Universität zu Köln

2022

Stuessel, L. G., Hollstein, R., Laugsch, M., Hochfeld, L. M., Welzenbach, J., Schroeder, J., Thieme, F., Ishorst, N., Romero, R. Olmos, Weinhold, L., Hess, T., Gehlen, J., Mostowska, A., Heilmann-Heimbach, S., Mangold, E., Rada-Iglesias, A., Knapp, M., Schaaf, C. P. and Ludwig, K. U. (2022). MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell Migration. J. Dent. Res., 101 (3). S. 323 - 331. THOUSAND OAKS: SAGE PUBLICATIONS INC. ISSN 1544-0591

2020

Hoelzel, S., Ishorst, N., Greve, C., Degenhardt, F., Drichel, D., Maj, C., Nothnagel, M. ORCID: 0000-0001-8305-7114, Hehir-Kwa, J. Y., Veltman, J. A., Kruse, T., Reutter, H., Nowak, S., Carels, C., van Rooij, I., Ludwig, K. U. and Mangold, E. (2020). Nonsyndromic orofacial clefts - Identifying putative causative genes by CNV analysis of whole exome sequencing data. Eur. J. Hum. Genet., 28 (SUPPL 1). S. 839 - 840. LONDON: SPRINGERNATURE. ISSN 1476-5438

Hollstein, R., Schroeder, J., Welzenbach, J., Bartusel, M., Rada-Iglesias, A. and Ludwig, K. U. (2020). Unraveling genomic interactions at nsCL/P associated GWAS loci using Circular Chromosome Conformation Capture (4C). Eur. J. Hum. Genet., 28 (SUPPL 1). S. 569 - 571. LONDON: SPRINGERNATURE. ISSN 1476-5438

2018

Koller, A. C., Strohmaier, J., Ludwig, K. U., Degenhardt, F. C., Wulff, M., Breuer, D., Winkler, L., Neukirch, F., Maaser, A., Forstner, A., Sivalingam, S., Reif, A., Ramirez, A., Maier, W., Rujescu, D., Giegling, I., Thiele, H., Nuernberg, P., Heilmann-Heimbach, S., Andlauer, T., Fischer, A., Jain, G., Kaurani, L., Klockmeier, K., Worf, K., Krumsiek, J., Wildenauer, D., Schwab, S., Rietschel, M., Noethen, M. M. and Degenhardt, F. (2018). Large family-based exome sequencing study provides new insight into schizophrenia. Eur. J. Hum. Genet., 26. S. 417 - 419. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5438

Ludwig, K. U., Boehmer, A. C., Bowes, J., Nikolic, M., Ishorst, N., Wyatt, N., Hammond, N., Goelz, L., Thieme, F., Spielmann, M., Aldhorae, K., Rojas-Martinez, A., Noethen, M. M., Rada-Iglesias, A., Dixon, M. J., Knapp, M. and Mangold, E. (2018). Comprehensive analyses of genome-wide data reveal novel insights into distinct etiologies of cleft lip with/without celft palate, and cleft palate only. Eur. J. Hum. Genet., 26. S. 243 - 244. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5438

2017

Hoebel, A. K., Drichel, D., van de Vorst, M., Boehmer, A. C., Sivalingam, S., Ishorst, N., Klamt, J., Goelz, L., Alblas, M., Maaser, A., Keppler, K., Zink, A. M., Dixon, M. J., Dixon, J., Hemprich, A., Kruse, T., Graf, I., Dunsche, A., Schmidt, G., Daratsianos, N., Nowak, S., Aldhorae, K. A., Noethen, M. M., Knapp, M., Thiele, H., Gilissen, C., Reutter, H., Hoischen, A., Mangold, E. and Ludwig, K. U. (2017). Candidate Genes for Nonsyndromic Cleft Palate Detected by Exome Sequencing. J. Dent. Res., 96 (11). S. 1314 - 1322. THOUSAND OAKS: SAGE PUBLICATIONS INC. ISSN 1544-0591

2014

Ludwig, K. U., Boehmer, A. C., Rubini, M., Mossey, P. A., Herms, S., Nowak, S., Reutter, H., Alblas, M. A., Lippke, B., Barth, S., Paredes-Zenteno, M., Munoz-Jimenez, S. G., Ortiz-Lopez, R., Kreusch, T., Hemprich, A., Martini, M., Braumann, B., Jaeger, A., Poetzsch, B., Molloy, A., Peterlin, B., Hoffmann, P., Noethen, M. M., Rojas-Martinez, A., Knapp, M., Steegers-Theunissen, R. P. and Mangold, E. (2014). Strong Association of Variants around FOXE1 and Orofacial Clefting. J. Dent. Res., 93 (4). S. 376 - 382. THOUSAND OAKS: SAGE PUBLICATIONS INC. ISSN 1544-0591