The DOI matches its Crossref record; 15 of the 15 references it cites were found in a registry or an index.
Familial myeloid malignancies with germline TET2 mutation
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In the citing paper
“Interestingly, families with germline heterozygous TET2 or DNMT3A mutations develop predominantly myeloid neoplasms [234][235][236][237][238] , whereas rare individuals with germline homozygous TET2 mutations develop either B or T cell lymphomas along with a lymphoproliferative syndrome characterized by autoimmune cytopenias and immunodeficiency 239 .”
From Clonal haematopoiesis and dysregulation of the immune system (2023) · cites this paper as [234]
Citations
Cites
Age-related clonal hematopoiesis associated with adverse outcomes
Jaiswal, S., Fontanillas, P., Flannick, J., Manning, A., Grauman, P. V., Mar, B. G., Lindsley, R. C., Mermel, C. H., Burtt, N., Chavez, A., et al. (2014) · New England Journal of Medicine · doi:10.1056/nejmoa1408617 · Cited by 4,841
Mutation in TET2 in Myeloid Cancers
Delhommeau, F., Dupont, S., Valle, V. D., James, C., Trannoy, S., Massé, A., Kosmider, O., Le Couedic, J.-P., Robert, F., Alberdi, A., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0810069 · Cited by 1,776
Molecular Minimal Residual Disease in Acute Myeloid Leukemia
Jongen-Lavrencic, M., Grob, T., Hanekamp, D., Kavelaars, F. G., al Hinai, A., Zeilemaker, A., Erpelinck-Verschueren, C. A. J., Gradowska, P. L., Meijer, R., Cloos, J., et al. (2018) · New England Journal of Medicine · doi:10.1056/nejmoa1716863 · Cited by 786
Genetic Analysis of 779 Advanced Differentiated and Anaplastic Thyroid Cancers
Pozdeyev, N., Gay, L. M., Sokol, E. S., Hartmaier, R., Deaver, K. E., Davis, S., French, J. D., Borre, P. V., LaBarbera, D. V., Tan, A.-C., et al. (2018) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-18-0373 · Cited by 533
Tefferi, A., Pardanani, A., Lim, K.-H., Abdel-Wahab, O., Lasho, T. L., Patel, J., Gangat, N., Finke, C. M., Schwager, S., Mullally, A., et al. (2009) · Leukemia · doi:10.1038/leu.2009.47 · Cited by 425
Lorsbach, R. B., Moore, J., Mathew, S., Raimondi, S. C., Mukatira, S. T., & Downing, J. R. (2003) · Leukemia · doi:10.1038/sj.leu.2402834 · Cited by 416
The Ten-Eleven Translocation-2 (TET2) gene in hematopoiesis and hematopoietic diseases
Solary, E., Bernard, O. A., Tefferi, A., Fuks, F., & Vainchenker, W. (2014) · Leukemia · doi:10.1038/leu.2013.337 · Cited by 288
TET2 mutation is an independent favorable prognostic factor in myelodysplastic syndromes (MDSs)
Kosmider, O., Gelsi-Boyer, V., Cheok, M., Grabar, S., Della-Valle, V., Picard, F., Viguié, F., Quesnel, B., Beyne-Rauzy, O., Solary, E., et al. (2009) · Blood · doi:10.1182/blood-2009-04-215814 · Cited by 276
Self-citationSelimoglu-Buet, D., Wagner-Ballon, O., Saada, V., Bardet, V., Itzykson, R., Bencheikh, L., Morabito, M., Met, E., Debord, C., Benayoun, E., et al. (2015) · Blood · doi:10.1182/blood-2015-01-620781 · Cited by 265
Self-citationTET2 gene mutation is a frequent and adverse event in chronic myelomonocytic leukemia
Kosmider, O., Gelsi‐Boyer, V., Ciudad, M., Racoeur, C., Jooste, V., Vey, N., Quesnel, B., Fenaux, P., Bastie, J.-N., Beyne‐Rauzy, O., et al. (2009) · Haematologica · doi:10.3324/haematol.2009.011205 · Cited by 255
Self-citation
Cited by
Arber, D. A., Orazi, A., Hasserjian, R. P., Borowitz, M. J., Calvo, K. R., Kvasnicka, H.-M., Wang, S. A., Bagg, A., Barbui, T., Branford, S., et al. (2022) · Blood · doi:10.1182/blood.2022015850 · Cited by 2,945
Clonal haematopoiesis and dysregulation of the immune system
Belizaire, R., Wong, W. J., Robinette, M. L., & Ebert, B. L. (2023) · Nature Reviews Immunology · doi:10.1038/s41577-023-00843-3 · Cited by 161
Metadata
- Authors
- Duployez, N., Goursaud, L., Fenwarth, L., Bories, C., Marceau-Renaut, A., Boyer, T., Fournier, E., Nibourel, O., Roche-Lestienne, C., Huet, G., Beauvais, D., Berthon, C., Cambier, N., Quesnel, B., & Preudhomme, C.
- Venue
- Leukemia
- Published
- 2019-12-11
- Volume
- 34
- Issue
- 5
- Pages
- 1450-1453
- ISSN
- 0887-6924
- 1476-5551
- Cited by
- 49
- References
- 15
- Language
- en
- Licence
- www.springer.com/tdm (tdm)
- www.springer.com/tdm (vor)
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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.
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Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Familial myeloid malignancies with germline TET2 mutation. https://app.cochat.ai/papers/10.1038/s41375-019-0675-6
- The paper
- Duployez, N., Goursaud, L., Fenwarth, L., Bories, C., Marceau-Renaut, A., Boyer, T., Fournier, E., Nibourel, O., Roche-Lestienne, C., Huet, G., Beauvais, D., Berthon, C., Cambier, N., Quesnel, B., & Preudhomme, C. (2020). Familial myeloid malignancies with germline TET2 mutation. Leukemia. https://doi.org/10.1038/s41375-019-0675-6
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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.
