Rich-club organization of the human connectome
Open accessAbstract
The human brain is a complex network of interlinked regions. Recent studies have demonstrated the existence of a number of highly connected and highly central neocortical hub regions, regions that play a key role in global information integration between different parts of the network. The potential functional importance of these "brain hubs" is underscored by recent studies showing that disturbances of their structural and functional connectivity profile are linked to neuropathology. This study aims to map out both the subcortical and neocortical hubs of the brain and examine their mutual relationship, particularly their structural linkages. Here, we demonstrate that brain hubs form a so-called "rich club," characterized by a tendency for high-degree nodes to be more densely connected among themselves than nodes of a lower degree, providing important information on the higher-level topology of the brain network. Whole-brain structural networks of 21 subjects were reconstructed using diffusion tensor imaging data. Examining the connectivity profile of these networks revealed a group of 12 strongly interconnected bihemispheric hub regions, comprising the precuneus, superior frontal and superior parietal cortex, as well as the subcortical hippocampus, putamen, and thalamus. Importantly, these hub regions were found to be more densely interconnected than would be expected based solely on their degree, together forming a rich club. We discuss the potential functional implications of the rich-club organization of the human connectome, particularly in light of its role in information integration and in conferring robustness to its structural core.
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Rich-club organization has been observed in several mesoscale connectomes: in humans, other mammals and light-level (not synaptic resolution) connectomes in Drosophila.
“Rich-club organization has been observed in several mesoscale connectomes: in humans, other mammals8,9,17 and light-level (not synaptic resolution) connectomes in Drosophila18,19.”
From Network statistics of the whole-brain connectome of Drosophila (2024) · cites this paper as [8]
Connectomic rich club networks have high centrality and interconnectivity that may allow systems with mostly local connections to achieve both integrated and differentiated processing.
“In terms of neuronal architecture, van den Heuvel and Sporns (2011) have identified connectomic “rich club” networks, whose high centrality and interconnectivity may allow systems with mostly local connections to achieve both integrated and differentiated processing (Sporns, 2013).”
From An Integrated World Modeling Theory (IWMT) of Consciousness (2020) · cites this paper as van den Heuvel and Sporns (2011)
The distribution of connections between hubs is often significantly nonrandom, with highly connected hubs even more strongly connected to each other in a so-called rich club.
“Furthermore, the distribution of connections between such hubs is often found to be significantly nonrandom, with highly connected hubs even more strongly connected to each other in a so-called “rich club.”97”
From Graph theory analysis of complex brain networks: new concepts in brain mapping applied to neurosurgery (2016) · cites this paper as [97]
The dynamics of the default mode, salience and frontoparietal control networks form the computational core of a brain's dynamic internal working model of the body in the world, entraining sensory and motor systems to create multi-sensory representations of the world at various time scales from the perspective of someone who has a body, all in the service of allostasis.
“My key hypothesis is that the dynamics of the default mode, salience and frontoparietal control networks form the computational core of a brain’s dynamic internal working model of the body in the world, entraining sensory and motor systems to create multi-sensory representations of the world at various time scales from the perspective of someone who has a body, all in the service of allostasis (”
From The theory of constructed emotion: an active inference account of interoception and categorization (2016) · cites this paper as van den Heuvel and Sporns, 2011
Cites
Modularity and community structure in networks
Newman, M. E. J. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601602103 · Cited by 12,256 · see citing works
Error and attack tolerance of complex networks
Albert, R., Jeong, H., & Barabási, A.-L. (2000) · Nature · doi:10.1038/35019019 · Cited by 7,534 · 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
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
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
Self-citationEfficiency of Functional Brain Networks and Intellectual Performance
van den Heuvel, M. P., Stam, C. J., Kahn, R. S., & Hulshoff Pol, H. E. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1443-09.2009 · Cited by 1,078 · see citing works
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
Dynamical consequences of lesions in cortical networks
Honey, C. J., & Sporns, O. (2008) · Human Brain Mapping · doi:10.1002/hbm.20579 · Cited by 353 · see citing works
Self-citationvan 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
A DTI-Derived Measure of Cortico-Cortical Connectivity
Zalesky, A., & Fornito, A. (2009) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2008.2012113 · Cited by 141 · see citing works
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The brain's default mode network
Raichle, M. E. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071013-014030 · Cited by 3,904 · see citing works
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Bullmore, E., & Sporns, O. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3214 · Cited by 3,284 · see citing works
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Self-citationStructural and Functional Brain Networks: From Connections to Cognition
Park, H.-J., & Friston, K. (2013) · Science · doi:10.1126/science.1238411 · Cited by 2,106 · see citing works
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Fornito, A., Zalesky, A., & Breakspear, M. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3901 · Cited by 1,734 · see citing works
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Barrett, L. F., & Simmons, W. K. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3950 · Cited by 1,766 · see citing works
Function in the human connectome: task-fMRI and individual differences in behavior
Barch, D. M., Burgess, G. C., Harms, M. P., Petersen, S. E., Schlaggar, B. L., Corbetta, M., Glasser, M. F., Curtiss, S., Dixit, S., Feldt, C., et al. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.033 · Cited by 1,529 · see citing works
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Barrett, L. F. (2016) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsw154 · Cited by 1,426 · see citing works
“…sensory and motor systems to create multi-sensory representations of the world at various time scales from the perspective of someone who has a body, all in the service of allostasis (for evidence consistent with this view, see van den Heuvel et al. , 2012; van den Heuvel and Sporns, 2011, 2013).”
Sporns, O., & Betzel, R. F. (2016) · Annual Review of Psychology · doi:10.1146/annurev-psych-122414-033634 · Cited by 1,334 · see citing works
Self-citationNetwork attributes for segregation and integration in the human brain
Sporns, O. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.11.015 · Cited by 1,067 · see citing works
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Alexander-Bloch, A., Giedd, J. N., & Bullmore, E. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3465 · Cited by 1,064 · see citing works
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Smallwood, J., Bernhardt, B. C., Leech, R., Bzdok, D., Jefferies, E., & Margulies, D. S. (2021) · Nature Reviews Neuroscience · doi:10.1038/s41583-021-00474-4 · Cited by 935 · see citing works
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Barrett, L. F. (2017) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsx060 · Cited by 950 · see citing works
“…sensory and motor systems to create multi-sensory representations of the world at various time scales from the perspective of someone who has a body, all in the service of allostasis (for evidence consistent with this view, see van den Heuvel et al., 2012; van den Heuvel and Sporns, 2011, 2013).”
Controllability of structural brain networks
Gu, S., Pasqualetti, F., Cieslak, M., Telesford, Q. K., Yu, A. B., Kahn, A. E., Medaglia, J. D., Vettel, J. M., Miller, M. B., Grafton, S. T., et al. (2015) · Nature Communications · doi:10.1038/ncomms9414 · Cited by 912 · see citing works
Betzel, R. F., Byrge, L., He, Y., Goñi, J., Zuo, X.-N., & Sporns, O. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.07.067 · Cited by 807 · see citing works
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Kleckner, I. R., Zhang, J., Touroutoglou, A., Chanes, L., Xia, C., Simmons, W. K., Quigley, K. S., Dickerson, B. C., & Feldman Barrett, L. (2017) · Nature Human Behaviour · doi:10.1038/s41562-017-0069 · Cited by 641 · see citing works
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Petersen, S. E., & Sporns, O. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.027 · Cited by 553 · see citing works
Self-citationAn active inference theory of allostasis and interoception in depression
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An Integrative Model of the Maturation of Cognitive Control
Luna, B., Marek, S., Larsen, B., Tervo-Clemmens, B., & Chahal, R. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-034054 · Cited by 550 · see citing works
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Smith, R., Thayer, J. F., Khalsa, S. S., & Lane, R. D. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.02.003 · Cited by 523 · see citing works
Increased global functional connectivity correlates with LSD-induced ego dissolution
Tagliazucchi, E., Roseman, L., Kaelen, M., Orban, C., Muthukumaraswamy, S. D., Murphy, K., Laufs, H., Leech, R., McGonigle, J., Crossley, N., et al. (2016) · Current Biology · doi:10.1016/j.cub.2016.02.010 · Cited by 503 · see citing works
A cross-disorder connectome landscape of brain dysconnectivity
van den Heuvel, M. P., & Sporns, O. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0177-6 · Cited by 462 · see citing works
Self-citationA Predictive Network Model of Cerebral Cortical Connectivity Based on a Distance Rule
Ercsey-Ravasz, M., Markov, N. T., Lamy, C., Van Essen, D. C., Knoblauch, K., Toroczkai, Z., & Kennedy, H. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.036 · Cited by 487 · 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
The connectome of an insect brain
Winding, M., Pedigo, B. D., Barnes, C. L., Patsolic, H. G., Park, Y., Kazimiers, T., Fushiki, A., Andrade, I. V., Khandelwal, A., Valdes-Aleman, J., et al. (2023) · Science · doi:10.1126/science.add9330 · Cited by 435 · see citing works
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Medaglia, J. D., Lynall, M.-E., & Bassett, D. S. (2015) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_00810 · Cited by 419 · see citing works
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Baum, G. L., Ciric, R., Roalf, D. R., Betzel, R. F., Moore, T. M., Shinohara, R. T., Kahn, A. E., Vandekar, S. N., Rupert, P. E., Quarmley, M., et al. (2017) · Current Biology · doi:10.1016/j.cub.2017.04.051 · Cited by 401 · see citing works
Understanding brain networks and brain organization
Pessoa, L. (2014) · Physics of Life Reviews · doi:10.1016/j.plrev.2014.03.005 · Cited by 464 · see citing works
“Based on structural human brain data, van den Heuvel and Sporns[36] (p. 15784) proposed that “the aggregation of hubs [i.e., regions of high connectivity] into a rich club suggests that the communication hubs of the brain do not operate as individual entities, but instead act as a strongly interlinked collective” (see…”
BackgroundInfluentialAn anatomical substrate for integration among functional networks in human cortex
van den Heuvel, M. P., & Sporns, O. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.2128-13.2013 · Cited by 404 · see citing works
Self-citationToward a computational theory of conscious processing
Dehaene, S., Charles, L., King, J.-R., & Marti, S. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.12.005 · Cited by 404 · see citing works
Alzheimer's disease: connecting findings from graph theoretical studies of brain networks
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The Neonatal Connectome During Preterm Brain Development
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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
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
Rich-club organization of the newborn human brain
Ball, G., Aljabar, P., Zebari, S., Tusor, N., Arichi, T., Merchant, N., Robinson, E. C., Ogundipe, E., Rueckert, D., Edwards, A. D., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1324118111 · Cited by 360 · see citing works
Transdiagnostic impairment of cognitive control in mental illness
McTeague, L. M., Goodkind, M. S., & Etkin, A. (2016) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2016.08.001 · Cited by 368 · see citing works
Default Mode Dynamics for Global Functional Integration
Vatansever, D., Menon, D. K., Manktelow, A. E., Sahakian, B. J., & Stamatakis, E. A. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.2135-15.2015 · Cited by 333 · see citing works
van den Heuvel, M. P., Bullmore, E. T., & Sporns, O. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2016.03.001 · Cited by 328 · see citing works
Self-citationThe Rich Club of the<i>C. elegans</i>Neuronal Connectome
Towlson, E. K., Vértes, P. E., Ahnert, S. E., Schafer, W. R., & Bullmore, E. T. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3784-12.2013 · Cited by 343 · see citing works
Network neuroscience theory of human intelligence
Barbey, A. K. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2017.10.001 · Cited by 355 · see citing works
The parcellation-based connectome: limitations and extensions
de Reus, M. A., & van den Heuvel, M. P. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.03.053 · Cited by 282 · see citing works
Self-citationMapping neuroplastic potential in brain-damaged patients
Herbet, G., Maheu, M., Costi, E., Lafargue, G., & Duffau, H. (2016) · Brain · doi:10.1093/brain/awv394 · Cited by 289 · see citing works
The Multilayer Connectome of Caenorhabditis elegans
Bentley, B., Branicky, R., Barnes, C. L., Chew, Y. L., Yemini, E., Bullmore, E. T., Vértes, P. E., & Schafer, W. R. (2016) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1005283 · Cited by 269 · see citing works
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Yu, M., Sporns, O., & Saykin, A. J. (2021) · Nature Reviews Neurology · doi:10.1038/s41582-021-00529-1 · Cited by 265 · see citing works
Self-citationNormative brain size variation and brain shape diversity in humans
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Ball, G., Pazderova, L., Chew, A., Tusor, N., Merchant, N., Arichi, T., Allsop, J. M., Cowan, F. M., Edwards, A. D., & Counsell, S. J. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu331 · Cited by 234 · see citing works
Adolfi, F., Couto, B., Richter, F., Decety, J., Lopez, J., Sigman, M., Manes, F., & Ibáñez, A. (2017) · Cortex · doi:10.1016/j.cortex.2016.12.019 · Cited by 238 · see citing works
Optimally controlling the human connectome: the role of network topology
Betzel, R. F., Gu, S., Medaglia, J. D., Pasqualetti, F., & Bassett, D. S. (2016) · Scientific Reports · doi:10.1038/srep30770 · Cited by 247 · see citing works
Development of Human Brain Structural Networks Through Infancy and Childhood
Huang, H., Shu, N., Mishra, V., Jeon, T., Chalak, L., Wang, Z. J., Rollins, N., Gong, G., Cheng, H., Peng, Y., et al. (2015) · Cerebral Cortex · doi:10.1093/cercor/bht335 · Cited by 223 · see citing works
Architecture of the cerebral cortical association connectome underlying cognition
Bota, M., Sporns, O., & Swanson, L. W. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1504394112 · Cited by 231 · see citing works
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The contribution of geometry to the human connectome
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Childhood maltreatment: altered network centrality of cingulate, precuneus, temporal pole and insula
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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
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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
Hellyer, P. J., Scott, G., Shanahan, M., Sharp, D. J., & Leech, R. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4648-14.2015 · Cited by 187 · see citing works
Structural network alterations and neurological dysfunction in cerebral amyloid angiopathy
Reijmer, Y. D., Fotiadis, P., Martinez-Ramirez, S., Salat, D. H., Schultz, A., Shoamanesh, A., Ayres, A. M., Vashkevich, A., Rosas, D., Schwab, K., et al. (2015) · Brain · doi:10.1093/brain/awu316 · Cited by 181 · see citing works
Mapping Structural Connectivity Using Diffusion <scp>MRI</scp> : Challenges and Opportunities
Yeh, C., Jones, D. K., Liang, X., Descoteaux, M., & Connelly, A. (2021) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.27188 · Cited by 187 · see citing works
Smallwood, J., Karapanagiotidis, T., Ruby, F., Medea, B., de Caso, I., Konishi, M., Wang, H.-T., Hallam, G., Margulies, D. S., & Jefferies, E. (2016) · PLOS ONE · doi:10.1371/journal.pone.0152272 · Cited by 165 · see citing works
Historical pitfalls and new directions in the neuroscience of emotion
Barrett, L. F., & Satpute, A. B. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2017.07.045 · Cited by 180 · see citing works
Scholtens, L. H., Schmidt, R., de Reus, M. A., & van den Heuvel, M. P. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.0752-14.2014 · Cited by 160 · see citing works
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Müller, F., Dolder, P. C., Schmidt, A., Liechti, M. E., & Borgwardt, S. (2018) · NeuroImage: Clinical · doi:10.1016/j.nicl.2018.03.005 · Cited by 174 · see citing works
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Daianu, M., Jahanshad, N., Nir, T. M., Toga, A. W., Jack, C. R., Weiner, M. W., & Thompson, F. T. A. D. (2013) · Brain Connectivity · doi:10.1089/brain.2012.0137 · Cited by 173 · see citing works
Drakesmith, M., Caeyenberghs, K., Dutt, A., Lewis, G., David, A. S., & Jones, D. K. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.05.011 · Cited by 157 · see citing works
Imaging human brain networks to improve the clinical efficacy of non-invasive brain stimulation
Sale, M. V., Mattingley, J. B., Zalesky, A., & Cocchi, L. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.09.010 · Cited by 145 · see citing works
Ray, S., Miller, M., Karalunas, S., Robertson, C., Grayson, D. S., Cary, R. P., Hawkey, E., Painter, J. G., Kriz, D., Fombonne, E., et al. (2014) · Human Brain Mapping · doi:10.1002/hbm.22603 · Cited by 149 · see citing works
Patejdl, R., Penner, I. K., Noack, T. K., & Zettl, U. K. (2016) · Autoimmunity Reviews · doi:10.1016/j.autrev.2015.11.005 · Cited by 141 · see citing works
Moon, J.-Y., Lee, U., Blain-Moraes, S., & Mashour, G. A. (2015) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1004225 · Cited by 136 · see citing works
Miranda-Dominguez, O., Mills, B. D., Grayson, D., Woodall, A., Grant, K. A., Kroenke, C. D., & Fair, D. A. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.4229-13.2014 · Cited by 130 · see citing works
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Powers, A. R., Kelley, M., & Corlett, P. R. (2016) · Biological Psychiatry: Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2016.04.003 · Cited by 138 · see citing works
van den Heuvel, M. P., de Reus, M. A., Feldman Barrett, L., Scholtens, L. H., Coopmans, F. M. T., Schmidt, R., Preuss, T. M., Rilling, J. K., & Li, L. (2015) · Human Brain Mapping · doi:10.1002/hbm.22828 · Cited by 131 · see citing works
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To, W. T., De Ridder, D., Hart Jr., J., & Vanneste, S. (2018) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2018.00128 · Cited by 135 · see citing works
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Bär, K.-J., de la Cruz, F., Schumann, A., Koehler, S., Sauer, H., Critchley, H., & Wagner, G. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.03.071 · Cited by 134 · see citing works
Safron, A. (2020) · Frontiers in Artificial Intelligence · doi:10.3389/frai.2020.00030 · Cited by 133 · see citing works
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Lin, A., Yang, R., Dorkenwald, S., Matsliah, A., Sterling, A. R., Schlegel, P., Yu, S.-C., McKellar, C. E., Costa, M., Eichler, K., et al. (2024) · Nature · doi:10.1038/s41586-024-07968-y · Cited by 147 · see citing works
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Kringelbach, M. L., Perl, Y. S., Tagliazucchi, E., & Deco, G. (2023) · Science Advances · doi:10.1126/sciadv.ade6049 · Cited by 105 · see citing works
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Baum, G. L., Roalf, D. R., Cook, P. A., Ciric, R., Rosen, A. F. G., Xia, C., Elliott, M. A., Ruparel, K., Verma, R., Tunç, B., et al. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.02.041 · Cited by 116 · see citing works
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Li, L., Hu, X., Preuss, T. M., Glasser, M. F., Damen, F. W., Qiu, Y., & Rilling, J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.04.024 · Cited by 109 · see citing works
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van den Heuvel, M. I., Turk, E., Manning, J. H., Hect, J., Hernandez-Andrade, E., Hassan, S. S., Romero, R., van den Heuvel, M. P., & Thomason, M. E. (2018) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2018.02.001 · Cited by 108 · see citing works
Albantakis, L., Hintze, A., Koch, C., Adami, C., & Tononi, G. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003966 · Cited by 101 · see citing works
Rayner, G., Jackson, G., & Wilson, S. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.09.022 · Cited by 104 · see citing works
Spoormaker, V. I., Gleiser, P. M., & Czisch, M. (2012) · Frontiers in Neurology · doi:10.3389/fneur.2012.00080 · Cited by 83 · see citing works
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Katsumi, Y., Theriault, J. E., Quigley, K. S., & Barrett, L. F. (2022) · Network Neuroscience · doi:10.1162/netn_a_00240 · Cited by 88 · see citing works
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De Asis-Cruz, J., Bouyssi-Kobar, M., Evangelou, I., Vezina, G., & Limperopoulos, C. (2015) · Scientific Reports · doi:10.1038/srep17755 · Cited by 85 · see citing works
Gaiteri, C., Chen, M., Szymanski, B., Kuzmin, K., Xie, J., Lee, C., Blanche, T., Chaibub Neto, E., Huang, S.-C., Grabowski, T., et al. (2015) · Scientific Reports · doi:10.1038/srep16361 · Cited by 76 · see citing works
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Meskaldji, D. E., Fischi-Gomez, E., Griffa, A., Hagmann, P., Morgenthaler, S., & Thiran, J.-P. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.04.084 · Cited by 77 · see citing works
Wirsich, J., Perry, A., Ridley, B., Proix, T., Golos, M., Bénar, C., Ranjeva, J.-P., Bartolomei, F., Breakspear, M., Jirsa, V., et al. (2016) · NeuroImage: Clinical · doi:10.1016/j.nicl.2016.05.010 · Cited by 77 · see citing works
Januszko, P., Niemcewicz, S., Gajda, T., Wołyńczyk-Gmaj, D., Piotrowska, A. J., Gmaj, B., Piotrowski, T., & Szelenberger, W. (2016) · Clinical Neurophysiology · doi:10.1016/j.clinph.2015.01.014 · Cited by 74 · see citing works
Hart, M. G., Ypma, R. J. F., Romero-Garcia, R., Price, S. J., & Suckling, J. (2016) · Journal of Neurosurgery · doi:10.3171/2015.4.jns142683 · Cited by 74 · see citing works
- Authors
- van den Heuvel, M. P., & Sporns, O.
- Affiliations
- Indiana University Bloomington (US)
- ORCID
- Sporns, Olaf
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2011-11-02
- Volume
- 31
- Issue
- 44
- Pages
- 15775-15786
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6623027
- OpenAlex
- W2012559638
- Cited by
- 2,354
- References
- 10
- Citations by year
- 2026: 112 · 2025: 147 · 2024: 135 · 2023: 153 · 2022: 205 · 2021: 185 · 2020: 188 · 2019: 207 · 2018: 166 · 2017: 196 · 2016: 202 · 2015: 184 · 2014: 129 · 2013: 98 · 2012: 41
- FWCI
- 44.52
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Pure Amsterdam UMC (publishedVersion, other-oa)
- Amsterdam UMC (VU Amsterdam) - Institutional Repository (submittedVersion, other-oa)
- Data Archiving and Networked Services (DANS) (submittedVersion, other-oa)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Physical Sciences › Physics and Astronomy › Statistical and Nonlinear Physics › Complex Network Analysis Techniques
- Keywords
- rich club, human connectome, brain network hubs, structural connectivity, brain network topology, precuneus, hippocampus, thalamus, putamen, information integration, network robustness, diffusion tensor imaging
- MeSH terms
- Adult, Brain, Brain Mapping, Female, Humans, Image Processing, Computer-Assisted, Male, Models, Neurological, Nerve Net, Neural Pathways, Young Adult, Diffusion Tensor Imaging
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