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| Deletions of 17p and p53 Mutations in Preneoplastic Lesions of the Lung G Sozzi, M Miozzo, R Donghi, S Pilotti, CT Cariani, U Pastorino, ... Cancer research 52 (21), 6079-6082, 1992 | 358 | 1992 |
| Frequency of monosomy X in women with primary biliary cirrhosis P Invernizzi, M Miozzo, PM Battezzati, I Bianchi, FR Grati, G Simoni, ... The Lancet 363 (9408), 533-535, 2004 | 284 | 2004 |
| Characterization of an inversion on the long arm of chromosome 10 juxtaposing D10S170 and RET and creating the oncogenic sequence RET/PTC. MA Pierotti, M Santoro, RB Jenkins, G Sozzi, I Bongarzone, M Grieco, ... Proceedings of the National Academy of Sciences 89 (5), 1616-1620, 1992 | 271 | 1992 |
| X chromosome monosomy: a common mechanism for autoimmune diseases P Invernizzi, M Miozzo, C Selmi, L Persani, PM Battezzati, M Zuin, ... The journal of immunology 175 (1), 575-578, 2005 | 214 | 2005 |
| Genetic evidence for an independent origin of multiple preneoplastic and neoplastic lung lesions G Sozzi, M Miozzo, U Pastorino, S Pilotti, R Donghi, M Giarola, ... Cancer research 55 (1), 135-140, 1995 | 188 | 1995 |
| Genetics of mayer–rokitansky–küster–hauser (MRKH) syndrome L Fontana, B Gentilin, L Fedele, C Gervasini, M Miozzo Clinical genetics 91 (2), 233-246, 2017 | 167 | 2017 |
| Microsatellite alterations in bronchial and sputum specimens of lung cancer patients M Miozzo, G Sozzi, K Musso, S Pilotti, M Incarbone, U Pastorino, ... Cancer research 56 (10), 2285-2288, 1996 | 165 | 1996 |
| Fragile X syndrome: a review of clinical and molecular diagnoses C Ciaccio, L Fontana, D Milani, S Tabano, M Miozzo, S Esposito Italian journal of pediatrics 43, 1-12, 2017 | 163 | 2017 |
| Cytogenetic abnormalities and overexpression of receptors for growth factors in normal bronchial epithelium and tumor samples of lung cancer patients G Sozzi, M Miozzo, E Tagliabue, C Calderone, L Lombardi, S Pilotti, ... Cancer research 51 (1), 400-404, 1991 | 157 | 1991 |
| Epigenetic modulation of the IGF2/H19 imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction S Tabano, P Colapietro, I Cetin, FR Grati, S Zanutto, C Mandò, ... Epigenetics 5 (4), 313-324, 2010 | 153 | 2010 |
| Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports L Bernardini, S Gimelli, C Gervasini, M Carella, A Baban, G Frontino, ... Orphanet journal of rare diseases 4, 1-6, 2009 | 149 | 2009 |
| Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis M Miozzo, C Selmi, B Gentilin, FR Grati, S Sirchia, S Oertelt, M Zuin, ... Hepatology 46 (2), 456-462, 2007 | 145 | 2007 |
| Fetal growth restriction: a workshop report I Cetin, JM Foidart, M Miozzo, T Raun, T Jansson, V Tsatsaris, W Reik, ... Placenta 25 (8-9), 753-757, 2004 | 135 | 2004 |
| HER-2/Neu alterations in non-small cell lung cancer: a comprehensive evaluation by real time reverse transcription-PCR, fluorescence in situ hybridization, and immunohistochemistry C Pellegrini, M Falleni, A Marchetti, B Cassani, M Miozzo, F Buttitta, ... Clinical cancer research 9 (10), 3645-3652, 2003 | 133 | 2003 |
| The role of imprinted genes in fetal growth M Miozzo, G Simoni Neonatology 81 (4), 217-228, 2002 | 120 | 2002 |
| Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells SM Sirchia, L Ramoscelli, FR Grati, F Barbera, D Coradini, F Rossella, ... Cancer research 65 (6), 2139-2146, 2005 | 116 | 2005 |
| Y chromosome loss in male patients with primary biliary cirrhosis A Lleo, S Oertelt-Prigione, I Bianchi, L Caliari, P Finelli, M Miozzo, ... Journal of autoimmunity 41, 87-91, 2013 | 113 | 2013 |
| SARS-CoV-2 specific serological pattern in healthcare workers of an Italian COVID-19 forefront hospital G Sotgiu, A Barassi, M Miozzo, L Saderi, A Piana, N Orfeo, C Colosio, ... BMC Pulmonary Medicine 20 (1), 1-6, 2020 | 110 | 2020 |
