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Andrea Riccio

Professor of Genetics

University Name

Italy

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Research Interests

Obstetrics And Gynecology

30%

Cell Biology

50%

Medical Science

100%

Epigenetic

60%

Polycystic Ovary Syndrome

50%

Immunogenetics

30%

Prenatal Diagnosis

30%

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Articles17

New insights into oocyte cytoplasmic lattice-associated proteins

Article Link

Year:

2024

A maternal-effectPadi6variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos

Article Link

Year:

2024

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

Article Link

Year:

2024

Imprinting disorders

Article Link

Year:

2023

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

Article Link

Year:

2023

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

Article Link

Year:

2023

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

Article Link

Year:

2023

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

Article Link

Year:

2023

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

Article Link

Year:

2023

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

Article Link

Year:

2023

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

Article Link

Year:

2022

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

Article Link

Year:

2022

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

Article Link

Year:

2022

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.

Article Link

Year:

2022

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

Article Link

Year:

2022

Epigenetic Alterations in Inborn Errors of Immunity

Article Link

Year:

2022

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

Article Link

Year:

2021

Collaborators9

achille iolascon

Prof of Medical Genetics

ITALY

Pierpaola Tannorella

Istituto Auxologico Italiano

ITALY

LUIGI TARANI

ASSOCIATE PROFESSOR

Sapienza University of Rome

ITALY

Zeynep Tumer

Professor

University of Copenhagen

DENMARK

Guiomar Perez de Nanclares

SPAIN

Irene NETCHINE

Head of department and head of research team

Sorbonne Université Faculté de Médecine

FRANCE

Maria Monticelli

ITALY

Flavia CERRATO

Università degli Studi della Campania Luigi Vanvitelli

ITALY

Antonio M. GALVAO

Babraham Institute

UNITED KINGDOM

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Andrea Riccio

Professor of Genetics

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Research Interests

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Articles17

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

Collaborators9

achille iolascon

Pierpaola Tannorella

LUIGI TARANI

Zeynep Tumer

Guiomar Perez de Nanclares

Irene NETCHINE

Maria Monticelli

Flavia CERRATO

Antonio M. GALVAO

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