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Andrea Riccio

16PUBLICATIONS

49CO-AUTHORS

Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Genetic immunologyCancer therapy (excl. chemotherapy and radiation therapy)Bioinformatic methods development

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Publications (16)

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|Mar 28, 2024

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

Francesca Cillo, Emma Coppola, Federico Habetswallner

|Mar 07, 2024

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.

Carlo Giaccari, Francesco Cecere, Lucia Argenziano

|Dec 23, 2023

ICF1-Syndrome-Associated <i>DNMT3B</i> Mutations Prevent De Novo Methylation at a Subset of Imprinted Loci during iPSC Reprogramming.

Ankit Verma, Varsha Poondi Krishnan, Francesco Cecere

|Jun 29, 2023

Imprinting disorders.

Thomas Eggermann, David Monk, Guiomar Perez de Nanclares

|Apr 13, 2023

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

Francesco Cecere, Laura Pignata, Bruno Hay Mele

|Feb 11, 2023

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

Maria Luca, Diana Carli, Simona Cardaropoli

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Frequent Collaborators

7 joint publications

Flavia Cerrato

6 joint publications

Laura Pignata

4 joint publications

Orazio Palumbo

3 joint publications

Francesco Cecere

3 joint publications

Angela Sparago

2 joint publications

Bruno Hay Mele

2 joint publications

Massimo Carella

2 joint publications

Giuseppe Merla

2 joint publications

Silvia Russo

2 joint publications

Claudia Angelini

Frequent Collaborators

7 joint publications

Flavia Cerrato

6 joint publications

Laura Pignata

4 joint publications

Orazio Palumbo

3 joint publications

Francesco Cecere

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