Lisenka Vissers

39PUBLICATIONS
290CO-AUTHORS
NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Immunogenetics (incl. genetic immunology)
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Publications (39)

|Aug 18, 2026
Genome sequencing reveals high diagnostic yield in children with severe sporadic developmental language disorder.

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

|Jul 17, 2026
NKX2-1 Downstream Regulatory Structural Variants Explain a Substantial Proportion of Molecular Diagnoses in Patients With Benign Hereditary Chorea.

|Jun 26, 2026
Near-perfect genome sequencing in medical genetics.

|Sep 09, 2025
The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease.

Vicente A Yépez, German Demidov, Kornelia Ellwanger

|Jul 16, 2025
Complexome profiling showed impaired immunoproteasome assembly in a novel PRAAS subtype caused by monoallelic PSMB8 variants.

Robin Wijngaard, Caspar I van der Made, Sema Kalkan Uçar

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Frequent Collaborators

18 joint publications

Christian Gilissen

7 joint publications

Steven Laurie

7 joint publications

Holm Graessner

6 joint publications

Erik-Jan Kamsteeg