| Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene E Di Pasquale, P Beck-Peccoz, L Persani The American Journal of Human Genetics 75 (1), 106-111, 2004 | 633 | 2004 |
| A novel mutation in the bone morphogenetic protein 15 gene causing defective protein secretion is associated with both increased ovulation rate and sterility in Lacaune sheep L Bodin, E Di Pasquale, S Fabre, M Bontoux, P Monget, L Persani, ... Endocrinology 148 (1), 393-400, 2007 | 312 | 2007 |
| Identification of New Variants of Human BMP15 Gene in a Large Cohort of Women with Premature Ovarian Failure E Di Pasquale, R Rossetti, A Marozzi, B Bodega, S Borgato, L Cavallo, ... The Journal of Clinical Endocrinology & Metabolism 91 (5), 1976-1979, 2006 | 280 | 2006 |
| Identification of New Variants of Human BMP15 Gene in a Large Cohort of Women with Premature Ovarian Failure E Di Pasquale, R Rossetti, A Marozzi, B Bodega, S Borgato, L Cavallo, ... The Journal of Clinical Endocrinology & Metabolism 91 (5), 1976-1979, 2006 | 280 | 2006 |
| Regulation of ovulation rate in mammals: contribution of sheep genetic models S Fabre, A Pierre, P Mulsant, L Bodin, E Di Pasquale, L Persani, ... Reproductive Biology and Endocrinology 4, 1-12, 2006 | 265 | 2006 |
| The fundamental role of bone morphogenetic protein 15 in ovarian function and its involvement in female fertility disorders L Persani, R Rossetti, E Di Pasquale, C Cacciatore, S Fabre Human reproduction update 20 (6), 869-883, 2014 | 262 | 2014 |
| BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein R Rossetti, E Di Pasquale, A Marozzi, S Bione, D Toniolo, P Grammatico, ... Human mutation 30 (5), 804-810, 2009 | 170 | 2009 |
| American heart association council on E, prevention statistics c, stroke statistics s. heart disease and stroke statistics-2019 update: a report from the American heart association EJ Benjamin, P Muntner, A Alonso, MS Bittencourt, CW Callaway, ... Circulation 139 (10), e56-e528, 2019 | 165 | 2019 |
| T cell costimulation blockade blunts pressure overload-induced heart failure M Kallikourdis, E Martini, P Carullo, C Sardi, G Roselli, CM Greco, ... Nature communications 8 (1), 14680, 2017 | 156 | 2017 |
| CaMKII inhibition rectifies arrhythmic phenotype in a patient-specific model of catecholaminergic polymorphic ventricular tachycardia E Di Pasquale, F Lodola, M Miragoli, M Denegri, JE Avelino-Cruz, ... Cell death & disease 4 (10), e843-e843, 2013 | 135 | 2013 |
| Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy R Roncarati, C Viviani Anselmi, P Krawitz, G Lattanzi, Y Von Kodolitsch, ... European Journal of Human Genetics 21 (10), 1105-1111, 2013 | 107 | 2013 |
| The K219T-Lamin mutation induces conduction defects through epigenetic inhibition of SCN5A in human cardiac laminopathy N Salvarani, S Crasto, M Miragoli, A Bertero, M Paulis, P Kunderfranco, ... Nature communications 10 (1), 2267, 2019 | 92 | 2019 |
| Induced pluripotent stem cell–derived cardiomyocytes in studies of inherited arrhythmias SG Priori, C Napolitano, E Di Pasquale, G Condorelli The Journal of clinical investigation 123 (1), 84-91, 2013 | 80 | 2013 |
| The broad spectrum of LMNA cardiac diseases: from molecular mechanisms to clinical phenotype S Crasto, I My, E Di Pasquale Frontiers in Physiology 11, 538082, 2020 | 73 | 2020 |
| Post-natal cardiomyocytes can generate iPS cells with an enhanced capacity toward cardiomyogenic re-differentation R Rizzi, E Di Pasquale, P Portararo, R Papait, P Cattaneo, MVG Latronico, ... Cell Death & Differentiation 19 (7), 1162-1174, 2012 | 71 | 2012 |
| DOT1L-mediated H3K79me2 modification critically regulates gene expression during cardiomyocyte differentiation P Cattaneo, P Kunderfranco, C Greco, A Guffanti, GG Stirparo, F Rusconi, ... Cell Death & Differentiation 23 (4), 555-564, 2016 | 70 | 2016 |
| Adeno-associated virus-mediated CASQ2 delivery rescues phenotypic alterations in a patient-specific model of recessive catecholaminergic polymorphic ventricular tachycardia F Lodola, D Morone, M Denegri, R Bongianino, H Nakahama, ... Cell death & disease 7 (10), e2393-e2393, 2016 | 64 | 2016 |
| Human iPSC modelling of a familial form of atrial fibrillation reveals a gain of function of If and ICaL in patient-derived cardiomyocytes P Benzoni, G Campostrini, S Landi, V Bertini, E Marchina, M Iascone, ... Cardiovascular Research 116 (6), 1147-1160, 2020 | 58 | 2020 |
| Cofilin-1 phosphorylation catalyzed by ERK1/2 alters cardiac actin dynamics in dilated cardiomyopathy caused by lamin A/C gene mutation M Chatzifrangkeskou, D Yadin, T Marais, S Chardonnet, ... Human Molecular Genetics 27 (17), 3060-3078, 2018 | 54 | 2018 |
| Growth hormone-releasing hormone attenuates cardiac hypertrophy and improves heart function in pressure overload-induced heart failure I Gesmundo, M Miragoli, P Carullo, L Trovato, V Larcher, E Di Pasquale, ... Proceedings of the National Academy of Sciences 114 (45), 12033-12038, 2017 | 53 | 2017 |
