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Published in JAMA : the journal of the American Medical Association (12.04.2016)
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Published in Current biology (23.11.2010)
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The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans
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Published in Nature genetics (01.03.2013)
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Published in Nature genetics (01.05.2013)
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Classification of patients with sepsis according to blood genomic endotype: a prospective cohort study
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Published in The lancet respiratory medicine (01.10.2017)
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TGFβ signaling directs serrated adenomas to the mesenchymal colorectal cancer subtype
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Published in EMBO molecular medicine (01.07.2016)
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Clonal dynamics towards the development of venetoclax resistance in chronic lymphocytic leukemia
Herling, Carmen D., Abedpour, Nima, Weiss, Jonathan, Schmitt, Anna, Jachimowicz, Ron Daniel, Merkel, Olaf, Cartolano, Maria, Oberbeck, Sebastian, Mayer, Petra, Berg, Valeska, Thomalla, Daniel, Kutsch, Nadine, Stiefelhagen, Marius, Cramer, Paula, Wendtner, Clemens-Martin, Persigehl, Thorsten, Saleh, Andreas, Altmüller, Janine, Nürnberg, Peter, Pallasch, Christian, Achter, Viktor, Lang, Ulrich, Eichhorst, Barbara, Castiglione, Roberta, Schäfer, Stephan C., Büttner, Reinhard, Kreuzer, Karl-Anton, Reinhardt, Hans Christian, Hallek, Michael, Frenzel, Lukas P., Peifer, Martin
Published in Nature communications (20.02.2018)
Published in Nature communications (20.02.2018)
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Published in American journal of human genetics (04.05.2012)
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Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas
Spier, Isabel, Holzapfel, Stefanie, Altmüller, Janine, Zhao, Bixiao, Horpaopan, Sukanya, Vogt, Stefanie, Chen, Sophia, Morak, Monika, Raeder, Susanne, Kayser, Katrin, Stienen, Dietlinde, Adam, Ronja, Nürnberg, Peter, Plotz, Guido, Holinski‐Feder, Elke, Lifton, Richard P., Thiele, Holger, Hoffmann, Per, Steinke, Verena, Aretz, Stefan
Published in International journal of cancer (15.07.2015)
Published in International journal of cancer (15.07.2015)
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Mutational dynamics between primary and relapse neuroblastomas
Schramm, Alexander, Köster, Johannes, Assenov, Yassen, Althoff, Kristina, Peifer, Martin, Mahlow, Ellen, Odersky, Andrea, Beisser, Daniela, Ernst, Corinna, Henssen, Anton G, Stephan, Harald, Schröder, Christopher, Heukamp, Lukas, Engesser, Anne, Kahlert, Yvonne, Theissen, Jessica, Hero, Barbara, Roels, Frederik, Altmüller, Janine, Nürnberg, Peter, Astrahantseff, Kathy, Gloeckner, Christian, De Preter, Katleen, Plass, Christoph, Lee, Sangkyun, Lode, Holger N, Henrich, Kai-Oliver, Gartlgruber, Moritz, Speleman, Frank, Schmezer, Peter, Westermann, Frank, Rahmann, Sven, Fischer, Matthias, Eggert, Angelika, Schulte, Johannes H
Published in Nature genetics (01.08.2015)
Published in Nature genetics (01.08.2015)
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Long‐lived macrophage reprogramming drives spike protein‐mediated inflammasome activation in COVID‐19
Theobald, Sebastian J, Simonis, Alexander, Georgomanolis, Theodoros, Kreer, Christoph, Zehner, Matthias, Eisfeld, Hannah S, Albert, Marie‐Christine, Chhen, Jason, Motameny, Susanne, Erger, Florian, Fischer, Julia, Malin, Jakob J, Gräb, Jessica, Winter, Sandra, Pouikli, Andromachi, David, Friederike, Böll, Boris, Koehler, Philipp, Vanshylla, Kanika, Gruell, Henning, Suárez, Isabelle, Hallek, Michael, Fätkenheuer, Gerd, Jung, Norma, Cornely, Oliver A, Lehmann, Clara, Tessarz, Peter, Altmüller, Janine, Nürnberg, Peter, Kashkar, Hamid, Klein, Florian, Koch, Manuel, Rybniker, Jan
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G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth
Pasternack, Sandra M, Molderings, Gerhard J, Voss, Katrin, Betz, Regina C, Nöthen, Markus M, Aboud, Khalid Al, Lee, Young-Ae, Hillmer, Axel M, Ramirez, Alfredo, Rüschendorf, Franz, Nürnberg, Peter, Franz, Thomas, von Kügelgen, Ivar
Published in Nature genetics (01.03.2008)
Published in Nature genetics (01.03.2008)
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Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration
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Published in Nature genetics (01.05.2015)
Published in Nature genetics (01.05.2015)
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A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome
Rutsch, Frank, MacDougall, Mary, Lu, Changming, Buers, Insa, Mamaeva, Olga, Nitschke, Yvonne, Rice, Gillian I., Erlandsen, Heidi, Kehl, Hans Gerd, Thiele, Holger, Nürnberg, Peter, Höhne, Wolfgang, Crow, Yanick J., Feigenbaum, Annette, Hennekam, Raoul C.
Published in American journal of human genetics (05.02.2015)
Published in American journal of human genetics (05.02.2015)
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Mutations in FAM134B , encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy
Gal, Andreas, Huebner, Antje K, Baets, Jonathan, De Jonghe, Peter, Soehendra, Désirée, Nürnberg, Gudrun, Rotthier, Annelies, Senderek, Jan, Kaether, Christoph, Hübner, Christian A, Hennings, J Christopher, Timmerman, Vincent, Farrell, Sandra A, Pamminger, Torsten, Kurth, Ingo, Topaloglu, Haluk, Nürnberg, Peter
Published in Nature genetics (01.11.2009)
Published in Nature genetics (01.11.2009)
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Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation
Gardella, Elena, Becker, Felicitas, Møller, Rikke S., Schubert, Julian, Lemke, Johannes R., Larsen, Line H. G., Eiberg, Hans, Nothnagel, Michael, Thiele, Holger, Altmüller, Janine, Syrbe, Steffen, Merkenschlager, Andreas, Bast, Thomas, Steinhoff, Bernhard, Nürnberg, Peter, Mang, Yuan, Bakke Møller, Louise, Gellert, Pia, Heron, Sarah E., Dibbens, Leanne M., Weckhuysen, Sarah, Dahl, Hans Atli, Biskup, Saskia, Tommerup, Niels, Hjalgrim, Helle, Lerche, Holger, Beniczky, Sándor, Weber, Yvonne G.
Published in Annals of neurology (01.03.2016)
Published in Annals of neurology (01.03.2016)
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