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Silvia Russo

Director

IRCCS Istituto Auxologico Italiano

Italy

Research Interests

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Professors in Italy

Articles (13)

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2026

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2025

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2025

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2023

Collaborators (16)

Francesca Cogliati

IRCCS Istituto Auxologico Italiano

ITALY

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Mohamad Maghnie

University of Genoa

ITALY

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Sara Guzzetti

IRCCS Istituto Auxologico Italiano

ITALY

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Laima Ambrozaityte

senior researcher, professor

Vilnius University

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Rosanna Asselta

Full Professor in Medical Genetics

Humanitas University

ITALY

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Pierpaola Tannorella

Istituto Auxologico Italiano

ITALY

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Niccolò Butti

Istituto di Ricovero e Cura a Carattere Scientifico Eugenio Medea

ITALY

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Andrea Riccio

Professor of Genetics

ITALY

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LUIGI TARANI

ASSOCIATE PROFESSOR

Sapienza University of Rome

ITALY

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Timothy Yu

Associate Member

Broad Institute

UNITED STATES

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Letizia Straniero

Assistant Professor of Medical Genetics

Humanitas University

ITALY

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José Ramón Fernández‐Fructuoso

SPAIN

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Alessandro Mussa

Deputy Director, Director for Research

Università degli Studi di Torino

ITALY

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roberta battini

University of Pisa

ITALY

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Angela Sparago

Associate Professor

Università degli Studi della Campania Luigi Vanvitelli

ITALY

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Ashley Hurst

Harvard University

UNITED STATES

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Silvia Russo

Research Interests

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Articles (13)

The Italian Angelman Syndrome Registry (IReAS): a tool for standardized data collection and genotype-phenotype analysis

Hypomethylation of the MEG8:Int2-DMR in patients with pathogenic PLAG1 variants suggests new role of the chr14q32 imprinting cluster in Silver-Russell syndrome.

Beckwith-Wiedemann spectrum (BWSp): an update on diagnosis, management, and follow-up from the scientific committee of the Italian BWSp association

PEG10 loss of function causes Silver-Russell syndrome: a familial case with paternal deletion

Clinical differences in monozygotic twins with Rett syndrome: case report and systematic review

Deletions in the <i>CDKL5</i> 5′ untranslated region lead to CDKL5 deficiency disorder

Low-grade parental gonosomal mosaicism in CHD2 siblings with Smith–Magenis-like syndrome

Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis

A long way to syndromic short stature

Performance Metrics of the Scoring System for the Diagnosis of the Beckwith–Wiedemann Spectrum (BWSp) and Its Correlation with Cancer Development

Corrigendum: Pubertal timing in children with Silver Russell syndrome compared to those born small for gestational age(Front. Endocrinol., (2022), 13, (975511), 10.3389/fendo.2022.975511)

Case report: a typical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum

Prenatal testing for imprinting disorders: A laboratory perspective

Collaborators (16)

Francesca Cogliati

Mohamad Maghnie

Sara Guzzetti

Laima Ambrozaityte

Rosanna Asselta

Pierpaola Tannorella

Niccolò Butti

Andrea Riccio

LUIGI TARANI

Timothy Yu

Letizia Straniero

José Ramón Fernández‐Fructuoso

Alessandro Mussa

roberta battini

Angela Sparago

Ashley Hurst

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