The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1
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Citations
Cites
Pevny, L., Simon, M. C., Robertson, E., Klein, W. H., Tsai, S.-F., D'Agati, V., Orkin, S. H., & Costantini, F. (1991) · Nature · doi:10.1038/349257a0 · Cited by 1,308
Self-citationWeiss, M. J., Keller, G., & Orkin, S. H. (1994) · Genes & Development · doi:10.1101/gad.8.10.1184 · Cited by 541
Self-citationTranscriptional activation and DNA binding by the erythroid factor GF-1/NF-E1/Eryf 1.
Martin, D. I., & Orkin, S. H. (1990) · Genes & Development · doi:10.1101/gad.4.11.1886 · Cited by 409
Self-citation
Cited by
Transcriptional Regulatory Elements in the Human Genome
Maston, G. A., Evans, S. K., & Green, M. R. (2006) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.7.080505.115623 · Cited by 937
Disruption of differentiation in human cancer: AML shows the way
Tenen, D. G. (2003) · Nature Reviews Cancer · doi:10.1038/nrc989 · Cited by 612
Proximity among Distant Regulatory Elements at the β-Globin Locus Requires GATA-1 and FOG-1
Vakoc, C. R., Letting, D. L., Gheldof, N., Sawado, T., Bender, M. A., Groudine, M., Weiss, M. J., Dekker, J., & Blobel, G. A. (2005) · Molecular Cell · doi:10.1016/j.molcel.2004.12.028 · Cited by 490
Self-citationExome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia
Sankaran, V. G., Ghazvinian, R., Do, R., Thiru, P., Vergilio, J.-A., Beggs, A. H., Sieff, C. A., Orkin, S. H., Nathan, D. G., Lander, E. S., et al. (2012) · Journal of Clinical Investigation · doi:10.1172/jci63597 · Cited by 342
RUNX1 and GATA-1 coexpression and cooperation in megakaryocytic differentiation.
Elagib, K. E., Racke, F. K., Mogass, M., Khetawat, R., Delehanty, L. L., & Goldfarb, A. N. (2003) · Blood · doi:10.1182/blood-2002-09-2708 · Cited by 332
Metadata
- Authors
- Nichols, K. E., Crispino, J. D., Poncz, M., White, J. G., Orkin, S. H., Maris, J. M., & Weiss, M. J.
- Venue
- Nature Genetics
- Published
- 2000-03
- Volume
- 24
- Issue
- 3
- Pages
- 266-270
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W1998602132
- Cited by
- 515
- References
- 3
- FWCI
- 17.60
- Type
- journal article
- Language
- en
- Open access
- green
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- CoChat. (2026). Citation check: Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1. https://app.cochat.ai/papers/10.1038/73480
- The paper
- Nichols, K. E., Crispino, J. D., Poncz, M., White, J. G., Orkin, S. H., Maris, J. M., & Weiss, M. J. (2000). Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1. Nature Genetics. https://doi.org/10.1038/73480
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.
