Claudia Wiese

This study identifies a direct physical and functional interaction between FBH1 and RAD54L, showing they cooperate to drive replication fork reversal.

This study shows that phosphorylation of RAD51AP1 at S277/282 regulates its function in homology-directed DNA repair, with phosphomimetic variants enhancing its activity.

This study identifies distinct roles of BRCA2's two DNA binding domains in DNA repair and replication fork stability using genetic and biochemical methods.

This study identifies TLK1-mediated phosphorylation of RAD54 at specific sites that regulate homologous recombination repair, with distinct effects on repair efficiency and cell survival.