Associated Papers
Monogenic disorders of immunity: Common variants are not so rare.
Béziat V et al.
Cell Genomics, 2026
A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunity.
Al Qureshah F et al.
The Journal of Experimental Medicine, 2025
Individual genetic variability mainly of Proinflammatory cytokines, cytokine receptors, and toll-like receptors dictates pathophysiology of COVID-19 disease.
Vakil MK et al.
Journal of Medical Virology, 2022
The association of COVID-19 severity and susceptibility and genetic risk factors: A systematic review of the literature.
Ishak A et al.
Gene, 2022
Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome.
Abolhassani H et al.
Journal of Clinical Immunology, 2022
An overview of human proteins and genes involved in SARS-CoV-2 infection.
Jahanafrooz Z et al.
Gene, 2022
Human genetic basis of severe or critical illness in COVID-19.
Ji XS et al.
Frontiers in Cellular and Infection Microbiology, 2022
IFNAR1 gene mutation may contribute to developmental stuttering in the Chinese population.
Sun Y et al.
Hereditas, 2021
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19.
Zhang Q et al.
Science (new York, N.y.), 2020
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