Connection

Laurent Abel to Female

This is a "connection" page, showing publications Laurent Abel has written about Female.
Connection Strength

0.052
  1. Preexisting autoantibodies to type I IFNs underlie critical COVID-19 pneumonia in patients with APS-1. J Exp Med. 2021 07 05; 218(7).
    View in: PubMed
    Score: 0.003
  2. Auto-antibodies to type I IFNs can underlie adverse reactions to yellow fever live attenuated vaccine. J Exp Med. 2021 04 05; 218(4).
    View in: PubMed
    Score: 0.003
  3. Inhibition of HECT E3 ligases as potential therapy for COVID-19. Cell Death Dis. 2021 03 24; 12(4):310.
    View in: PubMed
    Score: 0.003
  4. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19. Science. 2020 10 23; 370(6515).
    View in: PubMed
    Score: 0.003
  5. Autoantibodies against type I IFNs in patients with life-threatening COVID-19. Science. 2020 10 23; 370(6515).
    View in: PubMed
    Score: 0.003
  6. 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.
    View in: PubMed
    Score: 0.003
  7. 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.
    View in: PubMed
    Score: 0.003
  8. A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rß1 Deficiency. J Clin Immunol. 2018 07; 38(5):617-627.
    View in: PubMed
    Score: 0.003
  9. A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity. Sci Immunol. 2018 06 15; 3(24).
    View in: PubMed
    Score: 0.003
  10. Microdeletion on chromosome 8p23.1 in a familial form of severe Buruli ulcer. PLoS Negl Trop Dis. 2018 04; 12(4):e0006429.
    View in: PubMed
    Score: 0.003
  11. Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi Arabia. J Clin Immunol. 2018 04; 38(3):278-282.
    View in: PubMed
    Score: 0.003
  12. IRF4 haploinsufficiency in a family with Whipple's disease. Elife. 2018 03 14; 7.
    View in: PubMed
    Score: 0.003
  13. An in vitro diagnostic certified point of care single nucleotide test for IL28B polymorphisms. PLoS One. 2017; 12(9):e0183084.
    View in: PubMed
    Score: 0.002
  14. Recurrent rhinovirus infections in a child with inherited MDA5 deficiency. J Exp Med. 2017 Jul 03; 214(7):1949-1972.
    View in: PubMed
    Score: 0.002
  15. Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiency. J Clin Invest. 2017 May 01; 127(5):1991-2006.
    View in: PubMed
    Score: 0.002
  16. Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis. J Am Coll Cardiol. 2017 Apr 04; 69(13):1653-1665.
    View in: PubMed
    Score: 0.002
  17. A genome wide association study identifies a lncRna as risk factor for pathological inflammatory responses in leprosy. PLoS Genet. 2017 02; 13(2):e1006637.
    View in: PubMed
    Score: 0.002
  18. 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.
    View in: PubMed
    Score: 0.002
  19. Invasive pneumococcal disease in children can reveal a primary immunodeficiency. Clin Infect Dis. 2014 Jul 15; 59(2):244-51.
    View in: PubMed
    Score: 0.002
  20. 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.
    View in: PubMed
    Score: 0.001
  21. 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.
    View in: PubMed
    Score: 0.001
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.