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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:

The enigma of monosomy 7
Toshiya Inaba, Hiroaki Honda, Hirotaka Matsui
Blood (2018) Vol. 131, Iss. 26, pp. 2891-2898
Open Access | Times Cited: 74

Showing 1-25 of 74 citing articles:

Genetic predisposition to MDS: clinical features and clonal evolution
Alyssa L. Kennedy, Akiko Shimamura
Blood (2019) Vol. 133, Iss. 10, pp. 1071-1085
Open Access | Times Cited: 125
Genetic abnormalities and pathophysiology of MDS
Naoko Hosono
International Journal of Clinical Oncology (2019) Vol. 24, Iss. 8, pp. 885-892
Closed Access | Times Cited: 95
Treatment optimization and genomic outcomes in refractory severe aplastic anemia treated with eltrombopag
Thomas Winkler, Xing Fan, James Cooper, et al.
Blood (2019) Vol. 133, Iss. 24, pp. 2575-2585
Open Access | Times Cited: 93
Somatic genetic rescue in Mendelian haematopoietic diseases
Patrick Revy, Caroline Kannengiesser, Alain Fischer
Nature Reviews Genetics (2019) Vol. 20, Iss. 10, pp. 582-598
Closed Access | Times Cited: 92
Inherited Bone Marrow Failure Syndromes
Lorraine E. Canham, Jill L. O. de Jong
Elsevier eBooks (2024), pp. 51-94
Closed Access | Times Cited: 10
Predisposition to myeloid malignancies in Shwachman-Diamond syndrome: biological insights and clinical advances
Christopher R. Reilly, Akiko Shimamura
Blood (2022) Vol. 141, Iss. 13, pp. 1513-1523
Open Access | Times Cited: 37
Germline loss-of-function SAMD9 and SAMD9L alterations in adult myelodysplastic syndromes
Yasunobu Nagata, Satoshi Narumi, Yihong Guan, et al.
Blood (2018) Vol. 132, Iss. 21, pp. 2309-2313
Open Access | Times Cited: 52
Current Treatment of Juvenile Myelomonocytic Leukemia
Christina Mayerhofer, Charlotte M. Niemeyer, Christian Flotho
Journal of Clinical Medicine (2021) Vol. 10, Iss. 14, pp. 3084-3084
Open Access | Times Cited: 36
Structure and function of an effector domain in antiviral factors and tumor suppressors SAMD9 and SAMD9L
Shuxia Peng, Xiangzhi Meng, Fushun Zhang, et al.
Proceedings of the National Academy of Sciences (2022) Vol. 119, Iss. 4
Open Access | Times Cited: 25
Outcomes and genetic dynamics of acute myeloid leukemia at first relapse
Álex Bataller, Hagop M. Kantarjian, Alexandre Bazinet, et al.
Haematologica (2024)
Open Access | Times Cited: 5
Eltrombopag for patients with moderate aplastic anemia or uni-lineage cytopenias
Xing Fan, Ronan Desmond, Thomas Winkler, et al.
Blood Advances (2020) Vol. 4, Iss. 8, pp. 1700-1710
Open Access | Times Cited: 39
Outcomes of Hematopoietic Cell Transplantation in Patients with Germline SAMD9/SAMD9L Mutations
Ibrahim Ahmed, Midhat S. Farooqi, Mark T. Vander Lugt, et al.
Biology of Blood and Marrow Transplantation (2019) Vol. 25, Iss. 11, pp. 2186-2196
Open Access | Times Cited: 37
Understanding the Continuum between High-Risk Myelodysplastic Syndrome and Acute Myeloid Leukemia
Phaedon D. Zavras, Ilias Sinanidis, Panagiotis Tsakiroglou, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 5, pp. 5018-5018
Open Access | Times Cited: 11
Mutation dynamics from diagnosis to relapse in acute myeloid leukemia with chromosomal 7 deletions
Eitan Kugler, Enes Dasdemir, Álex Bataller, et al.
Leukemia & lymphoma/Leukemia and lymphoma (2025), pp. 1-13
Closed Access
Integrative study of EZH2 mutational status, copy number, protein expression and H3K27 trimethylation in AML/MDS patients
Julia Stomper, Ruth Meier, Tobias Ma, et al.
Clinical Epigenetics (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 21
Myelodysplastic Syndrome
Ota Fuchs
Elsevier eBooks (2024), pp. 144-169
Closed Access | Times Cited: 3
Identification of a shared gene signature and biological mechanism between diabetic foot ulcers and cutaneous lupus erythemnatosus by transcriptomic analysis
Siqi Wu, Yuetong Wang, Jingyi Duan, et al.
Frontiers in Physiology (2024) Vol. 15
Open Access | Times Cited: 3
Precision Medicine Approaches in Acute Myeloid Leukemia with Adverse Genetics
Nicole Santoro, Prassede Salutari, Mauro Di Ianni, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 8, pp. 4259-4259
Open Access | Times Cited: 3
Of gains and losses: SAMD9/SAMD9L and monosomy 7 in myelodysplastic syndrome
Jörg Cammenga
Experimental Hematology (2024) Vol. 134, pp. 104217-104217
Open Access | Times Cited: 3
Role of aneuploidy in the carcinogenic process: Part 3 of the report of the 2017 IWGT workgroup on assessing the risk of aneugens for carcinogenesis and hereditary diseases
David Tweats, David A. Eastmond, Anthony M. Lynch, et al.
Mutation Research/Genetic Toxicology and Environmental Mutagenesis (2019) Vol. 847, pp. 403032-403032
Closed Access | Times Cited: 24
Prevalence of germline GATA2 and SAMD9/9L variants in paediatric haematological disorders with monosomy 7
Masanori Yoshida, Kanako Tanase‐Nakao, Hirohito Shima, et al.
British Journal of Haematology (2020) Vol. 191, Iss. 5, pp. 835-843
Open Access | Times Cited: 23
Genomics of deletion 7 and 7q in myeloid neoplasm: from pathogenic culprits to potential synthetic lethal therapeutic targets
Minako Mori, Yasuo Kubota, Arda Durmaz, et al.
Leukemia (2023) Vol. 37, Iss. 10, pp. 2082-2093
Open Access | Times Cited: 8
Multiorgan failure with abnormal receptor metabolism in mice mimicking Samd9/9L syndromes
Akiko Nagamachi, Akinori Kanai, Megumi Nakamura, et al.
Journal of Clinical Investigation (2020) Vol. 131, Iss. 4
Open Access | Times Cited: 19
Molecular Drivers of Myelodysplastic Neoplasms (MDS)—Classification and Prognostic Relevance
Fieke W. Hoff, Yazan F. Madanat
Cells (2023) Vol. 12, Iss. 4, pp. 627-627
Open Access | Times Cited: 7
Rare NUP98::PRRX1 fusion transcript in a therapy-related acute myeloid leukemia associated with del(7q) following chemotherapy for diffuse large B-cell lymphoma
Yanfang Wang, Zhenghao Zhang, Lingli Wang, et al.
Cancer Genetics (2024) Vol. 284-285, pp. 12-15
Closed Access | Times Cited: 2
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