The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Recurrent RAS and PIK3CA mutations in Erdheim-Chester disease
Open accessAbstract
Key Points: PIK3CA and NRAS mutations are recurrent in BRAFV600E wild-type ECD patients. 57.5% (46/80) of ECD patients have a BRAFV600E mutation, and an additional 10.9% and 3.7% have PIK3CA and NRAS mutations, respectively.
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Ascierto, P. A., Schadendorf, D., Berking, C., Agarwala, S. S., van Herpen, C. M., Queirolo, P., Blank, C. U., Hauschild, A., Beck, J. T., St-Pierre, A., et al. (2013) · The Lancet Oncology · doi:10.1016/s1470-2045(13)70024-x · Cited by 640
Cangi, M. G., Biavasco, R., Cavalli, G., Grassini, G., Dal-Cin, E., Campochiaro, C., Guglielmi, B., Berti, A., Lampasona, V., von Deimling, A., et al. (2015) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2013-204924 · Cited by 112
Cited by
Mutually exclusive recurrent KRAS and MAP2K1 mutations in Rosai–Dorfman disease
Garces, S., Medeiros, L. J., Patel, K. P., Li, S., Pina-Oviedo, S., Li, J., Garces, J. C., Khoury, J. D., & Yin, C. C. (2017) · Modern Pathology · doi:10.1038/modpathol.2017.55 · Cited by 299
Metadata
- Authors
- Emile, J.-F., Diamond, E. L., Hélias-Rodzewicz, Z., Cohen-Aubart, F., Charlotte, F., Hyman, D. M., Kim, E., Rampal, R., Patel, M., Ganzel, C., Aumann, S., Faucher, G., Le Gall, C., Leroy, K., Colombat, M., Kahn, J.-E., Trad, S., Nizard, P., Donadieu, J., Taly, V., Amoura, Z., Abdel-Wahab, O., & Haroche, J.
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2014-11-06
- Volume
- 124
- Issue
- 19
- Pages
- 3016-3019
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- OpenAlex
- W2095514651
- Cited by
- 244
- References
- 2
- FWCI
- 15.94
- Type
- journal article
- Language
- en
- Open access
- green
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- The paper
- Emile, J.-F., Diamond, E. L., Hélias-Rodzewicz, Z., Cohen-Aubart, F., Charlotte, F., Hyman, D. M., Kim, E., Rampal, R., Patel, M., Ganzel, C., Aumann, S., Faucher, G., Le Gall, C., Leroy, K., Colombat, M., Kahn, J.-E., Trad, S., Nizard, P., Donadieu, J., . . . Haroche, J. (2014). Recurrent RAS and PIK3CA mutations in Erdheim-Chester disease. Blood. https://doi.org/10.1182/blood-2014-04-570937
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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.
