Pino D'Ambrosio

3PUBLICATIONS
26CO-AUTHORS
Paediatrics not elsewhere classifiedEpigenetics (incl. genome methylation and epigenomics)Respiratory diseases
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Publications (3)

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|Aug 27, 2026
A Clinical Genetics-Driven Dual Diagnosis of Prader-Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL.

|Apr 26, 2025
Clinical-Genetic Approach to Conditions with Macrocephaly and ASD/Behaviour Abnormalities: Variants in PTEN and PPP2R5D Are the Most Recurrent Gene Mutations in a Patient-Oriented Diagnostic Strategy.

Federica Francesca L'Erario, Annalisa Gazzellone, Ilaria Contaldo

|Dec 17, 2024
Sex-Specific HLA Alleles Contribute to the Modulation of COVID-19 Severity.

Serena Spartano, Maria Vittoria Faggiano, Giovanna Guidi

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Frequent Collaborators

2 joint publications

Marcella Zollino

2 joint publications

Maria Grazia Pomponi

1 joint publications

Serena Spartano

1 joint publications

Agnese Novelli

1 joint publications

Lorenza Lambertenghi

1 joint publications

Alessandro Visentin

1 joint publications

Annamaria Azzini

1 joint publications

Enrico Maria Trecarichi

1 joint publications

Antonio Liguori

1 joint publications

Massimo Fantoni

Frequent Collaborators

2 joint publications

Marcella Zollino

2 joint publications

Maria Grazia Pomponi

1 joint publications

Serena Spartano

1 joint publications

Agnese Novelli

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