| Regulatory Noncoding and Predicted Pathogenic Coding Variants of CCR5 Predispose to Severe COVID-19 S Cantalupo, VA Lasorsa, R Russo, I Andolfo, G D’Alterio, BE Rosato, ... International journal of molecular sciences 22 (10), 5372, 2021 | 27 | 2021 |
| Wee1 rather than Plk1 is inhibited by AZD1775 at therapeutically relevant concentrations AF Serpico, G D’Alterio, C Vetrei, R Della Monica, L Nardella, R Visconti, ... Cancers 11 (6), 819, 2019 | 27 | 2019 |
| Inherited rare variants in homologous recombination and neurodevelopmental genes are associated with increased risk of neuroblastoma F Bonfiglio, VA Lasorsa, S Cantalupo, G D'Alterio, V Aievola, A Boccia, ... EBioMedicine 87, 2023 | 14 | 2023 |
| Germline rare variants of lectin pathway genes predispose to asymptomatic SARS-CoV-2 infection in elderly individuals G D’Alterio, VA Lasorsa, F Bonfiglio, S Cantalupo, BE Rosato, I Andolfo, ... Genetics in Medicine 24 (8), 1653-1663, 2022 | 11 | 2022 |
| A novel variant in RAD21 in Cornelia De Lange syndrome type 4: Case report and Bioinformatic analysis A De Falco, D De Brasi, M Della Monica, C Cesario, S Petrocchi, A Novelli, ... Genes 14 (1), 119, 2023 | 3 | 2023 |
| Improving single nucleotide polymorphisms genotyping accuracy for dihydropyrimidine dehydrogenase testing in pharmacogenetics A Montella, S Cantalupo, G D’Alterio, V Damiano, A Iolascon, M Capasso Exploration of Targeted Anti-tumor Therapy 5 (2), 374, 2024 | 1 | 2024 |
| Comprehensive whole genome sequencing unravels the complex genomic landscape of Neuroblastoma G D'Alterio Università degli Studi di Milano, 2024 | | 2024 |
| Noncoding regulatory mutations as a driving event for the oncogenic core regulatory circuitries of neuroblastoma V Aievola, VA Lasorsa, A Montella, F Bonfiglio, M Avitabile, T Maiorino, ... Proceedings 100 (1), 18, 2024 | | 2024 |
| Noncoding regulatory mutations as driving event for the oncogenic core regulatory circuitries of neuroblastoma M Capasso, V Aievola, VA Lasorsa, A Montella, F Bonfiglio, M Avitabile, ... Cancer Research 84 (6_Supplement), 2850-2850, 2024 | | 2024 |
| Unraveling the Role of PIEZO1 in Stressed Erythropoiesis: Implications for Dyserythropoiesis and Potential Therapeutic Targets in Dehydrated Hereditary Stomatocytosis BE Rosato, V D'Onofrio, A Nostroso, R Marra, FM Esposito, M Raia, ... Blood 142, 2446, 2023 | | 2023 |
| P1470: IDENTIFICATION OF THE PRO20THR NOVEL VARIANT IN CDIN1 GENE ALLOWED EXPLORING THE BIOLOGICAL PROCESSES IMPAIRED IN CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE I R Marra, A Nostroso, FM Esposito, BE Rosato, V D’onofrio, G D’alterio, ... HemaSphere 7 (Suppl), e831813d, 2023 | | 2023 |
| P1468: PIEZO1 GAIN-OF-FUNCTION VARIANTS ACCOUNT FOR STRESSED ERYTHROPOIESIS BY ALTERING APOPTOSIS, HYPOXIA CELL RESPONSE, AND GLYCOLYSIS BE Rosato, V D’onofrio, A Nostroso, R Marra, FM Esposito, M Raia, ... HemaSphere 7 (Suppl), e70724eb, 2023 | | 2023 |
| Security testing semi-automatico di applicazioni basate su container G D’Alterio | | |
