Silvia Russo

19PUBLICATIONS
67CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Social program evaluationDevelopmental genetics (incl. sex determination)Bioinformatic methods developmentNeurogenetics
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Publications (19)

|Jun 25, 2026
Prenatal Genetic Testing for Beckwith-Wiedemann Syndrome: Considerations, Challenges and Observations (A Real-World Study).

|Dec 22, 2025
PEG10 loss of function causes Silver-Russell syndrome: a familial case with paternal deletion.

Alessandro Vimercati, Giuseppa Patti, Pierpaola Tannorella

|Sep 02, 2025
Clinical differences in monozygotic twins with Rett syndrome: case report and systematic review.

Silvia Boeri, Maria Piai, Silvia Russo

|Oct 16, 2024
Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver-Russell Syndrome and Focus on the IGF1R Gene.

Alessandro Vimercati, Pierpaola Tannorella, Sara Guzzetti

|Aug 29, 2024
Deletions in the CDKL5 5' untranslated region lead to CDKL5 deficiency disorder.

Isabel Haviland, Ralph D Hector, Lindsay C Swanson

|Feb 22, 2024
Low-grade parental gonosomal mosaicism in CHD2 siblings with Smith-Magenis-like syndrome.

Francesca Cogliati, Letizia Straniero, Valeria Rimoldi

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Frequent Collaborators

6 joint publications

Lidia Larizza

6 joint publications

Donatella Milani

4 joint publications

Francesca Cogliati

3 joint publications

Luciano Calzari