Researcher Database

243 researchers found.

Name Site Program Email / Phone
Dr. Malte von Bonin Dresden CI malte.bonin@uniklinikum-dresden.de Details
Prof. Dominik von Elverfeldt Freiburg ROI dominik.elverfeldt@uniklinik-freiburg.de Details
Prof.Dr. med. Juliane Walz Tubingen SoO, CI juliane.walz@med.uni-tuebingen.de Details
Prof. Dr. Alexander Weber Tubingen EOM, CI alexander.weber@uni-tuebingen.de Details
Prof. Dr. Wolfgang Weber Munich ROI w.weber@tum.de Details
Prof. Dr. med. Oliver Weigert Munich EOM oliver.weigert@med.uni-muenchen.de Details
Prof. Dr. med. Jürgen Weitz, MSc. Dresden EOM, MDEB, MTT juergen.weitz@uniklinikum-dresden.de Details
Prof. Dr. Winfried Wels Frankfurt/Mainz CI wels@em.uni-frankfurt.de Details
Prof. Dr. Martin Werner Freiburg MDEB, MTT direktion-pathologie@uniklinik-freiburg.de Details
Dr. med. Benedikt Westphalen Munich MDEB, MTT cwestpha@med.lmu.de Details
Prof. Dr. Wolfgang Wick Heidelberg CCP, MDEB, MTT Wolfgang.Wick@med.uni-heidelberg.de Details
Prof. Dr. Gerald Willimsky Berlin CI gerald.willimsky@charite.de / +49 30 450 513 607 Details
Prof. Dr. Pauline Wimberger Dresden EOM, MDEB, MTT frauenklinik@uniklinikum-dresden.de Details
Prof. Dr. Olaf Witt Heidelberg MTT o.witt@dkfz-heidelberg.de Details
Prof. Dr. Barbara Wollenberg Munich EOM, CI barbara.wollenberg@tum.de Details
Prof. Maxim Zaitsev Freiburg ROI maxim.zaitsev@uniklinik-freiburg.de Details
Prof. Robert Zeiser Freiburg MTT robert.zeiser@uniklinik-freiburg.de Details
Prof. Lars Zender Tubingen EOM, MTT lars.zender@med.uni-tuebingen.de Details

DKTK Junior Group Leader for Cancer Systems Biology

Single-cell approaches have not only revealed a wide variety of cell states, characterized by cells exhibiting striking differences in their transcriptional profile, but have also illuminated the mechanisms underlying state transitions in health and disease. Cellular plasticity and adaptive state changes have recently emerged as a basis for therapeutic resistance in cancer, and a better understanding of how cell state transitions are regulated is critical to develop therapeutic approaches that can overcome therapy resistance. 

Our research focuses on understanding the mechanisms driving non-genetic cellular heterogeneity and therapy resistance in malignancy. Using novel single-cell sequencing approaches, we seek to develop new experimental and computational strategies to define altered cell states in both, cancer and immune cells. Our aim is to leverage a data driven strategy combined with single cell genomics and systems biology to address the challenges posed by heterogeneity in cancer, and to develop new strategies to overcome it, with the aim of translating laboratory-based findings into the clinic.