| Human LH and hCG stimulate differently the early signalling pathways but result in equal testosterone synthesis in mouse Leydig cells in vitro L Riccetti, F De Pascali, L Gilioli, F Potì, LB Giva, M Marino, S Tagliavini, ... Reproductive Biology and Endocrinology 15, 1-12, 2017 | 121 | 2017 |
| FSHR POLYMORPHISM P.N680S MEDIATES DIFFERENT RESPONSES TO FSH IN VITRO. SM Casarini L, Moriondo V, Marino M, Adversi F, Capodanno F, Grisolia C, La ... Molecular and Cellular Endocrinology 393 (1-2), 83-91, 2014 | 100 | 2014 |
| Treatment with human, recombinant FSH improves sperm DNA fragmentation in idiopathic infertile men depending on the FSH receptor polymorphism p. N680S: a pharmacogenetic study M Simoni, D Santi, L Negri, I Hoffmann, M Muratori, E Baldi, M Cambi, ... Human Reproduction 31 (9), 1960-1969, 2016 | 98 | 2016 |
| Estrogen modulates specific life and death signals induced by LH and hCG in human primary granulosa cells in vitro L Casarini, L Riccetti, F De Pascali, L Gilioli, M Marino, E Vecchi, D Morini, ... International Journal of Molecular Sciences 18 (5), 926, 2017 | 68 | 2017 |
| Impact of gene polymorphisms of gonadotropins and their receptors on human reproductive success MM Casarini L, Santi D Reproduction, 2015 | 57 | 2015 |
| iVar, an interpretation-oriented tool to manage the update and revision of variant annotation and classification S Castellano, F Cestari, G Faglioni, E Tenedini, M Marino, L Artuso, ... Genes 12 (3), 384, 2021 | 29 | 2021 |
| PREVALENCE OF OLFACTORY AND OTHER DEVELOPMENTAL ANOMALIES IN PATIENTS WITH CENTRAL HYPOGONADOTROPIC HYPOGONADISM. SM Della Valle E, Vezzani S, Rochira V, Granata AR, Madeo B, Genovese E ... Frontiers in Endocrinology 4 (70), 2013 | 25 | 2013 |
| Hereditary pancreatic cancer: a retrospective single-center study of 5143 Italian families with history of BRCA-related malignancies A Toss, M Venturelli, E Molinaro, S Pipitone, E Barbieri, I Marchi, ... Cancers 11 (2), 193, 2019 | 20 | 2019 |
| Central hypogonadotropic hypogonadism: genetic complexity of a complex disease M Marino, V Moriondo, E Vighi, E Pignatti, M Simoni International Journal of Endocrinology 2014 (1), 649154, 2014 | 20 | 2014 |
| DOUBLE HETEROZYGOSITY FOR BRCA1 AND HMLH1 GENE MUTATIONS IN A 46-YEAR-OLD WOMAN WITH FIVE PRIMARY TUMORS. PLM Pedroni M, Di Gregorio C, Cortesi L, Reggiani Bonetti L, Magnani G ... Techniques in Coloproctology 18 (3), 285-289, 2013 | 18* | 2013 |
| Real-life use of BRAF-V600E mutation analysis in thyroid nodule fine needle aspiration: consequences on clinical decision-making G Brigante, A Craparo, E Pignatti, M Marino, ML Monzani, S De Vincentis, ... Endocrine 73, 625-632, 2021 | 15 | 2021 |
| ARE PRE-MIR-146A AND PTTG1 ASSOCIATED WITH PAPILLARY THYROID CANCER? LF Marco Marino, Valentina Cirello, Valentina Gnarini, Carla Colombo, Elisa ... Endocrine Connections 2 (4), 178-185, 2013 | 15 | 2013 |
| Altered methylation pattern of the SRD5A2 gene in the cerebrospinal fluid of post-finasteride patients: a pilot study RC Melcangi, L Casarini, M Marino, D Santi, S Sperduti, S Giatti, ... Endocrine connections 8 (8), 1118-1125, 2019 | 13 | 2019 |
| High Resolution Melting: a sensitive, cost-effective, time-Saving technique for BRAFV600E detection in thyroid FNAB Washing liquid. A prospective cohort study SM Marino M, Monzani ML, Brigante G, Cioni K, Madeo B, Santi D, Maiorana A ... Eur Thyroid J, 2015 | 13 | 2015 |
| THE TRHR GENE IS ASSOCIATED WITH HYPOTHALAMO-PITUITARY SENSITIVITY TO LEVOTHYROXINE. SM Brigante G, Spaggiari G, Santi D, Cioni K, Gnarini V, Diazzi C, Pignatti ... European Thyroid Journal 3, 101-108, 2014 | 12 | 2014 |
| A NOVEL DELETION OF BRCA1 GENE THAT ELIMINATES THE ATG INITIATION CODON WITHOUT AFFECTING THE PROMOTER REGION. LCSC Marco Marino, Claudio Rabacchi, Maria Luisa Simone, Veronica Medici Clinica Chimica Acta 403 (1-2), 249-253, 2009 | 12 | 2009 |
| Characterization of New ATM Deletion Associated with Hereditary Breast Cancer S Parenti, C Rabacchi, M Marino, E Tenedini, L Artuso, S Castellano, ... Genes 12 (2), 136, 2021 | 10 | 2021 |
| AN APPARENT INCONSISTENCY IN PARENT TO OFFSPRING TRANSMISSION OF POINT MUTATIONS OF LDLR GENE IN FAMILIAL HYPERCHOLESTEROLEMIA. SC Claudio Rabacchi, Alessia Wunsch, Margherita Ghisellini, Marco Marino ... Clinica Chimica Acta 406 (1-2), 75-80, 2009 | 10 | 2009 |
| Detection of germline variants in 450 breast/ovarian cancer families with a multi-gene panel including coding and regulatory regions C Guglielmi, R Scarpitta, G Gambino, E Conti, F Bellè, M Tancredi, ... International Journal of Molecular Sciences 22 (14), 7693, 2021 | 7 | 2021 |
| Complete aromatase deficiency in four adult men: detection of a novel mutation and two known mutations in the CYP19A1 gene E Pignatti, KM Ajlouni, N Khawaja, K Unluhizarci, E Kartal, C Carani, ... ENDOCRINE REVIEWS 34, FP22-1; SUN-527-FP22-1; SUN-527, 2013 | 6 | 2013 |
Manuela SimoniUniversity of Modena and Reggio Emilia, Italy在 unimore.it 的电子邮件经过验证
