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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:

RasGRP2 Structure, Function and Genetic Variants in Platelet Pathophysiology
Matthias Canault, Marie‐Christine Alessi
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 3, pp. 1075-1075
Open Access | Times Cited: 28

Showing 1-25 of 28 citing articles:

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
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
The Diagnostic Assessment of Platelet Function Defects
Karina Althaus, Gero Hoepner, Barbara Zieger, et al.
Hämostaseologie (2025)
Closed Access
RASGRP2 is a potential immune-related biomarker and regulates mitochondrial-dependent apoptosis in lung adenocarcinoma
Yongting Liu, Yanhong Ouyang, Ziyang Feng, et al.
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 12
Association between MAPK and PI3K/Akt signaling pathway‐related gene polymorphisms and migraine
Mingxue Wang, Yujia Gu, Shuhan Meng, et al.
Molecular Genetics & Genomic Medicine (2024) Vol. 12, Iss. 8
Open Access | Times Cited: 3
Ras guanine nucleotide-releasing protein-4 promotes renal inflammatory injury in type 2 diabetes mellitus
Shuai Huang, Junmei Wang, Li Zhang, et al.
Metabolism (2022) Vol. 131, pp. 155177-155177
Open Access | Times Cited: 13
Utility of thromboelastography with platelet mapping for monitoring platelet transfusion in qualitative platelet disorders
Robert H. Lee, Tanvi Rudran, Wolfgang Bergmeier
Journal of Thrombosis and Haemostasis (2024) Vol. 22, Iss. 10, pp. 2873-2878
Closed Access | Times Cited: 2
Inherited Platelet Disorders: A Short Introduction
Barbara Zieger, Doris Boeckelmann
Hämostaseologie (2023) Vol. 43, Iss. 01, pp. 052-059
Open Access | Times Cited: 6
The Role of RASGRP2 in Vascular Endothelial Cells—A Mini Review
Jun-ichi Takino, Shouhei Miyazaki, Kentaro Nagamine, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 20, pp. 11129-11129
Open Access | Times Cited: 12
NEDD4L-mediated RASGRP2 suppresses high-glucose and oxLDL-induced vascular endothelial cell dysfunctions by activating Rap1 and R-Ras
Guozhu Chen, Yisong Pei, Qiaoling Ye, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research (2024) Vol. 1871, Iss. 8, pp. 119844-119844
Closed Access | Times Cited: 1
Roles of G proteins and their GTPase-activating proteins in platelets
Lorna O’Donoghue, Albert Smolenski
Bioscience Reports (2024) Vol. 44, Iss. 5
Open Access | Times Cited: 1
Platelet transfusion for patients with platelet dysfunction: effectiveness, mechanisms, and unanswered questions
Robert H. Lee, Raj S. Kasthuri, Wolfgang Bergmeier
Current Opinion in Hematology (2020) Vol. 27, Iss. 6, pp. 378-385
Open Access | Times Cited: 9
Laboratory Techniques Used to Diagnose Constitutional Platelet Dysfunction
Manal Ibrahim‐Kosta, Marie‐Christine Alessi, Nathalie Hézard
Hämostaseologie (2020) Vol. 40, Iss. 04, pp. 444-459
Open Access | Times Cited: 8
Identification of Transcriptomic Differences between Lower Extremities Arterial Disease, Abdominal Aortic Aneurysm and Chronic Venous Disease in Peripheral Blood Mononuclear Cells Specimens
Daniel Zalewski, Karol P. Ruszel, Andrzej Stępniewski, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 6, pp. 3200-3200
Open Access | Times Cited: 6
Mutations in RASGRP2 gene identified in patients misdiagnosed as Glanzmann thrombasthenia patients
Nurit Rosenberg, Rima Dardik, Hagit Hauschner, et al.
Blood Cells Molecules and Diseases (2021) Vol. 89, pp. 102560-102560
Closed Access | Times Cited: 5
Utility of thromboelastography with platelet mapping (TEG-PM) for monitoring platelet transfusion in qualitative platelet disorders
Robert H. Lee, Tanvi Rudran, Wolfgang Bergmeier
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
A splice mutation in RASGRP2 gene in the patient with recurrent epistaxis and nasal vascular malformation
Zhongyu Shi, Qing-Ling Lei, Shaoqin Duan, et al.
Platelets (2024) Vol. 35, Iss. 1
Open Access
Pathologies plaquettaires constitutionnelles
Livia Claude, Véronique Baccini
Encyclopédie médico-chirurgicale. Hématologie (2024) Vol. 35, Iss. 2, pp. 1-18
Closed Access
Exploration de l’hémostase primaire
Georges Jourdi, Isabelle Gouin‐Thibault, Pascale Gaussem
Encyclopédie médico-chirurgicale. Hématologie (2024) Vol. 35, Iss. 4, pp. 1-14
Closed Access
Electron microscopy shows that binding of monoclonal antibody PT25-2 primes integrin αIIbβ3 for ligand binding
Dragana Nešić, Martin Bush, Aleksandar Spasic, et al.
Blood Advances (2021) Vol. 5, Iss. 7, pp. 1781-1790
Open Access | Times Cited: 3
Molecular Research on Platelet Activity in Health and Disease
Maria Valeria Catani, Isabella Savini, Valeria Gasperi
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 11, pp. 3804-3804
Open Access | Times Cited: 2
Genetic Confirmation and Identification of Novel Variants for Glanzmann Thrombasthenia and Other Inherited Platelet Function Disorders: A Study by the Korean Pediatric Hematology Oncology Group (KPHOG)
Eu Jeen Yang, Ye Jee Shim, Heung Soo Kim, et al.
Genes (2021) Vol. 12, Iss. 5, pp. 693-693
Open Access | Times Cited: 2
Severe Bleeding Diathesis in Siblings with Platelet Dysfunction due to a Novel Nonsense RASGRP2 Mutation
Julia Körholz, Nadja Lucas, Franziska Boiti, et al.
TH Open (2020) Vol. 04, Iss. 04, pp. e413-e416
Open Access | Times Cited: 1
Novel RASGRP2 variants in platelet function defects: Indian study
Nikesh Kawankar, Shrimati Shetty, Bipin Kulkarni
British Journal of Haematology (2022) Vol. 197, Iss. 3, pp. 377-380
Open Access | Times Cited: 1
CalDAG-GEFI Deficiency in a Family with Symptomatic Heterozygous and Homozygous Carriers of a Likely Pathogenic Variant in RASGRP2
Sara Moráis, Mónica Pereira, Catarina Lau, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 22, pp. 12423-12423
Open Access | Times Cited: 1
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