Co-Authors
This is a "connection" page, showing publications co-authored by Laurent Abel and Jean-Laurent Casanova.
Connection Strength
4.402
-
Human genetics of infectious diseases: Unique insights into immunological redundancy. Semin Immunol. 2018 04; 36:1-12.
Score: 0.746
-
Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths. Sci Immunol. 2021 08 19; 6(62).
Score: 0.241
-
X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19. Sci Immunol. 2021 08 19; 6(62).
Score: 0.241
-
Insufficient type I IFN immunity underlies life-threatening COVID-19 pneumonia. C R Biol. 2021 Jun 21; 344(1):19-25.
Score: 0.238
-
Auto-antibodies to type I IFNs can underlie adverse reactions to yellow fever live attenuated vaccine. J Exp Med. 2021 04 05; 218(4).
Score: 0.235
-
Life-Threatening COVID-19: Defective Interferons Unleash Excessive Inflammation. Med (N Y). 2020 Dec 18; 1(1):14-20.
Score: 0.230
-
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19. Science. 2020 10 23; 370(6515).
Score: 0.226
-
Autoantibodies against type I IFNs in patients with life-threatening COVID-19. Science. 2020 10 23; 370(6515).
Score: 0.226
-
Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons. Proc Natl Acad Sci U S A. 2018 08 21; 115(34):E8007-E8016.
Score: 0.195
-
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity. Sci Immunol. 2018 06 15; 3(24).
Score: 0.193
-
IRF4 haploinsufficiency in a family with Whipple's disease. Elife. 2018 03 14; 7.
Score: 0.190
-
An eQTL variant of ZXDC is associated with IFN-? production following Mycobacterium tuberculosis antigen-specific stimulation. Sci Rep. 2017 10 09; 7(1):12800.
Score: 0.184
-
Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis. J Am Coll Cardiol. 2017 Apr 04; 69(13):1653-1665.
Score: 0.178
-
Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I. J Exp Med. 2010 Feb 15; 207(2):291-7.
Score: 0.108
-
Inherited interleukin-12 deficiency: IL12B genotype and clinical phenotype of 13 patients from six kindreds. Am J Hum Genet. 2002 Feb; 70(2):336-48.
Score: 0.062
-
Association of rare predicted loss-of-function variants of influenza-related type I IFN genes with critical COVID-19 pneumonia. J Clin Invest. 2021 08 02; 131(15).
Score: 0.060
-
Preexisting autoantibodies to type I IFNs underlie critical COVID-19 pneumonia in patients with APS-1. J Exp Med. 2021 07 05; 218(7).
Score: 0.060
-
Harnessing Type I IFN Immunity Against SARS-CoV-2 with Early Administration of IFN-ß. J Clin Immunol. 2021 10; 41(7):1425-1442.
Score: 0.059
-
SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease? J Exp Med. 2021 06 07; 218(6).
Score: 0.059
-
Polyclonal expansion of TCR Vbeta 21.3+ CD4+ and CD8+ T cells is a hallmark of Multisystem Inflammatory Syndrome in Children. Sci Immunol. 2021 05 25; 6(59).
Score: 0.059
-
Inhibition of HECT E3 ligases as potential therapy for COVID-19. Cell Death Dis. 2021 03 24; 12(4):310.
Score: 0.059
-
SeqTailor: a user-friendly webserver for the extraction of DNA or protein sequences from next-generation sequencing data. Nucleic Acids Res. 2019 07 02; 47(W1):W623-W631.
Score: 0.052
-
A purely quantitative form of partial recessive IFN-?R2 deficiency caused by mutations of the initiation or second codon. Hum Mol Genet. 2019 02 01; 28(3):524.
Score: 0.050
-
A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rß1 Deficiency. J Clin Immunol. 2018 07; 38(5):617-627.
Score: 0.049
-
CDG: An Online Server for Detecting Biologically Closest Disease-Causing Genes and its Application to Primary Immunodeficiency. Front Immunol. 2018; 9:1340.
Score: 0.048
-
Microdeletion on chromosome 8p23.1 in a familial form of severe Buruli ulcer. PLoS Negl Trop Dis. 2018 04; 12(4):e0006429.
Score: 0.048
-
Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi Arabia. J Clin Immunol. 2018 04; 38(3):278-282.
Score: 0.048
-
Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections. J Clin Invest. 2017 Sep 01; 127(9):3543-3556.
Score: 0.045
-
Recurrent rhinovirus infections in a child with inherited MDA5 deficiency. J Exp Med. 2017 Jul 03; 214(7):1949-1972.
Score: 0.045
-
Kaposi sarcoma, oral malformations, mitral dysplasia, and scoliosis associated with 7q34-q36.3 heterozygous terminal deletion. Am J Med Genet A. 2017 Jul; 173(7):1858-1865.
Score: 0.045
-
Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiency. J Clin Invest. 2017 May 01; 127(5):1991-2006.
Score: 0.045
-
Inherited human IRAK-1 deficiency selectively impairs TLR signaling in fibroblasts. Proc Natl Acad Sci U S A. 2017 01 24; 114(4):E514-E523.
Score: 0.044
-
Invasive pneumococcal disease in children can reveal a primary immunodeficiency. Clin Infect Dis. 2014 Jul 15; 59(2):244-51.
Score: 0.036