Elena Andreucci

5PUBLICATIONS
36CO-AUTHORS
Neurology and neuromuscular diseasesChild language acquisitionEpigenetics (incl. genome methylation and epigenomics)Gene and molecular therapy
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Publications (5)

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

Andrea Gazzin, Marta Calvo, Federico Rondot

|Aug 07, 2023
Evidence for a Pathogenic Role of CSMD1 in Childhood Apraxia of Speech.

Daniela Formicola, Irina Podda, Marilena Pantaleo

|Apr 30, 2021
Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell Syndrome.

Laura Pignata, Angela Sparago, Orazio Palumbo

|Aug 14, 2020
Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications.

Christina Lissewski, Valérie Chune, Francesca Pantaleoni

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Frequent Collaborators

2 joint publications

Alessandro De Luca

2 joint publications

Marco Tartaglia

1 joint publications

Christina Lissewski

1 joint publications

Francesca Pantaleoni