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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:

The diagnosis of severe combined immunodeficiency: Implementation of the PIDTC 2022 Definitions
Christopher C. Dvorak, Élie Haddad, Jennifer Heimall, et al.
Journal of Allergy and Clinical Immunology (2022) Vol. 151, Iss. 2, pp. 547-555.e5
Open Access | Times Cited: 29

Showing 1-25 of 29 citing articles:

Current Status of Newborn Bloodspot Screening Worldwide 2024: A Comprehensive Review of Recent Activities (2020–2023)
Bradford L. Therrell, Carmencita D. Padilla, Gustavo Borrajo, et al.
International Journal of Neonatal Screening (2024) Vol. 10, Iss. 2, pp. 38-38
Open Access | Times Cited: 27
The diagnosis of severe combined immunodeficiency (SCID): The Primary Immune Deficiency Treatment Consortium (PIDTC) 2022 Definitions
Christopher C. Dvorak, Élie Haddad, Jennifer Heimall, et al.
Journal of Allergy and Clinical Immunology (2022) Vol. 151, Iss. 2, pp. 539-546
Open Access | Times Cited: 67
Prospective Newborn Screening for SCID in Germany: A First Analysis by the Pediatric Immunology Working Group (API)
Carsten Speckmann, U Nennstiel‐Ratzel, Manfred Hönig, et al.
Journal of Clinical Immunology (2023) Vol. 43, Iss. 5, pp. 965-978
Open Access | Times Cited: 31
Exonic knockout and knockin gene editing in hematopoietic stem and progenitor cells rescues RAG1 immunodeficiency
Maria Carmina Castiello, Chiara Brandas, Samuele Ferrari, et al.
Science Translational Medicine (2024) Vol. 16, Iss. 733
Open Access | Times Cited: 10
Expanding the PRAAS spectrum: De novo mutations of immunoproteasome subunit β-type 10 in six infants with SCID-Omenn syndrome
Caspar I. van der Made, Simone Kersten, Odelia Chorin, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 4, pp. 791-804
Open Access | Times Cited: 6
Preimplantation genetic testing for four families with severe combined immunodeficiency: Three unaffected livebirths
L. Y. Zhang, Lei Feng, Hao Shi, et al.
Orphanet Journal of Rare Diseases (2025) Vol. 20, Iss. 1
Open Access
Pulmonary Aspergillosis and Low HIES Score in a Family with STAT3 N-Terminal Domain Mutation
Suiane Lima de Souza, Takaki Asano, Virpi Glumoff, et al.
Journal of Clinical Immunology (2025) Vol. 45, Iss. 1
Open Access
Advancing precision care in pregnancy through a treatable fetal findings list
Jennifer L. Cohen, Michael H. Duyzend, Sophia Adelson, et al.
The American Journal of Human Genetics (2025)
Closed Access
Combined T and B Cell Deficiency - SCID Forms: T-B+
Fabio Candotti
Elsevier eBooks (2025)
Closed Access
Correlation Analysis of Human Immunological Indicators and Nosocomial Infections, Along With Evaluation Value for Prognosis
C.‐L. Wu, Jun Yan, Liping Sun, et al.
Journal of Immunology Research (2025) Vol. 2025, Iss. 1
Open Access
Assistance of next-generation sequencing for diagnosis of disseminated Bacillus Calmette-Guerin disease with X-SCID in an infant: a case report and literature review
Haiyang Zhang, Yi Liao, Zhensheng Zhu, et al.
Frontiers in Cellular and Infection Microbiology (2024) Vol. 14
Open Access | Times Cited: 3
European flow cytometry quality assurance guidelines for the diagnosis of primary immune deficiencies and assessment of immune reconstitution following B cell depletion therapies and transplantation
Peter Kelleher, Louise Greathead, Liam Whitby, et al.
Cytometry Part B Clinical Cytometry (2024)
Open Access | Times Cited: 3
Allogeneic Hematopoietic Stem Cell Transplantation Activity in Inborn Errors of Immunity in Russian Federation
Alexandra Laberko, Anna Mukhinа, Е. Б. Мачнева, et al.
Journal of Clinical Immunology (2023) Vol. 43, Iss. 6, pp. 1241-1249
Open Access | Times Cited: 5
Omenn Syndrome in Two Infants with Different Hypomorphic Variants in Janus Kinase 3
Christo Tsilifis, Jarmila Stremenova Spegarova, Ross Good, et al.
Journal of Clinical Immunology (2024) Vol. 44, Iss. 4
Open Access | Times Cited: 1
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
IL-7–dependent and –independent lineages of IL-7R–dependent human T cells
Carlos A. Arango-Franco, Masato Ogishi, Susanne Unger, et al.
Journal of Clinical Investigation (2024) Vol. 134, Iss. 19
Open Access | Times Cited: 1
Combined Immunodeficiencies
Tamar Rubin, Kelli W. Williams, Monica G. Lawrence
(2024), pp. 692-716
Closed Access | Times Cited: 1
Case report: Identification of a Chinese patient with RAG1 mutations initially presenting as autoimmune hemolytic anemia
Xin Chen, Chunxue Jiang, Wenliang Song, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 1
Purine Nucleoside Phosphorylase Deficient Severe Combined Immunodeficiencies: A Case Report and Systematic Review (1975–2022)
Syarifah Masyitah Habib Dzulkarnain, Ilie Fadzilah Hashim, Zarina Thasneem Zainudeen, et al.
Journal of Clinical Immunology (2023) Vol. 43, Iss. 7, pp. 1623-1639
Open Access | Times Cited: 2
Mutational analysis in different genes underlying severe combined immunodeficiency in seven consanguineous Pakistani families
Hajra Fayyaz, Atteaya Zaman, Sheeba Shabbir, et al.
Molecular Biology Reports (2024) Vol. 51, Iss. 1
Closed Access
Case report: Artificial thymic organoids facilitate clinical decisions for a patient with a TP63 variant and severe persistent T cell lymphopenia
Alevtina Gall, Marita Bosticardo, Stacey Ma, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access
Late effects following hematopoietic cell transplantation for severe combined immunodeficiency: critical factors and therapeutic options
Hesham Eissa, Morton J. Cowan, Jennifer Heimall
Expert Review of Clinical Immunology (2024), pp. 1-10
Closed Access
Hematopoietic cell transplantation for inborn errors of immunity: an update on approaches, outcomes and innovations
Olatundun Williams
Current Opinion in Pediatrics (2024) Vol. 36, Iss. 6, pp. 653-658
Closed Access
Omenn syndrome: A rare manifestation of severe combined immunodeficiency masquerading as drug reaction with eosinophilia and systemic symptoms
Elizabeth M. Forbes, Peter McNaughton
Journal of Paediatrics and Child Health (2024) Vol. 60, Iss. 12, pp. 880-882
Open Access
Late-Onset and Hypomorphic Presentation of Severe Combined Immune Deficiency
Lorenzo Salvati, Boaz Palterer, Lorenzo Cosmi
Rare diseases of the immune system (2024), pp. 91-101
Closed Access
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