ROSSETTI, RAFFAELLA
ROSSETTI, RAFFAELLA
Dipartimento di Scienze Cliniche e di Comunità
The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres
2022 L. Persani, M. Cools, S. Ioakim, S. Faisal Ahmed, S. Andonova, M. Avbelj-Stefanija, F. Baronio, J. Bouligand, H. T Bruggenwirth, J. H Davies, E. De Baere, I. Dzivite-Krisane, P. Fernandez-Alvarez, A. Gheldof, C. Giavoli, C. H Gravholt, O. Hiort, P. Holterhus, A. Juul, C. Krausz, K. Lagerstedt-Robinson, R. Mcgowan, U. Neumann, A. Novelli, X. Peyrassol, L. A Phylactou, J. Rohayem, P. Touraine, D. Westra, V. Vezzoli, R. Rossetti
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
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
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
Genetics of primary ovarian insufficiency
2017 R. Rossetti, I. Ferrari, M. Bonomi, L. Persani
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
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
The fundamental role of bone morphogenetic protein 15 in ovarian function and its involvement in female fertility disorders
2014 L. Persani, R. Rossetti, E. Di pasquale, C. Cacciatore, S. Fabre
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
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
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
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
Genetic defects of ovarian TGF-β-like factors and premature ovarian failure
2011 L. Persani, R. Rossetti, C. Cacciatore, S. Fabre
Genes involved in human premature ovarian failure
2010 L. Persani, R. Rossetti, C. Cacciatore
SCREENING OF SIX CANDIDATE GENES FOR PRIMARY OVARIAN INSUFFICIENCY (POI) IN A LARGE CAUCASIAN FEMALE POPULATION
2009 R. Rossetti, C. Cacciatore, A. Marozzi, D. Cordella, P. Beck-Peccoz, L. Persani, N. Italiano per lo studio dei Difetti Ovarici
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
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
BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein
2009 R. Rossetti, E. Di Pasquale, A. Marozzi, S. Bione, D. Toniolo, P. Grammatico, L. M. Nelson, P. Beck-Peccoz, L. Persani
Primary Ovarian Insufficiency : X chromosome defects and autoimmunity
2009 L. Persani, R. Rossetti, C. Cacciatore, M. Bonomi
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