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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:

Variable immune deficiency related to deletion size in chromosome 22q11.2 deletion syndrome
Blaine Crowley, Melanie A. Ruffner, Donna M. McDonald‐McGinn, et al.
American Journal of Medical Genetics Part A (2018) Vol. 176, Iss. 10, pp. 2082-2086
Open Access | Times Cited: 55

Showing 1-25 of 55 citing articles:

Chromosome 22q11.2 deletion syndrome and DiGeorge syndrome
Kathleen E. Sullivan
Immunological Reviews (2018) Vol. 287, Iss. 1, pp. 186-201
Closed Access | Times Cited: 107
Vitamin D status and the immune assessment in 22q11.2 deletion syndrome
Annalisa Legitimo, Veronica Bertini, Giorgio Costagliola, et al.
Clinical & Experimental Immunology (2020) Vol. 200, Iss. 3, pp. 272-286
Open Access | Times Cited: 89
Thymic Epithelium Abnormalities in DiGeorge and Down Syndrome Patients Contribute to Dysregulation in T Cell Development
Genni Enza Marcovecchio, Ileana Bortolomai, Francesca Ferrua, et al.
Frontiers in Immunology (2019) Vol. 10
Open Access | Times Cited: 76
Primary and secondary defects of the thymus
Sarah S. Dinges, Kayla Amini, Luigi D. Notarangelo, et al.
Immunological Reviews (2024) Vol. 322, Iss. 1, pp. 178-211
Closed Access | Times Cited: 10
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: 21
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
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
Shared Genetic Loci Between Schizophrenia and White Blood Cell Counts Suggest Genetically Determined Systemic Immune Abnormalities
Nils Eiel Steen, Zillur Rahman, Attila Szabó, et al.
Schizophrenia Bulletin (2023) Vol. 49, Iss. 5, pp. 1345-1354
Open Access | Times Cited: 17
Clinical and immunological features in a cohort of patients with partial DiGeorge syndrome followed at a single center
Giuliana Giardino, Nesrine Radwan, Patra Koletsi, et al.
Blood (2019) Vol. 133, Iss. 24, pp. 2586-2596
Open Access | Times Cited: 53
Untargeted metabolomic, and proteomic analysis identifies metabolic biomarkers and pathway alterations in individuals with 22q11.2 deletion syndrome
Marwa Zafarullah, Kathleen Angkustsiri, Austin Quach, et al.
Metabolomics (2024) Vol. 20, Iss. 2
Open Access | Times Cited: 5
Somatic copy number deletion of chromosome 22q in papillary thyroid carcinoma
Olivia W. Lee, Danielle M. Karyadi, Stephen W. Hartley, et al.
European Thyroid Journal (2025)
Open Access
When Should We Raise Clinical Suspicion of DiGeorge Syndrome: Two Case Reports from a Tertiary Hospital in Indonesia
Joni Indah Sari, Nydia Rena Benita Sihombing, Nani Maharani, et al.
OBM Genetics (2025) Vol. 09, Iss. 01, pp. 1-16
Open Access
Immune and Genetic Features of the Chromosome 22q11.2 Deletion (DiGeorge Syndrome)
Caroline Y. Kuo, Rebecca Signer, Sulagna C. Saitta
Current Allergy and Asthma Reports (2018) Vol. 18, Iss. 12
Closed Access | Times Cited: 32
Inborn Errors of Immunity and Cancer
Alessandra Tiri, Riccardo Masetti, Francesca Conti, et al.
Biology (2021) Vol. 10, Iss. 4, pp. 313-313
Open Access | Times Cited: 26
Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome
Kathleen Rooney, Michael A. Levy, Sadegheh Haghshenas, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 16, pp. 8611-8611
Open Access | Times Cited: 24
Congenital Athymia: Unmet Needs and Practical Guidance
Evey Howley, E. Graham Davies, Alexandra Y. Kreins
Therapeutics and Clinical Risk Management (2023) Vol. Volume 19, pp. 239-254
Open Access | Times Cited: 9
Inborn errors of thymic stromal cell development and function
Alexandra Y. Kreins, Stefano Maio, Fatima Dhalla
Seminars in Immunopathology (2020) Vol. 43, Iss. 1, pp. 85-100
Open Access | Times Cited: 27
Relationship Between Severity of T Cell Lymphopenia and Immune Dysregulation in Patients with DiGeorge Syndrome (22q11.2 Deletions and/or Related TBX1 Mutations): a USIDNET Study
Deepti Deshpande, Yeşim Yılmaz Demirdağ, Rebecca Marsh, et al.
Journal of Clinical Immunology (2020) Vol. 41, Iss. 1, pp. 29-37
Closed Access | Times Cited: 21
Distinct immune trajectories in patients with chromosome 22q11.2 deletion syndrome and immune-mediated diseases
T. Blaine Crowley, Ian M. Campbell, Emily J. Liebling, et al.
Journal of Allergy and Clinical Immunology (2021) Vol. 149, Iss. 1, pp. 445-450
Open Access | Times Cited: 19
Dendritic cells in inborn errors of immunity
Sudhir Gupta, Anshu Agrawal
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 7
Immunologic, Molecular, and Clinical Profile of Patients with Chromosome 22q11.2 Duplications
Dharmagat Bhattarai, Daniel E. McGinn, T. Blaine Crowley, et al.
Journal of Clinical Immunology (2023) Vol. 43, Iss. 4, pp. 794-807
Closed Access | Times Cited: 7
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
Copy Number Analysis in a Large Cohort Suggestive of Inborn Errors of Immunity Indicates a Wide Spectrum of Relevant Chromosomal Losses and Gains
Rensheng Wan, Maximilian Schieck, Andrés Caballero-Oteyza, et al.
Journal of Clinical Immunology (2022) Vol. 42, Iss. 5, pp. 1083-1092
Open Access | Times Cited: 10
Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype–Phenotype Correlation
Eva-Cristiana Gavril, Roxana Popescu, Irina Nucă, et al.
Genes (2022) Vol. 13, Iss. 11, pp. 2083-2083
Open Access | Times Cited: 9
Testing criteria for 22q11.2 deletion syndrome: preliminary results of a low cost strategy for public health
Ilária Cristina Sgardioli, Fabíola Paoli Monteiro, Paulo Fanti, et al.
Orphanet Journal of Rare Diseases (2019) Vol. 14, Iss. 1
Open Access | Times Cited: 14
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