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  1. Gogiel, Magdalena; Begemann, Matthias; Spengler, Sabrina; Soellner, Lukas; Göretzlehner, Ulf; Eggermann, Thomas; Strobl-Wildemann, Gertrud

    Genome-wide paternal uniparental disomy mosaicism in a woman with Beckwith–Wiedemann syndrome and ovarian steroid cell tumour

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    Springer Science and Business Media LLC, 2013

    Published in: European Journal of Human Genetics

  2. Rolles, Benjamin; Meyer, Robert; Begemann, Matthias; Elbracht, Miriam; Jost, Edgar; Stelljes, Matthias; Kurth, Ingo; Brümmendorf, Tim H.; Silling, Gerda

    DDX41 germline variants causing donor cell leukemia indicate a need for further genetic workup in the context of hematopoietic stem cell transplantation

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    Springer Science and Business Media LLC, 2023

    Published in: Blood Cancer Journal

  3. Trubetskoy, Vassily [Author]; Pardiñas, Antonio F. [Author]; Lam, Max [Author]; Giannitelli, Marianna [Author]; Giegling, Ina [Author]; Giusti-Rodríguez, Paola [Author]; Godard, Stephanie [Author]; Goldstein, Jacqueline I. [Author]; González Peñas, Javier [Author]; González-Pinto, Ana [Author]; Gopal, Srihari [Author]; Gratten, Jacob [Author]; Green, Michael F. [Author]; Watanabe, Kyoko [Author]; Greenwood, Tiffany A. [Author]; Guillin, Olivier [Author]; Gülöksüz, Sinan [Author]; Gur, Raquel E. [Author]; Gur, Ruben C. [Author]; Gutiérrez, Blanca [Author]; Hahn, Eric [Author]; Hakonarson, Hakon [Author]; Haroutunian, Vahram [Author]; Hartmann, Annette M. [Author]; [...]

    Mapping genomic loci implicates genes and synaptic biology in schizophrenia

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    Nature Publ. Group, 2022

    Published in: Nature <London> 604, 502–508 (2022). doi:10.1038/s41586-022-04434-5

  4. Eggermann, Thomas; Brück, Johanna; Knopp, Cordula; Fekete, György; Kratz, Christian; Tasic, Velibor; Kurth, Ingo; Elbracht, Miriam; Eggermann, Katja; Begemann, Matthias

    Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important

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    Springer Science and Business Media LLC, 2020

    Published in: Journal of Molecular Medicine

  5. Chantot-Bastaraud, Sandra; Stratmann, Svea; Brioude, Frédéric; Begemann, Matthias; Elbracht, Miriam; Graul-Neumann, Luitgard; Harbison, Madeleine; Netchine, Irène; Eggermann, Thomas

    Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction

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    Springer Science and Business Media LLC, 2017

    Published in: Molecular Cytogenetics