Matias Wagner

67PUBLICATIONS
570CO-AUTHORS
Gene and molecular therapyNanomanufacturingEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesInfant and child health
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Publications (67)

|Oct 08, 2026
KCNA2-Associated Hereditary Spastic Paraplegia: Clinical Characteristics and Rationale for Targeted Treatment.

|Sep 08, 2026
Pathogenicity of NUSAP1 Variants Is Defined by NMD-Escape: Evidence From Two Novel Cases and Systematic Population-Based Variant Analysis.

|Aug 28, 2026
Rare genetic variation in adults with surgically treated temporal lobe epilepsy: An exome sequencing study.

|Aug 14, 2026
Splice effect of a synonymous variant in AP4B1: multiomics approach establishes the diagnosis in two sisters with spastic paraplegia.

|Jun 11, 2026
Epilepsy surgery in pediatric patients with complex COL4A1/2-associated epilepsy.

|May 27, 2026
Prominent Movement Disorders in RNU2-2-Related Spliceosomopathy.

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Frequent Collaborators

15 joint publications

Theresa Brunet

11 joint publications

Martin Krenn

10 joint publications

Melanie Brugger

9 joint publications

Michael Zech