Elena Gardella

42PUBLICATIONS
251CO-AUTHORS
Medical molecular engineering of nucleic acids and proteinsCharacterisation of biological macromoleculesInfant and child healthNeonatologyGene expression (incl. microarray and other genome-wide approaches)
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Publications (42)

|Jun 02, 2026
Transfer learning enhances clinical utility of polygenic scores with small, phenotypically refined cohorts.

|Jun 02, 2026
Add-on treatment with vinpocetine reduces seizure frequency and improves comorbidities in patients with loss-of-function γ-aminobutyric acid type A receptor variants.

|Apr 28, 2026
Developmental and/or epileptic encephalopathy with spike-and-wave activation in sleep: Pathophysiological insights and treatment options.

|Apr 02, 2026
Neonatal developmental and epileptic encephalopathy with movement disorder and arthrogryposis: A shared phenotype across brain-expressed sodium channelopathies.

Sopio Gverdtsiteli, Sebastian Ortiz, Tobias Brünger

|Jan 28, 2026
Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variants.

Sebastian Ortiz, Leonardo Affronte, Chiara Bagliani

|Jan 13, 2026
Biallelic variants in CELSR1 cause brain malformations, neurodevelopmental disorders and epilepsy in humans.

Claudia M Bonardi, Rikke S Møller, Nuria Ruiz-Reig

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Frequent Collaborators

27 joint publications

Rikke Steensbjerre Møller

16 joint publications

Guido Rubboli

8 joint publications

Allan Bayat

8 joint publications

Gaetan Lesca