| Persistent cAMP-signals triggered by internalized G-protein–coupled receptors D Calebiro, VO Nikolaev, MC Gagliani, T De Filippis, C Dees, C Tacchetti, ... PLoS biology 7 (8), e1000172, 2009 | 700 | 2009 |
| Thyrotropin-secreting pituitary tumors P Beck-Peccoz, F Brucker-Davis, L Persani, RC Smallridge, ... Endocrine reviews 17 (6), 610-638, 1996 | 687 | 1996 |
| Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene E Di Pasquale, P Beck-Peccoz, L Persani The American Journal of Human Genetics 75 (1), 106-111, 2004 | 667 | 2004 |
| Congenital hypothyroidism: a 2020–2021 consensus guidelines update—an ENDO-European reference network initiative endorsed by the European society for pediatric endocrinology … P Van Trotsenburg, A Stoupa, J Léger, T Rohrer, C Peters, L Fugazzola, ... Thyroid 31 (3), 387-419, 2021 | 531 | 2021 |
| Premature ovarian failure P Beck-Peccoz, L Persani Orphanet journal of rare diseases 1 (1), 9, 2006 | 465 | 2006 |
| Central hypothyroidism: pathogenic, diagnostic, and therapeutic challenges L Persani The Journal of Clinical Endocrinology & Metabolism 97 (9), 3068-3078, 2012 | 437 | 2012 |
| Genes involved in human premature ovarian failure L Persani, R Rossetti, C Cacciatore Journal of molecular endocrinology 45 (5), 257, 2010 | 348 | 2010 |
| A novel mutation in the bone morphogenetic protein 15 gene causing defective protein secretion is associated with both increased ovulation rate and sterility in Lacaune sheep L Bodin, E Di Pasquale, S Fabre, M Bontoux, P Monget, L Persani, ... Endocrinology 148 (1), 393-400, 2007 | 340 | 2007 |
| A 7‐year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH) C Corbetta, G Weber, F Cortinovis, D Calebiro, A Passoni, MC Vigone, ... Clinical endocrinology 71 (5), 739-745, 2009 | 325 | 2009 |
| Signaling by internalized G-protein-coupled receptors D Calebiro, VO Nikolaev, L Persani, MJ Lohse Trends in pharmacological sciences 31 (5), 221-228, 2010 | 321 | 2010 |
| The fundamental role of bone morphogenetic protein 15 in ovarian function and its involvement in female fertility disorders L Persani, R Rossetti, E Di Pasquale, C Cacciatore, S Fabre Human reproduction update 20 (6), 869-883, 2014 | 311 | 2014 |
| TSH-secreting adenomas P Beck-Peccoz, L Persani, D Mannavola, I Campi Best Practice & Research Clinical Endocrinology & Metabolism 23 (5), 597-606, 2009 | 297 | 2009 |
| Regulation of ovulation rate in mammals: contribution of sheep genetic models S Fabre, A Pierre, P Mulsant, L Bodin, E Di Pasquale, L Persani, ... Reproductive Biology and Endocrinology 4 (1), 20, 2006 | 296 | 2006 |
| Identification of New Variants of Human BMP15 Gene in a Large Cohort of Women with Premature Ovarian Failure E Di Pasquale, R Rossetti, A Marozzi, B Bodega, S Borgato, L Cavallo, ... The Journal of Clinical Endocrinology & Metabolism 91 (5), 1976-1979, 2006 | 295 | 2006 |
| Autoimmunity and thyroid function in patients with chronic active hepatitis treated with recombinant interferon alpha-2a D Preziati, L La Rosa, G Covini, R Marcelli, S Rescalli, L Persani, ... European Journal of Endocrinology 132 (5), 587-593, 1995 | 284 | 1995 |
| A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function E Porcu, M Medici, G Pistis, CB Volpato, SG Wilson, AR Cappola, SD Bos, ... PLoS genetics 9 (2), e1003266, 2013 | 283 | 2013 |
| Luteinizing hormone signaling in preovulatory follicles involves early activation of the epidermal growth factor receptor pathway S Panigone, M Hsieh, M Fu, L Persani, M Conti Molecular endocrinology 22 (4), 924-936, 2008 | 272 | 2008 |
| Genetics of primary ovarian insufficiency R Rossetti, I Ferrari, M Bonomi, L Persani Clinical genetics 91 (2), 183-198, 2017 | 256 | 2017 |
| Thyroid gland development and function in the zebrafish model P Porazzi, D Calebiro, F Benato, N Tiso, L Persani Molecular and cellular endocrinology 312 (1-2), 14-23, 2009 | 249 | 2009 |
| Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement Y Sun, B Bak, N Schoenmakers, ASP van Trotsenburg, W Oostdijk, ... Nature genetics 44 (12), 1375-1381, 2012 | 248 | 2012 |
Laura FugazzolaUniversità degli Studi di MilanoVerified email at auxologico.it
