Author

Christina Vossler-Wolf

University of Tübingen

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· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Amelie T. van der VeniD· 1 shared An‐Sofie SchoonjansiD· 1 shared Andrea Rueegger· 1 shared Anna Esteve‐CodinaiD· 1 shared Anna JanseniD· 1 shared Anne Schulz· 1 shared Barbara CastellottiiD· 1 shared Bernd Axel NeubaueriD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Amelie T. van der VenORCID

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1 paper

Recent·Most cited

Long-read genome sequencing resolves complex structural variants in exome-negative developmental and epileptic encephalopathy

Joohyun Park, Zakaria Eddafir, Josua Kegele, Davide Mei, Noor Smal, Christina Vossler-Wolf, Kornelia Ellwanger, Charissa Millevert, Merel Swinnen, Robert J. Lauerer, Heidi Loeffler, Thomas Ott, German M. Demidov, Michael Alber, Francesca Bisulli, , Holger Lerche

This study evaluates the diagnostic value of long-read genome sequencing in DEE patients, finding it particularly effective for resolving complex structural variants not detected by short-read sequencing.

medRxiv · Oct 28, 2026 · PreprintGenetic & Genomic Medicine