Browsing Universitätsbibliographie by Author "Demidov, German"

DSpace Repository

Browsing Universitätsbibliographie by Author "Demidov, German"

Sort by: Order: Results:

  • Allele balance bias identifies systematic genotyping errors and false disease associations
    Muyas, Francesc; Bosio, Mattia; Puig, Anna; Susak, Hana; Domenech, Laura; Escaramis, Georgia; Zapata, Luis; Demidov, German; Estivill, Xavier; Rabionet, Raquel; Ossowski, Stephan (2019)
  • Cancer immune control needs senescence induction by interferon-dependent cell cycle regulator pathways in tumours
    Brenner, Ellen; Schoerg, Barbara F.; Ahmetlic, Fatima; Wieder, Thomas; Hilke, Franz Joachim; Simon, Nadine; Schroeder, Christopher; Demidov, German; Riedel, Tanja; Fehrenbacher, Birgit; Schaller, Martin; Forschner, Andrea; Eigentler, Thomas; Niessner, Heike; Sinnberg, Tobias; Boehm, Katharina S.; Hoemberg, Nadine; Braumueller, Heidi; Dauch, Daniel; Zwirner, Stefan; Zender, Lars; Sonanini, Dominik; Geishauser, Albert; Bauer, Juergen; Eichner, Martin; Jarick, Katja J.; Beilhack, Andreas; Biskup, Saskia; Doecker, Dennis; Schadendorf, Dirk; Quintanilla-Martinez, Leticia; Pichler, Bernd J.; Kneilling, Manfred; Mocikat, Ralph; Roecken, Martin (2020)
  • Circulating cell-free DNA: A potential biomarker to differentiate inflammation and infection during radiochemotherapy
    Zwirner, Kerstin; Hilke, Franz J.; Demidov, German; Ossowski, Stephan; Gani, Cihan; Riess, Olaf; Zips, Daniel; Welz, Stefan; Schroeder, Christopher (2018)
  • Distinct Mutation Patterns Reveal Melanoma Subtypes and Influence Immunotherapy Response in Advanced Melanoma Patients
    Hilke, Franz J.; Sinnberg, Tobias; Gschwind, Axel; Niessner, Heike; Demidov, German; Amaral, Teresa; Ossowski, Stephan; Bonzheim, Irina; Roecken, Martin; Riess, Olaf; Garbe, Claus; Schroeder, Christopher; Forschner, Andrea (2020)
  • Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation
    Susak, Hana; Serra-Saurina, Laura; Demidov, German; Rabionet, Raquel; Domenech, Laura; Bosio, Mattia; Muyas, Francesc; Estivill, Xavier; Escaramis, Georgia; Ossowski, Stephan (2021)
  • Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank
    Fawcett, Katherine A.; Demidov, German; Shrine, Nick; Paynton, Megan L.; Ossowski, Stephan; Sayers, Ian; Wain, Louise, V; Hollox, Edward J. (2022)
  • Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy
    Park, Joohyun; Tucci, Arianna; Cipriani, Valentina; Demidov, German; Rocca, Clarissa; Senderek, Jan; Butryn, Michaela; Velic, Ana; Lam, Tanya; Galanaki, Evangelia; Cali, Elisa; Vestito, Letizia; Maroofian, Reza; Deininger, Natalie; Rautenberg, Maren; Admard, Jakob; Hahn, Gesa-Astrid; Bartels, Claudius; van Os, Nienke J. H.; Horvath, Rita; Chinnery, Patrick F.; Tiet, May Yung; Hewamadduma, Channa; Hadjivassiliou, Marios; Tofaris, George K.; Wood, Nicholas W.; Hayer, Stefanie N.; Bender, Friedemann; Menden, Benita; Cordts, Isabell; Klein, Katrin; Huu Phuc Nguyen; Krauss, Joachim K.; Blahak, Christian; Strom, Tim M.; Sturm, Marc; van de Warrenburg, Bart; Lerche, Holger; Macek, Boris; Synofzik, Matthis; Ossowski, Stephan; Timmann, Dagmar; Wolf, Marc E.; Smedley, Damian; Riess, Olaf; Schoels, Ludger; Houlden, Henry; Haack, Tobias B.; Hengel, Holger (2022)
  • MDM2, MDM4 and EGFR Amplifications and Hyperprogression in Metastatic Acral and Mucosal Melanoma
    Forschner, Andrea; Hilke, Franz-Joachim; Bonzheim, Irina; Gschwind, Axel; Demidov, German; Amaral, Teresa; Ossowski, Stephan; Riess, Olaf; Schroeder, Christopher; Martus, Peter; Klumpp, Bernhard; Gonzalez-Menendez, Irene; Garbe, Claus; Niessner, Heike; Sinnberg, Tobias (2020)
  • Pan-cancer analysis of whole genomes
    Campbell, Peter J.; Getz, Gad; Korbel, Jan O.; Stuart, Joshua M.; Jennings, Jennifer L.; Stein, Lincoln D.; Perry, Marc D.; Nahal-Bose, Hardeep K.; Ouellette, B. F. Francis; Li, Constance H.; Rheinbay, Esther; Nielsen, G. Petur; Sgroi, Dennis C.; Wu, Chin-Lee; Faquin, William C.; Deshpande, Vikram; Boutros, Paul C.; Lazar, Alexander J.; Hoadley, Katherine A.; Louis, David N.; Dursi, L. Jonathan; Yung, Christina K.; Bailey, Matthew H.; Saksena, Gordon; Raine, Keiran M.; Buchhalter, Ivo; Kleinheinz, Kortine; Schlesner, Matthias; Zhang, Junjun; Wang, Wenyi; Wheeler, David A.; Ding, Li; Simpson, Jared T.; O'Connor, Brian D.; Yakneen, Sergei; Ellrott, Kyle; Miyoshi, Naoki; Butler, Adam P.; Royo, Romina; Shorser, Solomon, I; Vazquez, Miguel; Rausch, Tobias; Tiao, Grace; Waszak, Sebastian M.; Rodriguez-Martin, Bernardo; Shringarpure, Suyash; Wu, Dai-Ying; Demidov, German M.; Delaneau, Olivier; Hayashi, Shuto; Imoto, Seiya; Habermann, Nina; Segre, Ayellet, V; Garrison, Erik; Cafferkey, Andy; Alvarez, Eva G.; Maria Heredia-Genestar, Jose; Muyas, Francesc; Drechsel, Oliver; Bruzos, Alicia L.; Temes, Javier; Zamora, Jorge; Baez-Ortega, Adrian; Kim, Hyung-Lae; Mashl, R. Jay; Ye, Kai; DiBiase, Anthony; Huang, Kuan-lin; Letunic, Ivica; McLellan, Michael D.; Newhouse, Steven J.; Shmaya, Tal; Kumar, Sushant; Wedge, David C.; Wright, Mark H.; Yellapantula, Venkata D.; Gerstein, Mark; Khurana, Ekta; Marques-Bonet, Tomas; Navarro, Arcadi; Bustamante, Carlos D.; Siebert, Reiner; Nakagawa, Hidewaki; Easton, Douglas F.; Ossowski, Stephan; Tubio, Jose M. C.; De La Vega, Francisco M.; Estivill, Xavier; Yuen, Denis; Mihaiescu, George L.; Omberg, Larsson; Ferretti, Vincent; Sabarinathan, Radhakrishnan; Pich, Oriol; Gonzalez-Perez, Abel; Weiner, Amaro Taylor; Fittall, Matthew W.; Demeulemeester, Jonas; Tarabichi, Maxime; Roberts, Nicola D.; Van Loo, Peter (2020)
  • Radiogenomics in head and neck cancer: correlation of radiomic heterogeneity and somatic mutations in TP53, FAT1 and KMT2D
    Zwirner, Kerstin; Hilke, Franz J.; Demidov, German; Fernandez, Jairo Socarras; Ossowski, Stephan; Gani, Cihan; Thorwarth, Daniela; Riess, Olaf; Zips, Daniel; Schroeder, Christopher; Welz, Stefan (2019)
  • Transcript-Specific Loss-of-Function Variants in VPS16 Are Enriched in Patients With Dystonia
    Park, Joohyun; Reilaender, Annemarie; Petry-Schmelzer, Jan N.; Stoebe, Petra; Cordts, Isabell; Harmuth, Florian; Rautenberg, Maren; Woerz, Sarah E.; Demidov, German; Sturm, Marc; Ossowski, Stephan; Schwaibold, Eva M. C.; Wunderlich, Gilbert; Paus, Sebastian; Saft, Carsten; Haack, Tobias B. (2022)