Works by Kiess, Wieland

Results: 385
    1
    2
    3
    4
    5
    6
    7
    8
    9
    10
    11
    12
    13
    14
    15
    16
    17
    18
    19
    20
    21
    22

    A Rare Case of Congenital Choroid Plexus Carcinoma.

    Published in:
    Pediatric Hematology & Oncology, 2012, v. 29, n. 7, p. 643, doi. 10.3109/08880018.2012.710298
    By:
    • Wilhelm, Miriam;
    • Hirsch, Wolfgang;
    • Merkenschlager, Andreas;
    • Stepan, Holger;
    • Geyer, Christian;
    • Kiess, Wieland
    Publication type:
    Article
    23
    24
    25
    26
    27
    28
    29
    30
    31
    32
    33
    34
    35
    36
    37

    Ocular complications at the limits of viability.

    Published in:
    Acta Paediatrica, 2007, v. 96, n. 3, p. 353, doi. 10.1111/j.1651-2227.2007.00087.x
    By:
    • Pulzer, Ferdinand;
    • Robel-Tillig, Eva;
    • Knüpfer, Matthias;
    • Foja, Christian;
    • Gebauer, Corinna;
    • Kiess, Wieland
    Publication type:
    Article
    38
    39

    De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.

    Published in:
    Nature Genetics, 2015, v. 47, n. 4, p. 393, doi. 10.1038/ng.3239
    By:
    • Syrbe, Steffen;
    • Bertsche, Astrid;
    • Bernhard, Matthias K;
    • Merkenschlager, Andreas;
    • Kiess, Wieland;
    • Serratosa, José M;
    • Nothnagel, Michael;
    • May, Patrick;
    • Krause, Roland;
    • Dorn, Thomas;
    • Vogt, Heinrich;
    • Krämer, Günter;
    • Mullis, Primus E;
    • Linnankivi, Tarja;
    • Lehesjoki, Anna-Elina;
    • Sterbova, Katalin;
    • Craiu, Dana C;
    • Hoffman-Zacharska, Dorota;
    • Hedrich, Ulrike B S;
    • Müller, Stephan
    Publication type:
    Article
    40

    CEP152 is a genome maintenance protein disrupted in Seckel syndrome.

    Published in:
    Nature Genetics, 2011, v. 43, n. 1, p. 23, doi. 10.1038/ng.725
    By:
    • Kalay, Ersan;
    • Yigit, Gökhan;
    • Aslan, Yakup;
    • Brown, Karen E.;
    • Pohl, Esther;
    • Bicknell, Louise S.;
    • Kayserili, Hülya;
    • Yun Li;
    • Tüysüz, Beyhan;
    • Nürnberg, Gudrun;
    • Kiess, Wieland;
    • Koegl, Manfred;
    • Baessmann, Ingelore;
    • Buruk, Kurtulus;
    • Toraman, Bayram;
    • Kayipmaz, Saadettin;
    • Kul, Sibel;
    • Ikbal, Mevlit;
    • Turner, Daniel J.;
    • Taylor, Martin S.
    Publication type:
    Article
    41

    Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations.

    Published in:
    Nature Genetics, 2009, v. 41, n. 2, p. 157, doi. 10.1038/ng.301
    By:
    • Meyre, David;
    • Delplanque, Jérôme;
    • Chèvre, Jean-Claude;
    • Lecoeur, Cécile;
    • Lobbens, Stéphane;
    • Gallina, Sophie;
    • Durand, Emmanuelle;
    • Vatin, Vincent;
    • Degraeve, Franck;
    • Proença, Christine;
    • Gaget, Stefan;
    • Körner, Antje;
    • Kovacs, Peter;
    • Kiess, Wieland;
    • Tichet, Jean;
    • Marre, Michel;
    • Hartikainen, Anna-Liisa;
    • Horber, Fritz;
    • Potoczna, Natascha;
    • Hercberg, Serge
    Publication type:
    Article
    42

    Variation in FTO contributes to childhood obesity and severe adult obesity.

    Published in:
    Nature Genetics, 2007, v. 39, n. 6, p. 724, doi. 10.1038/ng2048
    By:
    • Dina, Christian;
    • Meyre, David;
    • Gallina, Sophie;
    • Durand, Emmanuelle;
    • Körner, Antje;
    • Jacobson, Peter;
    • Carlsson, Lena M. S.;
    • Kiess, Wieland;
    • Vatin, Vincent;
    • Lecoeur, Cecile;
    • Delplanque, Jérome;
    • Vaillant, Emmanuel;
    • Pattou, François;
    • Ruiz, Juan;
    • Weill, Jacques;
    • Levy-Marchal, Claire;
    • Horber, Fritz;
    • Potoczna, Natascha;
    • Hercberg, Serge;
    • Le Stunff, Catherine
    Publication type:
    Article
    43
    44
    45
    46
    47
    48
    49
    50