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Raffaella Rossetti
Raffaella Rossetti
IRCCS Istituo Auxologico Italiano
Verified email at auxologico.it
Title
Cited by
Cited by
Year
Genes involved in human premature ovarian failure
L Persani, R Rossetti, C Cacciatore
Journal of molecular endocrinology 45 (5), 257, 2010
3102010
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
2802006
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
2622014
Genome-Wide Association Studies Identify Two Novel BMP15 Mutations Responsible for an Atypical Hyperprolificacy Phenotype in Sheep
J Demars, S Fabre, J Sarry, R Rossetti, H Gilbert, L Persani, ...
PLoS genetics 9 (4), e1003482, 2013
2062013
Genetics of primary ovarian insufficiency
R Rossetti, I Ferrari, M Bonomi, L Persani
Clinical genetics 91 (2), 183-198, 2017
2032017
BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein
R Rossetti, E Di Pasquale, A Marozzi, S Bione, D Toniolo, P Grammatico, ...
Human mutation 30 (5), 804-810, 2009
1702009
Primary ovarian insufficiency: X chromosome defects and autoimmunity
L Persani, R Rossetti, C Cacciatore, M Bonomi
Journal of autoimmunity 33 (1), 35-41, 2009
1452009
Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies
MF Portnoi, MC Dumargne, S Rojo, SF Witchel, AJ Duncan, C Eozenou, ...
Human molecular genetics 27 (7), 1228-1240, 2018
812018
Blood cell mitochondrial DNA content and premature ovarian aging
M Bonomi, E Somigliana, C Cacciatore, M Busnelli, R Rossetti, S Bonetti, ...
Public Library of Science 7 (8), e42423, 2012
722012
Gene dosage as a relevant mechanism contributing to the determination of ovarian function in Turner syndrome
C Castronovo, R Rossetti, D Rusconi, MP Recalcati, C Cacciatore, ...
Human reproduction 29 (2), 368-379, 2014
682014
Genetic defects of ovarian TGF-β-like factors and premature ovarian failure
L Persani, R Rossetti, C Cacciatore, S Fabre
Journal of endocrinological investigation 34, 244-251, 2011
562011
A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure
T Corre, J Schuettler, S Bione, A Marozzi, L Persani, R Rossetti, ...
Human reproduction 24 (8), 2023-2028, 2009
472009
High-resolution array-CGH analysis on 46, XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function
I Bestetti, C Castronovo, A Sironi, C Caslini, C Sala, R Rossetti, M Crippa, ...
Human Reproduction 34 (3), 574-583, 2019
442019
Positive selection in bone morphogenetic protein 15 targets a natural mutation associated with primary ovarian insufficiency in human
S Auclair, R Rossetti, C Meslin, O Monestier, E Di Pasquale, G Pascal, ...
PLoS One 8 (10), e78199, 2013
282013
Fundamental role of BMP15 in human ovarian folliculogenesis revealed by null and missense mutations associated with primary ovarian insufficiency
R Rossetti, I Ferrari, I Bestetti, S Moleri, F Brancati, L Petrone, P Finelli, ...
Human mutation 41 (5), 983-997, 2020
262020
Impaired protein stability and nuclear localization of NOBOX variants associated with premature ovarian insufficiency
I Ferrari, J Bouilly, I Beau, F Guizzardi, A Ferlin, M Pollazzon, M Salerno, ...
Human Molecular Genetics 25 (23), 5223-5233, 2016
262016
A clinical research integration special program (CRISP) for young women with primary ovarian insufficiency
A Falorni, V Minarelli, CM Eads, CM Joachim, L Persani, R Rossetti, ...
Panminerva medica 56 (4), 245, 2014
202014
Mitochondrial DNA copy number in peripheral blood: a potential non-invasive biomarker for female subfertility
A Busnelli, D Lattuada, R Rossetti, A Paffoni, L Persani, L Fedele, ...
Journal of Assisted Reproduction and Genetics 35, 1987-1994, 2018
172018
Targeted next-generation sequencing indicates a frequent oligogenic involvement in primary ovarian insufficiency onset
R Rossetti, S Moleri, F Guizzardi, D Gentilini, L Libera, A Marozzi, ...
Frontiers in endocrinology 12, 664645, 2021
102021
The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres
L Persani, M Cools, S Ioakim, SF Ahmed, S Andonova, M Avbelj-Stefanija, ...
Endocrine Connections 11 (12), 2022
42022
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