Area of research
Molecular Biology · Cellular and Molecular Neuroscience
Research interest
Research interests include Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, RNA modifications and cancer, and Congenital heart defects research.
Unveiling the Therapeutic Potential of the Second-Generation Incretin Analogs Semaglutide and Tirzepatide in Type 1 Diabetes and Latent Autoimmune Diabetes in Adults
Trends in Precision Medicine and Pharmacogenetics as an Adjuvant in Establishing a Correct Immunosuppressive Therapy for Kidney Transplant: An Up-to-Date Historical Overview
The seven enigmas of SARS-CoV-2: From the past to the future
Deleterious variants in the autophagy-related gene RB1CC1/FIP200 impair immunity to SARS-CoV-2
A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunity
Heterozygous <i>BTNL8</i> variants in individuals with multisystem inflammatory syndrome in children (MIS-C)
Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection
Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
Additional file 2 of Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
Human genetic and immunological determinants of critical COVID-19 pneumonia
Studying severe long COVID to understand post-infectious disorders beyond COVID-19
Autoantibodies against type I IFNs in patients with critical influenza pneumonia
Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia
Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs
Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency
Patients with an Open Abdomen in Asian, American and European Continents: A Comparative Analysis from the International Register of Open Abdomen (IROA)
Decoding the Human Genetic and Immunological Basis of COVID-19 mRNA Vaccine-Induced Myocarditis
X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19
SARS-CoV-2–related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
A global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection
Inhibition of HECT E3 ligases as potential therapy for COVID-19
Harnessing Type I IFN Immunity Against SARS-CoV-2 with Early Administration of IFN-β
From Your Nose to Your Toes: A Review of Severe Acute Respiratory Syndrome Coronavirus 2 Pandemic‒Associated Pernio
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
Improving diagnosis for rare diseases: the experience of the Italian undiagnosed Rare diseases network
Tumor Necrosis Factor Receptor SF10A (TNFRSF10A) SNPs Correlate With Corticosteroid Response in Duchenne Muscular Dystrophy
Open abdomen management for severe peritonitis in elderly. Results from the prospective International Register of Open Abdomen (IROA): Cohort study
Prospective Observational Study on acute Appendicitis Worldwide (POSAW)