Universität zu Köln

Burgmaier, Kathrin ORCID: 0000-0001-9787-1096, Kilian, Samuel, Arbeiter, Klaus, Atmis, Bahriye, Boyer, Olivia ORCID: 0000-0002-3957-1359, Buescher, Anja, Dursun, Ismail, Erger, Florian ORCID: 0000-0002-2768-1702, Fila, Marc ORCID: 0000-0001-8857-7100, Galiano, Matthias, Gokce, Ibrahim, Haeffner, Karsten, Haffner, Dieter, Hooman, Nakysa, Klaus, Guenter, König, Jens, Lange-Sperandio, Bärbel ORCID: 0000-0001-8898-3459, Marlais, Matko, Massella, Laura, Mekahli, Djalila, Miklaszewska, Monika, Miloševski-Lomić, Gordana, Obrycki, Lukasz ORCID: 0000-0002-5134-8643, Ranchin, Bruno ORCID: 0000-0001-9073-4662, Seitz, Barbara, Stabouli, Stella ORCID: 0000-0001-9843-8198, Tabel, Yilmaz, Taranta-Janusz, Katarzyna, Weber, Lutz Thorsten ORCID: 0000-0003-4116-598X, Weitz, Marcus, Wühl, Elke ORCID: 0000-0002-1205-2620, Yilmaz, Alev, Dötsch, Jörg ORCID: 0000-0003-1529-7647, Schaefer, Franz, Liebau, Max Christoph ORCID: 0000-0003-0494-9080, Akinci, Nurver, Eid, Loai Akram, Ariceta, Gema, Bald, Martin, Benz, Marcus, Bernhardt, Wanja, Bienias, Beata, Buchholz, Björn, Afonso, Alberto Caldas, Candan, Cengiz, Collard, Laure, Derichs, Ute, Dittrich, Katalin, Dossier, Claire, Dunand, Oliver, Duzova, Ali, Feldkoetter, Markus, Gessner, Michaela, Gonzalez Rodriguez, Juan David, Gross, Oliver, Grundmann, Franziska, Harambat, Jerome, Henn, Michael, Jankauskiene, Augustina, Jilani, Houweyda, Lechner, Felix, Longo, Germana, Mastrangelo, Antonio, Mencarelli, Francesca, Mir, Sevgi, Nabhan, Marwa, Nalcacioglu, Hulya, Parvex, Paloma, Patzer, Ludwig, Prikhodina, Larisa, Rachisan, Andreea, Ranguelov, Nadejda, Barba, Adela Rodriguez, Rosenberger, Christian, Rus, Rina, Ruzgiene, Dovile, Santos, Fernando, Schalk, Gesa, Schild, Raphael, Schlevogt, Bernhard, Seeman, Tomas, Sever, Lale, Simon, Thomas, Soylu, Alper, Stanczyk, Malgorzata, Staude, Hagen, Szczepanska, Maria, Teixeira, Ana, Thumfart, Julia, Wurm, Donald, Zagozdzon, Ilona, Zaniew, Marcin and Zieg, Jakub (2025). A risk score to predict kidney survival in patients with autosomal recessive polycystic kidney disease at the age of two months. Kidney International, 107 (5). pp. 903-915. Elsevier. ISSN 0085-2538

Simonis, Alexander ORCID: 0000-0003-2945-9897, Theobald, Sebastian J., Koch, Anna E. ORCID: 0009-0003-1593-9715, Mummadavarapu, Ram ORCID: 0009-0009-4244-8982, Mudler, Julie M. ORCID: 0000-0003-1378-9648, Pouikli, Andromachi ORCID: 0000-0003-1868-6875, Göbel, Ulrike, Acton, Richard ORCID: 0000-0002-2574-9611, Winter, Sandra, Albus, Alexandra ORCID: 0000-0002-4897-6972, Holzmann, Dmitriy, Albert, Marie-Christine, Hallek, Michael ORCID: 0000-0002-7425-4455, Walczak, Henning ORCID: 0000-0002-6312-4591, Ulas, Thomas, Koch, Manuel ORCID: 0000-0002-2962-7814, Tessarz, Peter ORCID: 0000-0002-6953-9835, Hänsel-Hertsch, Robert ORCID: 0000-0002-2835-4471 and Rybniker, Jan ORCID: 0000-0001-8351-2690 (2025). Persistent epigenetic memory of SARS-CoV-2 mRNA vaccination in monocyte-derived macrophages. Molecular Systems Biology, 21 (4). pp. 341-360. Nature Publishing Group UK. ISSN 1744-4292

Veltman, Charlotte (2024). Characterization of novel potential binding partners of Plastin 3, a protective modifier of Spinal Muscular Atrophy. PhD thesis, Universität zu Köln.

Tjiang, Noah Song-Ming ORCID: 0000-0002-9957-0198 (2024). Mitochondrial Distribution and Dynamics at the Axon Initial Segment and their Influence on TAU-Trafficking. PhD thesis, Universität zu Köln.

Buchholz, Sarah ORCID: 0000-0002-3636-1364 (2023). Investigating human TAU isoform-specific functions and their toxicity in Alzheimer's disease and related tauopathies. PhD thesis, Universität zu Köln.

Kruse, Teresa ORCID: 0000-0002-3431-7749, Shamai, Sara ORCID: 0000-0001-5434-3920, Leflerovà, Diana, Wirth, Brunhilde ORCID: 0000-0003-4051-5191, Heller, Raoul, Schloss, Natalie, Lehmann, Helma C. ORCID: 0000-0001-6205-2293, Brakemeier, S., Hagenacker, T., Braumann, Bert ORCID: 0000-0002-5031-9816 and Wunderlich, Gilbert ORCID: 0000-0001-5544-335X (2023). Objective measurement of oral function in adults with spinal muscular atrophy. Orphanet Journal of Rare Diseases, 18 (1). p. 103. Springer Nature. ISSN 1750-1172

Tschernoster, Nikolai ORCID: 0000-0002-6058-9342, Erger, Florian ORCID: 0000-0002-2768-1702, Kohl, Stefan, Reusch, Björn ORCID: 0000-0002-8963-6835, Wenzel, Andrea ORCID: 0009-0005-3280-0947, Walsh, Stephen, Thiele, Holger ORCID: 0000-0003-4495-4597, Becker, Christian ORCID: 0009-0002-2964-4486, Franitza, Marek, Bartram, Malte P., Kömhoff, Martin, Schumacher, Anna-Lena ORCID: 0000-0001-7739-486X, Kukat, Christian ORCID: 0000-0003-1508-0229, Borodina, Tatiana, Quedenau, Claudia, Nürnberg, Peter ORCID: 0000-0002-7228-428X, Rinschen, Markus M, Driller, Jan H., Pedersen, Bjørn P., Schlingmann, Karl P., Hüttel, Bruno ORCID: 0000-0001-7165-1714, Bockenhauer, Detlef, Beck, Bodo Bernhard ORCID: 0000-0003-0495-7670 and Altmüller, Janine ORCID: 0000-0003-4372-1521 (2023). Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions. Genome Medicine, 15 (1). p. 62. Springer Nature. ISSN 1756-994X

Recker, Pia ORCID: 0000-0002-0337-9613, Beck, Bodo Bernhard ORCID: 0000-0003-0495-7670, Sikora, Przemyslaw ORCID: 0000-0002-5698-6863, Göbel, Heike ORCID: 0000-0002-0171-7025, Kemper, Markus Josef ORCID: 0000-0002-9205-7906, Nazco, Angel ORCID: 0000-0001-6685-7267, Martin-Higueras, Cristina ORCID: 0000-0003-1139-4642 and Hoppe, Bernd ORCID: 0000-0002-8120-3306 (2022). Chronic liver disease and hepatic calcium-oxalate deposition in patients with primary hyperoxaluria type I. Scientific Reports, 12 (1). p. 16725. Springer Nature. ISSN 2045-2322