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Barc, Julien; Tadros, Rafik; Glinge, Charlotte; Chiang, David Y.; Jouni, Mariam; Simonet, Floriane; Jurgens, Sean J.; Baudic, Manon; Nicastro, Michele; Potet, Franck; Offerhaus, Joost A.; Walsh, Roddy; Choi, Seung Hoan; Verkerk, Arie O.; Mizusawa, Yuka; Anys, Soraya; Minois, Damien; Arnaud, Marine; Duchateau, Josselin; Wijeyeratne, Yanushi D.; ... (2022). Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nature genetics, 54(3), pp. 232-239. Springer Nature 10.1038/s41588-021-01007-6
Lahrouchi, Najim; Tadros, Rafik; Crotti, Lia; Mizusawa, Yuka; Postema, Pieter G; Beekman, Leander; Walsh, Roddy; Hasegawa, Kanae; Barc, Julien; Ernsting, Marko; Turkowski, Kari L; Mazzanti, Andrea; Beckmann, Britt M; Shimamoto, Keiko; Diamant, Ulla-Britt; Wijeyeratne, Yanushi D; Kucho, Yu; Robyns, Tomas; Ishikawa, Taisuke; Arbelo, Elena; ... (2020). Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. Circulation, 142(4), pp. 324-338. American Heart Association 10.1161/CIRCULATIONAHA.120.045956
Christophersen, Ingrid E; Rienstra, Michiel; Roselli, Carolina; Yin, Xiaoyan; Geelhoed, Bastiaan; Barnard, John; Lin, Honghuang; Arking, Dan E; Smith, Albert V; Albert, Christine M; Chaffin, Mark; Tucker, Nathan R; Li, Molong; Klarin, Derek; Bihlmeyer, Nathan A; Low, Siew-Kee; Weeke, Peter E; Müller-Nurasyid, Martina; Smith, J Gustav; Brody, Jennifer A; ... (2017). Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nature genetics, 49(6), pp. 946-952. Nature America 10.1038/ng.3843
Andlauer, Till F M; Buck, Dorothea; Antony, Gisela; Bayas, Antonios; Bechmann, Lukas; Berthele, Achim; Chan, Andrew; Gasperi, Christiane; Gold, Ralf; Graetz, Christiane; Haas, Jürgen; Hecker, Michael; Infante-Duarte, Carmen; Knop, Matthias; Kümpfel, Tania; Limmroth, Volker; Linker, Ralf A; Loleit, Verena; Luessi, Felix; Meuth, Sven G; ... (2016). Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. Science Advances, 2(6), e1501678. American Association for the Advancement of Science 10.1126/sciadv.1501678
Rautanen, Anna; Mills, Tara C; Gordon, Anthony C; Hutton, Paula; Steffens, Michael; Nuamah, Rosamond; Chiche, Jean-Daniel; Parks, Tom; Chapman, Stephen J; Davenport, Emma E; Elliott, Katherine S; Bion, Julian; Lichtner, Peter; Meitinger, Thomas; Wienker, Thomas F; Caulfield, Mark J; Mein, Charles; Bloos, Frank; Bobek, Ilona; Cotogni, Paolo; ... (2015). Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study. The lancet. Respiratory medicine, 3(1), pp. 53-60. Elsevier 10.1016/S2213-2600(14)70290-5
Oexle, Konrad; Schormair, Barbara; Ried, Janina S.; Czamara, Darina; Heim, Katharina; Frauscher, Birgit; Högl, Birgit; Trenkwalder, Claudia; Fiedler, G. Martin; Thiery, Joachim; Lichtner, Peter; Prokisch, Holger; Specht, Michael; Müller-Myhsok, Bertram; Döring, Angela; Gieger, Christian; Peters, Annette; Wichmann, H.-Erich; Meitinger, Thomas and Winkelmann, Juliane (2013). Dilution of candidates: the case of iron-related genes in restless legs syndrome. European journal of human genetics, 21(4), pp. 410-414. Nature Publishing Group 10.1038/ejhg.2012.193
Faraco, Juliette; Lin, Ling; Kornum, Birgitte Rahbek; Kenny, Eimear E; Trynka, Gosia; Einen, Mali; Rico, Tom J; Lichtner, Peter; Dauvilliers, Yves; Arnulf, Isabelle; Lecendreux, Michel; Javidi, Sirous; Geisler, Peter; Mayer, Geert; Pizza, Fabio; Poli, Francesca; Plazzi, Giuseppe; Overeem, Sebastiaan; Lammers, Gert Jan; Kemlink, David; ... (2013). ImmunoChip study implicates antigen presentation to T cells in narcolepsy. PLoS genetics, 9(2), e1003270. San Francisco, Calif.: Public Library of Science 10.1371/journal.pgen.1003270
Testoni, Stefania; Bartolone, Elena; Rossi, Marco; Patrignani, Andrea; Bruggmann, Rémy; Lichtner, Peter; Tetens, Jens; Gentile, Arcangelo; Drögemüller, Cord (2012). KDM2B is implicated in bovine lethal multi-organic developmental dysplasia. PLoS ONE, 7(9), e45634. Lawrence, Kans.: Public Library of Science 10.1371/journal.pone.0045634
Menoud, Annie; Welle, Monika Maria; Tetens, Jens; Lichtner, Peter; Drögemüller, Cord; Szecsi, Pal Bela (2012). A COL7A1 Mutation Causes Dystrophic Epidermolysis Bullosa in Rotes Höhenvieh Cattle. PLoS ONE, 7(6), e38823. Public Library of Science 10.1371/journal.pone.0038823
Oexle, Konrad; Ried, Janina S; Hicks, Andrew A; Tanaka, Toshiko; Hayward, Caroline; Bruegel, Mathias; Gögele, Martin; Lichtner, Peter; Müller-Myhsok, Bertram; Döring, Angela; Illig, Thomas; Schwienbacher, Christine; Minelli, Cosetta; Pichler, Irene; Fiedler, G Martin; Thiery, Joachim; Rudan, Igor; Wright, Alan F; Campbell, Harry; Ferrucci, Luigi; ... (2011). Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. Human molecular genetics, 20(5), pp. 1042-7. Oxford: Oxford University Press 10.1093/hmg/ddq538
