Presentation
Scientific Publications
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2024Journal (source)HGG AdvLack of association between classical HLA genes and asymptomatic SARS-CoV-2 i...
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2020Journal (source)Science
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19.
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2020Journal (source)Science
Autoantibodies against type I IFNs in patients with life-threatening COVID-19.
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2021Journal (source)Sci Immunol
Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected indi...
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2021Journal (source)Sci Immunol
X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life...
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2022Journal (source)Nature
Human genetic and immunological determinants of critical COVID-19 pneumonia.
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Journal (source)Proc Natl Acad Sci U S A
The risk of COVID-19 death is much greater and age dependent with type I IFN ...
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2022Journal (source)J Exp Med
Recessive inborn errors of type I IFN immunity in children with COVID-19 pneu...
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2023Journal (source)Genome Med
Rare predicted loss-of-function variants of type I IFN immunity genes are ass...
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2023Journal (source)J Exp Med
Autoantibodies neutralizing type I IFNs underlie West Nile virus encephalitis...
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2024Journal (source)J Exp Med
Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-...
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2024Journal (source)HGG Adv
Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 i...
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2024Journal (source)J Exp Med
Incontinentia pigmenti underlies thymic dysplasia, autoantibodies to type I I...
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2022Journal (source)Nature
Human genetic and immunological determinants of critical COVID-19 pneumonia.
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2021Journal (source)J Exp Med
Auto-antibodies to type I IFNs can underlie adverse reactions to yellow fever...
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2020Journal (source)Science
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19.
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2020Journal (source)Science
Auto-antibodies against type I IFNs in patients with life-threatening COVID-19.
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2019Journal (source)J. Exp. Med.
Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reacti...
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Journal (source)Proc. Natl. Acad. Sci. U.S.A.
Homozygous NLRP1 gain-of-function mutation in siblings with a syndromic form ...
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2019Journal (source)Front Genet
Identification of an Endoglin Variant Associated With HCV-Related Liver Fibro...
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Journal (source)Proc. Natl. Acad. Sci. U.S.A.
Homozygous NLRP1 gain-of-function mutation in siblings with a syndromic form ...