Cited by 386Functional Brain Connectivity StudiesAdvanced Neuroimaging Techniques and ApplicationsComplex Network Analysis Techniques

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The Neonatal Connectome During Preterm Brain Development

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van den Heuvel, Martijn P., Kersbergen, Karina J., de Reus, Marcel A., Keunen, Kristin, Kahn, René S., Groenendaal, Floris, de Vries, Linda S., Benders, Manon J.N.L.·2015·Cerebral Cortex

DOI 10.1093/cercor/bhu095PMC PMC4537441

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Abstract

The human connectome is the result of an elaborate developmental trajectory. Acquiring diffusion-weighted imaging and resting-state fMRI, we studied connectome formation during the preterm phase of macroscopic connectome genesis. In total, 27 neonates were scanned at week 30 and/or week 40 gestational age (GA). Examining the architecture of the neonatal anatomical brain network revealed a clear presence of a small-world modular organization before term birth. Analysis of neonatal functional connectivity (FC) showed the early formation of resting-state networks, suggesting that functional networks are present in the preterm brain, albeit being in an immature state. Moreover, structural and FC patterns of the neonatal brain network showed strong overlap with connectome architecture of the adult brain (85 and 81%, respectively). Analysis of brain development between week 30 and week 40 GA revealed clear developmental effects in neonatal connectome architecture, including a significant increase in white matter microstructure (P < 0.01), small-world topology (P < 0.01) and interhemispheric FC (P < 0.01). Computational analysis further showed that developmental changes involved an increase in integration capacity of the connectivity network as a whole. Taken together, we conclude that hallmark organizational structures of the human connectome are present before term birth and subject to early development.

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Modularity and community structure in networks
Newman, M. E. J. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601602103 · Cited by 12,256
Complex brain networks: graph theoretical analysis of structural and functional systems
Bullmore, E., & Sporns, O. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2575 · Cited by 11,820
Complex network measures of brain connectivity: Uses and interpretations
Rubinov, M., & Sporns, O. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.10.003 · Cited by 11,522
Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion
Power, J. D., Barnes, K. A., Snyder, A. Z., Schlaggar, B. L., & Petersen, S. E. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.10.018 · Cited by 7,429
Incidence and evolution of subependymal and intraventricular hemorrhage: A study of infants with birth weights less than 1,500 gm
Papile, L. A., Burstein, J., Burstein, R., & Koffler, H. (1978) · The Journal of Pediatrics · doi:10.1016/s0022-3476(78)80282-0 · Cited by 6,435
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
Mapping the structural core of human cerebral cortex
Hagmann, P., Cammoun, L., Gigandet, X., Meuli, R., Honey, C. J., Wedeen, V. J., & Sporns, O. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060159 · Cited by 4,173
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
Predicting human resting-state functional connectivity from structural connectivity
Honey, C. J., Sporns, O., Cammoun, L., Gigandet, X., Thiran, J. P., Meuli, R., & Hagmann, P. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811168106 · Cited by 3,307
The Human Connectome: A Structural Description of the Human Brain
Sporns, O., Tononi, G., & Kötter, R. (2005) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0010042 · Cited by 3,260
Specificity and Stability in Topology of Protein Networks
Maslov, S., & Sneppen, K. (2002) · Science · doi:10.1126/science.1065103 · Cited by 3,051
Cortical Hubs Revealed by Intrinsic Functional Connectivity: Mapping, Assessment of Stability, and Relation to Alzheimer's Disease
Buckner, R. L., Sepulcre, J., Talukdar, T., Krienen, F. M., Liu, H., Hedden, T., Andrews-Hanna, J. R., Sperling, R. A., & Johnson, K. A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5062-08.2009 · Cited by 2,862
Distinct brain networks for adaptive and stable task control in humans
Dosenbach, N. U. F., Fair, D. A., Miezin, F. M., Cohen, A. L., Wenger, K. K., Dosenbach, R. A. T., Fox, M. D., Snyder, A. Z., Vincent, J. L., Raichle, M. E., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704320104 · Cited by 2,632
Small-World Brain Networks
Bassett, D. S., & Bullmore, E. (2006) · The Neuroscientist · doi:10.1177/1073858406293182 · Cited by 2,600
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
The influence of head motion on intrinsic functional connectivity MRI
Van Dijk, K. R. A., Sabuncu, M. R., & Buckner, R. L. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.07.044 · Cited by 2,344
Prediction of individual brain maturity using fMRI
Dosenbach, N. U. F., Nardos, B., Cohen, A. L., Fair, D. A., Power, J. D., Church, J. A., Nelson, S. M., Wig, G. S., Vogel, A. C., Lessov-Schlaggar, C. N., et al. (2010) · Science · doi:10.1126/science.1194144 · Cited by 2,183
Network hubs in the human brain
van den Heuvel, M. P., & Sporns, O. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.09.012 · Cited by 2,123 · cited 1×
“Other studies have shown the feasibility of reconstructing and examining brain networks at higher resolutions (e.g., Eguiluz et al. 2005; Hagmann et al. 2008; van den Heuvel et al. 2008; Bassett et al. 2010; Zalesky et al. 2010; van den Heuvel and Sporns 2013).”
Background
Structural and Functional Brain Networks: From Connections to Cognition
Park, H.-J., & Friston, K. (2013) · Science · doi:10.1126/science.1238411 · Cited by 2,106
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
The basics of brain development
Stiles, J., & Jernigan, T. L. (2010) · Neuropsychology Review · doi:10.1007/s11065-010-9148-4 · Cited by 2,009
Functional brain networks develop from a local to distributed organization
Fair, D. A., Cohen, A. L., Power, J. D., Dosenbach, N. U. F., Church, J. A., Miezin, F. M., Schlaggar, B. L., & Petersen, S. E. (2009) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000381 · Cited by 1,530
Scale-Free Brain Functional Networks
Eguı́luz, V. M., Chialvo, D. R., Cecchi, G., Baliki, M. N., & Apkarian, A. V. (2005) · Physical Review Letters · doi:10.1103/physrevlett.94.018102 · Cited by 1,464
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 1,440
Extraordinary neoteny of synaptic spines in the human prefrontal cortex
Petanjek, Z., Judaš, M., Šimić, G., Rašin, M. R., Uylings, H. B. M., Rakic, P., & Kostović, I. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105108108 · Cited by 1,411
Neonatal MRI to Predict Neurodevelopmental Outcomes in Preterm Infants
Woodward, L. J., Anderson, P. J., Austin, N. C., Howard, K., & Inder, T. E. (2006) · New England Journal of Medicine · doi:10.1056/nejmoa053792 · Cited by 1,344
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
The maturing architecture of the brain's default network
Fair, D. A., Cohen, A. L., Dosenbach, N. U. F., Church, J. A., Miezin, F. M., Barch, D. M., Raichle, M. E., Petersen, S. E., & Schlaggar, B. L. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800376105 · Cited by 1,314
Development of distinct control networks through segregation and integration
Fair, D. A., Dosenbach, N. U. F., Church, J. A., Cohen, A. L., Brahmbhatt, S., Miezin, F. M., Barch, D. M., Raichle, M. E., Petersen, S. E., & Schlaggar, B. L. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705843104 · Cited by 1,244
Network Centrality in the Human Functional Connectome
Zuo, X., Ehmke, R. C., Mennes, M., Imperati, D., Castellanos, F. X., Sporns, O., & Milham, M. P. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr269 · Cited by 1,190
Whole-brain anatomical networks: does the choice of nodes matter?
Zalesky, A., Fornito, A., Harding, I. H., Cocchi, L., Yücel, M., Pantelis, C., & Bullmore, E. T. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.12.027 · Cited by 1,169
Concurrent overproduction of synapses in diverse regions of the primate cerebral cortex
Rakic, P., Bourgeois, J.-P., Eckenhoff, M. F., Zecevic, N., & Goldman-Rakic, P. S. (1986) · Science · doi:10.1126/science.3952506 · Cited by 1,133 · cited 2×
“…(Lagercrantz 1998), indicating the start of a period of exuberant formation of synaptical connections, with a peak of synaptic connections occurring around year 2 of life (Rakic et al. 1986; Huttenlocher and Dabholkar 1997; Bruer 1999; Petanjek et al. 2011; Lagercrantz 1998; Kostovic et al. 2014).”
Background
Impact of in-scanner head motion on multiple measures of functional connectivity: relevance for studies of neurodevelopment in youth
Satterthwaite, T. D., Wolf, D. H., Loughead, J., Ruparel, K., Elliott, M. A., Hakonarson, H., Gur, R. C., & Gur, R. E. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.12.063 · Cited by 1,125
Mapping anatomical connectivity patterns of human cerebral cortex using in vivo diffusion tensor imaging tractography
Gong, G., He, Y., Concha, L., Lebel, C., Gross, D. W., Evans, A. C., & Beaulieu, C. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn102 · Cited by 1,112
Detecting rich-club ordering in complex networks
Colizza, V., Flammini, A., Serrano, M. A., & Vespignani, A. (2006) · Nature Physics · doi:10.1038/nphys209 · Cited by 1,001
Functionally linked resting‐state networks reflect the underlying structural connectivity architecture of the human brain
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
Self-citation
Development of the human cerebral cortex: Boulder Committee revisited
Bystron, I., Blakemore, C., & Rakic, P. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2252 · Cited by 977
Human brain networks in health and disease
Bassett, D. S., & Bullmore, E. T. (2009) · Current Opinion in Neurology · doi:10.1097/wco.0b013e32832d93dd · Cited by 922
Weight-conserving characterization of complex functional brain networks
Rubinov, M., & Sporns, O. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.03.069 · Cited by 903
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
Small-world and scale-free organization of voxel-based resting-state functional connectivity in the human brain
van den Heuvel, M. P., Stam, C. J., Boersma, M., & Pol, H. E. H. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.08.010 · Cited by 745
Microstructural Development of Human Newborn Cerebral White Matter Assessed in Vivo by Diffusion Tensor Magnetic Resonance Imaging
Hüppi, P. S., Maier, S. E., Peled, S., Zientara, G. P., Barnes, P. D., Jolesz, F. A., & Volpe, J. J. (1998) · Pediatric Research · doi:10.1203/00006450-199810000-00019 · Cited by 722
Schizophrenia, neuroimaging and connectomics
Fornito, A., Zalesky, A., Pantelis, C., & Bullmore, E. T. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.12.090 · Cited by 716
White matter maturation reshapes structural connectivity in the late developing human brain
Hagmann, P., Sporns, O., Madan, N., Cammoun, L., Pienaar, R., Wedeen, V. J., Meuli, R., Thiran, J.-P., & Grant, P. E. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009073107 · Cited by 700
Resting-state networks in the infant brain
Fransson, P., Skiöld, B., Horsch, S., Nordell, A., Blennow, M., Lagercrantz, H., & Åden, U. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704380104 · Cited by 696
Orientationally invariant indices of axon diameter and density from diffusion MRI
Alexander, D. C., Hubbard, P. L., Hall, M. G., Moore, E. A., Ptito, M., Parker, G. J. M., & Dyrby, T. B. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.05.043 · Cited by 683
Aberrant Frontal and Temporal Complex Network Structure in Schizophrenia: A Graph Theoretical Analysis
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 677
Self-citation
Abnormal Rich Club Organization and Functional Brain Dynamics in Schizophrenia
van den Heuvel, M. P., Sporns, O., Collin, G., Scheewe, T. W., Mandl, R. C. W., Cahn, W., Goñi, J., Pol, H. E. H., & Kahn, R. S. (2013) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2013.1328 · Cited by 649
Self-citation
Normal brain in human newborns: apparent diffusion coefficient and diffusion anisotropy measured by using diffusion tensor MR imaging.
Neil, J. J., Shiran, S. I., McKinstry, R. C., Schefft, G. L., Snyder, A. Z., Almli, C. R., Akbudak, E., Aronovitz, J. A., Miller, J. P., Lee, B. C., et al. (1998) · Radiology · doi:10.1148/radiology.209.1.9769812 · Cited by 645
Cortical high-density counterstream architectures
Markov, N. T., Ercsey-Ravasz, M., Van Essen, D. C., Knoblauch, K., Toroczkai, Z., & Kennedy, H. (2013) · Science · doi:10.1126/science.1238406 · Cited by 616
Tractography: Where Do We Go from Here?
Jbabdi, S., & Johansen-Berg, H. (2011) · Brain Connectivity · doi:10.1089/brain.2011.0033 · Cited by 614
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
The brainstem reticular formation is a small-world, not scale-free, network
Humphries, M. D., GURNEY, K. N., & Prescott, T. J. (2005) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2005.3354 · Cited by 610
The functional architecture of the infant brain as revealed by resting-state fMRI
Fransson, P., Åden, U., Blennow, M., & Lagercrantz, H. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq071 · Cited by 542
Brain Networks in Schizophrenia
van den Heuvel, M. P., & Fornito, A. (2014) · Neuropsychology Review · doi:10.1007/s11065-014-9248-7 · Cited by 531
Exuberance in the development of cortical networks
Innocenti, G. M., & Price, D. J. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1790 · Cited by 512
Axon overproduction and elimination in the corpus callosum of the developing rhesus monkey
LaMantia, A., & RAKIC, P. T. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-07-02156.1990 · Cited by 511
Studying connections in the living human brain with diffusion MRI
Jones, D. K. (2008) · Cortex · doi:10.1016/j.cortex.2008.05.002 · Cited by 497
Genetic control over the resting brain
Glahn, D. C., Winkler, A. M., Kochunov, P., Almasy, L., Duggirala, R., Carless, M. A., Curran, J. C., Olvera, R. L., Laird, A. R., Smith, S. M., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909969107 · Cited by 450
Diffusion-tensor MR imaging of gray and white matter development during normal human brain maturation.
Mukherjee, P., Miller, J. H., Shimony, J. S., Philip, J. V., Nehra, D., Snyder, A. Z., Conturo, T. E., Neil, J. J., & McKinstry, R. C. (2002) · PubMed Central · Cited by 445
Cognitive fitness of cost-efficient brain functional networks
Bassett, D. S., Bullmore, E. T., Meyer‐Lindenberg, A., Apud, J. A., Weinberger, D. R., & Coppola, R. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903641106 · Cited by 429
An anatomical substrate for integration among functional networks in human cortex
van den Heuvel, M. P., & Sporns, O. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.2128-13.2013 · Cited by 404
Development of Executive Function and Attention in Preterm Children: A Systematic Review
Mulder, H., Pitchford, N. J., Hagger, M. S., & Marlow, N. (2009) · Developmental Neuropsychology · doi:10.1080/87565640902964524 · Cited by 388
Weight consistency specifies regularities of macaque cortical networks
Markov, N. T., Misery, P., Falchier, A., Lamy, C., Vezoli, J., Quilodran, R., Gariel, M. A., Giroud, P., Ercsey-Ravasz, M., Pilaz, L. J., et al. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq201 · Cited by 386
The development of synapses in cerebral cortex of the human fetus
Molliver, M. E., Kostović, I., & der Loos, H. V. (1973) · Brain Research · doi:10.1016/0006-8993(73)90741-5 · Cited by 385
Conserved and variable architecture of human white matter connectivity
Bassett, D., Brown, J. A., Deshpande, V., Carlson, J., & Grafton, S. T. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.09.006 · Cited by 380
Discovering the Human Connectome
Sporns, O. (2012) · The MIT Press eBooks · doi:10.7551/mitpress/9266.001.0001 · Cited by 354
Dynamical consequences of lesions in cortical networks
Honey, C. J., & Sporns, O. (2008) · Human Brain Mapping · doi:10.1002/hbm.20579 · Cited by 353
Cortical hubs form a module for multisensory integration on top of the hierarchy of cortical networks
Zamora‐López, G. (2010) · Frontiers in Neuroinformatics · doi:10.3389/neuro.11.001.2010 · Cited by 333
Using Diffusion Imaging to Study Human Connectional Anatomy
Johansen‐Berg, H., & Rushworth, M. F. S. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135735 · Cited by 325
Rich Club Organization of Macaque Cerebral Cortex and Its Role in Network Communication
Harriger, L., van den Heuvel, M. P., & Sporns, O. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046497 · Cited by 309
Multi-contrast human neonatal brain atlas: Application to normal neonate development analysis
Oishi, K., Mori, S., Donohue, P., Ernst, T. M., Anderson, L. M., Buchthal, S. D., Faria, A. V., Jiang, H., Li, X., Miller, M. I., et al. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.01.051 · Cited by 303
Genetic Influences on Cost-Efficient Organization of Human Cortical Functional Networks
Fornito, A., Zalesky, A., Bassett, D. S., David Meunier, A., Ellison-Wright, I., Yücel, M., Wood, S. J., Shaw, K., O'Connor, J., Nertney, D. A., et al. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4858-10.2011 · Cited by 286
The parcellation-based connectome: limitations and extensions
de Reus, M. A., & van den Heuvel, M. P. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.03.053 · Cited by 282
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 273
Functional connectivity MRI in infants: Exploration of the functional organization of the developing brain
Smyser, C. D., Snyder, A. Z., & Neil, J. J. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.02.073 · Cited by 259
Structural and Functional Aspects Relating to Cost and Benefit of Rich Club Organization in the Human Cerebral Cortex
Collin, G., Sporns, O., Mandl, R. C. W., & van den Heuvel, M. P. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht064 · Cited by 257
Estimating false positives and negatives in brain networks
de Reus, M. A., & van den Heuvel, M. P. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.12.066 · Cited by 256
Changes in the interaction of resting-state neural networks from adolescence to adulthood
Stevens, M. C., Pearlson, G. D., & Calhoun, V. D. (2009) · Human Brain Mapping · doi:10.1002/hbm.20673 · Cited by 256
Spontaneous Brain Activity in the Newborn Brain During Natural Sleep—An fMRI Study in Infants Born at Full Term
Fransson, P., Skiöld, B., Engström, M., Hallberg, B., Mosskin, M., Ådén, U., Lagercrantz, H., & Blennow, M. (2009) · Pediatric Research · doi:10.1203/pdr.0b013e3181b1bd84 · Cited by 248
Water diffusion in the giant axon of the squid: implications for diffusion-weighted MRI of the nervous system
Beaulieu, C., & Allen, P. S. (1994) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910320506 · Cited by 240
Developmental Changes in Organization of Structural Brain Networks
Khundrakpam, B. S., Reid, A., Brauer, J., Carbonell, F., Lewis, J., Ameis, S., Karama, S., Lee, J., Chen, Z., Das, S., et al. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs187 · Cited by 234
The development of hub architecture in the human functional brain network
Hwang, K., Hallquist, M. N., & Luna, B. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs227 · Cited by 226
Quantitative diffusion tensor MRI fiber tractography of sensorimotor white matter development in premature infants
Berman, J., Mukherjee, P., Partridge, S. C., Miller, S. P., Ferriero, D. M., Barkovich, A. J., Vigneron, D. B., & Henry, R. G. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.05.018 · Cited by 225
Assessment of system dysfunction in the brain through MRI-based connectomics
Filippi, M., van den Heuvel, M. P., Fornito, A., Yong He, A., Pol, H. E. H., Agosta, F., Comı, G., & Rocca, M. A. (2013) · The Lancet Neurology · doi:10.1016/s1474-4422(13)70144-3 · Cited by 219
The Ontogeny of the Human Connectome: Development and Dynamic Changes of Brain Connectivity Across the Life Span
Collin, G., & van den Heuvel, M. P. (2013) · The Neuroscientist · doi:10.1177/1073858413503712 · Cited by 198
Development Trends of White Matter Connectivity in the First Years of Life
Yap, P.-T., Fan, Y., Chen, Y., Gilmore, J. H., Lin, W., & Shen, D. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024678 · Cited by 190
Perinatal and early postnatal reorganization of the subplate and related cellular compartments in the human cerebral wall as revealed by histological and MRI approaches
Kostović, I., Milošević, N. J., Radoš, M., Sedmak, G., Benjak, V., Srzentić, M. K., Vasung, L., Čuljat, M., Radoš, M., Hüppi, P. S., et al. (2012) · Brain Structure and Function · doi:10.1007/s00429-012-0496-0 · Cited by 179
Heritability of regional and global brain structure at the onset of puberty: a magnetic resonance imaging study in 9-year-old twin pairs
Peper, J. S., Schnack, H. G., Brouwer, R. M., Van Baal, G. C. M., Pjetri, E., Székely, E., van Leeuwen, M., van den Berg, S. M., Collins, D. L., Evans, A. C., et al. (2009) · Human Brain Mapping · doi:10.1002/hbm.20660 · Cited by 177
Self-citation
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Authors: van den Heuvel, M. P., Kersbergen, K. J., de Reus, M. A., Keunen, K., Kahn, R. S., Groenendaal, F., de Vries, L. S., & Benders, M. J. N. L.
Affiliations: University Medical Center Utrecht (NL)
ORCID: Kersbergen, Karina J.
Keunen, Kristin
Kahn, René S.
Groenendaal, Floris
Benders, Manon J.N.L.
Venue: Cerebral Cortex
Publisher: Oxford University Press (OUP)
Published: 2014-05-15
Volume: 25
Issue: 9
Pages: 3000-3013
ISSN: 1047-3211 (ISSN-L)
1460-2199
DOI: 10.1093/cercor/bhu095
PMC: PMC4537441
OpenAlex: W2133182819
Cited by: 386
References: 121
Citations by year: 2026: 17 · 2025: 32 · 2024: 29 · 2023: 25 · 2022: 31 · 2021: 37 · 2020: 62 · 2019: 28 · 2018: 38 · 2017: 34 · 2016: 24 · 2015: 20 · 2014: 7
FWCI: 15.67
Type: journal article
Language: en
Open access: green
europepmc.org
Licence: cc-by-nc
Locations: Cerebral Cortex (publishedVersion)
Europe PMC (PubMed Central) (publishedVersion, cc-by-nc)
PubMed Central (publishedVersion, cc-by-nc)
PubMed (publishedVersion)
Pure Amsterdam UMC (publishedVersion, cc-by)
Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion, other-oa)
Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
Utrecht University Repository (Utrecht University) (submittedVersion)
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
Physical Sciences › Physics and Astronomy › Statistical and Nonlinear Physics › Complex Network Analysis Techniques
Keywords: small-world networks, resting-state functional connectivity, resting-state networks, white matter microstructure, interhemispheric functional connectivity, gestational age, diffusion-weighted imaging, resting-state fMRI
MeSH terms: Adult, Brain, Female, Gestational Age, Humans, Image Processing, Computer-Assisted, Infant, Newborn, Magnetic Resonance Imaging, Male, Neural Pathways, Oxygen, Diffusion Magnetic Resonance Imaging, Premature Birth, Young Adult, Connectome, White Matter

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The Neonatal Connectome During Preterm Brain Development

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