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 diseases with normal platelet count: phenotypes, genotypes and diagnostic strategy
Paquita Nurden, Simon Stritt, Rémi Favier, et al.
Haematologica (2020) Vol. 106, Iss. 2, pp. 337-350
Open Access | Times Cited: 59

Showing 1-25 of 59 citing articles:

Organization, dynamics and mechanoregulation of integrin-mediated cell–ECM adhesions
Pakorn Kanchanawong, David Calderwood
Nature Reviews Molecular Cell Biology (2022) Vol. 24, Iss. 2, pp. 142-161
Open Access | Times Cited: 249

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

Chediak-Higashi syndrome
Mackenzie L. Talbert, May Christine V. Malicdan, Wendy J. Introne
Current Opinion in Hematology (2023) Vol. 30, Iss. 4, pp. 144-151
Closed Access | Times Cited: 23

SARS-CoV-2 Spike protein activates TMEM16F-mediated platelet procoagulant activity
Ambra Cappelletto, Harriet E. Allan, Marilena Crescente, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 9
Open Access | Times Cited: 13

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

Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities for ultra-rare inherited bleeding disorders
Diane J. Nugent, Suchitra S. Acharya, Kimberly J. Baumann, et al.
Expert Review of Hematology (2023) Vol. 16, Iss. sup1, pp. 55-70
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

The Diagnostic Assessment of Platelet Function Defects
Karina Althaus, Gero Hoepner, Barbara Zieger, et al.
Hämostaseologie (2025)
Closed Access

Idiopathic Mild Platelet Dysfunction: Baseline Characteristics and Clinical Courses
Nitchkan Wiwatsomwong, Ratchaneekorn Jantasing, Benjaporn Akkawat, et al.
International Journal of Laboratory Hematology (2025)
Closed Access

Platelet functional responses and signalling: the molecular relationship. Part 1: responses.
А. Н. Свешникова, M. G. Stepanyan, Mikhail A. Panteleev
System Biology and Physiology Reports (2021) Vol. 1, Iss. 1, pp. 20-28
Open Access | Times Cited: 24

How I manage pregnancy in women with Glanzmann thrombasthenia
Mathieu Fiore, Loı̈c Sentilhes, Roseline d’Oiron
Blood (2022) Vol. 139, Iss. 17, pp. 2632-2641
Open Access | Times Cited: 18

Molecular basis of clot retraction and its role in wound healing
Alan T. Nurden
Thrombosis Research (2022) Vol. 231, pp. 159-169
Closed Access | Times Cited: 18

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

The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants
Luca Stefanucci, Janine Collins, Matthew C. Sims, et al.
Blood (2023) Vol. 142, Iss. 24, pp. 2055-2068
Open Access | Times Cited: 10

Glanzmann Thrombasthenia 10 Years Later: Progress Made and Future Directions
Alan T. Nurden, Paquita Nurden
Seminars in Thrombosis and Hemostasis (2024)
Closed Access | Times Cited: 3

How to investigate mild to moderate bleeding disorders and bleeding disorder of unknown cause
Alessandro Casini, Johanna Gebhart
International Journal of Laboratory Hematology (2024) Vol. 46, Iss. S1, pp. 27-33
Open Access | Times Cited: 2

Targeting Tissue Factor Pathway Inhibitor with concizumab to improve haemostasis in patients with Glanzmann thrombasthenia: an in vitro study
Jade Dubut, Valérie Goin, Cloé Derray, et al.
Journal of Thrombosis and Haemostasis (2024) Vol. 22, Iss. 9, pp. 2589-2600
Open Access | Times Cited: 2

Hermansky-Pudlak Syndrome: Identification of Novel Variants in the Genes HPS3, HPS5, and DTNBP1 (HPS-7)
Doris Boeckelmann, Mira Wolter, Katharina Neubauer, et al.
Frontiers in Pharmacology (2022) Vol. 12
Open Access | Times Cited: 10

Age‐restricted functional and developmental differences of neonatal platelets
Zhaoyan Liu, Cecilia Avila, Lisa E. Malone, et al.
Journal of Thrombosis and Haemostasis (2022) Vol. 20, Iss. 11, pp. 2632-2645
Open Access | Times Cited: 9

Antagonistic Roles of Human Platelet Integrin αIIbβ3 and Chemokines in Regulating Neutrophil Activation and Fate on Arterial Thrombi Under Flow
Claudia Schönichen, Samantha J. Montague, Sanne L. N. Brouns, et al.
Arteriosclerosis Thrombosis and Vascular Biology (2023) Vol. 43, Iss. 9, pp. 1700-1712
Open Access | Times Cited: 5

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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