Research

Publications

Müller M, Zodel K, Abhari BA, Cuomo F, Nizamuddin S, Metzger P, Boerries MTimmers HTMFrew IJ. KDM5C and KDM5D mutations have different consequences in clear cell renal cell carcinoma cells. Commun Biol (2025). Pal J, Riester M, Ganner A, …, Frew IJ, Kotsis F, Neumann-Haefelin E, Spang A, Diederichs S. Nonstop mutations cause loss of renal tumor suppressor proteins VHL and BAP1 and affect multiple stages of protein translation. Sci Adv (2025). Felixberger PT, Andrieux G, Maul-Pavicic A, …, Boerries M, Nitschke L, Voll RE, Warnatz K, Keller B. CD21low B cells reveal a unique glycosylation pattern with hypersialylation and hyperfucosylation. Front Immunol (2025). Schumann A, Garbade SF, Beblo S, …, Thimm E, Weinhold N, Williams M, Wortmann S, Grünert SC. Kidney involvement in glycogen storage disease type I: Current knowledge and key challenges. Mol Genet Metab (2025). Braun LM, Giesler S, Andrieux G, …, Boerries M, …, Schell C, …, Becher B, Funke-Lorenz C, Placke JM, Apostolava P, Zeiser R. Adiponectin reduces immune checkpoint inhibitor-induced inflammation without blocking anti-tumor immunity. Cancer Cell (2025). Li MJ, Meyer LC, Meier N, Wittke J, Maldacker M, Seredynska A, Schueler J, Schilling O, Föll MC. Spatial Proteomics by Parallel Accumulation-Serial Fragmentation Supported MALDI MS/MS Imaging: A First Glance Into Multiplexed and Spatial Peptide Identification. Rapid Commun Mass Spectrom (2025). König L, Schmidts M. The role of chromatin-related epigenetic modulations in CAKUT. Curr Top Dev Biol (2025). Stölting G, Hellmig N, Dinh HA, Butz F, Secener AK, Volkert M, Scholl UI. Expression and function of Connexin 43 and Connexin 37 in the murine zona glomerulosa. Physiol Rep (2025). Brombacher E, Schilling O, Kreutz C. Characterizing the omics landscape based on 10,000+ datasets. Sci Rep (2025). Scherer N, Fässler D, Borisov O, Cheng Y, Schlosser PWuttke M, …, Sekula P, Hoppmann A, Schultheiss UT, …, Schmidts, Köttgen M, …, Grünert SC, Estrada K, Thiele I, Hertel J, Köttgen A. Coupling metabolomics and exome sequencing reveals graded effects of rare damaging heterozygous variants on gene function and human traits. Nat Genet (2025).