Universität zu Köln

Bartusel, Michaela (2019). Disruption of neural crest enhancer landscapes as an etiological mechanism for human neurocristopathies. PhD thesis, Universität zu Köln.

Bleckwehl, Tore, Crispatzu, Giuliano, Schaaf, Kaitlin, Respuela, Patricia, Bartusel, Michaela ORCID: 0000-0003-1008-1951, Benson, Laura, Clark, Stephen J., Dorighi, Kristel M., Barral, Antonio, Laugsch, Magdalena, van Ijcken, Wilfred F. J., Manzanares, Miguel ORCID: 0000-0003-4849-2836, Wysocka, Joanna, Reikf, Wolf and Rada-Iglesias, Alvaro ORCID: 0000-0001-7137-1341 (2021). Enhancer-associated H3K4 methylation safeguards in vitro germline competence. Nat. Commun., 12 (1). BERLIN: NATURE PORTFOLIO. ISSN 2041-1723

Ishorst, Nina, Henschel, Leonie, Thieme, Frederic, Drichel, Dmitriy, Sivalingam, Sugirthan, Mehrem, Sarah L., Fechtner, Ariane C., Fazaal, Julia, Welzenbach, Julia, Heimbach, Andre, Maj, Carlo, Borisov, Oleg, Hausen, Jonas, Raff, Ruth, Hoischen, Alexander ORCID: 0000-0002-8072-4476, Dixon, Michael, Rada-Iglesias, Alvaro, Bartusel, Michaela, Rojas-Martinez, Augusto, Aldhorae, Khalid, Braumann, Bert, Kruse, Teresa, Kirschneck, Christian, Spanier, Gerrit, Reutter, Heiko, Nowak, Stefanie, Goelz, Lina, Knapp, Michael, Buness, Andreas, Krawitz, Peter, Noethen, Markus M., Nothnagel, Michael, Becker, Tim, Ludwig, Kerstin U. and Mangold, Elisabeth (2023). Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores. Mol. Genet. Genom. Med., 11 (3). HOBOKEN: WILEY. ISSN 2324-9269

Koester, Janis ORCID: 0000-0002-5274-0591, Miroshnikova, Yekaterina A., Ghatak, Sushmita, Chacon-Martinez, Carlos Andres, Morgner, Jessica ORCID: 0000-0001-6374-8639, Li, Xinping ORCID: 0000-0002-7427-0017, Atanassov, Ilian ORCID: 0000-0001-8259-2545, Altmueller, Janine, Birk, David E., Koch, Manuel ORCID: 0000-0002-2962-7814, Bloch, Wilhelm, Bartusel, Michaela, Niessen, Carien M. ORCID: 0000-0002-4892-9391, Rada-Iglesias, Alvaro ORCID: 0000-0001-7137-1341 and Wickstroem, Sara A. (2021). Niche stiffening compromises hair follicle stem cell potential during ageing by reducing bivalent promoter accessibility. Nat. Cell Biol., 23 (7). S. 771 - 797. BERLIN: NATURE RESEARCH. ISSN 1476-4679

Laugsch, Magdalena, Bartusel, Michaela, Rehimi, Rizwan, Alirzayeva, Hafiza, Karaolidou, Agathi, Crispatzu, Giuliano, Zentis, Peter, Nikolic, Milos ORCID: 0000-0003-0029-7601, Bleckwehl, Tore, Kolovos, Petros ORCID: 0000-0002-0787-6158, van Ijcken, Wilfred F. J., Saric, Tomo, Koehler, Katrin, Frommolt, Peter ORCID: 0000-0002-1966-8014, Lachlan, Katherine, Baptista, Julia and Rada-Iglesias, Alvaro (2019). Modeling the Pathological Long-Range Regulatory Effects of Human Structural Variation with Patient-Specific hiPSCs. Cell Stem Cell, 24 (5). S. 736 - 765. CAMBRIDGE: CELL PRESS. ISSN 1875-9777

Rehimi, Rizwan, Bartusel, Michaela, Solinas, Francesca, Altmueller, Janine and Rada-Iglesias, Alvaro (2017). Chromatin Immunoprecipitation (ChIP) Protocol for Low-abundance Embryonic Samples. J. Vis. Exp. (126). CAMBRIDGE: JOURNAL OF VISUALIZED EXPERIMENTS. ISSN 1940-087X

Thues, Cedric, Valadas, Jorge S., Deaulmerie, Liesbeth, Geens, Ann, Chouhan, Amit K., Duran-Romana, Ramon ORCID: 0000-0002-2020-8672, Schymkowitz, Joost, Rousseau, Frederic, Bartusel, Michaela, Rehimi, Rizwan, Rada-Iglesias, Alvaro ORCID: 0000-0001-7137-1341, Verstreken, Patrik ORCID: 0000-0002-5073-5393 and Van Esch, Hilde (2021). MAPRE2 mutations result in altered human cranial neural crest migration, underlying craniofacial malformations in CSC-KT syndrome. Sci Rep, 11 (1). BERLIN: NATURE RESEARCH. ISSN 2045-2322