ROSSETTI, RAFFAELLA

ROSSETTI, RAFFAELLA  

Dipartimento di Scienze Cliniche e di Comunità  

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Titolo Data di pubblicazione Autori Tipo File Abstract
The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres 2022 Luca PersaniClaudia GiavoliValeria VezzoliRaffaella Rossetti + Article (author) -
Fundamental role of BMP15 in human ovarian folliculogenesis revealed by null and missense mutations associated with primary ovarian insufficiency 2020 Rossetti, RaffaellaFerrari, IlariaBestetti, IlariaMoleri, SilviaFinelli, PalmaPersani, Luca + Article (author) -
Mitochondrial DNA copy number in peripheral blood : a potential non-invasive biomarker for female subfertility 2018 Busnelli, AndreaLattuada, DeboraRossetti, RaffaellaPaffoni, AlessioPersani, LucaFedele, LuigiSomigliana, Edgardo Article (author) -
Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies 2018 Rossetti, RaffaellaPersani, Luca + Article (author) -
Genetics of primary ovarian insufficiency 2017 ROSSETTI, RAFFAELLAFERRARI, ILARIAM. BonomiL. Persani Article (author) -
Impaired protein stability and nuclear localization of NOBOX variants associated with premature ovarian insufficiency 2016 I. FerrariF. GuizzardiL. PersaniR. Rossetti + Article (author) -
Identification of rare CNVs involving genes acting in oocyte maturation and differentiation in a cohort of patients affected by Primary Ovarian Insufficiency 2014 I. BestettiC. CastronovoM. CrippaR. RossettiA. PistocchiC. CasliniL. PersaniA. MarozziP. Finelli + Conference Object -
A clinical research integration special program (CRISP) for young women with primary ovarian insufficiency 2014 L. PersaniR. Rossetti + Article (author) -
Gene dosage as a relevant mechanism contributing to the determination of ovarian function in Turner syndrome 2014 C. CastronovoR. RossettiD. RusconiM.P. RecalcatiCACCIATORE, CHIARAP. InvernizziP. FinelliL. Persani + Article (author) -
The fundamental role of bone morphogenetic protein 15 in ovarian function and its involvement in female fertility disorders 2014 L. PersaniR. RossettiE. Di pasqualeC. Cacciatore + Article (author) -
Genome-wide association studies identify two novel BMP15 mutations responsible for an atypical hyperprolificacy phenotype in sheep 2013 R. RossettiL. Persani + Article (author) -
Positive selection in bone morphogenetic protein 15 targets a natural mutation associated with primary ovarian insufficiency in human 2013 R. RossettiE. Di PasqualeL. Persani + Article (author) -
Genetic defects of ovarian TGF-β-like factors and premature ovarian failure 2011 L. PersaniR. Rossetti + Article (author) -
Genes involved in human premature ovarian failure 2010 L. PersaniR. Rossetti + Article (author) -
SCREENING OF SIX CANDIDATE GENES FOR PRIMARY OVARIAN INSUFFICIENCY (POI) IN A LARGE CAUCASIAN FEMALE POPULATION 2009 R. RossettiA. MarozziD. CordellaP. Beck-PeccozL. Persani + Conference Object -
Candidate gene analyses in Caucasian patients with Primary Ovarian Insufficiency (POI) 2009 R. RossettiA. MarozziD. CordellaP. Beck-PeccozL. Persani + Conference Object -
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure 2009 A. MarozziL. PersaniR. Rossetti + Article (author) -
BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein 2009 R. RossettiE. Di PasqualeA. MarozziP. Beck-PeccozL. Persani + Article (author) -
Primary Ovarian Insufficiency : X chromosome defects and autoimmunity 2009 L. PersaniR. RossettiM. Bonomi + Article (author) -
Molecular and functional characterization of BMP15 variants associated with secondary amenorrhea and Premature Ovarian Failure (POF) 2008 R. RossettiE. Di PasqualeA. MarozziP. Beck-PeccozL. Persani + Conference Object -