Studies
Genetics and Pathophysiology of Autoinflammatory Disorders
Genetics and Pathophysiology of Autoinflammatory Disorders
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Overview
Selected Publications (6)
Early-onset stroke and vasculopathy associated with mutations in ADA2.
Qing Zhou, Dan Yang, A. Ombrello, et al.. (2014). The New England journal of medicine. Cited 740 times.
https://doi.org/10.1056/NEJMoa1307361
Pyrin Inflammasome Activation and RhoA Signaling in the Autoinflammatory Diseases FMF and HIDS
Y. Park, G. Wood, D. Kastner, et al.. (2016). Nature immunology. Cited 485 times.
https://doi.org/10.1038/ni.3457
Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early onset autoinflammatory syndrome
Qing Zhou, Hongying Wang, D. Schwartz, et al.. (2015). Nature genetics. Cited 418 times.
https://doi.org/10.1038/ng.3459
The monogenic autoinflammatory diseases define new pathways in human innate immunity and inflammation
K. Manthiram, Qing Zhou, I. Aksentijevich, et al.. (2017). Nature Immunology. Cited 324 times.
https://doi.org/10.1038/ni.3777
Dense genotyping of immune-related loci implicates host responses to microbial exposure in Behçet’s disease susceptibility
M. Takeuchi, N. Mizuki, A. Meguro, et al.. (2017). Nature genetics. Cited 140 times.
https://doi.org/10.1038/ng.3786
Second Case of HOIP Deficiency Expands Clinical Features and Defines Inflammatory Transcriptome Regulated by LUBAC
H. Oda, D. Beck, H. Kuehn, et al.. (2019). Frontiers in Immunology. Cited 65 times.
https://doi.org/10.3389/fimmu.2019.00479
