01 / Regulatory DNA
Reading the noncoding genome
How do enhancers and inherited variants shape leukemia risk? We use CRISPR screens and dense base editing to resolve regulatory function.
Vienna · St. Anna CCRI & CeMM
We combine genome engineering, functional genomics and chromatin biology to understand leukemia and uncover new vulnerabilities.
What we study
01 / Regulatory DNA
How do enhancers and inherited variants shape leukemia risk? We use CRISPR screens and dense base editing to resolve regulatory function.
02 / Transcriptional machinery
We study how co-activator complexes assemble, control chromatin and expose vulnerabilities in leukemia cells.
03 / Disease models
We use experimental hematology and genomics to model and understand pediatric leukemia.
Selected publications · 2026
Functional genomics
A tiled base editing strategy couples sequence changes to an allelic readout of regulatory activity.
Nature Communications · 2026 ↗

Chromatin biology
Loss of the SAGA CORE triggers collateral degradation of its acetyltransferase and reduces histone acetylation.
Nature Communications · 2026 ↗

Leukemia predisposition
The leukemia risk factor ARID5B links to HDAC mediated control of gene expression.
Nucleic Acids Research · 2026 ↗

The people behind the work
We are an international team in Vienna studying gene regulation, hematopoiesis and childhood cancer.