Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Overview of inherited bone marrow failure syndromes
Meerim Park
Blood Research (2022) Vol. 57, Iss. S1, pp. S49-S54
Open Access | Times Cited: 23

Showing 23 citing articles:

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
Approach to Pancytopenia: From Blood Tests to the Bedside
Shaun Chew, Majeed Kamangar
Clinical Medicine (2024) Vol. 24, Iss. 5, pp. 100235-100235
Open Access | Times Cited: 4
ERCC6L2-Associated Inherited Bone Marrow Failure Syndrome: A Croatian Experience
Izabela Kranjčec, Nuša Matijašić, Katarina Vulin, et al.
Cureus (2025)
Open Access
Identification of TRAPPC4 as a Key Autoantigen in Immune-Related Pancytopenia: Epitope Characterization and Immune Activation Mechanisms
Shanfeng Hao, Yang Zhang, Na Xiao, et al.
Turkish Journal of Hematology (2025)
Open Access
Germline Testing in Hematopoietic Malignancies
Himachandana Atluri, Lucy A. Godley
Advances in Oncology (2025)
Closed Access
Reduced AKT activation accompanied with high TP53 expression is implicated in the impaired hematogenesis in Ziegler-Huang syndrome and the Znt7 null mice partially recapitulates the human disease linked to pancytopenia
Liping Huang, Stéphanie Nguyen, Zhongyue Yang, et al.
Journal of Trace Elements in Medicine and Biology (2025) Vol. 89, pp. 127658-127658
Open Access
Genomic insights into inherited bone marrow failure syndromes: a single-center clinical study
Kyle Dillahunt, Georgianne Younger, Madeline Van Der Graaf, et al.
Journal of Translational Genetics and Genomics (2025) Vol. 9, Iss. 2, pp. 76-89
Open Access
The effect of red blood cell disorders on male fertility and reproductive health
Bryan Naelitz, Prajit Khooblall, Neel Parekh, et al.
Nature Reviews Urology (2024) Vol. 21, Iss. 5, pp. 303-316
Closed Access | Times Cited: 3
Fanconi anemia and dyskeratosis congenita/telomere biology disorders: Two inherited bone marrow failure syndromes with genomic instability
Moisés Ó. Fiesco-Roa, Benilde García‐de Teresa, Paula Leal-Anaya, et al.
Frontiers in Oncology (2022) Vol. 12
Open Access | Times Cited: 16
An Introduction to the Complete Blood Count for Clinical Chemists: Red Blood Cells
Maximo J Marin, Xander M.R. van Wijk, Paul Boothe, et al.
The Journal of Applied Laboratory Medicine (2024) Vol. 9, Iss. 5, pp. 1025-1039
Closed Access | Times Cited: 2
Integrated proteogenomic analysis for inherited bone marrow failure syndrome
Manabu Wakamatsu, Hideki Muramatsu, Hironori Sato, et al.
Leukemia (2024) Vol. 38, Iss. 6, pp. 1256-1265
Open Access | Times Cited: 2
The Molecular and Genetic Mechanisms of Inherited Bone Marrow Failure Syndromes: The Role of Inflammatory Cytokines in Their Pathogenesis
Nozomu Kawashima, Valentino Bezzerri, Seth J. Corey
Biomolecules (2023) Vol. 13, Iss. 8, pp. 1249-1249
Open Access | Times Cited: 5
Pediatric Bone Marrow Failure: A Broad Landscape in Need of Personalized Management
Lotte Vissers, Mirjam van der Burg, Arjan C. Lankester, et al.
Journal of Clinical Medicine (2023) Vol. 12, Iss. 22, pp. 7185-7185
Open Access | Times Cited: 4
Genomic insights into inherited bone marrow failure syndromes in a Korean population
Jong‐Mi Lee, Hoon Seok Kim, Jaeeun Yoo, et al.
British Journal of Haematology (2024)
Open Access | Times Cited: 1
Allogeneic Hematopoietic Cell Transplantation for the Treatment of Severe Aplastic Anemia: Evidence-Based Guidelines from the American Society for Transplantation and Cellular Therapy
Raheel Iftikhar, Zachariah DeFilipp, Amy E. DeZern, et al.
Transplantation and Cellular Therapy (2024)
Open Access | Times Cited: 1
Germline Variants and Characteristic Features of Hereditary Hematological Malignancy Syndrome
Hironori Arai, Hirotaka Matsui, SungGi Chi, et al.
(2023)
Open Access | Times Cited: 2
Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico
Paula Leal-Anaya, Tamara N. Kimball, Ana Lucia Yanez‐Felix, et al.
Frontiers in Genetics (2024) Vol. 14
Open Access
Infrequent fractures and resilient bone mineral density: bone health in patients with Fanconi anemia
Jane Koo, Jonathan C. Howell, Lindsey Hornung, et al.
Haematologica (2024) Vol. 109, Iss. 10, pp. 3435-3438
Open Access
Disorders of bone marrow structure and function
Faramarz Naeim, P. Nagesh Rao, Sophie X. Song
Elsevier eBooks (2024), pp. 29-58
Closed Access
Detection of PNH clones can aid in the distinction of aplastic anemia vs inherited BM failure syndromes: a single center experience and review of the literature.
Patrice Nasnas, Jianhua Ling, Yoheved Gerstein, et al.
Clinical Lymphoma Myeloma & Leukemia (2024)
Closed Access
Genetic testing facilitates correct diagnosis and directs management of unexplained pediatric chronic cytopenia: case presentations of rare Inherited Bone Marrow Syndrome (ERCC6L2-associated disease)
Izabela Kranjčec, Nuša Matijašić, Katarina Vulin, et al.
Authorea (Authorea) (2024)
Open Access
Case report: Development of clonal hematologic disorders from inherited bone marrow failure
Jaroslav Čermák
Frontiers in Oncology (2024) Vol. 14
Open Access
Rare cytogenetic abnormalities in MDS evolving from fanconi anemia-A case report
Nidhi Rajendra, Subbaiah Ramanathan, Vishal Ashok, et al.
IP Journal of diagnostic pathology and oncology/IP journal of diagnostic pathology and oncology/Journal of diagnostic pathology and oncology (2023) Vol. 7, Iss. 4, pp. 252-254
Open Access | Times Cited: 1
Genetic Counseling and Family Screening Recommendations in Patients with Telomere Biology Disorders
Laura Ongie, Hannah A. Raj, Katie Barrett Stevens
Current Hematologic Malignancy Reports (2023) Vol. 18, Iss. 6, pp. 273-283
Closed Access | Times Cited: 1
Inherited Bone Marrow Failure Syndromes in Children
Mehmet Emin Ertunç, Ahmet Genar Çelik, Akif Tahiroğlu, et al.
The Journal of Pediatric Academy (2023) Vol. 4, Iss. 1, pp. 1-5
Open Access
Page 1

Scroll to top