Giorgio Casari
Università Vita-Salute San Raffaele
H-index: 71
Europe-Italy
Top articles of Giorgio Casari
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 | Genome Medicine | Daniela Matuozzo Estelle Talouarn Astrid Marchal Peng Zhang Jeremy Manry | 2024/1/6 |
Restrained memory CD8+ T cell responses favors viral persistence and elevated IgG responses in patients with severe Long COVID. | medRxiv | Lucie Rodriguez Ziyang Tan Lakshmi Kanth Tadepally Jun Wang Hugo Barcenilla | 2024 |
115 The mannose-binding lectin (MBL) in MIS-C: relationship between MBL genotype, levels, and functional activity against SARS-CoV-2 | Immunobiology | Matteo Stravalaci Isabel Pagani Hang Zhong Marina Sironi Simone Bondesan | 2023/9/1 |
Whole exome data prioritization unveils the hidden weight of Mendelian causes of male infertility. A report from the first Italian cohort | Plos one | Gioia Quarantani Anna Sorgente Massimo Alfano Giovanni Battista Pipitone Luca Boeri | 2023/8/4 |
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias | The American Journal of Human Genetics | Paulina Cunha Emilien Petit Marie Coutelier Giulia Coarelli Caterina Mariotti | 2023/7/6 |
Inflammation on endomyocardial biopsy predicts risk of MACE in undefined left ventricular Arrhythmogenic cardiomyopathy | Clinical Electrophysiology | Giovanni Peretto Michela Casella Marco Merlo Sara Benedetti Stefania Rizzo | 2023/7/1 |
Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 | Genome medicine | Daniela Matuozzo Estelle Talouarn Astrid Marchal Peng Zhang Jeremy Manry | 2023/4/5 |
A WFS1 variant disrupting acceptor splice site uncovers the impact of alternative splicing on ER-stress independent β cell apoptosis in a patient with Wolfram syndrome. | bioRxiv | Raniero Chimienti Silvia Torchio Valentina Zamarian Gabriel Siracusano Laura Monaco | 2023 |
The risk of Von Hippel Lindau disease according to individual sporadic cancer in a multidisciplinary program: external validation of the VHL alliance guidelines for genetic … | European Urology Open Science | A Larcher G Fallara I Rowe F Belladelli O Iliopoulos | 2022/10/1 |
Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes | Brain | Marcello Scala Masashi Nishikawa Hidenori Ito Hidenori Tabata Tayyaba Khan | 2022/9/1 |
The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies | Proceedings of the National Academy of Sciences | Jérémy Manry Paul Bastard Adrian Gervais Tom Le Voyer Jérémie Rosain | 2022/5/24 |
Prognostic role of myocardial inflammation in patients with undefined left ventricular arrhythmogenic cardiomyopathy | Europace | G Peretto M Casella M Merlo S Benedetti C Cappelletto | 2022/5/18 |
Studying severe long COVID to understand post-infectious disorders beyond COVID-19 | Nature medicine | Petter Brodin Giorgio Casari Liam Townsend Cliona O’Farrelly Ivan Tancevski | 2022/5 |
Solve-RD: the ITHACA perspective | European Journal of Human Genetics | AS Denommé-Pichon E de Boer E Benetti S Banka G Casari | 2022/4 |
Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant | European Journal of Medical Genetics | Elke de Boer Burcu Yaldiz Anne-Sophie Denommé-Pichon Leslie Matalonga Steve Laurie | 2022/1/1 |
VarGenius-HZD allows accurate detection of rare homozygous or hemizygous deletions in targeted sequencing leveraging breadth of coverage | Genes | Francesco Musacchia Marianthi Karali Annalaura Torella Steve Laurie Valeria Policastro | 2021/12/13 |
Brugada syndrome genetics is associated with phenotype severity | European heart journal | Giuseppe Ciconte Michelle M Monasky Vincenzo Santinelli Emanuele Micaglio Gabriele Vicedomini | 2021/3/14 |
From your nose to your toes: a review of severe acute respiratory syndrome coronavirus 2 pandemic‒associated pernio | Lisa M Arkin John J Moon Jennifer M Tran Samira Asgari Cliona O’Farrelly | 2021/12/1 | |
5P Anti-GD2 chimeric antigen receptor & TRAIL modified mesenchymal progenitors as novel strategy against Ewing’s sarcoma | Annals of Oncology | G Golinelli G Grisendi M Dall'Ora G Casari M Prapa | 2021/3/1 |
Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment | Genetics in Medicine | Thomas Roux Mathieu Barbier Mélanie Papin Claire-Sophie Davoine Sabrina Sayah | 2021/10 |
