Joachim Jankowski
Professor
Joachim Jankowski is an internationally recognised scientist whose pioneering work has substantially advanced vascular biology, molecular cardiovascular and cardiorenal research. He currently serves as Professor and Director of the Institute for Molecular Cardiovascular Research (IMCAR) at University Hospital RWTH Aachen. Before joining RWTH Aachen, he pursued a highly productive academic career in research and teaching at Charité - Universitätsmedizin Berlin. Trained in the natural sciences and holding a doctorate (Dr. rer. nat.), he has established internationally visible expertise in chromatographic separation, mass spectrometry and advanced analytical methods for isolating, identifying and functionally characterising endogenous cardiovascular mediators. His research bridges analytical biochemistry, nephrology, vascular biology and cardiovascular medicine and has generated new mechanistic concepts, biomarkers, therapeutic targets and treatment strategies for chronic kidney and cardiovascular disease. He has established highly visible interdisciplinary and international collaborations and successfully coordinated major research networks, including the DFG-funded SFB/TRR219 and SFB1739, as well as Marie Skłodowska-Curie Innovative Training Networks CaReSyAn (Aachen) and Lipidbrigt (UM). Joachim is founder of the “Aachen-Maastricht Institute for Cardiorenal research (AMICARE). Through his scientific leadership, translational focus and strong commitment to mentoring, he has made lasting contributions to cardiorenal research in Europe.
His research focuses on the molecular mechanisms linking chronic kidney disease to cardiovascular disease and other systemic disorders. Key topics include uremic toxins, post-translational protein modifications, vasoactive peptides, vascular calcification, cardiac remodeling, inflammation and inter-organ crosstalk. The laboratory combines high-resolution mass spectrometry, proteomics, peptidomics, metabolomics, lipidomics and mass-spectrometry imaging with cell and animal models and deeply phenotyped patient cohorts. The overarching goal is to identify causal mediators, clinically useful biomarkers and new therapeutic targets. Current work is embedded in major collaborative programs, including the DFG-funded SFB/TRR219 on cardiovascular complications in chronic kidney disease, SFB1739 on periodontal remodeling in systemic disease, SFB1382 on gut-liver communication, and KFO5011/InteraKD on acute kidney injury. Additional projects address peptide-based therapies, prevention of pathogenic protein modifications and multi-omics strategies for precision medicine in kidney and cardiovascular disease.




