| Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders T Wang, K Hoekzema, D Vecchio, H Wu, A Sulovari, BP Coe, ... Nature communications 11 (1), 4932, 2020 | 142 | 2020 |
| The increasing challenge of multidrug-resistant gram-negative bacilli: results of a 5-year active surveillance program in a neonatal intensive care unit M Giuffrè, DM Geraci, C Bonura, L Saporito, G Graziano, V Insinga, A Aleo, ... Medicine 95 (10), e3016, 2016 | 78 | 2016 |
| Communication about vaccination: A shared responsibility LR Biasio, G Corsello, C Costantino, GM Fara, G Giammanco, ... Human vaccines & immunotherapeutics 12 (11), 2984-2987, 2016 | 68 | 2016 |
| Media use during adolescence: The recommendations of the Italian Pediatric Society E Bozzola, G Spina, M Ruggiero, D Vecchio, C Caruso, M Bozzola, ... Italian journal of pediatrics 45, 1-9, 2019 | 59 | 2019 |
| A case of femoral-facial syndrome in a patient with autism spectrum disorders. D Vecchio, E Salzano, A Vecchio, T Di Filippo, M Roccella Minerva Pediatrica 63 (4), 341-344, 2011 | 36 | 2011 |
| The first case of myoclonic epilepsy in a child with a de novo 22q11. 2 microduplication M Piccione, D Vecchio, S Cavani, M Malacarne, M Pierluigi, G Corsello American Journal of Medical Genetics Part A 155 (12), 3054-3059, 2011 | 32 | 2011 |
| Outbreak of ST395 KPC-producing Klebsiella pneumoniae in a neonatal intensive care unit in Palermo, Italy CM Maida, C Bonura, DM Geraci, G Graziano, A Carattoli, A Rizzo, ... infection control & hospital epidemiology 39 (4), 496-498, 2018 | 27 | 2018 |
| MASTREE+: Time‐series of plant reproductive effort from six continents A Hacket‐Pain, JJ Foest, IS Pearse, JM LaMontagne, WD Koenig, ... Global change biology 28 (9), 3066-3082, 2022 | 25 | 2022 |
| Paternal uniparental disomy chromosome 14‐like syndrome due a maternal de novo 160 kb deletion at the 14q32. 2 region not encompassing the IG‐and the MEG3‐DMRs: Patient report … G Corsello, E Salzano, D Vecchio, V Antona, M Grasso, M Malacarne, ... American Journal of Medical Genetics Part A 167 (12), 3130-3138, 2015 | 24 | 2015 |
| Bi-allelic LoF NRROS variants impairing active TGF-β1 delivery cause a severe infantile-onset neurodegenerative condition with intracranial calcification X Dong, NB Tan, KB Howell, S Barresi, JL Freeman, D Vecchio, ... The American Journal of Human Genetics 106 (4), 559-569, 2020 | 20 | 2020 |
| Esophageal atresia and Beckwith–Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first report G Serra, V Antona, M Schierz, D Vecchio, E Piro, G Corsello Clinical Case Reports 6 (2), 399, 2018 | 19 | 2018 |
| TUBB3 E410K syndrome: Case report and review of the clinical spectrum of TUBB3 mutations ML Dentici, V Maglione, E Agolini, G Catena, R Capolino, V Lanari, ... American Journal of Medical Genetics Part A 182 (8), 1977-1984, 2020 | 17 | 2020 |
| Dysregulated miRNAs in bone cells of patients with Gorham‐Stout disease M Rossi, I Rana, PS Buonuomo, G Battafarano, E Mariani, M D’Agostini, ... The FASEB Journal 35 (3), e21424, 2021 | 14 | 2021 |
| Italian consensus on the therapeutic management of uncomplicated acute hematogenous osteomyelitis in children A Krzysztofiak, E Chiappini, E Venturini, L Gargiullo, M Roversi, ... Italian Journal of Pediatrics 47, 1-12, 2021 | 12 | 2021 |
| Clinical and molecular characterization of patients with adenylosuccinate lyase deficiency G Mastrogiorgio, M Macchiaiolo, PS Buonuomo, E Bellacchio, M Bordi, ... Orphanet Journal of Rare Diseases 16, 1-10, 2021 | 12 | 2021 |
| Facial masks in children: the position statement of the Italian pediatric society A Villani, E Bozzola, A Staiano, R Agostiniani, A Del Vecchio, N Zamperini, ... Italian Journal of Pediatrics 46 (1), 132, 2020 | 12 | 2020 |
| Management of pediatric post-infectious neurological syndromes E Bozzola, G Spina, M Valeriani, L Papetti, F Ursitti, R Agostiniani, ... Italian Journal of Pediatrics 47, 1-12, 2021 | 11 | 2021 |
| Diagnosis and follow-up of complex congenital malformations/mental retardation (MRA/MR) E Piro, V Consiglio, M Agrifoglio, F Sireci, A Ballacchino, P Salvago, ... Acta Médica Mediterránea 29, 321-325, 2013 | 11 | 2013 |
| Microcephaly a clinical-genetic and neurologic approach GC ETTORE PIRO, VINCENZO ANTONA, VALERIA CONSIGLIO, ANTONELLA BALLACCHINO ... Acta Medica Mediterranea, 327-31, 2002 | 8* | 2002 |
| A deep phenotyping experience: up to date in management and diagnosis of Malan syndrome in a single center surveillance report M Macchiaiolo, FM Panfili, D Vecchio, MV Gonfiantini, F Cortellessa, ... Orphanet Journal of Rare Diseases 17 (1), 235, 2022 | 7 | 2022 |
