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Andrea Riccio

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Professor of Genetics

Italy

Research Interests

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Recent Grants

Grant: Close

Role of maternal effect genes and epimutations in Beckwith-Wiedemann syndrome and adverse reproductive outcomes

Open Date: 2023-01-01

Close Date: 2025-01-01

Grant: Close

Causes and mechanisms of genomic imprinting disturbances in Beckwith-Wiedemann syndrome and Wilms Tumor

Open Date: 2021-01-02

Close Date: 2024-04-01

Grant: Close

Pathways and mechanisms for maintainance and loss of genomic imprinting in somatic cells

Open Date: 2020-01-02

Close Date: 2021-04-01

Grant: Close

Molecular bases of the Beckwith-Wiedemann Syndrome and Silver-Russell Syndrome

Open Date: 2015-12-01

Close Date: 2019-11-30

Grant: Close

Studying Physiology and Pathology of Imprinted Genes to understand the role of Epigenetic Mutations in Human Disease

Open Date: 2012-01-01

Close Date: 2016-01-01

Articles (19)

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Collaborators (16)

achille iolascon

Prof of Medical Genetics

ITALY

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Giuliana Giardino

Ricercatore a tempo determinato - Tipologia B

Federico II University Hospital

ITALY

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Pierpaola Tannorella

Istituto Auxologico Italiano

ITALY

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LUIGI TARANI

ASSOCIATE PROFESSOR

Sapienza University of Rome

ITALY

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Zeynep Tumer

Clinical Professor

University of Copenhagen

DENMARK

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Guiomar Perez de Nanclares

Principal investigator

SPAIN

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Irene NETCHINE

Head of department and head of research team

Sorbonne Université Faculté de Médecine

FRANCE

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Emilio Di Maria

Associate Professor

Università degli Studi di Torino

ITALY

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Angela Sparago

Associate Professor

Università degli Studi della Campania Luigi Vanvitelli

ITALY

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Maria Monticelli

Associate Professor

ITALY

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Giuseppe Merla

Full professor

Università degli Studi di Napoli Federico II

ITALY

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Silvia Russo

Director

IRCCS Istituto Auxologico Italiano

ITALY

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Corrado Romano

Docenti di ruolo di IIa fascia

University of Catania

ITALY

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Flavia CERRATO

Università degli Studi della Campania Luigi Vanvitelli

ITALY

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Antonio M. GALVAO

Royal Veterinary College

UNITED KINGDOM

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Flavio Faletra

Docenti di ruolo di IIa fascia

University of Udine

ITALY

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Andrea Riccio

Research Interests

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Recent Grants

Articles (19)

Highly variable genomic methylation in the Beckwith-Wiedemann syndrome associated with multi-locus imprinting disturbances

Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans

New insights into oocyte cytoplasmic lattice-associated proteins

A maternal-effect<i>Padi6</i>variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos

Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors

Imprinting disorders

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

Co-Occurrence of Beckwith–Wiedemann Syndrome and Early-Onset Colorectal Cancer

ICF1-Syndrome-Associated DNMT3B Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming

A novel missense variant in CDK5RAP2 associated with non-obstructive azoospermia

Beckwith-Wiedemann syndrome and twinning: case report and brief review of literature

Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?

Different Mechanisms Cause Hypomethylation of Both <i>H19</i> and <i>KCNQ1OT1</i> Imprinted Differentially Methylated Regions in Two Cases of Silver–Russell Syndrome Spectrum

First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders.

Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques.

Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances.

Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences.

Epigenetic Alterations in Inborn Errors of Immunity

Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell Syndrome

Collaborators (16)

achille iolascon

Giuliana Giardino

Pierpaola Tannorella

LUIGI TARANI

Zeynep Tumer

Guiomar Perez de Nanclares

Irene NETCHINE

Emilio Di Maria

Angela Sparago

Maria Monticelli

Giuseppe Merla

Silvia Russo

Corrado Romano

Flavia CERRATO

Antonio M. GALVAO

Flavio Faletra

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