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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:

T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency
Immacolata Brigida, Matteo Zoccolillo, Maria Pia Cicalese, et al.
Blood (2018) Vol. 132, Iss. 22, pp. 2362-2374
Open Access | Times Cited: 103

Showing 1-25 of 103 citing articles:

The Pyrin Inflammasome in Health and Disease
Oskar Schnappauf, Jae Jin Chae, Daniel L. Kastner, et al.
Frontiers in Immunology (2019) Vol. 10
Open Access | Times Cited: 288
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function
Michael T. Lam, Simona Coppola, Oliver H.F. Krumbach, et al.
The Journal of Experimental Medicine (2019) Vol. 216, Iss. 12, pp. 2778-2799
Open Access | Times Cited: 171
Hematopoietic Stem Cell Transplantation in Primary Immunodeficiency Diseases: Current Status and Future Perspectives
Riccardo Castagnoli, Ottavia M. Delmonte, Enrica Calzoni, et al.
Frontiers in Pediatrics (2019) Vol. 7
Open Access | Times Cited: 170
A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency
Stefano Volpi, Maria Pia Cicalese, Paul Tuijnenburg, et al.
Journal of Allergy and Clinical Immunology (2019) Vol. 143, Iss. 6, pp. 2296-2299
Open Access | Times Cited: 99
Somatic genetic rescue in Mendelian haematopoietic diseases
Patrick Revy, Caroline Kannengiesser, Alain Fischer
Nature Reviews Genetics (2019) Vol. 20, Iss. 10, pp. 582-598
Closed Access | Times Cited: 92
Loss of ARPC1B impairs cytotoxic T lymphocyte maintenance and cytolytic activity
Lyra O. Randzavola, Katharina Strege, Marie Juzans, et al.
Journal of Clinical Investigation (2019) Vol. 129, Iss. 12, pp. 5600-5614
Open Access | Times Cited: 79
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: 69
Actin Remodeling Defects Leading to Autoinflammation and Immune Dysregulation
Riccardo Papa, Federica Penco, Stefano Volpi, et al.
Frontiers in Immunology (2021) Vol. 11
Open Access | Times Cited: 63
Molecular mechanisms of phenotypic variability in monogenic autoinflammatory diseases
Ivona Aksentijevich, Oskar Schnappauf
Nature Reviews Rheumatology (2021) Vol. 17, Iss. 7, pp. 405-425
Closed Access | Times Cited: 61
Dominant activating RAC2 mutation with lymphopenia, immunodeficiency, and cytoskeletal defects
Amy P. Hsu, Ágnes Donkó, Megan E. Arrington, et al.
Blood (2019) Vol. 133, Iss. 18, pp. 1977-1988
Open Access | Times Cited: 71
Systemic autoinflammatory diseases: Clinical state of the art
Sophie Georgin‐Lavialle, Stéphanie Ducharme‐Bénard, Guillaume Sarrabay, et al.
Best Practice & Research Clinical Rheumatology (2020) Vol. 34, Iss. 4, pp. 101529-101529
Open Access | Times Cited: 54
Inherited thrombocytopenias: an updated guide for clinicians
Alessandro Pecci, Carlo L. Balduini
Blood Reviews (2020) Vol. 48, pp. 100784-100784
Closed Access | Times Cited: 54
Actin Dynamics at the T Cell Synapse as Revealed by Immune-Related Actinopathies
Loı̈c Dupré, Kaan Boztuğ, Laurène Pfajfer
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 48
MICAL2 enhances branched actin network disassembly by oxidizing Arp3B-containing Arp2/3 complexes
Chiara Galloni, Davide Carra, Jasmine V. Abella, et al.
The Journal of Cell Biology (2021) Vol. 220, Iss. 8
Open Access | Times Cited: 43
Identification of Tumor Antigens and Immune Subtypes of Glioblastoma for mRNA Vaccine Development
Lin Han, Kun Wang, Yuxin Xiong, et al.
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 38
Novel Genetic Discoveries in Primary Immunodeficiency Disorders
Margaret Redmond, Rebecca Scherzer, Benjamin T. Prince
Clinical Reviews in Allergy & Immunology (2022) Vol. 63, Iss. 1, pp. 55-74
Open Access | Times Cited: 29
Branching out in different directions: Emerging cellular functions for the Arp2/3 complex and WASP-family actin nucleation factors
Kenneth G. Campellone, Nadine M. Lebek, Virginia L. King
European Journal of Cell Biology (2023) Vol. 102, Iss. 2, pp. 151301-151301
Open Access | Times Cited: 22
Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies
Cristina Cifaldi, Immacolata Brigida, Federica Barzaghi, et al.
Frontiers in Immunology (2019) Vol. 10
Open Access | Times Cited: 50
Human inborn errors of the actin cytoskeleton affecting immunity: way beyond WAS and WIP
Stuart G. Tangye, Giorgia Bucciol, José Casas-Martín, et al.
Immunology and Cell Biology (2019) Vol. 97, Iss. 4, pp. 389-402
Open Access | Times Cited: 46
When Actin is Not Actin’ Like It Should: A New Category of Distinct Primary Immunodeficiency Disorders
Evelien G. G. Sprenkeler, Steven Webbers, Taco W. Kuijpers
Journal of Innate Immunity (2020) Vol. 13, Iss. 1, pp. 3-25
Open Access | Times Cited: 40
Inborn errors of immunity with atopic phenotypes: A practical guide for allergists
Riccardo Castagnoli, Vassilios Lougaris, Giuliana Giardino, et al.
World Allergy Organization Journal (2021) Vol. 14, Iss. 2, pp. 100513-100513
Open Access | Times Cited: 38
Neutrophil motility is regulated by both cell intrinsic and endothelial cell ARPC1B
Ashley Peterson, David A. Bennin, Michael Lasarev, et al.
Journal of Cell Science (2024) Vol. 137, Iss. 3
Open Access | Times Cited: 6
Clonal hematopoiesis in children with predisposing conditions
Enrico Attardi, Seth J. Corey, Marcin W. Włodarski
Seminars in Hematology (2024) Vol. 61, Iss. 1, pp. 35-42
Open Access | Times Cited: 6
Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network
Emilia Cirillo, Caterina Cancrini, Chiara Azzari, et al.
Frontiers in Immunology (2019) Vol. 10
Open Access | Times Cited: 37
Teasing out function from morphology: Similarities between primary cilia and immune synapses
Tiphaine Douanne, Jane C. Stinchcombe, Gillian M. Griffiths
The Journal of Cell Biology (2021) Vol. 220, Iss. 6
Open Access | Times Cited: 29
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