The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.
Uncovering Intrinsic Modular Organization of Spontaneous Brain Activity in Humans
Open accessAbstract
The characterization of topological architecture of complex brain networks is one of the most challenging issues in neuroscience. Slow (<0.1 Hz), spontaneous fluctuations of the blood oxygen level dependent (BOLD) signal in functional magnetic resonance imaging are thought to be potentially important for the reflection of spontaneous neuronal activity. Many studies have shown that these fluctuations are highly coherent within anatomically or functionally linked areas of the brain. However, the underlying topological mechanisms responsible for these coherent intrinsic or spontaneous fluctuations are still poorly understood. Here, we apply modern network analysis techniques to investigate how spontaneous neuronal activities in the human brain derived from the resting-state BOLD signals are topologically organized at both the temporal and spatial scales. We first show that the spontaneous brain functional networks have an intrinsically cohesive modular structure in which the connections between regions are much denser within modules than between them. These identified modules are found to be closely associated with several well known functionally interconnected subsystems such as the somatosensory/motor, auditory, attention, visual, subcortical, and the "default" system. Specifically, we demonstrate that the module-specific topological features can not be captured by means of computing the corresponding global network parameters, suggesting a unique organization within each module. Finally, we identify several pivotal network connectors and paths (predominantly associated with the association and limbic/paralimbic cortex regions) that are vital for the global coordination of information flow over the whole network, and we find that their lesions (deletions) critically affect the stability and robustness of the brain functional system. Together, our results demonstrate the highly organized modular architecture and associated topological properties in the temporal and spatial brain functional networks of the human brain that underlie spontaneous neuronal dynamics, which provides important implications for our understanding of how intrinsically coherent spontaneous brain activity has evolved into an optimal neuronal architecture to support global computation and information integration in the absence of specific stimuli or behaviors.
Overview
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
Verification
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.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Emergence of Scaling in Random Networks
Barabási, A.-L., & Albert, R. (1999) · Science · doi:10.1126/science.286.5439.509 · Cited by 36,135
Finding and evaluating community structure in networks
Newman, M. E. J., & Girvan, M. (2004) · Physical Review E · doi:10.1103/physreve.69.026113 · Cited by 13,931
Control of goal-directed and stimulus-driven attention in the brain
Corbetta, M., & Shulman, G. L. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn755 · Cited by 12,881
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
Functional connectivity in the motor cortex of resting human brain using echo‐planar mri
Biswal, B., Zerrin Yetkin, F., Haughton, V. M., & Hyde, J. S. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910340409 · Cited by 9,812
The Brain's Default Network: Anatomy, Function, and Relevance to Disease
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
Error and attack tolerance of complex networks
Albert, R., Jeong, H., & Barabási, A.-L. (2000) · Nature · doi:10.1038/35019019 · Cited by 7,534
Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging
Fox, M. D., & Raichle, M. E. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2201 · Cited by 6,700
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
(2023) · doi:10.1126/science · Cited by 6,063
Research works printed but not linked: 52
- Y He, 2007, Regional coherence changes in the early stages of Alzheimer's disease: a combined structural and resting-state functional MRI study., Neuroimage, 35, 488, 10.1016/j.neuroimage.2006.11.042 · DOI · Paper page
- AM Wink, 2006, Age and cholinergic effects on hemodynamics and functional coherence of human hippocampus., Neurobiology of Aging, 27, 1395, 10.1016/j.neurobiolaging.2005.08.011 · DOI
- KJ Friston, 1993, Functional connectivity: the principal-component analysis of large (PET) data sets., J Cereb Blood Flow Metab, 13, 5, 10.1038/jcbfm.1993.4 · DOI · Paper page
- T Jiang, 2004, Modulation of functional connectivity during the resting state and the motor task., Hum Brain Mapp, 22, 63, 10.1002/hbm.20012 · DOI
- MJ Lowe, 1998, Functional connectivity in single and multislice echoplanar imaging using resting-state fluctuations., Neuroimage, 7, 119, 10.1006/nimg.1997.0315 · DOI · Paper page
- D Cordes, 2001, Frequencies Contributing to Functional Connectivity in the Cerebral Cortex in “Resting-state” Data., AJNR Am J Neuroradiol, 22, 1326
- MD Fox, 2005, The human brain is intrinsically organized into dynamic, anticorrelated functional networks., Proc Natl Acad Sci U S A, 102, 9673, 10.1073/pnas.0504136102 · DOI · Paper page
- R Salvador, 2005, Neurophysiological architecture of functional magnetic resonance images of human brain., Cereb Cortex, 15, 1332, 10.1093/cercor/bhi016 · DOI · Paper page
- V Kiviniemi, 2003, Independent component analysis of nondeterministic fMRI signal sources., Neuroimage, 19, 253, 10.1016/S1053-8119(03)00097-1 · DOI · Paper page
- M De Luca, 2006, fMRI resting state networks define distinct modes of long-distance interactions in the human brain., NeuroImage, 29, 1359, 10.1016/j.neuroimage.2005.08.035 · DOI · Paper page
- SH Strogatz, 2001, Exploring complex networks., Nature, 410, 268, 10.1038/35065725 · DOI · Paper page
- S Boccaletti, 2006, Complex networks: structure and dynamics., Phys Reports, 175, 10.1016/j.physrep.2005.10.009 · DOI · Paper page
- S Achard, 2006, A resilient, low-frequency, small-world human brain functional network with highly connected association cortical hubs., J Neurosci, 26, 63, 10.1523/JNEUROSCI.3874-05.2006 · DOI · Paper page
- J Wang, 2008, Parcellation-dependent small-world brain functional networks: A resting-state fMRI study., Hum Brain Mapp
- Y Liu, 2008, Disrupted small-world networks in schizophrenia., Brain, 131, 945, 10.1093/brain/awn018 · DOI · Paper page
- L Wang, 2008, Altered small-world brain functional networks in children with attention-deficit/hyperactivity disorder., Hum Brain Mapp
- Y He, 2007, Small-world anatomical networks in the human brain revealed by cortical thickness from MRI., Cereb Cortex, 17, 2407, 10.1093/cercor/bhl149 · DOI · Paper page
- G Gong, 2008, Mapping Anatomical Connectivity Patterns of Human Cerebral Cortex Using In Vivo Diffusion Tensor Imaging Tractography., Cereb Cortex
- R Guimera, 2005, The worldwide air transportation network: Anomalous centrality, community structure, and cities' global roles., Proc Natl Acad Sci U S A, 102, 7794, 10.1073/pnas.0407994102 · DOI · Paper page
- JD Han, 2004, Evidence for dynamically organized modularity in the yeast protein-protein interaction network., Nature, 430, 88, 10.1038/nature02555 · DOI · Paper page
- LH Hartwell, 1999, From molecular to modular cell biology., Nature, 402, C47, 10.1038/35011540 · DOI · Paper page
- JW Scannell, 1999, The connectional organization of the cortico-thalamic system of the cat., Cereb Cortex, 9, 277, 10.1093/cercor/9.3.277 · DOI · Paper page
- C Zhou, 2006, Hierarchical organization unveiled by functional connectivity in complex brain networks., Phys Rev Lett, 97, 238103, 10.1103/PhysRevLett.97.238103 · DOI · Paper page
- ZJ Chen, 2008, Revealing Modular Architecture of Human Brain Structural Networks by Using Cortical Thickness from MRI., Cereb Cortex
- AJ Schwarz, 2008, Community structure and modularity in networks of correlated brain activity., Magn Reson Imaging, 26, 914, 10.1016/j.mri.2008.01.048 · DOI
- L Ferrarini, 2008, Hierarchical functional modularity in the resting-state human brain., Hum Brain Mapp
- D Meunier, 2009, Age-related changes in modular organization of human brain functional networks., Neuroimage, 44, 715, 10.1016/j.neuroimage.2008.09.062 · DOI · Paper page
- N Tzourio-Mazoyer, 2002, Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single-subject brain., Neuroimage, 15, 273, 10.1006/nimg.2001.0978 · DOI · Paper page
- R Guimera, 2005, Cartography of complex networks: modules and universal roles., J Stat Mech Theor Exp, P02001
- R Guimera, 2004, Modularity from fluctuations in random graphs and complex networks., Phys Rev E Stat Nonlin Soft Matter Phys, 70, 025101, 10.1103/PhysRevE.70.025101 · DOI · Paper page
- P Fransson, 2005, Spontaneous low-frequency BOLD signal fluctuations: an fMRI investigation of the resting-state default mode of brain function hypothesis., Hum Brain Mapp, 26, 15, 10.1002/hbm.20113 · DOI · Paper page
- CJ Stam, 2007, Small-world networks and functional connectivity in Alzheimer's disease., Cereb Cortex, 17, 92, 10.1093/cercor/bhj127 · DOI · Paper page
- DJ Watts, 1998, Collective dynamics of ‘small-world’ networks., Nature, 393, 440, 10.1038/30918 · DOI · Paper page
- V Latora, 2001, Efficient behavior of small-world networks., Phys Rev Lett, 87, 198701, 10.1103/PhysRevLett.87.198701 · DOI · Paper page
- R Guimera, 2007, Classes of complex networks defined by role-to-role connectivity profiles., Nat Phys, 3, 63, 10.1038/nphys489 · DOI · Paper page
- LC Freeman, 1977, A set of measures of centrality based upon betweenness., Sociometry, 35, 10.2307/3033543 · DOI · Paper page
- M Kaiser, 2004, Edge vulnerability in neural and metabolic networks., Biol Cybern, 90, 311, 10.1007/s00422-004-0479-1 · DOI
- JA Bullinaria, 2007, Understanding the emergence of modularity in neural systems., Cognitive Science, 31, 673, 10.1080/15326900701399939 · DOI
- O Sporns, 2000, Theoretical neuroanatomy: relating anatomical and functional connectivity in graphs and cortical connection matrices., Cereb Cortex, 10, 127, 10.1093/cercor/10.2.127 · DOI · Paper page
- R Kotter, 2003, Network participation indices: characterizing component roles for information processing in neural networks., Neural Netw, 16, 1261, 10.1016/j.neunet.2003.06.002 · DOI
- O Sporns, 2007, Identification and classification of hubs in brain networks., PLoS ONE, 2, e1049, 10.1371/journal.pone.0001049 · DOI · Paper page
- HB Fraser, 2005, Modularity and evolutionary constraint on proteins., Nat Genet, 37, 351, 10.1038/ng1530 · DOI
- V Spirin, 2006, A metabolic network in the evolutionary context: multiscale structure and modularity., Proc Natl Acad Sci U S A, 103, 8774, 10.1073/pnas.0510258103 · DOI
- A Hintze, 2008, Evolution of complex modular biological networks., PLoS Comput Biol, 4, e23, 10.1371/journal.pcbi.0040023 · DOI
- CJ Honey, 2007, Network structure of cerebral cortex shapes functional connectivity on multiple time scales., Proc Natl Acad Sci U S A, 104, 10240, 10.1073/pnas.0701519104 · DOI · Paper page
- R Salvador, 2005, Undirected graphs of frequency-dependent functional connectivity in whole brain networks., Philos Trans R Soc Lond B Biol Sci, 360, 937, 10.1098/rstb.2005.1645 · DOI · Paper page
- MX Cohen, 2008, Covariance-based subdivision of the human striatum using T1-weighted MRI., Eur J Neurosci, 27, 1534, 10.1111/j.1460-9568.2008.06117.x · DOI
- AL Cohen, 2008, Defining functional areas in individual human brains using resting functional connectivity MRI., Neuroimage, 41, 45, 10.1016/j.neuroimage.2008.01.066 · DOI · Paper page
- KE Stephan, 2003, Lateralized cognitive processes and lateralized task control in the human brain., Science, 301, 384, 10.1126/science.1086025 · DOI · Paper page
- RM Birn, 2006, Separating respiratory-variation-related fluctuations from neuronal-activity-related fluctuations in fMRI., Neuroimage, 31, 1536, 10.1016/j.neuroimage.2006.02.048 · DOI · Paper page
- LD-G Danon, 2005, Comparing community structure identification., J Stat mech Theor Exp, P09008
- DC Van Essen, 2005, A Population-Average, Landmark- and Surface-based (PALS) atlas of human cerebral cortex., Neuroimage, 28, 635, 10.1016/j.neuroimage.2005.06.058 · DOI · Paper page
Cited by
Functional Network Organization of the Human Brain
Power, J. D., Cohen, A. L., Nelson, S. M., Wig, G. S., Barnes, K. A., Church, J. A., Vogel, A. C., Laumann, T. O., Miezin, F. M., Schlaggar, B. L., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.006 · Cited by 4,124
BrainNet Viewer: A Network Visualization Tool for Human Brain Connectomics
Xia, M., Wang, J., & He, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068910 · Cited by 4,106
Self-citationThe economy of brain network organization
Bullmore, E., & Sporns, O. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3214 · Cited by 3,284
Toward discovery science of human brain function
Biswal, B. B., Mennes, M., Zuo, X.-N., Gohel, S., Kelly, C., Smith, S. M., Beckmann, C. F., Adelstein, J. S., Buckner, R. L., Colcombe, S., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911855107 · Cited by 2,970
Self-citationModular and hierarchically modular organization of brain networks
Meunier, D., Lambiotte, R., & Bullmore, E. T. (2010) · Frontiers in Neuroscience · doi:10.3389/fnins.2010.00200 · Cited by 1,156
Precuneus shares intrinsic functional architecture in humans and monkeys
Margulies, D. S., Vincent, J. L., Kelly, C., Lohmann, G., Uddin, L. Q., Biswal, B. B., Villringer, A., Castellanos, F. X., Milham, M. P., & Petrides, M. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905314106 · Cited by 965
The development of human functional brain networks
Power, J. D., Fair, D. A., Schlaggar, B. L., & Petersen, S. E. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.017 · Cited by 751
Evidence for hubs in human functional brain networks
Power, J. D., Schlaggar, B. L., Lessov-Schlaggar, C. N., & Petersen, S. E. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.035 · Cited by 716
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
Liang, X., Zou, Q., He, Y., & Yang, Y. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1214900110 · Cited by 677
Self-citationGraph-based network analysis of resting-state functional MRI
Wang, J. (2010) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2010.00016 · Cited by 614
Self-citationKapogiannis, D., & Mattson, M. P. (2011) · The Lancet Neurology · doi:10.1016/s1474-4422(10)70277-5 · Cited by 594
Betzel, R. F., & Bassett, D. S. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2016.11.006 · Cited by 587
Brain hyperconnectivity in children with autism and its links to social deficits
Supekar, K., Uddin, L. Q., Khouzam, A., Phillips, J., Gaillard, W. D., Kenworthy, L. E., Yerys, B. E., Vaidya, C. J., & Menon, V. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.10.001 · Cited by 538
Networks of anatomical covariance
Evans, A. C. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.05.054 · Cited by 429
Self-citationBraun, U., Plichta, M. M., Esslinger, C., Sauer, C., Haddad, L., Grimm, O., Mier, D., Mohnke, S., Heinz, A., Erk, S., et al. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.08.044 · Cited by 424
Wang, J.-H., Zuo, X.-N., Gohel, S., Milham, M. P., Biswal, B. B., & He, Y. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021976 · Cited by 416
Self-citationMachine learning in major depression: from classification to treatment outcome prediction
Gao, S., Calhoun, V. D., & Sui, J. (2018) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13048 · Cited by 370
Krienen, F. M., Yeo, B. T. T., & Buckner, R. L. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0526 · Cited by 372
Brain activity at rest: a multiscale hierarchical functional organization
Doucet, G., Naveau, M., Petit, L., Delcroix, N., Zago, L., Crivello, F., Jobard, G., Tzourio-Mazoyer, N., Mazoyer, B., Mellet, E., et al. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00895.2010 · Cited by 319
Temporal and spatial evolution of brain network topology during the first two years of life
Gao, W., Gilmore, J. H., Giovanello, K. S., Smith, J. K., Shen, D., Zhu, H., & Lin, W. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025278 · Cited by 272
Liang, X., Zou, Q., He, Y., & Yang, Y. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhu316 · Cited by 261
Wang, L., Dai, Z., Peng, H., Tan, L., Ding, Y., He, Z., Zhang, Y., Xia, M., Li, Z., Li, W., et al. (2014) · Human Brain Mapping · doi:10.1002/hbm.22241 · Cited by 236
Self-citationDevelopment 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
Kapogiannis, D., Reiter, D. A., Willette, A. A., & Mattson, M. P. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.09.029 · Cited by 211
Changes in Community Structure of Resting State Functional Connectivity in Unipolar Depression
Lord, A., Horn, D., Breakspear, M., & Walter, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041282 · Cited by 174
Wang, L., Xia, M., Li, K., Zeng, Y., Su, Y., Dai, W., Zhang, Q., Jin, Z., Mitchell, P. B., Yu, X., et al. (2015) · Human Brain Mapping · doi:10.1002/hbm.22663 · Cited by 166
Self-citationShin, D.-J., Jung, W. H., He, Y., Wang, J., Shim, G., Byun, M. S., Jang, J. H., Kim, S. N., Lee, T. Y., Park, H. Y., et al. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.09.002 · Cited by 162
Self-citationHou, J.-M., Zhao, M., Zhang, W., Song, L.-H., Wu, W.-J., Wang, J., Zhou, D.-Q., Xie, B., He, M., Guo, J.-W., et al. (2014) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.130220 · Cited by 163
Self-citationUehara, T., Yamasaki, T., Okamoto, T., Koike, T., Kan, S., Miyauchi, S., Kira, J.-I., & Tobimatsu, S. (2014) · Cerebral Cortex · doi:10.1093/cercor/bht004 · Cited by 136
Pereira, J. B., Mijalkov, M., Kakaei, E., Mecocci, P., Vellas, B., Tsolaki, M., Kłoszewska, I., Soininen, H., Spenger, C., Lovestone, S., et al. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw128 · Cited by 142
Wang, Y., Wang, J., Jia, Y., Zhong, S., Zhong, M., Sun, Y., Niu, M., Zhao, L., Zhao, L., Pan, J., et al. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.117 · Cited by 133
Self-citationAbnormal small-world architecture of top-down control networks in obsessive-compulsive disorder
Zhang, T. (2011) · Journal of Psychiatry & Neuroscience · doi:10.1503/jpn.100006 · Cited by 134
Information processing architecture of functionally defined clusters in the macaque cortex
Shen, K., Bezgin, G., Hutchison, R. M., Gati, J. S., Menon, R. S., Everling, S., & McIntosh, A. R. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.2709-12.2012 · Cited by 123
Intrinsic Functional Brain Architecture Derived from Graph Theoretical Analysis in the Human Fetus
Thomason, M. E., Brown, J. A., Dassanayake, M. T., Shastri, R., Marusak, H. A., Hernandez-Andrade, E., Yeo, L., Mody, S., Berman, S., Hassan, S. S., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0094423 · Cited by 130
Jiang, X., Shen, Y., Yao, J., Zhang, L., Xu, L., Feng, R., Cai, L., Liu, J., Chen, W., & Wang, J. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0467-9 · Cited by 120
Self-citationHan, K., Mac Donald, C. L., Johnson, A. M., Barnes, Y., Wierzechowski, L., Zonies, D., Oh, J., Flaherty, S., Fang, R., Raichle, M. E., et al. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.08.017 · Cited by 123
Sun, Y., Yin, Q., Fang, R., Yan, X., Wang, Y., Bezerianos, A., Tang, H., Miao, F., & Sun, J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096505 · Cited by 122
Self-citationA Monte Carlo evaluation of weighted community detection algorithms
Gates, K. M., Henry, T., Steinley, D., & Fair, D. A. (2016) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2016.00045 · Cited by 106
“Given the exceptional performance on large graphs (on the order of thousands), neuroimagers routinely apply community detection algorithms to graphs with node size on the order of hundreds (e.g., Power et al., 2011) and smaller (e.g., He et al., 2009).”
MethodPredicting 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
Ginestet, C. E., & Simmons, A. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.11.030 · Cited by 112
Yokoi, T., Watanabe, H., Yamaguchi, H., Bagarinao, E., Masuda, M., Imai, K., Ogura, A., Ohdake, R., Kawabata, K., Hara, K., et al. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00304 · Cited by 116
Kang, J., Wang, L., Yan, C., Wang, J., Liang, X., & He, Y. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.03.033 · Cited by 111
Self-citationRubia, K., Criaud, M., Wulff, M., Alegria, A., Brinson, H., Barker, G., Stahl, D., & Giampietro, V. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2018.11.055 · Cited by 111
Kim, K., Kim, S.-W., Myung, W., Han, C. E., Fava, M., Mischoulon, D., Papakostas, G. I., Seo, S. W., Cho, H., Seong, J.-K., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-15926-0 · Cited by 107
Functional properties of resting state networks in healthy full-term newborns
De Asis-Cruz, J., Bouyssi-Kobar, M., Evangelou, I., Vezina, G., & Limperopoulos, C. (2015) · Scientific Reports · doi:10.1038/srep17755 · Cited by 85
Graph theoretical analysis of developmental patterns of the white matter network
Chen, Z., Liu, M., Gross, D. W., & Beaulieu, C. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00716 · Cited by 77
Self-citationAltered brain network modules induce helplessness in major depressive disorder
Peng, D., Shi, F., Shen, T., Peng, Z., Zhang, C., Liu, X., Qiu, M., Liu, J., Jiang, K., Fang, Y., et al. (2014) · Journal of Affective Disorders · doi:10.1016/j.jad.2014.05.061 · Cited by 76
Balancing the Brain: Resting State Networks and Deep Brain Stimulation
Kringelbach, M. L., Green, A. L., & Aziz, T. Z. (2011) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2011.00008 · Cited by 72
Hosseini, S. M. H., & Kesler, S. R. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.04.032 · Cited by 59
Reconfiguration of Cortical Networks in MDD Uncovered by Multiscale Community Detection with fMRI
He, Y., Lim, S., Fortunato, S., Sporns, O., Zhang, L., Qiu, J., Xie, P., & Zuo, X.-N. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhx335 · Cited by 54
Self-citationAn, J., Wang, L., Li, K., Zeng, Y., Su, Y., Jin, Z., Yu, X., & Si, T. (2017) · Scientific Reports · doi:10.1038/s41598-017-10575-9 · Cited by 48
Self-citationDesign of a hierarchy modular neural network and its application in multimodal emotion recognition
Li, W., Chu, M., & Qiao, J. (2019) · Soft Computing · doi:10.1007/s00500-018-03735-0 · Cited by 13
Metadata
- Authors
- He, Y., Wang, J., Wang, L., Chen, Z. J., Yan, C., Yang, H., Tang, H., Zhu, C., Gong, Q., Zang, Y., & Evans, A. C.
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2009-04-21
- Volume
- 4
- Issue
- 4
- Pages
- e5226
- ISSN
- 1932-6203 (ISSN-L)
- OpenAlex
- W2028645759
- Cited by
- 630
- References
- 31
- FWCI
- 19.03
- Type
- journal article
- Language
- en
- Open access
- gold
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
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.