Davide Mei

23PUBLICATIONS
240CO-AUTHORS
Regenerative medicine (incl. stem cells)Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Neurogenetics
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Publications (23)

|Jan 06, 2026
Author Correction: The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease.

Vicente A Yépez, German Demidov, Kornelia Ellwanger

|Dec 26, 2025
DNAJC12 Disease: Clinical Spectrum and Long-Term Outcomes.

Filippo Manti, Giacomina Ricciardi, Francesca Nardecchia

|Oct 25, 2025
Clinical and genetic landscape of epilepsies with absence seizures and single-gene etiology.

Simona Balestrini, Ilaria Galli, Maria Luisa Ricci

|Sep 09, 2025
The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease.

Vicente A Yépez, German Demidov, Kornelia Ellwanger

|Jan 29, 2025
Fibroblast transcriptomics uncovers pathogenic genomic variants in individuals with exome-negative childhood onset epilepsy.

Noor Smal, Charissa Millevert, Matthias De Wachter

|Nov 29, 2024
National survey on the prevalence of single-gene aetiologies for genetic developmental and epileptic encephalopathies in Italy.

Davide Mei, Simona Balestrini, Elena Parrini

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Frequent Collaborators

14 joint publications

Renzo Guerrini

6 joint publications

Simona Balestrini

5 joint publications

Elena Parrini

4 joint publications

Anne-Sophie Denommé-Pichon