| MicroRNA expression profile helps to distinguish benign nodules from papillary thyroid carcinomas starting from cells of fine-needle aspiration P Agretti, E Ferrarini, T Rago, A Candelieri, G De Marco, A Dimida, ... European journal of endocrinology 167 (3), 393-400, 2012 | 87 | 2012 |
| Identification and functional analysis of novel dual oxidase 2 (DUOX2) mutations in children with congenital or subclinical hypothyroidism G De Marco, P Agretti, L Montanelli, C Di Cosmo, B Bagattini, M De Servi, ... The Journal of Clinical Endocrinology & Metabolism 96 (8), E1335-E1339, 2011 | 75 | 2011 |
| Similar frequency of paternal uniparental disomy involving chromosome 20q (patUPD20q) in Japanese and Caucasian patients affected by sporadic pseudohypoparathyroidism type Ib … R Takatani, M Minagawa, A Molinaro, M Reyes, K Kinoshita, T Takatani, ... Bone 79, 15-20, 2015 | 52 | 2015 |
| A mouse model for creatine transporter deficiency reveals early onset cognitive impairment and neuropathology associated with brain aging L Baroncelli, A Molinaro, F Cacciante, MG Alessandrì, D Napoli, ... Human molecular genetics 25 (19), 4186-4200, 2016 | 47 | 2016 |
| iPSC-derived neurons profiling reveals GABAergic circuit disruption and acetylated α-tubulin defect which improves after iHDAC6 treatment in Rett syndrome E Landucci, M Brindisi, L Bianciardi, LM Catania, S Daga, S Croci, ... Experimental cell research 368 (2), 225-235, 2018 | 46 | 2018 |
| TSH elevations as the first laboratory evidence for pseudohypoparathyroidism type Ib (PHP‐Ib) A Molinaro, D Tiosano, R Takatani, D Chrysis, W Russell, N Koscielniak, ... Journal of Bone and Mineral Research 30 (5), 906-912, 2015 | 43 | 2015 |
| Analysis of multiple families with single individuals affected by pseudohypoparathyroidism type Ib (PHP1B) reveals only one novel maternally inherited GNAS deletion R Takatani, A Molinaro, G Grigelioniene, O Tafaj, T Watanabe, M Reyes, ... Journal of Bone and Mineral Research 31 (4), 796-805, 2016 | 34 | 2016 |
| Presence in the pre-surgical fine-needle aspiration of potential thyroid biomarkers previously identified in the post-surgical one F Ciregia, L Giusti, A Molinaro, F Niccolai, P Agretti, T Rago, G Di Coscio, ... PLoS One 8 (9), e72911, 2013 | 28 | 2013 |
| Proteomic analysis of fine-needle aspiration in differential diagnosis of thyroid nodules F Ciregia, L Giusti, A Molinaro, F Niccolai, MR Mazzoni, T Rago, ... Translational Research 176, 81-94, 2016 | 27 | 2016 |
| BRAF mutation analysis in thyroid nodules with indeterminate cytology: our experience on surgical management of patients with thyroid nodules from an area of borderline iodine … P Agretti, F Niccolai, T Rago, G De Marco, A Molinaro, M Scutari, ... Journal of endocrinological investigation 37, 1009-1014, 2014 | 25 | 2014 |
| A Large Inversion Involving GNAS Exon A/B and All Exons Encoding Gsα Is Associated With Autosomal Dominant Pseudohypoparathyroidism Type Ib (PHP1B) G Grigelioniene, PI Nevalainen, M Reyes, S Thiele, O Tafaj, A Molinaro, ... Journal of Bone and Mineral Research 32 (4), 776-783, 2017 | 24 | 2017 |
| Genetic markers to discriminate benign and malignant thyroid nodules with undetermined cytology in an area of borderline iodine deficiency M Tonacchera, P Agretti, T Rago, G De Marco, F Niccolai, A Molinaro, ... Journal of endocrinological investigation 35 (8), 754-759, 2012 | 10 | 2012 |
