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OpenAlex Citation Counts

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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.

Requested Article:

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

Showing 1-25 of 217 citing articles:

Diagnosis and treatment of primary myelodysplastic syndromes in adults: recommendations from the European LeukemiaNet
Luca Malcovati, Eva Hellström‐Lindberg, David Bowen, et al.
Blood (2013) Vol. 122, Iss. 17, pp. 2943-2964
Open Access | Times Cited: 632
The genetics of myelodysplastic syndrome: from clonal haematopoiesis to secondary leukaemia
Adam S. Sperling, Christopher J. Gibson, Benjamin L. Ebert
Nature reviews. Cancer (2016) Vol. 17, Iss. 1, pp. 5-19
Open Access | Times Cited: 600
Novel mutations and their functional and clinical relevance in myeloproliferative neoplasms: JAK2, MPL, TET2, ASXL1, CBL, IDH and IKZF1
Ayalew Tefferi
Leukemia (2010) Vol. 24, Iss. 6, pp. 1128-1138
Open Access | Times Cited: 515
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
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
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
The lysosome as a command-and-control center for cellular metabolism
Chun-Yan Lim, Roberto Zoncu
The Journal of Cell Biology (2016) Vol. 214, Iss. 6, pp. 653-664
Open Access | Times Cited: 277
Impact of molecular mutations on treatment response to DNMT inhibitors in myelodysplasia and related neoplasms
Fabı́ola Traina, Valeria Visconte, Paul Elson, et al.
Leukemia (2013) Vol. 28, Iss. 1, pp. 78-87
Closed Access | Times Cited: 273
Protein tyrosine kinase regulation by ubiquitination: Critical roles of Cbl-family ubiquitin ligases
Bhopal Mohapatra, Gulzar Ahmad, Scott Nadeau, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research (2012) Vol. 1833, Iss. 1, pp. 122-139
Open Access | Times Cited: 213
Novel somatic and germline mutations in intracranial germ cell tumours
Linghua Wang, Shigeru Yamaguchi, Matthew D. Burstein, et al.
Nature (2014) Vol. 511, Iss. 7508, pp. 241-245
Open Access | Times Cited: 210
The RING finger protein family in health and disease
Chunmei Cai, Yan‐Dong Tang, Jingbo Zhai, et al.
Signal Transduction and Targeted Therapy (2022) Vol. 7, Iss. 1
Open Access | Times Cited: 99
Chronic myelomonocytic leukemia: 2022 update on diagnosis, risk stratification, and management
Mrinal M. Patnaik, Ayalew Tefferi
American Journal of Hematology (2022) Vol. 97, Iss. 3, pp. 352-372
Closed Access | Times Cited: 72
Chronic myelomonocytic leukemia: 2024 update on diagnosis, risk stratification and management
Mrinal M. Patnaik, Ayalew Tefferi
American Journal of Hematology (2024) Vol. 99, Iss. 6, pp. 1142-1165
Open Access | Times Cited: 23
Measurable Residual FLT3 Internal Tandem Duplication Before Allogeneic Transplant for Acute Myeloid Leukemia
Laura W. Dillon, Gege Gui, Niveditha Ravindra, et al.
JAMA Oncology (2024) Vol. 10, Iss. 8, pp. 1104-1104
Open Access | Times Cited: 17
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
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
ASXL1 mutation is associated with poor prognosis and acute transformation in chronic myelomonocytic leukaemia
Véronique Gelsi‐Boyer, Virginie Trouplin, Julien Roquain, et al.
British Journal of Haematology (2010) Vol. 151, Iss. 4, pp. 365-375
Open Access | Times Cited: 215
Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes
Christian P. Kratz, Suthee Rapisuwon, Helen E. Reed, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2011) Vol. 157, Iss. 2, pp. 83-89
Open Access | Times Cited: 209
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
Novel homo- and hemizygous mutations in EZH2 in myeloid malignancies
Hideki Makishima, Anna Jankowska, Ramón V. Tiu, et al.
Leukemia (2010) Vol. 24, Iss. 10, pp. 1799-1804
Closed Access | Times Cited: 179
Combined mutations of ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, RUNX1, TET2 and WT1 genes in myelodysplastic syndromes and acute myeloid leukemias
Julien Rocquain, Nadine Carbuccia, Virginie Trouplin, et al.
BMC Cancer (2010) Vol. 10, Iss. 1
Open Access | Times Cited: 168
Recent advances in the pathogenesis and treatment of juvenile myelomonocytic leukaemia
Mignon L. Loh
British Journal of Haematology (2011) Vol. 152, Iss. 6, pp. 677-687
Open Access | Times Cited: 155
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