Microstructural Organization of the Cingulum Tract and the Level of Default Mode Functional Connectivity
Open accessAbstract
The default mode network is a functionally connected network of brain regions that show highly synchronized intrinsic neuronal activation during rest. However, less is known about the structural connections of this network, which could play an important role in the observed functional connectivity patterns. In this study, we examined the microstructural organization of the cingulum tract in relation to the level of resting-state default mode functional synchronization. Resting-state functional magnetic resonance imaging and diffusion tensor imaging data of 45 healthy subjects were acquired on a 3 tesla scanner. Both structural and functional connectivity of the default mode network were examined. In all subjects, the cingulum tract was identified from the total collection of reconstructed tracts to interconnect the precuneus/posterior cingulate cortex and medial frontal cortex, key regions of the default mode network. A significant positive correlation was found between the average fractional anisotropy value of the cingulum tract and the level of functional connectivity between the precuneus/posterior cingulate cortex and medial frontal cortex. Our results suggest a direct relationship between the structural and functional connectivity measures of the default mode network and contribute to the understanding of default mode network connectivity.
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?
Cingulum FA correlates with default-mode functional connectivity.
“e.g., cingulum FA correlates with default-mode functional connectivity (van den Heuvel et al., 2008).”
From The cingulum bundle: Anatomy, function, and dysfunction (2018) · cites this paper as van den Heuvel et al., 2008
Higher FA is associated with better functional connectivity between anatomically distant gray matter regions using resting-state fMRI.
“higher FA has been associated with better functional connectivity between anatomically distant gray matter regions using resting-state fMRI (functional MRI) 35,47,48”
From Physical exercise keeps the brain connected: biking increases white matter integrity in patients with schizophrenia and healthy controls. (2015) · cites this paper as [35]
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
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 · see citing works
The human brain is intrinsically organized into dynamic, anticorrelated functional networks
Fox, M. D., Snyder, A. Z., Vincent, J. L., Corbetta, M., Van Essen, D. C., & Raichle, M. E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504136102 · Cited by 8,553 · see citing works
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 · 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
Consistent resting-state networks across healthy subjects
Damoiseaux, J. S., Rombouts, S. A. R. B., Barkhof, F., Scheltens, P., Stam, C. J., Smith, S. M., & Beckmann, C. F. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601417103 · Cited by 4,326 · see citing works
Greicius, M. D., Srivastava, G., Reiss, A. L., & Menon, V. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308627101 · Cited by 3,684 · see citing works
Three-dimensional tracking of axonal projections in the brain by magnetic resonance imaging
Mori, S., Crain, B. J., Chacko, V. P., & van Zijl, P. C. M. (1999) · Annals of Neurology · doi:10.1002/1531-8249(199902)45:2 · Cited by 3,479 · see citing works
Andersson, J. L. R., Skare, S., & Ashburner, J. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00336-7 · Cited by 3,469 · see citing works
Automatic 3D intersubject registration of MR volumetric data in standardized Talairach space
Collins, D. L., Neelin, P., Peters, T. M., & Evans, A. C. (1994) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-199403000-00005 · Cited by 3,431 · cited 1× · see citing works
“The T1 image was normalized to match the Montreal Neurological Institute 305 T1 template brain (Collins et al., 1994).”
MethodInvestigations into resting-state connectivity using independent component analysis
Beckmann, C. F., DeLuca, M., Devlin, J. T., & Smith, S. M. (2005) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2005.1634 · Cited by 3,398 · see citing works
Searching for a baseline: Functional imaging and the resting human brain
Gusnard, D. A., & Raichle, M. E. (2001) · Nature Reviews Neuroscience · doi:10.1038/35094500 · Cited by 3,371 · see citing works
Self-referential processing in our brain—A meta-analysis of imaging studies on the self
Northoff, G., Heinzel, A., de Greck, M., Bermpohl, F., Dobrowolny, H., & Panksepp, J. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.12.002 · Cited by 2,792 · see citing works
Wandering minds: the default network and stimulus-independent thought
Mason, M. F., Norton, M. I., Van Horn, J. D., Wegner, D. M., Grafton, S. T., & Macrae, C. N. (2007) · Science · doi:10.1126/science.1131295 · Cited by 2,792 · 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
Resting-State Functional Connectivity Reflects Structural Connectivity in the Default Mode Network
Greicius, M. D., Supekar, K., Menon, V., & Dougherty, R. F. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn059 · Cited by 2,175 · see citing works
A default mode of brain function: a brief history of an evolving idea
Raichle, M. E., & Snyder, A. Z. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.02.041 · Cited by 2,173 · see citing works
Fiber Tract–based Atlas of Human White Matter Anatomy
Wakana, S., Jiang, H., Nagae‐Poetscher, L. M., van Zijl, P. C. M., & Mori, S. (2004) · Radiology · doi:10.1148/radiol.2301021640 · Cited by 2,023 · see citing works
Fiber tracking: principles and strategies – a technical review
Mori, S., & van Zijl, P. C. M. (2002) · NMR in Biomedicine · doi:10.1002/nbm.781 · Cited by 2,019 · see citing works
Voluntary orienting is dissociated from target detection in human posterior parietal cortex
Corbetta, M., Kincade, J. M., Ollinger, J. M., McAvoy, M. P., & Shulman, G. L. (2000) · Nature Neuroscience · doi:10.1038/73009 · Cited by 1,816 · see citing works
Disruption of Large-Scale Brain Systems in Advanced Aging
Andrews-Hanna, J. R., Snyder, A. Z., Vincent, J. L., Lustig, C., Head, D., Raichle, M. E., & Buckner, R. L. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.038 · Cited by 1,592 · see citing works
Fiber tract-based atlas of human white matter anatomy
Wakana, S. (2006) · Medical Entomology and Zoology · Cited by 1,544 · see citing works
Cortical midline structures and the self
Northoff, G., & Bermpohl, F. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.01.004 · Cited by 1,446 · see citing works
Frequencies contributing to functional connectivity in the cerebral cortex in "resting-state" data.
Cordes, D., Haughton, V. M., Arfanakis, K., Carew, J. D., Turski, P. A., Moritz, C. H., Quigley, M., & Meyerand, M. E. (2001) · PubMed Central · Cited by 1,402 · see citing works
Neurophysiological Architecture of Functional Magnetic Resonance Images of Human Brain
Salvador, R. M., John Suckling, A., Coleman, M. R., Pickard, J. D., Menon, D. K., & Bullmore, E. T. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhi016 · Cited by 1,334 · see citing works
fMRI resting state networks define distinct modes of long-distance interactions in the human brain
De Luca, M., Beckmann, C. F., De Stefano, N., Matthews, P. M., & Smith, S. M. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.08.035 · Cited by 1,241 · see citing works
Reduced resting-state brain activity in the “default network” in normal aging
Damoiseaux, J. S., Beckmann, C. F., Arigita, E. J. S., Barkhof, F., Scheltens, P., Stam, C. J., Smith, S. M., & Rombouts, S. A. R. B. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm207 · Cited by 1,187 · see citing works
Schmahmann, J. D., Pandya, D. N., Wang, R., Dai, G., D'Arceuil, H. E., de Crespigny, A. J., & Wedeen, V. J. (2007) · Brain · doi:10.1093/brain/awl359 · Cited by 1,067 · see citing works
Disrupted small-world networks in schizophrenia
Liu, Y., Liang, M., Zhou, Y., Yong He, A., Hao, Y., Song, M., Yu, C., Liu, H., Liu, Z., & Jiang, T. (2008) · Brain · doi:10.1093/brain/awn018 · Cited by 1,020 · see citing works
Jones, D. K. (2004) · Magnetic Resonance in Medicine · doi:10.1002/mrm.20033 · Cited by 776 · see citing works
Rombouts, S. A. R. B., Barkhof, F., Goekoop, R., Stam, C. J., & Scheltens, P. (2005) · Human Brain Mapping · doi:10.1002/hbm.20160 · Cited by 734 · see citing works
Wise, R. G., Ide, K., Poulin, M. J., & Tracey, I. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.11.025 · Cited by 664 · see citing works
RESTORE: Robust estimation of tensors by outlier rejection
Chang, L., Jones, D. K., & Pierpaoli, C. M. (2005) · Magnetic Resonance in Medicine · doi:10.1002/mrm.20426 · Cited by 611 · see citing works
Bluhm, R. L., Miller, J., Lanius, R. A., Osuch, E. A., Boksman, K., Neufeld, R. W. J., Théberge, J., Schaefer, B., & Williamson, P. (2007) · Schizophrenia Bulletin · doi:10.1093/schbul/sbm052 · Cited by 568 · see citing works
Stam, C. J. (2003) · Neuroscience Letters · doi:10.1016/j.neulet.2003.10.063 · Cited by 550 · see citing works
Unrest at rest: Default activity and spontaneous network correlations
Buckner, R. L., & Vincent, J. L. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.01.010 · Cited by 523 · see citing works
An investigation of functional and anatomical connectivity using magnetic resonance imaging
Koch, M. A., Norris, D. G., & Hund-Georgiadis, M. (2002) · NeuroImage · doi:10.1006/nimg.2001.1052 · Cited by 509 · see citing works
Diffusion tensor imaging of cingulum fibers in mild cognitive impairment and Alzheimer disease
Zhang, Y., Schuff, N. W., Jahng, G., Bayne, W., Mori, S., Schad, L. R., Mueller, S. G., Du, A., Kramer, J. H., Yaffe, K. S., et al. (2007) · Neurology · doi:10.1212/01.wnl.0000250326.77323.01 · Cited by 508 · see citing works
Small-world networks and disturbed functional connectivity in schizophrenia
Micheloyannis, S., Pachou, E., Stam, C. J., Breakspear, M. J., Bitsios, P., Vourkas, M., Erimaki, S., & Zervakis, M. E. (2006) · Schizophrenia Research · doi:10.1016/j.schres.2006.06.028 · Cited by 435 · see citing works
Sun, F. T., Miller, L. M., & D’Esposito, M. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.09.056 · Cited by 406 · see citing works
Normalized Cut Group Clustering of Resting-State fMRI Data
van den Heuvel, M. P., Mandl, R. C. W., & Pol, H. E. H. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002001 · Cited by 403 · see citing works
Self-citationLiang, M., Zhou, Y., Jiang, T., Liu, Z., Tian, L., Liu, H., & Hao, Y. (2006) · Neuroreport · doi:10.1097/01.wnr.0000198434.06518.b8 · Cited by 402 · see citing works
Lawes, I. N. C., Barrick, T. R., Murugam, V., Spierings, N. M. K., Evans, D. R., Song, M., & Clark, C. A. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.06.041 · Cited by 369 · see citing works
Schizophrenia and the disconnection hypothesis
Friston, K. J. (1999) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.1999.tb05985.x · Cited by 321 · see citing works
Johnston, 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
A Model-Based Method for Retrospective Correction of Geometric Distortions in Diffusion-Weighted EPI
Andersson, J., & Skare, S. T. (2002) · NeuroImage · doi:10.1006/nimg.2001.1039 · Cited by 272 · see citing works
Relevance to self: A brief review and framework of neural systems underlying appraisal
Schmitz, T. W., & Johnson, S. C. (2007) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2006.12.003 · Cited by 271 · see citing works
Donahue, K. M., Krouwer, H. G. J., Rand, S. D., Pathak, A. P., Marszalkowski, C. S., Censky, S. C., & Prost, R. W. (2000) · Magnetic Resonance in Medicine · doi:10.1002/1522-2594(200006)43:6 · Cited by 241 · see citing works
Kim, J. H., Loy, D. N., Liang, H., Trinkaus, K. M., Schmidt, R. E., & Song, S. (2007) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21316 · Cited by 173 · see citing works
Abnormal anterior cingulum in patients with schizophrenia: a diffusion tensor imaging study
Sun, Z., Wang, F., Cui, L., Breeze, J. L., Du, X., Wang, X., Cong, Z., Zhang, H., Li, B., Hong, N., et al. (2003) · Neuroreport · doi:10.1097/00001756-200310060-00015 · Cited by 171 · see citing works
Toosy, A., Ciccarelli, O., Parker, G. J. M., Wheeler‐Kingshott, C. A. M. G., Miller, D. H., & Thompson, A. J. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.11.022 · Cited by 169 · see citing works
Are Anticorrelated Networks in the Brain Relevant to Schizophrenia?
Williamson, P. (2007) · Schizophrenia Bulletin · doi:10.1093/schbul/sbm043 · Cited by 120 · see citing works
Frontal connections and cognitive changes in normal aging rhesus monkeys: A DTI study.
Makris, N., Papadimitriou, G. M., van der Kouwe, A., Kennedy, D. N., Hodge, S. M., Dale, A. M., Benner, T., Wald, L. L., Wu, O., Tuch, D. S., et al. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.07.005 · Cited by 115 · see citing works
Neggers, S. F. W., Hermans, E. J., & Ramsey, N. F. (2008) · NMR in Biomedicine · doi:10.1002/nbm.1235 · Cited by 114 · see citing works
Attentional networks and cingulum bundle in chronic schizophrenia☆
Nestor, P. G., Kubicki, M. R., Spencer, K., Niznikiewicz, M. A., McCarley, R. W., & Shenton, M. E. (2006) · Schizophrenia Research · doi:10.1016/j.schres.2006.10.005 · Cited by 112 · see citing works
Salvador, R. M., Martínez-Pérez, Á., Pomarol‐Clotet, E., Sarró, S., John Suckling, A., & Bullmore, E. T. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.12.001 · Cited by 89 · see citing works
Region-specific changes of cerebral white matter during normal aging: A diffusion-tensor analysis
Yoon, B., Shim, Y., Lee, K., Shon, Y., & Yang, D. (2007) · Archives of Gerontology and Geriatrics · doi:10.1016/j.archger.2007.07.004 · Cited by 75 · see citing works
Evaluation of bilateral cingulum with tractography in patients with Alzheimer’s disease
Xie, S., Xiao, J. X., Wang, Y. H., Wu, H. K., Gong, G. L., & Jiang, X. X. (2005) · NeuroReport · doi:10.1097/01.wnr.0000174061.41897.ee · Cited by 68 · see citing works
Myelination shapes functional activity in the developing brain
Fornari, E., Knyazeva, M. G., Meuli, R. A., & Maeder, P. P. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.07.010 · Cited by 64 · see citing works
Diffusion Tensor Anisotropy in Adolescents and Adults
Schneiderman, J. S., Buchsbaum, M. S., Haznedar, M. M., Hazlett, E. A., Brickman, A. M., Shihabuddin, L., Brand, J. G., Torosjan, Y., Newmark, R. E., Tang, C. Y., et al. (2007) · Neuropsychobiology · doi:10.1159/000104277 · Cited by 51 · see citing works
Seo, Y., Shinar, H., Morita, Y., & Navon, G. (1999) · Magnetic Resonance in Medicine · doi:10.1002/(sici)1522-2594(199909)42:3 · Cited by 19 · see citing works
Biswal (1997) · doi:10.1002/(sici)1099-1492(199706/08)10:4/5
Flagged first, then by citations
Cited by
Sorted by citations
Exploring the brain network: A review on resting-state fMRI functional connectivity
van den Heuvel, M. P., & Hulshoff Pol, H. E. (2010) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2010.03.008 · Cited by 3,326 · see citing works
Rich-club organization of the human connectome
van den Heuvel, M. P., & Sporns, O. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.3539-11.2011 · Cited by 2,354 · see citing works
The human connectome: a complex network
Sporns, O. (2011) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05888.x · Cited by 1,399 · see citing works
Efficiency 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
Self-citationThe vascular depression hypothesis: mechanisms linking vascular disease with depression
Taylor, W. D., Aizenstein, H. J., & Alexopoulos, G. S. (2013) · Molecular Psychiatry · doi:10.1038/mp.2013.20 · Cited by 923 · see citing works
Disease and the brain's dark energy
Zhang, D., & Raichle, M. E. (2010) · Nature Reviews Neurology · doi:10.1038/nrneurol.2009.198 · Cited by 903 · see citing works
Damoiseaux, J. S., & Greicius, M. D. (2009) · Brain Structure and Function · doi:10.1007/s00429-009-0208-6 · Cited by 897 · see citing works
A hitchhiker's guide to diffusion tensor imaging
Soares, J. M., Marques, P., Alves, V., & Sousa, N. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00031 · Cited by 893 · see citing works
On the relationship between the “default mode network” and the “social brain
Mars, R. B., Neubert, F.-X., Noonan, M. P., Sallet, J., Toni, I., & Rushworth, M. F. S. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00189 · Cited by 766 · see citing works
Contributions and challenges for network models in cognitive neuroscience
Sporns, O. (2014) · Nature Neuroscience · doi:10.1038/nn.3690 · Cited by 743 · see citing works
The cingulum bundle: Anatomy, function, and dysfunction
Bubb, E. J., Metzler-Baddeley, C., & Aggleton, J. P. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.05.008 · Cited by 740 · see citing works
van den Heuvel, M. P., Mandl, R. C. W., Stam, C. J., Kahn, R. S., & Pol, H. E. H. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2874-10.2010 · Cited by 662 · see citing works
Self-citationKeeser, D., Meindl, T., Bor, J., Palm, U., Pogarell, O. M., Mulert, C., Brunelin, J., Möller, H., Reiser, M. F., & Padberg, F. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0542-11.2011 · Cited by 585 · see citing works
Zhang, Z., Liao, W., Chen, H., Mantini, D., Ding, J.-R., Xu, Q., Wang, Z., Yuan, C., Chen, G., Jiao, Q., et al. (2011) · Brain · doi:10.1093/brain/awr223 · Cited by 580 · see citing works
The default-mode, ego-functions and free-energy: a neurobiological account of Freudian ideas
Carhart-Harris, R. L., & Friston, K. J. (2010) · Brain · doi:10.1093/brain/awq010 · Cited by 574 · see citing works
Supekar, K., Uddin, L. Q., Prater, K. E., Amin, H., Greicius, M. D., & Menon, V. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.04.009 · Cited by 524 · see citing works
Uddin, L. Q., Supekar, K. S., Ryali, S., & Menon, V. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4465-11.2011 · Cited by 520 · see citing works
Cerebral White Matter Integrity and Cognitive Aging: Contributions from Diffusion Tensor Imaging
Madden, D. J., Bennett, I. J., & Song, A. W. (2009) · Neuropsychology Review · doi:10.1007/s11065-009-9113-2 · Cited by 463 · see citing works
Default Mode Network Connectivity Predicts Sustained Attention Deficits after Traumatic Brain Injury
Bonnelle, V., Leech, R., Kinnunen, K. M., Ham, T., Beckmann, C. F., Boissezon, X. D., Greenwood, R., & Sharp, D. J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1163-11.2011 · Cited by 463 · see citing works
Caeyenberghs, K., Leemans, A., Leunissen, I., Michiels, K., & Swinnen, S. P. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00726 · Cited by 462 · see citing works
Uddin, L. Q., Supekar, K., Amin, H., Rykhlevskaia, E. I., Nguyen, D. A., Greicius, M. D., & Menon, V. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq011 · Cited by 449 · see citing works
Stimulation mapping of white matter tracts to study brain functional connectivity.
Duffau, H. (2015) · Nature Reviews Neurology · doi:10.1038/nrneurol.2015.51 · Cited by 437 · see citing works
Development of the Brain's Default Mode Network from Wakefulness to Slow Wave Sleep
Sämann, P. G., Wehrle, R., Hoehn, D., Spoormaker, V. I., Peters, H., Tully, C., Holsboer, F., & Czisch, M. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq295 · Cited by 399 · see citing works
Fox, M. D., Halko, M. A., Eldaief, M. C., & Pascual-Leone, A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.03.035 · Cited by 395 · see citing works
The Default Mode Network in Autism
Padmanabhan, A., Lynch, C. J., Schaer, M., & Menon, V. (2017) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2017.04.004 · Cited by 381 · see citing works
The structural–functional connectome and the default mode network of the human brain
Horn, A., Ostwald, D., Reisert, M., & Blankenburg, F. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.09.069 · Cited by 355 · see citing works
Noninvasive Functional and Structural Connectivity Mapping of the Human Thalamocortical System
Zhang, D., Snyder, A. Z., Shimony, J. S., Fox, M., & Raichle, M. E. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp182 · Cited by 344 · 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
Default mode network abnormalities in mesial temporal lobe epilepsy: A study combining fMRI and DTI
Liao, W., Zhang, Z., Pan, Z., Mantini, D., Ding, J., Duan, X., Luo, C., Wang, Z., Tan, Q., Lu, G., et al. (2010) · Human Brain Mapping · doi:10.1002/hbm.21076 · Cited by 325 · see citing works
Default-mode network dysfunction and cognitive impairment in progressive MS
Rocca, M. A., Valsasina, P., Absinta, M., Riccitelli, G. C., Rodegher, M., Misci, P., Rossi, P., Falini, A., Comi, G., & Filippi, M. (2010) · Neurology · doi:10.1212/wnl.0b013e3181d9ed91 · Cited by 323 · see citing works
Andrews-Hanna, J. R., Saxe, R., & Yarkoni, T. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.01.032 · Cited by 313 · see citing works
Fibre-specific white matter reductions in Alzheimer’s disease and mild cognitive impairment
Mito, R., Raffelt, D., Dhollander, T., Vaughan, D. N., Tournier, J.-D., Salvado, O., Brodtmann, A., Rowe, C. C., Villemagne, V. L., & Connelly, A. (2018) · Brain · doi:10.1093/brain/awx355 · Cited by 309 · see citing works
The Default Mode Network in Healthy Aging and Alzheimer′s Disease
Mevel, K., Chételat, G., Eustache, F., & Desgranges, B. (2011) · International Journal of Alzheimer’s Disease · doi:10.4061/2011/535816 · Cited by 302 · see citing works
Herbet, G., & Duffau, H. (2020) · Physiological Reviews · doi:10.1152/physrev.00033.2019 · Cited by 299 · see citing works
Guye, M., Bettus, G., Bartoloméi, F., & Cozzone, P. J. (2010) · Magnetic Resonance Materials in Physics Biology and Medicine · doi:10.1007/s10334-010-0205-z · Cited by 298 · see citing works
Raznahan, A., Lerch, J. P., Lee, N., Greenstein, D. K., Wallace, G. L., Stockman, M., CLASEN, L. S., Shaw, P. W., & Giedd, J. N. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.028 · Cited by 297 · see citing works
A role for the default mode network in the bases of disorders of consciousness
Fernández‐Espejo, D., Soddu, A., Cruse, D., Palacios, E. M., Junqué, C., Vanhaudenhuyse, A., Rivas, E., Newcombe, V., Menon, D. K., Pickard, J. D., et al. (2012) · Annals of Neurology · doi:10.1002/ana.23635 · Cited by 277 · see citing works
MR connectomics: Principles and challenges
Hagmann, P., Cammoun, L., Gigandet, X., Gerhard, S., Grant, P. E., Wedeen, V. J., Meuli, R. A., Thiran, J., Honey, C. J., & Sporns, O. (2010) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2010.01.014 · Cited by 271 · see citing works
Abdelnour, F., Voss, H. U., & Raj, A. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2013.12.039 · Cited by 260 · see citing works
Long-term effects of marijuana use on the brain
Filbey, F. M., Aslan, S., Calhoun, V. D., Spence, J. S., Damaraju, E., Caprihan, A., & Segall, J. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1415297111 · Cited by 249 · see citing works
Behrens, T. E. J., & Sporns, O. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.08.005 · Cited by 245 · see citing works
Early development of structural networks and the impact of prematurity on brain connectivity
Batallé, D., Hughes, E., Zhang, H. G., Tournier, J., Tusor, N., Aljabar, P., Wali, L., Alexander, D. C., Hajnal, J. V., Nosarti, C., et al. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.01.065 · Cited by 243 · see citing works
Smyser, C. D., Snyder, A. Z., & Neil, J. J. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.02.073 · Cited by 241 · see citing works
Large-scale topology and the default mode network in the mouse connectome
Stafford, J. M., Jarrett, B. R., Miranda-Dominguez, O., Mills, B. D., Cain, N., Mihalas, S., Lahvis, G. P., Lattal, K. M., Mitchell, S. H., David, S. V., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1404346111 · Cited by 229 · see citing works
Understanding Structural-Functional Relationships in the Human Brain
Wang, Z., Dai, Z., Gong, G., Zhou, C., & Yong He, A. (2014) · The Neuroscientist · doi:10.1177/1073858414537560 · Cited by 222 · see citing works
Functional and structural brain changes in anti–N‐methyl‐D‐aspartate receptor encephalitis
Finke, C., Kopp, U. A., Scheel, M., Pech, L., Soemmer, C., Schlichting, J., Leypoldt, F., Brandt, A. U., Wuerfel, J. T., Probst, C., et al. (2013) · Annals of Neurology · doi:10.1002/ana.23932 · Cited by 208 · see citing works
Kelly, C. A. M., Uddin, L. Q., Shehzad, Z. E., Margulies, D. S., Castellanos, F. X., Milham, M. P., & Petrides, M. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07279.x · Cited by 207 · see citing works
White matter microstructure underlying default mode network connectivity in the human brain
Teipel, S. J., Bokde, A. L. W., Meindl, T., Amaro, E., Soldner, J., Reiser, M. F., Herpertz, S. C., Möller, H., & Hampel, H. J. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.10.067 · Cited by 200 · see citing works
Distributed changes in default-mode resting-state connectivity in multiple sclerosis
Bonavita, S., Gallo, A., Sacco, R., Corte, M. D., Bisecco, A., Docimo, R., Lavorgna, L., Corbo, D., Costanzo, A. D., Tortora, F., et al. (2011) · Multiple Sclerosis Journal · doi:10.1177/1352458510394609 · Cited by 190 · see citing works
Deep learning predictions of survival based on MRI in amyotrophic lateral sclerosis
van der Burgh, H. K., Schmidt, R., Westeneng, H., de Reus, M. A., van den Berg, L. H., & van den Heuvel, M. P. (2016) · NeuroImage Clinical · doi:10.1016/j.nicl.2016.10.008 · Cited by 184 · see citing works
Inferring a dual-stream model of mentalizing from associative white matter fibres disconnection.
Herbet, G., Lafargue, G., Bonnetblanc, F., Moritz-Gasser, S., de Champfleur, N. M., & Duffau, H. (2014) · Brain : a journal of neurology · doi:10.1093/brain/awt370 · Cited by 181 · see citing works
Verstraete, E., van den Heuvel, M. P., Veldink, J. H., Blanken, N., Mandl, R. C. W., Pol, H. E. H., & van den Berg, L. H. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013664 · Cited by 179 · see citing works
Self-citationEfficiency of weak brain connections support general cognitive functioning
Santarnecchi, E., Galli, G., Polizzotto, N. R., Rossi, A., & Rossi, S. (2014) · Human Brain Mapping · doi:10.1002/hbm.22495 · Cited by 169 · see citing works
Stam, C. J. (2010) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2010.06.024 · Cited by 169 · see citing works
Wang, L. Y., Li, Y., Metzak, P. D., Yong He, A., & Woodward, T. S. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.01.044 · Cited by 159 · see citing works
Deep brain stimulation targets for treating depression
Drobisz, D., & Damborská, A. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.11.004 · Cited by 159 · see citing works
Di, X., & Biswal, B. B. (2012) · Brain Connectivity · doi:10.1089/brain.2012.0086 · Cited by 158 · see citing works
Structural substrates for resting network disruption in temporal lobe epilepsy
Voets, N., Beckmann, C. F., Cole, D. M., Hong, S., Bernasconi, A., & Bernasconi, N. (2012) · Brain · doi:10.1093/brain/aws137 · Cited by 150 · see citing works
Impaired Structural Motor Connectome in Amyotrophic Lateral Sclerosis
Verstraete, E., Veldink, J. H., Mandl, R. C. W., van den Berg, L. H., & van den Heuvel, M. P. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024239 · Cited by 145 · see citing works
Self-citationDi, X., & Biswal, B. B. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.07.071 · Cited by 143 · see citing works
Hoogenboom, W. S., Marder, T. J., Flores, V. L., Huisman, S., Eaton, H. P., Schneiderman, J. S., Bolo, N. R., Simonson, D. C., Jacobson, A. M., Kubicki, M. R., et al. (2013) · Diabetes · doi:10.2337/db13-1219 · Cited by 137 · see citing works
Jacobson, S. C., Kelleher, I., Harley, M., Murtagh, A., Clarke, M. C., Blanchard, M. M., Connolly, C. G., O’Hanlon, E., Garavan, H., & Cannon, M. D. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.09.015 · Cited by 136 · see citing works
Fusing DTI and fMRI data: A survey of methods and applications
Zhu, D., Zhang, T., Jiang, X., Hu, X., Chen, H., Yang, N., Lv, J., Han, J., Guo, L., & Liu, T. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.09.071 · Cited by 133 · see citing works
Altered Functional and Structural Connectivity Networks in Psychogenic Non-Epileptic Seizures
Ding, J.-R., An, D., Liao, W., Li, J., Wu, G.-R., Xu, Q., Long, Z., Gong, Q., Zhou, D., Sporns, O., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0063850 · Cited by 132 · see citing works
Verstraete, E., Veldink, J. H., van den Berg, L. H., & van den Heuvel, M. P. (2013) · Human Brain Mapping · doi:10.1002/hbm.22258 · Cited by 132 · see citing works
The structural and functional brain networks that support human social networks
Noonan, M. P., Mars, R. B., Sallet, J., Dunbar, R. I. M., & Fellows, L. K. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.02.019 · Cited by 131 · see citing works
Hierarchical Alteration of Brain Structural and Functional Networks in Female Migraine Sufferers
Liu, J., Zhao, L., Li, G., Xiong, S., Nan, J., Li, J., Yuan, K., von Deneen, K. M., Liang, F., Qin, W., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0051250 · Cited by 128 · see citing works
Yuan, K., Qin, W., Liu, P., Zhao, L., Yu, D., Zhao, L., Dong, M., Liu, J., Yang, X., von Deneen, K. M., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0045476 · Cited by 127 · see citing works
Dídac Vidal-piñeiro, A., eValls-Pedret, C., Fernández‐Cabello, S., Arenaza‐Urquijo, E. M., Sala-Llonch, R., Solana, E., Bargalló, N., Junqué, C., Ros, E., & David Bartrés-faz, A. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00256 · Cited by 126 · see citing works
Brain Connectivity and Visual Attention
Parks, E. L., & Madden, D. J. (2013) · Brain Connectivity · doi:10.1089/brain.2012.0139 · Cited by 124 · see citing works
Marstaller, L., Williams, M., Rich, A. N., Savage, G. R., & Burianová, H. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.01.049 · Cited by 123 · see citing works
Svatkova, A., Mandl, R. C. W., Scheewe, T. W., Cahn, W., Kahn, R. S., & Hulshoff Pol, H. E. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv033 · Cited by 120 · see citing works
Self-citationSemantic memory activation in amnestic mild cognitive impairment
Woodard, J. L., Seidenberg, M., Nielson, K. A., Antuono, P., Guidotti, L. M., Durgerian, S., Zhang, Q., Lancaster, M. A., Hantke, N. C., Butts, A. M., et al. (2009) · Brain · doi:10.1093/brain/awp157 · Cited by 120 · see citing works
Tan, G. C. Y., Doke, T. F., Ashburner, J., Wood, N. W., & Frackowiak, R. S. J. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.02.018 · Cited by 116 · see citing works
Reduced functional coupling in the default-mode network during self-referential processing
van Buuren, M., Gladwin, T. E., Zandbelt, B. B., Kahn, R. S., & Vink, M. (2010) · Human Brain Mapping · doi:10.1002/hbm.20920 · Cited by 115 · see citing works
Teipel, S. J., Grothe, M. J., Zhou, J. H., Sepulcre, J., Dyrba, M., Sorg, C., & Babiloni, C. (2016) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617715000995 · Cited by 115 · see citing works
Meta-analysis of functional network alterations in Alzheimer's disease: Toward a network biomarker
Jacobs, H. I. L., Raduà, J., Lückmann, H. C., & Sack, A. T. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.03.009 · Cited by 114 · see citing works
Fjell, A. M., Sneve, M. H., Grydeland, H., Storsve, A. B., Amlien, I. K., Yendiki, A., & Walhovd, K. B. (2016) · Human Brain Mapping · doi:10.1002/hbm.23403 · Cited by 113 · see citing works
Perspectives in affective disorders: Clocks and sleep
Wirz‐Justice, A., & Benedetti, F. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14362 · Cited by 108 · see citing works
Wiggins, J. L., Peltier, S., Ashinoff, S., Weng, S.-J., Carrasco, M., Welsh, R. C., Lord, C., & Monk, C. S. (2010) · Brain Research · doi:10.1016/j.brainres.2010.10.102 · Cited by 106 · see citing works
White matter pathways and social cognition
Wang, Y., Metoki, A., Alm, K. H., & Olson, I. R. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.04.015 · Cited by 104 · see citing works
Neural pathways subserving face-based mentalizing
Yordanova, Y. N., Duffau, H., & Herbet, G. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1388-0 · Cited by 102 · see citing works
Visualizing the human connectome
Margulies, D. S., Böttger, J., Watanabe, A., & Gorgolewski, K. J. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.04.111 · Cited by 102 · see citing works
Evidence for exercise-related plasticity in functional and structural neural network connectivity
Won, J., Callow, D. D., Pena, G. S., Gogniat, M. A., Kommula, Y., Arnold-Nedimala, N. A., Jordan, L. S., & Smith, J. C. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.10.013 · Cited by 102 · see citing works
Constituents and functional implications of the rat default mode network
Hsu, L., Liang, X., Gu, H., Brynildsen, J. K., Stark, J. A., Ash, J. A., Lin, C., Lu, H., Rapp, P. R., Stein, E. A., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1601485113 · Cited by 101 · see citing works
Liégeois, R., Santos, A., Matta, V., Ville, D. V. D., & Sayed, A. H. (2020) · Network Neuroscience · doi:10.1162/netn_a_00166 · Cited by 100 · see citing works
Disrupted structural and functional connectivity networks in ischemic stroke patients
Zhang, J., Zhang, Y., Wang, L., Sang, L., Yang, J., Yan, R., Li, P., Wang, J., & Qiu, M. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.09.009 · Cited by 99 · see citing works
Mandl, R. C. W., Schnack, H. G., Luigjes, J., van den Heuvel, M. P., Cahn, W., Kahn, R. S., & Pol, H. E. H. (2008) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn161 · Cited by 99 · see citing works
Self-citationMR connectomics: a conceptual framework for studying the developing brain
Hagmann, P., Grant, P. E., & Fair, D. A. (2012) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2012.00043 · Cited by 96 · see citing works
Paquola, C., Garber, M., Frässle, S., Royer, J., Zhou, Y., Tavakol, S., Rodríguez‐Cruces, R., Cabalo, D. G., Valk, S. L., Eickhoff, S. B., et al. (2025) · Nature Neuroscience · doi:10.1038/s41593-024-01868-0 · Cited by 95 · see citing works
Lin, P., Yang, Y., Jovicich, J., Pisapia, N. D., Wang, X., Zuo, C. S., & Levitt, J. J. (2015) · Brain Imaging and Behavior · doi:10.1007/s11682-015-9384-6 · Cited by 91 · see citing works
Use of resting-state functional MRI to study brain development and injury in neonates
Smyser, C. D., & Neil, J. J. (2015) · Seminars in Perinatology · doi:10.1053/j.semperi.2015.01.006 · Cited by 90 · see citing works
Apolipoprotein E genotype, gender and age modulate connectivity of the hippocampus in healthy adults
Heise, V., Filippini, N., Trachtenberg, A. J., Suri, S., Ebmeier, K. P., & Mackay, C. E. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.04.081 · Cited by 90 · see citing works
Filippi, M., & Agosta, F. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-101854 · Cited by 89 · see citing works
Sharaev, M., Zavyalova, V. V., Ushakov, V., Kartashov, S., & Velichkovsky, B. M. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00014 · Cited by 89 · see citing works
Jung, M., Tu, Y., Lang, C., Ortiz, A., Park, J., Jorgenson, K., Kong, X., & Kong, J. (2017) · NeuroImage · doi:10.1016/j.neuroimage.2017.09.031 · Cited by 86 · see citing works
Neural substrates for late-life depression: A selective review of structural neuroimaging studies
Kim, Y., & Han, K. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.110010 · Cited by 86 · see citing works
Cerebral small vessel disease affects white matter microstructure in mild cognitive impairment
Papma, J. M., de Groot, M., de Koning, I., Mattace-Raso, F. U. S., van der Lugt, A., Vernooij, M. W., Niessen, W. J., Swieten, J. C. V., Koudstaal, P. J., Prins, N. D., et al. (2013) · Human Brain Mapping · doi:10.1002/hbm.22370 · Cited by 84 · see citing works
Hirsiger, S., Koppelmans, V., Mérillat, S., Liem, F., Erdeniz, B., Seidler, R. D., & Jäncke, L. (2015) · Human Brain Mapping · doi:10.1002/hbm.23067 · Cited by 84 · see citing works
- Authors
- van den Heuvel, M., Mandl, R., Luigjes, J., & Hulshoff Pol, H.
- Affiliations
- Utrecht University (NL)
- ORCID
- Mandl, René
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2008-10-22
- Volume
- 28
- Issue
- 43
- Pages
- 10844-10851
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6671361
- OpenAlex
- W1997491128
- Cited by
- 349
- References
- 63
- Citations by year
- 2026: 5 · 2025: 6 · 2024: 15 · 2023: 14 · 2022: 13 · 2021: 20 · 2020: 16 · 2019: 12 · 2018: 25 · 2017: 33 · 2016: 21 · 2015: 22 · 2014: 29 · 2013: 27 · 2012: 24
- FWCI
- 11.39
- 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 (publishedVersion, other-oa)
- Data Archiving and Networked Services (DANS) (submittedVersion, other-oa)
- Funders
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Life Sciences › Neuroscience › Cognitive Neuroscience › Mind wandering and attention
- Keywords
- default mode network, resting-state functional connectivity, structural connectivity, fractional anisotropy, precuneus, posterior cingulate cortex, medial frontal cortex, white matter tracts
- MeSH terms
- Adult, Brain Mapping, Cerebral Cortex, Female, Gyrus Cinguli, Humans, Image Processing, Computer-Assisted, Functional Laterality, Magnetic Resonance Imaging, Male, Models, Neurological, Nerve Net, Neural Pathways, Oxygen, Rest
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