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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:

RUNX1 isoform disequilibrium promotes the development of trisomy 21–associated myeloid leukemia
S Gialesaki, Daniela Bräuer-Hartmann, H Issa, et al.
Blood (2022) Vol. 141, Iss. 10, pp. 1105-1118
Open Access | Times Cited: 24

Showing 24 citing articles:

Cancer, metastasis, and the epigenome
Saurav Kiri, Tyrone Ryba
Molecular Cancer (2024) Vol. 23, Iss. 1
Open Access | Times Cited: 29
Landscape of driver mutations and their clinical effects on Down syndrome–related myeloid neoplasms
Tomohiko Sato, Kenichi Yoshida, Tsutomu Toki, et al.
Blood (2024) Vol. 143, Iss. 25, pp. 2627-2643
Closed Access | Times Cited: 9
Down syndrome and leukemia: from basic mechanisms to clinical advances
André Baruchel, Jean‐Pierre Bourquin, John D. Crispino, et al.
Haematologica (2023) Vol. 108, Iss. 10, pp. 2570-2581
Open Access | Times Cited: 16
Insights into the Clinical, Biological and Therapeutic Impact of Copy Number Alteration in Cancer
Shannon L. Carey-Smith, Rishi S. Kotecha, Laurence C. Cheung, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 13, pp. 6815-6815
Open Access | Times Cited: 4
RUNX1A isoform is overexpressed in acute myeloid leukemia and is associated with FLT3 internal tandem duplications
Cosimo Cumbo, Francesco Tarantini, Elisa Parciante, et al.
Research Square (Research Square) (2025)
Closed Access
Disease characteristics and outcomes of acute myeloid leukemia in germline RUNX1 deficiency (Familial Platelet Disorder with associated Myeloid Malignancy)
Martijn P. T. Ernst, Jurjen Versluis, Peter J.M. Valk, et al.
HemaSphere (2025) Vol. 9, Iss. 1
Open Access
Using Zebrafish to Study the Mechanisms That Underlie Down Syndrome
Anna J. Moyer, Summer B. Thyme
(2025), pp. 187-232
Closed Access
Myeloid Leukemia of Down Syndrome
Aikaterini Kosmidou, Athanasios Tragiannidis, Eleni Gavriilaki
Cancers (2023) Vol. 15, Iss. 13, pp. 3265-3265
Open Access | Times Cited: 8
RUNX1 Isoforms Regulate RUNX1 and Target-Genes Differentially in Platelets-Megakaryocytes: Association with Clinical Cardiovascular Events
Liying Guan, Deepak Voora, Rachel A. Myers, et al.
Journal of Thrombosis and Haemostasis (2024) Vol. 22, Iss. 12, pp. 3581-3598
Open Access | Times Cited: 3
RUN(X) out of blood: emerging RUNX1 functions beyond hematopoiesis and links to Down syndrome
Esteban J. Rozen, Christopher D. Ozeroff, Mary A. Allen
Human Genomics (2023) Vol. 17, Iss. 1
Open Access | Times Cited: 7
Aberrant stem cell and developmental programs in pediatric leukemia
Rebecca E. Ling, Joe W. Cross, Anindita Roy
Frontiers in Cell and Developmental Biology (2024) Vol. 12
Open Access | Times Cited: 2
Selection forces underlying aneuploidy patterns in cancer
Tamara C. Klockner, Christopher S. Campbell
Molecular & Cellular Oncology (2024) Vol. 11, Iss. 1
Open Access | Times Cited: 2
Down syndrome-associated leukaemias: current evidence and challenges
N. Mason, Hilary Cahill, Yonatan Diamond, et al.
Therapeutic Advances in Hematology (2024) Vol. 15
Open Access | Times Cited: 2
Synergistic roles of DYRK1A and GATA1 in trisomy 21 megakaryopoiesis
Ying Ting Sit, Kaoru Takasaki, Hyun Hyung An, et al.
JCI Insight (2023) Vol. 8, Iss. 23
Open Access | Times Cited: 4
Single-cell transcriptomics dissects the transcriptome alterations of hematopoietic stem cells in myelodysplastic neoplasms
Xiangzong Zeng, Yichen Wang, Min Dai, et al.
Journal of Translational Medicine (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 1
The clinical phenotype of germline RUNX1 mutations in relation to the accompanying somatic variants and RUNX1 isoform expression
David Cabrerizo Granados, Indira Barbosa, Panagiotis Baliakas, et al.
Genes Chromosomes and Cancer (2023) Vol. 62, Iss. 11, pp. 672-677
Open Access | Times Cited: 2
Down syndrome and leukemia: An insight into the disease biology and current treatment options
Sonali P. Barwe, E. Anders Kolb, Anilkumar Gopalakrishnapillai
Blood Reviews (2023) Vol. 64, pp. 101154-101154
Closed Access | Times Cited: 2
ROBO1 deficiency impairs HSPC homeostasis and erythropoiesis via CDC42 and predicts poor prognosis in MDS
Jiacheng Jin, Bingyi Chen, Chuhan Deng, et al.
Science Advances (2023) Vol. 9, Iss. 48
Open Access | Times Cited: 1
MYC-stery of Down syndrome unraveled
Jan‐Henning Klusmann
Blood (2024) Vol. 143, Iss. 25, pp. 2566-2567
Closed Access
RUNX1 Isoforms Regulate RUNX1 and Target-Genes Differentially in Platelets-Megakaryocytes: Association with Clinical Cardiovascular Events
Liying Guan, Deepak Voora, Rachel A. Myers, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Deciphering the miR-200a-3p/RUNX1 Axis: A Novel Oncogene Signature in Colorectal Cancer
Xingkai Su, Xia Jiang, Fangjian Shang, et al.
Research Square (Research Square) (2024)
Open Access
Four Cases of Myeloproliferative Disorders Associated With Down Syndrome: Distinguishing ML‐DS From TAM‐DS
Kévin Boumeghar, Sylvie Daliphard, Nimrod Buchbinder, et al.
Case Reports in Hematology (2024) Vol. 2024, Iss. 1
Open Access
ERG: the good, the bad, and the ugly
Ron Rabinowicz, Shai Izraeli
Blood (2024) Vol. 144, Iss. 17, pp. 1755-1756
Open Access
It is more “unbalanced” than you think
Sébastien Malinge
Blood (2023) Vol. 141, Iss. 10, pp. 1095-1096
Open Access
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