Modeling the impact of lesions in the human brain
Open accessAbstract
Lesions of anatomical brain networks result in functional disturbances of brain systems and behavior which depend sensitively, often unpredictably, on the lesion site. The availability of whole-brain maps of structural connections within the human cerebrum and our increased understanding of the physiology and large-scale dynamics of cortical networks allow us to investigate the functional consequences of focal brain lesions in a computational model. We simulate the dynamic effects of lesions placed in different regions of the cerebral cortex by recording changes in the pattern of endogenous ("resting-state") neural activity. We find that lesions produce specific patterns of altered functional connectivity among distant regions of cortex, often affecting both cortical hemispheres. The magnitude of these dynamic effects depends on the lesion location and is partly predicted by structural network properties of the lesion site. In the model, lesions along the cortical midline and in the vicinity of the temporo-parietal junction result in large and widely distributed changes in functional connectivity, while lesions of primary sensory or motor regions remain more localized. The model suggests that dynamic lesion effects can be predicted on the basis of specific network measures of structural brain networks and that these effects may be related to known behavioral and cognitive consequences of brain lesions.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Simulated dynamic effects of lesions varied in size and spatial pattern depending on lesion location, with midline, temporoparietal junction, and superior frontal gyrus lesions tending to have the greatest effect on neural dynamics.
“Simulated dynamic effects of lesions varied in size and spatial pattern depending on the lesion location, with lesions in the midline as well as those involving the temporoparietal junction and superior frontal gyrus tending to have the greatest effect on neural dynamics.”
From Graph theory analysis of complex brain networks: new concepts in brain mapping applied to neurosurgery (2016) · cites this paper as [4]
In general, lesions reduced functional connectivity, with effects most pronounced in the ipsilateral hemisphere, but also extending nonlocally to the contralateral hemisphere.
“In general, lesions reduced functional connectivity, with effects most pronounced in the ipsilateral hemisphere, but also extending in a nonlocal manner to the contralateral hemisphere.”
From Graph theory analysis of complex brain networks: new concepts in brain mapping applied to neurosurgery (2016) · cites this paper as [4]
The extent that alterations of the structural network produced dynamic consequences was most accurately predicted by injury to the DMN rather than by the degree or strength of connections directly incorporated by the lesion.
“the extent that alterations of the structural network produced dynamic consequences was most accurately predicted by injury to the DMN rather than, for instance, the degree or strength of connections directly incorporated by the lesion.”
From Graph theory analysis of complex brain networks: new concepts in brain mapping applied to neurosurgery (2016) · cites this paper as [4]
Simulation experiments using structure-function models predict that purely focal and transient perturbations in activity result in diffuse network reorganization affecting distant brain systems.
“simulation experiments using structure-function models have predicted that even purely focal and transient perturbations in activity should result in diffuse network reorganization that affects distant brain systems (Alstott et al., 2009; Honey and Sporns, 2008; Misic et al., 2015).”
From Development of large-scale functional networks from birth to adulthood: A guide to the neuroimaging literature (2017) · cites this paper as Alstott et al., 2009
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
A default mode of brain function
Raichle, M. E., MacLeod, A. M., Snyder, A. Z., Powers, W. J., Gusnard, D. A., & Shulman, G. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.2.676 · Cited by 12,190 · see citing works
Complex brain networks: graph theoretical analysis of structural and functional systems
Bullmore, E., & Sporns, O. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2575 · Cited by 11,820 · see citing works
Self-citationA set of measures of centrality based upon betweenness
Freeman, L. (1977) · Sociometry · doi:10.2307/3033543 · Cited by 10,557 · see citing works
<i>The Brain's Default Network</i>: <i>Anatomy, Function, and Relevance to Disease</i>
Buckner, R. L., Andrews‐Hanna, J. R., & Schacter, D. L. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1440.011 · Cited by 9,761 · see citing works
Network biology: understanding the cell's functional organization
Barabási, A.-L., & Oltvai, Z. N. (2004) · Nature Reviews Genetics · doi:10.1038/nrg1272 · Cited by 7,903 · 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
Error and attack tolerance of complex networksPreprint
Albert, R., Jeong, H., & Barabási, A.-Ĺ. (2000) · Cited by 6,554 · 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
Cognitive and emotional influences in anterior cingulate cortex
Bush, G., Luu, P., & Posner, M. I. (2000) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01483-2 · Cited by 6,259 · see citing works
Lethality and centrality in protein networks
Jeong, H., Mason, S., Barabási, A., & Oltvai, Z. (2001) · Nature · doi:10.1038/35075138 · Cited by 5,327 · see citing works
Efficient behavior of small-world networks
Latora, V., & Marchiori, M. (2001) · Physical Review Letters · doi:10.1103/physrevlett.87.198701 · Cited by 5,119 · see citing works
Spectral Analysis and its Applications.
Freiberger, W. F., Jenkins, G. M., & Watts, D. G. (1969) · Journal of the American Statistical Association · doi:10.2307/2286100 · Cited by 5,022 · 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-citationDISCONNEXION SYNDROMES IN ANIMALS AND MAN
Geschwind, N. (1965) · Brain · doi:10.1093/brain/88.2.237 · Cited by 3,419 · 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
Self-citationThe Human Connectome: A Structural Description of the Human Brain
Sporns, O., Tononi, G., & Kötter, R. (2005) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0010042 · Cited by 3,260 · see citing works
Self-citationBuckner, R. L., Sepulcre, J., Talukdar, T., Krienen, F. M., Liu, H., Hedden, T., Andrews-Hanna, J. R., Sperling, R. A., & Johnson, K. A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5062-08.2009 · Cited by 2,862 · see citing works
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
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
Self-citationPrinciples of Behavioral and Cognitive Neurology
(2000) · doi:10.1093/oso/9780195134759.001.0001 · Cited by 1,448 · see citing works
Whitfield-Gabrieli, S., Thermenos, H. W., Milanovic, S., Tsuang, M. T., Faraone, S. V., McCarley, R. W., Shenton, M. E., Green, A. I., Nieto-Castanon, A., LaViolette, P., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809141106 · Cited by 1,435 · see citing works
Identification and classification of hubs in brain networks
Sporns, O., Honey, C. J., & Kötter, R. (2007) · PLoS ONE · doi:10.1371/journal.pone.0001049 · Cited by 1,165 · see citing works
Self-citationNonlinear Responses in fMRI: The Balloon Model, Volterra Kernels, and Other Hemodynamics
Friston, K. J., Mechelli, A., Turner, R., & Price, C. J. (2000) · NeuroImage · doi:10.1006/nimg.2000.0630 · Cited by 1,131 · see citing works
Gong, G., He, Y., Concha, L., Lebel, C., Gross, D. W., Evans, A. C., & Beaulieu, C. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn102 · Cited by 1,112 · see citing works
Network thinking in ecology and evolution
Proulx, S. R., Promislow, D., & PHILLIPS, P. (2005) · Trends in Ecology & Evolution · doi:10.1016/j.tree.2005.04.004 · Cited by 941 · see citing works
He, B. J., Snyder, A. Z., Vincent, J. L., Epstein, A. A., Shulman, G. L., & Corbetta, M. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.013 · Cited by 916 · see citing works
Neural basis and recovery of spatial attention deficits in spatial neglect
Corbetta, M., Kincade, M. J., Lewis, C., Snyder, A. Z., & Sapir, A. (2005) · Nature Neuroscience · doi:10.1038/nn1574 · Cited by 892 · see citing works
Lesion analysis in neuropsychology
Damásio, H., & Damásio, A. R. (1989) · Oxford University Press eBooks · Cited by 881 · see citing works
Spatial awareness is a function of the temporal not the posterior parietal lobe
Karnath, H., Ferber, S., & Himmelbach, M. (2001) · Nature · doi:10.1038/35082075 · Cited by 813 · see citing works
Mapping Human Whole-Brain Structural Networks with Diffusion MRI
Hagmann, P., Kurant, M., Gigandet, X., Thiran, P., Wedeen, V. J., Meuli, R., & Thiran, J.-P. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000597 · Cited by 788 · see citing works
Self-citationDiffusion MRI : from quantitative measurement to in vivo neuroanatomy
Johansen‐Berg, H., & Behrens, T. E. J. (2014) · doi:10.1016/b978-0-12-374709-9.x0001-6 · Cited by 703 · see citing works
Functional connectivity of the angular gyrus in normal reading and dyslexia
Horwitz, B., Rumsey, J. M., & Donohue, B. C. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.15.8939 · Cited by 607 · see citing works
Noise during Rest Enables the Exploration of the Brain's Dynamic Repertoire
Ghosh, A., Rho, Y.-A., McIntosh, A. R., Kötter, R., & Jirsa, V. (2008) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000196 · Cited by 550 · see citing works
Lesion Analysis in Neuropsychology
Poeck, K. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90028-9 · Cited by 528 · see citing works
Studying the human brain anatomical network via diffusion-weighted MRI and graph theory
Iturria-Medina, Y., Sotero, R. C., Canales-Rodríguez, E. J., Alemán-Gómez, Y., & Melie-García, L. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2007.10.060 · Cited by 506 · see citing works
The “robust yet fragile” nature of the Internet
Doyle, J. C., Alderson, D., Li, L., Low, S. H., Roughan, M., Shalunov, S., Tanaka, R., & Willinger, W. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501426102 · Cited by 475 · see citing works
Small‐world properties of nonlinear brain activity in schizophrenia
Rubinov, M., Knock, S. A., Stam, C. J., Micheloyannis, S., Harris, A. W. F., Williams, L. M., & Breakspear, M. J. (2007) · Human Brain Mapping · doi:10.1002/hbm.20517 · Cited by 458 · see citing works
Self-citationDie Lokalisation im Grosshirn und der Abbau der Funktion durch Kortikale Herde.
(1914) · JAMA · doi:10.1001/jama.1914.02570090083033 · Cited by 453 · see citing works
Measuring brain connectivity: Diffusion tensor imaging validates resting state temporal correlations
Skudlarski, P., Jagannathan, K., Calhoun, V. D., Hampson, M., Skudlarska, B. A., & Pearlson, G. D. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.07.063 · Cited by 450 · 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-citationJohnston, J. M., Vaishnavi, S. N., Smyth, M. D., Zhang, D., He, B. J., Zempel, J. M., Shimony, J. S., Snyder, A. Z., & Raichle, M. E. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0573-08.2008 · Cited by 296 · see citing works
Bartolomei, F., Bosma, I., Klein, M., Baayen, J. C., Reijneveld, J. C., Postma, T. J., Heimans, J. J., van Dijk, B. W., de Munck, J. C., de Jongh, A., et al. (2006) · Clinical Neurophysiology · doi:10.1016/j.clinph.2006.05.018 · Cited by 276 · see citing works
Simulation of robustness against lesions of cortical networks
Kaiser, M., Martin, R., Andras, P., & Young, M. P. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05574.x · Cited by 244 · see citing works
Breakspear, M. J., Terry, J. R., & Friston, K. J. (2003) · Network Computation in Neural Systems · doi:10.1088/0954-898x/14/4/305 · Cited by 176 · see citing works
Self-citationResidual 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
Breakspear, M. J., Terry, J. R., & Friston, K. J. (2003) · Network Computation in Neural Systems · doi:10.1088/0954-898x_14_4_305 · Cited by 107 · see citing works
Self-citationEdge vulnerability in neural and metabolic networks
Kaiser, M., & Hilgetag, C. C. (2004) · Biological Cybernetics · doi:10.1007/s00422-004-0479-1 · Cited by 106 · see citing works
On imputing function to structure from the behavioural effects of brain lesions
Young, M. P., Hilgetag, C. C., & Scannell, J. W. (2000) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2000.0555 · Cited by 103 · see citing works
(2001) · Cambridge University Press eBooks · doi:10.1017/cbo9780511586521 · Cited by 62 · see citing works
Rubinov, M., McIntosh, A. R., Valenzuela, M., & Breakspear, M. J. (2008) · American Journal of Geriatric Psychiatry · doi:10.1097/jgp.0b013e318187137a · Cited by 37 · see citing works
Self-citationConnectivity‐Based Parcellation of the Cortical Mantle Usingq‐Ball Diffusion Imaging
Perrin, M., Cointepas, Y., Cachia, A., Poupon, C., Thirion, B., Rivière, D., Cathier, P., Kouby, V. E., Constantinesco, A., Bihan, D. L., et al. (2008) · International Journal of Biomedical Imaging · doi:10.1155/2008/368406 · Cited by 32 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Large-scale brain networks and psychopathology: a unifying triple network model
Menon, V. (2011) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2011.08.003 · Cited by 4,168 · see citing works
Functional and Effective Connectivity: A Review
Friston, K. J. (2011) · Brain Connectivity · doi:10.1089/brain.2011.0008 · Cited by 3,415 · see citing works
The economy of brain network organization
Bullmore, E., & Sporns, O. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3214 · Cited by 3,284 · see citing works
Self-citationNetwork 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
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
The connectomics of brain disorders
Fornito, A., Zalesky, A., & Breakspear, M. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3901 · Cited by 1,734 · 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
Self-citationControllability 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
Disruptions of network connectivity predict impairment in multiple behavioral domains after stroke
Siegel, J. S., Ramsey, L. E., Snyder, A. Z., Metcalf, N. V., Chacko, R. V., Weinberger, K., Baldassarre, A., Hacker, C. D., Shulman, G. L., & Corbetta, M. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1521083113 · Cited by 656 · see citing works
Boveroux, P., Vanhaudenhuyse, A., Bruno, M.-A., Noirhomme, Q., Lauwick, S., Luxen, A., Degueldre, C., Plenevaux, A., Schnakers, C., Phillips, C., et al. (2010) · Anesthesiology · doi:10.1097/aln.0b013e3181f697f5 · Cited by 630 · see citing works
Can structure predict function in the human brain?
Honey, C. J., Thivierge, J.-P., & Sporns, O. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.01.071 · Cited by 629 · see citing works
Self-citationA 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-citationFunctional network disruption in the degenerative dementias
Pievani, M., de Haan, W., Wu, T., Seeley, W. W., & Frisoni, G. B. (2011) · The Lancet Neurology · doi:10.1016/s1474-4422(11)70158-2 · Cited by 481 · see citing works
Intrinsic Coupling Modes: Multiscale Interactions in Ongoing Brain Activity
Engel, A. K., Gerloff, C., Hilgetag, C. C., & Nolte, G. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.038 · Cited by 471 · see citing works
Grayson, D. S., & Fair, D. A. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.01.079 · Cited by 411 · see citing works
“As an example, simulation experiments using structure-function models have predicted that even purely focal and transient perturbations in activity should result in diffuse network reorganization that affects distant brain systems (Alstott et al., 2009; Honey and Sporns, 2008; Misic et al., 2015).”
MethodBrain reward circuitry beyond the mesolimbic dopamine system: a neurobiological theory
Ikemoto, S. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.02.001 · Cited by 454 · see citing works
Exploring the network dynamics underlying brain activity during rest
Cabral, J., Kringelbach, M. L., & Deco, G. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.12.005 · Cited by 351 · see citing works
Mathematical framework for large-scale brain network modeling in The Virtual Brain
Sanz-Leon, P., Knock, S. A., Spiegler, A., & Jirsa, V. K. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.01.002 · Cited by 356 · see citing works
Duffau, H. (2014) · Cortex · doi:10.1016/j.cortex.2013.08.005 · Cited by 331 · see citing works
Key, B. (2016) · Animal Sentience · doi:10.51291/2377-7478.1011 · Cited by 318 · see citing works
Mapping 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
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
Insects have the capacity for subjective experience
Klein, C., & Barron, A. B. (2016) · Animal Sentience · doi:10.51291/2377-7478.1113 · Cited by 243 · see citing works
Adachi, Y., Osada, T., Sporns, O., Watanabe, T., Matsui, T., Miyamoto, K., & Miyashita, Y. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr234 · Cited by 211 · see citing works
Self-citationStructural disconnections explain brain network dysfunction after stroke
Griffis, J. C., Metcalf, N. V., Corbetta, M., & Shulman, G. L. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.07.100 · Cited by 213 · see citing works
Ekstrom, A. D., Huffman, D. J., & Starrett, M. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00531.2017 · Cited by 186 · see citing works
Mapping Connectivity Damage in the Case of Phineas Gage
Van Horn, J. D., Irimia, A., Torgerson, C. M., Chambers, M. C., Kikinis, R., & Toga, A. W. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037454 · Cited by 196 · 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
Revisiting the global workspace orchestrating the hierarchical organization of the human brain
Deco, G., Vidaurre, D., & Kringelbach, M. L. (2021) · Nature Human Behaviour · doi:10.1038/s41562-020-01003-6 · Cited by 162 · see citing works
Grayson, D. S., Bliss-Moreau, E., Machado, C. J., Bennett, J., Shen, K., Grant, K. A., Fair, D. A., & Amaral, D. G. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.005 · Cited by 172 · 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
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
Computational and dynamic models in neuroimaging
Friston, K. J., & Dolan, R. J. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.12.068 · Cited by 131 · see citing works
Caeyenberghs, K., Leemans, A., Heitger, M. H., Leunissen, I., Dhollander, T., Sunaert, S., Dupont, P., & Swinnen, S. P. (2012) · Brain · doi:10.1093/brain/aws048 · Cited by 129 · see citing works
Kringelbach, M. L., Perl, Y. S., Tagliazucchi, E., & Deco, G. (2023) · Science Advances · doi:10.1126/sciadv.ade6049 · Cited by 105 · see citing works
Principles of recovery from traumatic brain injury: Reorganization of functional networks
Castellanos, N. P., Leyva, I., Buldú, J. M., Bajo, R., Paúl, N., Cuesta, P., Ordóñez, V. E., Pascua, C. L., Boccaletti, S., Maestú, F., et al. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.12.046 · Cited by 96 · see citing works
Brain functional connectivity correlates of coping styles
Santarnecchi, E., Sprugnoli, G., Tatti, E., Mencarelli, L., Neri, F., Momi, D., Di Lorenzo, G., Pascual-Leone, A., Rossi, S., & Rossi, A. (2018) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/s13415-018-0583-7 · Cited by 85 · see citing works
Age-specific effects of voluntary exercise on memory and the older brain
Siette, J., Westbrook, R. F., Cotman, C., Sidhu, K., Zhu, W., Sachdev, P., & Valenzuela, M. J. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.05.034 · Cited by 78 · see citing works
Fellrath, J., Mottaz, A., Schnider, A., Guggisberg, A. G., & Ptak, R. (2016) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2016.07.012 · Cited by 77 · 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
Functional Neuroimaging in Traumatic Brain Injury: From Nodes to Networks
Medaglia, J. D. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00407 · Cited by 63 · see citing works
Disturbed Small-World Networks and Neurocognitive Function in Frontal Lobe Low-Grade Glioma Patients
Huang, Q., Zhang, R., Hu, X., Ding, S., Qian, J., Lei, T., Cao, X., Tao, L., Qian, Z., & Liu, H. (2014) · PLoS ONE · doi:10.1371/journal.pone.0094095 · Cited by 55 · see citing works
Tian, L., Meng, C., Yan, H., Zhao, Q., Liu, Q., Yan, J., Han, Y., Yuan, H., Wang, L., Yue, W., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028794 · Cited by 44 · see citing works
- Authors
- Alstott, J., Breakspear, M., Hagmann, P., Cammoun, L., & Sporns, O.
- Affiliations
- Indiana University Bloomington (US)
- Black Dog Institute (AU)
- École Polytechnique (FR)
- Corresponding author
- Sporns, Olaf
- Venue
- PLoS Computational Biology
- Publisher
- Public Library of Science (PLoS)
- Published
- 2009-06-12
- Volume
- 5
- Issue
- 6
- Pages
- e1000408
- ISSN
- 1553-734X (ISSN-L)
- 1553-7358
- PMC
- PMC2688028
- OpenAlex
- W2088905367
- Cited by
- 561
- References
- 51
- Citations by year
- 2026: 14 · 2025: 25 · 2024: 28 · 2023: 34 · 2022: 40 · 2021: 42 · 2020: 28 · 2019: 33 · 2018: 28 · 2017: 54 · 2016: 47 · 2015: 30 · 2014: 39 · 2013: 38 · 2012: 31
- FWCI
- 13.07
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- PLoS Computational Biology (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- IRIS (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion, cc-by-nc-nd)
- SERVAL (Université de Lausanne) (submittedVersion, other-oa)
- Funders
- National Science Foundation
- James S. McDonnell Foundation
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- Université de Lausanne
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Keywords
- brain lesions, functional connectivity, resting-state brain activity, cortical networks, structural connectivity, temporoparietal junction, network metrics, computational models of the brain, hemispheric lateralization
- MeSH terms
- Algorithms, Brain Diseases, Brain Mapping, Cerebral Cortex, Computer Simulation, Humans, Models, Neurological, Nerve Net, Reproducibility of Results
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review