Giorgio Casari

Milan, Italy

Last Updated: 09/26/2026

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Found 52 publications

Pharmacological restoration of mitochondrial permeability transition pore flickering by high-content drug repurposing.

Pharmacological restoration of mitochondrial permeability transition pore flickering by high-content drug repurposing.

Journal: Pharmacological research

Published: January 29, 2026

The seven enigmas of SARS-CoV-2: from the past to the future.

The seven enigmas of SARS-CoV-2: from the past to the future.

Journal: Journal of human immunity

Published: December 05, 2025

Telethon Undiagnosed Disease Program: Structured approach to solving rare childhood-onset genetic diseases.

Telethon Undiagnosed Disease Program: Structured approach to solving rare childhood-onset genetic diseases.

Journal: Genetics in medicine open

Published: May 05, 2025

A WFS1 variant disrupting acceptor splice site uncovers the impact of alternative splicing on beta cell apoptosis in a patient with Wolfram syndrome.

A WFS1 variant disrupting acceptor splice site uncovers the impact of alternative splicing on beta cell apoptosis in a patient with Wolfram syndrome.

Journal: Diabetologia

Published: March 12, 2024

Severe West Nile Virus and Severe Acute Respiratory Syndrome Coronavirus 2 Infections in a Patient With Thymoma and Anti-Type I Interferon Antibodies.

Severe West Nile Virus and Severe Acute Respiratory Syndrome Coronavirus 2 Infections in a Patient With Thymoma and Anti-Type I Interferon Antibodies.

Journal: The Journal of infectious diseases

Published: January 18, 2024

Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.

Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.

Journal: Genome medicine

Published: January 06, 2024

Whole exome data prioritization unveils the hidden weight of Mendelian causes of male infertility. A report from the first Italian cohort.

Whole exome data prioritization unveils the hidden weight of Mendelian causes of male infertility. A report from the first Italian cohort.

Journal: PloS one

Published: April 26, 2023

Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias.

Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias.

Journal: American journal of human genetics

Published: March 26, 2023

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.

Journal: medRxiv : the preprint server for health sciences

Published: November 03, 2022

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.

Journal: Genome medicine

Published: September 15, 2022

Inflammation on Endomyocardial Biopsy Predicts Risk of MACE in Undefined Left Ventricular Arrhythmogenic Cardiomyopathy.

Inflammation on Endomyocardial Biopsy Predicts Risk of MACE in Undefined Left Ventricular Arrhythmogenic Cardiomyopathy.

Journal: JACC. Clinical electrophysiology

Published: July 28, 2022

The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies.

The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: May 16, 2022

Showing 1-12 of 52

Last Updated: 09/26/2026