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  3. Bens, Jonas [Editor]; Kleinfeld, Susanne [Editor]; Noack, Karoline [Editor]

    Fußball. Macht. Politik : interdisziplinäre Perspektiven auf Fußball und Gesellschaft

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    Berlin: De Gruyter, ©2014 ; Bielefeld: transcript, ©2014

    Published in: Kultur und soziale Praxis- De Gruyter eBook-Paket Sozialwissenschaften

  4. Siebert, Reiner [Author]; Bens, Susanne [Author]; Kolarova, Julia [Author] ; Institut für Humangenetik Kiel, Universitätsklinikum Ulm Institut für Humangenetik

    Schlussbericht zu dem BMBF geförderten Projekt: Imprintingerkrankungen: "Diseases caused by imprinting defects: clinical spectrum and pathogenetic mechanisms" - Teilprojekt 4

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    [Ulm]: Universität Ulm, [2018?]

  5. Barbaro, Michela [Author]; Bens, Susanne [Author]; Haake, Andrea [Author]; Peter, Michael [Author]; Brämswig, Jürgen [Author]; Holterhus, Paul-Martin [Author]; Lopez-Siguero, Juan Pedro [Author]; Menken, Udo [Author]; Mix, Monika [Author]; Sippell, Wolfgang [Author]; Wedell, Anna [Author]; Riepe, Felix Günther [Author]

    Multiplex ligation-dependent probe amplification analysis of the NR0B1(DAX1) locus enables explanation of phenotypic differences in patients with X-linked congenital adrenal hypoplasia

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    Basel: S. Karger, 23 March 2012

    Published in: Hormone research in paediatrics ; 77, (2012), 2

  6. Bens, Susanne [Author]; Ammerpohl, Ole [Author]; Martin-Subero, Jose Ignacio [Author]; Appari, Mahesh [Author]; Richter, Julia [Author]; Hiort, Olaf [Author]; Werner, Ralf [Author]; Riepe, Felix [Author]; Siebert, Reiner [Author]; Holterhus, Paul-Martin [Author]

    Androgen receptor mutations are associated with altered epigenomic programming as evidenced by HOXA5 methylation

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    Basel: Karger, 2011

    Published in: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation ; 5 (2011), 2

  7. Federico, Aniello [Author]; Thomas, Christian [Author]; Miskiewicz, Katarzyna [Author]; Woltering, Niklas [Author]; Zin, Francesca [Author]; Nemes, Karolina [Author]; Bison, Brigitte [Author]; Johann, Pascal-David [Author]; Hawes, Debra [Author]; Bens, Susanne [Author]; Kordes, Uwe [Author]; Albrecht, Steffen [Author]; Dohmen, Hildegard [Author]; Hauser, Peter [Author]; Keyvani, Kathy [Author]; Landeghem, Frank Karel Hendrik van [Author]; Løbner Lund, Eva [Author]; Scheie, David [Author]; Mawrin, Christian [Author]; Monoranu, Camelia Maria [Author]; Parm Ulhøi, Benedicte [Author]; Pietsch, Torsten [Author]; Reinhard, Harald [Author]; Riemenschneider, Markus Johannes [Author]; [...]

    ATRT-SHH comprises three molecular subgroups with characteristic clinical and histopathological features and prognostic significance

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    2022

    Published in: Acta neuropathologica ; 143(2022), 6, Seite 697-711

  11. Elgaafary, Shaymaa; Nagel, Inga; López, Cristina; Bens, Susanne; Szczepanowski, Monika; Wagener, Rabea; Klapper, Wolfram; Siebert, Reiner

    Double-hit lymphoma of the male breast: a case report

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    Springer Science and Business Media LLC, 2020

    Published in: Journal of Medical Case Reports

  13. Elbracht, Miriam; Buiting, Karin; Bens, Susanne; Siebert, Reiner; Horsthemke, Bernhard; Gillessen-Kaesbach, Gabriele; Eggermann, Thomas

    Chromosom 14-assoziierte Imprintingsyndrome – Temple- und Kagami-Ogata-Syndrome : Ein klinisches und molekulares Update : Ein klinisches und molekulares Update

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    Walter de Gruyter GmbH, 2015

    Published in: Medizinische Genetik