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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:

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

Showing 1-25 of 28 citing articles:

Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee
Stuart G. Tangye, Waleed Al‐Herz, Aziz Bousfiha, et al.
Journal of Clinical Immunology (2022) Vol. 42, Iss. 7, pp. 1473-1507
Open Access | Times Cited: 833
The Ever-Increasing Array of Novel Inborn Errors of Immunity: an Interim Update by the IUIS Committee
Stuart G. Tangye, Waleed Al‐Herz, Aziz Bousfiha, et al.
Journal of Clinical Immunology (2021) Vol. 41, Iss. 3, pp. 666-679
Open Access | Times Cited: 198
Novel Genetic Discoveries in Primary Immunodeficiency Disorders
Margaret Redmond, Rebecca Scherzer, Benjamin T. Prince
Clinical Reviews in Allergy & Immunology (2022) Vol. 63, Iss. 1, pp. 55-74
Open Access | Times Cited: 29
Lessons Learned From Five Years of Newborn Screening for Severe Combined Immunodeficiency in Israel
Atar Lev, Idan Sharir, Amos J. Simon, et al.
The Journal of Allergy and Clinical Immunology In Practice (2022) Vol. 10, Iss. 10, pp. 2722-2731.e9
Closed Access | Times Cited: 20
Outcome of hematopoietic stem cell transplantation for SCID and impact of newborn screening on overall survival – A single referral center study
Chen Anchoo, Atar Lev, Amos J. Simon, et al.
Journal of Allergy and Clinical Immunology (2025)
Closed Access
Combined T and B Cell Deficiency - SCID Forms: T-B+
Fabio Candotti
Elsevier eBooks (2025)
Closed Access
A partial human LCK defect causes a T cell immunodeficiency with intestinal inflammation
Victor G. Lui, Manfred Hoenig, Berenice Cabrera-Martinez, et al.
The Journal of Experimental Medicine (2023) Vol. 221, Iss. 1
Open Access | Times Cited: 10
The Multiple Roles of the Cytosolic Adapter Proteins ADAP, SKAP1 and SKAP2 for TCR/CD3 -Mediated Signaling Events
Nirdosh Dadwal, Charlie Mix, Annegret Reinhold, et al.
Frontiers in Immunology (2021) Vol. 12
Open Access | Times Cited: 22
A Novel Biallelic LCK Variant Resulting in Profound T-Cell Immune Deficiency and Review of the Literature
Anna-Lisa Lanz, Şerife Erdem, Alper Özcan, et al.
Journal of Clinical Immunology (2023) Vol. 44, Iss. 1
Open Access | Times Cited: 8
New primary immunodeficiencies 2021 context and future
Yeşim Yılmaz Demirdağ, Ramsay Fuleihan, Jordan S. Orange, et al.
Current Opinion in Pediatrics (2021) Vol. 33, Iss. 6, pp. 657-675
Closed Access | Times Cited: 20
Imagine CRISPR cures
Fyodor D. Urnov
Molecular Therapy (2021) Vol. 29, Iss. 11, pp. 3103-3106
Open Access | Times Cited: 15
Host genetics of innate immune system in infection
Amy P. Hsu, Steven M. Holland
Current Opinion in Immunology (2022) Vol. 74, pp. 140-149
Open Access | Times Cited: 9
SLP76 Mutation Associated with Combined Immunodeficiency and EBV-Related Lymphoma
Atar Lev, Mahdi Asleh, Shiran Levy, et al.
Journal of Clinical Immunology (2022) Vol. 43, Iss. 3, pp. 625-635
Closed Access | Times Cited: 9
Disaster cassification net: A disaster classification algorithm on remote sensing imagery
Jianye Yuan, Xinwang Ding, Fangyuan Liu, et al.
Frontiers in Environmental Science (2023) Vol. 10
Open Access | Times Cited: 5
The Clinical Aspect of Adaptor Molecules in T Cell Signaling: Lessons Learnt From Inborn Errors of Immunity
Yael Dinur-Schejter, Irina Zaidman, Hagar Mor‐Shaked, et al.
Frontiers in Immunology (2021) Vol. 12
Open Access | Times Cited: 12
Combined immunodeficiency and impaired PI3K signaling in a patient with biallelic LCP2 variants
Emily S.J. Edwards, Samar Ojaimi, James Ngui, et al.
Journal of Allergy and Clinical Immunology (2023) Vol. 152, Iss. 3, pp. 807-813.e7
Open Access | Times Cited: 4
Hyperactivation of the PI3K Pathway in Inborn Errors of Immunity: current understanding and therapeutic perspectives
Hanna IJspeert, Virgil A. S. H. Dalm, Menno C. van Zelm, et al.
Immunotherapy Advances (2024) Vol. 4, Iss. 1
Open Access | Times Cited: 1
Low Efficacy of Genetic Tests for the Diagnosis of Primary Lymphedema Prompts Novel Insights into the Underlying Molecular Pathways
G Bonetti, Stefano Paolacci, Michele Samaja, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 13, pp. 7414-7414
Open Access | Times Cited: 7
Inherited immunodeficiencies associated with proximal and distal defects in T cell receptor signaling and co-signaling
Sylvain Latour
Biomedical Journal (2022) Vol. 45, Iss. 2, pp. 321-333
Open Access | Times Cited: 6
Combined Immunodeficiency Caused by a Novel Nonsense Mutation in LCK
Baerbel Keller, Shlomit Kfir‐Erenfeld, Paul Matusewicz, et al.
Journal of Clinical Immunology (2023) Vol. 44, Iss. 1
Open Access | Times Cited: 3
Distinct Proteomic Profiling of Plasma Extracellular Vesicles from Moderate-to-Severe Atopic Dermatitis Patients
Chih‐Jung Chang, Haiqing Wang, Jing Zhang, et al.
Clinical Cosmetic and Investigational Dermatology (2021) Vol. Volume 14, pp. 1033-1043
Open Access | Times Cited: 7
Complex Inheritance of Rare Missense Variants in PAK2, TAP2, and PLCL1 Genes in a Consanguineous Arab Family With Multiple Autoimmune Diseases Including Celiac Disease
Arwa Mastoor Alharthi, Babajan Banaganapalli, Sabah M. Hassan, et al.
Frontiers in Pediatrics (2022) Vol. 10
Open Access | Times Cited: 4
Perspective - Was it All for Nothing?
Raz Somech
Journal of Clinical Immunology (2024) Vol. 44, Iss. 5
Closed Access
Defects in T Cell Activation and Signaling
Sylvain Latour
Elsevier eBooks (2024)
Closed Access
The opposing effects of two gene defects in STX11 and SLP76 on the disease in a patient with an inborn error of immunity
Rana Mansour, Rana El-Hassan, Youmna El-Orfali, et al.
Journal of Allergy and Clinical Immunology (2023) Vol. 152, Iss. 6, pp. 1597-1606
Closed Access | Times Cited: 1
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