Matias Wagner

62PUBLICATIONS

545CO-AUTHORS

Infant and child healthNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Major global burdens of diseaseLife histories

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Publications (62)

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|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

|Nov 15, 2025

The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency.

Kajus Merkevicius, Dmitrii Smirnov, Lea D Schlieben

|Oct 07, 2025

Mutations in the Key Autophagy Tethering Factor EPG5 Link Neurodevelopmental and Neurodegenerative Disorders Including Early-Onset Parkinsonism.

Hormos Salimi Dafsari, Celine Deneubourg, Kritarth Singh

|Oct 01, 2025

Integrating Long-Read Nanopore Sequencing for Precision Resolution of Genomic Variants in Dystonia.

Ugo Sorrentino, Martin Pavlov, Nazanin Mirza-Schreiber

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Frequent Collaborators

13 joint publications

Theresa Brunet

Martin Krenn

Melanie Brugger

Dominik S Westphal

Michael Zech

Jakob Rath

Henry Houlden

Felix Distelmaier

Korbinian Maria Riedhammer

4 joint publications

Frederic Tran Mau-Them

Frequent Collaborators

13 joint publications

Theresa Brunet

9 joint publications

Martin Krenn

9 joint publications

Melanie Brugger

6 joint publications

Dominik S Westphal