| Effects of melatonin treatment in septic newborns E Gitto, M Karbownik, RJ Reiter, DX Tan, S Cuzzocrea, P Chiurazzi, ... Pediatric research 50 (6), 756-760, 2001 | 662 | 2001 |
| A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability F Zalfa, B Eleuteri, KS Dickson, V Mercaldo, S De Rubeis, A di Penta, ... Nature neuroscience 10 (5), 578-587, 2007 | 423 | 2007 |
| Synergistic Effect of Histone Hyperacetylation and DNA Demethylation in the Reactivation of the FMR1 Gene P Chiurazzi, M Grazia Pomponi, R Pietrobono, CE Bakker, G Neri, ... Human molecular genetics 8 (12), 2317-2323, 1999 | 283 | 1999 |
| In Vitro Reactivation of the FMR1 Gene Involved in Fragile X Syndrome P Chiurazzi, MG Pomponi, R Willemsen, BA Oostra, G Neri Human molecular genetics 7 (1), 109-113, 1998 | 238 | 1998 |
| XLMR genes: update 2007 P Chiurazzi, CE Schwartz, J Gecz, G Neri European Journal of Human Genetics 16 (4), 422-434, 2008 | 229 | 2008 |
| Oxidative and inflammatory parameters in respiratory distress syndrome of preterm newborns: beneficial effects of melatonin E Gitto, RJ Reiter, SP Cordaro, M La Rosa, P Chiurazzi, G Trimarchi, ... American journal of perinatology 21 (04), 209-216, 2004 | 209 | 2004 |
| Advances in understanding–genetic basis of intellectual disability P Chiurazzi, F Pirozzi F1000Research 5, 2016 | 189 | 2016 |
| Mutations in KANSL1 cause the 17q21. 31 microdeletion syndrome phenotype M Zollino, D Orteschi, M Murdolo, S Lattante, D Battaglia, C Stefanini, ... Nature genetics 44 (6), 636-638, 2012 | 188 | 2012 |
| Natural small molecules as inhibitors of coronavirus lipid-dependent attachment to host cells: a possible strategy for reducing SARS-COV-2 infectivity? M Baglivo, M Baronio, G Natalini, T Beccari, P Chiurazzi, E Fulcheri, ... Acta Bio Medica: Atenei Parmensis 91 (1), 161, 2020 | 169 | 2020 |
| SMT3A, a human homologue of theS. cerevisiae SMT3gene, maps to chromosome 21qter and defines a novel gene family V Lapenta, P Chiurazzi, P van der Spek, A Pizzuti, F Hanaoka, C Brahe Genomics 40 (2), 362-366, 1997 | 161 | 1997 |
| Molecular dissection of the events leading to inactivation of the FMR1 gene R Pietrobono, E Tabolacci, F Zalfa, I Zito, A Terracciano, U Moscato, ... Human molecular genetics 14 (2), 267-277, 2005 | 148 | 2005 |
| Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström syndromes C Redin, S Le Gras, O Mhamdi, V Geoffroy, C Stoetzel, MC Vincent, ... Journal of medical genetics 49 (8), 502-512, 2012 | 135 | 2012 |
| A double‐blind, parallel, multicenter comparison of L‐acetylcarnitine with placebo on the attention deficit hyperactivity disorder in fragile X syndrome boys MG Torrioli, S Vernacotola, L Peruzzi, E Tabolacci, M Mila, R Militerni, ... American Journal of Medical Genetics Part A 146 (7), 803-812, 2008 | 129 | 2008 |
| Fragile X syndrome A Terracciano, P Chiurazzi, G Neri American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2005 | 126 | 2005 |
| Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5‐azadeoxycytidine R Pietrobono, MG Pomponi, E Tabolacci, B Oostra, P Chiurazzi, G Neri Nucleic acids research 30 (14), 3278-3285, 2002 | 123 | 2002 |
| XLMR genes: update 2000 P Chiurazzi, BCJ Hamel, G Neri European Journal of Human Genetics 9 (2), 71-81, 2001 | 118 | 2001 |
| Molecular analysis, pathogenic mechanisms, and readthrough therapy on a large cohort of K abuki syndrome patients L Micale, B Augello, C Maffeo, A Selicorni, F Zucchetti, C Fusco, ... Human mutation 35 (7), 841-850, 2014 | 111 | 2014 |
| Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments E Tabolacci, R Pietrobono, U Moscato, BA Oostra, P Chiurazzi, G Neri European journal of human genetics 13 (5), 641-648, 2005 | 107 | 2005 |
| XLMRgenes: Update 1996 HA Lubs, P Chiurazzi, JF Arena, C Schwartz, L Tranebjaerg, G Neri American journal of medical genetics 64 (1), 147-157, 1996 | 106 | 1996 |
| Epigenetic analysis reveals a euchromatic configuration in the FMR1 unmethylated full mutations E Tabolacci, U Moscato, F Zalfa, C Bagni, P Chiurazzi, G Neri European journal of human genetics 16 (12), 1487-1498, 2008 | 105 | 2008 |
