Vincenzo Nigro

14PUBLICATIONS
97CO-AUTHORS
Immunogenetics (incl. genetic immunology)Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Medical infection agents (incl. prions)Neurogenetics
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Publications (14)

|Jul 31, 2026
A novel ZNF699 mutation in a patient with DEGCAGS syndrome and severe B cell depletion.

|Jul 06, 2026
KCTD3 deficiency disrupts axon initial segment organization and neurite outgrowth in a neurodevelopmental disorder mouse model.

|Oct 23, 2025
Reanalysis of Undiagnosed Neurodevelopmental Disorder Cases: From RNU4-2 Variants to Clinical Phenotypes.

Pasquale Di Letto, Chiara De Leonibus, Francesca Pia Palmieri

|May 15, 2025
Deletion Testing of the DEGS1 Gene Should Be Part of the Diagnostic Pipeline for Hypomyelinating Leukodystrophy (HLD18).

Mariateresa Zanobio, Francesca Nardecchia, Gerarda Cappuccio

|Jun 10, 2023
Alu-Mediated Insertions in the DMD Gene: A Difficult Puzzle to Interpret Clinically.

Annalaura Torella, Alberto Budillon, Mariateresa Zanobio

|Apr 24, 2023
Neurologic, Neuropsychologic, and Neuroradiologic Features of EBF3-Related Syndrome.

Claudia Ciaccio, Chiara Pantaleoni, Marco Moscatelli

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Frequent Collaborators

5 joint publications

Giulio Piluso

4 joint publications

Nicola Brunetti-Pierri

4 joint publications

Annalaura Torella

3 joint publications

Mariateresa Zanobio