| Practical guidelines for managing patients with 22q11. 2 deletion syndrome AS Bassett, DM McDonald-McGinn, K Devriendt, MC Digilio, ... The Journal of pediatrics 159 (2), 332-339. e1, 2011 | 682 | 2011 |
| MicroRNA 217 modulates endothelial cell senescence via silent information regulator 1 R Menghini, V Casagrande, M Cardellini, E Martelli, A Terrinoni, F Amati, ... Circulation 120 (15), 1524-1532, 2009 | 566 | 2009 |
| Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot A Pizzuti, A Sarkozy, AL Newton, E Conti, E Flex, M Cristina Digilio, ... Human mutation 22 (5), 372-377, 2003 | 168 | 2003 |
| 22q11 deletions in isolated and syndromic patients with tetralogy of Fallot F Amati, A Mari, MC Digilio, R Mingarelli, B Marino, A Giannotti, G Novelli, ... Human genetics 95, 479-482, 1995 | 144 | 1995 |
| In Vivo and In Vitro Studies Support That a New Splicing Isoform of OLR1 Gene Is Protective Against Acute Myocardial Infarction R Mango, S Biocca, F del Vecchio, F Clementi, F Sangiuolo, F Amati, ... Circulation Research 97 (2), 152-158, 2005 | 138 | 2005 |
| UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome A Pizzuti, G Novelli, A Ratti, F Amati, A Mari, G Calabrese, S Nicolis, ... Human molecular genetics 6 (2), 259-265, 1997 | 115 | 1997 |
| Atypical deletions suggest five 22q11. 2 critical regions related to the DiGeorge/velo-cardio-facial syndrome F Amati, E Conti, A Novelli, M Bengala, MC Digilio, B Marino, A Giannotti, ... European Journal of Human Genetics 7 (8), 903-909, 1999 | 105 | 1999 |
| cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene A Pizzuti, F Amati, G Calabrese, A Mari, A Colosimo, V Silani, L Giardino, ... Human molecular genetics 5 (7), 953-958, 1996 | 101 | 1996 |
| Biased T-cell receptor repertoires in patients with chromosome 22q11. 2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) M Pierdominici, F Mazzetta, E Caprini, M Marziali, MC Digilio, B Marino, ... Clinical & Experimental Immunology 132 (2), 323-331, 2003 | 74 | 2003 |
| Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome A Mari, F Amati, R Mingarelli, A Giannotti, G Sebastio, V Colloridi, ... Human genetics 96, 444-448, 1995 | 73 | 1995 |
| Epigenetic Modification in Coronary Atherosclerosis: JACC Review Topic of the Week B Rizzacasa, F Amati, F Romeo, G Novelli, JL Mehta Journal of the American College of Cardiology 74 (10), 1352-1365, 2019 | 69 | 2019 |
| Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome. A Pizzuti, G Novelli, A Mari, A Ratti, A Colosimo, F Amati, D Penso, ... American journal of human genetics 58 (4), 722, 1996 | 65 | 1996 |
| Epidermal growth factor-like domain 7 promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways M Massimiani, L Vecchione, D Piccirilli, P Spitalieri, F Amati, S Salvi, ... MHR: Basic science of reproductive medicine 21 (5), 435-451, 2015 | 64 | 2015 |
| Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2 A Botta, L Vallo, F Rinaldi, E Bonifazi, F Amati, M Biancolella, ... Gene expression 13 (6), 339, 2007 | 62 | 2007 |
| Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit L Berti, G Mittler, GKH Przemeck, G Stelzer, B Günzler, F Amati, E Conti, ... Genomics 74 (3), 320-332, 2001 | 57 | 2001 |
| Valproic acid induces neuroendocrine differentiation and UGT2B7 up-regulation in human prostate carcinoma cell line A Valentini, M Biancolella, F Amati, P Gravina, R Miano, G Chillemi, ... Drug metabolism and disposition 35 (6), 968-972, 2007 | 53 | 2007 |
| Application of Next Generation Sequencing for personalized medicine for sudden cardiac death E Morini, F Sangiuolo, D Caporossi, G Novelli, F Amati Frontiers in genetics 6, 127339, 2015 | 51 | 2015 |
| Association study of a promoter polymorphism of UFD1L gene with schizophrenia A De Luca, A Pasini, F Amati, A Botta, G Spalletta, S Alimenti, F Caccamo, ... American journal of medical genetics 105 (6), 529-533, 2001 | 49 | 2001 |
| Fractionated ionizing radiation exposure induces apoptosis through caspase-3 activation and reactive oxygen species generation B Bucci, S Misiti, A Cannizzaro, R Marchese, GH Raza, R Miceli, ... Anticancer research 26 (6B), 4549-4557, 2006 | 45 | 2006 |
| MiR-423 is differentially expressed in patients with stable and unstable coronary artery disease: A pilot study B Rizzacasa, E Morini, R Mango, C Vancheri, S Budassi, G Massaro, ... PLoS One 14 (5), e0216363, 2019 | 43 | 2019 |
