Giovanni Battista Ferrero

29PUBLICATIONS
174CO-AUTHORS
NeurogeneticsNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Gene mappingGene expression (incl. microarray and other genome-wide approaches)
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Publications (29)

|Jul 08, 2026
The NeuroWES project: lessons learned from comprehensive phenotyping and genetic analysis of neurodevelopmental disorders over a decade.

|Mar 26, 2026
DNA methylation signature and clinical delineation of PACS1-related disorder in 24 unreported individuals.

Quentin Sabbagh, Camille Cenni, Sadegheh Haghshenas

|Feb 09, 2026
Additive effect of multiple genetic variants in SEC23B and PIEZO1 on iron metabolism dyshomeostasis in hereditary anemias.

Antonella Nostroso, Roberta Marra, Barbara Eleni Rosato

|Jan 08, 2026
Domain-specific phenotypic profiles in RAF1-related Noonan syndrome.

Andrea Gazzin, Marta Calvo, Federico Rondot

|Dec 30, 2025
Systems-Level Integration of Multi-Omics Identifies Genetic Modifiers of TANGO2 Deficiency Disorder.

Manuel Airoldi, Heather Bondi, Veronica Remori

|Oct 29, 2025
Expanding Clinical and Genetic Landscape of SATB2-Associated Syndrome.

Verdiana Pullano, Federico Rondot, Ilaria Carelli

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Frequent Collaborators

12 joint publications

Diana Carli

10 joint publications

Alfredo Brusco

9 joint publications

Alessandro Mussa

9 joint publications

Marco Tartaglia