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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:

Hereditary platelet disorders associated with germ line variants in RUNX1, ETV6, and ANKRD26
Claire C. Homan, Hamish S. Scott, Anna Brown
Blood (2023) Vol. 141, Iss. 13, pp. 1533-1543
Open Access | Times Cited: 28

Showing 1-25 of 28 citing articles:

Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41
Claire C. Homan, Michael W. Drazer, Kai Yu, et al.
Blood Advances (2023) Vol. 7, Iss. 20, pp. 6092-6107
Open Access | Times Cited: 19
Inherited blood cancer predisposition through altered transcription elongation
Jiawei Zhao, Liam D. Cato, Uma P. Arora, et al.
Cell (2024) Vol. 187, Iss. 3, pp. 642-658.e19
Open Access | Times Cited: 6
Clonal hematopoiesis in children with predisposing conditions
Enrico Attardi, Seth J. Corey, Marcin W. Włodarski
Seminars in Hematology (2024) Vol. 61, Iss. 1, pp. 35-42
Open Access | Times Cited: 5
Insights into the Molecular Mechanisms of Genetic Predisposition to Hematopoietic Malignancies: The Importance of Gene–Environment Interactions
César Cobaleda, Lucy A. Godley, Kim E. Nichols, et al.
Cancer Discovery (2024) Vol. 14, Iss. 3, pp. 396-405
Open Access | Times Cited: 5
Germline Variants and Characteristic Features of Hereditary Hematological Malignancy Syndrome
Hironori Arai, Hirotaka Matsui, SungGi Chi, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 1, pp. 652-652
Open Access | Times Cited: 4
Myelodysplastic syndrome with dual germline RUNX1 and DDX41 variants: a rare genetic predisposition case
Virginia Bove, María Noel Spangenberg, Carolina Ottati, et al.
Familial Cancer (2025) Vol. 24, Iss. 1
Closed Access
Purpura thrombopénique immunologique réfractaire révélant un syndrome MYH9 chez un homme de 64 ans
Q. Bodard, G. Fredon, A. Riché, et al.
La Revue de Médecine Interne (2025)
Closed Access
Germline Testing in Hematopoietic Malignancies
Himachandana Atluri, Lucy A. Godley
Advances in Oncology (2025)
Closed Access
Germline copy number variants in RUNX1: An updated case report and a decade-old red herring
Natalie Deuitch, Amra Kajdic, Erica Bresciani, et al.
BJC Reports (2025) Vol. 3, Iss. 1
Open Access
The CRISPR-Cas System and Clinical Applications of CRISPR-Based Gene Editing in Hematology with a Focus on Inherited Germline Predisposition to Hematologic Malignancies
Rina Kansal
Genes (2024) Vol. 15, Iss. 7, pp. 863-863
Open Access | Times Cited: 2
Thrombopénies constitutionnelles
Cécile Lavenu‐Bombled, Céline Falaise, Adeline Blandinières, et al.
Perfectionnement en Pédiatrie (2024) Vol. 7, Iss. 1, pp. 48-60
Open Access | Times Cited: 1
Genomic testing for germline predisposition to hematologic malignancies
Sang Mee Hwang
Blood Research (2024) Vol. 59, Iss. 1
Open Access | Times Cited: 1
Genetic Predisposition to Myelodysplastic Syndrome: Genetic Counseling and Transplant Implications
Yi Liu, Kathleen A. Calzone, Lisa J. McReynolds
Seminars in Hematology (2024)
Closed Access | Times Cited: 1
Transcription factor genetics and biology in predisposition to bone marrow failure and hematological malignancy
Jiarna R. Zerella, Claire C. Homan, Peer Arts, et al.
Frontiers in Oncology (2023) Vol. 13
Open Access | Times Cited: 3
Human leucocyte antigen‐matched related haematopoietic stem cell transplantation using low‐dose cyclophosphamide, fludarabine and thymoglobulin in children with severe aplastic anaemia
Abdulrahman Alsultan, Rodaina Abujoub, Reem Al‐Sudairy, et al.
British Journal of Haematology (2023) Vol. 203, Iss. 2, pp. 255-263
Open Access | Times Cited: 3
A Novel Constitutional t(3;8)(p26;q21) and ANKRD26 and SRP72 Variants in a Child with Myelodysplastic Neoplasm: Clinical Implications
Viviane Lamim Lovatel, Ana Paula Silva Bueno, Elaiza Almeida Antônio de Kós, et al.
Journal of Clinical Medicine (2023) Vol. 12, Iss. 9, pp. 3171-3171
Open Access | Times Cited: 2
Diagnostic work-up of hematological malignancies with underlying germline predisposition disorders (GPD)
Rashmi Kanagal‐Shamanna, Kristian T. Schafernak, Katherine R. Calvo
Seminars in Diagnostic Pathology (2023) Vol. 40, Iss. 6, pp. 443-456
Closed Access | Times Cited: 2
When to consider inherited marrow failure syndromes in adults
Fernanda Gutierrez‐Rodrigues, Bhavisha A. Patel, Emma M. Groarke
Hematology (2023) Vol. 2023, Iss. 1, pp. 548-555
Closed Access | Times Cited: 2
RUNX1 C-terminal Mutations Impair Blood Cell Differentiation by Perturbing Specific Enhancer-Promoter Networks
Nathan D. Jayne, Zhengyu Liang, Do‐Hwan Lim, et al.
Blood Advances (2024) Vol. 8, Iss. 10, pp. 2410-2423
Open Access
Inherited thrombocytopenia associated with a variant in the FLI1 binding site in the 5′ UTR of ANKRD26
Caitlin Dunstan‐Harrison, Ian M. Morison, Elizabeth C. Ledgerwood
Clinical Genetics (2024) Vol. 106, Iss. 3, pp. 315-320
Open Access
Germline Predisposition to Hematopoietic Malignancies: An Overview
Yogameenakshi Haribabu, Emma Bhote, Lucy A. Godley
Annual Review of Cancer Biology (2024) Vol. 8, Iss. 1, pp. 309-329
Open Access
Molecular pathophysiology of germline mutations in acute myeloid leukemia
Yasunobu Nagata
International Journal of Hematology (2024) Vol. 120, Iss. 4, pp. 417-426
Closed Access
Impact of thrombocytopenia-associated c.-118C>T and c.-140C>G ANKRD26 5’UTR variants in three-generational pedigree
Jakub Trizuljak, Paulína Likavcová, Kateřina Staňo Kozubík, et al.
Platelets (2024) Vol. 35, Iss. 1
Open Access
How we diagnose Myelodysplastic syndromes
Howard S. Oster, Moshe Mittelman
Frontiers in Oncology (2024) Vol. 14
Open Access
Gene Therapy for Germline Predisposition to Myeloid Malignancies: Insights from a Nonhuman Primate RUNX1 Model
Christine M. McMahon
The Hematologist (2023) Vol. 20, Iss. 3
Open Access
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