First Case of Complete Bladder Duplication in the Coronal Plane with Concomitant Duplication of the Urethra in an Adult Male

Por Karpathakis, Nikolaos, Vasileiou, Georgia, Fasoulakis, Konstantinos, Heretis, Ioannis
Publicado em 2013

Chromatin-Remodeling-Factor ARID1B Represses Wnt/β-Catenin Signaling

Por Vasileiou, Georgia, Ekici, Arif B., Uebe, Steffen, Zweier, Christiane, Hoyer, Juliane, Engels, Hartmut, Behrens, Jürgen, Reis, André, Hadjihannas, Michel V.
Publicado no Am J Hum Genet (2015)

Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria

Por Hoyer, Juliane, Vasileiou, Georgia, Uebe, Steffen, Wunderle, Marius, Kraus, Cornelia, Fasching, Peter A., Thiel, Christian T., Hartmann, Arndt, Beckmann, Matthias W., Lux, Michael P., Reis, André
Publicado no BMC Cancer (2018)

Gender-based analysis of cortical thickness and structural connectivity in Parkinson’s disease

Por Yadav, Santosh K., Kathiresan, Nagarajan, Mohan, Suyash, Vasileiou, Georgia, Singh, Anup, Kaura, Deepak, Melhem, Elias R., Gupta, Rakesh K., Wang, Ena, Marincola, Francesco M., Borthakur, Arijitt, Haris, Mohammad
Publicado no J Neurol (2016)

De Novo Mutations in the Genome Organizer CTCF Cause Intellectual Disability

Por Gregor, Anne, Oti, Martin, Kouwenhoven, Evelyn N., Hoyer, Juliane, Sticht, Heinrich, Ekici, Arif B., Kjaergaard, Susanne, Rauch, Anita, Stunnenberg, Hendrik G., Uebe, Steffen, Vasileiou, Georgia, Reis, André, Zhou, Huiqing, Zweier, Christiane
Publicado em 2013

Risk, Prediction and Prevention of Hereditary Breast Cancer – Large-Scale Genomic Studies in Times of Big and Smart Data

Por Wunderle, Marius, Olmes, Gregor, Nabieva, Naiba, Häberle, Lothar, Jud, Sebastian M., Hein, Alexander, Rauh, Claudia, Hack, Carolin C., Erber, Ramona, Ekici, Arif B., Hoyer, Juliane, Vasileiou, Georgia, Kraus, Cornelia, Reis, André, Hartmann, Arndt, Schulz-Wendtland, Rüdiger, Lux, Michael P., Beckmann, Matthias W., Fasching, Peter A.
Publicado no Geburtshilfe Frauenheilkd (2018)

Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome

Por Vasileiou, Georgia, Vergarajauregui, Silvia, Endele, Sabine, Popp, Bernt, Büttner, Christian, Ekici, Arif B., Gerard, Marion, Bramswig, Nuria C., Albrecht, Beate, Clayton-Smith, Jill, Morton, Jenny, Tomkins, Susan, Low, Karen, Weber, Astrid, Wenzel, Maren, Altmüller, Janine, Li, Yun, Wollnik, Bernd, Hoganson, George, Plona, Maria-Renée, Cho, Megan T., Thiel, Christian T., Lüdecke, Hermann-Josef, Strom, Tim M., Calpena, Eduardo, Wilkie, Andrew O.M., Wieczorek, Dagmar, Engel, Felix B., Reis, André
Publicado no Am J Hum Genet (2018)