Works by Schumacher, Johannes

Results: 75
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    MCM3AP and POMP Mutations Cause a DNA-Repair and DNA-Damage-Signaling Defect in an Immunodeficient Child.

    Published in:
    Human Mutation, 2016, v. 37, n. 3, p. 257, doi. 10.1002/humu.22939
    By:
    • Gatz, Susanne A.;
    • Salles, Daniela;
    • Jacobsen, Eva‐Maria;
    • Dörk, Thilo;
    • Rausch, Tobias;
    • Aydin, Sevtap;
    • Surowy, Harald;
    • Volcic, Meta;
    • Vogel, Walther;
    • Debatin, Klaus‐Michael;
    • Stütz, Adrian M.;
    • Schwarz, Klaus;
    • Pannicke, Ulrich;
    • Hess, Timo;
    • Korbel, Jan O.;
    • Schulz, Ansgar S.;
    • Schumacher, Johannes;
    • Wiesmüller, Lisa
    Publication type:
    Article
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    Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31.

    Published in:
    Bipolar Disorders, 2009, v. 11, n. 6, p. 610, doi. 10.1111/j.1399-5618.2009.00736.x
    By:
    • Hamshere, Marian L;
    • Schulze, Thomas G;
    • Schumacher, Johannes;
    • Corvin, Aiden;
    • Owen, Michael J;
    • Jamra, Rami Abou;
    • Propping, Peter;
    • Maier, Wolfgang;
    • Orozco y Diaz, Guillermo;
    • Mayoral, Fermin;
    • Rivas, Fabio;
    • Jones, Ian;
    • Jones, Lisa;
    • Kirov, George;
    • Gill, Michael;
    • Holmans, Peter A;
    • Nöthen, Markus M;
    • Cichon, Sven;
    • Rietschel, Marcella;
    • Craddock, Nick
    Publication type:
    Article
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    RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection.

    Published in:
    Nature Genetics, 2009, v. 41, n. 7, p. 773, doi. 10.1038/ng.398
    By:
    • Henneke, Marco;
    • Diekmann, Simone;
    • Ohlenbusch, Andreas;
    • Kaiser, Jens;
    • Engelbrecht, Volkher;
    • Kohlschütter, Alfried;
    • Krätzner, Ralph;
    • Madruga-Garrido, Marcos;
    • Mayer, Michèle;
    • Opitz, Lennart;
    • Rodriguez, Diana;
    • Rüschendorf, Franz;
    • Schumacher, Johannes;
    • Thiele, Holger;
    • Thoms, Sven;
    • Steinfeld, Robert;
    • Nürnberg, Peter;
    • Gärtner, Jutta
    Publication type:
    Article
    11

    Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin.

    Published in:
    2004
    By:
    • Cichon, Sven;
    • Buervenich, Silvia;
    • Kirov, George;
    • Akula, Nirmala;
    • Dimitrova, Albena;
    • Green, Elaine;
    • Schumacher, Johannes;
    • Klopp, Norman;
    • Becker, Tim;
    • Ohlraun, Stephanie;
    • Schulze, Thomas G.;
    • Tullius, Monja;
    • Gross, Magdalena M.;
    • Jones, Lisa;
    • Krastev, Stefan;
    • Nikolov, Ivan;
    • Hamshere, Marian;
    • Jones, Ian;
    • Czerski, Piotr M.;
    • Leszczynska-Rodziewicz, Anna
    Publication type:
    Letter
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    Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.

    Published in:
    Journal of Human Genetics, 2015, v. 60, n. 7, p. 399, doi. 10.1038/jhg.2015.37
    By:
    • Matsson, Hans;
    • Huss, Mikael;
    • Persson, Helena;
    • Einarsdottir, Elisabet;
    • Tiraboschi, Ettore;
    • Nopola-Hemmi, Jaana;
    • Schumacher, Johannes;
    • Neuhoff, Nina;
    • Warnke, Andreas;
    • Lyytinen, Heikki;
    • Schulte-Körne, Gert;
    • Nöthen, Markus M;
    • Leppänen, Paavo HT;
    • Peyrard-Janvid, Myriam;
    • Kere, Juha
    Publication type:
    Article
    20

    Pathogen-specific innate immune response patterns are distinctly affected by genetic diversity.

    Published in:
    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38994-5
    By:
    • Häder, Antje;
    • Schäuble, Sascha;
    • Gehlen, Jan;
    • Thielemann, Nadja;
    • Buerfent, Benedikt C.;
    • Schüller, Vitalia;
    • Hess, Timo;
    • Wolf, Thomas;
    • Schröder, Julia;
    • Weber, Michael;
    • Hünniger, Kerstin;
    • Löffler, Jürgen;
    • Vylkova, Slavena;
    • Panagiotou, Gianni;
    • Schumacher, Johannes;
    • Kurzai, Oliver
    Publication type:
    Article
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    Achalasia: will genetic studies provide insights?

    Published in:
    Human Genetics, 2010, v. 128, n. 4, p. 353, doi. 10.1007/s00439-010-0874-8
    By:
    • Gockel, Henning R.;
    • Schumacher, Johannes;
    • Gockel, Ines;
    • Lang, Hauke;
    • Haaf, Thomas;
    • Nöthen, Markus M.
    Publication type:
    Article
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    Identification of shared risk loci and pathways for bipolar disorder and schizophrenia.

    Published in:
    PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0171595
    By:
    • Forstner, Andreas J.;
    • Hecker, Julian;
    • Hofmann, Andrea;
    • Maaser, Anna;
    • Reinbold, Céline S.;
    • Mühleisen, Thomas W.;
    • Leber, Markus;
    • Strohmaier, Jana;
    • Degenhardt, Franziska;
    • Treutlein, Jens;
    • Mattheisen, Manuel;
    • Schumacher, Johannes;
    • Streit, Fabian;
    • Meier, Sandra;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Lacour, André;
    • Witt, Stephanie H.;
    • Reif, Andreas;
    • Müller-Myhsok, Bertram
    Publication type:
    Article
    30

    The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language.

    Published in:
    Behavior Genetics, 2012, v. 42, n. 4, p. 509, doi. 10.1007/s10519-012-9532-3
    By:
    • Anthoni, Heidi;
    • Sucheston, Lara;
    • Lewis, Barbara;
    • Tapia-Páez, Isabel;
    • Fan, Xiaotang;
    • Zucchelli, Marco;
    • Taipale, Mikko;
    • Stein, Catherine;
    • Hokkanen, Marie-Estelle;
    • Castrén, Eero;
    • Pennington, Bruce;
    • Smith, Shelley;
    • Olson, Richard;
    • Tomblin, J.;
    • Schulte-Körne, Gerd;
    • Nöthen, Markus;
    • Schumacher, Johannes;
    • Müller-Myhsok, Bertram;
    • Hoffmann, Per;
    • Gilger, Jeffrey
    Publication type:
    Article
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    Genome-wide transcriptome induced by Porphyromonas gingivalis LPS supports the notion of host-derived periodontal destruction and its association with systemic diseases.

    Published in:
    Innate Immunity, 2016, v. 22, n. 1, p. 72, doi. 10.1177/1753425915616685
    By:
    • Gölz, Lina;
    • Buerfent, Benedikt C.;
    • Hofmann, Andrea;
    • Hübner, Marc P.;
    • Rühl, Heiko;
    • Fricker, Nadine;
    • Schmidt, David;
    • Johannes, Oldenburg;
    • Jepsen, Søren;
    • Deschner, James;
    • Hoerauf, Achim;
    • Nöthen, Markus M.;
    • Schumacher, Johannes;
    • Jäger, Andreas
    Publication type:
    Article
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    The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.

    Published in:
    Human Molecular Genetics, 2009, v. 18, n. 14, p. 2719, doi. 10.1093/hmg/ddp204
    By:
    • Schumacher, Johannes;
    • Laje, Gonzalo;
    • Jamra, Rami Abou;
    • Becker, Tim;
    • Mühleisen, Thomas W.;
    • Vasilescu, Catalina;
    • Mattheisen, Manuel;
    • Herms, Stefan;
    • Hoffmann, Per;
    • Hillmer, Axel M.;
    • Georgi, Alexander;
    • Herold, Christine;
    • Schulze, Thomas G.;
    • Propping, Peter;
    • Rietschel, Marcella;
    • McMahon, Francis J.;
    • Nöthen, Markus M.;
    • Cichon, Sven
    Publication type:
    Article
    38

    Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5′-region are associated with bipolar affective disorder.

    Published in:
    Human Molecular Genetics, 2008, v. 17, n. 1, p. 87
    By:
    • Cichon, Sven;
    • Winge, Ingeborg;
    • Mattheisen, Manuel;
    • Georgi, Alexander;
    • Karpushova, Anna;
    • Freudenberg, Jan;
    • Freudenberg-Hua, Yun;
    • Babadjanova, Gulia;
    • Van Den Bogaert, Ann;
    • Abramova, Lilia I.;
    • Kapiletti, Sofia;
    • Knappskog, Per M.;
    • McKinney, Jeffrey;
    • Maier, Wolfgang;
    • Abou Jamra, Rami;
    • Schulze, Thomas G.;
    • Schumacher, Johannes;
    • Propping, Peter;
    • Rietschel, Marcella;
    • Haavik, Jan
    Publication type:
    Article
    39

    A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.

    Published in:
    Human Molecular Genetics, 2007, v. 16, n. 6, p. 667, doi. 10.1093/hmg/ddm009
    By:
    • Anthoni, Heidi;
    • Zucchelli, Marco;
    • Matsson, Hans;
    • Müller-Myhsok, Bertram;
    • Fransson, Ingegerd;
    • Schumacher, Johannes;
    • Massinen, Satu;
    • Onkamo, Päivi;
    • Warnke, Andreas;
    • Griesemann, Heide;
    • Hoffmann, Per;
    • Nopola-Hemmi, Jaana;
    • Lyytinen, Heikki;
    • Schulte-Körne, Gerd;
    • Kere, Juha;
    • Nöthen, Markus M.;
    • Peyrard-Janvid, Myriam
    Publication type:
    Article
    40

    A genome screen for genes predisposing to bipolar affective disorder detects a new susceptibility locus on 8q.

    Published in:
    Human Molecular Genetics, 2002, v. 11, n. 14, p. 1685, doi. 10.1093/hmg/11.14.1685
    By:
    • Cichon, Sven;
    • Schumacher, Johannes;
    • Müller, Daniel J.;
    • Hürter, Martina;
    • Windemuth, Christine;
    • Strauch, Konstantin;
    • Hemmer, Susanne;
    • Schulze, Thomas G.;
    • Schmidt-Wolf, Gabriele;
    • Albus, Margot;
    • Borrmann-Hassenbach, Margitta;
    • Franzek, Ernst;
    • Lanczik, Mario;
    • Fritze, Jürgen;
    • Kreiner, Roland;
    • Reuner, Ulrike;
    • Weigelt, Bettina;
    • Minges, Jürgen;
    • Lichtermann, Dirk;
    • Lerer, Bernhard
    Publication type:
    Article
    41

    Can long-range microsatellite data be used to predict short-range linkage disequilibrium?

    Published in:
    Human Molecular Genetics, 2002, v. 11, n. 12, p. 1363, doi. 10.1093/hmg/11.12.1363
    By:
    • Schulze, Thomas G.;
    • Chen, Yu-Sheng;
    • Akula, Nirmala;
    • Hennessy, Kathleen;
    • Badner, Judith A.;
    • McInnis, Melvin G.;
    • DePaulo, J. Raymond;
    • Schumacher, Johannes;
    • Cichon, Sven;
    • Propping, Peter;
    • Maier, Wolfgang;
    • Rietschel, Marcella;
    • Nöthen, Markus M.;
    • McMahon, Francis J.
    Publication type:
    Article
    42

    A genome screen for genes predisposingto bipolar affective disorder detects a new susceptibility locus on 8q.

    Published in:
    Human Molecular Genetics, 2001, v. 10, n. 25, p. 2933, doi. 10.1093/hmg/10.25.2933
    By:
    • Cichon, Sven;
    • Schumacher, Johannes;
    • Müller, Daniel J.;
    • Windemuth, Christine;
    • Strauch, Konstantin;
    • Hemmer, Susanne;
    • Schulze, Thomas G.;
    • Schmidt-Wolf, Gabriele;
    • Albus, Margot;
    • Borrmann-Hassenbach, Margitta;
    • Franzek, Ernst;
    • Lanczik, Mario;
    • Fritze, Jürgen;
    • Kreiner, Roland;
    • Reuner, Ulrike;
    • Weigelt, Bettina;
    • Minges, Jürgen;
    • Lichtermann, Dirk;
    • Lerer, Bernhard;
    • Kanyas, Kyra
    Publication type:
    Article
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    Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity.

    Published in:
    European Journal of Human Genetics, 2011, v. 19, n. 11, p. 1161, doi. 10.1038/ejhg.2011.98
    By:
    • Abou Jamra, R;
    • Wohlfart, Sigrun;
    • Zweier, Markus;
    • Uebe, Steffen;
    • Priebe, Lutz;
    • Ekici, Arif;
    • Giesebrecht, Susanne;
    • Abboud, Ahmad;
    • Al Khateeb, Mohammed Ayman;
    • Fakher, Mahmoud;
    • Hamdan, Saber;
    • Ismael, Amina;
    • Muhammad, Safia;
    • Nöthen, Markus M;
    • Schumacher, Johannes;
    • Reis, André
    Publication type:
    Article
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    Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations.

    Published in:
    Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00366-1
    By:
    • Kim-Hellmuth, Sarah;
    • Bechheim, Matthias;
    • Pütz, Benno;
    • Mohammadi, Pejman;
    • Nédélec, Yohann;
    • Giangreco, Nicholas;
    • Becker, Jessica;
    • Kaiser, Vera;
    • Fricker, Nadine;
    • Beier, Esther;
    • Boor, Peter;
    • Castel, Stephane E.;
    • Nöthen, Markus M.;
    • Barreiro, Luis B.;
    • Pickrell, Joseph K.;
    • Müller-Myhsok, Bertram;
    • Lappalainen, Tuuli;
    • Schumacher, Johannes;
    • Hornung, Veit
    Publication type:
    Article