Universität zu Köln

2024

Valdez Capuccino, Lucas (2024). Harnessing cell death vulnerabilities for the treatment of Small Cell Lung Cancer. PhD thesis, Universität zu Köln.

2023

Brünger, Tobias ORCID: 0000-0003-2591-432X (2023). Bioinformatic approaches to determine pathogenicity and function of clinical genetic variants across ion channels and neurodevelopmental disorder associated genes. PhD thesis, Universität zu Köln.

Adesoji, Oluyomi Modupe ORCID: 0000-0002-8583-7170 (2023). Benchmarking of univariate pleiotropy detection methods, with an application to epilepsy phenotypes. PhD thesis, Universität zu Köln.

Zhu, Mengjie ORCID: 0000-0001-7961-6542, Metzen, Fabian ORCID: 0000-0002-5248-8218, Hopkinson, Mark, Betz, Janina, Heilig, Juliane, Sodhi, Jassi, Imhof, Thomas ORCID: 0000-0002-0554-7617, Niehoff, Anja ORCID: 0000-0002-4165-0929, Birk, David E., Izu, Yayoi, Krüger, Marcus ORCID: 0000-0002-5846-6941, Pitsillides, Andrew A., Altmüller, Janine ORCID: 0000-0003-4372-1521, van Osch, Gerjo J.V.M., Straub, Volker, Schreiber, Gudrun, Paulsson, Mats ORCID: 0000-0002-6846-857X, Koch, Manuel ORCID: 0000-0002-2962-7814 and Brachvogel, Bent ORCID: 0000-0002-3923-0554 (2023). Ablation of collagen XII disturbs joint extracellular matrix organization and causes patellar subluxation. iScience, 26 (7). p. 107225. Elsevier. ISSN 25890042

Abo Zed, Seif El Din, Hackl, Agnes, Bohl, Katrin ORCID: 0000-0003-3746-4047, Ebert, Lena Kathrin ORCID: 0009-0000-6583-3220, Kieckhöfer, Emilia ORCID: 0009-0004-7888-9185, Müller, Carsten, Becker, Kerstin ORCID: 0009-0009-7897-7181, Fink, Gregor ORCID: 0000-0001-7042-1706, Nüsken, Kai-Dietrich ORCID: 0000-0001-5749-7183, Nüsken, Eva ORCID: 0000-0002-0674-804X, Müller, Roman-Ulrich ORCID: 0000-0001-6910-0745, Schermer, Bernhard ORCID: 0000-0002-5194-9000 and Weber, Lutz T. ORCID: 0000-0003-4116-598X (2023). Mycophenolic acid directly protects podocytes by preserving the actin cytoskeleton and increasing cell survival. Scientific Reports, 13 (1). p. 4281. Springer Nature. ISSN 2045-2322

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

Tschernoster, Nikolai (2023). Genomic profiling in rare kidney disease. PhD thesis, Universität zu Köln.

2022

Heß, Sarah Aurora (2022). Eine Strategie zur STR-Analyse telogener Einzelhaare in der forensischen Genetik. PhD thesis, Universität zu Köln.

2020

Asif, Maria ORCID: 0000-0003-3578-6229 (2020). Delineating genetic underpinnings and disease pathogenesis of primary microcephaly and Filippi syndrome. PhD thesis, Universität zu Köln.

2018

Arora, Ankit (2018). Development of Web-Application for High-Throughput Sequencing Data and In Silico Dissection of LINE-1 Retrotransposons in Cellular Senescence. PhD thesis, Universität zu Köln.