Publications

Baranzehi T, Kordi-Tamandani DM, Najafi M, Khajeh A, Schmidts M. Identification of a TPP1 Q278X Mutation in an Iranian Patient with Neuronal Ceroid Lipofuscinosis 2: Literature Review and Mutations Update. J Clin Med (2022). Kocylowski MK, Aypek H, Bildl W, Helmstädter M, Trachte P, …, Köttgen A, …, Huber TB, Fakler B, Grahammer F. A slit-diaphragm-associated protein network for dynamic control of renal filtration. Nat Commun (2022). Westermann L, Li Y, Göcmen B, Niedermoser M, Rhein K, …, Köttgen A, Köttgen M, Busch T. Wildtype heterogeneity contributes to clonal variability in genome edited cells. Sci Rep (2022). Bauer J, Köhler N, Maringer Y, Bucher P, Bilich T, …, Börries M, …, Rammensee HG, Hailfinger S, Walz JS. The oncogenic fusion protein DNAJB1-PRKACA can be specifically targeted by peptide-based immunotherapy in fibrolamellar hepatocellular carcinoma. Nat Commun (2022). Brombacher E, Hackenberg M, Kreutz C, Binder H, Treppner M. The performance of deep generative models for learning joint embeddings of single-cell multi-omics data. Front Mol Biosci (2022). Strohmeier V, Andrieux G, Unger S, Pascual-Reguant A, Klocperk A, …, Schell C, …, Börries M, Hasselblatt P, Warnatz K. Interferon-Driven Immune Dysregulation in Common Variable Immunodeficiency-Associated Villous Atrophy and Norovirus Infection. J Clin Immunol (2022). Rottmann FA, Breiden AK, Bemtgen X, Welte T, Supady A, Wengenmayer T, Staudacher DL. Levosimendan in acute heart failure with severely reduced kidney function, a propensity score matched registry study. Front Cardiovasc Med (2022). Bona A, Seifert M, Thünauer R, Zodel K, Frew IJ, Römer W, Walz G, Yakulov TA. MARVEL domain containing CMTM4 affects CXCR4 trafficking. Mol Biol Cell (2022). Yengo L, Vedantam S, Marouli E, Sidorenko J, Bartell E, …, Wuttke M, …, Köttgen A, …, Wood AR, Visscher PM, Hirschhorn JN. A saturated map of common genetic variants associated with human height. Nature (2022). Marinescu IM, Rogg M, Spohn S, von Büren M, Kamps M, …, Grosu AL, Schell C, Zamboglou C. Ex vivo γH2AX assay for tumor radiosensitivity in primary prostate cancer patients and correlation with clinical parameters. Radiat Oncol (2022). Milosavljevic J, Lempicki C, Lang K, Heinkele H, Kampf L, …, Walz G, Pollak M, Hermle T. Nephrotic Syndrome Gene TBC1D8B is Required for Endosomal Maturation and Nephrin Endocytosis in Drosophila. J Am Soc Nephrol (2022). Najafi M, Riedhammer KM, Rad A, Torbati PN, Berutti R, …, Köttgen A, Backofen R, Karimiani EG, Hoefele J, Schmidts M. High detection rate for disease-causing variants in a cohort of 30 Iranian pediatric steroid resistant nephrotic syndrome cases. Front Pediatr (2022). Chakraborty S, Andrieux G, Kastl P, Adlung L, Altamura S, …, Börries M, Busch H, Muckenthaler MU, Schilling M, Klingmüller U. Erythropoietin-driven dynamic proteome adaptations during erythropoiesis prevent iron overload in the developing embryo. Cell Rep (2022). Arnold F, Huzly D, Tanriver Y, Welte T. Response to SARS-CoV-2 vaccines in patients receiving B-cell modulating antibodies for renal autoimmune disease. BMC Infect Dis (2022). Sierks D, Schönauer R, Friedrich A, Hantmann E, de Fallois J, …, Bergmann C, Berg T, Halbritter J. Modelling polycystic liver disease progression using age-adjusted liver volumes and targeted mutational analysis. JHEP Rep (2022). Braig D, Runkel A, Eisenhardt AE, Schmid A, Zeller J, …, Kiefer J, Börries M, Eisenhardt SU. Individualized Mini-Panel Sequencing of ctDNA Allows Tumor Monitoring in Complex Karyotype Sarcomas. Int J Mol Sci (2022).