The DOI matches its Crossref record; 25 of the 25 references it cites were found in a registry or an index.
Clinical implications of genetic advances in Charcot–Marie–Tooth disease
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Citations
Cites
Schouten, J. P. (2002) · Nucleic Acids Research · doi:10.1093/nar/gnf056 · Cited by 2,699
Whole-Genome Sequencing in a Patient with Charcot–Marie–Tooth Neuropathy
Lupski, J. R., Reid, J. G., Gonzaga-Jauregui, C., Rio Deiros, D., Chen, D. C. Y., Nazareth, L., Bainbridge, M., Dinh, H., Jing, C., Wheeler, D. A., et al. (2010) · New England Journal of Medicine · doi:10.1056/nejmoa0908094 · Cited by 759
Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)
Raeymaekers, P., Timmerman, V, Nelis, E., De Jonghe, P., Hoogenduk, J. E., Baas, F., Barker, D. F., Martin, J. J., De Visser, M., Bolhuis, P. A., et al. (1991) · Neuromuscular Disorders · doi:10.1016/0960-8966(91)90055-w · Cited by 607
Charcot‐marie‐tooth disease subtypes and genetic testing strategies
Saporta, A. S. D., Sottile, S. L., Miller, L. J., Feely, S. M. E., Siskind, C. E., & Shy, M. E. (2011) · Annals of Neurology · doi:10.1002/ana.22166 · Cited by 542
d'Ydewalle, C., Krishnan, J., Chiheb, D. M., Van Damme, P., Irobi, J., Kozikowski, A. P., Berghe, P. V., Timmerman, V., Robberecht, W., & Van Den Bosch, L. (2011) · Nature Medicine · doi:10.1038/nm.2396 · Cited by 454
Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss
Klein, C. J., Botuyan, M.-V., Wu, Y., Ward, C. J., Nicholson, G. A., Hammans, S., Hojo, K., Yamanishi, H., Karpf, A. R., Wallace, D. C., et al. (2011) · Nature Genetics · doi:10.1038/ng.830 · Cited by 405
Charcot–Marie–Tooth disease: frequency of genetic subtypes and guidelines for genetic testing
Murphy, S. M., Laura, M., Fawcett, K., Pandraud, A., Liu, Y.-T., Davidson, G. L., Rossor, A. M., Polke, J. M., Castleman, V., Manji, H., et al. (2012) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp-2012-302451 · Cited by 378
Self-citationDisease-targeted sequencing: a cornerstone in the clinic
Rehm, H. L. (2013) · Nature Reviews Genetics · doi:10.1038/nrg3463 · Cited by 377
Ascorbic acid treatment corrects the phenotype of a mouse model of Charcot-Marie-Tooth disease
Passage, E., Norreel, J. C., Noack-Fraissignes, P., Sanguedolce, V., Pizant, J., Thirion, X., Robaglia-Schlupp, A., Pellissier, J. F., & Fontés, M. (2004) · Nature Medicine · doi:10.1038/nm1023 · Cited by 349
Sereda, M. W., Meyer zu Hörste, G., Suter, U., Uzma, N., & Nave, K.-A. (2003) · Nature Medicine · doi:10.1038/nm957 · Cited by 310
Cited by
Salzer, J. L. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020529 · Cited by 364
Regulation of the epigenome by vitamin C
Young, J. I., Züchner, S., & Wang, G. (2015) · Annual Review of Nutrition · doi:10.1146/annurev-nutr-071714-034228 · Cited by 319
Myelin lipid metabolism and its role in myelination and myelin maintenance
Barnes-Vélez, J. A., Aksoy Yasar, F. B., & Hu, J. (2023) · The Innovation · doi:10.1016/j.xinn.2022.100360 · Cited by 73
Yagi, T., Ito, D., & Suzuki, N. (2016) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlw009 · Cited by 33
Disrupting the transmembrane domain interface between PMP22 and MPZ causes peripheral neuropathy
(2024) · doi:10.1016/j.isci.2024.110989 · Cited by 15
Metadata
- Authors
- Rossor, A. M., Polke, J. M., Houlden, H., & Reilly, M. M.
- Venue
- Nature Reviews Neurology
- Published
- 2013-09-10
- Volume
- 9
- Issue
- 10
- Pages
- 562-571
- ISSN
- 1759-4758 (ISSN-L)
- 1759-4766
- OpenAlex
- W1965759164
- Cited by
- 358
- References
- 25
- FWCI
- 2.55
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Clinical implications of genetic advances in Charcot–Marie–Tooth disease. https://app.cochat.ai/papers/10.1038/nrneurol.2013.179
- The paper
- Rossor, A. M., Polke, J. M., Houlden, H., & Reilly, M. M. (2013). Clinical implications of genetic advances in Charcot–Marie–Tooth disease. Nature Reviews Neurology. https://doi.org/10.1038/nrneurol.2013.179
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
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.
