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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:

MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia
Manuela Germeshausen, Phil Ancliff, Jaime Estrada, et al.
Blood Advances (2018) Vol. 2, Iss. 6, pp. 586-596
Open Access | Times Cited: 95

Showing 1-25 of 95 citing articles:

Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee
Stuart G. Tangye, Waleed Al–Herz, Aziz Bousfiha, et al.
Journal of Clinical Immunology (2022) Vol. 42, Iss. 7, pp. 1473-1507
Open Access | Times Cited: 846
Human inborn errors of immunity: 2024 update on the classification from the International Union of Immunological Societies Expert Committee
M. Cecilia Poli, Ivona Aksentijevich, Ahmed Aziz Bousfiha, et al.
(2025) Vol. 1, Iss. 1
Open Access | Times Cited: 5
Inherited Platelet Disorders: An Updated Overview
Verónica Palma‐Barqueros, Nuria Revilla, Ana B. Sánchez, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 9, pp. 4521-4521
Open Access | Times Cited: 69
Acquired severe aplastic anaemia: how medical therapy evolved in the 20th and 21st centuries
Phillip Scheinberg
British Journal of Haematology (2021) Vol. 194, Iss. 6, pp. 954-969
Open Access | Times Cited: 57
Inherited thrombocytopenias: an updated guide for clinicians
Alessandro Pecci, Carlo L. Balduini
Blood Reviews (2020) Vol. 48, pp. 100784-100784
Closed Access | Times Cited: 54
A genetic disorder reveals a hematopoietic stem cell regulatory network co-opted in leukemia
Richard A. Voit, Liming Tao, Fulong Yu, et al.
Nature Immunology (2022) Vol. 24, Iss. 1, pp. 69-83
Open Access | Times Cited: 35
Acquired and germline predisposition to bone marrow failure: Diagnostic features and clinical implications
Michael E. Kallen, Alina Dulau‐Florea, Weixin Wang, et al.
Seminars in Hematology (2018) Vol. 56, Iss. 1, pp. 69-82
Closed Access | Times Cited: 55
Inherited Thrombocytopenia: Update on Genes and Genetic Variants Which may be Associated With Bleeding
Ibrahim Almazni, Rachel J. Stapley, Neil V. Morgan
Frontiers in Cardiovascular Medicine (2019) Vol. 6
Open Access | Times Cited: 48
Overview of inherited bone marrow failure syndromes
Meerim Park
Blood Research (2022) Vol. 57, Iss. S1, pp. S49-S54
Open Access | Times Cited: 25
Molecular Diagnosis of Inherited Coagulation and Bleeding Disorders
José María Bastida, Rocí­o Benito, Marı́a Luisa Lozano, et al.
Seminars in Thrombosis and Hemostasis (2019) Vol. 45, Iss. 07, pp. 695-707
Closed Access | Times Cited: 39
CAMT-MPL: congenital amegakaryocytic thrombocytopenia caused by MPL mutations - heterogeneity of a monogenic disorder - a comprehensive analysis of 56 patients
Manuela Germeshausen, Matthias Ballmaier
Haematologica (2020) Vol. 106, Iss. 9, pp. 2439-2448
Open Access | Times Cited: 35
Genetics of inherited thrombocytopenias
Julia T. Warren, Jorge Di Paola
Blood (2022) Vol. 139, Iss. 22, pp. 3264-3277
Open Access | Times Cited: 20
ALWAYS STRESSED BUT NEVER EXHAUSTED: HOW STEM CELLS IN MYELOID NEOPLASMS AVOID EXTINCTION IN INFLAMMATORY CONDITIONS
Helong Zhao, Michael W. Deininger
Blood (2023)
Open Access | Times Cited: 13
MECOM Deficiency: from Bone Marrow Failure to Impaired B-Cell Development
Richard A. Voit, Vijay G. Sankaran
Journal of Clinical Immunology (2023) Vol. 43, Iss. 6, pp. 1052-1066
Closed Access | Times Cited: 11
Hereditary Predisposition to Hematopoietic Neoplasms
Abhishek A. Mangaonkar, Mrinal M. Patnaik
Mayo Clinic Proceedings (2020) Vol. 95, Iss. 7, pp. 1482-1498
Open Access | Times Cited: 32
Inherited Susceptibility to Hematopoietic Malignancies in the Era of Precision Oncology
Gregory W. Roloff, Michael W. Drazer, Lucy A. Godley
JCO Precision Oncology (2021), Iss. 5, pp. 107-122
Closed Access | Times Cited: 27
Megakaryopoiesis and Platelet Biology: Roles of Transcription Factors and Emerging Clinical Implications
Ji-Yoon Noh
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 17, pp. 9615-9615
Open Access | Times Cited: 25
Lessons From Pediatric MDS: Approaches to Germline Predisposition to Hematologic Malignancies
Serine Avagyan, Akiko Shimamura
Frontiers in Oncology (2022) Vol. 12
Open Access | Times Cited: 17
A genetikai eredetű gyermekkori krónikus cytopeniák felismerése a molekuláris medicina érájában
Bálint Egyed, Kristóf Árvai, Erik Zajta, et al.
Orvosi Hetilap (2025) Vol. 166, Iss. 1, pp. 3-19
Closed Access
A novel MECOM gene variant causes severe thrombocytopenia in a neonate: a case report and review of the literature
Jiayan Li, Ting Peng, Guoqiang Cheng, et al.
Journal of Medical Case Reports (2025) Vol. 19, Iss. 1
Open Access
Rare Genetic and Uncommon Morphological Entities in Adults with Acute Myeloid Leukemia
Xavier Thomas
Current Oncology Reports (2025)
Closed Access
Inherited predisposition to haematopoietic malignancies: overcoming barriers and exploring opportunities
Amy M. Trottier, Lucy A. Godley
British Journal of Haematology (2020) Vol. 194, Iss. 4, pp. 663-676
Open Access | Times Cited: 27
Special pre- and posttransplant considerations in inherited bone marrow failure and hematopoietic malignancy predisposition syndromes
Carmem Bonfim
Hematology (2020) Vol. 2020, Iss. 1, pp. 107-114
Open Access | Times Cited: 24
Aberrant EVI1 splicing contributes to EVI1-rearranged leukemia
Atsushi Tanaka, Taizo A. Nakano, Masaki Nomura, et al.
Blood (2022) Vol. 140, Iss. 8, pp. 875-888
Open Access | Times Cited: 15
Expanded phenotypic and hematologic abnormalities beyond bone marrow failure in MECOM‐associated syndromes
Michell M. Lozano Chinga, Alison A. Bertuch, Zeinab Afify, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 7, pp. 1826-1835
Open Access | Times Cited: 9
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