürgen, K. (2004) · Cited by 1,482 · see citing works

Separating respiratory-variation-related fluctuations from neuronal-activity-related fluctuations in fMRI

Birn, R. M., Diamond, J. B., Smith, M. A., & Bandettini, P. A. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.02.048 · Cited by 1,342 · see citing works

An Insular View of Anxiety

Paulus, M. P., & Stein, M. B. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.03.042 · Cited by 1,325 · see citing works

The maturing architecture of the brain's default network

Fair, D. A., Cohen, A. L., Dosenbach, N. U. F., Church, J. A., Miezin, F. M., Barch, D. M., Raichle, M. E., Petersen, S. E., & Schlaggar, B. L. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800376105 · Cited by 1,314 · see citing works

A link between the systems: functional differentiation and integration within the human insula revealed by meta-analysis

Kurth, F., Zilles, K., Fox, P. T., Laird, A. R., & Eickhoff, S. B. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0255-z · Cited by 1,293 · see citing works

fMRI resting state networks define distinct modes of long-distance interactions in the human brain

De Luca, M., Beckmann, C. F., De Stefano, N., Matthews, P. M., & Smith, S. M. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.08.035 · Cited by 1,241 · see citing works

Reduced resting-state brain activity in the “default network” in normal aging

Damoiseaux, J. S., Beckmann, C. F., Arigita, E. J. S., Barkhof, F., Scheltens, P., Stam, C. J., Smith, S. M., & Rombouts, S. A. R. B. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm207 · Cited by 1,187 · see citing works

Analysis of functional image analysis contest (FIAC) data with brainvoyager QX: From single‐subject to cortically aligned group general linear model analysis and self‐organizing group independent component analysis

Goebel, R., Esposito, F., & Formisano, E. (2006) · Human Brain Mapping · doi:10.1002/hbm.20249 · Cited by 1,053 · see citing works

Characterizing the hemodynamic response: effects of presentation rate, sampling procedure, and the possibility of ordering brain activity based on relative timing.

Miezin, F. M., Maccotta, L., Ollinger, J., Petersen, S., & Buckner, R. (2000) · NeuroImage · doi:10.1006/nimg.2000.0568 · Cited by 1,033 · see citing works

Insula of the old world monkey. III: Efferent cortical output and comments on function

Mesulam, M. ‐., & Mufson, E. J. (1982) · Journal of Comparative Neurology · doi:10.1002/cne.902120104 · Cited by 1,013 · see citing works

The Resting Brain: Unconstrained yet Reliable

Shehzad, Z. E., Kelly, C. A. M., Reiss, P. T., Gee, D. G., Gotimer, K., Uddin, L. Q., Lee, S. H., Margulies, D. S., Roy, A. K., Biswal, B. B., et al. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn256 · Cited by 913 · see citing works

The elusive concept of brain connectivity

Horwitz, B. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00112-5 · Cited by 779 · see citing works

Correlations and anticorrelations in resting-state functional connectivity MRI: A quantitative comparison of preprocessing strategies

Weissenbacher, A., Kasess, C., Gerstl, F., Lanzenberger, R., Moser, E., & Windischberger, C. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.05.005 · Cited by 776 · see citing works

Mapping the functional connectivity of anterior cingulate cortex

Margulies, D. S., Kelly, C. A. M., Uddin, L. Q., Biswal, B. B., Castellanos, F. X., & Milham, M. P. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.05.019 · Cited by 751 · see citing works

Detection of functional connectivity using temporal correlations in MR images

Hampson, M., Peterson, B. S., Skudlarski, P., Gatenby, J. C., & Gore, J. C. (2002) · Human Brain Mapping · doi:10.1002/hbm.10022 · Cited by 699 · see citing works

Changes in connectivity profiles define functionally distinct regions in human medial frontal cortex

Johansen‐Berg, H., Behrens, T. E. J., Robson, M. D., Drobnjak, I., Rushworth, M. F. S., Brady, J. M., Smith, S. M., Higham, D. J., & Matthews, P. M. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0403743101 · Cited by 684 · see citing works

Two systems of resting state connectivity between the insula and cingulate cortex

Taylor, K. S., Seminowicz, D. A., & Davis, K. D. (2009) · Human Brain Mapping · doi:10.1002/hbm.20705 · Cited by 665 · see citing works

Insula of the old world monkey. Architectonics in the insulo‐orbito‐temporal component of the paralimbic brain

Mesulam, M. M., & Mufson, E. J. (1982) · The Journal of Comparative Neurology · doi:10.1002/cne.902120102 · Cited by 654 · see citing works

Areal differences in the laminar distribution of thalamic afferents in cortical fields of the insular, parietal and temporal regions of primates

Jones, E. G., & Burton, H. (1976) · The Journal of Comparative Neurology · doi:10.1002/cne.901680203 · Cited by 653 · see citing works

The respiration response function: The temporal dynamics of fMRI signal fluctuations related to changes in respiration

Birn, R. M., Smith, M. A., Jones, T. B., & Bandettini, P. A. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2007.11.059 · Cited by 645 · see citing works

Forebrain emotional asymmetry: a neuroanatomical basis?

Craig, A. D. (. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.10.005 · Cited by 626 · see citing works

How default is the default mode of brain function?

Fransson, P. (2006) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.06.017 · Cited by 611 · see citing works

Cortical and subcortical afferents to the amygdala of the rhesus monkey (Macaca mulatta)

Aggleton, J. P., Burton, M. J., & Passingham, R. E. (1980) · Brain Research · doi:10.1016/0006-8993(80)90279-6 · Cited by 610 · see citing works

THE INSULA: FURTHER OBSERVATIONS ON ITS FUNCTION

PENFIELD, W., & FAULK, M. E. (1955) · Brain · doi:10.1093/brain/78.4.445 · Cited by 606 · see citing works

Cingulate cortex of the rhesus monkey: I. Cytoarchitecture and thalamic afferents

Vogt, B. A., Pandya, D. N., & Rosene, D. L. (1987) · Journal of Comparative Neurology · doi:10.1002/cne.902620207 · Cited by 604 · see citing works

The sentient self

Craig, A. D. (. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0248-y · Cited by 600 · see citing works

Representation of Pain and Somatic Sensation in the Human Insula: a Study of Responses to Direct Electrical Cortical Stimulation

Ostrowsky‐Coste, K. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.4.376 · Cited by 573 · see citing works

The role of anterior insular cortex in social emotions

Lamm, C., & Singer, T. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0251-3 · Cited by 566 · see citing works

Insula of the old world monkey. II: Afferent cortical input and comments on the claustrum

Mufson, E. J., & Mesulam, M. ‐. (1982) · Journal of Comparative Neurology · doi:10.1002/cne.902120103 · Cited by 559 · see citing works

Tre test clinici di ricerca e produzione lessicale: taratura su soggetti normali

Novelli, C., Papagno, C., Capitani, E., Laiacona, M., Vallar, G., & Cappa, S. (1986) · Archivio di psicologia, neurologia e psichiatria · Cited by 559 · see citing works

The posterior thalamic region and its cortical projection in new world and old world monkeys

Burton, H., & Jones, E. G. (1976) · Journal of Comparative Neurology · doi:10.1002/cne.901680204 · Cited by 555 · see citing works

Intuition and autism: a possible role for Von Economo neurons

Allman, J. M., Watson, K. K., Tetreault, N. A., & Hakeem, A. Y. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.06.008 · Cited by 484 · see citing works

Human feelings: why are some more aware than others?

Craig, A. D. (. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.04.004 · Cited by 445 · see citing works

Topographic anatomy of the insular region

Türe, U., Yaşargil, D. C. H., Al-Mefty, O., & Yaşargil, M. G. (1999) · Journal of Neurosurgery · doi:10.3171/jns.1999.90.4.0720 · Cited by 439 · see citing works

Role of the anterior insula in task-level control and focal attention

Nelson, S. M., Dosenbach, N. U. F., Cohen, A. L., Wheeler, M. E., Schlaggar, B. L., & Petersen, S. E. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0260-2 · Cited by 435 · see citing works

The von Economo neurons in frontoinsular and anterior cingulate cortex in great apes and humans

Allman, J., Tetreault, N. A., Hakeem, A. Y., Manaye, K., Semendeferi, K., Erwin, J., Park, S. Q., Goubert, V., & Hof, P. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0254-0 · Cited by 429 · see citing works

The anterior insula in autism: Under-connected and under-examined

Uddin, L. Q., & Menon, V. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.06.002 · Cited by 424 · see citing works

Core Text of Neuroanatomy

Carpenter, M. B. (1978) · Andalas University Repository (Andalas University) · Cited by 403 · see citing works

The insula (Island of Reil) and its role in auditory processing

Bamiou, D., Musiek, F. E., & LUXON, L. M. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(03)00172-3 · Cited by 397 · see citing works

Neurobiology of cingulate cortex and limbic thalamus : a comprehensive handbook

Vogt, B. A., & Gabriel, M. (1993) · Medical Entomology and Zoology · Cited by 378 · see citing works

Somatotopic organisation of the human insula to painful heat studied with high resolution functional imaging

Brooks, J. C. W., Zambreanu, L., Godinez, A., Craig, A. D. (., & Tracey, I. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.03.041 · Cited by 355 · see citing works

Brain structures mediating cardiovascular arousal and interoceptive awareness

Pollatos, O., Schandry, R., Auer, D. P., & Kaufmann, C. (2007) · Brain Research · doi:10.1016/j.brainres.2007.01.026 · Cited by 351 · see citing works

Brain correlates of autonomic modulation: Combining heart rate variability with fMRI

Napadow, V., Dhond, R. P., Conti, G., Makris, N., Brown, E. N., & Barbieri, R. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.04.238 · Cited by 347 · see citing works

Insular cortex and neuropsychiatric disorders: A review of recent literature

Nagai, M., Kishi, K., & Kato, S. (2007) · European Psychiatry · doi:10.1016/j.eurpsy.2007.02.006 · Cited by 332 · see citing works

Cytochrome Oxidase, Acetylcholinesterase, and NADPH-Diaphorase Staining in Human Supratemporal and Insular Cortex: Evidence for Multiple Auditory Areas

Rivier, F., & Clarke, S. (1997) · NeuroImage · doi:10.1006/nimg.1997.0304 · Cited by 311 · see citing works

Interoception and emotion: A neuroanatomical perspective.

Craig, A. D. (2008) · Cited by 289 · see citing works

Defining functional SMA and pre-SMA subregions in human MFC using resting state fMRI: Functional connectivity-based parcellation method

Kim, J., Lee, J., Jo, H. J., Kim, S. H., Lee, J. H., Kim, S. T., Seo, S. W., Cox, R. W., Na, D. L., Kim, S. I., et al. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.10.016 · Cited by 281 · see citing works

Anatomy of the insula functional and clinical correlates

Flynn, F. G. (1999) · Aphasiology · doi:10.1080/026870399402325 · Cited by 271 · see citing works

A new correlation‐based fuzzy logic clustering algorithm for FMRI

Golay, X., Kollias, S., Stoll, G., Meier, D., Valavanis, A., & Boesiger, P. (1998) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910400211 · Cited by 253 · see citing works

Functional neural networks underlying response inhibition in adolescents and adults

Stevens, M. C., Kiehl, K. A., Pearlson, G. D., & Calhoun, V. D. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.03.023 · Cited by 241 · see citing works

Cytoarchitecture and Probabilistic Maps of the Human Posterior Insular Cortex

Kurth, F., Eickhoff, S. B., Schleicher, A., Hömke, L., Zilles, K., & Amunts, K. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp208 · Cited by 241 · see citing works

Functional organization of the human anterior insular cortex

Mutschler, I., Wieckhorst, B., Kowalevski, S., Derix, J., Wentlandt, J., Schulze‐Bonhage, A., & Tonio Ball, A. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.03.101 · Cited by 240 · see citing works

Specificity in the Projections of Prefrontal and Insular Cortex to Ventral Striatopallidum and the Extended Amygdala

Reynolds, S. M., & Zahm, D. S. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3432-05.2005 · Cited by 239 · see citing works

Pain sensitivity and fMRI pain-related brain activity in Alzheimer's disease

Cole, L. J., Farrell, M. J., Duff, E. P., Barber, J. B., Egan, G. F., & Gibson, S. J. (2006) · Brain · doi:10.1093/brain/awl228 · Cited by 229 · see citing works

The insular lobe in primates including humans

Augustine, J. R. (1985) · Neurological Research · doi:10.1080/01616412.1985.11739692 · Cited by 224 · see citing works

Right insula for our sense of limb ownership and self-awareness of actions

Karnath, H.-O., & Baier, B. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0250-4 · Cited by 223 · see citing works

Spindle neurons of the human anterior cingul. Ate cortex

Nimchinsky, E. A., Vogt, B. A., Morrison, J. H., & Hof, P. R. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903550106 · Cited by 220 · see citing works

Core Text of Neuroanatomy

Graham, J. G. (1978) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.41.12.1147-b · Cited by 196 · see citing works

An fMRI study of cerebral processing of brush-evoked allodynia in neuropathic pain patients

Schweinhardt, P., Glynn, C. J., Brooks, J. C. W., McQuay, H., Jack, T., Chessell, I. P., Bountra, C., & Tracey, I. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.03.024 · Cited by 194 · see citing works

Cortical and thalamic afferent connections of the insular and adjacent cortex of the rat

Guldin, W. O., & Markowitsch, H. J. (1983) · The Journal of Comparative Neurology · doi:10.1002/cne.902150203 · Cited by 181 · see citing works

Striatum forever, despite sequence learning variability: A random effect analysis of PET data

Peigneux, P., Maquet, P., Meulemans, T., Destrebecqz, A., Laureys, S., Degueldre, C., Delfiore, G., Aerts, J. J., Luxen, A., Franck, G., et al. (2000) · Human Brain Mapping · doi:10.1002/1097-0193(200008)10:4 · Cited by 172 · see citing works

The insula: anatomic study and MR imaging display at 1.5 T.

Naidich, T. P., Kang, E., Fatterpekar, G. M., Delman, B. N., Gultekin, S. H., WOLFE, D. E., Ortiz, O. A., Yousry, I., Weismann, M., & Yousry, T. A. (2004) · PubMed Central · Cited by 169 · see citing works

Structural Organization of Cingulate Cortex: Areas, Neurons, and Somatodendritic Transmitter Receptors

Vogt, B. A. (1993) · Neurobiology of Cingulate Cortex and Limbic Thalamus · doi:10.1007/978-1-4899-6704-6_2 · Cited by 139 · see citing works

The Insular Cortex: Morphological and Vascular Anatomic Characteristics

Varnavas, G., & Grand, W. (1999) · Neurosurgery · doi:10.1097/00006123-199901000-00079 · Cited by 132 · see citing works

Functional Connectivity of the Posteromedial Cortex

Cauda, F., Geminiani, G. C., D’Agata, F., Sacco, K., Duca, S., Bagshaw, A. P., & Cavanna, A. E. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013107 · Cited by 129 · see citing works

Pathology of the Insular Cortex in Alzheimer Disease Depends on Cortical Architecture

Bonthius, D. J., Solodkin, A., & Hoesen, G. W. V. (2005) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/01.jnen.0000182983.87106.d1 · Cited by 128 · see citing works

Cortical network dynamics with time delays reveals functional connectivity in the resting brain

Ghosh, A., Rho, Y.-A., McIntosh, A. R., Kötter, R., & Jirsa, V. (2008) · Cognitive Neurodynamics · doi:10.1007/s11571-008-9044-2 · Cited by 127 · see citing works

Cardiorespiratory effects on default‐mode network activity as measured with fMRI

van Buuren, M., Gladwin, T. E., Zandbelt, B. B., van den Heuvel, M. P., Ramsey, N. F., Kahn, R. S., & Vink, M. (2009) · Human Brain Mapping · doi:10.1002/hbm.20729 · Cited by 119 · see citing works

Group analyses of connectivity-based cortical parcellation using repeated k-means clustering

Nanetti, L., Cerliani, L., Gazzola, V., Renken, R. J., & Keysers, C. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.06.014 · Cited by 113 · see citing works

On the number of clusters and the fuzziness index for unsupervised FCA application to BOLD fMRI time series

Fadili, J. M., Ruan, S., Bloyet, D., & Mazoyer, B. M. (2001) · Medical Image Analysis · doi:10.1016/s1361-8415(00)00035-9 · Cited by 75 · see citing works

Feelings of warmth correlate with neural activity in right anterior insular cortex

Olausson, H., Charron, J., Marchand, S., Villemure, C., Strigo, I. A., & Bushnell, M. C. (2005) · Neuroscience Letters · doi:10.1016/j.neulet.2005.06.065 · Cited by 71 · see citing works

Cortical and thalamic afferent connections of the insular and adjacent cortex of the cat

Guldin, W. O., & Markowitsch, H. J. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902290309 · Cited by 56 · see citing works

Raven's Progressive Matrices: Construct Validity

Bingham, W. C., Burke, H. R., & Murray, S. (1966) · The Journal of Psychology · doi:10.1080/00223980.1966.10543785 · Cited by 42 · see citing works

Discovering the somatotopic organization of the motor areas of the medial wall using low‐frequency bold fluctuations

Cauda, F., Giuliano, G., D’Agata, F., Sergio, D., & Sacco, K. (2010) · Human Brain Mapping · doi:10.1002/hbm.21132 · Cited by 41 · see citing works

Dissecting cognitive stages with time-resolved fMRI data: a comparison of fuzzy clustering and independent component analysis

Smolders, A., Martino, F. D., Staeren, N., et al. (2007) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2007.02.018 · Cited by 41 · see citing works

Endogenous oscillations and networks in functional magnetic resonance imaging

Bandettini, P. A., & Bullmore, E. T. (2008) · Human Brain Mapping · doi:10.1002/hbm.20607 · Cited by 32 · see citing works

How to Avoid Spurious Cluster Validation? A Methodological Investigation on Simulated and fMRI Data

Möller, U., Ligges, M., Georgiewa, P., Ligges, C., Kaiser, W. A., Witte, H., & Blanz, B. (2002) · NeuroImage · doi:10.1006/nimg.2002.1166 · Cited by 25 · see citing works

Testing the Equality of Two or More Split-Half Reliability Coefficients

Charter, R. A. (2001) · Psychological Reports · doi:10.2466/pr0.2001.88.3.844 · Cited by 12 · see citing works

Classification and clustering : proceedings of an advanced seminar conducted by the Mathematics Research Center, the University of Wisconsin at Madison, May 3-5, 1976

Ryzin, J. V. (1977) · Academic Press eBooks · Cited by 9 · see citing works

022 Functional connectivity of the posteromedial cortex

Cavanna, A. E., Geminiani, G. C., D’Agata, F., Sacco, K., Duca, S., Bagshaw, A. P., & Cauda, F. (2010) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2010.217554.22 · Cited by 4 · see citing works

Transient fetal structure, the gangliothalamic body, connects telencephalic germinal zone with all thalamic regions in the developing human brain

Letinić, K., & Kostović, I. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970804)384:3 · Cited by 3 · see citing works

Salience processing and insular cortical function and dysfunction

Uddin, L. Q. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3857 · Cited by 2,083 · see citing works

The integration of negative affect, pain and cognitive control in the cingulate cortex

Shackman, A. J., Salomons, T. V., Slagter, H. A., Fox, A. S., Winter, J. J., & Davidson, R. J. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn2994 · Cited by 2,082 · see citing works

Uncertainty and anticipation in anxiety: an integrated neurobiological and psychological perspective

Grupe, D. W., & Nitschke, J. B. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3524 · Cited by 2,007 · see citing works

Gut feelings: the emerging biology of gut-brain communication

Mayer, E. A. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3071 · Cited by 1,726 · see citing works

Behavioral interpretations of intrinsic connectivity networks

Laird, A. R., Fox, P. M., Eickhoff, S. B., Turner, J. A., Ray, K. L., McKay, D. R., Glahn, D. C., Beckmann, C. F., Smith, S. M., & Fox, P. T. (2011) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00077 · Cited by 1,023 · see citing works

Modelling neural correlates of working memory: A coordinate-based meta-analysis

Rottschy, C., Langner, R., Dogan, I., Reetz, K., Laird, A. R., Schulz, J. B., Fox, P. T., & Eickhoff, S. B. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.11.050 · Cited by 951 · see citing works

Decoding the Role of the Insula in Human Cognition: Functional Parcellation and Large-Scale Reverse Inference

Chang, L. J., Yarkoni, T., Khaw, M. W., & Sanfey, A. G. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs065 · Cited by 879 · see citing works

Anterior insular cortex and emotional awareness

Gu, X., Hof, P. R., Friston, K. J., & Fan, J. (2013) · Journal of Comparative Neurology · doi:10.1002/cne.23368 · Cited by 712 · see citing works

Co-activation patterns distinguish cortical modules, their connectivity and functional differentiation

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 · see citing works

Salience Network

Menon, V. (2015) · Brain Mapping · doi:10.1016/b978-0-12-397025-1.00052-x · Cited by 625 · see citing works

Distinct Global Brain Dynamics and Spatiotemporal Organization of the Salience Network

Chen, T., Cai, W., Ryali, S., Supekar, K., & Menon, V. (2016) · PLOS Biology · doi:10.1371/journal.pbio.1002469 · Cited by 480 · see citing works

Keeping the body in mind: insula functional organization and functional connectivity integrate interoceptive, exteroceptive, and emotional awareness

Simmons, W. K., Avery, J. A., Barcalow, J. C., Bodurka, J., Drevets, W. C., & Bellgowan, P. (2013) · Human Brain Mapping · doi:10.1002/hbm.22113 · Cited by 401 · see citing works

Neural Dysregulation in Posttraumatic Stress Disorder: Evidence for Disrupted Equilibrium Between Salience and Default Mode Brain Networks

Sripada, R. K., King, A. P., Welsh, R. C., Garfinkel, S. N., Wang, X., Sripada, C. S., & Liberzon, I. (2012) · Psychosomatic Medicine · doi:10.1097/psy.0b013e318273bf33 · Cited by 412 · see citing works

A convergent functional architecture of the insula emerges across imaging modalities

Kelly, C., Toro, R., Di Martino, A., Cox, C. L., Bellec, P., Castellanos, F. X., & Milham, M. P. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.021 · Cited by 374 · see citing works

Connectivity-based parcellation of the human orbitofrontal cortex

Kahnt, T., Chang, L. J., Park, S. Q., Heinzle, J., & Haynes, J.-D. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.0257-12.2012 · Cited by 299 · see citing works

Dissociable large-scale networks anchored in the right anterior insula subserve affective experience and attention

Touroutoglou, A., Hollenbeck, M., Dickerson, B. C., & Feldman Barrett, L. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.02.012 · Cited by 276 · see citing works

Coupling Inner and Outer Body for Self-Consciousness

Park, H.-D., & Blanke, O. (2019) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2019.02.002 · Cited by 266 · see citing works

Prenatal maternal depression alters amygdala functional connectivity in 6-month-old infants

Qiu, A., Anh, T. T., Li, Y., Chen, H., Rifkin-Graboi, A., Broekman, B. F. P., Kwek, K., Saw, S.-M., Chong, Y.-S., Gluckman, P. D., et al. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.3 · Cited by 282 · see citing works

Resting-state functional and structural connectivity within an insula–amygdala route specifically index state and trait anxiety

Baur, V., Hänggi, J., Langer, N., & Jäncke, L. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.06.003 · Cited by 258 · see citing works

Oxytocin facilitates protective responses to aversive social stimuli in males

Striepens, N., Scheele, D., Kendrick, K. M., Becker, B., Schäfer, L., Schwalba, K., Reul, J., Maier, W., & Hurlemann, R. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1208852109 · Cited by 242 · see citing works

Pain and analgesia: the value of salience circuits

Borsook, D., Edwards, R., Elman, I., Becerra, L., & Levine, J. (2013) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.02.003 · Cited by 215 · see citing works

Error awareness and the insula: links to neurological and psychiatric diseases

Klein, T. A., Ullsperger, M., & Danielmeier, C. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00014 · Cited by 210 · see citing works

The insular cortex and the regulation of cardiac function

Oppenheimer, S., & Cechetto, D. (2016) · Comprehensive Physiology · doi:10.1002/cphy.c140076 · Cited by 191 · see citing works

Atypical interoception as a common risk factor for psychopathology: A review

Brewer, R., Murphy, J., & Bird, G. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.07.036 · Cited by 180 · see citing works

Networks of task co-activations

Laird, A. R., Eickhoff, S. B., Rottschy, C., Bzdok, D., Ray, K. L., & Fox, P. T. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.04.073 · Cited by 168 · see citing works

Effects of craving behavioral intervention on neural substrates of cue-induced craving in Internet gaming disorder

Zhang, J.-T., Yao, Y.-W., Potenza, M. N., Xia, C.-C., Lan, J., Liu, L., Wang, L.-J., Liu, B., Ma, S.-S., & Fang, X.-Y. (2016) · NeuroImage: Clinical · doi:10.1016/j.nicl.2016.09.004 · Cited by 177 · see citing works

An oxytocin-induced facilitation of neural and emotional responses to social touch correlates inversely with autism traits

Scheele, D., Kendrick, K. M., Khouri, C., Kretzer, E., Schläpfer, T. E., Stoffel-Wagner, B., Güntürkün, O., Maier, W., & Hurlemann, R. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.78 · Cited by 171 · see citing works

The neural crossroads of psychiatric illness: an emerging target for brain stimulation

Downar, J., Blumberger, D. M., & Daskalakis, Z. J. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.10.007 · Cited by 166 · see citing works

Brain systems for baroreflex suppression during stress in humans

Gianaros, P. J., Onyewuenyi, I. C., Sheu, L. K., Christie, I. C., & Critchley, H. D. (2012) · Human Brain Mapping · doi:10.1002/hbm.21315 · Cited by 166 · see citing works

Insular and hippocampal gray matter volume reductions in patients with major depressive disorder

Stratmann, M., Konrad, C., Kugel, H., Krug, A., Schöning, S., Ohrmann, P., Uhlmann, C., Postert, C., Suslow, T., Heindel, W., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0102692 · Cited by 164 · see citing works

Auditory feedback differentially modulates behavioral and neural markers of objective and subjective performance when tapping to your heartbeat

Canales-Johnson, A., Silva, C., Huepe, D., Rivera-Rei, Á., Noreika, V., Garcia, M. D. C., Silva, W., Ciraolo, C., Vaucheret, E., Sedeño, L., et al. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv076 · Cited by 146 · see citing works

Distinct intrinsic network connectivity patterns of post‐traumatic stress disorder symptom clusters

Tursich, M., Ros, T., Frewen, P. A., Kluetsch, R. C., Calhoun, V. D., & Lanius, R. A. (2015) · Acta Psychiatrica Scandinavica · doi:10.1111/acps.12387 · Cited by 148 · see citing works

The Insula: A “Hub of Activity” in Migraine

Borsook, D., Veggeberg, R., Erpelding, N., Borra, R., Linnman, C., Burstein, R., & Becerra, L. (2016) · The Neuroscientist · doi:10.1177/1073858415601369 · Cited by 146 · see citing works

Meta-analytic investigations of structural grey matter, executive domain-related functional activations, and white matter diffusivity in obsessive compulsive disorder: an integrative review

Eng, G. K., Sim, K., & Chen, S.-H. A. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.03.002 · Cited by 148 · see citing works

Preserved Self-Awareness following Extensive Bilateral Brain Damage to the Insula, Anterior Cingulate, and Medial Prefrontal Cortices

Philippi, C. L., Feinstein, J. S., Khalsa, S. S., Damasio, A., Tranel, D., Landini, G., Williford, K., & Rudrauf, D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038413 · Cited by 144 · see citing works

Large-scale brain network dynamics supporting adolescent cognitive control

Dwyer, D. B., Harrison, B. J., Yücel, M., Whittle, S., Zalesky, A., Pantelis, C., Allen, N. B., & Fornito, A. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.1634-14.2014 · Cited by 143 · see citing works

Unique insula subregion resting-state functional connectivity with amygdala complexes in posttraumatic stress disorder and its dissociative subtype.

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 · see citing works

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 · see citing works

Increased anterior insula activity in anxious individuals is linked to diminished perceived control

Alvarez, R. P., Kirlic, N., Misaki, M., Bodurka, J., Rhudy, J. L., Paulus, M. P., & Drevets, W. C. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.84 · Cited by 113 · see citing works

PTSD and its dissociative subtype through the lens of the insula: Anterior and posterior insula resting‐state functional connectivity and its predictive validity using machine learning

Harricharan, S., Nicholson, A. A., Thome, J., Densmore, M., McKinnon, M. C., Théberge, J., Frewen, P. A., Neufeld, R. W. J., & Lanius, R. A. (2020) · Psychophysiology · doi:10.1111/psyp.13472 · Cited by 94 · see citing works

Approach/avoidance

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 · see citing works

Variety in emotional life: Within-category typicality of emotional experiences is associated with neural activity in large-scale brain networks

Wilson-Mendenhall, C. D., Barrett, L. F., & Barsalou, L. W. (2015) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsu037 · Cited by 98 · see citing works

Altered functional connectivity of the insular cortex across prefrontal networks in cocaine addiction

Cisler, J. M., Elton, A., Kennedy, A. P., Young, J., Smitherman, S., Andrew James, G., & Kilts, C. D. (2013) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2013.02.007 · Cited by 99 · see citing works

Structural basis of empathy and the domain general region in the anterior insular cortex

Mutschler, I., Reinbold, C., Wankerl, J., Seifritz, E., & Ball, T. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00177 · Cited by 92 · see citing works

Task-Induced Deactivation from Rest Extends beyond the Default Mode Brain Network

Harrison, B. J., Pujol, J., Contreras-Rodríguez, O., Soriano-Mas, C., López-Solà, M., Deus, J., Ortiz, H., Blanco-Hinojo, L., Alonso, P., Hernández-Ribas, R., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0022964 · Cited by 92 · see citing works

Individual Differences in Reward and Somatosensory-Motor Brain Regions Correlate with Adiposity in Adolescents

Rapuano, K. M., Huckins, J. F., Sargent, J. D., Heatherton, T. F., & Kelley, W. M. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv097 · Cited by 90 · see citing works

Insula’s functional connectivity with ventromedial prefrontal cortex mediates the impact of trait alexithymia on state tobacco craving

Sutherland, M. T., Carroll, A. J., Salmeron, B. J., Ross, T. J., & Stein, E. A. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3018-8 · Cited by 89 · see citing works

Increased functional connectivity in an insula-based network is associated with improved smoking cessation outcomes

Addicott, M. A., Sweitzer, M. M., Froeliger, B., Rose, J. E., & McClernon, F. J. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.114 · Cited by 85 · see citing works

Brain Structure and Subclinical Symptoms: A Dimensional Perspective of Psychopathology in the Depression and Anxiety Spectrum

Besteher, B., Gaser, C., & Nenadić, I. (2020) · Neuropsychobiology · doi:10.1159/000501024 · Cited by 83 · see citing works

Interoceptive and multimodal functions of the operculo-insular cortex: tactile, nociceptive and vestibular representations

zu Eulenburg, P., Baumgärtner, U., Treede, R.-D., & Dieterich, M. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.06.057 · Cited by 82 · see citing works

Maternal stress during pregnancy alters fetal cortico-cerebellar connectivity in utero and increases child sleep problems after birth

van den Heuvel, M. I., Hect, J. L., Smarr, B. L., Qawasmeh, T., Kriegsfeld, L. J., Barcelona, J., Hijazi, K. E., & Thomason, M. E. (2021) · Scientific Reports · doi:10.1038/s41598-021-81681-y · Cited by 76 · see citing works

The neurosteroids allopregnanolone and dehydroepiandrosterone modulate resting-state amygdala connectivity: Neurosteroids Modulate Amygdala Resting fcMRI

Sripada, R. K., Welsh, R. C., Marx, C. E., & Liberzon, I. (2014) · Human Brain Mapping · doi:10.1002/hbm.22399 · Cited by 66 · see citing works

An fMRI investigation of the relationship between future imagination and cognitive flexibility

Roberts, R. P., Wiebels, K., Sumner, R. L., van Mulukom, V., Grady, C. L., Schacter, D. L., & Addis, D. R. (2017) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2016.11.019 · Cited by 58 · see citing works

Concurrent TMS-fMRI reveals interactions between dorsal and ventral attentional systems

Leitao, J., Thielscher, A., Tunnerhoff, J., & Noppeney, U. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0939-15.2015 · Cited by 58 · see citing works

Increased amygdala response to shame in remitted major depressive disorder

Pulcu, E., Lythe, K., Elliott, R., Green, S., Moll, J., Deakin, J. F. W., & Zahn, R. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086900 · Cited by 57 · see citing works

Neuropathology of the Anterior Midcingulate Cortex in Young Children With Autism

Uppal, N., Wicinski, B., Buxbaum, J. D., Heinsen, H., Schmitz, C., & Hof, P. R. (2014) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0000000000000108 · Cited by 52 · see citing works

Disentangling interoception: insights from focal strokes affecting the perception of external and internal milieus

Couto, B., Adolfi, F., Sedeño, L., Salles, A., Canales-Johnson, A., Alvarez-Abut, P., Garcia-Cordero, I., Pietto, M., Bekinschtein, T., Sigman, M., et al. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.00503 · Cited by 51 · see citing works

Altered functional organization within the insular cortex in adult males with high-functioning autism spectrum disorder: evidence from connectivity-based parcellation

Yamada, T., Itahashi, T., Nakamura, M., Watanabe, H., Kuroda, M., Ohta, H., Kanai, C., Kato, N., & Hashimoto, R.-I. (2016) · Molecular Autism · doi:10.1186/s13229-016-0106-8 · Cited by 50 · see citing works

Altered functional connectivity between medial prefrontal cortex and the inferior brainstem in major depression during appraisal of subjective emotional responses: a preliminary study

Smith, R., Allen, J. J. B., Thayer, J. F., & Lane, R. D. (2015) · Biological Psychology · doi:10.1016/j.biopsycho.2015.03.007 · Cited by 49 · see citing works

Neuroimaging the traumatized self: fMRI reveals altered response in cortical midline structures and occipital cortex during visual and verbal self- and other-referential processing in women with PTSD.

Frewen, P., Thornley, E., Rabellino, D., & Lanius, R. (2017) · European Journal of Psychotraumatology · doi:10.1080/20008198.2017.1314164 · Cited by 36 · see citing works

Salience network activity in perceptual decisions

Lamichhane, B., Adhikari, B. M., & Dhamala, M. (2016) · Brain Connectivity · doi:10.1089/brain.2015.0392 · Cited by 33 · see citing works

Gender- and Age-Specific Differences in Resting-State Functional Connectivity of the Central Autonomic Network in Adulthood

Sie, J.-H., Chen, Y.-H., Shiau, Y.-H., & Chu, W.-C. (2019) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2019.00369 · Cited by 35 · see citing works

Distinct functional connectivity of limbic network in the washing type obsessive–compulsive disorder

Jhung, K., Ku, J., Kim, S. J., Lee, H., Kim, K. R., An, S. K., Kim, S. I., Yoon, K.-J., & Lee, E. (2014) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2014.04.007 · Cited by 26 · see citing works

Hemispheric contributions toward interoception and emotion recognition in left-vs right-semantic dementia

Hazelton, J. L., Devenney, E., Ahmed, R., Burrell, J., Hwang, Y., Piguet, O., & Kumfor, F. (2023) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2023.108628 · Cited by 16 · see citing works

Gray matter volumes of insular subregions are not correlated with smoking cessation outcomes but negatively correlated with nicotine dependence severity in chronic smokers

Wang, C., Huang, P., Shen, Z., Qian, W., Li, K., Luo, X., Zeng, Q., Guo, T., Yu, H., Yang, Y., et al. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2018.12.013 · Cited by 16 · see citing works

Role of the healthy hemisphere in recovery after resection of the supplementary motor area

Krainik, A., Duffau, H., Capelle, L., Cornu, P., Boch, A., Mangin, J.-F., Bihan, D. L., Marsault, C., Jacques Chiras, C., & Lehéricy, S. (2004) · Neurology · doi:10.1212/01.wnl.0000120547.83482.b1 · Cited by 205 · see citing works

Interconnections between the prefrontal cortex and the premotor areas in the frontal lobe

Lu, M., Preston, J. B., & Strick, P. L. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903410308 · Cited by 501 · see citing works

Premotor areas in man

Freund, H. (1984) · Trends in Neurosciences · doi:10.1016/s0166-2236(84)80260-x · Cited by 22 · see citing works

Activation of frontal premotor areas during suprathreshold transcranial magnetic stimulation of the left primary sensorimotor cortex: A glucose metabolic PET study

(2001) · doi:10.1002/1097-0193(200103)12:3

Frontal lobe inputs to the shoulder region of the dorsal premotor area (PMd)

Hirata, Y., Inoue, K., Takahara, D., Ninomiya, T., Miyachi, S., Tanji, J., Takada, M., & Hoshi, E. (2009) · Neuroscience Research · doi:10.1016/j.neures.2009.09.1105