Federico Rondot

4PUBLICATIONS
28CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)NanomedicineNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)
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Publications (4)

|Jun 26, 2026
TRAPPC9-Related Intellectual Developmental Disorder: A Systematic Review and a Novel Case of a Complex Structural Variant.

|Jun 26, 2026
PPP1CB-Related Noonan Syndrome with Loose Anagen Hair: A Systematic Review.

|Jan 08, 2026
Domain-specific phenotypic profiles in RAF1-related Noonan syndrome.

Andrea Gazzin, Marta Calvo, Federico Rondot

|Oct 29, 2025
Expanding Clinical and Genetic Landscape of SATB2-Associated Syndrome.

Verdiana Pullano, Federico Rondot, Ilaria Carelli

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Frequent Collaborators

4 joint publications

Simona Cardaropoli

4 joint publications

Giuseppe Reynolds

3 joint publications

Diana Carli

3 joint publications

Marta Calvo