Open Access Helper

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:

Exome and genome sequencing for inborn errors of immunity
Isabelle Meyts, Barbara Bosch, Alexandre Bolze, et al.
Journal of Allergy and Clinical Immunology (2016) Vol. 138, Iss. 4, pp. 957-969
Open Access | Times Cited: 179

Showing 1-25 of 179 citing articles:

Human Inborn Errors of Immunity: 2019 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 (2020) Vol. 40, Iss. 1, pp. 24-64
Open Access | Times Cited: 1028
The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity
Markus G. Seidel, Gerhard Kindle, Benjamin Gathmann, et al.
The Journal of Allergy and Clinical Immunology In Practice (2019) Vol. 7, Iss. 6, pp. 1763-1770
Open Access | Times Cited: 490
Type 2 immunity in the skin and lungs
Cezmi A. Akdiş, Peter D. Arkwright, Marie‐Charlotte Brüggen, et al.
Allergy (2020) Vol. 75, Iss. 7, pp. 1582-1605
Open Access | Times Cited: 424
Deficiency of Adenosine Deaminase 2 (DADA2): Updates on the Phenotype, Genetics, Pathogenesis, and Treatment
Isabelle Meyts, Ivona Aksentijevich
Journal of Clinical Immunology (2018) Vol. 38, Iss. 5, pp. 569-578
Open Access | Times Cited: 354
Primary immunodeficiency
Christine McCusker, Julia Upton, Richard Warrington
Allergy Asthma and Clinical Immunology (2018) Vol. 14, Iss. S2
Open Access | Times Cited: 201
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
Mendelian susceptibility to mycobacterial disease: 2014–2018 update
Jérémie Rosain, Xiao‐Fei Kong, Rubén Martínez‐Barricarte, et al.
Immunology and Cell Biology (2018) Vol. 97, Iss. 4, pp. 360-367
Open Access | Times Cited: 185
Inherited CARD9 Deficiency: Invasive Disease Caused by Ascomycete Fungi in Previously Healthy Children and Adults
Emilie Corvilain, Jean‐Laurent Casanova, Anne Puel
Journal of Clinical Immunology (2018) Vol. 38, Iss. 6, pp. 656-693
Open Access | Times Cited: 137
Global report on primary immunodeficiencies: 2018 update from the Jeffrey Modell Centers Network on disease classification, regional trends, treatment modalities, and physician reported outcomes
Vicki Modell, Jordan S. Orange, Jessica Quinn, et al.
Immunologic Research (2018) Vol. 66, Iss. 3, pp. 367-380
Closed Access | Times Cited: 133
Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic disease
Batsukh Dorjbal, Jeffrey R. Stinson, Chi A., et al.
Journal of Allergy and Clinical Immunology (2018) Vol. 143, Iss. 4, pp. 1482-1495
Open Access | Times Cited: 129
Lethal Infectious Diseases as Inborn Errors of Immunity: Toward a Synthesis of the Germ and Genetic Theories
Jean‐Laurent Casanova, Laurent Abel
Annual Review of Pathology Mechanisms of Disease (2020) Vol. 16, Iss. 1, pp. 23-50
Open Access | Times Cited: 106
T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency
Immacolata Brigida, Matteo Zoccolillo, Maria Pia Cicalese, et al.
Blood (2018) Vol. 132, Iss. 22, pp. 2362-2374
Open Access | Times Cited: 103
Clinical implications of systematic phenotyping and exome sequencing in patients with primary antibody deficiency
Hassan Abolhassani, Asghar Aghamohammadi, Mingyan Fang, et al.
Genetics in Medicine (2018) Vol. 21, Iss. 1, pp. 243-251
Open Access | Times Cited: 97
Primary immunodeficiencies reveal the molecular requirements for effective host defense against EBV infection
Stuart G. Tangye, Sylvain Latour
Blood (2020) Vol. 135, Iss. 9, pp. 644-655
Open Access | Times Cited: 96
A global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection
Evangelos Andreakos, Laurent Abel, Donald C. Vinh, et al.
Nature Immunology (2021) Vol. 23, Iss. 2, pp. 159-164
Open Access | Times Cited: 57
Growth in diagnosis and treatment of primary immunodeficiency within the global Jeffrey Modell Centers Network
Jessica Quinn, Vicki Modell, Jordan S. Orange, et al.
Allergy Asthma and Clinical Immunology (2022) Vol. 18, Iss. 1
Open Access | Times Cited: 52
Multi-omics research in sarcopenia: Current progress and future prospects
Jiachen Liu, Shan‐Shan Dong, Hui Shen, et al.
Ageing Research Reviews (2022) Vol. 76, pp. 101576-101576
Closed Access | Times Cited: 48
Inborn errors of immunity: an expanding universe of disease and genetic architecture
Yemsratch T. Akalu, Dusan Bogunovic
Nature Reviews Genetics (2023) Vol. 25, Iss. 3, pp. 184-195
Closed Access | Times Cited: 24
Human germline gain-of-function in STAT6: from severe allergic disease to lymphoma and beyond
Mehul Sharma, Narissara Suratannon, Daniel Leung, et al.
Trends in Immunology (2024) Vol. 45, Iss. 2, pp. 138-153
Open Access | Times Cited: 16
Heterozygous mutations in the C-terminal domain of COPA underlie a complex autoinflammatory syndrome
Selket Delafontaine, Alberto Iannuzzo, Tarin M. Bigley, et al.
Journal of Clinical Investigation (2024) Vol. 134, Iss. 4
Open Access | Times Cited: 12
Health-related quality of life in patients with inborn errors of immunity: a bibliometric analysis
Ningkun Xiao, Xin‐Lin Huang, Wanli Zang, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 11
Inborn errors of immunity (primary immunodeficiencies)
Vy H.D. Kim, Julia Upton, Beáta Dérfalvi, et al.
Allergy Asthma and Clinical Immunology (2025) Vol. 20, Iss. S3
Open Access | Times Cited: 1
Ex vivo T-lymphopoiesis assays assisting corrective treatment choice for genetically undefined T-lymphocytopaenia
Zainab Golwala, Helena Spiridou Goncalves, Ranjita Devi Moirangthem, et al.
Clinical Immunology (2025), pp. 110453-110453
Open Access | Times Cited: 1
Uses of Next-Generation Sequencing Technologies for the Diagnosis of Primary Immunodeficiencies
Michael Seleman, Rodrigo Hoyos‐Bachiloglu, Raif S. Geha, et al.
Frontiers in Immunology (2017) Vol. 8
Open Access | Times Cited: 86
Diagnostic interpretation of genetic studies in patients with primary immunodeficiency diseases: A working group report of the Primary Immunodeficiency Diseases Committee of the American Academy of Allergy, Asthma & Immunology
Iván K. Chinn, Alice Chan, Karin Chen, et al.
Journal of Allergy and Clinical Immunology (2019) Vol. 145, Iss. 1, pp. 46-69
Open Access | Times Cited: 72
Page 1 - Next Page

Scroll to top