Rikke Steensjerre Moller

70PUBLICATIONS
430CO-AUTHORS
Characterisation of biological macromoleculesCircuits and systemsNeonatologyGene expression (incl. microarray and other genome-wide approaches)Other European languages
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Publications (70)

|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 22, 2026
Collapse of feed-forward inhibition underpins hyperexcitability in GABAA gain-of-function epilepsy.

|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

|Mar 13, 2026
Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant Classification.

Tobias Brünger, Ilona Krey, Suyeon Kim

|Feb 05, 2026
Mechanisms of SCN2A loss of function do not predict presence or phenotype of epilepsy.

Marsha Tan, Beatrice Southby Goad, Meagan Allen

|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

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Frequent Collaborators

27 joint publications

Elena Gardella

20 joint publications

Guido Rubboli

14 joint publications

Katrine Marie Johannesen

12 joint publications

Gaetan Lesca