Author

Christoph Much

University of Lübeck

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Approach:experimental assay· 1 Approach:statistical model· 1

Frequent Co-Authors

Christine KleiniD· 2 shared Joanne TrinhiD· 2 shared Susen SchaakeiD· 2 shared Theresa LüthiD· 2 shared Anne GrünewaldiD· 1 shared Carolin GabbertiD· 1 shared Hansi WeißensteineriD· 1 shared Jan Olav AaslyiD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Christine KleinORCID

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2 papers

Recent·Most cited

Long-read sequencing enables high-accuracy mitochondrial heteroplasmy detection in Parkinson's disease

Theresa Lüth, Susen Schaake, Christoph Much, Mary Megan Belyea, Philip Seibler, Anne Grünewald, Patrick May, Christine Klein, Hansi Weißensteiner, Joanne Trinh

This study uses long-read sequencing to accurately detect low-frequency mitochondrial heteroplasmy in Parkinson's disease patients and carriers.

medRxiv · Jun 15, 2026 · PreprintGenetic & Genomic Medicine

GBA in Parkinson's disease: variant detection and pathogenicity scoring matters

Carolin Gabbert, Susen Schaake, Theresa Lüth, Christoph Much, Christine Klein, Jan Olav Aasly, Matthew James Farrer, Joanne Trinh

The paper evaluates Oxford Nanopore sequencing for detecting GBA variants in Parkinson's disease patients and controls, finding high true-positive rates and identifying two pathogenic variants.

medRxiv · Feb 3, 2023 · PreprintGenetic & Genomic Medicine