Author

Marius Möller

University of LübeckORCID 0009-0005-9746-6804Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Assay:long-read sequencing· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Christine KleiniD· 2 shared Hauke S. BuschiD· 2 shared Katja LohmanniD· 2 shared Ai Huey TaniD· 1 shared Aleš MaveriD· 1 shared Alexander Munchau· 1 shared Ana L. de Almeida Marcelino· 1 shared Ana MarjanovićiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Christine KleinORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 21, 2026

A coding CAG repeat expansion in EP400 causes Spinocerebellar Ataxia

Stijn V. Weckesser, Nataša Mišković, Mirja Thomsen…·Katja Lohmann

This study identifies a CAG repeat expansion in EP400 as a novel cause of spinocerebellar ataxia in Serbian patients, with an inverse correlation between repeat number and age at onset.

DOI 10.64898/2026.10.16.26365393

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintAug 20, 2025

Complementarity of long-read sequencing and optical genome mapping in Parkinson's disease

André Fienemann, Theresa Lüth, Susen Schaake…·Joanne Trinh

This study compares long-read sequencing and optical genome mapping in detecting structural variants in Parkinson's disease, finding OGM better detects large variants while ONT provides high-resolution refinement.

DOI 10.1101/2025.08.20.25333965

humanlong-read sequencing

𝕏 PostBluesky