Silvia Maria Sirchia
Università degli Studi di Milano
H-index: 27
Europe-Italy
Top articles of Silvia Maria Sirchia
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Non-invasive biomarkers for sperm retrieval in non-obstructive patients: a comprehensive review | Laura Fontana Silvia M Sirchia Chiara Pesenti Giovanni Maria Colpi Monica R Miozzo | 2024/4/16 | |
Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith–Wiedemann Syndrome Cell Lines | International Journal of Molecular Sciences | Silvana Pileggi Elisa A Colombo Silvia Ancona Roberto Quadri Clara Bernardelli | 2024/3/22 |
Violence against women and stress-related disorders: Seeking for associated epigenetic signatures, a pilot study | Healthcare | Andrea Piccinini Paolo Bailo Giussy Barbara Monica Miozzo Silvia Tabano | 2023/1/6 |
A perspective on diet, epigenetics and complex diseases: where is the field headed next? | Fabio Coppedè Marica Franzago Emiliano Giardina Cristiana Lo Nigro Giuseppe Matullo | 2022/10 | |
Primary TSC2-/meth Cells Induce Follicular Neogenesis in an Innovative TSC Mouse Model | International Journal of Molecular Sciences | Clara Bernardelli Eloisa Chiaramonte Silvia Ancona Silvia M Sirchia Amilcare Cerri | 2022/8/26 |
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes | Pediatric research | Jole Costanza Margherita Camanni Maria Maddalena Ferrari Valentina De Cosmi Silvia Tabano | 2022/6 |
Correction: Rondinone et al. Extensive Placental Methylation Profiling in Normal Pregnancies. Int. J. Mol. Sci. 2021, 22, 2136 | International Journal of Molecular Sciences | Ornella Rondinone Alessio Murgia Jole Costanza Silvia Tabano Margherita Camanni | 2022/5/10 |
Cohesin Mutations Induce Chromatin Conformation Perturbation of the H19/IGF2 Imprinted Region and Gene Expression Dysregulation in Cornelia de Lange … | Biomolecules | Silvana Pileggi Marta La Vecchia Elisa Adele Colombo Laura Fontana Patrizia Colapietro | 2021/11/2 |
Clinical and molecular diagnosis of Beckwith-Wiedemann Syndrome with single-or multi-locus imprinting disturbance | Laura Fontana Silvia Tabano Silvia Maitz Patrizia Colapietro Emanuele Garzia | 2021/3/26 | |
(Epi) genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome | Molecular Genetics & Genomic Medicine | Laura Fontana Maria F Bedeschi Giulia A Cagnoli Jole Costanza Nicola Persico | 2020/9 |
Profound alterations of the chromatin architecture at chromosome 11p15. 5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients | Scientific reports | Davide Rovina Marta La Vecchia Alice Cortesi Laura Fontana Matthieu Pesant | 2020/5/19 |
DNA methylation in the diagnosis of monogenic diseases | Flavia Cerrato Angela Sparago Francesca Ariani Fulvia Brugnoletti Luciano Calzari | 2020/3/26 |
