Paola Carrera

6PUBLICATIONS
33CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Major global burdens of diseaseGene and molecular therapyPersonality and individual differencesGene mapping
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Publications (6)

|Oct 28, 2023
Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights.

Anthony Frosio, Emanuele Micaglio, Ivan Polsinelli

|Oct 28, 2023
Combined Presence in Heterozygosis of Two Variant Usher Syndrome Genes in Two Siblings Affected by Isolated Profound Age-Related Hearing Loss.

Nica Borgese, Andrés Guillén-Samander, Sara Francesca Colombo

|Oct 09, 2023
Behavioral Phenotype, Electroclinical Features, and Treatment Options in Twins with Lrp2 Candidate Variants (Donnay-Barrow/Foar Syndrome).

Alessia Mingarelli, Giovanni Battista Pipitone, Giacomo Torini

|Jul 29, 2023
APC-Related Phenotypes and Intellectual Disability in 5q Interstitial Deletions: A New Case and Review of the Literature.

Flavia Privitera, Flavia Piccini, Maria Paola Recalcati

|Jun 10, 2023
Functional Characterisation of the Rare SCN5A p.E1225K Variant, Segregating in a Brugada Syndrome Familial Case, in Human Cardiomyocytes from Pluripotent Stem Cells.

Nicolò Salvarani, Giovanni Peretto, Crasto Silvia

|Dec 20, 2017
Surfactant proteins gene variants in premature newborn infants with severe respiratory distress syndrome.

Marco Somaschini, Silvia Presi, Maurizio Ferrari

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Frequent Collaborators

2 joint publications

Silvia Presi

1 joint publications

Nicolò Salvarani

1 joint publications

Giovanni Peretto

1 joint publications

Crasto Silvia