Matias Wagner

65PUBLICATIONS
554CO-AUTHORS
NanomanufacturingEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesInfant and child healthGene expression (incl. microarray and other genome-wide approaches)
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Publications (65)

|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.

|Feb 02, 2026
Fibroblast Transcriptomics in Molecular Diagnostics of a Comprehensive Dystonia Cohort.

Alice Saparov, Ivana Dzinovic, Theresa Brunet

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Frequent Collaborators

15 joint publications

Theresa Brunet

10 joint publications

Martin Krenn

10 joint publications

Melanie Brugger

8 joint publications

Michael Zech