OpenAlex Citation Counts

OpenAlex Citations Logo

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:

There is no gene for CVID — novel monogenetic causes for primary antibody deficiency
Neftali Jose Ramirez, Sara Posadas‐Cantera, Andrés Caballero-Oteyza, et al.
Current Opinion in Immunology (2021) Vol. 72, pp. 176-185
Closed Access | Times Cited: 39

Showing 1-25 of 39 citing articles:

The Rapidly Expanding Genetic Spectrum of Common Variable Immunodeficiency–Like Disorders
Rohan Ameratunga, Emily S.J. Edwards, Klaus Lehnert, et al.
The Journal of Allergy and Clinical Immunology In Practice (2023) Vol. 11, Iss. 6, pp. 1646-1664
Closed Access | Times Cited: 25

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

Impact of SARS-CoV-2 infection and COVID-19 on patients with inborn errors of immunity
Stuart G. Tangye, Laurent Abel, Salah Al-Muhsen, et al.
Journal of Allergy and Clinical Immunology (2022) Vol. 151, Iss. 4, pp. 818-831
Open Access | Times Cited: 29

Therapeutic gene editing of T cells to correct CTLA-4 insufficiency
Thomas A. Fox, Benjamin C. Houghton, Lina Petersone, et al.
Science Translational Medicine (2022) Vol. 14, Iss. 668
Open Access | Times Cited: 23

Enrichment of Immune Dysregulation Disorders in Adult Patients with Human Inborn Errors of Immunity
Alejandro Segura‐Tudela, Marta López-Nevado, Celia Nieto-López, et al.
Journal of Clinical Immunology (2024) Vol. 44, Iss. 3
Open Access | Times Cited: 4

Electronic health record signatures identify undiagnosed patients with common variable immunodeficiency disease
Ruth Johnson, Alexis V. Stephens, Rachel Mester, et al.
Science Translational Medicine (2024) Vol. 16, Iss. 745
Open Access | Times Cited: 4

Decreased expression of hsa-miR-142-3p and hsa-miR-155-5p in common variable immunodeficiency and involvement of their target genes and biological pathways
Tayebeh Ranjbarnejad, Alieh Gholaminejad, Hassan Abolhassani, et al.
Allergologia et Immunopathologia (2025) Vol. 53, Iss. 1, pp. 153-169
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

The pediatric common variable immunodeficiency — from genetics to therapy: a review
Aleksandra Szczawińska-Popłonyk, Eyal Schwartzmann, Ewelina Bukowska‐Olech, et al.
European Journal of Pediatrics (2021) Vol. 181, Iss. 4, pp. 1371-1383
Open Access | Times Cited: 25

Immune Dysregulation in Pediatric Common Variable Immunodeficiency: Implications for the Diagnostic Approach
Aleksandra Szczawińska-Popłonyk, Katarzyna Tąpolska‐Jóźwiak, Eyal Schwartzmann, et al.
Frontiers in Pediatrics (2022) Vol. 10
Open Access | Times Cited: 12

Genomic crossroads between non-Hodgkin’s lymphoma and common variable immunodeficiency
Kissy Guevara‐Hoyer, Jesús Fuentes‐Antrás, E. de la Fuente, et al.
Frontiers in Immunology (2022) Vol. 13
Open Access | Times Cited: 12

Association Between Cytometric Biomarkers, Clinical Phenotype, and Complications of Common Variable Immunodeficiency
Adam Markocsy, Anna Bobčáková, Otilia Petrovicova, et al.
Cureus (2024)
Open Access | Times Cited: 2

An Exploratory Approach of Clinically Useful Biomarkers of Cvid by Logistic Regression
Teresa Guerra-Galán, María Palacios-Ortega, Adolfo Jiménez‐Huete, et al.
Journal of Clinical Immunology (2024) Vol. 44, Iss. 6
Open Access | Times Cited: 2

Monogenic forms of common variable immunodeficiency and implications on target therapeutic approaches
Giulio Tessarin, Manuela Baronio, Vassilios Lougaris
Current Opinion in Allergy and Clinical Immunology (2023) Vol. 23, Iss. 6, pp. 461-466
Open Access | Times Cited: 5

The Scope and Impact of Viral Infections in Common Variable Immunodeficiency (CVID) and CVID-like Disorders: A Literature Review
Adam Al‐Hakim, Mark Kačar, Sinisa Savic
Journal of Clinical Medicine (2024) Vol. 13, Iss. 6, pp. 1717-1717
Open Access | Times Cited: 1

Immunogenetic Landscape in Pediatric Common Variable Immunodeficiency
Aleksandra Szczawińska-Popłonyk, Wiktoria Ciesielska, Marta Konarczak, et al.
(2024)
Open Access | Times Cited: 1

Common variable immunodeficiency: autoimmune cytopenias and advances in molecular diagnosis
Charlotte Cunningham-Rundles, Jean‐Laurent Casanova, Bertrand Boisson
Hematology (2024) Vol. 2024, Iss. 1, pp. 137-142
Closed Access | Times Cited: 1

Incidence, Management Experience and Characteristics of Patients with Giardiasis and Common Variable Immunodeficiency
Irene Díaz-Alberola, Juan Francisco Gutiérrez‐Bautista, A. Espuch-Oliver, et al.
Journal of Clinical Medicine (2022) Vol. 11, Iss. 23, pp. 7007-7007
Open Access | Times Cited: 7

Patients with CVID have their own “gut feeling” for viruses
Raffaele De Palma
Journal of Allergy and Clinical Immunology (2023) Vol. 151, Iss. 3, pp. 697-699
Open Access | Times Cited: 3

Phenotype from SAMD9 Mutation at 7p21.2 Appears Attenuated by Novel Compound Heterozygous Variants at RUNX2 and SALL1
E. Scott Sills, Samuel H. Wood
Global Medical Genetics (2021) Vol. 09, Iss. 02, pp. 124-128
Open Access | Times Cited: 7

Telomere biology disorders may manifest as common variable immunodeficiency (CVID)
Benjamin Rolles, Andrés Caballero-Oteyza, Michele Proietti, et al.
Clinical Immunology (2023) Vol. 257, pp. 109837-109837
Closed Access | Times Cited: 2

Challenges for gene editing in common variable immunodeficiency disorders: Current and future prospects
Rohan Ameratunga, Euphemia Leung, See‐Tarn Woon, et al.
Clinical Immunology (2023) Vol. 258, pp. 109854-109854
Closed Access | Times Cited: 2

Common variable immunodeficiency, cross currents, and prevailing winds
Neil Romberg, Carole Le Coz
Immunological Reviews (2023) Vol. 322, Iss. 1, pp. 233-243
Closed Access | Times Cited: 2

Common Variable Immunodeficiency Associated with a De Novo IKZF1 Variant and a Low Humoral Immune Response to the SARS-CoV-2 Vaccine
Irene Díaz-Alberola, A. Espuch-Oliver, José María García-Aznar, et al.
Journal of Clinical Medicine (2022) Vol. 11, Iss. 9, pp. 2303-2303
Open Access | Times Cited: 4

Case Report: Common variable immunodeficiency phenotype and granulomatous–lymphocytic interstitial lung disease with a novel SOCS1 variant
María Soledad Caldirola, Espantoso Daiana, Andrea Cecilia Gómez Raccio, et al.
Frontiers in Pediatrics (2024) Vol. 12
Open Access

Page 1 - Next Page

Scroll to top