Evelin Schröck
8PUBLICATIONS
99CO-AUTHORS
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Publications (8)
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|Nov 10, 2025
Targeted therapy in patients with genetic tumor syndromes.Arne Jahn, Christoph Heining, Stefan Fröhling
|Jun 24, 2025
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.Axel Schmidt, Magdalena Danyel, Kathrin Grundmann
|Apr 03, 2025
Long-read genome and RNA sequencing resolve a pathogenic intronic germline LINE-1 insertion in APC.Alexandra A Baumann, Lisanne I Knol, Marie Arlt
|Jul 22, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.Axel Schmidt, Magdalena Danyel, Kathrin Grundmann
|Mar 16, 2024
Author Correction: Proteogenomic analysis reveals RNA as a source for tumor-agnostic neoantigen identification.Celina Tretter, Niklas de Andrade Krätzig, Matteo Pecoraro
|Oct 26, 2023
NCT/DKFZ MASTER handbook of interpreting whole-genome, transcriptome, and methylome data for precision oncology.Andreas Mock, Maria-Veronica Teleanu, Simon Kreutzfeldt
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Frequent Collaborators
4 joint publications
Stefan Fröhling
3 joint publications
Barbara Klink
2 joint publications
Sebastian Ochsenreither
2 joint publications
Karl Hackmann
2 joint publications
Celina Tretter
2 joint publications
Niklas de Andrade Krätzig
2 joint publications
Sebastian Lange
2 joint publications
Johannes Untch
2 joint publications
Gabriela Zuleger
2 joint publications
Mathias Wilhelm
