Martin Krenn

23PUBLICATIONS
126CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesAutonomic nervous systemPeripheral nervous systemGene expression (incl. microarray and other genome-wide approaches)
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Publications (23)

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

|Sep 26, 2025
Screening for Congenital Myasthenic Syndromes in Adults With Seronegative Myasthenia Gravis Using Next-Generation Sequencing.

Martin Krenn, Matias Wagner, Helena Schuller

|Sep 05, 2025
AlphaMissense prediction for the evaluation of missense variants in the diagnostic setting of neuromuscular disorders.

Martin Krenn, Axel Schmidt, Matias Wagner

|Aug 05, 2025
The rs10191329 Risk Allele Is Associated With Pronounced Retinal Layer Atrophy in Multiple Sclerosis.

Gabriel Bsteh, Ruchi Tanavade, Nik Krajnc

|May 09, 2025
Holistic Exome-Based Genetic Testing in Adults With Epilepsy.

Martin Krenn, Matias Wagner, Karin Trimmel

|Apr 25, 2025
Expanding the Allelic and Clinical Heterogeneity of Movement Disorders Linked to Defects of Mitochondrial Adenosine Triphosphate Synthase.

Philip Harrer, Magdalena Krygier, Martin Krenn

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Frequent Collaborators

10 joint publications

Matias Wagner

5 joint publications

Jakob Rath

4 joint publications

Michael Zech

3 joint publications

Hakan Cetin