Nika Schuermans

3PUBLICATIONS
28CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Medical genetics (excl. cancer genetics)
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Publications (3)

|Jul 28, 2026
Consensus recommendations for next-generation sequencing-based genetic testing in Rare Neurological diseases.

|Oct 27, 2024
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses.

German Demidov, Burcu Yaldiz, José Garcia-Pelaez

|May 23, 2022
Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA).

Nika Schuermans, Dimitri Hemelsoet, Wim Terryn

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Frequent Collaborators

1 joint publications

German Demidov

1 joint publications

Burcu Yaldiz

1 joint publications

José Garcia-Pelaez

1 joint publications

Liedewei Van de Vondel