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:

Genetics and clinical phenotypes in common variable immunodeficiency
Charlotte Cunningham‐Rundles, Jean‐Laurent Casanova, Bertrand Boisson
Frontiers in Genetics (2024) Vol. 14
Open Access | Times Cited: 14

Showing 14 citing articles:

Clinical, Immunological, and Genetic Features in Patients with NFKB1 and NFKB2 Mutations: a Systematic Review
Nazanin Fathi, Matineh Nirouei, Zahra Salimian Rizi, et al.
Journal of Clinical Immunology (2024) Vol. 44, Iss. 7
Closed Access | Times Cited: 4

Monogenic Common Variable Immunodeficiency (Mo‐CVID) Score for Optimizing the Genetic Diagnosis in Pediatric CVID Cohort
Federica Barbati, Lorenzo Lodi, Silvia Boscia, et al.
European Journal of Immunology (2025) Vol. 55, Iss. 3
Open Access

The Burden of Non-Infectious Organ-Specific Immunopathology in Pediatric Common Variable Immunodeficiency
Aleksandra Szczawińska-Popłonyk, Julia Bekalarska, Kacper Jęch, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 6, pp. 2653-2653
Open Access

Exploring Monogenic, Polygenic, and Epigenetic Models of Common Variable Immunodeficiency
Tayebeh Ranjbarnejad, Hassan Abolhassani, Roya Sherkat, et al.
Human Mutation (2025) Vol. 2025, Iss. 1
Open Access

Flow cytometry-based diagnostic approach for inborn errors of immunity: experience from Algeria
Azzeddine Tahiat, Reda Belbouab, Abdelghani Yagoubi, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 1

A Novel Heterozygous NFKB2 Variant in a Multiplex Family with Common Variable Immune Deficiency and Autoantibodies Against Type I IFNs
Alperen Baran, Aysima Atılgan Lülecioğlu, Liwei Gao, et al.
Journal of Clinical Immunology (2024) Vol. 45, Iss. 1
Closed Access | Times Cited: 1

Immunophenotype, Clinical Effect, and Comparison of TNFRSF13B/TACI Mutations: A Single-Center Retrospective Cohort Study of 34 Patients
E Bekar Çepniler, Emin Abdullayev, Şefika İlknur Kökçü Karadağ, et al.
Turkish Journal of Immunology (2024), pp. 117-126
Open Access

Altered Genome-Wide DNA Methylation in the Duodenum of Common Variable Immunodeficiency Patients
Mingyi Yang, Mari Kaarbø, Vegard Myhre, et al.
Journal of Clinical Immunology (2024) Vol. 44, Iss. 6
Open Access

Overview of Immunodeficiency (Encyclopedie d’Immunologie)
Marina Cavazzana
Elsevier eBooks (2024)
Closed Access

Uniparental Disomy of Chromosome 4: A Case of Whole Chromosome UPD Presenting with LRBA Deficiency
Bilgesu Ak, Erhan Parıltay, Reyhan Gümüşburun, et al.
Journal of Clinical Immunology (2024) Vol. 45, Iss. 1
Closed Access

Analysis of rare genetic variants in All of Us cohort patients with common variable immunodeficiency
Troy von Beck, Meera Patel, Niraj Patel, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access

Clinical characterization of NOD2 variants in patients with common variable immunodeficiency
Ashley Sang Eun Lee, Jin Feng, Alp Kazancioglu, et al.
Clinical Immunology (2024) Vol. 270, pp. 110401-110401
Closed Access

Primary Versus Secondary Immune Thrombocytopenia (ITP): A Meeting Report from the 2023 McMaster ITP Summit
Dimpy Modi, Saifur Rahman Chowdhury, Syed Mahamad, et al.
Thrombosis and Haemostasis (2024)
Open Access

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