Works matching AU Becker, Tim

Results: 104
    1
    2
    3
    4
    5
    6
    7
    8
    9
    10
    11

    GENESTAT: an information portal for design and analysis of genetic association studies.

    Published in:
    European Journal of Human Genetics, 2009, v. 17, n. 4, p. 533, doi. 10.1038/ejhg.2008.216
    By:
    • Ripatti, Samuli;
    • Becker, Tim;
    • Bickeböller, Heike;
    • Dominicus, Annica;
    • Fischer, Christine;
    • Humphreys, Keith;
    • Jonasdottir, Gudrun;
    • Moreau, Yves;
    • Olsson, Marita;
    • Ploner, Alexander;
    • Sheehan, Nuala;
    • Van Steen, Kristel;
    • Baur, Max;
    • van Duijn, Cornelia;
    • Palmgren, Juni
    Publication type:
    Article
    12
    13
    14
    15

    Susceptibility variants for male-pattern baldness on chromosome 20p11.

    Published in:
    Nature Genetics, 2008, v. 40, n. 11, p. 1279, doi. 10.1038/ng.228
    By:
    • Hillmer, Axel M;
    • Brockschmit, Felix F;
    • Hanneken, Sandra;
    • Eigelshoven, Sibylle;
    • Steffens, Michael;
    • Flaquer, Antonia;
    • Herms, Stefan;
    • Becker, Tim;
    • Kortüm, Anne-Katrin;
    • Nyholt, Dale R;
    • Zhao, Zhen Zhen;
    • Montgomery, Grant W;
    • Martin, Nicholas G;
    • Mühleisen, Thomas W;
    • Alblas, Margrieta A;
    • Moebus, Susanne;
    • Jöckel, Karl-Heinz;
    • Bröcker-Preuss, Martina;
    • Erbel, Raimund;
    • Reinartz, Roman
    Publication type:
    Article
    16

    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
    17
    18
    19
    20

    High-Throughput miRNA and mRNA Sequencing of Paired Colorectal Normal, Tumor and Metastasis Tissues and Bioinformatic Modeling of miRNA-1 Therapeutic Applications.

    Published in:
    PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0067461
    By:
    • Röhr, Christina;
    • Kerick, Martin;
    • Fischer, Axel;
    • Kühn, Alexander;
    • Kashofer, Karl;
    • Timmermann, Bernd;
    • Daskalaki, Andriani;
    • Meinel, Thomas;
    • Drichel, Dmitriy;
    • Börno, Stefan T.;
    • Nowka, Anja;
    • Krobitsch, Sylvia;
    • McHardy, Alice C.;
    • Kratsch, Christina;
    • Becker, Tim;
    • Wunderlich, Andrea;
    • Barmeyer, Christian;
    • Viertler, Christian;
    • Zatloukal, Kurt;
    • Wierling, Christoph
    Publication type:
    Article
    21
    22

    CFH, C3 and ARMS2 Are Significant Risk Loci for Susceptibility but Not for Disease Progression of Geographic Atrophy Due to AMD.

    Published in:
    PLoS ONE, 2009, v. 4, n. 10, p. 1, doi. 10.1371/journal.pone.0007418
    By:
    • Scholl, Hendrik P. N.;
    • Fleckenstein, Monika;
    • Fritsche, Lars G.;
    • Schmitz-Valckenberg, Steffen;
    • Göbel, Arno;
    • Adrion, Christine;
    • Herold, Christine;
    • Keilhauer, Claudia N.;
    • Mackensen, Friederike;
    • Mößner, Andreas;
    • Pauleikhoff, Daniel;
    • Weinberger, Andreas W. A.;
    • Mansmann, Ulrich;
    • Holz, Frank G.;
    • Becker, Tim;
    • Weber, Bernhard H. F.
    Publication type:
    Article
    23
    24
    25
    26
    27

    Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 20, p. 5536, doi. 10.1093/hmg/ddu259
    By:
    • Reutter, Heiko;
    • Draaken, Markus;
    • Pennimpede, Tracie;
    • Wittler, Lars;
    • Brockschmidt, Felix F.;
    • Ebert, Anne-Karolin;
    • Bartels, Enrika;
    • Rösch, Wolfgang;
    • Boemers, Thomas M.;
    • Hirsch, Karin;
    • Schmiedeke, Eberhard;
    • Meesters, Christian;
    • Becker, Tim;
    • Stein, Raimund;
    • Utsch, Boris;
    • Mangold, Elisabeth;
    • Nordenskjöld, Agneta;
    • Barker, Gillian;
    • Kockum, Christina Clementsson;
    • Zwink, Nadine
    Publication type:
    Article
    28
    29
    30
    31
    32
    33
    34
    35
    36
    37
    38
    39
    40

    DNA sequence variants of the FKBP5 gene are associated with unipolar depression.

    Published in:
    International Journal of Neuropsychopharmacology, 2010, v. 13, n. 5, p. 649, doi. 10.1017/S1461145709991155
    By:
    • Zobel, Astrid;
    • Schuhmacher, Anna;
    • Jessen, Frank;
    • Höfels, Susanne;
    • von Widdern, Olrik;
    • Metten, Martin;
    • Pfeiffer, Ute;
    • Hanses, Claudia;
    • Becker, Tim;
    • Rietschel, Marcella;
    • Scheef, Lukas;
    • Block, Wolfgang;
    • Schild, Hans H.;
    • Maier, Wolfgang;
    • Schwab, Sibylle G.
    Publication type:
    Article
    41

    Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss.

    Published in:
    Archives of Dermatological Research, 2014, v. 306, n. 4, p. 413, doi. 10.1007/s00403-013-1436-4
    By:
    • Nuwaihyd, Rima;
    • Redler, Silke;
    • Heilmann, Stefanie;
    • Drichel, Dmitriy;
    • Wolf, Sabrina;
    • Birch, Pattie;
    • Dobson, Kathy;
    • Lutz, Gerhard;
    • Giehl, Kathrin;
    • Kruse, Roland;
    • Tazi-Ahnini, Rachid;
    • Hanneken, Sandra;
    • Böhm, Markus;
    • Miesel, Anja;
    • Fischer, Tobias;
    • Wolff, Hans;
    • Becker, Tim;
    • Garcia-Bartels, Natalie;
    • Blume-Peytavi, Ulrike;
    • Nöthen, Markus
    Publication type:
    Article
    42

    Selected variants of the melanocortin 4 receptor gene ( MC4R) do not confer susceptibility to female pattern hair loss.

    Published in:
    Archives of Dermatological Research, 2013, v. 305, n. 3, p. 249, doi. 10.1007/s00403-012-1296-3
    By:
    • Mahmoudi, Hassnaa;
    • Redler, Silke;
    • Birch, Pattie;
    • Drichel, Dmitriy;
    • Dobson, Kathy;
    • Tazi-Ahnini, Rachid;
    • Teßmann, Peter;
    • Giehl, Kathrin;
    • Kruse, Roland;
    • Lutz, Gerhard;
    • Hanneken, Sandra;
    • Wolff, Hans;
    • Blume-Peytavi, Ulrike;
    • Becker, Tim;
    • Nöthen, Markus;
    • Messenger, Andrew;
    • Böhm, Markus;
    • Betz, Regina
    Publication type:
    Article
    43
    44
    45

    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
    46
    47
    48
    49
    50