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2021
Royer-Pokora, Brigitte, Busch, Maike Anna, Tenbusch, Sarah, Schmidt, Mathias 
ORCID: 0000-0001-5554-9920, Beier, Manfred ORCID: 0000-0002-2482-1626, Woods, Andrew D., Thiele, Holger and Mora, Jaume
(2021).
Comprehensive Biology and Genetics Compendium of Wilms Tumor Cell Lines with Different WT1 Mutations.
Cancers, 13 (1).
BASEL:
MDPI.
ISSN 2072-6694
2017
Binder, Hans, Hopp, Lydia, Schweiger, Michal R., Hoffmann, Steve, Juehling, Frank, Kerick, Martin ORCID: 0000-0002-6298-4514, Timmermann, Bernd, Siebert, Susann, Grimm, Christina ORCID: 0000-0002-4676-8870, Nersisyan, Lilit ORCID: 0000-0001-8525-420X, Arakelyan, Arsen ORCID: 0000-0002-6851-1056, Herberg, Maria, Buske, Peter, Loeffler-Wirth, Henry, Rosolowski, Maciej, Engel, Christoph ORCID: 0000-0002-7247-282X, Przybilla, Jens, Peifer, Martin ORCID: 0000-0002-5243-5503, Friedrichs, Nicolaus, Moeslein, Gabriela, Odenthal, Margarete, Hussong, Michelle, Peters, Sophia, Holzapfel, Stefanie, Nattermann, Jacob, Hueneburg, Robert, Schmiegel, Wolff, Royer-Pokora, Brigitte, Aretz, Stefan ORCID: 0000-0002-5228-1890, Kloth, Michael, Kloor, Matthias, Buettner, Reinhard, Galle, Joerg and Loeffler, Markus
(2017).
Genomic and transcriptomic heterogeneity of colorectal tumours arising in Lynch syndrome.
J. Pathol., 243 (2).
S. 242 - 255.
HOBOKEN:
WILEY.
ISSN 1096-9896
2016
Rahner, Nils, Nuernberg, Gudrun, Finis, David, Nuernberg, Peter and Royer-Pokora, Brigitte (2016). A novel C8orf37 splice mutation and genotype-phenotype correlation for cone-rod dystrophy. Ophthalmic Genet., 37 (3). S. 294 - 301. PHILADELPHIA: TAYLOR & FRANCIS INC. ISSN 1744-5094
2014
Steinke, Verena, Holzapfel, Stefanie, Loeffler, Markus, Holinski-Feder, Elke, Morak, Monika, Schackert, Hans K., Goergens, Heike, Pox, Christian, Royer-Pokora, Brigitte, von Knebel-Doeberitz, Magnus, Buettner, Reinhard, Propping, Peter and Engel, Christoph ORCID: 0000-0002-7247-282X
(2014).
Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: A comprehensive analysis of 3,671 families.
Int. J. Cancer, 135 (1).
S. 69 - 78.
HOBOKEN:
WILEY.
ISSN 1097-0215
Yang, Rongxi, Chen, Bowang, Pfuetze, Katrin, Buch, Stephan, Steinke, Verena, Holinski-Feder, Elke, Stoecker, Sarah, von schoenfels, Witigo, Becker, Thomas, Schackert, Hans K., Royer-Pokora, Brigitte, Kloor, Matthias, Schmiegel, Wolff H., Buettner, Reinhard, Engel, Christoph ORCID: 0000-0002-7247-282X, Puertolas, Jesus Lascorz, Foersti, Asta, Kunkel, Nelli, Bugert, Peter, Schreiber, Stefan, Krawczak, Michael ORCID: 0000-0003-2603-1502, Schafmayer, Clemens, Propping, Peter, Hampe, Jochen ORCID: 0000-0002-2421-6127, Hemminki, Kari and Burwinkel, Barbara
(2014).
Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3.
Carcinogenesis, 35 (2).
S. 315 - 324.
OXFORD:
OXFORD UNIV PRESS.
ISSN 1460-2180