Author

Andreas Dalski

Christian-Albrechts-Universität zu Kiel

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

Frequent Co-Authors

Norbert BrüggemanniD· 2 shared Ai Huey TaniD· 1 shared Aleš MaveriD· 1 shared Alexander Erich VolkiD· 1 shared Alexander Maximilian MünchauiD· 1 shared Alexander Munchau· 1 shared Almuth CaliebeiD· 1 shared Amelie T. van der VeniD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Norbert BrüggemannORCID

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2 papers

Recent·Most cited

A coding CAG repeat expansion in EP400 causes Spinocerebellar Ataxia

Stijn V. Weckesser, Nataša Mišković, Mirja Thomsen, Marius Möller, Andona Milovanović, Frauke Hinrichs, Max Borsche, Andreas Dalski, Ana L. de Almeida Marcelino, Soren Franzenburg, Vladimir Kostić, Nikola D. Kresojević, Shen-Yang Lim, Sebastian Loens, Ana Marjanović, , 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.

medRxiv · Oct 21, 2026 · PreprintGenetic & Genomic Medicine

Evaluating Genome Sequencing Strategies: Trio, Singleton, and Standard Testing in Rare Disease Diagnosis

Daniel Kaschta, Christina Post, Franziska Gaass, Milad Al-Tawil, Vincent Arriens, Saranya Balachandran, Tobias Bäumer, Valerie Berge, Friederike Birgel, Andreas Dalski, Maike Dittmar, André Franke, Sören Franzenburg, Janina Fuß, Bettina Gehring, , Malte Spielmann

This study compares trio, singleton, and standard genome sequencing in rare disease diagnosis, finding trio sequencing has the highest diagnostic yield.

Genome Medicine · Sep 17, 2025Peer-reviewedGenetic & Genomic Medicine