Federica Ruscitti
4PUBLICATIONS
45CO-AUTHORS
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Publications (4)
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|Apr 09, 2026
Identification of an episignature for CHD3-related Snijders Blok-Campeau syndrome reveals heterogeneity in the CHARGE syndrome episignature: towards a better characterisation of chromatinopathies.Amandine Santini, Angelo Tognon, Anne-Claire Richard
|Dec 13, 2024
Advances and Challenges in Prenatal Detection and Genetic Diagnosis of Upper Limb Anomalies: Analysis of a South London and Kent Cohort.Federica Ruscitti, Tara Giacchino, Lemonia Koutoulas
|Oct 14, 2022
A case of Huntington disease-like 2 in a patient of African ancestry: the everlasting support of clinical examination in the molecular era.Federica Ruscitti, Paola Origone, Giulia Rosti
|Jun 25, 2022
An example of parenchymal renal sparing in the context of complex malformations due to a novel mutation in the PBX1 gene.Federica Ruscitti, Maria Cerminara, Maria Iascone
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Frequent Collaborators
1 joint publications
Giulia Rosti
1 joint publications
Lucia Trevisan
1 joint publications
Paola Mandich
1 joint publications
Amandine Santini
1 joint publications
Angelo Tognon
1 joint publications
Guillaume Velasco
1 joint publications
Gilles Phan
1 joint publications
Pauline Marzin
1 joint publications
Fabien Maury
1 joint publications
Caroline Michot
