Vienna · St. Anna CCRI & CeMM

Decoding gene regulation in childhood cancer.

We combine genome engineering, functional genomics and chromatin biology to understand leukemia and uncover new vulnerabilities.

What we study

Our research

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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.

02 / Transcriptional machinery

Dissecting the SAGA complex

We study how co-activator complexes assemble, control chromatin and expose vulnerabilities in leukemia cells.

03 / Disease models

Connecting mechanism to disease

We use experimental hematology and genomics to model and understand pediatric leukemia.

Selected publications · 2026

Recent discoveries

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Functional genomics

Mapping enhancers one nucleotide at a time

A tiled base editing strategy couples sequence changes to an allelic readout of regulatory activity.

Nature Communications · 2026   ↗

First page of Nucleotide-resolution mapping of regulatory elements via allelic readout of tiled base editing
PDF first page · Open paper ↗

Chromatin biology

Disrupting SAGA destabilizes KAT2A

Loss of the SAGA CORE triggers collateral degradation of its acetyltransferase and reduces histone acetylation.

Nature Communications · 2026   ↗

First page of Disruption of the SAGA CORE triggers collateral degradation of KAT2A
PDF first page · Open paper ↗

Leukemia predisposition

ARID5B coordinates transcriptional repression

The leukemia risk factor ARID5B links to HDAC mediated control of gene expression.

Nucleic Acids Research · 2026   ↗

First page of Leukemia risk factor ARID5B coordinates HDAC-mediated transcriptional repression
PDF first page · Open paper ↗

The people behind the work

We hunt for mechanisms that explain disease

We are an international team in Vienna studying gene regulation, hematopoiesis and childhood cancer.

Meet the team ↗

St. Anna Children’s Cancer Research Institute · CeMM