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Stepwise Connectivity of the Modal Cortex Reveals the Multimodal Organization of the Human Brain
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How human beings integrate information from external sources and internal cognition to produce a coherent experience is still not well understood. During the past decades, anatomical, neurophysiological and neuroimaging research in multimodal integration have stood out in the effort to understand the perceptual binding properties of the brain. Areas in the human lateral occipitotemporal, prefrontal, and posterior parietal cortices have been associated with sensory multimodal processing. Even though this, rather patchy, organization of brain regions gives us a glimpse of the perceptual convergence, the articulation of the flow of information from modality-related to the more parallel cognitive processing systems remains elusive. Using a method called stepwise functional connectivity analysis, the present study analyzes the functional connectome and transitions from primary sensory cortices to higher-order brain systems. We identify the large-scale multimodal integration network and essential connectivity axes for perceptual integration in the human brain.
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“Additionally, it has been demonstrated that aMCC is as a key region in a multimodal network that integrates information originating from primary sensory regions (e.g., visual, auditory, and somatosensory) (Sepulcre et al., 2012).”
From Motivation in the Service of Allostasis: The Role of Anterior Mid-Cingulate Cortex (2019) · cites this paper as Sepulcre et al., 2012
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“Moreover, the inverse correlation between the dorsal attention network and the default-mode network, interpreted by most as a sign of ‘competition’ between the processing of external and internal events in the mature brain106, also emerges during the first year of life112.”
From Imaging structural and functional brain development in early childhood (2018) · cites this paper as [112]
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Cites
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
Benjamini, Y., & Hochberg, Y. (1995) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1995.tb02031.x · Cited by 109,482
Receptive fields, binocular interaction and functional architecture in the cat’s visual cortex
Hubel, D. H., & Wiesel, T. N. (1962) · The Journal of Physiology · doi:10.1113/jphysiol.1962.sp006837 · Cited by 13,680
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
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
The organization of the human cerebral cortex estimated by intrinsic functional connectivity
Thomas Yeo, B. T., Krienen, F. M., Sepulcre, J., Sabuncu, M. R., Lashkari, D., Hollinshead, M., Roffman, J. L., Smoller, J. W., Zöllei, L., Polimeni, J. R., et al. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00338.2011 · Cited by 9,182
Self-citationThe 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
Distributed hierarchical processing in the primate cerebral cortex
Felleman, D. J., & Van Essen, D. C. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1 · Cited by 7,783
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
The organization of the human cerebellum estimated by intrinsic functional connectivity
Buckner, R. L., Krienen, F. M., Castellanos, A., Diaz, J. C., & Yeo, B. T. T. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00339.2011 · Cited by 7,304
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Items 101–200 of 323
Braga, R. M., & Leech, R. (2015) · The Neuroscientist · doi:10.1177/1073858415585730 · Cited by 42
Integration of visual and motor functional streams in the human brain
Sepulcre, J. (2014) · Neuroscience Letters · doi:10.1016/j.neulet.2014.03.050 · Cited by 44
Self-citationCross-modal transfer of statistical information benefits from sleep
Durrant, S. J., Cairney, S. A., & Lewis, P. A. (2016) · Cortex · doi:10.1016/j.cortex.2016.02.011 · Cited by 39
Development of top-down cortical propagations in youth
Pines, A. R., Keller, A. S., Larsen, B., Bertolero, M. A., Ashourvan, A., Bassett, D. S., Cieslak, M., Covitz, S. C., Yong Fan, A., Feczko, E., et al. (2023) · Neuron · doi:10.1016/j.neuron.2023.01.014 · Cited by 41
Ortiz-Terán, L., Diez, I. P., Ortiz, T., Perez, D. L., Aragón, J. I., Costumero, V., Pascual‐Leone, Á., Fakhri, G. E., & Sepulcre, J. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1619121114 · Cited by 43
Self-citationFriedemann Pulvermüller, A. (2023) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2023.102511 · Cited by 50
Spehl, T. S., Hellwig, S., Amtage, F., Weiller, C., Bormann, T., Weber, W., Hüll, M., Meyer, P. T., & Frings, L. (2014) · Journal of Neuroimaging · doi:10.1111/jon.12104 · Cited by 38
Aberrant Cortical Integration in First-Episode Psychosis During Natural Audiovisual Processing
Mäntylä, T. J. S., Nummenmaa, L., Rikandi, E., Lindgren, M., Kieseppä, T., Hari, R., Suvisaari, J., & Raij, T. T. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.04.014 · Cited by 34
Resting State Networks' Corticotopy: The Dual Intertwined Rings Architecture
Mesmoudi, S., Perlbarg, V., Rudrauf, D., Messé, A., Pinsard, B., Hasboun, D., Cioli, C., Marrelec, G., Toro, R., Benali, H., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0067444 · Cited by 38
Gao, Q. C., Yu, Y. Q., Su, X., Tao, Z., Zhang, M., Wang, Y., Leng, J., Sepulcre, J., & Chen, H. (2018) · Human Brain Mapping · doi:10.1002/hbm.24382 · Cited by 35
Self-citationAge-related vulnerability of the human brain connectome
Filippi, M., Cividini, C., Basaia, S., Spinelli, E. G., Castelnovo, V., Leocadi, M., Canu, E., & Agosta, F. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02157-1 · Cited by 36
Diveica, V., Riedel, M. C., Salo, T., Laird, A. R., Jackson, R. L., & Binney, R. J. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad373 · Cited by 38
Positive Connectivity Predicts the Dynamic Intrinsic Topology of the Human Brain Network
Qian, J., Diez, I. P., Ortiz-Terán, L., Bonadio, C., Liddell, T., Goñi, J., & Sepulcre, J. (2018) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00038 · Cited by 32
Self-citationAtypical functional connectome hierarchy impacts cognition in temporal lobe epilepsy
Fadaie, F., Lee, H. M., Caldairou, B., Gill, R. S., Sziklas, V., Crane, J., Bernhardt, B. C., Hong, S., Bernasconi, A., & Bernasconi, N. (2021) · Epilepsia · doi:10.1111/epi.17032 · Cited by 33
Signal processing in the vagus nerve: Hypotheses based on new genetic and anatomical evidence
Shaffer, C., Barrett, L. F., & Quigley, K. S. (2023) · Biological Psychology · doi:10.1016/j.biopsycho.2023.108626 · Cited by 34
Tanaka, S., & Kirino, E. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00328 · Cited by 33
Proulx, C. E., Jean, M. T. L., Higgins, J., Gagnon, D. H., & Dancause, N. (2022) · Frontiers in Rehabilitation Sciences · doi:10.3389/fresc.2022.789479 · Cited by 33
de Winckel, A. V., Patre, D. D., Rigoni, M., Fiecas, M. J. A., Hendrickson, T. J., Larson, M., Jagadeesan, B., Mueller, B. A., Elvendahl, W., Streib, C. D., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-77272-y · Cited by 31
Brain Plasticity in Blind Subjects Centralizes Beyond the Modal Cortices
Ortiz-Terán, L., Ortiz, T., Perez, D. L., Aragón, J. I., Diez, I. P., Pascual‐Leone, Á., & Sepulcre, J. (2016) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2016.00061 · Cited by 36
Self-citationModularity and granularity across the language network-A primary progressive aphasia perspective
Mesulam, M. M., Coventry, C., Rader, B. M., Kuang, A., Sridhar, J., Martersteck, A., Zhang, H., Thompson, C. K., Weıntraub, S., & Rogalski, E. J. (2021) · Cortex · doi:10.1016/j.cortex.2021.05.002 · Cited by 29
The parietal opercular auditory-sensorimotor network in musicians: A resting-state fMRI study
Tanaka, S., & Kirino, E. (2017) · Brain and Cognition · doi:10.1016/j.bandc.2017.11.001 · Cited by 30
Combining neighborhood separable subspaces for classification via sparsity regularized optimization
Zhu, P., Hu, Q., Han, Y., Zhang, C., & Du, Y. (2016) · Information Sciences · doi:10.1016/j.ins.2016.08.004 · Cited by 29
Spatiotemporal Network Markers of Individual Variability in the Human Functional Connectome
Peña-Gómez, C., Avena‐Koenigsberger, A., Sepulcre, J., & Sporns, O. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx170 · Cited by 33
Self-citationA role for the serotonin 2A receptor in the expansion and functioning of human transmodal cortex
Luppi, A. I., Girn, M., Rosas, F. E., Timmermann, C., Roseman, L., Erritzøe, D., Nutt, D., Stamatakis, E. A., Spreng, R. N., Xing, L., et al. (2023) · Brain · doi:10.1093/brain/awad311 · Cited by 31
Central neurogenetic signatures of the visuomotor integration system
Bueichekú, E., Aznárez‐Sanado, M., Diez, I. P., Uquillas, F. D., Ortiz-Terán, L., Qureshi, A. Y., Suñol, M., Basaia, S., Ortiz-Terán, E., Pastor, M. A., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1912429117 · Cited by 29
Self-citationMesulam, M. M., Gefen, T. D., Flanagan, M. E., Castellani, R. J., Jamshidi, P., Barbieri, E., Sridhar, J., Kawles, A., Weıntraub, S., Geula, C., et al. (2023) · Annals of Neurology · doi:10.1002/ana.26677 · Cited by 28
Motivation in the Service of Allostasis: The Role of Anterior Mid-Cingulate Cortex
Touroutoglou, A., Andreano, J. M., Adebayo, M., Lyons, S., & Barrett, L. F. (2019) · Advances in Motivation Science · doi:10.1016/bs.adms.2018.09.002 · Cited by 25
“, visual, auditory, and somatosensory) (Sepulcre et al., 2012).”
Cortical Surface Thickness in the Middle-Aged Brain with White Matter Hyperintense Lesions
Zhuang, Y., Zeng, X., Wang, B., Huang, M., Gong, H., & Zhou, F. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00225 · Cited by 27
Hierarchical complexity of the adult human structural connectome
Smith, K., Bastin, M. E., Cox, S. R., Hernández, M. V., Wiseman, S. J., Escudero, J., & Sudlow, C. L. M. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.02.028 · Cited by 25
Emergence of canonical functional networks from the structural connectome
Xie, X., Cai, C., Damasceno, P. F., Nagarajan, S. S., & Raj, A. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118190 · Cited by 24
Katsumi, Y., Wong, B., Cavallari, M., Fong, T. G., Alsop, D. C., Andreano, J. M., Carvalho, N., Brickhouse, M. J., Jones, R. N., Libermann, T. A., et al. (2022) · Brain Communications · doi:10.1093/braincomms/fcac163 · Cited by 28
Delegation to automaticity: the driving force for cognitive evolution?
Shine, J. M., & Shine, R. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00090 · Cited by 25
Pretus, C., Vidal, L. M., Martínez‐Garcia, M., Picado, M., Ramos‐Quiroga, J. A., Vanesa Richarte, B., Castellanos, F. X., Sepulcre, J., Desco, M., Vilarroya, Ó., et al. (2019) · Human Brain Mapping · doi:10.1002/hbm.24727 · Cited by 24
Self-citationXu, Z., Xia, M., Wang, X., Liao, X., Zhao, T., & Yong He, A. (2022) · Communications Biology · doi:10.1038/s42003-022-04028-x · Cited by 29
Cingulate-centered large-scale networks: Normal functions, aging, and neurodegenerative disease
Touroutoglou, A., & Dickerson, B. C. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-444-64196-0.00008-x · Cited by 23
Dintica, C. S., Marseglia, A., Wårdh, I., Stjernfeldt, P. E., Rizzuto, D., Shang, Y., Xu, W., & Pedersen, N. L. (2020) · Aging · doi:10.18632/aging.103156 · Cited by 25
Emergence of a hierarchical brain during infancy reflected by stepwise functional connectivity
Pendl, S. L., Salzwedel, A., Goldman, B. D., Barrett, L. F., Lin, W., Gilmore, J. H., & Gao, W. (2017) · Human Brain Mapping · doi:10.1002/hbm.23552 · Cited by 29
Altered brain connectivity in hyperkinetic movement disorders: A review of resting-state fMRI
Marapin, R. S., van der Horn, H. J., van der Stouwe, A. M. M., Dalenberg, J. R., de Jong, B. M., & Tijssen, M. A. J. (2022) · NeuroImage Clinical · doi:10.1016/j.nicl.2022.103302 · Cited by 24
Omnipresence of the sensorimotor-association axis topography in the human connectome
Nenning, K., Xu, T., Franco, A. R., Swallow, K. M., Tambini, A., Margulies, D. S., Smallwood, J., Colcombe, S. J., & Milham, M. P. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120059 · Cited by 25
An OP4 Functional Stream in the Language-Related Neuroarchitecture
Sepulcre, J. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht256 · Cited by 28
Self-citationFunctional Connectivity From Disease Epicenters in Frontotemporal Dementia
Agosta, F., Spinelli, E. G., Basaia, S., Cividini, C., Falbo, F., Pavone, C., Riva, N., Canu, E., Castelnovo, V., Magnani, G., et al. (2023) · Neurology · doi:10.1212/wnl.0000000000207277 · Cited by 23
Zheng, H., Ford, B. N., Kuplicki, R., Burrows, K., Hunt, P. W., Bodurka, J., Teague, T. K., Irwin, M. R., Yolken, R. H., Paulus, M. P., et al. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01558-6 · Cited by 23
Xiao, Y., Zhao, L., Zang, X., & Xue, S. (2023) · Human Brain Mapping · doi:10.1002/hbm.26485 · Cited by 20
Genetic risk factors underlying white matter hyperintensities and cortical atrophy
Patel, Y., Shin, J., Sliz, E., Tang, A., Mishra, A., Xia, R., Hofer, E., Rajula, H. S. R., Wang, R., Beyer, F., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-53689-1 · Cited by 24
A function-based mapping of sensory integration along the cortical hierarchy
Wei, W., Benn, R. A., Scholz, R., Shevchenko, V., Klatzmann, U., Alberti, F., Chiou, R. Y.-C., Wassermann, D., Vanderwal, T., Smallwood, J., et al. (2024) · Communications Biology · doi:10.1038/s42003-024-07224-z · Cited by 22
Wang, X., Li, Q., Zhao, Y. M., He, Y., Ma, B., Fu, Z., & Li, S. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118252 · Cited by 21
Connectome Computation System: 2015–2021 updates
Xing, X.-X., Xu, T., Jiang, C., Wang, Y., & Zuo, X. (2021) · 中国科学通报：英文版 · doi:10.1016/j.scib.2021.11.021 · Cited by 21
Neurodegeneration trajectory in pediatric and adult/late DM1: A follow‐up MRI study across a decade
Labayru, G., Jiménez-Marín, A., Fernández, E., Villanúa, J., Zulaica, M., Cortés, J. M., Diez, I. P., Sepulcre, J., de Munaín, A. L., & Sistiaga, A. (2020) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.51163 · Cited by 24
Self-citationBartrés‐Faz, D., González‐Escamilla, G., Vaqué‐Alcázar, L., Abellaneda‐Pérez, K., Valls‐Pedret, C., Ros, E., & Grothe, M. J. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2370-18.2019 · Cited by 22
Updated review on the link between cortical spreading depression and headache disorders
Vurallı, D., Karataş, H., Yemişçi, M., & Bolay, H. (2021) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2021.1947797 · Cited by 21
Fujimoto, U., Ogawa, A., Osada, T., Tanaka, M., Suda, A., Hattori, N., Kamagata, K., Aoki, S., & Konishi, S. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.03.010 · Cited by 21
Dental deafferentation and brain damage: A review and a hypothesis
Jou, Y. (2018) · The Kaohsiung Journal of Medical Sciences · doi:10.1016/j.kjms.2018.01.013 · Cited by 22
Large-scale cortical functional networks are organized in structured cycles
van Es, M. W. J., Higgins, C., Gohil, C., Quinn, A. J., Vidaurre, D., & Woolrich, M. W. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-02052-8 · Cited by 19
Fu, C., Aisikaer, A., Chen, Z., Yu, Q. B., Yin, J., & Yang, W. (2021) · Frontiers in Neurology · doi:10.3389/fneur.2021.668856 · Cited by 19
Jiang, S., Pei, H., Huang, Y., Chen, Y., Liu, L., Li, J., He, H., Yao, D., & Luo, C. (2020) · International Journal of Neural Systems · doi:10.1142/s0129065720500653 · Cited by 19
Cognitive Enhancement via Neuromodulation and Video Games: Synergistic Effects?
Palaus, M., Viejo-Sobera, R., Redolar-Ripoll, E., & Marrón, E. M. (2020) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2020.00235 · Cited by 18
Alexandrou, A. M., Saarinen, T., Kujala, J., & Salmelin, R. H. (2018) · Journal of Cognitive Neuroscience · doi:10.1162/jocn_a_01295 · Cited by 17
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Lee, H., Kwon, J., Lee, J., Park, B., & Park, H. (2022) · Communications Biology · doi:10.1038/s42003-021-02957-7 · Cited by 15
Gao, Q. C., Luo, N., Liang, M., Zhou, W., Li, Y., Li, R., Hu, X., Zou, T., Wang, X., Yu, J., et al. (2022) · IEEE Transactions on Neural Networks and Learning Systems · doi:10.1109/tnnls.2022.3202535 · Cited by 16
Filippi, M., Spinelli, E. G., Cividini, C., Ghirelli, A., Basaia, S., & Agosta, F. (2023) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2023.2174016 · Cited by 16
Task-Modulated Corticocortical Synchrony in the Cognitive-Motor Network Supporting Handwriting
Saarinen, T., Kujala, J., Laaksonen, H., Jalava, A., & Salmelin, R. H. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz210 · Cited by 15
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Costumero, V., Uquillas, F. D., Diez, I. P., Andorrà, M., Basaia, S., Bueichekú, E., Ortiz-Terán, L., Belloch, V., Escudero, J. V., Ávila, C., et al. (2019) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2019.12.005 · Cited by 16
Self-citationNishida, D., Mizuno, K., Yamada, E., Hanakawa, T., Liu, M., & Tsuji, T. (2021) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2021.02.010 · Cited by 16
Multistability in a star network of Kuramoto-type oscillators with synaptic plasticity
Ratas, I., Pyragas, K., & Tass, P. A. (2021) · Scientific Reports · doi:10.1038/s41598-021-89198-0 · Cited by 16
Neurogenetic traits outline vulnerability to cortical disruption in Parkinson’s disease
Basaia, S., Agosta, F., Diez, I. P., Bueichekú, E., Uquillas, F. D., Delgado‐Alvarado, M., Caballero‐Gaudes, C., Rodriguez-Oroz, M., Stojković, T., Kostić, V., et al. (2022) · NeuroImage Clinical · doi:10.1016/j.nicl.2022.102941 · Cited by 16
Self-citationAtypically high influence of subcortical activity on primary sensory regions in autism
Lorenzini, L., van Wingen, G. A., & Cerliani, L. (2021) · NeuroImage Clinical · doi:10.1016/j.nicl.2021.102839 · Cited by 15
Burger, B., Nenning, K., Schwartz, E., Margulies, D. S., Goulas, A., Liu, H., Neubauer, S., Dauwels, J., Prayer, D., & Langs, G. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118770 · Cited by 19
Self-citationSaarinen, T., Jalava, A., Kujala, J., Stevenson, C. M., & Salmelin, R. H. (2015) · Human Brain Mapping · doi:10.1002/hbm.22784 · Cited by 15
Bridging structural and functional biomarkers in functional movement disorder using network mapping
Sojka, P., Slovák, M., Věchetová, G., Jech, R., Perez, D. L., & Serranová, T. (2022) · Brain and Behavior · doi:10.1002/brb3.2576 · Cited by 13
Between-network connectivity occurs in brain regions lacking layer IV input
Wylie, K. P., Kronberg, E., Maharajh, K., Smucny, J., Cornier, M., & Tregellas, J. R. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.05.010 · Cited by 14
Fernandino, L., & Binder, J. R. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-820480-1.00155-8 · Cited by 14
Zhang, Y., Huang, G., Liu, M., Li, M., Wang, Z., Wang, R., & Yang, D. (2021) · Epilepsy Research · doi:10.1016/j.eplepsyres.2021.106595 · Cited by 13
Brain activations supporting linking of action phases in a sequential manual task
Säfström, D., & Domellöf, E. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2018.02.014 · Cited by 13
de Winckel, A. V., Carpentier, S. T., Deng, W., Bottale, S., Zhang, L., Hendrickson, T. J., Linnman, C., Lim, K. O., Mueller, B. A., Philippus, A. H., et al. (2023) · medRxiv · doi:10.1101/2023.02.09.23285713 · Cited by 13
The chronnectome as a model for Charcot’s ‘dynamic lesion’ in functional movement disorders
Marapin, R. S., van der Stouwe, A. M. M., de Jong, B. M., Gelauff, J., Vergara, V. M., Calhoun, V. D., Dalenberg, J. R., Dreissen, Y. E. M., Koelman, J. H. T. M., Tijssen, M. A. J., et al. (2020) · NeuroImage Clinical · doi:10.1016/j.nicl.2020.102381 · Cited by 13
Brain network reconfiguration for narrative and argumentative thought
Xu, Y., Vignali, L., Collignon, O., Crepaldi, D., & Bottini, R. (2021) · Communications Biology · doi:10.1038/s42003-021-02151-9 · Cited by 16
Brain connectivity and cognitive functioning in individuals six months after multiorgan failure
Jiménez-Marín, A., Rivera, D., Boado, V., Diez, I. P., Labayen, F., Garrido, I., Ramos‐Usuga, D., Benito-Sánchez, I., Rasero, J., Cabrera‐Zubizarreta, A., et al. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.102137 · Cited by 12
Small variation in dynamic functional connectivity in cerebellar networks
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Evrard, H., & Craig, A. D. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-397025-1.00237-2 · Cited by 13
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Orwig, W., Diez, I. P., Bueichekú, E., Vannini, P., Beaty, R. E., & Sepulcre, J. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2021.694274 · Cited by 12
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Jiang, S., Pei, H., Chen, J., Li, H., Liu, Z., Wang, Y., Gong, J., Wang, S., Li, Q., Duan, M., et al. (2024) · International Journal of Neural Systems · doi:10.1142/s0129065724500175 · Cited by 8
Metadata
- Authors
- Sepulcre, J., Sabuncu, M. R., Yeo, T. B., Liu, H., & Johnson, K. A.
- Affiliations
- Harvard University (US)
- Athinoula A. Martinos Center for Biomedical Imaging (US)
- Brigham and Women's Hospital (US)
- Venue
- Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2012-08-01
- Volume
- 32
- Issue
- 31
- Pages
- 10649-10661
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC3483645
- OpenAlex
- W2054260111
- Cited by
- 323
- References
- 72
- Citations by year
- 2026: 18 · 2025: 29 · 2024: 30 · 2023: 36 · 2022: 25 · 2021: 36 · 2020: 22 · 2019: 22 · 2018: 18 · 2017: 19 · 2016: 26 · 2015: 15 · 2014: 9 · 2013: 16 · 2012: 2
- FWCI
- 6.79
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc)
- Funders
- Alzheimer's Association (NIRG-11-205690)
- National Institutes of Health
- National Institute on Aging (R01AG036694, R01AG037497, P01AG036694)
- National Institute of Neurological Disorders and Stroke (K25NS069805)
- National Institute of Biomedical Imaging and Bioengineering (K25EB013649)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Multisensory perception and integration
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Keywords
- multimodal integration, functional connectivity, functional connectome, perceptual binding, sensory modalities, primary sensory cortex, lateral occipitotemporal cortex, prefrontal cortex, posterior parietal cortex
- MeSH terms
- Brain Mapping, Cerebral Cortex, Female, Humans, Image Processing, Computer-Assisted, Functional Laterality, Magnetic Resonance Imaging, Male, Mental Processes, Models, Neurological, Neural Pathways, Oxygen, Sensation, Linear Models, Young Adult
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