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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:

Shwachman-Diamond syndromes: clinical, genetic, and biochemical insights from the rare variants
Nozomu Kawashima, Usua Oyarbide, Marco Cipolli, et al.
Haematologica (2023) Vol. 108, Iss. 10, pp. 2594-2605
Open Access | Times Cited: 21

Showing 21 citing articles:

TREC and KREC profiles in patients with inborn errors of immunity
L. Yu. Barycheva, L. I. Bachieva, N. A. Kozmova, et al.
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) (2025) Vol. 69, Iss. 6, pp. 51-58
Open Access
Constitutive systemic inflammation in Shwachman-Diamond Syndrome
G Sabbioni, Elisabetta D’Aversa, Giulia Breveglieri, et al.
Molecular Medicine (2025) Vol. 31, Iss. 1
Open Access
Clinical and genetic spectrum of SBDS and DNAJC21 gene variants in bone marrow failure cases: Atypical and cryptic presentations
Swetha Palla, Prateek Bhatia, Sudhanshi Raina, et al.
Blood Cells Molecules and Diseases (2025), pp. 102924-102924
Closed Access
Discerning clinicopathological features of congenital neutropenia syndromes: an approach to diagnostically challenging differential diagnoses
Xenia Parisi, Jacob Bledsoe
Journal of Clinical Pathology (2024) Vol. 77, Iss. 9, pp. 586-604
Closed Access | Times Cited: 2
Dissecting thrombus-directed chemotaxis and random movement in neutrophil near-thrombus motion in flow chambers
Julia-Jessica D. Korobkin, Е. А. Деордиева, Ivan Tesakov, et al.
BMC Biology (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 2
CRISPR RNA-Guided Gene Editing and its Clinical Research Applications in Hematology with Focus on Inherited Germline Predisposition to Hematologic Malignancies
Rina Kansal
(2024)
Open Access | Times Cited: 2
Lipomatoses
H. Dupuis, Madleen Lemaître, Arnaud Jannin, et al.
Annales d Endocrinologie (2024) Vol. 85, Iss. 3, pp. 231-247
Open Access | Times Cited: 2
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
Update on Recommendations for Surveillance for Children with Predisposition to Hematopoietic Malignancy
Luke Maese, Marcin W. Włodarski, Sun Young Kim, et al.
Clinical Cancer Research (2024) Vol. 30, Iss. 19, pp. 4286-4295
Closed 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
Germline Predisposition in Hematologic Malignancies
Rina Kansal
Elsevier eBooks (2024), pp. 1-38
Closed Access | Times Cited: 1
Potentials of ribosomopathy gene as pharmaceutical targets for cancer treatment
Mengxin Wang, Stephen Vulcano, Changlu Xu, et al.
Journal of Pharmaceutical Analysis (2023) Vol. 14, Iss. 3, pp. 308-320
Open Access | Times Cited: 2
Hereditary syndromes in pediatric hematooncology
В. М. Козлова, Ekaterina E. Zelenova, Т. Т. Валиев, et al.
Педиатрическая фармакология (2024) Vol. 20, Iss. 6, pp. 557-573
Open Access
A Rare Inherited Bone Marrow Failure Syndrome Disclosed by Reanalysis of the Exome Data of a Patient Evaluated for Cytopenia and Dysmorphic Features
Durmus Durmaz, Ayça Aslanger, Zehra Yavaş Abalı, et al.
Journal of Pediatric Hematology/Oncology (2024) Vol. 46, Iss. 3, pp. e214-e219
Open Access
Growth Charts for Shwachman–Diamond Syndrome at Ages 0 to 18 Years
Anna Pegoraro, Valentino Bezzerri, Gloria Tridello, et al.
Cancers (2024) Vol. 16, Iss. 7, pp. 1420-1420
Open Access
Lethal Complications and Complex Genotypes in Shwachman Diamond Syndrome: Report of a Family with Recurrent Neonatal Deaths and a Case-Based Brief Review of the Literature
Danai Veltra, Nikolaos M. Marinakis, Ioannis Kotsios, et al.
Children (2024) Vol. 11, Iss. 6, pp. 705-705
Open Access
Oral Diseases as a Manifestation of Inborn Errors of Immunity
Katarzyna Napiórkowska-Baran, Samira Darwish, Justyna Kaczor, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 17, pp. 5079-5079
Open Access
Outcomes of allogeneic hematopoietic stem cell transplantation in Shwachman-Diamond Syndrome: a systematic review and meta-analysis
MA Cui-ping, Xiaohua Huang, Yuhan Chen, et al.
Cytotherapy (2024)
Closed 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
Shwachman–Diamond syndrome due to biallelic EFL1 variants with complex and fatal clinical course in early infancy
Holger Cario, Alexis Bertrand, Shengjiang Tan, et al.
British Journal of Haematology (2024)
Open Access
The metabolic basis of inherited neutropenias
Usua Oyarbide, Genevieve M. Crane, Seth J. Corey
British Journal of Haematology (2023) Vol. 204, Iss. 1, pp. 45-55
Closed Access
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