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Cited by 426

The DOI matches its Crossref record; 57 of the 57 references it cites were found in a registry or an index.

Childhood cerebellar tumours mirror conserved fetal transcriptional programs

Open access
Vladoiu, Maria C., El-Hamamy, Ibrahim, Donovan, Laura K., Farooq, Hamza, Holgado, Borja L., Sundaravadanam, Yogi, Ramaswamy, Vijay, Hendrikse, Liam D., Kumar, Sachin, Mack, Stephen C., Lee, John J. Y., Fong, Vernon, Juraschka, Kyle, Przelicki, David, Michealraj, Antony, Skowron, Patryk, Luu, Betty, Suzuki, Hiromichi, Morrissy, A. Sorana, Cavalli, Florence M. G., Garzia, Livia, Daniels, Craig, Wu, Xiaochong, Qazi, Maleeha A., Singh, Sheila K., Chan, Jennifer A., Marra, Marco A., Malkin, David, Dirks, Peter, Heisler, Lawrence, Pugh, Trevor, Ng, Karen, Notta, Faiyaz, Thompson, Eric M., Kleinman, Claudia L., Joyner, Alexandra L., Jabado, Nada, Stein, Lincoln, Taylor, Michael D.·2019·Nature

Abstract

Study of the origin and development of cerebellar tumours has been hampered by the complexity and heterogeneity of cerebellar cells that change over the course of development. Here we use single-cell transcriptomics to study more than 60,000 cells from the developing mouse cerebellum and show that different molecular subgroups of childhood cerebellar tumours mirror the transcription of cells from distinct, temporally restricted cerebellar lineages. The Sonic Hedgehog medulloblastoma subgroup transcriptionally mirrors the granule cell hierarchy as expected, while group 3 medulloblastoma resembles Nestin+ stem cells, group 4 medulloblastoma resembles unipolar brush cells, and PFA/PFB ependymoma and cerebellar pilocytic astrocytoma resemble the prenatal gliogenic progenitor cells. Furthermore, single-cell transcriptomics of human childhood cerebellar tumours demonstrates that many bulk tumours contain a mixed population of cells with divergent differentiation. Our data highlight cerebellar tumours as a disorder of early brain development and provide a proximate explanation for the peak incidence of cerebellar tumours in early childhood. Sequencing data from the developing cerebellum are compared with bulk sequencing data from paediatric tumours, providing insights into their potential origins and suggesting that many cerebellar tumours have their origins early in utero.

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Metadata

Authors
Vladoiu, M. C., El-Hamamy, I., Donovan, L. K., Farooq, H., Holgado, B. L., Sundaravadanam, Y., Ramaswamy, V., Hendrikse, L. D., Kumar, S., Mack, S. C., Lee, J. J. Y., Fong, V., Juraschka, K., Przelicki, D., Michealraj, A., Skowron, P., Luu, B., Suzuki, H., Morrissy, A. S., Cavalli, F. M. G., Garzia, L., Daniels, C., Wu, X., Qazi, M. A., Singh, S. K., Chan, J. A., Marra, M. A., Malkin, D., Dirks, P., Heisler, L., Pugh, T., Ng, K., Notta, F., Thompson, E. M., Kleinman, C. L., Joyner, A. L., Jabado, N., Stein, L., & Taylor, M. D.
Venue
Nature
Published
2019-05-01
Volume
572
Issue
7767
Pages
67-73
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
OpenAlex
W2808584871
Cited by
426
References
57
FWCI
25.59
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Childhood cerebellar tumours mirror conserved fetal transcriptional programs. https://app.cochat.ai/papers/10.1038/s41586-019-1158-7
The paper
Vladoiu, M. C., El-Hamamy, I., Donovan, L. K., Farooq, H., Holgado, B. L., Sundaravadanam, Y., Ramaswamy, V., Hendrikse, L. D., Kumar, S., Mack, S. C., Lee, J. J. Y., Fong, V., Juraschka, K., Przelicki, D., Michealraj, A., Skowron, P., Luu, B., Suzuki, H., Morrissy, A. S., . . . Taylor, M. D. (2019). Childhood cerebellar tumours mirror conserved fetal transcriptional programs. Nature. https://doi.org/10.1038/s41586-019-1158-7

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.