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:

Severe combined immunodeficiency—an update
Emilia Cirillo, Giuliana Giardino, Vera Gallo, et al.
Annals of the New York Academy of Sciences (2015) Vol. 1356, Iss. 1, pp. 90-106
Closed Access | Times Cited: 93

Showing 1-25 of 93 citing articles:

Primary Immunodeficiency Diseases and Bacillus Calmette-Guérin (BCG)-Vaccine–Derived Complications: A Systematic Review
Saba Fekrvand, Reza Yazdani, Peter Olbrich, et al.
The Journal of Allergy and Clinical Immunology In Practice (2020) Vol. 8, Iss. 4, pp. 1371-1386
Closed Access | Times Cited: 66

Diagnostics of Primary Immunodeficiencies through Next-Generation Sequencing
Vera Gallo, Laura Dotta, Giuliana Giardino, et al.
Frontiers in Immunology (2016) Vol. 7
Open Access | Times Cited: 65

Increasing CRISPR Efficiency and Measuring Its Specificity in HSPCs Using a Clinically Relevant System
Jenny Shapiro, Ortal Iancu, Ashley M. Jacobi, et al.
Molecular Therapy — Methods & Clinical Development (2020) Vol. 17, pp. 1097-1107
Open Access | Times Cited: 53

Recent advances in lentiviral vectors for gene therapy
Xiaoyu Wang, Cuicui Ma, Roberto Rodríguez‐Labrada, et al.
Science China Life Sciences (2021) Vol. 64, Iss. 11, pp. 1842-1857
Closed Access | Times Cited: 43

Multiplex HDR for disease and correction modeling of SCID by CRISPR genome editing in human HSPCs
Ortal Iancu, Daniel Allen, Orli Knop, et al.
Molecular Therapy — Nucleic Acids (2022) Vol. 31, pp. 105-121
Open Access | Times Cited: 28

Exploration of the therapeutic aspects of Lck: A kinase target in inflammatory mediated pathological conditions
Pankaj Kumar Singh, Aanchal Kashyap, Om Silakari
Biomedicine & Pharmacotherapy (2018) Vol. 108, pp. 1565-1571
Open Access | Times Cited: 59

Autoimmunity in Primary Immunodeficiency Disorders: An Updated Review on Pathogenic and Clinical Implications
Giorgio Costagliola, Susanna Cappelli, Rita Consolini
Journal of Clinical Medicine (2021) Vol. 10, Iss. 20, pp. 4729-4729
Open Access | Times Cited: 39

Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency
Jessica C. Barry, T. Blaine Crowley, Soma Jyonouchi, et al.
Journal of Clinical Immunology (2017) Vol. 37, Iss. 5, pp. 476-485
Closed Access | Times Cited: 44

B-cell receptor repertoire sequencing in patients with primary immunodeficiency: a review
Marie Ghraichy, Jacob D. Galson, Dominic F. Kelly, et al.
Immunology (2017) Vol. 153, Iss. 2, pp. 145-160
Open Access | Times Cited: 42

Severe Combined Immunodeficiency—Classification, Microbiology Association and Treatment
Angel A Justiz-Vaillant, Darren Gopaul, Patrick Eberechi Akpaka, et al.
Microorganisms (2023) Vol. 11, Iss. 6, pp. 1589-1589
Open Access | Times Cited: 12

Janus Kinase 3 (JAK3): A Critical Conserved Node in Immunity Disrupted in Immune Cell Cancer and Immunodeficiency
Clifford Liongue, Tarindhi Ratnayake, Faiza Basheer, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 5, pp. 2977-2977
Open Access | Times Cited: 4

Methylene-Tetrahydrofolate Dehydrogenase 1 (MTHFD1) Deficiency
Parinaz Sedighi, Sara Hanaei
(2025), pp. 1-3
Closed Access

JAK/STAT disruption induces immuno-deficiency: Rationale for the development of JAK inhibitors as immunosuppressive drugs
Isabelle Cornez, Sowmya Parampalli Yajnanarayana, Anna Wolf, et al.
Molecular and Cellular Endocrinology (2017) Vol. 451, pp. 88-96
Closed Access | Times Cited: 34

FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
Vera Gallo, Emilia Cirillo, Giuliana Giardino, et al.
Journal of Clinical Immunology (2017) Vol. 37, Iss. 8, pp. 751-758
Closed Access | Times Cited: 34

Unbalanced Immune System: Immunodeficiencies and Autoimmunity
Giuliana Giardino, Vera Gallo, Rosaria Prencipe, et al.
Frontiers in Pediatrics (2016) Vol. 4
Open Access | Times Cited: 33

Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defects
Atar Lev, Yu Nee Lee, Guangping Sun, et al.
The Journal of Experimental Medicine (2020) Vol. 218, Iss. 3
Open Access | Times Cited: 28

Immune Response in Pneumocystis Infections According to the Host Immune System Status
Éléna Charpentier, Sandie Ménard, Catherine Marques, et al.
Journal of Fungi (2021) Vol. 7, Iss. 8, pp. 625-625
Open Access | Times Cited: 27

CRISPR-Cas9 engineering of the RAG2 locus via complete coding sequence replacement for therapeutic applications
Daniel Allen, Orli Knop, Bryan Itkowitz, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 10

Newborn screening using TREC/KREC assay for severe T and B cell lymphopenia in Iran
Maryam Nourizadeh, Leila Shakerian, Stephan Borte, et al.
Scandinavian Journal of Immunology (2018) Vol. 88, Iss. 2
Open Access | Times Cited: 32

Lymphadenopathy at the crossroad between immunodeficiency and autoinflammation: An intriguing challenge
Giorgio Costagliola, Rita Consolini
Clinical & Experimental Immunology (2021) Vol. 205, Iss. 3, pp. 288-305
Open Access | Times Cited: 23

Establishment and Maintenance of the Human Naïve CD4+ T-Cell Compartment
Susana L. Silva, Ana E. Sousa
Frontiers in Pediatrics (2016) Vol. 4
Open Access | Times Cited: 23

Consensus of the Italian Primary Immunodeficiency Network on transition management from pediatric to adult care in patients affected with childhood-onset inborn errors of immunity
Emilia Cirillo, Giuliana Giardino, Silvia Ricci, et al.
Journal of Allergy and Clinical Immunology (2020) Vol. 146, Iss. 5, pp. 967-983
Open Access | Times Cited: 19

Clinical, immunologic, and genetic characteristics of RAG mutations in 15 Chinese patients with SCID and Omenn syndrome
Xiaoming Bai, Jing Liu, Zhiyong Zhang, et al.
Immunologic Research (2015) Vol. 64, Iss. 2, pp. 497-507
Closed Access | Times Cited: 20

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