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Publications

featured publications

  • Cis-epistasis at the LPA locus and risk of cardiovascular diseases.

    Cardiovascular research

    Authors: Lingyao Zeng, Sylvain Moser, Nazanin Mirza-Schreiber, Claudia Lamina, Stefan Coassin, Christopher P Nelson, Tarmo Annilo, Oscar Franzén, Marcus E Kleber, Salome Mack, Till F M Andlauer, Beibei Jiang, Barbara Stiller, Ling Li, Christina Willenborg, Matthias Munz, Thorsten Kessler, Adnan Kastrati, Karl-Ludwig Laugwitz, Jeanette Erdmann, Susanne Moebus, Markus M Nöthen, Annette Peters, Konstantin Strauch, Martina Müller-Nurasyid, Christian Gieger, Thomas Meitinger, Elisabeth Steinhagen-Thiessen, Winfried März, Andres Metspalu, Johan L M Björkegren, Nilesh J Samani, Florian Kronenberg, Bertram Müller-Myhsok, Heribert Schunkert

  • Global Seroprevalence of Pre-existing Immunity Against AAV5 and Other AAV Serotypes in People with Hemophilia A.

    Human gene therapy

    Authors: Robert Klamroth, Gregory Hayes, Tatiana Andreeva, Keith Gregg, Takashi Suzuki, Ismail Haroon Mitha, Brandon Hardesty, Midori Shima, Toni Pollock, Patricia Slev, Johannes Oldenburg, Margareth C Ozelo, Natalie Stieltjes, Sabine-Marie Castet, Johnny Mahlangu, Flora Peyvandi, Rashid Kazmi, Jean-François Schved, Andrew D Leavitt, Michael Callaghan, Brigitte Pan-Petesch, Doris V Quon, Jayson Andrews, Alex Trinh, Mingjin Li, Wing Yen Wong

  • Functional characterization of the human Cdk10/Cyclin Q complex.

    Open biology

    Authors: Robert Düster, Yanlong Ji, Kuan-Ting Pan, Henning Urlaub, Matthias Geyer

  • Effects of a Fully Humanized Type II Anti-CD20 Monoclonal Antibody on Peripheral and CNS B Cells in a Transgenic Mouse Model of Multiple Sclerosis.

    International journal of molecular sciences

    Authors: Sabine Tacke, Rittika Chunder, Verena Schropp, Eduard Urich, Stefanie Kuerten

  • A genetic risk score of alleles related to MGUS interacts with socioeconomic position in a population-based cohort.

    Scientific reports

    Authors: Lisa Baak, Mirjam Frank, Jan Dürig, Ulrich Dührsen, Per Hoffmann, Markus M Nöthen, Nico Dragano, Raimund Erbel, Karl-Heinz Jöckel, Börge Schmidt

  • Descriptive analysis of 179 German reports of melanoma reported to an adverse drug reaction database as a drug-related adverse effect, and comparison with melanoma cases contained in German cancer registries.

    Clinical and experimental dermatology

    Authors: Bernhardt Sachs, Diana Dubrall, Klaus Kraywinkel, Maike Schulz, Matthias Schmid, Jens Bate, Wilma Fischer-Barth

  • The arginine methyltransferase PRMT7 promotes extravasation of monocytes resulting in tissue injury in COPD.

    Nature communications

    Authors: Gizem Günes Günsel, Thomas M Conlon, Aicha Jeridi, Rinho Kim, Zeynep Ertüz, Niklas J Lang, Meshal Ansari, Mariia Novikova, Dongsheng Jiang, Maximilian Strunz, Mariia Gaianova, Christine Hollauer, Christina Gabriel, Ilias Angelidis, Sebastian Doll, Jeanine C Pestoni, Stephanie L Edelmann, Marlene Sophia Kohlhepp, Adrien Guillot, Kevin Bassler, Hannelore P Van Eeckhoutte, Özgecan Kayalar, Nur Konyalilar, Tamara Kanashova, Sophie Rodius, Carolina Ballester-López, Carlos M Genes Robles, Natalia Smirnova, Markus Rehberg, Charu Agarwal, Ioanna Krikki, Benoit Piavaux, Stijn E Verleden, Bart Vanaudenaerde, Melanie Königshoff, Gunnar Dittmar, Ken R Bracke, Joachim L Schultze, Henrik Watz, Oliver Eickelberg, Tobias Stoeger, Gerald Burgstaller, Frank Tacke, Vigo Heissmeyer, Yuval Rinkevich, Hasan Bayram, Herbert B Schiller, Marcus Conrad, Robert Schneider, Ali Önder Yildirim

  • Real world considerations for newly approved CGRP receptor antagonists in migraine care.

    Expert review of neurotherapeutics

    Authors: Damiana Scuteri, Paolo Tonin, Pierluigi Nicotera, Giacinto Bagetta, Maria Tiziana Corasaniti

  • A Homozygous Deep Intronic Variant Causes Von Willebrand Factor Deficiency and Lack of Endothelial-Specific Secretory Organelles, Weibel-Palade Bodies.

    International journal of molecular sciences

    Authors: Hamideh Yadegari, Muhammad Ahmer Jamil, Natascha Marquardt, Johannes Oldenburg

  • A girl with unruly locks: molecular genetics makes a diagnosis of uncombable hair syndrome.

    Lancet (London, England)

    Authors: Jakob Lillemoen Drivenes, Regina C Betz, Anette Bygum