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Elife|March 15, 2018
IRF4 haploinsufficiency in a family with Whipple's diseaseAntoine Guérin, Gaspard Kerner, Nico Marr, et al.The Journal of Experimental Medicine|September 2, 2021
Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiencyJuan Li, Wei-Te Lei, Peng Zhang, et al.Cell Death & Disease|March 25, 2021
Inhibition of HECT E3 ligases as potential therapy for COVID-19Giuseppe Novelli, Jing Liu, Michela Biancolella, et al.Proceedings of the National Academy of Sciences of the United States of America|April 20, 2021
Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial diseaseTom Le Voyer, Anna-Lena Neehus, Rui Yang, et al.Science Immunology|December 23, 2018
Human IFN-γ immunity to mycobacteria is governed by both IL-12 and IL-23Rubén Martínez-Barricarte, Janet G Markle, Cindy S Ma, et al.The Journal of Experimental Medicine|April 20, 2022
A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotesPaul Bastard, Kuang-Chih Hsiao, Qian Zhang, et al.Science (New York, N.Y.)|December 20, 2022
Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in childrenDanyel Lee, Jérémie Le Pen, Ahmad Yatim, et al.Science (New York, N.Y.)|September 25, 2020
Autoantibodies against type I IFNs in patients with life-threatening COVID-19Paul Bastard, Lindsey B Rosen, Qian Zhang, et al.Science Immunology|August 20, 2021
X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19Takaki Asano, Bertrand Boisson, Fanny Onodi, et al.Science (New York, N.Y.)|September 25, 2020
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19Qian Zhang, Paul Bastard, Zhiyong Liu, et al.Pageof 4