Katrine Marie Johannesen

23PUBLICATIONS
106CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Cancer geneticsSystem and network securityNeurology and neuromuscular diseasesPsychology of ageing
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Publications (23)

|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

|Jan 10, 2025
A Novel Case of Biallelic MLH3 Variants in a Patient With Rectal Cancer and Polyps.

Katrine M Johannesen, John Gásdal Karstensen, Andreas Ørslev Rasmussen

|Oct 03, 2024
Sleep disturbances in SCN8A-related disorders.

Francesca Furia, Katrine M Johannesen, Claudia M Bonardi

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

Claudia Cuccurullo, Emanuele Cerulli Irelli, Lorenzo Ugga

|Jun 05, 2024
Genetic testing in adults with developmental and epileptic encephalopathy - what do we know?

Ilona Krey, Kathrine M Johannesen, Oona Kohnen

|Sep 26, 2023
Solving the unsolved genetic epilepsies: Current and future perspectives.

Katrine M Johannesen, Zeynep Tümer, Sarah Weckhuysen

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Frequent Collaborators

14 joint publications

Rikke Steensjerre Moller

7 joint publications

Guido Rubboli

7 joint publications

Elena Gardella

3 joint publications

Katherine L Helbig