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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:

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: 66

Showing 1-25 of 66 citing articles:

Assessment of a complete and classified platelet proteome from genome-wide transcripts of human platelets and megakaryocytes covering platelet functions
Jingnan Huang, Frauke Swieringa, Fiorella A. Solari, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 68
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: 29
Combining Diagnostics and Research in an Academic Laboratory
Grit Waitz, Stefan Handtke, Carlo Zaninetti, et al.
Hämostaseologie (2025) Vol. 45, Iss. 01, pp. 063-069
Closed Access | Times Cited: 1
Validation of immunofluorescence analysis of blood smears in patients with inherited platelet disorders
Carlo Zaninetti, Eva Leinøe, Marı́a Luisa Lozano, et al.
Journal of Thrombosis and Haemostasis (2023) Vol. 21, Iss. 4, pp. 1010-1019
Open Access | Times Cited: 13
Bernard-Soulier syndrome case caused by novel compound heterozygous variants in the GP1BA gene: Case report
Chenxia Xu, Chunhua Lai, Zhang Sheng, et al.
Gene Reports (2025), pp. 102133-102133
Closed Access
Uniform impact on individual megakaryocytes is essential for efficient in vitro platelet production
Andrei K. Garzon Dasgupta, Anaïs Pongérard, Léa Mallo, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
mBAT: a newly developed mobile application for self-screening of pediatric bleeding disorders – a multi-center study
Arpatsorn Sermcheep, Rungrote Natesirinilkul, Patcharee Komvilaisak, et al.
Annals of Hematology (2025)
Open Access
The Diagnostic Assessment of Platelet Function Defects
Karina Althaus, Gero Hoepner, Barbara Zieger, et al.
Hämostaseologie (2025)
Closed Access
Acoustic Activation of Human Circulatory Parameters
Vytautas Ostaševičius, Vytautas Jūrėnas, Mantas Venslauskas, et al.
Synthesis lectures on biomedical engineering (2025), pp. 13-73
Closed Access
Epidemiological and clinical characteristics of children and young adults with Glanzmann’s thrombasthenia in upper Egypt: a multicenter cross-sectional study
Gehan Lotfy Abdel Hakeem, Ahmed El-Sayed, Zahraa Elmasry, et al.
Annals of Hematology (2025)
Open Access
Descripción de una serie de casos de trombocitopenias de origen genético diagnosticadas en el servicio de Hematología del Hospital de San José entre los años 2000-2021 y revisión narrativa de la literatura
Claudia Patricia Casas Patarroyo, María Helena Solano Trujillo, Gerson Menoyo-Caballero, et al.
IATREIA (2025) Vol. 38, Iss. 3
Open Access
Management of a twin pregnancy patient with Glanzmann thrombasthenia might be caused by a novel ITGA2B gene mutation (c.2822G>A): a case report and family investigation
Xiangcheng Liao, Ruikai Zhu, Zhigang Yang, et al.
Platelets (2025) Vol. 36, Iss. 1
Open Access
Platelet parameters for distinguishing between inherited macrothrombocytopenia and acquired thrombocytopenia: a retrospective case–control study
Wenlan Chen, Yajie Ding, Li Cai, et al.
Platelets (2025) Vol. 36, Iss. 1
Open Access
Genetics of inherited thrombocytopenias
Julia T. Warren, Jorge Di Paola
Blood (2022) Vol. 139, Iss. 22, pp. 3264-3277
Open Access | Times Cited: 20
Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities for mucocutaneous bleeding disorders
Robert F. Sidonio, Paulette Bryant, Jorge Di Paola, et al.
Expert Review of Hematology (2023) Vol. 16, Iss. sup1, pp. 39-54
Open Access | Times Cited: 12
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
Screening and diagnosis of inherited platelet disorders
Alex Bourguignon, Subia Tasneem, Catherine P.M. Hayward
Critical Reviews in Clinical Laboratory Sciences (2022) Vol. 59, Iss. 6, pp. 405-444
Open Access | Times Cited: 16
Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases
Hrushikesh Vyas, Ahmad Alcheikh, Gillian Lowe, et al.
Platelets (2022) Vol. 33, Iss. 8, pp. 1107-1112
Open Access | Times Cited: 16
Interleukins in Platelet Biology: Unraveling the Complex Regulatory Network
Miao Huang, Long Wang, Qianhui Zhang, et al.
Pharmaceuticals (2024) Vol. 17, Iss. 1, pp. 109-109
Open Access | Times Cited: 3
Treatment of Inherited Platelet Disorders: Current Status and Future Options
Caroline Bargehr, Ralf Knöfler, Werner Streif
Hämostaseologie (2023) Vol. 43, Iss. 04, pp. 261-270
Open Access | Times Cited: 8
Expanding the genetic spectrum of TUBB1-related thrombocytopenia
Verónica Palma‐Barqueros, Loredana Bury, Shinji Kunishima, et al.
Blood Advances (2021) Vol. 5, Iss. 24, pp. 5453-5467
Open Access | Times Cited: 18
Inherited Thrombocytopenia Caused by Variants in Crucial Genes for Glycosylation
Ana Marín‐Quílez, Lorena Díaz‐Ajenjo, Christian A. Di Buduo, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 6, pp. 5109-5109
Open Access | Times Cited: 7
Treatment of inherited thrombocytopenias
Carlo L. Balduini
Haematologica (2022) Vol. 107, Iss. 6, pp. 1278-1292
Open Access | Times Cited: 11
Novel variants in GALE cause syndromic macrothrombocytopenia by disrupting glycosylation and thrombopoiesis
Ana Marín‐Quílez, Christian A. Di Buduo, Lorena Díaz‐Ajenjo, et al.
Blood (2022) Vol. 141, Iss. 4, pp. 406-421
Open Access | Times Cited: 11
A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger
José María Bastida, Stefano Malvestiti, Doris Boeckelmann, et al.
Cells (2022) Vol. 11, Iss. 20, pp. 3223-3223
Open Access | Times Cited: 8
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