Connection

Giuseppe Novelli to Alleles

This is a "connection" page, showing publications Giuseppe Novelli has written about Alleles.
Connection Strength

0.282
  1. Biallelic variants in the ciliary gene TMEM67 cause RHYNS syndrome. Eur J Hum Genet. 2018 09; 26(9):1266-1271.
    View in: PubMed
    Score: 0.117
  2. 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).
    View in: PubMed
    Score: 0.036
  3. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19. Science. 2020 10 23; 370(6515).
    View in: PubMed
    Score: 0.034
  4. HLA allele frequencies and susceptibility to COVID-19 in a group of 99 Italian patients. HLA. 2020 11; 96(5):610-614.
    View in: PubMed
    Score: 0.034
  5. STAT4, TRAF3IP2, IL10, and HCP5 Polymorphisms in Sjögren's Syndrome: Association with Disease Susceptibility and Clinical Aspects. J Immunol Res. 2019; 2019:7682827.
    View in: PubMed
    Score: 0.031
  6. A multivariate genetic analysis confirms rs5010528 in the human leucocyte antigen-C locus as a significant contributor to Stevens-Johnson syndrome/toxic epidermal necrolysis susceptibility in a Mozambique HIV population treated with nevirapine. J Antimicrob Chemother. 2018 08 01; 73(8):2137-2140.
    View in: PubMed
    Score: 0.030
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.