| Disease spreading modeling and analysis: A survey P Hiram Guzzi, F Petrizzelli, T Mazza Briefings in Bioinformatics 23 (4), bbac230, 2022 | 29 | 2022 |
| MitImpact 3: modeling the residue interaction network of the Respiratory Chain subunits S Castellana, T Biagini, F Petrizzelli, L Parca, N Panzironi, V Caputo, ... Nucleic acids research 49 (D1), D1282-D1288, 2021 | 22 | 2021 |
| Are gaming-enabled graphic processing unit cards convenient for molecular dynamics simulation? T Biagini, F Petrizzelli, M Truglio, R Cespa, A Barbieri, D Capocefalo, ... Evolutionary Bioinformatics 15, 1176934319850144, 2019 | 20 | 2019 |
| Beyond COVID-19 pandemic: Topology-aware optimization of vaccination strategy for minimizing virus spreading F Petrizzelli, PH Guzzi, T Mazza Computational and Structural Biotechnology Journal 20, 2664-2671, 2022 | 13 | 2022 |
| Pyntacle: a parallel computing-enabled framework for large-scale network biology analysis L Parca, M Truglio, T Biagini, S Castellana, F Petrizzelli, D Capocefalo, ... GigaScience 9 (10), giaa115, 2020 | 13 | 2020 |
| Phosphorylation within Intrinsic Disordered Region Discriminates Histone Variant macroH2A1 Splicing Isoforms—macroH2A1. 1 and macroH2A1. 2 S Giallongo, O Lo Re, G Lochmanová, L Parca, F Petrizzelli, Z Zdráhal, ... Biology 10 (7), 659, 2021 | 10 | 2021 |
| GDF5 mutation case report and a systematic review of molecular and clinical spectrum: Expanding current knowledge on genotype-phenotype correlations ML Genovesi, D Guadagnolo, E Marchionni, A Giovannetti, A Traversa, ... Bone 144, 115803, 2021 | 8 | 2021 |
| Mechanisms of pathogenesis of missense mutations on the KDM6A-H3 interaction in type 2 Kabuki Syndrome F Petrizzelli, T Biagini, A Barbieri, L Parca, N Panzironi, S Castellana, ... Computational and Structural Biotechnology Journal 18, 2033-2042, 2020 | 8 | 2020 |
| APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants SD Bianco, L Parca, F Petrizzelli, T Biagini, A Giovannetti, N Liorni, ... Nature Communications 14 (1), 5058, 2023 | 7 | 2023 |
| Clinical variability in DYNC2H1-related skeletal ciliopathies includes Ellis-van Creveld syndrome F Piceci-Sparascio, L Micale, B Torres, V Guida, F Consoli, I Torrente, ... European Journal of Human Genetics 31 (4), 479-484, 2023 | 6 | 2023 |
| Potassium channel KCNH1 activating variants cause altered functional and morphological ciliogenesis G Napoli, N Panzironi, A Traversa, C Catalanotto, V Pace, F Petrizzelli, ... Molecular Neurobiology 59 (8), 4825-4838, 2022 | 6 | 2022 |
| Molecular dynamics analysis of superoxide dismutase 1 mutations suggests decoupling between mechanisms underlying ALS onset and progression M Kalia, M Miotto, D Ness, S Opie-Martin, TP Spargo, L Di Rienzo, ... Computational and Structural Biotechnology Journal 21, 5296-5308, 2023 | 5 | 2023 |
| RhythmicDB: a database of predicted multi-frequency rhythmic transcripts S Castellana, T Biagini, F Petrizzelli, A Cabibbo, G Mazzoccoli, T Mazza Frontiers in Genetics 13, 882044, 2022 | 5 | 2022 |
| Investigating Mitochondrial Gene Expression Patterns in Drosophila melanogaster Using Network Analysis to Understand Aging Mechanisms M Mangoni, F Petrizzelli, N Liorni, SD Bianco, T Biagini, A Napoli, ... Applied Sciences 13 (12), 7342, 2023 | 4 | 2023 |
| A comparative benchmark of classic DNA motif discovery tools on synthetic data S Castellana, T Biagini, L Parca, F Petrizzelli, SD Bianco, AL Vescovi, ... Briefings in Bioinformatics 22 (6), bbab303, 2021 | 4 | 2021 |
| Exploiting in silico structural analysis to introduce emerging genotype–phenotype correlations in DHCR24-related sterol biosynthesis disorder: a case study D Cocciadiferro, T Mazza, D Vecchio, T Biagini, F Petrizzelli, E Agolini, ... Frontiers in Genetics 14, 1307934, 2024 | 3 | 2024 |
| KDM6A missense variants hamper H3 histone demethylation in lung squamous cell carcinoma T Biagini, F Petrizzelli, SD Bianco, N Liorni, A Napoli, S Castellana, ... Computational and Structural Biotechnology Journal 20, 3151-3160, 2022 | 3 | 2022 |
| Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co … A Traversa, E Marchionni, A Giovannetti, ML Genovesi, N Panzironi, ... Molecular Genetics & Genomic Medicine 8 (8), e1336, 2020 | 3 | 2020 |
| Small RNAs and tooth development: The role of microRNAs in tooth agenesis and impaction A Giovannetti, R Guarnieri, F Petrizzelli, S Lazzari, G Padalino, A Traversa, ... Journal of Dental Sciences, 2024 | | 2024 |
| Clinical and molecular description of the first Italian cohort of 33 subjects with hypophosphatasia L Cinque, F Pugliese, AS Salcuni, D Trombetta, C Battista, T Biagini, ... Frontiers in Endocrinology 14, 1205977, 2023 | | 2023 |
Tommaso MazzaIRCCS Casa Sollievo della SofferenzaVerified email at css-mendel.it
