Works by Rahmann, Sven

Results: 80
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    Epigenetic dynamics of monocyteto-macrophage differentiation.

    Published in:
    Epigenetics & Chromatin, 2016, v. 8, p. 1, doi. 10.1186/s13072-016-0079-z
    By:
    • Wallner, Stefan;
    • Schröder, Christopher;
    • Leitão, Elsa;
    • Berulava, Tea;
    • Haak, Claudia;
    • Beiβer, Daniela;
    • Rahmann, Sven;
    • Richter, Andreas S.;
    • Manke, Thomas;
    • Bönisch, Ulrike;
    • Arrigoni, Laura;
    • Fröhler, Sebastian;
    • Klironomos, Filippos;
    • Wei Chen;
    • Rajewsky, Nikolaus;
    • Müller, Fabian;
    • Ebert, Peter;
    • Lengauer, Thomas;
    • Barann, Matthias;
    • Rosenstiel, Philip
    Publication type:
    Article
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    Mutational dynamics between primary and relapse neuroblastomas.

    Published in:
    Nature Genetics, 2015, v. 47, n. 8, p. 872, doi. 10.1038/ng.3349
    By:
    • Schramm, Alexander;
    • Althoff, Kristina;
    • Mahlow, Ellen;
    • Odersky, Andrea;
    • Henssen, Anton G;
    • Stephan, Harald;
    • De Preter, Katleen;
    • Speleman, Frank;
    • Plass, Christoph;
    • Lee, Sangkyun;
    • Lode, Holger N;
    • Henrich, Kai-Oliver;
    • Gartlgruber, Moritz;
    • Westermann, Frank;
    • Rahmann, Sven;
    • Fischer, Matthias;
    • Eggert, Angelika;
    • Schulte, Johannes H;
    • Köster, Johannes;
    • Beisser, Daniela
    Publication type:
    Article
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    SimLoRD: Simulation of Long Read Data.

    Published in:
    Bioinformatics, 2016, v. 32, n. 17, p. 2704, doi. 10.1093/bioinformatics/btw286
    By:
    • Stöcker, Bianca K.;
    • Köster, Johannes;
    • Rahmann, Sven
    Publication type:
    Article
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    Efficient exact motif discovery.

    Published in:
    Bioinformatics, 2009, v. 25, n. 12, p. i356, doi. 10.1093/bioinformatics/btp188
    By:
    • Tobias Marschall;
    • Sven Rahmann
    Publication type:
    Article
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    Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations.

    Published in:
    Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-110
    By:
    • Voigt, Claudia;
    • Mégarbané, André;
    • Neveling, Kornelia;
    • Czeschik, Johanna Christina;
    • Albrecht, Beate;
    • Callewaert, Bert;
    • Deimling, Florian von;
    • Hehr, Andreas;
    • Smeland, Marie Falkenberg;
    • König, Rainer;
    • Kuechler, Alma;
    • Marcelis, Carlo;
    • Puiu, Maria;
    • Reardon, Willie;
    • Riise Stensland, Hilde Monica Frostad;
    • Schweiger, Bernd;
    • Steehouwer, Marloes;
    • Teller, Christopher;
    • Martin, Marcel;
    • Rahmann, Sven
    Publication type:
    Article
    32

    Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations.

    Published in:
    2013
    By:
    • Voigt, Claudia;
    • Mégarbané, André;
    • Neveling, Kornelia;
    • Czeschik, Johanna Christina;
    • Albrecht, Beate;
    • Callewaert, Bert;
    • von Deimling, Florian;
    • Hehr, Andreas;
    • Falkenberg Smeland, Marie;
    • König, Rainer;
    • Kuechler, Alma;
    • Marcelis, Carlo;
    • Puiu, Maria;
    • Reardon, Willie;
    • Riise Stensland, Hilde Monica Frostad;
    • Schweiger, Bernd;
    • Steehouwer, Marloes;
    • Teller, Christopher;
    • Martin, Marcel;
    • Rahmann, Sven
    Publication type:
    journal article
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    A germ cell‐specific ageing pattern in otherwise healthy men.

    Published in:
    Aging Cell, 2020, v. 19, n. 10, p. 1, doi. 10.1111/acel.13242
    By:
    • Laurentino, Sandra;
    • Cremers, Jann‐Frederik;
    • Horsthemke, Bernhard;
    • Tüttelmann, Frank;
    • Czeloth, Karen;
    • Zitzmann, Michael;
    • Pohl, Eva;
    • Rahmann, Sven;
    • Schröder, Christopher;
    • Berres, Sven;
    • Redmann, Klaus;
    • Krallmann, Claudia;
    • Schlatt, Stefan;
    • Kliesch, Sabine;
    • Gromoll, Jörg
    Publication type:
    Article
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    Recurrent alterations of TNFAIP 3 ( A20) in T-cell large granular lymphocytic leukemia.

    Published in:
    International Journal of Cancer, 2016, v. 138, n. 1, p. 121, doi. 10.1002/ijc.29697
    By:
    • Johansson, Patricia;
    • Bergmann, Anke;
    • Rahmann, Sven;
    • Wohlers, Inken;
    • Scholtysik, René;
    • Przekopowitz, Martina;
    • Seifert, Marc;
    • Tschurtschenthaler, Gertraud;
    • Webersinke, Gerald;
    • Jäger, Ulrich;
    • Siebert, Reiner;
    • Klein ‐ Hitpass, Ludger;
    • Dührsen, Ulrich;
    • Dürig, Jan;
    • Küppers, Ralf
    Publication type:
    Article
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    Next-generation RNA sequencing reveals differential expression of MYCN target genes and suggests the mTOR pathway as a promising therapy target in MYCN-amplified neuroblastoma.

    Published in:
    International Journal of Cancer, 2013, v. 132, n. 3, p. E106, doi. 10.1002/ijc.27787
    By:
    • Schramm, Alexander;
    • Köster, Johannes;
    • Marschall, Tobias;
    • Martin, Marcel;
    • Schwermer, Melanie;
    • Fielitz, Kathrin;
    • Büchel, Gabriele;
    • Barann, Matthias;
    • Esser, Daniela;
    • RosENstiel, Philip;
    • Rahmann, SvEN;
    • Eggert, Angelika;
    • Schulte, Johannes H.
    Publication type:
    Article
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    Discovering motifs that induce sequencing errors.

    Published in:
    BMC Bioinformatics, 2013, v. 14, n. Suppl 5, p. 1, doi. 10.1186/1471-2105-14-S5-S1
    By:
    • Allhoff, Manuel;
    • Schönhuth, Alexander;
    • Martin, Marcel;
    • Costa, Ivan G.;
    • Rahmann, Sven;
    • Marschall, Tobias
    Publication type:
    Article