| Clinical exome sequencing is a powerful tool in the diagnostic flow of monogenic kidney diseases: an Italian experience T Vaisitti, M Sorbini, M Callegari, S Kalantari, V Bracciamà, F Arruga, ... Journal of Nephrology 34, 1767-1781, 2021 | 16 | 2021 |
| HLA-DRB1 mismatch-based identification of donor-derived cell free DNA (dd-cfDNA) as a marker of rejection in heart transplant recipients: A single-institution pilot study M Sorbini, GM Togliatto, E Simonato, M Boffini, M Cappuccio, A Gambella, ... The Journal of Heart and Lung Transplantation 40 (8), 794-804, 2021 | 15 | 2021 |
| Validation of a simple, rapid, and cost-effective method for acute rejection monitoring in lung transplant recipients M Sorbini, G Togliatto, F Mioli, E Simonato, M Marro, M Cappuccio, ... Transplant International 35, 10546, 2022 | 9 | 2022 |
| A novel COLEC10 mutation in a child with 3MC syndrome M Migliorero, S Kalantari, V Bracciamà, M Sorbini, F Arruga, L Peruzzi, ... European Journal of Medical Genetics 64 (12), 104374, 2021 | 4 | 2021 |
| Technical Advances in Circulating Cell-Free DNA Detection and Analysis for Personalized Medicine in Patients’ Care M Sorbini, T Carradori, GM Togliatto, T Vaisitti, S Deaglio Biomolecules 14 (4), 498, 2024 | | 2024 |
| Molecular signature of multiple hepatocellular adenomas from a patient harboring a germline variant in HNF1A: the role of somatic mutations AC Faini, F Arruga, M Pinon, V Bracciama, F Mioli, M Sorbini, A Gambella, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 391-392, 2024 | | 2024 |
| Design and validation of a new primers and probes panel for droplet digital PCR to quantify and monitor donor-derived cell-free DNA after solid organ transplantation targeting … M Sorbini, GM Togliatto, M Cappuccio, F Arruga, C Caorsi, M Mansouri, ... HLA 99 (5), 456-457, 2022 | | 2022 |
| COLEC10 and 3MC syndrome: expanding the genotypic and phenotypic spectrum of a very rare disease M Migliorero, S Kalantari, V Bracciama, M Sorbini, F Arruga, L Peruzzi, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 326-326, 2022 | | 2022 |
| MO059 COLEC10 AND 3MC SYNDROME: EXPANDING THE GENOTYPIC AND PHENOTYPIC SPECTRUM OF A VERY RARE DISEASE M Migliorero, S Kalantari, V Bracciamà, M Sorbini, F Arruga, L Peruzzi, ... Nephrology Dialysis Transplantation 36 (Supplement_1), gfab080. 0031, 2021 | | 2021 |
| P0051 NOVEL AND KNOWN MUTATIONS IDENTIFIED BY CLINICAL EXOME SEQUENCING FOR THE DIAGNOSIS OF POLYCYSTIC KIDNEY DISEASE T Vaisitti, M Sorbini, M Callegari, S Kalantari, V Bracciamà, F Arruga, ... Nephrology Dialysis Transplantation 35 (Supplement_3), gfaa142. P0051, 2020 | | 2020 |
| P0056 USE OF CLINICAL EXOME SEQUENCING IN THE DIAGNOSTIC FLOW OF MONOGENIC KIDNEY DISEASES: THE PIEDMONT EXPERIENCE T Vaisitti, M Sorbini, M Callegari, S Kalantari, V Bracciamà, F Arruga, ... Nephrology Dialysis Transplantation 35 (Supplement_3), gfaa142. P0056, 2020 | | 2020 |
| NOVEL AND KNOWN MUTATIONS IDENTIFIED BY CLINICAL EXOME SEQUENCING FOR THE DIAGNOSIS OF POLYCYSTIC KIDNEY DISEASE T Vaisitti, M Sorbini, M Callegari, S Kalantari, V Bracciama, F Arruga, ... NEPHROLOGY DIALYSIS TRANSPLANTATION 35, 347-347, 2020 | | 2020 |
| USE OF CLINICAL EXOME SEQUENCING IN THE DIAGNOSTIC FLOW OF MONOGENIC KIDNEY DISEASES: THE PIEDMONT EXPERIENCE T Vaisitti, M Sorbini, M Callegari, S Kalantari, V Bracciama, F Arruga, ... NEPHROLOGY DIALYSIS TRANSPLANTATION 35, 352-352, 2020 | | 2020 |
| Routine Monitoring of Donor-Derived Cell-Free DNA to Avoid Surveillance Endomyocardial Biopsies in Pediatric Heart Transplant Recipients M Sorbini, E Aidala, T Carradori, GM Togliatto, C Caorsi, M Mansouri, ... Available at SSRN 4567108, 0 | | |
