ROSSETTI, RAFFAELLA
ROSSETTI, RAFFAELLA
Dipartimento di Scienze Cliniche e di Comunità
A clinical research integration special program (CRISP) for young women with primary ovarian insufficiency
2014 A. Falorni, V. Minarelli, C.M. Eads, C.M. Joachim, L. Persani, R. Rossetti, P. Yurttas Beim, V.A. Pellegrini, P.F. Schnatz, S. Rafique, K. Kissell, K.A. Calis, V. Popat, L.M. Nelson
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure
2009 T. Corre, J. Schuettler, S. Bione, A. Marozzi, L. Persani, R. Rossetti, F. Torricelli, I. Giotti, P. Vogt, D. Toniolo, I. Network for the study of Ovarian Dysfunctions
Candidate gene analyses in Caucasian patients with Primary Ovarian Insufficiency (POI)
2009 R. Rossetti, C. Cacciatore, A. Marozzi, D. Cordella, S. Bione, S. Cannavo, D. Bernard, T. Cole, J. Clayton Smith, P. Beck-Peccoz, L. Persani
Fundamental role of BMP15 in human ovarian folliculogenesis revealed by null and missense mutations associated with primary ovarian insufficiency
2020 R. Rossetti, I. Ferrari, I. Bestetti, S. Moleri, F. Brancati, L. Petrone, P. Finelli, L. Persani
Gene dosage as a relevant mechanism contributing to the determination of ovarian function in Turner syndrome
2014 C. Castronovo, R. Rossetti, D. Rusconi, M.P. Recalcati, C. Cacciatore, E. Beccaria, V. Calcaterra, P. Invernizzi, D. Larizza, P. Finelli, L. Persani
Genes involved in human premature ovarian failure
2010 L. Persani, R. Rossetti, C. Cacciatore
Genetic defects of ovarian TGF-β-like factors and premature ovarian failure
2011 L. Persani, R. Rossetti, C. Cacciatore, S. Fabre
Genetics of primary ovarian insufficiency
2017 R. Rossetti, I. Ferrari, M. Bonomi, L. Persani
Genome-wide association studies identify two novel BMP15 mutations responsible for an atypical hyperprolificacy phenotype in sheep
2013 J. Demars, S. Fabre, J. Sarry, R. Rossetti, H. Gilbert, L. Persani, G. Tosser Klopp, P. Mulsant, Z. Nowak, W. Drobik, E. Martyniuk, L. Bodin
Identification of new variants of GDF9 gene in large cohort of women with Premature Ovarian Failure
2006 R. Rossetti, E. Di Pasquale, B. Bodega, S. Borgato, P. Beck-Peccoz, A. Marozzi, L. Persani
Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure
2006 E. Di Pasquale, R. Rossetti, A. Marozzi, B. Bodega, S. Borgato, L. Cavallo, S. Einaudi, G. Radetti, G. Russo, M. Sacco, M. Wasniewska, T. Cole, P. Beck-Peccoz, L.M. Nelson, L. Persani
Identification of rare CNVs involving genes acting in oocyte maturation and differentiation in a cohort of patients affected by Primary Ovarian Insufficiency
2014 I. Bestetti, C. Castronovo, M. Crippa, R. Rossetti, A. Pistocchi, C. Caslini, C. Sala, D. Toniollo, L. Persani, A. Marozzi, P. Finelli
Impaired protein stability and nuclear localization of NOBOX variants associated with premature ovarian insufficiency
2016 I. Ferrari, J. Bouilly, I. Beau, F. Guizzardi, A. Ferlin, M. Pollazzon, M. Salerno, N. Binart, L. Persani, R. Rossetti
In Vitro Molecular And Functional Studies Of Bmp15 Mutations Associated With Premature Ovarian Failure
2008 R. Rossetti, A. Marozzi, S. Bione, E. Di Pasquale, P. Beck-Peccoz, L. Persani
Mitochondrial DNA copy number in peripheral blood : a potential non-invasive biomarker for female subfertility
2018 A. Busnelli, D. Lattuada, R. Rossetti, A. Paffoni, L. Persani, L. Fedele, E. Somigliana
Molecular and functional characterization of BMP15 variants associated with secondary amenorrhea and Premature Ovarian Failure (POF)
2008 R. Rossetti, E. Di Pasquale, A. Marozzi, S. Bione, P. Beck-Peccoz, L. Persani
Molecular and functional characterization of BMP15 variants associated with secondary amenorrhea and premature ovarian failure (POF)
2008 R. Rossetti, E. Di Pasquale, A. Marozzi, S. Bione, P.L.M. Beck Peccoz, L. Persani
Molecular studies of BMP15 variants associated with secondary amenorrhea and premature ovarian failure (POF)
2007 R. Rossetti, E. Di Pasquale, S. Borgato, S. Bione, A. Marozzi, P. Beck-Peccoz, L. Persani
Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies
2018 M. Portnoi, M. Dumargne, S. Rojo, S.F. Witchel, A.J. Duncan, C. Eozenou, J. Bignon-Topalovic, S.A. Yatsenko, A. Rajkovic, M. Reyes-Mugica, K. Almstrup, L. Fusee, Y. Srivastava, S. Chantot-Bastaraud, C. Hyon, C. Louis-Sylvestre, P. Validire, C. de Malleray Pichard, C. Ravel, S. Christin-Maitre, R. Brauner, R. Rossetti, L. Persani, E.H. Charreau, L. Dain, V.A. Chiauzzi, I. Mazen, H. Rouba, C. Schluth-Bolard, S. Macgowan, W.H.I. Mclean, E. Patin, E. Rajpert-De Meyts, R. Jauch, J.C. Achermann, J. Siffroi, K. Mcelreavey, A. Bashamboo
Positive selection in bone morphogenetic protein 15 targets a natural mutation associated with primary ovarian insufficiency in human
2013 S. Auclair, R. Rossetti, C. Meslin, O. Monestier, E. Di Pasquale, G. Pascal, L. Persani, S. Fabre