Laurent Abel to Female
This is a "connection" page, showing publications Laurent Abel has written about Female.
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0.052
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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: 0.003
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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: 0.003
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Inhibition of HECT E3 ligases as potential therapy for COVID-19. Cell Death Dis. 2021 03 24; 12(4):310.
Score: 0.003
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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19. Science. 2020 10 23; 370(6515).
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Autoantibodies against type I IFNs in patients with life-threatening COVID-19. Science. 2020 10 23; 370(6515).
Score: 0.003
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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: 0.003
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Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Genome Med. 2018 07 27; 10(1):59.
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A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rß1 Deficiency. J Clin Immunol. 2018 07; 38(5):617-627.
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A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity. Sci Immunol. 2018 06 15; 3(24).
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Microdeletion on chromosome 8p23.1 in a familial form of severe Buruli ulcer. PLoS Negl Trop Dis. 2018 04; 12(4):e0006429.
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Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi Arabia. J Clin Immunol. 2018 04; 38(3):278-282.
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IRF4 haploinsufficiency in a family with Whipple's disease. Elife. 2018 03 14; 7.
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An in vitro diagnostic certified point of care single nucleotide test for IL28B polymorphisms. PLoS One. 2017; 12(9):e0183084.
Score: 0.002
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Recurrent rhinovirus infections in a child with inherited MDA5 deficiency. J Exp Med. 2017 Jul 03; 214(7):1949-1972.
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Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiency. J Clin Invest. 2017 May 01; 127(5):1991-2006.
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Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis. J Am Coll Cardiol. 2017 Apr 04; 69(13):1653-1665.
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A genome wide association study identifies a lncRna as risk factor for pathological inflammatory responses in leprosy. PLoS Genet. 2017 02; 13(2):e1006637.
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Trichodysplasia Spinulosa Polyomavirus Infection Occurs during Early Childhood with Intrafamilial Transmission, Especially from Mother to Child. J Invest Dermatol. 2017 05; 137(5):1181-1183.
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Invasive pneumococcal disease in children can reveal a primary immunodeficiency. Clin Infect Dis. 2014 Jul 15; 59(2):244-51.
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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: 0.001
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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: 0.001