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)

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|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

12 joint publications

Allan Bayat

Nicola Specchio

Sarah Weckhuysen

Philip K Ahring

Johannes R Lemke

Pasquale Striano

Frequent Collaborators

27 joint publications

Elena Gardella

20 joint publications

Guido Rubboli

14 joint publications

Katrine Marie Johannesen

12 joint publications

Gaetan Lesca