Giuseppe Novelli
Researcher Next ID · RN-035005
Researcher · Biochemistry, Genetics and Molecular Biology
University of Rome Tor Vergata
Rome, Italy
- Works count
- 1,020
- Citation count
- 38,663
- H-index
- 82
- i10-index
- 519
Research interests
Publications
Human genetic and immunological determinants of critical COVID-19 pneumonia
Nature · 2022 · https://doi.org/10.1038/s41586-022-04447-0
Autoantibodies against type I IFNs in patients with critical influenza pneumonia
The Journal of Experimental Medicine · 2022 · https://doi.org/10.1084/jem.20220514
Studying severe long COVID to understand post-infectious disorders beyond COVID-19
Nature Medicine · 2022 · https://doi.org/10.1038/s41591-022-01766-7
SARS-CoV-2–related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
The Journal of Experimental Medicine · 2021 · https://doi.org/10.1084/jem.20210446
X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19
Science Immunology · 2021 · https://doi.org/10.1126/sciimmunol.abl4348
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
Science · 2020 · https://doi.org/10.1126/science.abd4570
Prospective Observational Study on acute Appendicitis Worldwide (POSAW)
World Journal of Emergency Surgery · 2018 · https://doi.org/10.1186/s13017-018-0179-0
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
Nature Genetics · 2012 · https://doi.org/10.1038/ng.2467
Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis
Nature Genetics · 2010 · https://doi.org/10.1038/ng.688
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1
Nature Genetics · 2010 · https://doi.org/10.1038/ng.694
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis
Nature Genetics · 2009 · https://doi.org/10.1038/ng.313
Mandibuloacral Dysplasia Is Caused by a Mutation in LMNA-Encoding Lamin A/C
The American Journal of Human Genetics · 2002 · https://doi.org/10.1086/341908
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
Journal of Medical Genetics · 1997 · https://doi.org/10.1136/jmg.34.10.798
The origin of the major cystic fibrosis mutation (ΔF508) in European populations
Nature Genetics · 1994 · https://doi.org/10.1038/ng0694-169
Current projects
No projects listed.