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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:

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome
Vivien Béziat, Simon J. Tavernier, Yin‐Huai Chen, et al.
The Journal of Experimental Medicine (2020) Vol. 217, Iss. 6
Open Access | Times Cited: 92

Showing 1-25 of 92 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: 840
Human inborn errors of immunity: An expanding universe
Luigi D. Notarangelo, Rosa Bacchetta, Jean‐Laurent Casanova, et al.
Science Immunology (2020) Vol. 5, Iss. 49
Open Access | Times Cited: 206
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
Human autoantibodies underlying infectious diseases
Anne Puel, Paul Bastard, Jacinta Bustamante, et al.
The Journal of Experimental Medicine (2022) Vol. 219, Iss. 4
Open Access | Times Cited: 96
Human germline heterozygous gain-of-functionSTAT6variants cause severe allergic disease
Mehul Sharma, Daniel Leung, Mana Momenilandi, et al.
The Journal of Experimental Medicine (2023) Vol. 220, Iss. 5
Open Access | Times Cited: 63
JAKs and STATs from a Clinical Perspective: Loss-of-Function Mutations, Gain-of-Function Mutations, and Their Multidimensional Consequences
Nils Ott, Laura Faletti, Maximilian Heeg, et al.
Journal of Clinical Immunology (2023) Vol. 43, Iss. 6, pp. 1326-1359
Open Access | Times Cited: 43
The ouroboros of autoimmunity
Jean‐Laurent Casanova, Jessica N. Peel, Jean Donadieu, et al.
Nature Immunology (2024) Vol. 25, Iss. 5, pp. 743-754
Closed Access | Times Cited: 22
Human STAT1 Gain-of-Function Heterozygous Mutations: Chronic Mucocutaneous Candidiasis and Type I Interferonopathy
Satoshi Okada, Takaki Asano, Kunihiko Moriya, et al.
Journal of Clinical Immunology (2020) Vol. 40, Iss. 8, pp. 1065-1081
Open Access | Times Cited: 127
STAT3 Hyper-IgE Syndrome—an Update and Unanswered Questions
Christo Tsilifis, Alexandra F. Freeman, Andrew R. Gennery
Journal of Clinical Immunology (2021) Vol. 41, Iss. 5, pp. 864-880
Open Access | Times Cited: 101
Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency
Paul Bastard, Jérémy Manry, Jie Chen, et al.
Journal of Clinical Investigation (2020) Vol. 131, Iss. 1
Open Access | Times Cited: 87
Autoantibodies against cytokines: phenocopies of primary immunodeficiencies?
Cheng‐Lung Ku, Francesco Bianchi-Demicheli, Horst von Bernuth, et al.
Human Genetics (2020) Vol. 139, Iss. 6-7, pp. 783-794
Open Access | Times Cited: 81
Emerging roles for IL-11 in inflammatory diseases
Ka Yee Fung, Cynthia Louis, Riley D. Metcalfe, et al.
Cytokine (2021) Vol. 149, pp. 155750-155750
Open Access | Times Cited: 71
STAT3 is critical for skeletal development and bone homeostasis by regulating osteogenesis
Siru Zhou, Qinggang Dai, Xiangru Huang, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 66
Impaired IL-23–dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency
Masato Ogishi, Andrés A. Arias, Rui Yang, et al.
The Journal of Experimental Medicine (2022) Vol. 219, Iss. 10
Open Access | Times Cited: 42
Understanding the development of Th2 cell-driven allergic airway disease in early life
Beatriz León
Frontiers in Allergy (2023) Vol. 3
Open Access | Times Cited: 29
Inborn errors of human B cell development, differentiation, and function
Stuart G. Tangye, Tina Nguyen, Elissa K. Deenick, et al.
The Journal of Experimental Medicine (2023) Vol. 220, Iss. 7
Open Access | Times Cited: 26
French guidelines for the etiological workup of eosinophilia and the management of hypereosinophilic syndromes
Matthieu Groh, Julien Rohmer, Nicolas Etienne, et al.
Orphanet Journal of Rare Diseases (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 24
IL-6 prevents Th2 cell polarization by promoting SOCS3-dependent suppression of IL-2 signaling
Holly Bachus, Erin McLaughlin, Crystal Lewis, et al.
Cellular and Molecular Immunology (2023) Vol. 20, Iss. 6, pp. 651-665
Open Access | Times Cited: 23
FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice
Mana Momenilandi, Romain Lévy, Steicy Sobrino, et al.
Cell (2024) Vol. 187, Iss. 11, pp. 2817-2837.e31
Open Access | Times Cited: 13
The genetics of hyper IgE syndromes
Randa S AlYafie, Dinesh Velayutham, Nicholas van Panhuys, et al.
Frontiers in Immunology (2025) Vol. 16
Open Access | Times Cited: 1
Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance
Takaki Asano, Joëlle Khourieh, Peng Zhang, et al.
The Journal of Experimental Medicine (2021) Vol. 218, Iss. 8
Open Access | Times Cited: 41
Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity
Kunihiko Moriya, Tomohiro Nakano, Yoshitaka Honda, et al.
The Journal of Experimental Medicine (2023) Vol. 220, Iss. 9
Open Access | Times Cited: 17
Hyper-IgE syndrome, 2021 update
Yoshiyuki Minegishi
Allergology International (2021) Vol. 70, Iss. 4, pp. 407-414
Open Access | Times Cited: 41
Similarities and differences between IL11 and IL11RA1 knockout mice for lung fibro-inflammation, fertility and craniosynostosis
Benjamin Ng, Anissa A. Widjaja, Sivakumar Viswanathan, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 39
Inborn errors of immunity with atopic phenotypes: A practical guide for allergists
Riccardo Castagnoli, Vassilios Lougaris, Giuliana Giardino, et al.
World Allergy Organization Journal (2021) Vol. 14, Iss. 2, pp. 100513-100513
Open Access | Times Cited: 38
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