Incidence and prognostic impact of new-onset atrial fibrillation in patients with septic shock: a prospective observational study von Meierhenrich, Rainer, Steinhilber, Elisa, Eggermann, Christian, Weiss, Manfred, Voglic, Sami, Bögelein, Daniela, Gauss, Albrecht, Georgieff, Michael, Stahl, Wolfgang

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Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement von Brioude, Frédéric, Kalish, Jennifer M., Mussa, Alessandro, Foster, Alison C., Bliek, Jet, Ferrero, Giovanni Battista, Boonen, Susanne E., Cole, Trevor, Baker, Robert, Bertoletti, Monica, Cocchi, Guido, Coze, Carole, De Pellegrin, Maurizio, Hussain, Khalid, Ibrahim, Abdulla, Kilby, Mark D., Krajewska-Walasek, Malgorzata, Kratz, Christian P., Ladusans, Edmund J., Lapunzina, Pablo, Le Bouc, Yves, Maas, Saskia M., Macdonald, Fiona, Õunap, Katrin, Peruzzi, Licia, Rossignol, Sylvie, Russo, Silvia, Shipster, Caroleen, Skórka, Agata, Tatton-Brown, Katrina, Tenorio, Jair, Tortora, Chiara, Grønskov, Karen, Netchine, Irène, Hennekam, Raoul C., Prawitt, Dirk, Tümer, Zeynep, Eggermann, Thomas, Mackay, Deborah J. G., Riccio, Andrea, Maher, Eamonn R.

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Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important von Eggermann, Thomas, Brück, Johanna, Knopp, Cordula, Fekete, György, Kratz, Christian, Tasic, Velibor, Kurth, Ingo, Elbracht, Miriam, Eggermann, Katja, Begemann, Matthias

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Novel phenotype with prominent cerebellar oculomotor dysfunction in spastic paraplegia type 39 von Viertauer, Sebastian, Kurth, Ingo, Eggermann, Katja, Eggers, Christian

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Automatized detection of uniparental disomies in a large cohort von Moch, Johanna, Radtke, Maximilian, Liehr, Thomas, Eggermann, Thomas, Gilissen, Christian, Pfundt, Rolph, Astuti, Galuh, Hentschel, Julia, Schumann, Isabell

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One test for all: whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver-Russell syndrome von Meyer, Robert, Begemann, Matthias, Hübner, Christian Thomas, Dey, Daniela, Kuechler, Alma, Elgizouli, Magdeldin, Schara, Ulrike, Ambrozaityte, Laima, Burnyte, Birute, Schröder, Carmen, Kenawy, Asmaa, Kroisel, Peter, Demuth, Stephanie, Fekete, Gyorgy, Opladen, Thomas, Elbracht, Miriam, Eggermann, Thomas

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Molecular Basis of Beckwith–Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice von Eggermann, Thomas, Maher, Eamonn R., Kratz, Christian P., Prawitt, Dirk

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HMGA2 Variants in Silver-Russell Syndrome: Homozygous and Heterozygous Occurrence von Hübner, Christian Thomas, Meyer, Robert, Kenawy, Asmaa, Ambrozaityte, Laima, Matuleviciene, Ausra, Kraft, Florian, Begemann, Matthias, Elbracht, Miriam, Eggermann, Thomas

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Cancer incidence and spectrum among children with genetically confirmed Beckwith-Wiedemann spectrum in Germany: a retrospective cohort study von Cöktü, Sümeyye, Spix, Claudia, Kaiser, Melanie, Beygo, Jasmin, Kleinle, Stephanie, Bachmann, Nadine, Kohlschmidt, Nicolai, Prawitt, Dirk, Beckmann, Alf, Klaes, Ruediger, Nevinny-Stickel-Hinzpeter, Claudia, Döhnert, Steffi, Kraus, Cornelia, Kadgien, Gundula, Vater, Inga, Biskup, Saskia, Kutsche, Michael, Kohlhase, Jürgen, Eggermann, Thomas, Zenker, Martin, Kratz, Christian P.

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Genetic Variants in the Promoter Region of the Macrophage Migration Inhibitory Factor are Associated with the Severity of Hepatitis C Virus-Induced Liver Fibrosis von Wirtz, Theresa Hildegard, Fischer, Petra, Backhaus, Christina, Bergmann, Irina, Brandt, Elisa Fabiana, Heinrichs, Daniel, Koenen, Maria Teresa, Schneider, Kai Markus, Eggermann, Thomas, Kurth, Ingo, Stoppe, Christian, Bernhagen, Jürgen, Bruns, Tony, Fischer, Janett, Berg, Thomas, Trautwein, Christian, Berres, Marie-Luise

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Differential diagnosis of vacuolar myopathies in the NGS era von Mair, Dorothea, Biskup, Saskia, Kress, Wolfram, Abicht, Angela, Brück, Wolfgang, Zechel, Sabrina, Knop, Karl Christian, Koenig, Fatima Barbara, Tey, Shelisa, Nikolin, Stefan, Eggermann, Katja, Kurth, Ingo, Ferbert, Andreas, Weis, Joachim

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Endothelial progenitor cell culture and differentiation in vitro: a methodological comparison using human umbilical cord blood von EGGERMANN, Juliane, KLICHE, Stefanie, JARMY, Gergely, HOFFMANN, Karin, MAYR-BEYRLE, Ulrike, DEBATIN, Klaus-Michael, WALTENBERGER, Johannes, BELTINGER, Christian

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Systematic assessment of COVID-19 host genetics using whole genome sequencing data von Schmidt, Axel, Casadei, Nicolas, Brand, Fabian, Demidov, German, Vojgani, Elaheh, Abolhassani, Ayda, Aldisi, Rana, Butler-Laporte, Guillaume, Alawathurage, T Madhusankha, Augustin, Max, Bals, Robert, Bellinghausen, Carla, Berger, Marc Moritz, Bitzer, Michael, Bode, Christian, Boos, Jannik, Brenner, Thorsten, Cornely, Oliver A, Eggermann, Thomas, Erber, Johanna, Feldt, Torsten, Fuchsberger, Christian, Gagneur, Julien, Göpel, Siri, Haack, Tobias, Häberle, Helene, Hanses, Frank, Heggemann, Julia, Hehr, Ute, Hellmuth, Johannes C, Herr, Christian, Hinney, Anke, Hoffmann, Per, Illig, Thomas, Jensen, Björn-Erik Ole, Keitel, Verena, Kim-Hellmuth, Sarah, Koehler, Philipp, Kurth, Ingo, Lanz, Anna-Lisa, Latz, Eicke, Lehmann, Clara, Luedde, Tom, Maj, Carlo, Mian, Michael, Miller, Abigail, Muenchhoff, Maximilian, Pink, Isabell, Protzer, Ulrike, Rohn, Hana, Rybniker, Jan, Scaggiante, Federica, Schaffeldt, Anna, Scherer, Clemens, Schieck, Maximilian, Schmidt, Susanne V, Schommers, Philipp, Spinner, Christoph D, Vehreschild, Maria J G T, Velavan, Thirumalaisamy P, Volland, Sonja, Wilfling, Sibylle, Winter, Christof, Richards, J Brent, Heimbach, André, Becker, Kerstin, Ossowski, Stephan, Schultze, Joachim L, Nürnberg, Peter, Nöthen, Markus M, Motameny, Susanne, Nothnagel, Michael, Riess, Olaf, Schulte, Eva C, Ludwig, Kerstin U

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Mosaic Variegated Aneuploidy Syndrome and Noonan Syndrome in the Same Family von Hübner, Christian T., Amin, Asmaa K., Dey, Daniela, Meyer, Robert, Eggermann, Thomas

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FRI-262-Genetic variants in the promotor region of the macrophage migration inhibitory factor are associated with severity of HCV-induced liver fibrosis von Wirtz, Theresa Hildegard, Christina, Backhaus, Fischer, Petra, Irina, Bergmann, Thomas, Eggermann, Ingo, Kurth, Stoppe, Christian, Bernhagen, Jürgen, Berg, Thomas, Trautwein, Christian, Berres, Marie-Luise

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The genetic landscape of axonal neuropathies in the middle-aged and elderly: Focus on MME von Senderek, Jan, Lassuthova, Petra, Kabzińska, Dagmara, Abreu, Lisa, Baets, Jonathan, Beetz, Christian, Braathen, Geir J., Brenner, David, Dalton, Joline, Dankwa, Lois, Deconinck, Tine, De Jonghe, Peter, Dräger, Bianca, Eggermann, Katja, Ellis, Melina, Fischer, Carina, Stojkovic, Tanya, Herrmann, David N., Horvath, Rita, Høyer, Helle, Iglseder, Stephan, Kennerson, Marina, Kinslechner, Katharina, Kohler, Jennefer N., Kurth, Ingo, Laing, Nigel G., Lamont, Phillipa J., N. Löscher, Wolfgang, Ludolph, Albert, Marques, Wilson, Nicholson, Garth, Ong, Royston, Petri, Susanne, Ravenscroft, Gianina, Rebelo, Adriana, Ricci, Giulia, Rudnik-Schöneborn, Sabine, Schirmacher, Anja, Schlotter-Weigel, Beate, Schoels, Ludger, Schüle, Rebecca, Synofzik, Matthis, Francou, Bruno, Strom, Tim M., Wagner, Johannes, Walk, David, Wanschitz, Julia, Weinmann, Daniela, Weishaupt, Jochen, Wiessner, Manuela, Windhager, Reinhard, Young, Peter, Züchner, Stephan, Toegel, Stefan, Seeman, Pavel, Kochański, Andrzej, Auer-Grumbach, Michaela

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Balance between macrophage migration inhibitory factor and sCD74 predicts outcome in patients with acute decompensation of cirrhosis von Wirtz, Theresa H., Reuken, Philipp A., Jansen, Christian, Fischer, Petra, Bergmann, Irina, Backhaus, Christina, Emontzpohl, Christoph, Reißing, Johanna, Brandt, Elisa F., Koenen, M. Teresa, Schneider, Kai M., Schierwagen, Robert, Brol, Maximilian J., Chang, Johannes, Zimmermann, Henning W., Köse-Vogel, Nilay, Eggermann, Thomas, Kurth, Ingo, Stoppe, Christian, Bucala, Richard, Bernhagen, Jürgen, Praktiknjo, Michael, Stallmach, Andreas, Trautwein, Christian, Trebicka, Jonel, Bruns, Tony, Berres, Marie-Luise

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Genetic pain loss disorders von Lischka, Annette, Lassuthova, Petra, Çakar, Arman, Record, Christopher J., Van Lent, Jonas, Baets, Jonathan, Dohrn, Maike F., Senderek, Jan, Lampert, Angelika, Bennett, David L., Wood, John N., Timmerman, Vincent, Hornemann, Thorsten, Auer-Grumbach, Michaela, Parman, Yesim, Hübner, Christian A., Elbracht, Miriam, Eggermann, Katja, Geoffrey Woods, C., Cox, James J., Reilly, Mary M., Kurth, Ingo

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Autosomal recessive postlingual hearing loss (DFNB8): compound heterozygosity for two novel TMPRSS3 mutations in German siblings von Elbracht, Miriam, Senderek, Jan, Eggermann, Thomas, Thürmer, Christian, Park, Jonas, Westhofen, Martin, Zerres, Klaus

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One test for all: whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver-Russell syndrome von Meyer, Robert, Begemann, Matthias, Hübner, Christian Thomas, Dey, Daniela, Kuechler, Alma, Elgizouli, Magdeldin, Schara, Ulrike, Ambrozaityte, Laima, Burnyte, Birute, Schröder, Carmen, Kenawy, Asmaa, Kroisel, Peter, Demuth, Stephanie, Fekete, Gyorgy, Opladen, Thomas, Elbracht, Miriam, Eggermann, Thomas

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