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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:

Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development
Peter Mustillo, Kathleen E. Sullivan, Iván K. Chinn, et al.
Journal of Clinical Immunology (2023) Vol. 43, Iss. 2, pp. 247-270
Open Access | Times Cited: 20

Showing 20 citing articles:

Vaccine immunity in patients with 22q11.2 microdeletion syndrome
Leila Farpour, Renato Gualtieri, Tereza Kotalova, et al.
Pediatric Allergy and Immunology (2025) Vol. 36, Iss. 2
Closed Access | Times Cited: 2
Chromosome 22q11.2 Deletion (DiGeorge Syndrome): Immunologic Features, Diagnosis, and Management
Sarah E. Biggs, Bailee Gilchrist, Kathleen R. May
Current Allergy and Asthma Reports (2023) Vol. 23, Iss. 4, pp. 213-222
Open Access | Times Cited: 23
Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach
Aleksandra Szczawińska-Popłonyk, Eyal Schwartzmann, Zuzanna Chmara, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 9, pp. 8317-8317
Open Access | Times Cited: 17
Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors
Francesca Cillo, Emma Coppola, Federico Habetswallner, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 321-321
Open Access | Times Cited: 7
Thymic Atrophy and Immune Dysregulation in Infants with Complex Congenital Heart Disease
S. J. Bremer, Annika Boxnick, Laura Glau, et al.
Journal of Clinical Immunology (2024) Vol. 44, Iss. 3
Open Access | Times Cited: 4
Inborn Errors of Immunity Presenting with Early-Onset Severe Atopy
Nipat Chuleerarux, Nadia Makkoukdji, Travis Satnarine, et al.
Medicina (2025) Vol. 61, Iss. 1, pp. 62-62
Open Access
TREC and KREC profiles in patients with inborn errors of immunity
L. Yu. Barycheva, L. I. Bachieva, N. A. Kozmova, et al.
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) (2025) Vol. 69, Iss. 6, pp. 51-58
Open Access
Review of the Pathophysiology and Clinical Manifestations of 22q11.2 Deletion and Duplication Syndromes
Jeremy Purow, Lauren Waidner, Hanadys Ale
Clinical Reviews in Allergy & Immunology (2025) Vol. 68, Iss. 1
Closed Access
Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Cinical Approach
Aleksandra Szczawińska-Popłonyk, Eyal Schwartzmann, Zuzanna Chmara, et al.
(2023)
Open Access | Times Cited: 7
Genetically-determined defects of T cell development
Luigi D. Notarangelo
Allergy and Asthma Proceedings (2024) Vol. 45, Iss. 5, pp. 326-331
Closed Access | Times Cited: 2
European Society of Immunodeficiencies guidelines for the management of patients with congenital athymia
Alexandra Y. Kreins, Fatima Dhalla, Aisling M. Flinn, et al.
Journal of Allergy and Clinical Immunology (2024)
Open Access | Times Cited: 2
Evans syndrome in the background of 22q11.2 deletion syndrome
Mohmmad M. Alawajneh, Waseem Sameer, Mohamed Al Zobi, et al.
Pediatric Blood & Cancer (2024) Vol. 71, Iss. 7
Open Access | Times Cited: 1
Newborn screening for SCID and severe T lymphocytopenia in Europe
Maartje Blom, Maarja Soomann, Pere Soler‐Palacín, et al.
Journal of Allergy and Clinical Immunology (2024)
Open Access | Times Cited: 1
Integrating TREC/KREC assay and some cytokines in the evaluation of the immune status of patients with DiGeorge Syndrome
Assem Metwally Abo-Shanab, Haiam Abdel Raouf, Alaaeldin Fayez, et al.
Research Square (Research Square) (2024)
Closed Access
Mortality in Patients with 22q11.2 Rearrangements
Melisa Cilio Arroyuelo, Jair Tenorio, Luís Fernández, et al.
Genes (2024) Vol. 15, Iss. 9, pp. 1146-1146
Open Access
Case report: Artificial thymic organoids facilitate clinical decisions for a patient with a TP63 variant and severe persistent T cell lymphopenia
Alevtina Gall, Marita Bosticardo, Stacey Ma, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access
TREC and KREC values in patients with congenital heart defects — neonatal screening data
L. Yu. Barycheva, L. I. Bachieva, Andrey Anatolyevich Puchkov, et al.
Allergology and Immunology in Pediatrics (2024), Iss. 3, pp. 42-53
Open Access
Lymphoproliferation, Autoimmunity, and Recurrent Infections: Which Primary Immunodeficiency?
Gökcan Öztürk, Şule Haskoloğlu, Nazlı Deveci, et al.
Turkish Archives of Pediatrics (2023) Vol. 59, Iss. 1, pp. 106-108
Open Access
22q11.2 Deletion Syndrome in Taiwan: Clinical Presentation and Immune System Status of Patients
Chung‐Lin Lee, Shan‐Miao Lin, Ming‐Ren Chen, et al.
International Journal of Medical Sciences (2023) Vol. 20, Iss. 11, pp. 1377-1385
Open Access
Inborn errors of immunity present with neuropsychiatric symptoms overlapping with autistic behavioral symptoms
Harumi Jyonouchi
Journal of Translational Genetics and Genomics (2023) Vol. 7, Iss. 4, pp. 274-90
Open Access
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