Browsing Universitätsbibliographie by Author "Ossowski, Stephan"

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Browsing Universitätsbibliographie by Author "Ossowski, Stephan"

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  • A Genomic-Scale Artificial MicroRNA Library as a Tool to Investigate the Functionally Redundant Gene Space in Arabidopsis
    Hauser, Felix; Chen, Wenxiao; Deinlein, Ulrich; Chang, Kenneth; Ossowski, Stephan; Fitz, Joffrey; Hannon, Gregory J.; Schroeder, Julian I. (2013)
  • A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagy
    Figueroa, Karla P.; Gross, Caspar; Buena-Atienza, Elena; Paul, Sharan; Gandelman, Mandi; Kakar, Naseebullah; Sturm, Marc; Casadei, Nicolas; Admard, Jakob; Park, Joohyun; Zuehlke, Christine; Hellenbroich, Yorck; Pozojevic, Jelena; Balachandran, Saranya; Haendler, Kristian; Zittel, Simone; Timmann, Dagmar; Erdlenbruch, Friedrich; Herrmann, Laura; Feindt, Thomas; Zenker, Martin; Klopstock, Thomas; Dufke, Claudia; Scoles, Daniel R.; Koeppen, Arnulf; Spielmann, Malte; Riess, Olaf; Ossowski, Stephan; Haack, Tobias B.; Pulst, Stefan M. (2024)
  • A global metagenomic map of urban microbiomes and antimicrobial resistance
    Danko, David; Bezdan, Daniela; Afshin, Evan E.; Ahsanuddin, Sofia; Bhattacharya, Chandrima; Butler, Daniel J.; Chng, Kern Rei; Donnellan, Daisy; Hecht, Jochen; Jackson, Katelyn; Kuchin, Katerina; Karasikov, Mikhail; Lyons, Abigail; Mak, Lauren; Meleshko, Dmitry; Mustafa, Harun; Mutai, Beth; Neches, Russell Y.; Ng, Amanda; Nikolayeva, Olga; Nikolayeva, Tatyana; Png, Eileen; Ryon, Krista A.; Sanchez, Jorge L.; Shaaban, Heba; Sierra, Maria A.; Thomas, Dominique; Young, Ben; Abudayyeh, Omar O.; Alicea, Josue; Bhattacharyya, Malay; Blekhman, Ran; Castro-Nallar, Eduardo; Canas, Ana M.; Chatziefthimiou, Aspassia D.; Crawford, Robert W.; De Filippis, Francesca; Deng, Youping; Desnues, Christelle; Dias-Neto, Emmanuel; Dybwad, Marius; Elhaik, Eran; Ercolini, Danilo; Frolova, Alina; Gankin, Dennis; Gootenberg, Jonathan S.; Graf, Alexandra B.; Green, David C.; Hajirasouliha, Iman; Hastings, Jaden J. A.; Hernandez, Mark; Iraola, Gregorio; Jang, Soojin; Kahles, Andre; Kelly, Frank J.; Knights, Kaymisha; Kyrpides, Nikos C.; Labaj, Pawel P.; Lee, Patrick K. H.; Leung, Marcus H. Y.; Ljungdahl, Per O.; Mason-Buck, Gabriella; McGrath, Ken; Meydan, Cem; Mongodin, Emmanuel F.; Moraes, Milton Ozorio; Nagarajan, Niranjan; Nieto-Caballero, Marina; Noushmehr, Houtan; Oliveira, Manuela; Ossowski, Stephan; Osuolale, Olayinka O.; Ozcan, Orhan; Paez-Espino, David; Rascovan, Nicolas; Richard, Hugues; Ratsch, Gunnar; Schriml, Lynn M.; Semmler, Torsten; Sezerman, Osman U.; Shi, Leming; Shi, Tieliu; Siam, Rania; Song, Le Huu; Suzuki, Haruo; Court, Denise Syndercombe; Tighe, Scott W.; Tong, Xinzhao; Udekwu, Klas, I; Ugalde, Juan A.; Valentine, Brandon; Vassilev, Dimitar, I; Vayndorf, Elena M.; Velavan, Thirumalaisamy P.; Wu, Jun; Zambrano, Maria M.; Zhu, Jifeng; Zhu, Sibo; Mason, Christopher E. (2021)
  • A single center experience of prenatal parent-fetus trio exome sequencing for pregnancies with congenital anomalies
    Dufke, Andreas; Hoopmann, Markus; Waldmuller, Stephan; Prodan, Natalia Carmen; Beck-Woedl, Stefanie; Grasshoff, Ute; Heinrich, Tilman; Riess, Angelika; Kehrer, Martin; Falb, Ruth J.; Liebmann, Alexandra; Roggia, Cristiana; Stampfer, Miriam; Schadeck, Malou; Mueller, Amelie J.; Grimmel, Mona; Stoebe, Petra; Gauck, Darja; Buchert-Lo, Rebecca; Baumann, Sarah; Schaeferhoff, Karin; Bertrand, Miriam; Menden, Benita; Sturm, Marc; Schuetz, Leon; Riess, Olaf; Ossowski, Stephan; Haack, Tobias B.; Kagan, Karl Oliver (2022)
  • Absence of Non-Canonical, Inhibitory MYD88 Splice Variants in B Cell Lymphomas Correlates With Sustained NF-kappa B Signaling
    Gloria, Yamel Cardona; Bernhart, Stephan H.; Fillinger, Sven; Wolz, Olaf-Oliver; Dickhoefer, Sabine; Admard, Jakob; Ossowski, Stephan; Nahnsen, Sven; Siebert, Reiner; Weber, Alexander N. R. (2021)
  • AI Model for Predicting Anti-PD1 Response in Melanoma Using Multi-Omics Biomarkers
    Gschwind, Axel; Ossowski, Stephan (2025)
  • 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)
  • An interconnected data infrastructure to support large-scale rare disease research
    Johansson, Lennart F.; Laurie, Steve; Spalding, Dylan; Gibson, Spencer; Ruvolo, David; Thomas, Coline; Piscia, Davide; de Andrade, Fernanda; Been, Gerieke; Bijlsma, Marieke; Brunner, Han; Cimerman, Sandi; Dizjikan, Farid Yavari; Ellwanger, Kornelia; Fernandez, Marcos; Freeberg, Mallory; van de Geijn, Gert-Jan; Kanninga, Roan; Maddi, Vatsalya; Mehtarizadeh, Mehdi; Neerincx, Pieter; Ossowski, Stephan; Rath, Ana; Roelofs-Prins, Dieuwke; Stok-Benjamins, Marloes; van der Velde, K. Joeri; Veal, Cohn; van der Vries, Gerben; Wadsley, Marc; Warren, Gregory; Zurek, Birte; Keane, Thomas; Graessner, Holm; Beltran, Sergi; Swertz, Morris A.; Brookes, Anthony J. (2024)
  • Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
    Rheinbay, Esther; Nielsen, Morten Muhlig; Abascal, Federico; Wala, Jeremiah A.; Shapira, Ofer; Tiao, Grace; Hornshoj, Henrik; Hess, Julian M.; Juul, Randi Istrup; Lin, Ziao; Feuerbach, Lars; Sabarinathan, Radhakrishnan; Madsen, Tobias; Kim, Jaegil; Mularoni, Loris; Shuai, Shimin; Lanzos, Andres; Herrmann, Carl; Maruvka, Yosef E.; Shen, Ciyue; Amin, Samirkumar B.; Bandopadhayay, Pratiti; Bertl, Johanna; Boroevich, Keith A.; Busanovich, John; Carlevaro-Fita, Joana; Chakravarty, Dimple; Chan, Calvin Wing Yiu; Craft, David; Dhingra, Priyanka; Diamanti, Klev; Fonseca, Nuno A.; Gonzalez-Perez, Abel; Guo, Qianyun; Hamilton, Mark P.; Haradhvala, Nicholas J.; Hong, Chen; Isaev, Keren; Johnson, Todd A.; Juul, Malene; Kahles, Andre; Kahraman, Abdullah; Kim, Youngwook; Komorowski, Jan; Kumar, Kiran; Kumar, Sushant; Lee, Donghoon; Lehmann, Kjong-Van; Li, Yilong; Liu, Eric Minwei; Lochovsky, Lucas; Park, Keunchil; Pich, Oriol; Roberts, Nicola D.; Saksena, Gordon; Schumacher, Steven E.; Sidiropoulos, Nikos; Sieverling, Lina; Sinnott-Armstrong, Nasa; Stewart, Chip; Tamborero, David; Tubio, Jose M. C.; Umer, Husen M.; Uuskula-Reimand, Liis; Wadelius, Claes; Wadi, Lina; Yao, Xiaotong; Zhang, Cheng-Zhong; Zhang, Jing; Haber, James E.; Hobolth, Asger; Imielinski, Marcin; Kellis, Manolis; Lawrence, Michael S.; von Mering, Christian; Nakagawa, Hidewaki; Raphael, Benjamin J.; Rubin, Mark A.; Sander, Chris; Stein, Lincoln D.; Stuart, Joshua M.; Tsunoda, Tatsuhiko; Wheeler, David A.; Johnson, Rory; Reimand, Juri; Gerstein, Mark; Khurana, Ekta; Campbell, Peter J.; Lopez-Bigas, Nuria; Weischenfeldt, Joachim; Beroukhim, Rameen; Martincorena, Inigo; Pedersen, Jakob Skou; Getz, Gad; Bader, Gary D.; Barenboim, Jonathan; Brunak, Soren; Chen, Ken; Choi, Jung Kyoon; Deu-Pons, Jordi; Fink, J. Lynn (2020)
  • Benchmarking whole exome sequencing in the German network for personalized medicine
    Menzel, Michael; Martis-Thiele, Mihaela; Goldschmid, Hannah; Ott, Alexander; Romanovsky, Eva; Siemanowski-Hrach, Janna; Seillier, Lancelot; Bruechle, Nadina Ortiz; Maurer, Angela; Lehmann, Kjong-Van; Begemann, Matthias; Elbracht, Miriam; Meyer, Robert; Dintner, Sebastian; Claus, Rainer; Meier-Kolthoff, Jan P.; Blanc, Eric; Moebs, Markus; Joosten, Maria; Benary, Manuela; Basitta, Patrick; Hoelscher, Florian; Tischler, Verena; Gross, Thomas; Kutz, Oliver; Prause, Rebecca; William, Doreen; Horny, Kai; Goering, Wolfgang; Sivalingam, Sugirthan; Borkhardt, Arndt; Blank, Cornelia; Junk, Stefanie V.; Yasin, Layal; Moskalev, Evgeny A.; Carta, Maria Giulia; Ferrazzi, Fulvia; Toegel, Lars; Wolter, Steffen; Adam, Eugen; Matysiak, Uta; Rosenthal, Tessa; Doenitz, Juergen; Lehmann, Ulrich; Schmidt, Gunnar; Bartels, Stephan; Hofmann, Winfried; Hirsch, Steffen; Dikow, Nicola; Goebel, Kirsten; Banan, Rouzbeh; Hamelmann, Stefan; Fink, Annette; Ball, Markus; Neumann, Olaf; Rehker, Jan; Kloth, Michael; Murtagh, Justin; Hartmann, Nils; Jurmeister, Phillip; Mock, Andreas; Kumbrink, Joerg; Jung, Andreas; Mayr, Eva-Maria; Jacob, Anne; Trautmann, Marcel; Kirmse, Santina; Falkenberg, Kim; Ruckert, Christian; Hirsch, Daniela; Immel, Alexander; Dietmaier, Wolfgang; Haack, Tobias; Marienfeld, Ralf; Fuerstberger, Axel; Niewoehner, Jakob; Gerstenmaier, Uwe; Eberhardt, Timo; Greif, Philipp A.; Appenzeller, Silke; Maurus, Katja; Doll, Julia; Jelting, Yvonne; Jonigk, Danny; Maerkl, Bruno; Beule, Dieter; Horst, David; Wulf, Anna-Lena; Aust, Daniela; Werner, Martin; Reuter-Jessen, Kirsten; Stroebel, Philipp; Auber, Bernd; Sahm, Felix; Merkelbach-Bruse, Sabine; Siebolts, Udo; Roth, Wilfried; Lassmann, Silke; Klauschen, Frederick; Gaisa, Nadine T.; Weichert, Wilko (2024)
  • Bi-allelic loss-of-function variants in BCAS3 cause a syndromic neurodevelopmental disorder
    Hengel, Holger; Hannan, Shabab B.; Dyack, Sarah; MacKay, Sara B.; Schatz, Ulrich; Fleger, Martin; Kurringer, Andreas; Balousha, Ghassan; Ghanim, Zaid; Alkuraya, Fowzan S.; Alzaidan, Hamad; Alsaif, Hessa S.; Mitani, Tadahiro; Bozdogan, Sevcan; Pehlivan, Davut; Lupski, James R.; Gleeson, Joseph J.; Dehghani, Mohammadreza; Mehrjardi, Mohammad Y., V; Sherr, Elliott H.; Parks, Kendall C.; Argilli, Emanuela; Begtrup, Amber; Galehdari, Hamid; Balousha, Osama; Shariati, Gholamreza; Mazaheri, Neda; Malamiri, Reza A.; Pagnamenta, Alistair T.; Kingston, Helen; Banka, Siddharth; Jackson, Adam; Osmond, Mathew; Riess, Angelika; Haack, Tobias B.; Naegele, Thomas; Schuster, Stefanie; Hauser, Stefan; Admard, Jakob; Casadei, Nicolas; Velic, Ana; Macek, Boris; Ossowski, Stephan; Houlden, Henry; Maroofian, Reza; Schoels, Ludger (2021)
  • Bi-allelic loss-of-function variants in KIF21A cause severe fetal akinesia with arthrogryposis multiplex
    Falb, Ruth J.; Mueller, Amelie J.; Klein, Wolfram; Grimmel, Mona; Grasshoff, Ute; Spranger, Stephanie; Stoebe, Petra; Gauck, Darja; Kuechler, Alma; Dikow, Nicola; Schwaibold, Eva M. C.; Schmidt, Christoph; Averdunk, Luisa; Buchert, Rebecca; Heinrich, Tilman; Prodan, Natalia; Park, Joohyun; Kehrer, Martin; Sturm, Marc; Kelemen, Olga; Hartmann, Silke; Horn, Denise; Emmerich, Dirk; Hirt, Nina; Neumann, Armin; Kristiansen, Glen; Gembruch, Ulrich; Haen, Susanne; Siebert, Reiner; Hentze, Sabine; Hoopmann, Markus; Ossowski, Stephan; Waldmueller, Stephan; Beck-Woedl, Stefanie; Glaeser, Dieter; Tekesin, Ismail; Distelmaier, Felix; Riess, Olaf; Kagan, Karl-Oliver; Dufke, Andreas; Haack, Tobias B. (2023)
  • Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis
    Rabionet, Raquel; Remesal, Agustin; Mensa-Vilaro, Anna; Murias, Sara; Alcobendas, Rosa; Gonzalez-Roca, Eva; Ruiz-Ortiz, Estibaliz; Anton, Jordi; Iglesias, Estibaliz; Modesto, Consuelo; Comas, David; Puig, Anna; Drechsel, Oliver; Ossowski, Stephan; Yague, Jordi; Merino, Rosa; Estivill, Xavier; Arosteguis, Juan, I (2019)
  • Biallelic MAD2L1BP (p31comet) mutation is associated with mosaic aneuploidy and juvenile granulosa cell tumors
    Abdel-Salam, Ghada M. H.; Hellmuth, Susanne; Gradhand, Elise; Kaeseberg, Stephan; Winter, Jennifer; Pabst, Ann-Sophie; Eid, Maha M.; Thiele, Holger; Nuernberg, Peter; Budde, Birgit S.; Toliat, Mohammad Reza; Brecht, Ines B.; Schroeder, Christopher; Gschwind, Axel; Ossowski, Stephan; Haeuser, Friederike; Rossmann, Heidi; Abdel-Hamid, Mohamed S.; Hegazy, Ibrahim; Mohamed, Ahmed G.; Schneider, Dominik T.; Bertoli-Avella, Aida; Bauer, Peter; Pearring, Jillian N.; Pfundt, Rolph; Hoischen, Alexander; Gilissen, Christian; Strand, Dennis; Zechner, Ulrich; Tashkandi, Soha A.; Faqeih, Eissa A.; Stemmann, Olaf; Strand, Susanne; Bolz, Hanno J. (2023)
  • Cartography of opportunistic pathogens and antibiotic resistance genes in a tertiary hospital environment
    Chng, Kern Rei; Li, Chenhao; Bertrand, Denis; Ng, Amanda Hui Qi; Kwah, Junmei Samantha; Low, Hwee Meng; Tong, Chengxuan; Natrajan, Maanasa; Zhang, Michael Hongjie; Xu, Licheng; Ko, Karrie Kwan Ki; Ho, Eliza Xin Pei; Av-Shalom, Tamar, V; Teo, Jeanette Woon Pei; Khor, Chiea Chuen; Chen, Swaine L.; Mason, Christopher E.; Ng, Oon Tek; Marimuthu, Kalisvar; Ang, Brenda; Nagarajan, Niranjan; Danko, David; Bezdan, Daniela; Afshinnekoo, Ebrahim; Ahsanuddin, Sofia; Bhattacharya, Chandrima; Butler, Daniel J.; De Filippis, Francesca; Hecht, Jochen; Kahles, Andre; Karasikov, Mikhail; Kyrpides, Nikos C.; Leung, Marcus H. Y.; Meleshko, Dmitry; Mustafa, Harun; Mutai, Beth; Neches, Russell Y.; Ng, Amanda; Nieto-Caballero, Marina; Nikolayeva, Olga; Nikolayeva, Tatyana; Png, Eileen; Sanchez, Jorge L.; Shaaban, Heba; Sierra, Maria A.; Tong, Xinzhao; Young, Ben; Alicea, Josue; Bhattacharyya, Malay; Blekhman, Ran; Castro-Nallar, Eduardo; Canas, Ana M.; Chatziefthimiou, Aspassia D.; Crawford, Robert W.; Deng, Youping; Desnues, Christelle; Dias-Neto, Emmanuel; Donnellan, Daisy; Dybwad, Marius; Elhaik, Eran; Ercolini, Danilo; Frolova, Alina; Graf, Alexandra B.; Green, David C.; Hajirasouliha, Iman; Hernandez, Mark; Iraola, Gregorio; Jang, Soojin; Jones, Angela; Kelly, Frank J.; Knights, Kaymisha; Labaj, Pawel P.; Lee, Patrick K. H.; Shawn, Levy; Ljungdahl, Per; Lyons, Abigail; Mason-Buck, Gabriella; McGrath, Ken; Mongodin, Emmanuel F.; Moraes, Milton Ozorio; Noushmehr, Houtan; Oliveira, Manuela; Ossowski, Stephan; Osuolale, Olayinka O.; Ozcan, Orhan; Paez-Espino, David; Rascovan, Nicolas; Richard, Hugues; Raetsch, Gunnar; Schriml, Lynn M.; Semmler, Torsten; Sezerman, Osman U.; Shi, Leming; Song, Le Huu; Suzuki, Haruo; Court, Denise Syndercombe; Thomas, Dominique; Tighe, Scott W.; Udekwu, Klas, I; Ugalde, Juan A.; Valentine, Brandon (2020)
  • Cell-free DNA (cfDNA) and Exosome Profiling from a Year-Long Human Spaceflight Reveals Circulating Biomarkers
    Bezdan, Daniela; Grigorev, Kirill; Meydan, Cem; Vatter, Fanny A. Pelissier; Cioffi, Michele; Rao, Varsha; MacKay, Matthew; Nakahira, Kiichi; Burnham, Philip; Afshinnekoo, Ebrahim; Westover, Craig; Butler, Daniel; Mozsary, Chris; Donahoe, Timothy; Foox, Jonathan; Mishra, Tejaswini; Lucotti, Serena; Rana, Brinda K.; Melnick, Ari M.; Zhang, Haiying; Matei, Irina; Kelsen, David; Yu, Kenneth; Lyden, David C.; Taylor, Lynn; Bailey, Susan M.; Snyder, Michael P.; Garrett-Bakelman, Francine E.; Ossowski, Stephan; De Vlaminck, Iwijn; Mason, Christopher E. (2020)
  • Characterization of Genetic Heterogeneity in Recurrent Metastases of Renal Cell Carcinoma
    Sauter-Meyerhoff, Carolin; Bohnert, Regina; Mazzola, Pascale; Stuehler, Viktoria; Kandabarau, Siarhei; Buettner, Florian A.; Winter, Stefan; Herrmann, Lisa; Rausch, Steffen; Hennenlotter, Joerg; Fend, Falko; Scharpf, Marcus; Stenzl, Arnulf; Ossowski, Stephan; Bedke, Jens; Schwab, Matthias; Schaeffeler, Elke (2021)
  • Chemotherapy-free neoadjuvant pembrolizumab combined with trastuzumab and pertuzumab in HER2-enriched early breast cancer (WSG-KEYRICHED-1) a single-arm, phase 2 trial
    Kuemmel, Sherko; Graeser, Monika; Schmid, Peter; Reinisch, Mattea; Feuerhake, Friedrich; Volk, Valery; Armeanu-Ebinger, Sorin; Schuetz, Leon; Kelemen, Olga; Schroeder, Christopher; Ossowski, Stephan; Jozwiak, Katarzyna; Kostara, Athina; Scheffen, Iris; Luedtke-Heckenkamp, Kerstin; Hilpert, Felix; Kentsch, Angela; Ziske, Carsten; Depenbusch, Reinhard; Braun, Michael; Blohmer, Jens Uwe; zu Eulenburg, Christine; Christgen, Matthias; Bartels, Stephan; Kreipe, Hans Heinrich; Wuerstlein, Rachel; Biehl, Claudia; Pelz, Enrico; Hartkopf, Andreas; Harbeck, Nadia; Gluz, Oleg (2025)
  • CHIP mutations affect the heat shock response differently in human fibroblasts and iPSC-derived neurons
    Schuster, S.; Heuten, E.; Velic, A.; Admard, J.; Synofzik, M.; Ossowski, S.; Macek, B.; Hauser, S.; Schoels, L. (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)