Dynamic reconfiguration of structural and functional connectivity across core neurocognitive brain networks with development

Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single subject brain

Tzourio-Mazoyer, N., Landeau, B., Papathanassiou, D., Crivello, F., Etard, O., Delcroix, N., Mazoyer, B., & Joliot, M. (2002) · NeuroImage · doi:10.1006/nimg.2001.0978 · Cited by 16,319 · 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

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 1× · 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

The basis of anisotropic water diffusion in the nervous system—A technical review.

Beaulieu, C. (2002) · NMR in Biomedicine · doi:10.1002/nbm.782 · Cited by 4,653 · see citing works

Numerical Recipes in C: The Art of Scientific Computing.

Birchenhall, C. R., Press, W. H., Teukolsky, S. A., Vetterling, W. T., & Flannery, B. P. (1994) · The Economic Journal · doi:10.2307/2234664 · Cited by 4,355 · 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

Microstructural and physiological features of tissues elucidated by quantitative-diffusion-tensor MRI

Basser, P. J., & Pierpaoli, C. (1996) · Journal of Magnetic Resonance, Series B · doi:10.1006/jmrb.1996.0086 · Cited by 4,306 · 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

Default-mode network activity distinguishes Alzheimer’s disease from healthy aging: evidence from functional MRI

Greicius, M. D., Srivastava, G., Reiss, A. L., & Menon, V. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308627101 · Cited by 3,684 · see citing works

Three-dimensional tracking of axonal projections in the brain by magnetic resonance imaging

Mori, S., Crain, B. J., Chacko, V. P., & van Zijl, P. C. M. (1999) · Annals of Neurology · doi:10.1002/1531-8249(199902)45:2 · Cited by 3,479 · see citing works

Predicting human resting-state functional connectivity from structural connectivity

Honey, C. J., Sporns, O., Cammoun, L., Gigandet, X., Thiran, J. P., Meuli, R., & Hagmann, P. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811168106 · Cited by 3,307 · see citing works

From sensation to cognition

Mesulam, M. (1998) · Brain · doi:10.1093/brain/121.6.1013 · Cited by 3,072 · 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

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

Large-scale brain networks in cognition: emerging methods and principles

Bressler, S. L., & Menon, V. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.04.004 · Cited by 2,348 · see citing works

Network modelling methods for FMRI

Smith, S. M., Miller, K. L., Salimi-Khorshidi, G., Webster, M., Beckmann, C. F., Nichols, T. E., Ramsey, J. D., & Woolrich, M. W. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.08.063 · Cited by 1,878 · see citing works

Brain development in children and adolescents: Insights from anatomical magnetic resonance imaging

Lenroot, R. K., & Giedd, J. N. (2006) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2006.06.001 · Cited by 1,863 · see citing works

Tracking neuronal fiber pathways in the living human brain

Conturo, T. E., Lori, N. F., Cull, T. S., Akbudak, E., Snyder, A. Z., Shimony, J. S., McKinstry, R. C., Burton, H., & Raichle, M. E. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.18.10422 · Cited by 1,774 · see citing works

Reproducibility of quantitative tractography methods applied to cerebral white matter

Wakana, S., Caprihan, A., Panzenboeck, M. M., Fallon, J. H., Perry, M., Gollub, R. L., Hua, K., Zhang, J., Jiang, H., Dubey, P., et al. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.02.049 · Cited by 1,686 · see citing works

Network structure of cerebral cortex shapes functional connectivity on multiple time scales

Honey, C. J., Kötter, R., Breakspear, M. J., & Sporns, O. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701519104 · Cited by 1,683 · see citing works

Functional brain networks develop from a local to distributed organization

Fair, D. A., Cohen, A. L., Power, J. D., Dosenbach, N. U. F., Church, J. A., Miezin, F. M., Schlaggar, B. L., & Petersen, S. E. (2009) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000381 · Cited by 1,530 · see citing works

Inferring microstructural features and the physiological state of tissues from diffusion‐weighted images

Basser, P. J. (1995) · NMR in Biomedicine · doi:10.1002/nbm.1940080707 · Cited by 1,526 · see citing works

Autism spectrum disorders: developmental disconnection syndromes

Geschwind, D. H., & Levitt, P. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.01.009 · Cited by 1,411 · see citing works

Neurophysiological Architecture of Functional Magnetic Resonance Images of Human Brain

Salvador, R. M., John Suckling, A., Coleman, M. R., Pickard, J. D., Menon, D. K., & Bullmore, E. T. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhi016 · Cited by 1,334 · 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

Development of distinct control networks through segregation and integration

Fair, D. A., Dosenbach, N. U. F., Church, J. A., Cohen, A. L., Brahmbhatt, S., Miezin, F. M., Barch, D. M., Raichle, M. E., Petersen, S. E., & Schlaggar, B. L. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705843104 · Cited by 1,244 · 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

Lateral prefrontal cortex: architectonic and functional organization

Petrides, M. (2005) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2005.1631 · Cited by 1,212 · see citing works

Association fibre pathways of the brain: parallel observations from diffusion spectrum imaging and autoradiography

Schmahmann, J. D., Pandya, D. N., Wang, R., Dai, G., D'Arceuil, H. E., de Crespigny, A. J., & Wedeen, V. J. (2007) · Brain · doi:10.1093/brain/awl359 · Cited by 1,067 · see citing works

Mapping directed influence over the brain using Granger causality and fMRI

Roebroeck, A. F., Formisano, E., & Goebel, R. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2004.11.017 · Cited by 1,024 · see citing works

Disrupted small-world networks in schizophrenia

Liu, Y., Liang, M., Zhou, Y., Yong He, A., Hao, Y., Song, M., Yu, C., Liu, H., Liu, Z., & Jiang, T. (2008) · Brain · doi:10.1093/brain/awn018 · Cited by 1,020 · see citing works

Functionally linked resting‐state networks reflect the underlying structural connectivity architecture of the human brain

van den Heuvel, M. P., Mandl, R. C. W., Kahn, R. S., & Hulshoff Pol, H. E. (2009) · Human Brain Mapping · doi:10.1002/hbm.20737 · Cited by 987 · see citing works

White matter development during childhood and adolescence: a cross-sectional diffusion tensor imaging study

Barnea-Goraly, N., Menon, V., Eckert, M., Tamm, L., Bammer, R., Karchemskiy, A., Dant, C. C., & Reiss, A. L. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhi062 · Cited by 848 · see citing works

Structural MRI of pediatric brain development: what have we learned and where are we going?

Giedd, J. N., & Rapoport, J. L. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.040 · Cited by 836 · see citing works

Twenty‐five pitfalls in the analysis of diffusion MRI data

Jones, D. K., & Cercignani, M. (2010) · NMR in Biomedicine · doi:10.1002/nbm.1543 · Cited by 827 · see citing works

Development of large-scale functional brain networks in children

Supekar, K., Musen, M., & Menon, V. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000157 · Cited by 807 · see citing works

The effect of gradient sampling schemes on measures derived from diffusion tensor MRI: A Monte Carlo study†

Jones, D. K. (2004) · Magnetic Resonance in Medicine · doi:10.1002/mrm.20033 · Cited by 776 · see citing works

A MATLAB toolbox for Granger causal connectivity analysis

Seth, A. K. (2009) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2009.11.020 · Cited by 746 · see citing works

White matter maturation reshapes structural connectivity in the late developing human brain

Hagmann, P., Sporns, O., Madan, N., Cammoun, L., Pienaar, R., Wedeen, V. J., Meuli, R., Thiran, J.-P., & Grant, P. E. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009073107 · Cited by 700 · see citing works

Investigating directed cortical interactions in time-resolved fMRI data using vector autoregressive modeling and Granger causality mapping

Goebel, R., Roebroeck, A. F., Kim, D., & Formisano, E. (2003) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2003.08.026 · Cited by 687 · see citing works

Developmental neurobiology of cognitive control and motivational systems.

Somerville, L. H., & Casey, B. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.01.006 · Cited by 634 · see citing works

Conjoint activity of anterior insular and anterior cingulate cortex: awareness and response

Medford, N., & Critchley, H. D. (2010) · Brain Structure and Function · doi:10.1007/s00429-010-0265-x · Cited by 627 · see citing works

Cognitive control and right ventrolateral prefrontal cortex: Reflexive reorienting, motor inhibition, and action updating

Levy, B. J., & Wagner, A. D. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2011.05958.x · Cited by 625 · see citing works

Spatial transformations of diffusion tensor magnetic resonance images

Alexander, D. C., Pierpaoli, C., Basser, P. J., & Gee, J. C. (2001) · IEEE Transactions on Medical Imaging · doi:10.1109/42.963816 · Cited by 610 · see citing works

Spiral‐in/out BOLD fMRI for increased SNR and reduced susceptibility artifacts

Glover, G. H., & Law, C. S. W. (2001) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1222 · Cited by 600 · see citing works

Development of Anterior Cingulate Functional Connectivity from Late Childhood to Early Adulthood

Kelly, A. M. C., Di Martino, A., Uddin, L. Q., Shehzad, Z., Gee, D. G., Reiss, P. T., Margulies, D. S., Castellanos, F. X., & Milham, M. P. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn117 · Cited by 572 · see citing works

Development of functional and structural connectivity within the default mode network in young children

Supekar, K., Uddin, L. Q., Prater, K. E., Amin, H., Greicius, M. D., & Menon, V. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.04.009 · Cited by 524 · see citing works

Self‐navigated spiral fMRI: Interleaved versus single‐shot

Glover, G. H., & Lai, S. (1998) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910390305 · Cited by 476 · see citing works

Dissociable Connectivity within Human Angular Gyrus and Intraparietal Sulcus: Evidence from Functional and Structural Connectivity

Uddin, L. Q., Supekar, K., Amin, H., Rykhlevskaia, E. I., Nguyen, D. A., Greicius, M. D., & Menon, V. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq011 · Cited by 449 · see citing works

Causal Modelling and Brain Connectivity in Functional Magnetic Resonance Imaging

Friston, K. J. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000033 · Cited by 444 · see citing works

Growth of white matter in the adolescent brain: Myelin or axon?

Paus, T. (2010) · Brain and Cognition · doi:10.1016/j.bandc.2009.06.002 · Cited by 424 · 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

Measuring interregional functional connectivity using coherence and partial coherence analyses of fMRI data

Sun, F. T., Miller, L. M., & D’Esposito, M. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.09.056 · Cited by 406 · see citing works

Microstructural Organization of the Cingulum Tract and the Level of Default Mode Functional Connectivity

van den Heuvel, M., Mandl, R., Luigjes, J., & Hulshoff Pol, H. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2964-08.2008 · Cited by 349 · see citing works

Typical and atypical development of functional human brain networks: insights from resting-state fMRI

Uddin, L. Q. (2010) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2010.00021 · Cited by 343 · see citing works

Diffusion tensor imaging using single‐shot SENSE‐EPI

Bammer, R., Auer, M., Keeling, S. L., Augustin, M., Stables, L. A., PROKESCH, R. W., Stollberger, R., Moseley, M. E., & Fazekas, F. (2002) · Magnetic Resonance in Medicine · doi:10.1002/mrm.10184 · Cited by 279 · see citing works

Altered intrinsic functional connectivity of anterior and posterior insula regions in high-functioning participants with autism spectrum disorder

Ebisch, S. J. H., D, V. G. M., Willems, R. M., Mantini, D., Groen, W. B., Romani, G. L., Buitelaar, J. K., & Harold Bekkering, A. (2010) · Human Brain Mapping · doi:10.1002/hbm.21085 · Cited by 278 · see citing works

Changes in the interaction of resting-state neural networks from adolescence to adulthood

Stevens, M. C., Pearlson, G. D., & Calhoun, V. D. (2009) · Human Brain Mapping · doi:10.1002/hbm.20673 · Cited by 256 · see citing works

The identification of interacting networks in the brain using fMRI: Model selection, causality and deconvolution

Roebroeck, A. F., Formisano, E., & Goebel, R. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.09.036 · Cited by 238 · see citing works

Frontal parietal control network regulates the anti‐correlated default and dorsal attention networks

Gao, W., & Lin, W. (2011) · Human Brain Mapping · doi:10.1002/hbm.21204 · Cited by 216 · see citing works

Relationship Between Cingulo-Insular Functional Connectivity and Autistic Traits in Neurotypical Adults

Di Martino, A., Shehzad, Z., Kelly, C., Roy, A. K., Gee, D. G., Uddin, L. Q., Gotimer, K., Klein, D. F., Castellanos, F. X., & Milham, M. P. (2009) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2009.08121894 · Cited by 213 · see citing works

Residual functional connectivity in the split-brain revealed with resting-state functional MRI

Uddin, L. Q., Mooshagian, E., Zaidel, E., Scheres, A., Margulies, D. S., Kelly, A. M. C., Shehzad, Z., Adelstein, J. S., Castellanos, F. X., Biswal, B. B., et al. (2008) · NeuroReport · doi:10.1097/wnr.0b013e3282fb8203 · Cited by 170 · see citing works

Diffusion Tensor Imaging

CASCIO, C. J., GERIG, G., & PIVEN, J. (2007) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1097/01.chi.0000246064.93200.e8 · Cited by 167 · see citing works

White matter atlases based on diffusion tensor imaging

Mori, S., Oishi, K., & Faria, A. V. (2009) · Current Opinion in Neurology · doi:10.1097/wco.0b013e32832d954b · Cited by 166 · see citing works

Distributed and causal influence of frontal operculum in task control

Higo, T., Mars, R. B., Boorman, E. D., Buch, E. R., & Rushworth, M. F. S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1013361108 · Cited by 164 · see citing works

Instantaneous and causal connectivity in resting state brain networks derived from functional MRI data

Deshpande, G., Santhanam, P., & Hu, X. P. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.09.024 · Cited by 163 · see citing works

A Continuous Tensor Field Approximation of Discrete DT-MRI Data for Extracting Microstructural and Architectural Features of Tissue

Pajevic, S., Aldroubi, A., & Basser, P. J. (2002) · Journal of Magnetic Resonance · doi:10.1006/jmre.2001.2452 · Cited by 148 · see citing works

Resting-state networks in awake five- to eight-year old children

de Bie, H. M. A., Boersma, M., Adriaanse, S., Veltman, D. J., Wink, A. M., Roosendaal, S. D., Barkhof, F., Stam, C. J., Oostrom, K. J., Delemarre‐van de Waal, H. A., et al. (2012) · Human Brain Mapping · doi:10.1002/hbm.21280 · Cited by 143 · see citing works

Multivariate dynamical systems models for estimating causal interactions in fMRI

Ryali, S., Supekar, K., Chen, T., & Menon, V. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.09.052 · Cited by 110 · see citing works

The effect of intra- and inter-subject variability of hemodynamic responses on group level Granger causality analyses

Schippers, M. B., Renken, R. J., & Keysers, C. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.02.008 · Cited by 105 · see citing works

Measuringin VivoMyelination of Human White Matter Fiber Tracts with Magnetization Transfer MR

Rademacher, J., Engelbrecht, V., Bürgel, U., Freund, H., & Zilles, K. (1999) · NeuroImage · doi:10.1006/nimg.1998.0416 · Cited by 94 · see citing works

Neural correlates of the development of cognitive control

Bunge, S. A., & Crone, E. A. (2009) · Cambridge University Press eBooks · doi:10.1017/cbo9780511757402.005 · Cited by 73 · see citing works

Strength of default mode resting‐state connectivity relates to white matter integrity in children

Gordon, E. M., Lee, P. S., Maisog, J. M., Foss‐Feig, J. H., Billington, M. E., VanMeter, J. W., & Vaidya, C. J. (2010) · Developmental Science · doi:10.1111/j.1467-7687.2010.01020.x · Cited by 62 · see citing works

Network Analysis: Applications for the Developing Brain

Chu, C. J., Kramer, M., Bianchi, M. T., Caviness, V. S., & Cash, S. S. (2011) · Journal of Child Neurology · doi:10.1177/0883073810385345 · Cited by 26 · see citing works

Untitled work

Basser (2000) · doi:10.1002/1522-2594(200010)44:4

Network hubs in the human brain

van den Heuvel, M. P., & Sporns, O. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.09.012 · Cited by 2,123 · 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

Structure and Function of the Human Insula

Uddin, L. Q., Nomi, J. S., Hébert-Seropian, B., Ghaziri, J., & Boucher, O. (2017) · Journal of Clinical Neurophysiology · doi:10.1097/wnp.0000000000000377 · Cited by 1,262 · see citing works

Demystifying cognitive flexibility: Implications for clinical and developmental neuroscience

Dajani, D. R., & Uddin, L. Q. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.07.003 · Cited by 1,046 · see citing works

The salience network is responsible for switching between the default mode network and the central executive network: replication from DCM

Goulden, N., Khusnulina, A., Davis, N. J., Bracewell, R. M., Bokde, A. L., McNulty, J. P., & Mullins, P. G. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.05.052 · Cited by 810 · see citing works

Intrinsic Architecture Underlying the Relations among the Default, Dorsal Attention, and Frontoparietal Control Networks of the Human Brain

Spreng, R. N., Sepulcre, J., Turner, G. R., Stevens, W. D., & Schacter, D. L. (2013) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00281 · Cited by 668 · see citing works

Salience Network–Based Classification and Prediction of Symptom Severity in Children With Autism

Uddin, L. Q., Supekar, K., Lynch, C. J., Khouzam, A., Phillips, J., Feinstein, C., Ryali, S., & Menon, V. (2013) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2013.104 · Cited by 621 · see citing works

Salience network integrity predicts default mode network function after traumatic brain injury

Bonnelle, V., Ham, T. E., Leech, R., Kinnunen, K. M., Mehta, M. A., Greenwood, R. J., & Sharp, D. J. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1113455109 · Cited by 606 · 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

Topological organization of the human brain functional connectome across the lifespan

Cao, M., Wang, J.-H., Dai, Z.-J., Cao, X.-Y., Jiang, L.-L., Fan, F.-M., Song, X.-W., Xia, M.-R., Shu, N., Dong, Q., et al. (2014) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2013.11.004 · Cited by 440 · see citing works

Development of large-scale functional networks from birth to adulthood: A guide to the neuroimaging literature

Grayson, D. S., & Fair, D. A. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.01.079 · Cited by 411 · see citing works

Growing a social brain

Atzil, S., Gao, W., Fradkin, I., & Barrett, L. F. (2018) · Nature Human Behaviour · doi:10.1038/s41562-018-0384-6 · Cited by 415 · see citing works

Insular dysfunction within the salience network is associated with severity of symptoms and aberrant inter-network connectivity in major depressive disorder

Manoliu, A., Meng, C., Brandl, F., Doll, A., Tahmasian, M., Scherr, M., Schwerthöffer, D., Zimmer, C., Förstl, H., Bäuml, J., et al. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00930 · Cited by 382 · see citing works

Task-Based Core-Periphery Organization of Human Brain Dynamics

Bassett, D. S., Wymbs, N. F., Rombach, M. P., Porter, M. A., Mucha, P. J., & Grafton, S. T. (2013) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003171 · Cited by 356 · see citing works

Resting-state functional connectivity of subgenual anterior cingulate cortex in depressed adolescents

Connolly, C. G., Wu, J., Ho, T. C., Hoeft, F., Wolkowitz, O., Eisendrath, S., Frank, G., Hendren, R., Max, J. E., Paulus, M. P., et al. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.05.036 · Cited by 356 · see citing works

The contribution of network organization and integration to the development of cognitive control

Marek, S., Hwang, K., Foran, W., Hallquist, M. N., & Luna, B. (2015) · PLOS Biology · doi:10.1371/journal.pbio.1002328 · Cited by 337 · see citing works

Revisiting the role of the insula in addiction

Droutman, V., Read, S. J., & Bechara, A. (2015) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2015.05.005 · Cited by 317 · see citing works

Developmental changes in large-scale network connectivity in autism

Nomi, J. S., & Uddin, L. Q. (2015) · NeuroImage: Clinical · doi:10.1016/j.nicl.2015.02.024 · Cited by 274 · see citing works

Beyond the Tripartite Cognition–Emotion–Interoception Model of the Human Insular Cortex

Uddin, L. Q., Kinnison, J., Pessoa, L., & Anderson, M. L. (2014) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00462 · Cited by 275 · see citing works

The implications of brain connectivity in the neuropsychology of autism

Maximo, J. O., Cadena, E. J., & Kana, R. K. (2014) · Neuropsychology Review · doi:10.1007/s11065-014-9250-0 · Cited by 259 · see citing works

Functional alignment with anatomical networks is associated with cognitive flexibility

Medaglia, J. D., Huang, W., Karuza, E. A., Kelkar, A., Thompson-Schill, S. L., Ribeiro, A., & Bassett, D. S. (2017) · Nature Human Behaviour · doi:10.1038/s41562-017-0260-9 · Cited by 223 · see citing works

Annual research review: growth connectomics--the organization and reorganization of brain networks during normal and abnormal development

Vértes, P. E., & Bullmore, E. T. (2015) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.12365 · Cited by 197 · see citing works

Developmental changes in brain network hub connectivity in late adolescence

Baker, S. T. E., Lubman, D. I., Yucel, M., Allen, N. B., Whittle, S., Fulcher, B. D., Zalesky, A., & Fornito, A. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.5043-14.2015 · Cited by 168 · see citing works

Structural and functional rich club organization of the brain in children and adults

Grayson, D. S., Ray, S., Carpenter, S., Iyer, S., Dias, T. G. C., Stevens, C., Nigg, J. T., & Fair, D. A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0088297 · Cited by 187 · see citing works

Disruption of anterior insula modulation of large-scale brain networks in schizophrenia

Moran, L. V., Tagamets, M. A., Sampath, H., O’Donnell, A., Stein, E. A., Kochunov, P., & Hong, L. E. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.02.029 · Cited by 181 · see citing works

Adolescent Neurodevelopment and Vulnerability to Psychosis

Patel, P. K., Leathem, L. D., Currin, D. L., & Karlsgodt, K. H. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.06.028 · Cited by 152 · 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

Insular dysfunction reflects altered between-network connectivity and severity of negative symptoms in schizophrenia during psychotic remission

Manoliu, A., Riedl, V., Doll, A., Bäuml, J. G., Mühlau, M., Schwerthöffer, D., Scherr, M., Zimmer, C., Förstl, H., Bäuml, J., et al. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00216 · Cited by 128 · see citing works

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Kaunhoven, R. J., & Dorjee, D. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.01.007 · Cited by 130 · see citing works

Adolescent nicotine induces persisting changes in development of neural connectivity.

Smith, R. F., McDonald, C. G., Bergstrom, H. C., Ehlinger, D. G., & Brielmaier, J. M. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.05.019 · Cited by 120 · see citing works

Brain Mechanisms Supporting Flexible Cognition and Behavior in Adolescents With Autism Spectrum Disorder

Uddin, L. Q. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.05.010 · Cited by 116 · see citing works

Predicting individual brain maturity using dynamic functional connectivity

Qin, J., Chen, S.-G., Hu, D., Zeng, L.-L., Fan, Y.-M., Chen, X.-P., & Shen, H. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00418 · Cited by 117 · see citing works

Altered connectivity of the right anterior insula drives the pain connectome changes in chronic knee osteoarthritis

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 · see citing works

Associations between white matter microstructure and infants' working memory

Short, S. J., Elison, J. T., Goldman, B. D., Styner, M., Gu, H., Connelly, M., Maltbie, E., Woolson, S., Lin, W., Gerig, G., et al. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.09.021 · Cited by 105 · see citing works

Insula response and connectivity during social and non-social attention in children with autism

Odriozola, P., Uddin, L. Q., Lynch, C. J., Kochalka, J., Chen, T., & Menon, V. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsv126 · Cited by 95 · see citing works

Amygdala subnuclei resting-state functional connectivity sex and estrogen differences

Engman, J., Linnman, C., Van Dijk, K. R. A., & Milad, M. R. (2016) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.09.012 · Cited by 89 · see citing works

The link between testosterone and amygdala-orbitofrontal cortex connectivity in adolescent alcohol use

Peters, S., Jolles, D. J., Duijvenvoorde, A. C. K. V., Crone, E. A., & Peper, J. S. (2015) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.01.004 · Cited by 88 · see citing works

Neurofunctional maps of the ‘maternal brain’ and the effects of oxytocin: a multimodal voxel-based meta-analysis

Rocchetti, M., Radua, J., Paloyelis, Y., Xenaki, L., Frascarelli, M., Caverzasi, E., Politi, P., & Fusar‐Poli, P. (2014) · Psychiatry and Clinical Neurosciences · doi:10.1111/pcn.12185 · Cited by 83 · see citing works

Neurostructural abnormalities in pediatric anxiety disorders

Strawn, J. R., Hamm, L., Fitzgerald, D. A., Fitzgerald, K. D., Monk, C. S., & Phan, K. L. (2015) · Journal of Anxiety Disorders · doi:10.1016/j.janxdis.2015.03.004 · Cited by 81 · see citing works

Development of brain networks and relevance of environmental and genetic factors: A systematic review

Richmond, S., Johnson, K. A., Seal, M. L., Allen, N. B., & Whittle, S. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.08.024 · Cited by 70 · see citing works

Resting-state time-varying analysis reveals aberrant variations of functional connectivity in autism

Yao, Z., Hu, B., Xie, Y., Zheng, F., Liu, G., Chen, X., & Zheng, W. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00463 · Cited by 74 · see citing works

Differentially disrupted functional connectivity of the subregions of the inferior parietal lobule in Alzheimer’s disease

Wang, Z., Xia, M., Dai, Z., Liang, X., Song, H., He, Y., & Li, K. (2015) · Brain Structure and Function · doi:10.1007/s00429-013-0681-9 · Cited by 73 · see citing works

Correlations between social–emotional feelings and anterior insula activity are independent from visceral states but influenced by culture

Immordino-Yang, M. H., Yang, X.-F., & Damasio, H. (2014) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2014.00728 · Cited by 67 · see citing works

Aberrant development of functional connectivity among resting state-related functional networks in medication-naive ADHD children

Choi, J., Jeong, B., Lee, S. W., & Go, H.-J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0083516 · Cited by 58 · see citing works

Hyperconnectivity of the right posterior temporo-parietal junction predicts social difficulties in boys with autism spectrum disorder

Chien, H., Lin, H., Lai, M., Gau, S. S., & Tseng, W. I. (2015) · Autism Research · doi:10.1002/aur.1457 · Cited by 54 · see citing works

Morphological brain measures of cortico‐limbic inhibition related to resilience

Gupta, A., Love, A., Kilpatrick, L. A., Labus, J. S., Bhatt, R., Chang, L., Tillisch, K., Naliboff, B., & Mayer, E. A. (2017) · Journal of Neuroscience Research · doi:10.1002/jnr.24007 · Cited by 54 · see citing works

Dysfunction between dorsal caudate and salience network associated with impaired cognitive flexibility in obsessive-compulsive disorder: A resting-state fMRI study

Tomiyama, H., Nakao, T., Murayama, K., Nemoto, K., Ikari, K., Yamada, S., Kuwano, M., Hasuzawa, S., Togao, O., Hiwatashi, A., et al. (2019) · NeuroImage: Clinical · doi:10.1016/j.nicl.2019.102004 · Cited by 47 · see citing works

Underconnectivity Between Visual and Salience Networks and Links With Sensory Abnormalities in Autism Spectrum Disorders

Jao Keehn, R. J., Pueschel, E. B., Gao, Y., Jahedi, A., Alemu, K., Carper, R., Fishman, I., & Müller, R.-A. (2021) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2020.02.007 · Cited by 34 · see citing works

Salience network dynamics underlying successful resistance of temptation

Steimke, R., Nomi, J. S., Calhoun, V. D., Stelzel, C., Paschke, L. M., Gaschler, R., Goschke, T., Walter, H., & Uddin, L. Q. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsx123 · Cited by 30 · see citing works

Reduced functional connectivity to the frontal cortex during processing of social cues in autism spectrum disorder

Hoffmann, E., Brück, C., Kreifelts, B., Ethofer, T., & Wildgruber, D. (2016) · Journal of Neural Transmission · doi:10.1007/s00702-016-1544-3 · Cited by 30 · see citing works

Measuring Cognitive Flexibility with the Flexible Item Selection Task: From fMRI Adaptation to Individual Connectome Mapping

Dajani, D. R., Odriozola, P., Winters, M., Voorhies, W., Marcano, S., Baez, A., Gates, K. M., Dick, A. S., & Uddin, L. Q. (2020) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01536 · Cited by 27 · see citing works

Effects of Physical Exercise Breaks on Executive Function in a Simulated Classroom Setting: Uncovering a Window into the Brain

Yu, Q., Zhang, Z., Ludyga, S., Erickson, K. I., Cheval, B., Hou, M., Pindus, D. M., Hillman, C. H., Kramer, A. F., Falck, R. S., et al. (2025) · Advanced Science · doi:10.1002/advs.202406631 · Cited by 27 · see citing works

Creative thinking and brain network development in schoolchildren

Duval, P. E., Fornari, E., Décaillet, M., Ledoux, J., Beaty, R. E., & Denervaud, S. (2023) · Developmental Science · doi:10.1111/desc.13389 · Cited by 15 · see citing works

Infraslow closed-loop brain training for anxiety and depression (ISAD): a protocol for a randomized, double-blind, sham-controlled pilot trial in adult females with internalizing disorders

Perez, T. M., Glue, P., Adhia, D. B., Navid, M. S., Zeng, J., Dillingham, P., Smith, M., Niazi, I. K., Young, C. K., & De Ridder, D. (2022) · Trials · doi:10.1186/s13063-022-06863-z · Cited by 8 · see citing works

Changes in default mode network connectivity in patients with postmastectomy syndrome

Ternovykh, I., Bukkieva, T., Kasumova, A. A., et al. (2021) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2021.118307

Functional connectivity tracks clinical deterioration in Alzheimer's disease

Damoiseaux, J. S., Prater, K. E., Miller, B. L., & Greicius, M. D. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.06.024 · Cited by 504 · see citing works

Preliminary findings of altered functional connectivity of the default mode network linked to functional outcomes one year after pediatric traumatic brain injury

Stephens, J. A., Salorio, C. F., Barber, A. D., Risen, S., Mostofsky, S. H., & Suskauer, S. J. (2017) · Developmental Neurorehabilitation · doi:10.1080/17518423.2017.1338777 · Cited by 29 · see citing works

Functional Connectivity in Glioma patients using Resting State fMRI: Effect on Default Mode and Attention Networks

Jain, R., & Tordjman, M. (2020) · doi:10.26226/morressier.5e8335ba7cb08a046ef7c724

Negative BOLD Response and Functional Connectivity in the Default Mode Network are Representative of Two Overlapping but Separate Neurophysiological Processes (P4.191)

Parker, D., & Razlighi, Q. R. (2018) · Neurology · doi:10.1212/wnl.90.15_supplement.p4.191