Raffaella Rossetti
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Explore the profile of Raffaella Rossetti including associated specialties, affiliations and a list of published articles.
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18
Citations
514
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Recent Articles
1.
Cohen A, Rossetti R, Florsheim N, Samson A, Renbaum P, Carbone E, et al.
J Endocr Soc
. 2025 Jan;
9(2):bvae221.
PMID: 39850788
Context: Despite a growing number of studies, the genetic etiology in many cases of ovarian dysgenesis is incompletely understood. Objectives: This work aimed to study the genetic etiology causing absence...
2.
Federici S, Rossetti R, Moleri S, Munari E, Frixou M, Bonomi M, et al.
Front Endocrinol (Lausanne)
. 2024 Oct;
15:1464803.
PMID: 39391877
Primary ovarian insufficiency (POI) is a disorder of insufficient ovarian follicle function before the age of 40 years with an estimated prevalence of 3.7% worldwide. Its relevance is emerging due...
3.
Persani L, Cools M, Ioakim S, Ahmed S, Andonova S, Avbelj-Stefanija M, et al.
Endocr Connect
. 2022 Oct;
11(12).
PMID: 36228316
Differences of sex development and maturation (SDM) represent a heterogeneous puzzle of rare conditions with a large genetic component whose management and treatment could be improved by an accurate classification...
4.
Rossetti R, Moleri S, Guizzardi F, Gentilini D, Libera L, Marozzi A, et al.
Front Endocrinol (Lausanne)
. 2021 Nov;
12:664645.
PMID: 34803902
Primary ovarian insufficiency (POI) is one of the major causes of female infertility associated with the premature loss of ovarian function in about 3.7% of women before the age of...
5.
Cattoni A, Spano A, Tulone A, Boneschi A, Masera N, Maitz S, et al.
Front Endocrinol (Lausanne)
. 2020 Oct;
11:540683.
PMID: 33101191
Non-syndromic primary ovarian insufficiency due to ovarian dysgenesis in 46,XX patients is an uncommon finding in the general population, even though several monogenic variants have been reported as causative factors....
6.
Rossetti R, Ferrari I, Bestetti I, Moleri S, Brancati F, Petrone L, et al.
Hum Mutat
. 2020 Jan;
41(5):983-997.
PMID: 31957178
Bone morphogenetic protein 15 (BMP15) encodes an oocyte factor with a relevant role for folliculogenesis as homodimer or cumulin heterodimer (BMP15-GDF9). Heterozygous BMP15 variants in the precursor or mature peptide...
7.
Busnelli A, Lattuada D, Rossetti R, Paffoni A, Persani L, Fedele L, et al.
J Assist Reprod Genet
. 2018 Aug;
35(11):1987-1994.
PMID: 30120634
Purpose: Low mitochondrial DNA (mtDNA) content in oocytes and in cumulus cells is an indicator of poor oocyte quality. Moreover, initial evidence showed a correlation between mtDNA content in cumulus...
8.
Portnoi M, Dumargne M, Rojo S, Witchel S, Duncan A, Eozenou C, et al.
Hum Mol Genet
. 2018 Jan;
27(7):1228-1240.
PMID: 29373757
SOX8 is an HMG-box transcription factor closely related to SRY and SOX9. Deletion of the gene encoding Sox8 in mice causes reproductive dysfunction but the role of SOX8 in humans...
9.
Ferrari I, Bouilly J, Beau I, Guizzardi F, Ferlin A, Pollazzon M, et al.
Hum Mol Genet
. 2016 Nov;
25(23):5223-5233.
PMID: 27798098
Premature ovarian insufficiency (POI) is a clinical syndrome defined by a loss of ovarian activity before the age of 40. Its pathogenesis is still largely unknown, but increasing evidences support...
10.
Persani L, Rossetti R, Di Pasquale E, Cacciatore C, Fabre S
Hum Reprod Update
. 2014 Jul;
20(6):869-83.
PMID: 24980253
Background: A large number of studies have contributed to understanding the general mechanisms driving ovarian folliculogenesis in humans and show a complex endocrine dialog between the central nervous system, the...