The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia
Open accessAbstract
Key Points: Mutations of key transcription factor in myeloid malignancies.
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.
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
Song, W.-J., Sullivan, M. G., Legare, R. D., Hutchings, S., Tan, X., Kufrin, D., Ratajczak, J., Resende, I. C., Haworth, C., Hock, R., et al. (1999) · Nature Genetics · doi:10.1038/13793 · Cited by 1,100
Kirwan, M., Vulliamy, T., Marrone, A., Walne, A. J., Beswick, R., Hillmen, P., Kelly, R., Stewart, A., Bowen, D., Schonland, S. O., et al. (2009) · Human Mutation · doi:10.1002/humu.21115 · Cited by 109 · cited 3×
“La prot eine GATA2 est soumise a de nombreuses r egulations post-transcriptionnelles comme la phosphorylation [4-6], l’ac etylation affectant de nombreuses lysines localis ees au niveau des deux doigts de zinc [7], la sumoylation [8] et l’ubiquitinylation [9].”
Background
Cited by
The genetic basis of myelodysplasia and its clinical relevance
Cazzola, M., Della Porta, M. G., & Malcovati, L. (2013) · Blood · doi:10.1182/blood-2013-09-381665 · Cited by 346
Perez-Andreu, V., Roberts, K. G., Harvey, R. C., Yang, W., Cheng, C., Pei, D., Xu, H., Gastier-Foster, J., E, S., Lim, J. Y.-S., et al. (2013) · Nature Genetics · doi:10.1038/ng.2803 · Cited by 305
Metadata
- Authors
- Pasquet, M., Bellanné-Chantelot, C., Tavitian, S., Prade, N., Beaupain, B., LaRochelle, O., Petit, A., Rohrlich, P., Ferrand, C., Van Den Neste, E., Poirel, H. A., Lamy, T., Ouachée-Chardin, M., Mansat-De Mas, V., Corre, J., Récher, C., Plat, G., Bachelerie, F., Donadieu, J., & Delabesse, E.
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2013-01-31
- Volume
- 121
- Issue
- 5
- Pages
- 822-829
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- OpenAlex
- W2060073480
- Cited by
- 217
- References
- 2
- FWCI
- 11.16
- Type
- journal article
- Language
- en
- Open access
- green
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
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia. https://app.cochat.ai/papers/10.1182/blood-2012-08-447367
- The paper
- Pasquet, M., Bellanné-Chantelot, C., Tavitian, S., Prade, N., Beaupain, B., LaRochelle, O., Petit, A., Rohrlich, P., Ferrand, C., Van Den Neste, E., Poirel, H. A., Lamy, T., Ouachée-Chardin, M., Mansat-De Mas, V., Corre, J., Récher, C., Plat, G., Bachelerie, F., Donadieu, J., & Delabesse, E. (2013). High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia. Blood. https://doi.org/10.1182/blood-2012-08-447367
Data sources
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.
