scispace - formally typeset
G

Giorgio Casari

Researcher at Vita-Salute San Raffaele University

Publications -  171
Citations -  21211

Giorgio Casari is an academic researcher from Vita-Salute San Raffaele University. The author has contributed to research in topics: Gene & Genetic linkage. The author has an hindex of 59, co-authored 160 publications receiving 18048 citations. Previous affiliations of Giorgio Casari include Seattle Children's Research Institute & International Centre for Genetic Engineering and Biotechnology.

Papers
More filters
Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy

Daniel J. Klionsky, +1287 more
- 01 Apr 2012 - 
TL;DR: These guidelines are presented for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
Journal ArticleDOI

Autoantibodies against type I IFNs in patients with life-threatening COVID-19.

Paul Bastard, +140 more
- 23 Oct 2020 - 
TL;DR: A means by which individuals at highest risk of life-threatening COVID-19 can be identified is identified, and the hypothesis that neutralizing auto-Abs against type I IFNs may underlie critical CO VID-19 is tested.
Journal ArticleDOI

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.

Sekar Kathiresan, +118 more
- 08 Feb 2009 - 
TL;DR: SNPs at nine loci were reproducibly associated with myocardial infarction, but tests of common and rare CNVs failed to identify additional associations with my Cardiovascular Infarction risk.
Journal ArticleDOI

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.

TL;DR: Results show that mutations in the gene ATP1A2 that encodes the α2 subunit of the Na+/K+ pump are associated with familial hemiplegic migraine type 2 (FHM2) linked to chromosome 1q23 (OMIM 602481).