Research program
02Replication Stress & Genome Stability
Understanding how transcription, replication, and DNA repair intersect in cancer.

We investigate transcription-replication conflicts and replication stress, and how cancer cells engage DNA-damage signaling and repair pathways to survive these challenges.
- Transcription-Replication Conflicts
- ABL1
- Replication Stress
- Replication Forks
- DNA Repair
- Chromatin

Key publications
ABL kinase inactivation induces transcription-replication conflicts and impairs replication fork progression in metastatic small cell lung cancer
Multifaceted roles of PDS5B in RAD51-dependent homology-directed DNA repair and replication fork protection
DSS1 restrains BRCA2's engagement with dsDNA for homologous recombination, replication fork protection, and R-loop homeostasis