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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.

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Showing 1-25 of 72 citing articles:

The Human Phenotype Ontology in 2024: phenotypes around the world
Michael Gargano, Nicolas Matentzoglu, Ben Coleman, et al.
Nucleic Acids Research (2023) Vol. 52, Iss. D1, pp. D1333-D1346
Open Access | Times Cited: 102
Complement and systemic lupus erythematosus
Chau‐Ching Liu, Susan Manzi, Joseph M. Ahearn
Elsevier eBooks (2024), pp. 245-264
Closed Access | Times Cited: 20
The diagnosis of severe combined immunodeficiency (SCID): The Primary Immune Deficiency Treatment Consortium (PIDTC) 2022 Definitions
Christopher C. Dvorak, Élie Haddad, Jennifer Heimall, et al.
Journal of Allergy and Clinical Immunology (2022) Vol. 151, Iss. 2, pp. 539-546
Open Access | Times Cited: 70
Common Variable Immunodeficiency: More Pathways than Roads to Rome
Xiao Peng, Andrés Caballero-Oteyza, Bodo Grimbacher
Annual Review of Pathology Mechanisms of Disease (2022) Vol. 18, Iss. 1, pp. 283-310
Open Access | Times Cited: 42
Inborn errors of immunity (primary immunodeficiencies)
Vy H.D. Kim, Julia Upton, Beáta Dérfalvi, et al.
Allergy Asthma and Clinical Immunology (2025) Vol. 20, Iss. S3
Open Access | Times Cited: 1
The immunogenetic basis of severe herpes simplex infections in neonates and children: a review
Megan H. Tucker, Maria Kalamvoki, Kedar Tilak, et al.
Pediatric Research (2025)
Closed Access | Times Cited: 1
Efficacy and economics of targeted panel versus whole-exome sequencing in 878 patients with suspected primary immunodeficiency
Craig D. Platt, Fatima Zaman, Wayne Bainter, et al.
Journal of Allergy and Clinical Immunology (2020) Vol. 147, Iss. 2, pp. 723-726
Open Access | Times Cited: 55
ALPS, FAS, and beyond: from inborn errors of immunity to acquired immunodeficiencies
Filippo Consonni, Eleonora Gambineri, Claudio Favre
Annals of Hematology (2022) Vol. 101, Iss. 3, pp. 469-484
Open Access | Times Cited: 32
Somatic mosaicism in inborn errors of immunity: Current knowledge, challenges, and future perspectives
Jahnavi Aluri, Megan A. Cooper
Seminars in Immunology (2023) Vol. 67, pp. 101761-101761
Open Access | Times Cited: 17
Atopy as Immune Dysregulation: Offender Genes and Targets
Maryam Vaseghi‐Shanjani, Andrew L. Snow, David J. Margolis, et al.
The Journal of Allergy and Clinical Immunology In Practice (2022) Vol. 10, Iss. 7, pp. 1737-1756
Closed Access | Times Cited: 23
Inborn errors of immunity in adulthood
Joanne Wang, Arün Dhir, Kyla J. Hildebrand, et al.
Allergy Asthma and Clinical Immunology (2024) Vol. 20, Iss. 1
Open Access | Times Cited: 6
Current genetic diagnostics in inborn errors of immunity
Sandra von Hardenberg, Isabel Klefenz, Doris Steinemann, et al.
Frontiers in Pediatrics (2024) Vol. 12
Open Access | Times Cited: 6
Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency
Francesco Saettini, M. Cecilia Poli, Jaime Vengoechea, et al.
Blood (2020) Vol. 137, Iss. 4, pp. 493-499
Open Access | Times Cited: 39
Rapid identification of primary atopic disorders (PAD) by a clinical landmarkguided, upfront use of genomic sequencing
Tim Niehues, Sandra von Hardenberg, Eunike Velleuer
Allergologie select (2024) Vol. 8, Iss. 01, pp. 304-323
Closed Access | Times Cited: 4
Beyond monogenetic rare variants: tackling the low rate of genetic diagnoses in predominantly antibody deficiency
Emily S.J. Edwards, Julian J. Bosco, Samar Ojaimi, et al.
Cellular and Molecular Immunology (2020) Vol. 18, Iss. 3, pp. 588-603
Open Access | Times Cited: 29
Integrating next-generation sequencing and artificial intelligence for the identification and validation of pathogenic variants in colorectal cancer
Juliana Rodriguez-Salamanca, Mariana Angulo-Aguado, Sarah Orjuela-Amarillo, et al.
Frontiers in Oncology (2025) Vol. 15
Open Access
Primary Immunodeficiencies in India: Molecular Diagnosis and the Role of Next-Generation Sequencing
Arun Kumar Arunachalam, Madhavi Maddali, Fouzia N. Aboobacker, et al.
Journal of Clinical Immunology (2020) Vol. 41, Iss. 2, pp. 393-413
Open Access | Times Cited: 26
Curation and expansion of Human Phenotype Ontology for defined groups of inborn errors of immunity
Matthias Haimel, Júlia Pázmándi, Raúl Jiménez Heredia, et al.
Journal of Allergy and Clinical Immunology (2021) Vol. 149, Iss. 1, pp. 369-378
Open Access | Times Cited: 22
A 2020 update on the use of genetic testing for patients with primary immunodeficiency
Iván K. Chinn, Jordan S. Orange
Expert Review of Clinical Immunology (2020) Vol. 16, Iss. 9, pp. 897-909
Closed Access | Times Cited: 23
The scary world of variants of uncertain significance (VUS): A hitchhiker’s guide to interpretation
Kathleen E. Sullivan
Journal of Allergy and Clinical Immunology (2020) Vol. 147, Iss. 2, pp. 492-494
Open Access | Times Cited: 21
Next-generation sequencing for inborn errors of immunity
Kristy Lee, Roshini S. Abraham
Human Immunology (2021) Vol. 82, Iss. 11, pp. 871-882
Closed Access | Times Cited: 19
Impact of Genetic Diagnosis on the Outcome of Hematopoietic Stem Cell Transplant in Primary Immunodeficiency Disorders
Federica Forlanini, Alice Chan, Jasmeen Dara, et al.
Journal of Clinical Immunology (2022) Vol. 43, Iss. 3, pp. 636-646
Open Access | Times Cited: 14
The lung in inborn errors of immunity: From clinical disease patterns to molecular pathogenesis
María J. Gutiérrez, Gustavo Niño, Di Sun, et al.
Journal of Allergy and Clinical Immunology (2022) Vol. 150, Iss. 6, pp. 1314-1324
Open Access | Times Cited: 13
Perspective: Application of the American College of Medical Genetics Variant Interpretation Criteria to Common Variable Immunodeficiency Disorders
Rohan Ameratunga, Caroline Allan, Klaus Lehnert, et al.
Clinical Reviews in Allergy & Immunology (2021) Vol. 61, Iss. 2, pp. 226-235
Closed Access | Times Cited: 15
Phenomic Analysis of Chronic Granulomatous Disease Reveals More Severe Integumentary Infections in X-Linked Compared With Autosomal Recessive Chronic Granulomatous Disease
Timothy Lok-Hin Chiu, Daniel Leung, Koon-Wing Chan, et al.
Frontiers in Immunology (2022) Vol. 12
Open Access | Times Cited: 11
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