Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk
Mitja Mitrovič(Yale University), Nadia Barizzone(Università degli Studi del Piemonte Orientale “Amedeo Avogadro”), Isabelle Cournu‐Rebeix, Ralf A. Linker(University Hospital Regensburg), An Goris(University of Cambridge), Brigitte Wildemann(Heidelberg University), Philip Van Damme(Universitair Ziekenhuis Leuven), Martin Stangel(Novartis (Switzerland)), Henrik Ullum(Statens Serum Institut), Efthimios Dardiotis(University of Thessaly), Tania Kümpfel(Ludwig-Maximilians-Universität München), Robin Lemmens(VIB-KU Leuven Center for Microbiology), Benjamin Knier(Evangelisches Diakoniekrankenhaus), Björn Tackenberg(Universitätsklinikum Gießen und Marburg), Bernhard Hemmer(Munich Cluster for Systems Neurology), Theresa Dankowski, Sandra Vukusik(Inserm), Pierre‐Antoine Gourraud, Verena Grummel(Tampere University), Christoph Heesen(Universität Hamburg), Ashley Beecham, Thomas Werge(Cardiff University), Uwe K. Zettl(University of Rostock), Friedemann Paul(Max Delbrück Center), Lise Wegner Thørner, Marie D’hooghe, Hayrettin Tumani, Felix Luessi, Viola Pongratz, Ralf Gold(St. Josef-Hospital), Bertrand Fontaine(Institut du Cerveau), Nikolaos A. Patsopoulos(Broad Institute), Cristina Agliardi(Don Carlo Gnocchi Foundation), Ulf Ziemann(TH Bingen University of Applied Sciences), Janna Saarela(University of Helsinki), Till F. M. Andlauer(TUM Klinikum), Clemens Warnke(Philipps University of Marburg), Florian Then Bergh(Leipzig University), Christiane Gasperi, Antonios Bayas(University of Augsburg), Vincent Damotte, Helle Bach Søndergaard, Bénédicte Dubois(University of California, San Francisco), Heinz Wiendl(Heidelberg University), Léna Guillot‐Noël(Centre National de la Recherche Scientifique), Per Soelberg Sorensen, Dorothea Buck, Christina M. Lill(University of Münster), Mark Lathrop(McGill Genome Centre), Finn Sellebjerg(Kaiser Permanente)
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