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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

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Showing 1-25 of 292 citing articles:

Acquired mutations in TET2 are common in myelodysplastic syndromes
Saskia Langemeijer, Roland P. Kuiper, M Berends, et al.
Nature Genetics (2009) Vol. 41, Iss. 7, pp. 838-842
Closed Access | Times Cited: 732
Mutations of polycomb‐associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia
Véronique Gelsi‐Boyer, Virginie Trouplin, José Adélaı̈de, et al.
British Journal of Haematology (2009) Vol. 145, Iss. 6, pp. 788-800
Open Access | Times Cited: 563
Prognostic Score Including Gene Mutations in Chronic Myelomonocytic Leukemia
Raphaël Itzykson, Olivier Kosmider, Aline Renneville, et al.
Journal of Clinical Oncology (2013) Vol. 31, Iss. 19, pp. 2428-2436
Open Access | Times Cited: 504
Loss of Mismatched HLA in Leukemia after Stem-Cell Transplantation
Luca Vago, Serena K. Perna, Monica Zanussi, et al.
New England Journal of Medicine (2009) Vol. 361, Iss. 5, pp. 478-488
Open Access | Times Cited: 473
Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms
Masashi Sanada, Takahiro Suzuki, Lee‐Yung Shih, et al.
Nature (2009) Vol. 460, Iss. 7257, pp. 904-908
Closed Access | Times Cited: 389
Dynamics of clonal evolution in myelodysplastic syndromes
Hideki Makishima, Tetsuichi Yoshizato, Kenichi Yoshida, et al.
Nature Genetics (2016) Vol. 49, Iss. 2, pp. 204-212
Open Access | Times Cited: 381
Loss of heterozygosity 4q24 and TET2 mutations associated with myelodysplastic/myeloproliferative neoplasms
A. Jankowska, Hadrian Szpurka, Ramón V. Tiu, et al.
Blood (2009) Vol. 113, Iss. 25, pp. 6403-6410
Open Access | Times Cited: 376
Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms
Francis Grand, Claire Hidalgo-Curtis, Thomas Ernst, et al.
Blood (2009) Vol. 113, Iss. 24, pp. 6182-6192
Open Access | Times Cited: 366
Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis
Hideki Makishima, Valeria Visconte, Hirotoshi Sakaguchi, et al.
Blood (2012) Vol. 119, Iss. 14, pp. 3203-3210
Open Access | Times Cited: 364
Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia
Charlotte M. Niemeyer, Michelle Kang, Danielle H. Shin, et al.
Nature Genetics (2010) Vol. 42, Iss. 9, pp. 794-800
Open Access | Times Cited: 350
Mutational spectrum analysis of chronic myelomonocytic leukemia includes genes associated with epigenetic regulation: UTX, EZH2, and DNMT3A
A. Jankowska, Hideki Makishima, Ramón V. Tiu, et al.
Blood (2011) Vol. 118, Iss. 14, pp. 3932-3941
Open Access | Times Cited: 317
Unraveling the Molecular Pathophysiology of Myelodysplastic Syndromes
Rafael Bejar, Ross L. Levine, Benjamin L. Ebert
Journal of Clinical Oncology (2011) Vol. 29, Iss. 5, pp. 504-515
Open Access | Times Cited: 305
Next-Generation Sequencing Technology Reveals a Characteristic Pattern of Molecular Mutations in 72.8% of Chronic Myelomonocytic Leukemia by Detecting Frequent Alterations in TET2, CBL, RAS, and RUNX1
Alexander Kohlmann, Vera Großmann, Hans‐Ulrich Klein, et al.
Journal of Clinical Oncology (2010) Vol. 28, Iss. 24, pp. 3858-3865
Closed Access | Times Cited: 288
Mutations in CBL occur frequently in juvenile myelomonocytic leukemia
Mignon L. Loh, Debbie S. Sakai, Christian Flotho, et al.
Blood (2009) Vol. 114, Iss. 9, pp. 1859-1863
Open Access | Times Cited: 282
Clonal architecture of chronic myelomonocytic leukemias
Raphaël Itzykson, Olivier Kosmider, Aline Renneville, et al.
Blood (2013) Vol. 121, Iss. 12, pp. 2186-2198
Open Access | Times Cited: 253
Somatic SETBP1 mutations in myeloid malignancies
Hideki Makishima, Kenichi Yoshida, Nhu Nguyen, et al.
Nature Genetics (2013) Vol. 45, Iss. 8, pp. 942-946
Open Access | Times Cited: 248
Comprehensive mutational profiling of core binding factor acute myeloid leukemia
Nicolas Duployez, Alice Marceau‐Renaut, Nicolas Boissel, et al.
Blood (2016) Vol. 127, Iss. 20, pp. 2451-2459
Open Access | Times Cited: 217
Mutation allele burden remains unchanged in chronic myelomonocytic leukaemia responding to hypomethylating agents
Jane Merlevede, Nathalie Droin, Tingting Qin, et al.
Nature Communications (2016) Vol. 7, Iss. 1
Open Access | Times Cited: 200
Non canonical c-CBL mutations define a specific phenotype of myeloid neoplasia
Luca Guarnera, Carmelo Gurnari, Carlos Bravo‐Pérez, et al.
Leukemia (2025)
Open Access | Times Cited: 2
Heterozygous Germline Mutations in the CBL Tumor-Suppressor Gene Cause a Noonan Syndrome-like Phenotype
Simone Martinelli, Alessandro De Luca, Emilia Stellacci, et al.
The American Journal of Human Genetics (2010) Vol. 87, Iss. 2, pp. 250-257
Open Access | Times Cited: 248
TET2 gene mutation is a frequent and adverse event in chronic myelomonocytic leukemia
Olivier Kosmider, Véronique Gelsi‐Boyer, Marion Ciudad, et al.
Haematologica (2009) Vol. 94, Iss. 12, pp. 1676-1681
Open Access | Times Cited: 238
Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies
Christine L. O’Keefe, Michael A. McDevitt, Jaroslaw P. Maciejewski
Blood (2010) Vol. 115, Iss. 14, pp. 2731-2739
Open Access | Times Cited: 219
Mutations of E3 Ubiquitin Ligase Cbl Family Members Constitute a Novel Common Pathogenic Lesion in Myeloid Malignancies
Hideki Makishima, Heather Cazzolli, Hadrian Szpurka, et al.
Journal of Clinical Oncology (2009) Vol. 27, Iss. 36, pp. 6109-6116
Open Access | Times Cited: 217
Targeting oncogenic Ras signaling in hematologic malignancies
Ashley F. Ward, Benjamin S. Braun, Kevin Shannon
Blood (2012) Vol. 120, Iss. 17, pp. 3397-3406
Open Access | Times Cited: 195
Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies
Ramón V. Tiu, Lukasz P. Gondek, Christine L. O’Keefe, et al.
Blood (2011) Vol. 117, Iss. 17, pp. 4552-4560
Open Access | Times Cited: 193
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