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  2. Steinmann, Johannes L.; Boltz, Tobias; Brosi, Miriam; Bründermann, Erik; Caselle, Michele; Kehrer, Benjamin; Rota, Lorenzo; Schönfeldt, Patrik; Schuh, Marcel; Siegel, Michael; Weber, Marc; Müller, Anke-Susanne

    Continuous bunch-by-bunch spectroscopic investigation of the microbunching instability

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    American Physical Society (APS), 2018

    Published in: Physical Review Accelerators and Beams

  3. Brosi, Miriam; Steinmann, Johannes L.; Blomley, Edmund; Boltz, Tobias; Bründermann, Erik; Gethmann, Julian; Kehrer, Benjamin; Mathis, Yves-Laurent; Papash, Alexander; Schedler, Manuel; Schönfeldt, Patrik; Schreiber, Patrick; Schuh, Marcel; Schwarz, Markus; Müller, Anke-Susanne; Caselle, Michele; Rota, Lorenzo; Weber, Marc; Kuske, Peter

    Systematic studies of the microbunching instability at very low bunch charges

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    American Physical Society (APS), 2019

    Published in: Physical Review Accelerators and Beams

  4. Dufke, Andreas; Hoopmann, Markus; Waldmüller, Stephan; Prodan, Natalia Carmen; Beck‐Wödl, Stefanie; Grasshoff, Ute; Heinrich, Tilman; Riess, Angelika; Kehrer, Martin; Falb, Ruth J.; Liebmann, Alexandra; Roggia, Cristiana; Stampfer, Miriam; Schadeck, Malou; Müller, Amelie J.; Grimmel, Mona; Stöbe, Petra; Gauck, Darja; Buchert‐Lo, Rebecca; Baumann, Sarah; Schäferhoff, Karin; Bertrand, Miriam; Menden, Benita; Sturm, Marc; [...]

    A single center experience of prenatal parent‐fetus trio exome sequencing for pregnancies with congenital anomalies

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    Wiley, 2022

    Published in: Prenatal Diagnosis

  5. Falb, Ruth J; Müller, Amelie J; Klein, Wolfram; Grimmel, Mona; Grasshoff, Ute; Spranger, Stephanie; Stöbe, Petra; Gauck, Darja; Kuechler, Alma; Dikow, Nicola; Schwaibold, Eva M C; Schmidt, Christoph; Averdunk, Luisa; Buchert, Rebecca; Heinrich, Tilman; Prodan, Natalia; Park, Joohyun; Kehrer, Martin; Sturm, Marc; Kelemen, Olga; Hartmann, Silke; Horn, Denise; Emmerich, Dirk; Hirt, Nina; [...]

    Bi-allelic loss-of-function variants inKIF21Acause severe fetal akinesia with arthrogryposis multiplex

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    BMJ, 2023

    Published in: Journal of Medical Genetics

  6. Szakszon, Katalin; Lourenco, Charles Marques; Callewaert, Bert Louis; Geneviève, David; Rouxel, Flavien; Morin, Denis; Denommé-Pichon, Anne-Sophie; Vitobello, Antonio; Patterson, Wesley G; Louie, Raymond; Pinto e Vairo, Filippo; Klee, Eric; Kaiwar, Charu; Gavrilova, Ralitza H; Agre, Katherine E; Jacquemont, Sebastien; Khadijé, Jizi; Giltay, Jacques; van Gassen, Koen; Merő, Gabriella; Gerkes, Erica; Van Bon, Bregje W; Rinne, Tuula; Pfundt, Rolph; [...]

    Further delineation of the rare GDACCF (global developmental delay, absent or hypoplastic corpus callosum, dysmorphic facies syndrome): genotype and phenotype of 22 patients withZNF148mutations

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    BMJ, 2024

    Published in: Journal of Medical Genetics