Publikationen von 0000-0002-8072-4476
(ORCID: 0000-0002-8072-4476)

Ishorst, Nina, Henschel, Leonie, Thieme, Frederic, Drichel, Dmitriy, Sivalingam, Sugirthan, Mehrem, Sarah L., Fechtner, Ariane C., Fazaal, Julia, Welzenbach, Julia, Heimbach, André, Maj, Carlo, Borisov, Oleg, Hausen, Jonas, Raff, Ruth, Hoischen, Alexander , Dixon, Michael, Rada‐Iglesias, Alvaro, Bartusel, Michaela, Rojas‐Martinez, Augusto, Aldhorae, Khalid, Braumann, Bert, Kruse, Teresa, Kirschneck, Christian, Spanier, Gerrit, Reutter, Heiko, Nowak, Stefanie, Gölz, Lina, Knapp, Michael, Buness, Andreas, Krawitz, Peter , Nöthen, Markus M., Nothnagel, Michael, Becker, Tim, Ludwig, Kerstin U. und Mangold, Elisabeth (2023) Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores. Molecular Genetics & Genomic Medicine 11 (3). Volltext nicht vorhanden.

Khan, Mubeen, Cornelis, Stéphanie S., Pozo-Valero, Marta Del, Whelan, Laura, Runhart, Esmee H., Mishra, Ketan , Bults, Femke, AlSwaiti, Yahya, AlTalbishi, Alaa, De Baere, Elfride, Banfi, Sandro, Banin, Eyal, Bauwens, Miriam, Ben-Yosef, Tamar, Boon, Camiel J. F., van den Born, L. Ingeborgh, Defoort, Sabine, Devos, Aurore, Dockery, Adrian , Dudakova, Lubica , Fakin, Ana, Farrar, G. Jane, Sallum, Juliana Maria Ferraz, Fujinami, Kaoru, Gilissen, Christian , Glavač, Damjan, Gorin, Michael B., Greenberg, Jacquie, Hayashi, Takaaki, Hettinga, Ymkje M., Hoischen, Alexander , Hoyng, Carel B., Hufendiek, Karsten, Jägle, Herbert, Kamakari, Smaragda, Karali, Marianthi, Kellner, Ulrich, Klaver, Caroline C. W., Kousal, Bohdan , Lamey, Tina M., MacDonald, Ian M., Matynia, Anna, McLaren, Terri L., Mena, Marcela D. , Meunier, Isabelle, Miller, Rianne, Newman, Hadas, Ntozini, Buhle, Oldak, Monika , Pieterse, Marc, Podhajcer, Osvaldo L., Puech, Bernard, Ramesar, Raj, Rüther, Klaus, Salameh, Manar, Salles, Mariana Vallim, Sharon, Dror, Simonelli, Francesca, Spital, Georg, Steehouwer, Marloes, Szaflik, Jacek P., Thompson, Jennifer A., Thuillier, Caroline, Tracewska, Anna M. , van Zweeden, Martine, Vincent, Andrea L., Zanlonghi, Xavier, Liskova, Petra , Stöhr, Heidi, Roach, John N. De, Ayuso, Carmen, Roberts, Lisa , Weber, Bernhard H. F., Dhaenens, Claire‐Marie und Cremers, Frans P. M. (2020) Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics. Genetics in Medicine 22 (7), S. 1235-1246. Volltext nicht vorhanden.

Timal, Sharita, Hoischen, Alexander , Lehle, Ludwig, Adamowicz, Maciej, Huijben, Karin, Sykut-Cegielska, Jolanta, Paprocka, Justyna, Jamroz, Ewa, van Spronsen, Francjan J., Körner, Christian, Gilissen, Christian , Rodenburg, Richard J. , Eidhof, Ilse , Van den Heuvel, Lambert, Thiel, Christian, Wevers, Ron A. , Morava, Eva, Veltman, Joris und Lefeber, Dirk J. (2012) Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing. Human Molecular Genetics 21 (19), S. 4151-4161. Volltext nicht vorhanden.