| Regulatory mutations in transforming growth factor-β3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1 G Beffagna, G Occhi, A Nava, L Vitiello, A Ditadi, C Basso, B Bauce, ... Cardiovascular research 65 (2), 366-373, 2005 | 543 | 2005 |
| Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don't forget MEN1 genetic analysis T Cuny, M Pertuit, M Sahnoun-Fathallah, A Daly, G Occhi, MF Odou, ... European Journal of Endocrinology 168 (4), 533-541, 2013 | 173 | 2013 |
| A Novel Mutation in the Upstream Open Reading Frame of the CDKN1B Gene Causes a MEN4 Phenotype G Occhi, D Regazzo, G Trivellin, F Boaretto, D Ciato, S Bobisse, S Ferasin, ... PLoS genetics 9 (3), e1003350, 2013 | 163 | 2013 |
| Missense mutations in desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro G Beffagna, M De Bortoli, A Nava, M Salamon, A Lorenzon, M Zaccolo, ... BMC Medical Genetics 8, 1-10, 2007 | 95 | 2007 |
| An analysis of different therapeutic options in patients with C ushing's syndrome due to bilateral macronodular adrenal hyperplasia: a single‐centre experience NM Albiger, F Ceccato, M Zilio, M Barbot, G Occhi, S Rizzati, A Fassina, ... Clinical endocrinology 82 (6), 808-815, 2015 | 88 | 2015 |
| Performance of salivary cortisol in the diagnosis of Cushing's syndrome, adrenal incidentaloma, and adrenal insufficiency F Ceccato, M Barbot, M Zilio, S Ferasin, G Occhi, A Daniele, S Mazzocut, ... European Journal of Endocrinology 169 (1), 31-36, 2013 | 88 | 2013 |
| Arrhythmogenic right ventricular cardiomyopathy type 1 (ARVD1): confirmation of locus assignment and mutation screening of four candidate genes A Rampazzo, G Beffagna, A Nava, G Occhi, B Bauce, M Noiato, C Basso, ... European Journal of Human Genetics 11 (1), 69-76, 2003 | 78 | 2003 |
| Somatostatin analogues increase AIP expression in somatotropinomas, irrespective of Gsp mutations ML Jaffrain-Rea, S Rotondi, A Turchi, G Occhi, A Barlier, E Peverelli, ... Endocrine-Related Cancer 20 (5), 753-766, 2013 | 64 | 2013 |
| Temozolomide and pasireotide treatment for aggressive pituitary adenoma: expertise at a tertiary care center F Ceccato, G Lombardi, R Manara, E Emanuelli, L Denaro, L Milanese, ... Journal of Neuro-Oncology 122, 189-196, 2015 | 62 | 2015 |
| Prevalence of AIP mutations in a large series of sporadic Italian acromegalic patients and evaluation of CDKN1B status in acromegalic patients with multiple … G Occhi, G Trivellin, F Ceccato, P De Lazzari, G Giorgi, S Dematte, ... European Journal of Endocrinology 163 (3), 369-376, 2010 | 62 | 2010 |
| Characterization of C14orf4, a novel intronless human gene containing a polyglutamine repeat, mapped to the ARVD1 critical region A Rampazzo, F Pivotto, G Occhi, N Tiso, S Bortoluzzi, L Rowen, L Hood, ... Biochemical and Biophysical Research Communications 278 (3), 766-774, 2000 | 58 | 2000 |
| The R304X mutation of the aryl hydrocarbon receptor interacting protein gene in familial isolated pituitary adenomas: mutational hot-spot or founder effect? G Occhi, ML Jaffrain-Rea, G Trivellin, N Albiger, F Ceccato, E De Menis, ... Journal of Endocrinological Investigation 33, 800-805, 2010 | 57 | 2010 |
| Food-dependent Cushing's syndrome: from molecular characterization to therapeutical results NM Albiger, G Occhi, B Mariniello, M Iacobone, G Favia, A Fassina, ... European Journal of Endocrinology 157 (6), 771-778, 2007 | 55 | 2007 |
| The usefulness of combined biochemical tests in the diagnosis of Cushing’s disease with negative pituitary magnetic resonance imaging RM Testa, N Albiger, G Occhi, F Sanguin, M Scanarini, S Berlucchi, ... European journal of endocrinology 156 (2), 241-248, 2007 | 54 | 2007 |
| The GIP/GIPR axis is functionally linked to GH-secretion increase in a significant proportion of gsp− somatotropinomas D Regazzo, M Losa, NM Albiger, MR Terreni, G Vazza, F Ceccato, ... European journal of endocrinology 176 (5), 543-553, 2017 | 49 | 2017 |
| The Glucose‐Dependent Insulinotropic Polypeptide Receptor is Overexpressed Amongst GNAS1 Mutation‐Negative Somatotropinomas and Drives Growth … G Occhi, M Losa, N Albiger, G Trivellin, D Regazzo, M Scanarini, ... Journal of neuroendocrinology 23 (7), 641-649, 2011 | 48 | 2011 |
| Acromegaly Is More Severe in Patients With AHR or AIP Gene Variants Living in Highly Polluted Areas S Cannavo, M Ragonese, S Puglisi, PD Romeo, ML Torre, A Alibrandi, ... The Journal of Clinical Endocrinology & Metabolism 101 (4), 1872-1879, 2016 | 47 | 2016 |
| Homozygous desmocollin-2 mutations and arrhythmogenic cardiomyopathy A Lorenzon, K Pilichou, I Rigato, G Vazza, M De Bortoli, M Calore, ... The American Journal of Cardiology 116 (8), 1245-1251, 2015 | 46 | 2015 |
| Large genomic rearrangements of desmosomal genes in Italian arrhythmogenic cardiomyopathy patients K Pilichou, E Lazzarini, I Rigato, R Celeghin, M De Bortoli, ... Circulation: Arrhythmia and Electrophysiology 10 (10), e005324, 2017 | 44 | 2017 |
| Venous thromboembolism in patients with Cushing’s syndrome: need of a careful investigation of the prothrombotic risk profile S Koutroumpi, V Daidone, MT Sartori, MG Cattini, NM Albiger, G Occhi, ... Pituitary 16, 175-181, 2013 | 44 | 2013 |