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Cited by 404

The DOI matches its Crossref record; 10 of the 10 references it cites were found in a registry or an index.

Type I interferonopathies: a novel set of inborn errors of immunity

Open access
Crow, Yanick J.·2011·Annals of the New York Academy of Sciences

Abstract

The concept of grouping Mendelian disorders associated with an upregulation of type I interferon is not currently recognized in the medical literature. Here, we argue that such a concept has scientific validity and clinical utility. Specifically, we discuss a group of conditions, including Aicardi–Goutières syndrome, spondyloenchondrodysplasia, and cases of systemic lupus erythematosus with complement deficiency, in which an upregulation of type I interferons is apparently central to their pathogenesis. We believe that these diseases can usefully be considered to represent a novel set of inborn errors of immunity, and that the recognition of such diseases as type I interferonopathies will have significance in the development and use of targeted therapies.

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Crossref · 10.1111/j.1749-6632.2011.06220.x

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Metadata

Authors
Crow, Y. J.
Venue
Annals of the New York Academy of Sciences
Publisher
Wiley
Published
2011-11
Volume
1238
Issue
1
Pages
91-98
ISSN
  • 0077-8923 (ISSN-L)
  • 1749-6632
OpenAlex
W2160849060
Cited by
404
References
10
FWCI
6.63
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Type I interferonopathies: a novel set of inborn errors of immunity. https://app.cochat.ai/papers/10.1111/j.1749-6632.2011.06220.x
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Crow, Y. J. (2011). Type I interferonopathies: a novel set of inborn errors of immunity. Annals of the New York Academy of Sciences. https://doi.org/10.1111/j.1749-6632.2011.06220.x

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.