Auflistung Universitätsbibliographie nach Autor "Atasu, Burcu"

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Auflistung Universitätsbibliographie nach Autor "Atasu, Burcu"

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  • A multi-omics dataset for the analysis of frontotemporal dementia genetic subtypes
    Menden, Kevin; Francescatto, Margherita; Nyima, Tenzin; Blauwendraat, Cornelis; Dhingra, Ashutosh; Castillo-Lizardo, Melissa; Fernandes, Noemia; Kaurani, Lalit; Kronenberg-Versteeg, Deborah; Atasu, Burcu; Sadikoglou, Eldem; Borroni, Barbara; Rodriguez-Nieto, Salvador; Simon-Sanchez, Javier; Fischer, Andre; Craig, David Wesley; Neumann, Manuela; Bonn, Stefan; Rizzu, Patrizia; Heutink, Peter (2023)
  • Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia
    Mencacci, Niccolo E.; Brockmann, Marisa M.; Dai, Jinye; Pajusalu, Sander; Atasu, Burcu; Campos, Joaquin; Pino, Gabriela; Gonzalez-Latapi, Paulina; Patzke, Christopher; Schwake, Michael; Tucci, Arianna; Pittman, Alan; Simon-Sanchez, Javier; Carvill, Gemma L.; Balint, Bettina; Wiethoff, Sarah; Warner, Thomas T.; Papandreou, Apostolos; Soo, Audrey; Rein, Reet; Kadastik-Eerme, Liis; Puusepp, Sanna; Reinson, Karit; Tomberg, Tiiu; Hanagasi, Hasmet; Gasser, Thomas; Bhatia, Kailash P.; Kurian, Manju A.; Lohmann, Ebba; Ounap, Katrin; Rosenmund, Christian; Sudhof, Thomas C.; Wood, Nicholas W.; Krainc, Dimitri; Acuna, Claudio (2021)
  • Genotype-Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature review
    Atasu, Burcu; Acarli, Ayse Nur Ozdag; Bilgic, Basar; Baykan, Betul; Demir, Erol; Ozluk, Yasemin; Turkmen, Aydin; Hauser, Ann-Kathrin; Guven, Gamze; Hanagasi, Hasmet; Gurvit, Hakan; Emre, Murat; Gasser, Thomas; Lohmann, Ebba (2022)
  • HPCA Confirmed as a Genetic Cause of DYT2-Like Dystonia Phenotype
    Atasu, Burcu; Hanagasi, Hasmet; Bilgic, Basar; Pak, Meltem; Erginel-Unaltuna, Nihan; Hauser, Ann-Kathrin; Guven, Gamze; Simon-Sanchez, Javier; Heutink, Peter; Gasser, Thomas; Lohmann, Ebba (2018)
  • Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia
    Minnerop, Martina; Kurzwelly, Delia; Wagner, Holger; Soehn, Anne S.; Reichbauer, Jennifer; Tao, Feifei; Rattay, Tim W.; Peitz, Michael; Rehbach, Kristina; Giorgetti, Alejandro; Pyle, Angela; Thiele, Holger; Altmueller, Janine; Timmann, Dagmar; Karaca, Ilker; Lennarz, Martina; Baets, Jonathan; Hengel, Holger; Synofzik, Matthis; Atasu, Burcu; Feely, Shawna; Kennerson, Marina; Stendel, Claudia; Lindig, Tobias; Gonzalez, Michael A.; Stirnberg, Ruediger; Sturm, Marc; Roeske, Sandra; Jung, Johanna; Bauer, Peter; Lohmann, Ebba; Herms, Stefan; Heilmann-Heimbach, Stefanie; Nicholson, Garth; Mahanjah, Muhammad; Sharkia, Rajech; Carloni, Paolo; Bruestle, Oliver; Klopstock, Thomas; Mathews, Katherine D.; Shy, Michael E.; de Jonghe, Peter; Chinnery, Patrick F.; Horvath, Rita; Kohlhase, Juergen; Schmitt, Ina; Wolf, Michael; Greschus, Susanne; Amunts, Katrin; Maier, Wolfgang; Schoels, Ludger; Nuernberg, Peter; Zuchner, Stephan; Klockgether, Thomas; Ramirez, Alfredo; Schuele, Rebecca (2017)
  • Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey
    Kessler, Christoph; Atasu, Burcu; Hanagasi, Hasmet; Simon-Sanchez, Javier; Hauser, Ann-Kathrin; Pak, Meltem; Bilgic, Basar; Erginel-Unaltuna, Nihan; Gurvit, Hakan; Gasser, Thomas; Lohmann, Ebba (2018)