Federica Natacci

8PUBLICATIONS
37CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Medical biotechnology diagnostics (incl. biosensors)Epigenetics (incl. genome methylation and epigenomics)Cancer geneticsNeurology and neuromuscular diseases
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Publications (8)

|Sep 26, 2026
From Misdiagnosis to Discovery: Expanding the Spectrum of Spliceosomopathies.

|Jan 28, 2026
Prenatal Exome Sequencing: When Does Diagnostic Yield Meet Clinical Utility?

Alessia Carrer, Francesco Maria Crupano, Berardo Rinaldi

|Nov 27, 2024
Looks Can Be Deceiving: Diagnostic Power of Exome Sequencing in Debunking 15q11.2 Copy Number Variations.

Camilla Meossi, Alessia Carrer, Claudia Ciaccio

|Jun 14, 2024
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes.

Viviana Tritto, Paola Bettinaglio, Eleonora Mangano

|Aug 26, 2023
The Contribution of Oxidative Stress to NF1-Altered Tumors.

Elisabetta Kuhn, Federica Natacci, Massimo Corbo

|Jan 08, 2023
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort.

Rosina Paterra, Paola Bettinaglio, Arianna Borghi

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Frequent Collaborators

4 joint publications

Claudia Cesaretti

3 joint publications

Laura Pezzoli

3 joint publications

Marica Eoli

3 joint publications

Paola Riva