The DOI matches its Crossref record; 49 of the 49 references it cites were found in a registry or an index.
Dynamics of Oligodendrocyte Generation and Myelination in the Human Brain
Open accessAbstract
The myelination of axons by oligodendrocytes has been suggested to be modulated by experience, which could mediate neural plasticity by optimizing the performance of the circuitry. We have assessed the dynamics of oligodendrocyte generation and myelination in the human brain. The number of oligodendrocytes in the corpus callosum is established in childhood and remains stable after that. Analysis of the integration of nuclear bomb test-derived (14)C revealed that myelin is exchanged at a high rate, whereas the oligodendrocyte population in white matter is remarkably stable in humans, with an annual exchange of 1/300 oligodendrocytes. We conclude that oligodendrocyte turnover contributes minimally to myelin modulation in human white matter and that this instead may be carried out by mature oligodendrocytes, which may facilitate rapid neural plasticity.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In addition, birth dating of oligodendrocytes by analysis of integrated nuclear bomb test-derived 14C revealed that few oligodendrocytes were newly generated in shadow plaques of MS patients”
From BCAS1-positive oligodendrocytes enable efficient cortical remyelination in multiple sclerosis (2025) · cites this paper as [22]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Birth dating of oligodendrocytes, by analysis of the integration of nuclear bomb test-derived14C into cells, provided evidence for the generation of only few new oligodendrocytes in the adult human corpus callosum (15), suggesting that adaptive myelination in the white matter of humans may be more limited as compared to mice.”
From BCAS1 expression defines a population of early myelinating oligodendrocytes in multiple sclerosis lesions (2017) · cites this paper as [15]
The cited source says what the claim attributes to it.
In the citing paper
“Birth dating of oligodendrocytes, by analysis of the integration of nuclear bomb test-derived14C into cells, provided evidence for the generation of only few new oligodendrocytes in the adult human corpus callosum (15), suggesting that adaptive myelination in the white matter of humans may be more limited as compared to mice.”
From BCAS1 expression defines a population of early myelinating oligodendrocytes in multiple sclerosis lesions (2017) · cites this paper as [15]
The cited source says what the claim attributes to it.
In the citing paper
“These data are in good agreement with the birth dating of oligodendrocytes by14C integration, which showed that the number of oligodendrocytes in the white matter is largely established during the first years, whereas gray matter oligodendrocytes continue to be generated in adulthood (15).”
From BCAS1 expression defines a population of early myelinating oligodendrocytes in multiple sclerosis lesions (2017) · cites this paper as [15]
In the citing paper
“In the corpus callosum, oligodendrocyte numbers increase until age 5 years and are stable thereafter; a study of nuclear bomb test-derived 14C suggest that there is little turnover of oligodendrocytes after age 5 years217.”
From Imaging structural and functional brain development in early childhood (2018) · cites this paper as [217]
In the citing paper
“These and other studies have shown that myelination changes can occur in a time frame much less than the six-week intervention used here (Yeung et al., 2014; Gibson et al., 2014).”
From Multi-modal characterization of rapid anterior hippocampal volume increase associated with aerobic exercise (2016) · cites this paper as Yeung et al., 2014
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Evidence for Cardiomyocyte Renewal in Humans
Bergmann, O., Bhardwaj, R. D., Bernard, S., Zdunek, S., Barnabé-Heider, F., Walsh, S., Zupicich, J., Alkass, K., Buchholz, B. A., Druid, H., et al. (2009) · Science · doi:10.1126/science.1164680 · Cited by 3,130
Self-citationDynamics of hippocampal neurogenesis in adult humans
Spalding, K. L., Bergmann, O., Alkass, K., Bernard, S., Salehpour, M., Huttner, H. B., Boström, E., Westerlund, I., Vial, C., Buchholz, B. A., et al. (2013) · Cell · doi:10.1016/j.cell.2013.05.002 · Cited by 1,841
Self-citationTraining 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
Neuronal activity promotes oligodendrogenesis and adaptive myelination in the mammalian brain
Gibson, E. M., Purger, D., Mount, C. W., Goldstein, A. K., Lin, G. L., Wood, L. S., Inema, I., Miller, S. E., Bieri, G., Zuchero, J. B., et al. (2014) · Science · doi:10.1126/science.1252304 · Cited by 1,472
White matter in learning, cognition, and psychiatric disorders
Fields, R. D. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2008.04.001 · Cited by 1,337
Extensive piano practicing has regionally specific effects on white matter development
Bengtsson, S. L., Nagy, Z., Skare, S., Forsman, L., Forssberg, H., & Ullén, F. (2005) · Nature Neuroscience · doi:10.1038/nn1516 · Cited by 1,193
Unbiased stereological estimation of the number of neurons in the human hippocampus
West, M. J., & Gundersen, H. J. G. (1990) · Journal of Comparative Neurology · doi:10.1002/cne.902960102 · Cited by 1,153
Diffusion tensor imaging of white matter tract evolution over the lifespan
Lebel, C., Gee, M., Camicioli, R., Wieler, M., Martin, W., & Beaulieu, C. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.11.094 · Cited by 1,100
PDGFRA/NG2 glia generate myelinating oligodendrocytes and piriform projection neurons in adult mice
Rivers, L. E., Young, K. M., Rizzi, M., Jamen, F., Psachoulia, K., Wade, A., Kessaris, N., & Richardson, W. D. (2008) · Nature Neuroscience · doi:10.1038/nn.2220 · Cited by 961
Neurogenesis in the striatum of the adult human brain
Ernst, A., Alkass, K., Bernard, S., Salehpour, M., Perl, S., Tisdale, J., Possnert, G., Druid, H., & Frisén, J. (2014) · Cell · doi:10.1016/j.cell.2014.01.044 · Cited by 937
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Items 401–500 of 536
Cranial radiotherapy profoundly affects glia without inducing widespread cellular senescence
Kuil, L. E., van Scheppingen, R. H., Leter, Y. M., Röring, B. H., de Gooijer, M. C., Heijningen, C. L. V., Preković, S., Compter, A., van Tellingen, O., & Schagen, S. B. (2025) · Neuro-Oncology · doi:10.1093/neuonc/noaf146 · Cited by 3
Neuron–glial interactions and neurotransmitter signaling to cells of the oligodendrocyte lineage
Call, C. L., Biase, L. M. D., & Bergles, D. E. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00036-9 · Cited by 3
The dynamics of oligodendrocyte generation: how distinct is the mouse from the human?Preprint
Gonsalvez, D. G., Craig, G. A., Walsh, D. M., Hughes, B. D., Wood, R. J., Yoo, S. W., Murray, S. S., & Xiao, J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2019.12.23.887174 · Cited by 3
A COMPARATIVE ANALYSIS OF CONVECTIVE HEAT TRANSFER IN A NUCLEAR ROCKET NOZZLE
Neumann, H., & Bettinger, P. J. (1963) · University of Michigan Library Repository · Cited by 3
Sharma, M., Prakash, S., Mathur, P., Suri, V. S., Subramanian, A., Agrawal, D. K., Pandey, R. M., Raina, A., Malhotra, R., & Lalwani, S. (2023) · Journal of Forensic and Legal Medicine · doi:10.1016/j.jflm.2023.102557 · Cited by 3
Peterson, B. S., Delavari, S., Sadik, J., Ersland, L., Elgen, I., Sawardekar, S., Bansal, R., & Aukland, S. M. (2024) · Journal of Child Psychology and Psychiatry and Allied Disciplines · doi:10.1111/jcpp.14069 · Cited by 2
Winkler, I., Posod, A., Gizewski, E. R., Mangesius, S., Neubauer, V., Peglow, U. P., Kiechl-Kohlendorfer, U., & Griesmaier, E. (2025) · Neonatology · doi:10.1159/000543328 · Cited by 2
Ferreira, G. A. M., & Pinto, L. (2025) · Glia · doi:10.1002/glia.70031 · Cited by 2
GPR17 in Glioblastoma: Structure, Ligand Interactions, and Therapeutic Targeting
Ramalakshmi, S., Chaitanya, S. S., Kumar, I. S., Ramesh, T., Sureka, C., Abass, K. S., Saravanan, K. M., Anand, T., & Kandhavelu, M. (2025) · ACS Omega · doi:10.1021/acsomega.5c04079 · Cited by 2
G Protein‐Coupled Receptor Signaling in CNS (Re)Myelination
McDonald, J. K., Ang, S. Y., Langmead, C. J., & Stewart, G. D. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70286 · Cited by 2
Akbari, H., Kashani, I. R., Yazdi, F. R., & Pasbakhsh, P. (2026) · PLoS ONE · doi:10.1371/journal.pone.0343039 · Cited by 2
Enhanced myelination potential of human mature oligodendrocytes by TNF and IFNG combination
Mohammadnia, A., Cui, Q., Yaqubi, M., Blaszczyk, G. J., Weng, C., Hall, J. A., Dudley, R., Stratton, J. A., Zandee, S., Kennedy, T. E., et al. (2026) · Journal of Neuroinflammation · doi:10.1186/s12974-026-03753-y · Cited by 2
Chauca, J. M. N., VanDyck, M. V., Oseguera, A. L. G., Ramírez, C. M., Escobar, A. D. G., Orozco, I. P., & Sanchez, M. B. R. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27083603 · Cited by 3
Adiponectin Fortifies White Matter After Chronic Hypoperfusion–Induced Vascular Dementia
Miao, W., Xu, F., Pu, H., Shan, J., Lyu, J., Mai, T.-W., Tian, Q., Pandya, A., Barreiro, J., Jiang, L., et al. (2026) · Stroke · doi:10.1161/strokeaha.126.055924 · Cited by 2
Cortical and white matter myelination proceed in concert during early infancy
Zika, S., Chang, K., Orhon, A., Kruper, J., Tyagi, C., Yan, X., Tung, S. S., Kalanit Grill-spector, A., Rokem, A., & Grotheer, M. (2026) · Nature Communications · doi:10.1038/s41467-026-73366-9 · Cited by 2
Gene choice in cancer cells is exclusive in ion transport but concurrent in DNA replication
Mondal, S., & Becskei, A. (2024) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2024.06.004 · Cited by 2
Chabrol, T., & Wion, D. (2019) · Medical Hypotheses · doi:10.1016/j.mehy.2019.109417 · Cited by 2
DNA Methylation in Multiple Sclerosis
Kular, L., & Jagodic, M. (2019) · RNA technologies · doi:10.1007/978-3-030-14792-1_8 · Cited by 2
Signaling pathways that regulate glial development and early migration—oligodendrocytes
Fancy, S. P. J., & Miller, R. H. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00035-7 · Cited by 2
In vitro models for human neuroglia
Lendemeijer, B., & de Vrij, F. M. S. (2025) · Handbook of clinical neurology · doi:10.1016/b978-0-443-19104-6.00015-2 · Cited by 1
Myelin Maintenance and Addition Regulate Synaptic Plasticity in the Adult Mouse Cortex
Pepper, R., Makowiecki, K., Pitman, K. A., Ricci, R., Nicoli, A. L., Nguyen, P. T., Blizzard, C. L., Emery, B., Cullen, C. L., & Young, K. M. (2026) · Glia · doi:10.64898/2025.12.18.695322 · Cited by 1
Oligodendrocyte dysfunction in human age-related cognitive decline
Craig, G. A., Merour, E., Seeker, L. A., Haughian, A. J., Arbabi, K., Rose, J. L., Hoffmann, A., Thapar, J., Corsinotti, A., Mitchell, S., et al. (2026) · Nature Medicine · doi:10.1038/s41591-026-04608-y · Cited by 1
Education and Health as Social Determinants: The Econeurobiology of Brain Development
Shance, S. (2024) · Frontiers research topics · doi:10.3389/978-2-8325-5722-8 · Cited by 2
Gene Therapy of Adrenomyeloneuropathy: Challenges, Target Cells, and Prospectives
Bougneres, P. F., Stunff, C. L., & Badin, R. A. (2025) · Biomedicines · doi:10.3390/biomedicines13081892 · Cited by 1
Alpha synuclein-mediated cytoskeletal dysfunction impairs myelination in human oligodendrocytes
Wihan, J., Battis, K., Hoffmann, A., Windener, F., Himmler, M., Varghese, A., Koller, A., Karnatz, I., Schubert, D. W., Zunke, F., et al. (2025) · Acta Neuropathologica · doi:10.1007/s00401-025-02933-z · Cited by 1
Enhancer dynamics and cellular architecture in the human spinal cord
Kandror, E. K., Wang, A., Carriere, M., Peterson, A., Liao, W., Tjärnberg, A., Fung, J. H., Mahbubani, K. T. A., Loper, J., Pangburn, W., et al. (2026) · Neuron · doi:10.1016/j.neuron.2025.12.035 · Cited by 2
Reactive OPCs in CNS Injury: From Functional Diversity to Therapeutic Translation
Wang, S., Liu, H., Li, J., Yuan, Y., Dai, Z., Lan, Z., Huang, C., Wei, X., He, C., Su, Z., et al. (2026) · Neuroscience Bulletin · doi:10.1007/s12264-026-01601-w · Cited by 1
RXR Gamma Enables Oligodendrocyte Differentiation by Suppressing Sonic Hedgehog Signaling
Baldassarro, V. A., Brassart, Q., Fraulob, V., Calzà, L., & Krężel, W. (2026) · Glia · doi:10.1002/glia.70151 · Cited by 1
Bansal, R., Hellerstein, D. J., Sawardekar, S., Chen, Y., & Peterson, B. S. (2026) · NeuroImage Clinical · doi:10.1016/j.nicl.2026.104013 · Cited by 1
Congenital blindness reduces myelination in human visual cortex
Stroh, A., Edwards, L., Haenelt, D., Attar, F. M., Pine, K., Trampel, R., Marcin Szwed, A., & Weiskopf, N. (2026) · Science Advances · doi:10.1126/sciadv.aec2348 · Cited by 2
Neurodevelopment, Intestinal Function, and Autism
Yu, E. C.-L. (2018) · Neonatal and Pediatric Medicine · doi:10.4172/2572-4983.1000166 · Cited by 1
Ye, D., Qu, S., Yang, Y., Wang, Z., Wang, Q., Liu, W., Zhang, F., Guan, Q., Wang, X., Zang, J., et al. (2023) · iScience · doi:10.1016/j.isci.2023.106647 · Cited by 1
Манолова, А. О., & Gulyaeva, N. V. (2023) · Journal of Evolutionary Biochemistry and Physiology · doi:10.1134/s0022093023050125 · Cited by 1
Recchia, A. D., Dominicis, A., D’Amore, V. M., Fabiano, T., Jaf, A. I. A. A., Peria, S., Basoli, F., Rainer, A., Marinelli, L., Leva, F. S. D., et al. (2024) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2024.1473960 · Cited by 1
Oligodendroglial changes in ageing human white matter
Rivera, A. D., Azim, K., & Butt, A. M. (2025) · Ageing & Longevity · doi:10.47855/jal9020-2025-2-6 · Cited by 1
Modeling Down Syndrome Neurodevelopment with Dosage Compensation
Czerminski, J. T. (2019) · eScholarship@UMassChan · doi:10.13028/j7xf-1q21 · Cited by 1
Neurogenesis in the damaged mammalian brain
Nakafuku, M., & Grande, A. W. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00023-0 · Cited by 1
Talwar, P., Deantoni, M., Egroo, M. V., Muto, V., Chylinski, D., Koshmanova, E., Jaspar, M., Meyer, C., Degueldre, C., Berthomier, C., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-47753-x · Cited by 1
Lyons, D. A., & Almeida, R. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.732872241.793545529 · Cited by 1
Quantitative Grey/White Matter Myelin differences in Neurofibromatosis Type-1 using T1W/T2W ratioPreprint
Chandran, V. A., Lea‐Carnall, C., Stivaros, S. M., Vassallo, G., Muhlert, N., & Garg, S. (2025) · medRxiv · doi:10.1101/2025.03.28.25324840 · Cited by 1
Späte, E., Higgins, K. P., Kim, Y., Mangana, C., Komarek, L., Teymouri, M., Gerwig, U. C., Melzer, S., Sadowski, B., Ruhwedel, T., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.05.692364 · Cited by 1
mTOR Signaling and Endoplasmic Reticulum Stress in Mixed Glial Cultures
Schreiber-Stainthorp, W. T. (2015) · Trinity College Digital Repository (Trinity College, Hartford CT)
ANALYSIS OF CARDIAC CELL TURNOVER IN HUMANS BY RADIOCARBON DATING AND MATHEMATICAL MODELING
Zdunek, S. (2015) · Figshare
Self-citationMOLECULAR SUBCLASSIFICATION, STEM CELL MARKERS AND GROWTH REGULATORY PATHWAYS IN GLIOMAS
Olausson, K. H. (2015) · Figshare
Transcriptional control of myelin maintenance in the adult CNS
Koenning, M. (2015) · Minerva Access (University of Melbourne)
Genetic Evidence For Neuron-Glia Metabolic Coupling In The CNS
Supplie, L. M. (2016) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5775
The oligodendrocyte "processosome": novel regulators of differentiation and myelination
da Silva, A. F. B. (2015) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · doi:10.34626/1zbe-vq61
Developing brain and systemic inflammation: a "Toll-like" link with consequences
Mottahedin, A. (2017) · Gothenburg University Publications Electronic Archive (Gothenburg University)
Cerebral bases of cognitive training in working memory executive tasks
Padilla, A. M. (2018) · Tesis Doctorals en Xarxa (Consorci de Serveis Universitaris de Catalunya) · doi:10.6035/14109.2018.208792
Demyelinating conditions regulated by ROS pathways outside and inside the brain
Carlström, K. E. (2020) · Figshare
LRP1 is a negative regulator of oligodendrogenesis in the adult mouse central nervous system
Auderset, L. (2020) · UTAS Research Repository · doi:10.25959/100.00034806
Sterling, K. (2020) · York University Digital Library (York University)
Dynamic myelin regulation as a novel form of neural plasticity
Yuliana, Y. (2021) · Journal of the Medical Sciences (Berkala Ilmu Kedokteran) · doi:10.19106/jmedsci005301202107
Laine, M. A. (2021) · Työväentutkimus Vuosikirja
Investigation of myelin maintenance and turnover by inducible MBP knock-out in adult mice
Meschkat, M. (2019) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7679
Louie, A. Y., Kim, J., Soto‐Díaz, K., Dibaeinia, P., Koito, H., Sinha, S., Nowak, R. A., Das, A., & Steelman, A. J. (2021) · Research Square · doi:10.21203/rs.3.rs-310861/v1
Liang, Y., Wei, K., Liu, L., & Cao, W. (2021) · Research Square · doi:10.21203/rs.3.rs-664110/v1
Luo, J. X. X. (2021) · eScholarship@McGill (McGill) · doi:10.82308/21669
Mak, J. (2021) · TSpace (University of Toronto)
Role of microglia in myelin turnover
Safaiyan, S. (2016) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5727
Emery, B., & Duncan, G. J. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.736924641.793568752
Faculty Opinions recommendation of A hypothalamus-habenula circuit controls aversion.
Sajikumar, S., & Raghuraman, R. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735071584.793557290
Faculty Opinions recommendation of The adult oligodendrocyte can participate in remyelination.
Salzer, J. L. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.734522413.793557896
Engineering Adult Neurogenesis and Gliogenesis
(2021) · Frontiers research topics · doi:10.3389/978-2-88966-510-5
Lyons, D. A., & Almeida, R. (2020) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.738031512.793575106
Advances in Oligodendrocyte Research
朱, 秀. (2022) · Advances in Clinical Medicine · doi:10.12677/acm.2022.1291261 · Cited by 1
Gallego, J., Nevin, M., & Eisenstat, D. D. (2023) · Springer eBooks · doi:10.1007/978-3-031-20792-1_7
Graneri, L., Mamo, J. C. L., Takechi, R., & Lam, V. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-89834-8.00018-0 · Cited by 1
Vitamin D mechanisms of protection in multiple sclerosis
Hayes, C. E., Astier, A., & Lincoln, M. R. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-91338-6.00051-3
Author response: Fetal influence on the human brain through the lifespan
Walhovd, K. B., Krogsrud, S. K., Amlien, I. K., Sørensen, Ø., Wang, Y., Bråthen, A. C. S., Øverbye, K., Kransberg, J., Mowinckel, A. M., Magnussen, F., et al. (2024) · eLife · doi:10.7554/elife.86812.3.sa3
Манолова, А. О., & Gulyaeva, N. V. (2023) · Российский физиологический журнал им И М Сеченова · doi:10.31857/s0869813923090078 · Cited by 1
Role of clathrin-mediated endocytosis in myelinating oligodendrocytes
Siems, S. B. (2024) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-10475
Konopka, G., & Caglayan, E. (2024) · Oxford University Press eBooks · doi:10.1093/med/9780197676592.003.0006
Cellular biology of the central nervous system
Leyendecker, J., Prasse, T., Karp, A., & Khaing, Z. Z. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-95730-4.00016-0
Schuurmans, I. M. E., Mordelt, A., & de Witte, L. D. (2025) · Handbook of clinical neurology · doi:10.1016/b978-0-443-19104-6.00011-5
Morphology of Oligodendroglial Cells
Butt, A. M., Willis, A., Stevens, R., Hunter, I., & Nishiyama, A. (2025) · Advances in neurobiology · doi:10.1007/978-3-031-87919-7_5
Siems, S. B., Jung, R. B., Jahn, O., Meschkat, M., Michanski, S., Łukasik, N., Hümmert, S., Sasmita, A. O., Möbius, W., Benseler, F., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.02.673641
Epigenomic regulation of human oligodendrocyte myelination properties – relation to age and lineagePreprint
Mohammadnia, A., Dansu, D. K., Cui, Q., Yaqubi, M., Dudley, R., Stratton, J. A., Zandee, S., Kennedy, T. E., Srour, M., Casaccia, P., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.04.674347
Ding, T., Schweickart, G., Kaiser, K., Rivaldi, A., Marchal, N., Harrington, C. A., Varghese, A., Qin, K., Kelly, B., Sunkel, B. D., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.21.677597 · Cited by 1
Evolution of glia in humans and other hominoids
Falcone, C. (2025) · Evolution of Nervous Systems · doi:10.1016/b978-0-443-27380-3.00065-8
Han, X., Zuo, L., Zhang, Z., Yu, Y., Hu, J., Qian, L., Tian, X., Wei, J., Zhang, R., & Luo, F. (2026) · Communications Biology · doi:10.1038/s42003-026-11256-y
WWOX deficiency uncovers a cell-autonomous mechanism impairing myelin repairPreprint
Abudiab, B., Manenti, C., Repudi, S., Abu‐Swai, S., Akkawi, R., Jbara, T., Dávila-Velderrain, J., & Aqeilan, R. I. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.22.689900
GPR17 structure and agonism with small molecules and oxysterolsPreprint
Metrick, C. M., Zhang, L., Hercher, M., Dodge, G. J., Cherry, D., Rebollar, J. V., Brickelmaier, M., Wang, J., Martin, J. G., Hronowski, X. L., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.26.690757
Cepeda-Prado, E., Stamouli, C. A., Nocera, G., Aretio-Medina, C., Kidnapillai, S., Bruzelius, A., Giacomoni, J., Kajtez, J., Parmar, M., & Ottosson, D. R. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.02.691915
Chandran, V. A., Lea‐Carnall, C., Yang, Y., Wild, A., McCowen, M., Vassallo, G., Green, J., Haroon, H. A., Lloyd, W. K., Stivaros, S. M., et al. (2025) · medRxiv · doi:10.64898/2025.12.09.25341878
Language lateralization and neuroplasticity in pediatric drug-resistant focal epilepsy: A case study
Agudelo-Ríos, M., Salcedo-Posso, D., Correa-Rodríguez, W., Herrera-Trujillo, A., Tolosa-Gaviria, C., Cerón, C. A. R., Becerra-Hernández, L. V., Buriticá, E., & González-Acosta, C. A. (2025) · The Clinical Neuropsychologist · doi:10.1080/13854046.2025.2594019
Louie, A. Y., Kim, J., Drnevich, J., Dibaeinia, P., Koito, H., Sinha, S., McKim, D. B., Soto‐Díaz, K., Nowak, R. A., Das, A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26611526
Louie, A. Y., Kim, J., Drnevich, J., Dibaeinia, P., Koito, H., Sinha, S., McKim, D. B., Soto‐Díaz, K., Nowak, R. A., Das, A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26611523
Louie, A. Y., Kim, J., Drnevich, J., Dibaeinia, P., Koito, H., Sinha, S., McKim, D. B., Soto‐Díaz, K., Nowak, R. A., Das, A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26611514
Louie, A. Y., Kim, J., Drnevich, J., Dibaeinia, P., Koito, H., Sinha, S., McKim, D. B., Soto‐Díaz, K., Nowak, R. A., Das, A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26611505
Wu, X., Shen, Q., Zhang, Z., Zhang, D., Gu, Y., & Xing, D. (2021) · Figshare · doi:10.6084/m9.figshare.14773927
Louie, A. Y., Kim, J., Drnevich, J., Dibaeinia, P., Koito, H., Sinha, S., McKim, D. B., Soto‐Díaz, K., Nowak, R. A., Das, A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26611511
Louie, A. Y., Kim, J., Drnevich, J., Dibaeinia, P., Koito, H., Sinha, S., McKim, D. B., Soto‐Díaz, K., Nowak, R. A., Das, A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26611520
Louie, A. Y., Kim, J., Drnevich, J., Dibaeinia, P., Koito, H., Sinha, S., McKim, D. B., Soto‐Díaz, K., Nowak, R. A., Das, A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26611517
Louie, A. Y., Kim, J., Drnevich, J., Dibaeinia, P., Koito, H., Sinha, S., McKim, D. B., Soto‐Díaz, K., Nowak, R. A., Das, A., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26611508
Kamte, Y. S., Potosnak, C. E., London, N. M., Singh, V. R., Thompson, K., Fadare, A., Chandwani, M. N., Leak, R. K., & O’Donnell, L. A. (2026) · Research Square · doi:10.21203/rs.3.rs-8563506/v1
Metadata
- Authors
- Yeung, M. S. Y., Zdunek, S., Bergmann, O., Bernard, S., Salehpour, M., Alkass, K., Perl, S., Tisdale, J., Possnert, G., Brundin, L., Druid, H., & Frisén, J.
- Affiliations
- Karolinska Institutet (SE)
- Centre National de la Recherche Scientifique (FR)
- Uppsala University (SE)
- National Institutes of Health (US)
- Karolinska University Hospital (SE)
- Corresponding author
- Frisén, Jonas
- ORCID
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2014-11
- Volume
- 159
- Issue
- 4
- Pages
- 766-774
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2044216636
- Cited by
- 541
- References
- 49
- Citations by year
- 2026: 42 · 2025: 46 · 2024: 47 · 2023: 53 · 2022: 43 · 2021: 66 · 2020: 39 · 2019: 56 · 2018: 33 · 2017: 47 · 2016: 42 · 2015: 26
- FWCI
- 13.31
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion, other-oa)
- Uppsala University Publications (Uppsala University) (submittedVersion, other-oa)
- Funders
- Cancerfonden
- Vetenskapsrådet
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- oligodendrocyte generation, myelination, corpus callosum, white matter, neuroplasticity, human brain development
- MeSH terms
- Adolescent, Adult, Aged, Aged, 80 and over, Aging, Brain, Carbon Isotopes, Child, Child, Preschool, Corpus Callosum, Humans, Infant, Middle Aged, Myelin Sheath, Neuronal Plasticity, Oligodendroglia, Nuclear Weapons, Young Adult, White Matter
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