Silvia Morlino

5PUBLICATIONS
23CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)Epigenetics (incl. genome methylation and epigenomics)Gene mapping
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Publications (5)

|Jun 16, 2026
The evaluation of copy number variants in an unselected population of patients with inherited cardiac conditions: the INTERACTION study.

|Apr 30, 2025
Variant sub-tiering, disease-gene associations and strictness of clinical criteria improves the interpretation of variants of uncertain significance in hereditary cardiomyopathies and rhythm disorders.

Marco Castori, Sandra Mastroianno, Andrea Fontana

|Mar 06, 2024
Combined exome and whole transcriptome sequencing identifies a de novo intronic SRCAP variant causing DEHMBA syndrome with severe sleep disorder.

Silvia Morlino, Lorenzo Vaccaro, Maria Pia Leone

|Dec 29, 2020
Clinical presentation and molecular characterization of a novel patient with variant POC1A-related syndrome.

Silvia Majore, Emanuele Agolini, Lucia Micale

|Dec 22, 2020
Exon-Trapping Assay Improves Clinical Interpretation of COL11A1 and COL11A2 Intronic Variants in Stickler Syndrome Type 2 and Otospondylomegaepiphyseal Dysplasia.

Lucia Micale, Silvia Morlino, Annalisa Schirizzi

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Frequent Collaborators

3 joint publications

Marco Castori

2 joint publications

Lorenzo Vaccaro

2 joint publications

Antonio Novelli

2 joint publications

Emanuele Agolini