Abel L

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Family name Abel
Given name Laurent
Initials L
ORCID

ORCID 0000-0001-7016-6493
Affiliations Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France.
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.

9 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
Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children.
Bastard P, Gervais A, Taniguchi M, ..., Cobat A, Casanova JL
J. Exp. Med. 221 (2) - [2024-02-05; online 2024-01-04]
Clinical Genomics Stockholm [Service]
PubMed DOI Crossref
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
Matuozzo D, Talouarn E, Marchal A, ..., Abel L, Cobat A
Genome Med 15 (1) - [2023-04-05; online 2023-04-05]
Clinical Genomics Stockholm [Service]
PubMed DOI Crossref
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
Matuozzo D, Talouarn E, Marchal A, ..., Abel L, Cobat A
Genome Med 15 (1) - [2023-04-05; online 2023-04-05]
Clinical Genomics Stockholm [Service]
PubMed DOI Crossref
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
Matuozzo D, Talouarn E, Marchal A, ..., Abel L, Cobat A
Genome Med 15 (1) - [2023-04-05; online 2023-04-05]
Clinical Genomics Stockholm [Service]
PubMed DOI Crossref
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
Matuozzo D, Talouarn E, Marchal A, ..., Abel L, Cobat A
Genome Med 15 (1) - [2023-04-05; online 2023-04-05]
Clinical Genomics Stockholm [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
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