Connection

Giuseppe Novelli to Polymorphism, Single Nucleotide

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This is a "connection" page, showing publications Giuseppe Novelli has written about Polymorphism, Single Nucleotide.
Giuseppe Novelli
Connection Strength
0.577
Polymorphism, Single Nucleotide
  1. COVID-19 and Genetic Variants of Protein Involved in the SARS-CoV-2 Entry into the Host Cells. Genes (Basel). 2020 08 27; 11(9).
    View in: PubMed
    Score: 0.082
  2. Keratoderma-Deafness-Mucocutaneous Syndrome Associated with Phe142Leu in the GJB2 Gene. Acta Derm Venereol. 2019 Nov 01; 99(12):1192-1194.
    View in: PubMed
    Score: 0.078
  3. Association between a MIR499A polymorphism and diabetic neuropathy in type 2 diabetes. J Diabetes Complications. 2018 01; 32(1):11-17.
    View in: PubMed
    Score: 0.068
  4. Pharmacogenetics of inflammatory bowel disease: a focus on Crohn's disease. Pharmacogenomics. 2017 Jul; 18(11):1095-1114.
    View in: PubMed
    Score: 0.066
  5. Genome-wide association study of nevirapine hypersensitivity in a sub-Saharan African HIV-infected population. J Antimicrob Chemother. 2017 04 01; 72(4):1152-1162.
    View in: PubMed
    Score: 0.065
  6. Polymorphisms in STAT4, PTPN2, PSORS1C1 and TRAF3IP2 Genes Are Associated with the Response to TNF Inhibitors in Patients with Rheumatoid Arthritis. PLoS One. 2017; 12(1):e0169956.
    View in: PubMed
    Score: 0.064
  7. Typing of ARMS2 and CFH in age-related macular degeneration: case-control study and assessment of frequency in the Italian population. Arch Ophthalmol. 2009 Oct; 127(10):1368-72.
    View in: PubMed
    Score: 0.039
  8. Update on human genetic susceptibility to COVID-19: susceptibility to virus and response. Hum Genomics. 2021 08 25; 15(1):57.
    View in: PubMed
    Score: 0.022
  9. Analysis of ACE2 Genetic Variability among Populations Highlights a Possible Link with COVID-19-Related Neurological Complications. Genes (Basel). 2020 07 03; 11(7).
    View in: PubMed
    Score: 0.020
  10. The differential response to anti IL-6 treatment in COVID-19: the genetic counterpart. Clin Exp Rheumatol. 2020 May-Jun; 38(3):580.
    View in: PubMed
    Score: 0.020
  11. 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: 0.019
  12. 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: 0.018
  13. Targeted Next Generation Sequencing in patients with Myotonia Congenita. Clin Chim Acta. 2017 Jul; 470:1-7.
    View in: PubMed
    Score: 0.016
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