| Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy K Pilichou, A Nava, C Basso, G Beffagna, B Bauce, A Lorenzon, G Frigo, ... Circulation 113 (9), 1171-1179, 2006 | 731 | 2006 |
| Analysis of the human VPS13 gene family A Velayos-Baeza, A Vettori, RR Copley, C Dobson-Stone, AP Monaco Genomics 84 (3), 536-549, 2004 | 257 | 2004 |
| A locus for migraine without aura maps on chromosome 14q21. 2-q22. 3 D Soragna, A Vettori, G Carraro, E Marchioni, G Vazza, S Bellini, R Tupler, ... The American Journal of Human Genetics 72 (1), 161-167, 2003 | 126 | 2003 |
| Optical mapping of neuronal activity during seizures in zebrafish L Turrini, C Fornetto, G Marchetto, MC Müllenbroich, N Tiso, A Vettori, ... Scientific reports 7 (1), 3025, 2017 | 106 | 2017 |
| Loss-of-function mutations in the SIGMAR1 gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca2+ signalling E Gregianin, G Pallafacchina, S Zanin, V Crippa, P Rusmini, A Poletti, ... Human molecular genetics 25 (17), 3741-3753, 2016 | 104 | 2016 |
| Generation and application of signaling pathway reporter lines in zebrafish E Moro, A Vettori, P Porazzi, M Schiavone, E Rampazzo, A Casari, O Ek, ... Molecular Genetics and Genomics 288, 231-242, 2013 | 86 | 2013 |
| Different atrophy-hypertrophy transcription pathways in muscles affected by severe and mild spinal muscular atrophy C Millino, M Fanin, A Vettori, P Laveder, ML Mostacciuolo, C Angelini, ... BMC medicine 7, 1-9, 2009 | 85 | 2009 |
| Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26 G Vazza, C Bertolin, E Scudellaro, A Vettori, F Boaretto, S Rampinelli, ... Molecular psychiatry 12 (1), 87-93, 2007 | 74 | 2007 |
| A Smad3 transgenic reporter reveals TGF-beta control of zebrafish spinal cord development A Casari, M Schiavone, N Facchinello, A Vettori, D Meyer, N Tiso, E Moro, ... Developmental biology 396 (1), 81-93, 2014 | 61 | 2014 |
| Glucocorticoids promote von hippel lindau degradation and hif-1α stabilization A Vettori, D Greenald, GK Wilson, M Peron, N Facchinello, E Markham, ... Proceedings of the National Academy of Sciences 114 (37), 9948-9953, 2017 | 60 | 2017 |
| Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23. 3-q24. 1 M Zortea, A Vettori, CP Trevisan, S Bellini, G Vazza, M Armani, A Simonati, ... Journal of medical genetics 39 (6), 387-390, 2002 | 57 | 2002 |
| Loss of cardiac Wnt/β-catenin signalling in desmoplakin-deficient AC8 zebrafish models is rescuable by genetic and pharmacological intervention A Giuliodori, G Beffagna, G Marchetto, C Fornetto, F Vanzi, S Toppo, ... Cardiovascular research 114 (8), 1082-1097, 2018 | 55 | 2018 |
| Zebrafish mutants and TEAD reporters reveal essential functions for Yap and Taz in posterior cardinal vein development M Astone, JKH Lai, S Dupont, DYR Stainier, F Argenton, A Vettori Scientific reports 8 (1), 10189, 2018 | 53 | 2018 |
| Mutant MYO1F alters the mitochondrial network and induces tumor proliferation in thyroid cancer C Diquigiovanni, C Bergamini, C Evangelisti, F Isidori, A Vettori, N Tiso, ... International journal of cancer 143 (7), 1706-1719, 2018 | 48 | 2018 |
| Developmental defects and neuromuscular alterations due to mitofusin 2 gene (MFN2) silencing in zebrafish: a new model for Charcot-Marie-Tooth type 2A neuropathy A Vettori, G Bergamin, E Moro, G Vazza, G Polo, N Tiso, F Argenton, ... Neuromuscular disorders 21 (1), 58-67, 2011 | 48 | 2011 |
| Genetic background, nutrition and obesity: a review. A Vettori, G Pompucci, B Paolini, I Del Ciondolo, S Bressan, M Dundar, ... European Review for Medical & Pharmacological Sciences 23 (4), 2019 | 47 | 2019 |
| X‐inactivation pattern in multiple tissues from two leber's hereditary optic neuropathy (LHON) patients E Pegoraro, A Vettori, ML Valentino, A Molon, ML Mostacciuolo, N Howell, ... American Journal of Medical Genetics Part A 119 (1), 37-40, 2003 | 39 | 2003 |
| Mutation Analysis of MFN2, GJB1, MPZ and PMP22 in Italian Patients with Axonal Charcot–Marie–Tooth Disease G Bergamin, F Boaretto, C Briani, E Pegoraro, M Cacciavillani, ... Neuromolecular medicine 16, 540-550, 2014 | 35 | 2014 |
| A novel SACS mutation results in non‐ataxic spastic paraplegia and peripheral neuropathy E Gregianin, G Vazza, E Scaramel, F Boaretto, A Vettori, E Leonardi, ... European Journal of Neurology 20 (11), 1486-1491, 2013 | 34 | 2013 |
| SEVERE CMT TYPE 2 WITH FATAL ENCEPHALOPATHY ASSOCIATED WITH A NOVEL MFN2 SPLICING MUTATION F Boaretto, A Vettori, A Casarin, G Vazza, M Muglia, MG Rossetto, ... Neurology 74 (23), 1919-1921, 2010 | 34 | 2010 |
