Dynamics of the human structural connectome underlying working memory training
Open accessAbstract
Brain region-specific changes have been demonstrated with a variety of cognitive training interventions. The effect of cognitive training on brain subnetworks in humans, however, remains largely unknown, with studies limited to functional networks. Here, we used a well-established working memory training program and state-of-the art neuroimaging methods in 40 healthy adults (21 females, mean age 26.5 years). Near and far-transfer training effects were assessed using computerized working memory and executive function tasks. Adaptive working memory training led to improvement on (non)trained working memory tasks and generalization to tasks of reasoning and inhibition. Graph theoretical analysis of the structural (white matter) network connectivity ("connectome") revealed increased global integration within a frontoparietal attention network following adaptive working memory training compared with the nonadaptive group. Furthermore, the impact on the outcome of graph theoretical analyses of different white matter metrics to infer "connection strength" was evaluated. Increased efficiency of the frontoparietal network was best captured when using connection strengths derived from MR metrics that are thought to be more sensitive to differences in myelination (putatively indexed by the [quantitative] longitudinal relaxation rate, R1) than previously used diffusion MRI metrics (fractional anisotropy or fiber-tracking recovered streamlines). Our findings emphasize the critical role of specific microstructural markers in providing important hints toward the mechanisms underpinning training-induced plasticity that may drive working memory improvement in clinical populations. SIGNIFICANCE STATEMENT: This is the first study to explore training-induced changes in the structural connectome using a well-controlled design to examine cognitive training with up-to-date neuroimaging methods. We found changes in global integration based on white matter connectivity within a frontoparietal attention network following adaptive working memory training compared with a nonadaptive comparison group. Furthermore, the impact of different diffusion MR metrics and more specific markers of white matter on the graph theoretical findings was evaluated. An increase in network global efficiency following working memory training was best captured when connection strengths were weighted by MR relaxation rates (influenced by myelination). These results are important for the optimization of cognitive training programs for healthy individuals and people with brain disease.
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Two months of working memory training can cause dMRI changes in healthy young adults, including within the left parahippocampal cingulum.
“It has, for example, been shown that two months of working memory training can cause dMRI changes in healthy young adults, including within the left parahippocampal cingulum (Caeyenberghs et al., 2016; Metzler-Baddeley et al., 2017).”
From The cingulum bundle: Anatomy, function, and dysfunction (2018) · cites this paper as Caeyenberghs et al., 2016
The Participants and Abstract sections describe eight weeks of working-memory training in healthy adults (mean age 26.5 years), and the Results report training-related structural-network changes. But the Results describe diffusion-derived network effects as only marginally significant, while the significant global-efficiency effect used an MR relaxation metric. The regional analyses identify the right anterior cingulate and right inferior ventrolateral prefrontal cortex, not the left parahippocampal cingulum; page numbers are unavailable in our copy. (LLM, conf=0.88)
Experimental — accuracy not yet measuredEnhancements in cognitive performance following training are mirrored by changes in neural activity and connectivity of the brain networks serving working memory.
“Enhancements in cognitive performance following training are mirrored by changes in the neural activity and connectivity of the brain networks serving WM (Astle et al., 2015; Barnes et al., 2016; Caeyenberghs et al., 2016; Constantinidis & Klingberg, 2016; Dahlin, Neely, Larsson, Backman, & Nyberg, 2008; Kundu, Sutterer, Emrich, & Postle, 2013; Olesen, Westerberg, & Klingberg, 2004; Takeuchi & Kaw”
From Working memory training involves learning new skills (2019) · cites this paper as Caeyenberghs et al., 2016
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Studies of interference in serial verbal reactions
Stroop, J. R. (1935) · Journal of Experimental Psychology · doi:10.1037/h0054651 · Cited by 18,622 · see citing works
Tzourio-Mazoyer, N., Landeau, B., Papathanassiou, D., Crivello, F., Etard, O., Delcroix, N., Mazoyer, B., & Joliot, M. (2002) · NeuroImage · doi:10.1006/nimg.2001.0978 · Cited by 16,319 · see citing works
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 · see citing works
Fischl, B. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.01.021 · Cited by 9,526 · see citing works
Efficient behavior of small-world networks
Latora, V., & Marchiori, M. (2001) · Physical Review Letters · doi:10.1103/physrevlett.87.198701 · Cited by 5,119 · see citing works
Wechsler Abbreviated Scale of Intelligence
Wechsler, D. (1999) · PsycTESTS Dataset · doi:10.1037/t15170-000 · Cited by 4,681 · see citing works
Elastix: a toolbox for intensity-based medical image registration
Klein, S., Staring, M., Murphy, K., Viergever, M. A., & Pluim, J. (2010) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2009.2035616 · Cited by 4,311 · see citing works
The reorienting system of the human brain: from environment to theory of mind
Corbetta, M., Patel, G., & Shulman, G. L. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.017 · Cited by 3,889 · see citing works
Specific impairments of planning
Shallice, T. (1982) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1982.0082 · Cited by 3,741 · see citing works
Diffusion tensor MR imaging of the human brain
Pierpaoli, C., Jezzard, P., Basser, P. J., Barnett, A., & Di Chiro, G. (1996) · Radiology · doi:10.1148/radiology.201.3.8939209 · Cited by 2,664 · see citing works
White matter integrity, fiber count, and other fallacies: The do's and don'ts of diffusion MRI
Jones, D. K., Knösche, T. R., & Turner, R. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2012.06.081 · Cited by 2,479 · cited 2× · see citing works
“Although frequently concluded that increased myelination underpins traininginduced FA changes, FA can be modulated by a variety of biological factors, including myelination, packing density, and diameter of the axonal fibers (Jones et al., 2013).”
BackgroundSelf-citationWithin-subject template estimation for unbiased longitudinal image analysis
Reuter, M., Schmansky, N. J., Rosas, H. D., & Fischl, B. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.02.084 · Cited by 2,356 · see citing works
Large-scale brain networks in cognition: emerging methods and principles
Bressler, S. L., & Menon, V. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.04.004 · Cited by 2,348 · see citing works
Computerized training of working memory in children with ADHD – a randomized, controlled trial
Klingberg, T., Fernell, E., Olesen, P. J., Johnson, M., Gustafsson, P., Dahlström, K., Gillberg, C. G., Forssberg, H., & Westerberg, H. (2005) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1097/00004583-200502000-00010 · Cited by 1,949 · see citing works
An automated version of the operation span task
Unsworth, N., Heitz, R. P., Schrock, J. C., & Engle, R. W. (2005) · Behavior Research Methods · doi:10.3758/bf03192720 · Cited by 1,861 · see citing works
Is working memory training effective? A meta-analytic review
Melby-Lervåg, M., & Hulme, C. (2013) · Developmental Psychology · doi:10.1037/a0028228 · Cited by 1,782 · see citing works
Plasticity in gray and white: neuroimaging changes in brain structure during learning
Zatorre, R. J., Fields, R. D., & Johansen-Berg, H. (2012) · Nature Neuroscience · doi:10.1038/nn.3045 · Cited by 1,685 · see citing works
Training and plasticity of working memory
Klingberg, T. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.05.002 · Cited by 1,585 · see citing works
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 · see citing works
Training induces changes in white-matter architecture
Scholz, J., Klein, M. C., Behrens, T. E. J., & Johansen-Berg, H. (2009) · Nature Neuroscience · doi:10.1038/nn.2412 · Cited by 1,508 · see citing works
Small-World Anatomical Networks in the Human Brain Revealed by Cortical Thickness from MRI
Yong He, A., Chen, Z. J., & Evans, A. C. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhl149 · Cited by 1,341 · see citing works
Increased prefrontal and parietal activity after training of working memory
Olesen, P. J., Westerberg, H., & Klingberg, T. (2004) · Nature Neuroscience · doi:10.1038/nn1165 · Cited by 1,317 · see citing works
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 · see citing works
The B‐matrix must be rotated when correcting for subject motion in DTI data
Leemans, A., & Jones, D. K. (2009) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21890 · Cited by 1,266 · see citing works
Self-citationTraining of Working Memory in Children With ADHD
Klingberg, T., Forssberg, H., & Westerberg, H. (2002) · Journal of Clinical and Experimental Neuropsychology · doi:10.1076/jcen.24.6.781.8395 · Cited by 1,225 · see citing works
Hierarchical Organization of Human Cortical Networks in Health and Schizophrenia
Bassett, D. S., Bullmore, E. T., Verchinski, B. A., Mattay, V. S., Weinberger, D. R., & Meyer‐Lindenberg, A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1929-08.2008 · Cited by 1,203 · see citing works
Free water elimination and mapping from diffusion MRI
Pasternak, O., Sochen, N., Gur, Y., Intrator, N., & Assaf, Y. (2009) · Magnetic Resonance in Medicine · doi:10.1002/mrm.22055 · Cited by 1,092 · see citing works
Intensity and coherence of motifs in weighted complex networks.
Onnela, J., Saramäki, J., Kertész, J., & Kaski, K. (2004) · Physical review. E, Statistical, nonlinear, and soft matter physics · doi:10.1103/physreve.71.065103 · Cited by 1,087 · see citing works
Putting brain training to the test
Owen, A. M., Hampshire, A., Grahn, J. A., Stenton, R., Dajani, S., Burns, A. S., Howard, R. J., & Ballard, C. G. (2010) · Nature · doi:10.1038/nature09042 · Cited by 1,056 · see citing works
Clustering in weighted networks
Opsahl, T., & Panzarasa, P. (2009) · Social Networks · doi:10.1016/j.socnet.2009.02.002 · Cited by 1,037 · see citing works
Adaptive training leads to sustained enhancement of poor working memory in children
Holmes, J., Gathercole, S. E., & Dunning, D. L. (2009) · Developmental Science · doi:10.1111/j.1467-7687.2009.00848.x · Cited by 961 · see citing works
In vivo visualization of myelin water in brain by magnetic resonance
MacKay, A. L., Whittall, K. P., Adler, J., Li, D. K. B., Paty, D. W., & Graeb, D. A. (1994) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910310614 · Cited by 916 · see citing works
Oligodendrocyte Dynamics in the Healthy Adult CNS: Evidence for Myelin Remodeling
Young, K. M., Psachoulia, K., Tripathi, R. B., Dunn, S.-J., Cossell, L., Attwell, D., Tohyama, K., & Richardson, W. D. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.006 · Cited by 872 · cited 1× · see citing works
“This induced myelin formation is probably a process of myelin remodeling in healthy adults, whereby additional myelin internodes are added to partially myelinated axons in such a way that the total number of myelinating cells increases without a concomitant increase in the total length of myelin sheath (Young et al.,…”
BackgroundComposite hindered and restricted model of diffusion (CHARMED) MR imaging of the human brain
Assaf, Y., & Basser, P. J. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.03.042 · Cited by 856 · 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
Graph analysis of the human connectome: Promise, progress, and pitfalls
Fornito, A., Zalesky, A., & Breakspear, M. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.04.087 · Cited by 743 · see citing works
Improving fluid intelligence with training on working memory: a meta-analysis
Au, J., Sheehan, E., Tsai, N., Duncan, G. J., Buschkuehl, M., & Jaeggi, S. M. (2015) · Psychonomic Bulletin & Review · doi:10.3758/s13423-014-0699-x · Cited by 671 · 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
A 3 min reasoning test based on grammatical transformation
Baddeley, A. (1968) · Psychonomic Science · doi:10.3758/bf03331551 · Cited by 648 · see citing works
Cortese, S., Ferrin, M., Brandeis, D., Buitelaar, J., Daley, D., Dittmann, R. W., Holtmann, M., Santosh, P., Stevenson, J., Stringaris, A., et al. (2015) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2014.12.010 · Cited by 627 · see citing works
Karbach, J., & Verhaeghen, P. (2014) · Psychological Science · doi:10.1177/0956797614548725 · Cited by 589 · see citing works
Jovicich, J., Czanner, S., Han, X., Salat, D. H., van der Kouwe, A. J. W., Quinn, B. T., Pacheco, J., Albert, M., Killiany, R., & Blacker, D. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.02.010 · Cited by 549 · see citing works
Training of Working Memory Impacts Structural Connectivity
Takeuchi, H., Sekiguchi, A., Taki, Y., Yokoyama, S., Yomogida, Y., Komuro, N., Yamanouchi, T., Suzuki, S., & Kawashima, R. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4611-09.2010 · Cited by 531 · see citing works
Mapping Infant Brain Myelination with Magnetic Resonance Imaging
Deoni, S. C. L., Mercure, E., Blasi, A., Gasston, D., Thomson, A., Johnson, M., Williams, S. C. R., & Murphy, D. G. M. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2106-10.2011 · Cited by 497 · see citing works
Normalized Accurate Measurement of Longitudinal Brain Change
Smith, S. M., Stefano, N. D., Jenkinson, M., & Matthews, P. M. (2001) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-200105000-00022 · Cited by 489 · see citing works
Gleaning multicomponent T 1 and T 2 information from steady‐state imaging data
Deoni, S., Rutt, B. K., Arun, T., Pierpaoli, C. M., & Jones, D. K. (2008) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21704 · Cited by 473 · see citing works
Self-citationBernhardt, B. C., Chen, Z., Yong He, A., Evans, A. C., & Bernasconi, N. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq291 · Cited by 463 · see citing works
Alexander, A. L., Hurley, S. A., Samsonov, A. A., Adluru, N., Hosseinbor, A. P., Mossahebi, P., Tromp, D., Zakszewski, E., & Field, A. S. (2011) · Brain Connectivity · doi:10.1089/brain.2011.0071 · Cited by 450 · see citing works
Computerized working memory training after stroke–A pilot study
Westerberg, H., Jacobaeus, H., Hirvikoski, T., Clevberger, P., Östensson, M.-L., Bartfai, A., & Klingberg, T. (2007) · Brain Injury · doi:10.1080/02699050601148726 · Cited by 439 · see citing works
Deoni, S. C. L., Dean, D. C., O'Muircheartaigh, J., Dirks, H., & Jerskey, B. A. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.07.037 · Cited by 390 · see citing works
Effects of memory training on cortical thickness in the elderly
Engvig, A., Fjell, A., Westlye, L., Moberget, T., Sundseth, Ø., Larsen, V. A., & Walhovd, K. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.05.041 · Cited by 383 · see citing works
Hosseini, S. M. H., Hoeft, F., & Kesler, S. R. (2012) · PLoS ONE · doi:10.1371/journal.pone.0040709 · Cited by 361 · see citing works
Does Working Memory Training Transfer? A Meta-Analysis Including Training Conditions as Moderators
Schwaighofer, M., Fischer, F., & Bühner, M. (2015) · Educational Psychologist · doi:10.1080/00461520.2015.1036274 · Cited by 332 · see citing works
Dell'Acqua, F., Scifo, P., Rizzo, G., Catani, M., Simmons, A., Scotti, G., & Fazio, F. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2009.09.033 · Cited by 320 · see citing works
Cognitive Training for Improving Executive Function in Chemotherapy-Treated Breast Cancer Survivors
Kesler, S., Hadi Hosseini, S. M., Heckler, C., Janelsins, M., Palesh, O., Mustian, K., & Morrow, G. (2013) · Clinical Breast Cancer · doi:10.1016/j.clbc.2013.02.004 · Cited by 300 · see citing works
High field MRI correlates of myelin content and axonal density in multiple sclerosis
Mottershead, J. P., Schmierer, K., Clemence, M., Thornton, J. S., Scaravilli, F., Barker, G. J., Tofts, P. S., Newcombe, J., Cuzner, M. L., Ordidge, R. J., et al. (2003) · Journal of Neurology · doi:10.1007/s00415-003-0192-3 · Cited by 296 · see citing works
How and how not to correct for CSF-contamination in diffusion MRI
Metzler-Baddeley, C., O'Sullivan, M. J., Bells, S., Pasternak, O., & Jones, D. K. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.08.043 · Cited by 291 · see citing works
Self-citationQuantitative magnetic resonance of postmortem multiple sclerosis brain before and after fixation
Schmierer, K., Wheeler‐Kingshott, C. A. M., Tozer, D. J., Boulby, P. A., Parkes, H. G., Yousry, T. A., Scaravilli, F., Barker, G. J., Tofts, P. S., & Miller, D. H. (2008) · Magnetic Resonance in Medicine · doi:10.1002/mrm.21487 · Cited by 281 · see citing works
Ortiz, E., Pasquini, J. M., Thompson, K., Felt, B. T., Butkus, G., Beard, J. L., & Connor, J. R. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20207 · Cited by 260 · see citing works
Spencer‐Smith, M. M., & Klingberg, T. (2015) · PLoS ONE · doi:10.1371/journal.pone.0119522 · Cited by 230 · see citing works
Is diffusion anisotropy an accurate monitor of myelination?
Mädler, B., Drabycz, S. A., Kolind, S. H., Whittall, K. P., & MacKay, A. L. (2008) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2008.01.047 · Cited by 227 · see citing works
Brain anatomical networks in early human brain development
Fan, Y., Shi, F., Smith, J. K., Lin, W., Gilmore, J. H., & Shen, D. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.07.025 · Cited by 225 · see citing works
Irfanoglu, M. O., Walker, L., Sarlls, J. E., Marenco, S., & Pierpaoli, C. M. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.02.054 · Cited by 216 · see citing works
Neuronal effects following working memory training.
Buschkuehl, M., Jaeggi, S. M., & Jonides, J. (2012) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2011.10.001 · Cited by 212 · see citing works
Is the magnetization transfer ratio a marker for myelin in multiple sclerosis?
Vavasour, I. M., Laule, C., Li, D. K. B., Traboulsee, A. L., & MacKay, A. L. (2011) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.22441 · Cited by 201 · see citing works
Collin, G., & van den Heuvel, M. P. (2013) · The Neuroscientist · doi:10.1177/1073858413503712 · Cited by 198 · see citing works
Functional brain connectivity at rest changes after working memory training
Jolles, D. D., van Buchem, M. A., Crone, E. A., & Rombouts, S. A. R. B. (2013) · Human Brain Mapping · doi:10.1002/hbm.21444 · Cited by 183 · see citing works
The effects of working memory training on functional brain network efficiency
Langer, N., von Bastian, C. C., Wirz, H., Oberauer, K., & Jäncke, L. (2013) · Cortex · doi:10.1016/j.cortex.2013.01.008 · Cited by 175 · see citing works
White matter plasticity in adulthood
Wang, S., & Young, K. M. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.10.018 · Cited by 172 · see citing works
Takeuchi, H., Taki, Y., Sassa, Y., Hashizume, H., Sekiguchi, A., Fukushima, A., & Kawashima, R. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023175 · Cited by 166 · see citing works
Kundu, B., Sutterer, D. W., Emrich, S. M., & Postle, B. R. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.5565-12.2013 · Cited by 161 · see citing works
Ullman, H., Almeida, R., & Klingberg, T. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0842-13.2014 · Cited by 155 · see citing works
A cognitive training intervention increases resting cerebral blood flow in healthy older adults
Mozolic, J. L. (2010) · Frontiers in Human Neuroscience · doi:10.3389/neuro.09.016.2010 · Cited by 142 · see citing works
Peijnenborgh, J., Hurks, P. P. M., Aldenkamp, A. P., Vles, J. S. H., & Hendriksen, J. G. M. (2015) · Neuropsychological Rehabilitation · doi:10.1080/09602011.2015.1026356 · Cited by 134 · see citing works
Myelin water imaging reflects clinical variability in multiple sclerosis
Kolind, S., Matthews, L., Johansen‐Berg, H., Leite, M. I., Williams, S., Deoni, S., & Palace, J. A. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.11.070 · Cited by 131 · see citing works
Cognitive training enhances intrinsic brain connectivity in childhood
Astle, D. E., Barnes, J. J., Baker, K., Colclough, G. L., & Woolrich, M. W. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.4517-14.2015 · Cited by 123 · see citing works
Brain enhancement through cognitive training: a new insight from brain connectome
Taya, F., Sun, Y., Babiloni, F., Thakor, N. V., & Bezerianos, A. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00044 · Cited by 102 · see citing works
White-matter relaxation time and myelin water fraction differences in young adults with autism
Deoni, S., Zinkstok, J., Daly, E., Ecker, C., Williams, S., & Murphy, D. (2014) · Psychological Medicine · doi:10.1017/s0033291714001858 · Cited by 80 · see citing works
Deficient MWF mapping in multiple sclerosis using 3D whole-brain multi-component relaxation MRI
Kitzler, H. H., Su, J., Zeineh, M., Harper-Little, C., Leung, A., Kremenchutzky, M., Deoni, S., & Rutt, B. K. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.08.052 · Cited by 77 · see citing works
Motion correction and registration of high b‐value diffusion weighted images
Ben-Amitay, S., Jones, D. K., & Assaf, Y. (2011) · Magnetic Resonance in Medicine · doi:10.1002/mrm.23186 · Cited by 70 · see citing works
Self-citationSantis, S. D., Assaf, Y., Evans, C. J., & Jones, D. (2014) · Magnetic Resonance in Medicine · doi:10.1002/mrm.24717 · Cited by 53 · see citing works
Self-citationJeurissen, B., Leemans, A., Jones, D. K., Tournier, J., & Sijbers, J. (2010) · Cited by 46 · see citing works
Self-citationWolf, D. G. F., Fischer, F. U., Fesenbeckh, J., Yakushev, I. Y., Lelieveld, I. M., Scheurich, A., Schermuly, I., Zschutschke, L., & Fellgiebel, A. (2012) · Human Brain Mapping · doi:10.1002/hbm.22177 · Cited by 35 · see citing works
Changing iron content of the mouse brain during development
Holmes‐Hampton, G. P., Chakrabarti, M., Cockrell, A. L., McCormick, S. P., Abbott, L. C., Lindahl, L. S., & Lindahl, P. A. (2012) · Metallomics · doi:10.1039/c2mt20086d · Cited by 31 · see citing works
Spencer‐Smith, M. M., & Klingberg, T. (2016) · PLoS ONE · doi:10.1371/journal.pone.0167373 · Cited by 31 · see citing works
Rehabilitation of endogenous task shift processes in closed head injury patients
Stablum, F., Umiltà, C. A., Mazzoldi, M., et al. (2006) · Neuropsychological Rehabilitation · doi:10.1080/13506280500411111 · Cited by 29 · 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
TESTING THE MENTAL ABILITY OF ADULTS
Raven, J. (1942) · The Lancet · doi:10.1016/s0140-6736(00)79361-5 · Cited by 14 · see citing works
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Research works printed but not linked: 1
- Hurley S, Mossahebi P, Samsonov A, Alexander A, Deoni S, Fisher R, Duncan I, Field A (2010) Multicomponent relaxometry (mcDESPOT) in the shaking pup model of dysmyelination. In: Proceedings of the 18th Meet- ing of the International Society for Magnetic Resonance in Medicine, p 4516, Stockholm.
Cited by
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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
“It has, for example, been shown that two months of working memory training can cause dMRI changes in healthy young adults, including within the left parahippocampal cingulum (Caeyenberghs et al., 2016; MetzlerBaddeley et al., 2017).”
Self-citationWorking memory training involves learning new skills
Gathercole, S. E., Dunning, D. L., Holmes, J., & Norris, D. (2019) · Journal of Memory and Language · doi:10.1016/j.jml.2018.10.003 · Cited by 225 · see citing works
“Enhancements in cognitive performance following training are mirrored by changes in the neural activity and connectivity of the brain networks serving WM (Astle et al., 2015; Barnes et al., 2016; Caeyenberghs et al., 2016; Constantinidis & Klingberg, 2016; Dahlin, Neely, Larsson, Backman, & Nyberg, 2008; Kundu, Sutter…”
BackgroundBrooks, S. J., Burch, K. H., Maiorana, S. A., Cocolas, E., Schioth, H. B., Nilsson, E. K., Kamaloodien, K., & Stein, D. J. (2016) · NeuroImage: Clinical · doi:10.1016/j.nicl.2016.08.019 · Cited by 50 · see citing works
- Authors
- Caeyenberghs, K., Metzler-Baddeley, C., Foley, S., & Jones, D. K.
- Affiliations
- Australian Catholic University (AU)
- Cardiff University (GB)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2016-04-06
- Volume
- 36
- Issue
- 14
- Pages
- 4056-4066
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC4821915
- OpenAlex
- W2266839507
- Cited by
- 91
- References
- 88
- Citations by year
- 2026: 4 · 2025: 7 · 2024: 4 · 2023: 6 · 2022: 11 · 2021: 12 · 2020: 11 · 2019: 10 · 2018: 12 · 2017: 9 · 2016: 4
- FWCI
- 10.12
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion, cc-by)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- ORCA Online Research @Cardiff (Cardiff University) (submittedVersion)
- Research Bank (Australian Catholic University) (submittedVersion)
- Own your potential (DEAKIN) (submittedVersion)
- Figshare (submittedVersion, cc-by)
- Funders
- Wellcome Trust (096646/Z/11/Z)
- Vlaamse regering
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Cognitive Abilities and Testing
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Keywords
- working memory training, structural connectome, white matter connectivity, frontoparietal attention network, network efficiency, myelination, R1 relaxation rate, training-induced plasticity, transfer of training, executive function, graph theory
- MeSH terms
- Adult, Algorithms, Brain Mapping, Cognition, Female, Humans, Learning, Male, Memory, Short-Term, Mental Processes, Myelin Sheath, Nerve Net, Neuronal Plasticity, Psychomotor Performance, Diffusion Magnetic Resonance Imaging, Young Adult, Executive Function, Neuroimaging, Connectome, Gray Matter
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