Publications

Devane J, Ott E, Olinger EG, Epting D, Decker E, Friedrich A, Bachmann N, Renschler G, Eisenberger T, Briem-Richter A, Grabhorn EF, Powell L, Wilson IJ, Rice SJ, Miles CG, Wood K; Genomics England Research Consortium, Trivedi P, Hirschfield G, Pietrobattista A, Wohler E, Mezina A, Sobreira N, Agolini E, Maggiore G, Dahmer-Heath M, Yilmaz A, Boerries M, Metzger P, Schell C, Grünewald I, Konrad M, König J, Schlevogt B, Sayer JA, Bergmann C. Am J Hum Genet. 2022.  Progressive liver, kidney, and heart degeneration in children and adults affected by TULP3 mutations. Published 2022 May 5;109(5):928-943. doi: 10.1016/j.ajhg.2022.03.015. Epub 2022 Apr 8. PMID: 35397207

Lang-Meli, J., H. Luxenburger, K. Wild, V. Karl, V. Oberhardt, E. Salimi Alizei, A. Graeser, M. Reinscheid, N. Roehlen, D. B. Reeg, S. Giese, K. Ciminski, V. Gotz, D. August, S. Rieg, C. F. Waller, T. Wengenmayer, D. Staudacher, D. Huzly, B. Bengsch, G. Kochs, M. Schwemmle, F. Emmerich, T. Boettler, R. Thimme, M. Hofmann, and C. Neumann-Haefelin. 2022. SARS-CoV-2-specific T-cell epitope repertoire in convalescent and mRNA-vaccinated individuals. Nat Microbiol 7: 675-679. doi: 10.1038/s41564-022-01106-y.

Wan, R., M. Schieck, A. Caballero-Oteyza, W. Hofmann, A. V. Cochino, A. Shcherbina, R. Sherkat, C. Wache-Mainier, A. Fernandez, M. Sultan, T. Illig, B. Grimbacher, M. Proietti, and D. Steinemann. 2022. Copy Number Analysis in a Large Cohort Suggestive of Inborn Errors of Immunity Indicates a Wide Spectrum of Relevant Chromosomal Losses and Gains. J Clin Immunol 42: 1083-1092. doi: 10.1007/s10875-022-01276-8.

Boettler, T., B. Csernalabics, H. Salie, H. Luxenburger, L. Wischer, E. Salimi Alizei, K. Zoldan, L. Krimmel, P. Bronsert, M. Schwabenland, M. Prinz, C. Mogler, C. Neumann-Haefelin, R. Thimme, M. Hofmann, and B. Bengsch. 2022. SARS-CoV-2 vaccination can elicit a CD8 T-cell dominant hepatitis. J Hepatol 77: 653-659. doi: 10.1016/j.jhep.2022.03.040.

Masuda, T., L. Amann, G. Monaco, R. Sankowski, O. Staszewski, M. Krueger, F. Del Gaudio, L. He, N. Paterson, E. Nent, F. Fernandez-Klett, A. Yamasaki, M. Frosch, M. Fliegauf, L. F. P. Bosch, H. Ulupinar, N. Hagemeyer, D. Schreiner, C. Dorrier, M. Tsuda, C. Grothe, A. Joutel, R. Daneman, C. Betsholtz, U. Lendahl, K. P. Knobeloch, T. Lammermann, J. Priller, K. Kierdorf, and M. Prinz. 2022. Specification of CNS macrophage subsets occurs postnatally in defined niches. Nature 604: 740-748. doi: 10.1038/s41586-022-04596-2.

Susana Minguet, Alexander Nyström, Dimitra Kiritsi, Marta Rizzi. 2022. Inborn errors of immunity and immunodeficiencies: Antibody-mediated pathology and autoimmunity as a consequence of impaired immune reactions. Eur J Immunol, First published: 20 April 2022; doi.org/10.1002/eji.202149529

Schauer F, Nyström A, Kunz M, Hübner S, Scholl S, Athanasiou I, Alter S, Fischer J, Has C, Kiritsi D. 2022. Case Report: Diagnostic and Therapeutic Challenges in Severe Mechanobullous Epidermolysis Bullosa Acquisita. Front Immunol. 13:883967.  doi: 10.3389/fimmu.2022.883967.

Haimovici A, Höfer C, Badr MT, Bavafaye Haghighi E, Amer T, Boerries M, Bronsert P, Glavynskyi I, Fanfone D, Ichim G, Thilmany N, Weber A, Brummer T, Spohr C, Öllinger R, Janssen KP, Rad R, Häcker G. 2022. Spontaneous activity of the mitochondrial apoptosis pathway drives chromosomal defects, the appearance of micronuclei and cancer metastasis through the Caspase-Activated DNAse. Cell Death Dis. 2022 13(4):315. doi: 10.1038/s41419-022-04768-y.

Unberath, P., L. Mahlmeister, N. Reimer, H. Busch, M. Boerries, and J. Christoph. 2022. Searching of Clinical Trials Made Easier in cBioPortal Using Patients’ Genetic and Clinical Profiles. Appl Clin Inform 13: 363-369. doi: 10.1055/s-0042-1743560.

Wanner, N., G. Andrieux, I. M. P. Badia, C. Edler, S. Pfefferle, M. T. Lindenmeyer, C. Schmidt-Lauber, J. Czogalla, M. N. Wong, Y. Okabayashi, F. Braun, M. Lutgehetmann, E. Meister, S. Lu, M. L. M. Noriega, T. Gunther, A. Grundhoff, N. Fischer, H. Brauninger, D. Lindner, D. Westermann, F. Haas, K. Roedl, S. Kluge, M. M. Addo, S. Huber, A. W. Lohse, J. Reiser, B. Ondruschka, J. P. Sperhake, J. Saez-Rodriguez, M. Boerries, S. S. Hayek, M. Aepfelbacher, P. Scaturro, V. G. Puelles, and T. B. Huber. 2022. Molecular consequences of SARS-CoV-2 liver tropism. Nat Metab 4: 310-319. doi: 10.1038/s42255-022-00552-6.

Zeiser R, Warnatz K, Rosshart S, Sagar, Tanriver Y. 2022. GVHD, IBD and primary immunodeficiencies: The gut as a target of immunopathology resulting from impaired immunity. Eur J Immunol. 52(9):1406-1418. doi: 10.1002/eji.202149530.

Mossad, O., B. Batut, B. Yilmaz, N. Dokalis, C. Mezo, E. Nent, L. S. Nabavi, M. Mayer, F. J. M. Maron, J. M. Buescher, M. G. de Aguero, A. Szalay, T. Lammermann, A. J. Macpherson, S. C. Ganal-Vonarburg, R. Backofen, D. Erny, M. Prinz, and T. Blank. 2022. Gut microbiota drives age-related oxidative stress and mitochondrial damage in microglia via the metabolite N(6)-carboxymethyllysine. Nat Neurosci 25: 295-305

Flum, M., S. Dicks, Y. H. Teng, M. Schrempp, A. Nystrom, M. Boerries, and A. Hecht. 2022. Canonical TGFbeta signaling induces collective invasion in colorectal carcinogenesis through a Snail1- and Zeb1-independent partial EMT. Oncogene. pii: 10.1038/s41388-022-02190-4. doi: 10.1038/s41388-022-02190-4.

Vogelmann A, Schiedel M, Wössner N, Merz A, Herp D, Hammelmann S, Colcerasa A, Komaniecki G, Hong JY, Sum M, Metzger E, Neuwirt E, Zhang L, Einsle O, Groß O, Schüle R, Lin H, Sippl W, Jung M. 2022. Development of a NanoBRET assay to validate inhibitors of Sirt2-mediated lysine deacetylation and defatty-acylation that block prostate cancer cell migration. RSC Chem Biol 3(4):468-485. doi: 10.1039/d1cb00244a.

Erny, D., N. Dokalis, C. Mezo, O. Mossad, T. Blank, and M. Prinz. 2022. Flow-cytometry-based protocol to analyze respiratory chain function in mouse microglia. STAR Protoc 3: 101186.

Sharma, R., S. S. Sahoo, M. Honda, S. L. Granger, C. Goodings, L. Sanchez, A. Kunstner, H. Busch, F. Beier, S. M. Pruett-Miller, M. B. Valentine, A. G. Fernandez, T. C. Chang, V. Geli, D. Churikov, S. Hirschi, V. B. Pastor, M. Boerries, M. Lauten, C. Kelaidi, M. A. Cooper, S. Nicholas, J. A. Rosenfeld, S. Polychronopoulou, C. Kannengiesser, C. Saintome, C. M. Niemeyer, P. Revy, M. S. Wold, M. Spies, M. Erlacher, S. Coulon, and M. W. Wlodarski. 2022. Gain-of-function mutations in RPA1 cause a syndrome with short telomeres and somatic genetic rescue. Blood 139: 1039-1051