| Nosology and classification of genetic skeletal disorders: 2015 revision L Bonafe, V Cormier‐Daire, C Hall, R Lachman, G Mortier, S Mundlos, ... American journal of medical genetics Part A 167 (12), 2869-2892, 2015 | 677 | 2015 |
| Platelet-derived growth factors enhance proliferation of human stromal stem cells E Lucarelli, A Beccheroni, D Donati, L Sangiorgi, A Cenacchi, ... Biomaterials 24 (18), 3095-3100, 2003 | 620 | 2003 |
| Nosology and classification of genetic skeletal disorders: 2019 revision GR Mortier, DH Cohn, V Cormier‐Daire, C Hall, D Krakow, S Mundlos, ... American journal of medical genetics Part A 179 (12), 2393-2419, 2019 | 595 | 2019 |
| Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome TC Pansuriya, R van Eijk, P d'Adamo, MAJH van Ruler, ML Kuijjer, ... Nature genetics 43 (12), 1256-1261, 2011 | 584 | 2011 |
| Relationship of chemotherapy-induced necrosis and surgical margins to local recurrence in osteosarcoma. P Picci, L Sangiorgi, BT Rougraff, JR Neff, R Casadei, M Campanacci Journal of clinical oncology 12 (12), 2699-2705, 1994 | 383 | 1994 |
| Chemotherapy-induced tumor necrosis as a prognostic factor in localized Ewing's sarcoma of the extremities. P Picci, T Böhling, G Bacci, S Ferrari, L Sangiorgi, M Mercuri, P Ruggieri, ... Journal of clinical oncology 15 (4), 1553-1559, 1997 | 303 | 1997 |
| Canine tumor cross-species genomics uncovers targets linked to osteosarcoma progression M Paoloni, S Davis, S Lana, S Withrow, L Sangiorgi, P Picci, S Hewitt, ... BMC genomics 10, 1-13, 2009 | 301 | 2009 |
| Aging and imaging assessment of body composition: from fat to facts F Ponti, A Santoro, D Mercatelli, C Gasperini, M Conte, M Martucci, ... Frontiers in endocrinology 10, 861, 2020 | 299 | 2020 |
| Prognostic significance of histopathologic response to chemotherapy in nonmetastatic Ewing's sarcoma of the extremities. P Picci, BT Rougraff, G Bacci, JR Neff, L Sangiorgi, A Cazzola, N Baldini, ... Journal of Clinical Oncology 11 (9), 1763-1769, 1993 | 244 | 1993 |
| Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb) I Jennes, E Pedrini, M Zuntini, M Mordenti, S Balkassmi, CG Asteggiano, ... Human mutation 30 (12), 1620-1627, 2009 | 221 | 2009 |
| Stromal stem cells and platelet-rich plasma improve bone allograft integration E Lucarelli, M Fini, A Beccheroni, G Giavaresi, C Di Bella, NN Aldini, ... Clinical Orthopaedics and Related Research® 435, 62-68, 2005 | 192 | 2005 |
| Genotype-phenotype correlation study in 529 patients with multiple hereditary exostoses: identification of “protective” and “risk” factors E Pedrini, I Jennes, M Tremosini, A Milanesi, M Mordenti, A Parra, ... JBJS 93 (24), 2294-2302, 2011 | 158 | 2011 |
| Loss-of-Function Mutations in PTPN11 Cause Metachondromatosis, but Not Ollier Disease or Maffucci Syndrome ME Bowen, ED Boyden, IA Holm, B Campos-Xavier, L Bonafé, ... PLoS genetics 7 (4), e1002050, 2011 | 128 | 2011 |
| Risk factors for local recurrences after limb-salvage surgery for high-grade osteosarcoma of the extremities P Picci, L Sangiorgi, L Bahamonde, P Aluigi, J Bibiloni, M Zavatta, ... Annals of oncology 8 (9), 899-903, 1997 | 114 | 1997 |
| Congenital joint dislocations caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis P Hermanns, S Unger, A Rossi, A Perez-Aytes, H Cortina, L Bonafé, ... The American Journal of Human Genetics 82 (6), 1368-1374, 2008 | 111 | 2008 |
| Enchondromatosis (Ollier disease, Maffucci syndrome) is not caused by the PTHR1 mutation p. R150C LB Rozeman, L Sangiorgi, IHB Bruijn, P Mainil‐Varlet, F Bertoni, ... Human mutation 24 (6), 466-473, 2004 | 107 | 2004 |
| Genotype–phenotype correlation study in 364 osteogenesis imperfecta Italian patients M Maioli, M Gnoli, M Boarini, M Tremosini, A Zambrano, E Pedrini, ... European Journal of Human Genetics 27 (7), 1090-1100, 2019 | 83 | 2019 |
| Changes of the p16 gene but not the p53 gene in human chondrosarcoma tissues J Asp, L Sangiorgi, SE Inerot, A Lindahl, L Molendini, MS Benassi, P Picci International journal of cancer 85 (6), 782-786, 2000 | 83 | 2000 |
| Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype FKR Swinnen, PJ Coucke, AM De Paepe, S Symoens, F Malfait, ... Orphanet journal of rare diseases 6, 1-8, 2011 | 76 | 2011 |
| Cytokeratin expression and distribution in adamantinoma of the long bones and osteofibrous dysplasia of tibia and fibula. An immunohistochemical study correlated to histogenesis MS Benassi, L Campanacci, G Gamberi, C Ferrari, P Picci, L Sangiorgi, ... Histopathology 25 (1), 71-76, 1994 | 72 | 1994 |
