
We investigate the generation and functional consequences of somatic mosaicism within tissues, with a focus on variation in the mitochondrial DNA. By mapping genotype-to-phenotype relationships, we study how mutations shape cellular behavior in both health and disease.

We develop and apply single-cell genomics and transcriptomics tools to dissect complex tissues at high resolution – focusing on joint measurements of DNA and RNA. These technologies enable the identification of rare events, clonal dynamics, and the genetic diversity.

We employ human intestinal organoids and cancer models to study human disease-relevant processes. These models enable mapping of the molecular and cellular phenotypes directly in human tissue biology, bridging the gap between experimental studies and clinical relevance.

We want you!

We're recruiting
We are looking for motivated students interested in exploring how genetic variation shapes cellular function.
We welcome students from diverse backgrounds, including:
In the lab, you will have the opportunity to:
If you are interested in joining the lab, please send a short statement of interest and your CV.