Davide Mei

26PUBLICATIONS
257CO-AUTHORS
NeurogeneticsNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Cancer genetics
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Journal

Publications (26)

|Aug 22, 2026
A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

|Aug 20, 2026
Biallelic protein truncating EXOSC6 variants cause a neurodevelopmental disorder with cerebellar atrophy, ataxia, and global developmental delay.

|Aug 06, 2026
Associations of Cortical and Subcortical White Matter Morphometric Abnormalities With Clinical and Genetic Findings in STXBP1 Encephalopathy.

|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

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Frequent Collaborators

16 joint publications

Renzo Guerrini

7 joint publications

Simona Balestrini

6 joint publications

Elena Parrini

4 joint publications

Nicola Specchio