Laura Licchetta

18PUBLICATIONS
106CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Lexicography and semanticsForensic epidemiology
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Publications (18)

|Jul 04, 2026
Diagnostic yield and copy number variants findings in 219 adult patients with developmental and epileptic encephalopathy.

|Jul 03, 2026
Expanding the electroclinical spectrum of TANC2-related disorders: Lennox-Gastaut syndrome and related developmental epileptic phenotypes.

|Dec 06, 2025
Early neurological symptoms and epilepsy outcomes in individuals with the recurrent GABRG2 p.(Ala106Thr) gain-of-function variant: Structural and phenotypic insights.

Sebastian Ortiz, Chiara Bagliani, Susan X N Lin

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

Simona Balestrini, Ilaria Galli, Maria Luisa Ricci

|Sep 26, 2025
The challenge of ultra-rarity: Dual diagnosis of Lafora disease and developmental encephalopathies linked to TRIO and SHANK3 pathogenic variants.

Lorenzo Muccioli, Francesca Bisulli, Raffaella Minardi

|Jul 02, 2024
Clinical features and genotype-phenotype correlations in epilepsy patients with de novo DYNC1H1 variants.

Claudia Cuccurullo, Emanuele Cerulli Irelli, Lorenzo Ugga

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Frequent Collaborators

14 joint publications

Francesca Bisulli

6 joint publications

Lorenzo Muccioli

3 joint publications

Antonietta Coppola

3 joint publications

Raffaella Minardi