Elena Andreucci

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 3

Top Topics

Atrial Fibrillation

Gold Nanoparticles

Cell Proliferation

Top Venues

European journal of human genetics : EJHG

Neuropediatrics

This page only lists publications with an associated author ORCID identifier.

Publications

Daniela Formicola, Irina Podda, Marilena Pantaleo, Elena Andreucci, Diego Lopergolo, Sabrina Giglio, Filippo Maria Santorelli, Anna Chilosi
Evidence for a Pathogenic Role of CSMD1 in Childhood Apraxia of Speech. Neuropediatrics (2023)
Laura Pignata, Angela Sparago, Orazio Palumbo, Elena Andreucci, Elisabetta Lapi, Romano Tenconi, Massimo Carella, Andrea Riccio, Flavia Cerrato
Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell Syndrome. Genes 12 (4) (2021)
Christina Lissewski, Valérie Chune, Francesca Pantaleoni, Alessandro De Luca, Yline Capri, Julia Brinkmann, Francesca Lepri, Paola Daniele, Erika Leenders, Laura Mazzanti, Emanuela Scarano, Francesca Clementina Radio, Kerstin Kutsche, Alma Kuechler, Marion Gérard, Kara Ranguin, Marine Legendre, Yoann Vial, Ineke van der Burgt, Tuula Rinne, Elena Andreucci, Gioia Mastromoro, Maria Cristina Digilio, Hélène Cave, Tartaglia Marco, Martin Zenker
Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications. European journal of human genetics : EJHG 29 (1) (2020)