Katri Silvennoinen

11PUBLICATIONS
62CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Social epidemiologyGene mappingCircuits and systems
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Publications (11)

|Jul 13, 2026
Genetic testing among patients evaluated for epilepsy surgery.

|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

|Apr 06, 2023
Sex-based electroclinical differences and prognostic factors in epilepsy with eyelid myoclonia.

Emanuele Cerulli Irelli, Enrico Cocchi, Georgia Ramantani

|Apr 03, 2023
Widespread genomic influences on phenotype in Dravet syndrome, a 'monogenic' condition.

Helena Martins Custodio, Lisa M Clayton, Ravishankara Bellampalli

|Nov 18, 2022
Short- and long-interval intracortical inhibition in EPM1 is related to genotype.

Katri Silvennoinen, Laura Säisänen, Jelena Hyppönen

|Oct 29, 2022
The spectrum of epilepsy with eyelid myoclonia: delineation of disease subtypes from a large multicenter study.

Emanuele Cerulli Irelli, Enrico Cocchi, Georgia Ramantani

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Frequent Collaborators

8 joint publications

Sanjay M Sisodiya

7 joint publications

Simona Balestrini

3 joint publications

Reetta Kälviäinen

3 joint publications

Pasquale Striano