Casanova JL

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Family name Casanova
Given name Jean-Laurent
Initials JL
ORCID

ORCID 0000-0002-7782-4169
Affiliations Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France. jean-laurent.casanova@rockefeller.edu paul.bastard@institutimagine.org.
University of Paris, Imagine Institute, Paris, France.
St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA.
Howard Hughes Medical Institute, New York, NY, USA.
Pediatric Hematology and Immunology Unit, Necker Hospital for Sick Children, AP-HP, Paris, France.

7 publications

PubMed DOI Crossref
Incontinentia pigmenti underlies thymic dysplasia, autoantibodies to type I IFNs, and viral diseases.
Rosain J, Le Voyer T, Liu X, ..., Anderson MS, Casanova JL
J. Exp. Med. 221 (11) - [2024-11-04; online 2024-10-01]
Autoimmunity and Serology Profiling [Service]
PubMed DOI Crossref
Inherited human RelB deficiency impairs innate and adaptive immunity to infection.
Le Voyer T, Maglorius Renkilaraj MRL, Moriya K, ..., Tangye SG, Puel A
Proc. Natl. Acad. Sci. U.S.A. 121 (37) e2321794121 [2024-09-10; online 2024-09-04]
Autoimmunity and Serology Profiling [Service]
PubMed DOI Crossref
Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency.
Le Voyer T, Parent AV, Liu X, ..., Casanova JL, Puel A
Nature - (-) - [2023-11-08; online 2023-11-08]
Autoimmunity and Serology Profiling [Service]
PubMed DOI Crossref
Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia.
Zhang Q, Matuozzo D, Le Pen J, ..., Cobat A, Casanova JL
J. Exp. Med. 219 (8) - [2022-08-01; online 2022-06-16]
Clinical Genomics Stockholm [Service]
PubMed DOI Crossref
Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency.
Campbell TM, Liu Z, Zhang Q, ..., Meyts I, Bryceson YT
J. Exp. Med. 219 (7) - [2022-07-04; online 2022-06-07]
Clinical Genomics Stockholm [Service]
PubMed DOI Crossref
Identification of driver genes for critical forms of COVID-19 in a deeply phenotyped young patient cohort
Carapito R, Li R, Helms J, ..., Chittenden TW, Bahram S
Sci. Transl. Med. 14 (628) eabj7521 [2022-01-19; online 2022-01-19]
Autoimmunity and Serology Profiling [Service]
PubMed DOI Crossref
X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19.
Asano T, Boisson B, Onodi F, ..., Zhang Q, Casanova JL
Sci Immunol 6 (62) - [2021-08-19; online 2021-08-21]
Clinical Genomics Stockholm [Service]
SciLifeLab Data Centre
Publications 9.5.1