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Gehlen, Jan; Stundl, Anja; Debiec, Radoslaw; Fontana, Federica; Krane, Markus; Sharipova, Dinara; Nelson, Christopher P; Al-Kassou, Baravan; Giel, Ann-Sophie; Sinning, Jan-Malte; Bruenger, Christopher M H; Zelck, Carolin F; Koebbe, Laura L; Braund, Peter S; Webb, Thomas R; Hetherington, Simon; Ensminger, Stephan; Fujita, Buntaro; Mohamed, Salah A; Shrestha, Malakh; ... (2023). Elucidation of the genetic causes of bicuspid aortic valve disease. Cardiovascular research, 119(3), pp. 857-866. Oxford University Press 10.1093/cvr/cvac099
Schulz, Herbert; Ruppert, Ann-Kathrin; Zara, Federico; Madia, Francesca; Iacomino, Michele; S Vari, Maria; Balagura, Ganna; Minetti, Carlo; Striano, Pasquale; Bianchi, Amedeo; Marini, Carla; Guerrini, Renzo; Weber, Yvonne G; Becker, Felicitas; Lerche, Holger; Kapser, Claudia; Schankin, Christoph J.; Kunz, Wolfram S; Møller, Rikke S; Oliver, Karen L; ... (2019). No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy. Epilepsia, 60(5), e31-e36. Wiley-Blackwell 10.1111/epi.14657
Kröger, Annika; Hülsmann, Claudia; Fickl, Stefan; Spinell, Thomas; Hüttig, Fabian; Kaufmann, Frederic; Heimbach, André; Hoffmann, Per; Enkling, Norbert; Renvert, Stefan; Schwarz, Frank; Demmer, Ryan T; Papapanou, Panos N; Jepsen, Søren; Kebschull, Moritz (2018). The severity of human peri-implantitis lesions correlates with the level of submucosal microbial dysbiosis. Journal of clinical periodontology, 45(12), pp. 1498-1509. Wiley 10.1111/jcpe.13023
Anttila, Verneri; Bulik-Sullivan, Brendan; Finucane, Hilary K; Walters, Raymond K; Bras, Jose; Duncan, Laramie; Escott-Price, Valentina; Falcone, Guido J; Gormley, Padhraig; Malik, Rainer; Patsopoulos, Nikolaos A; Ripke, Stephan; Wei, Zhi; Yu, Dongmei; Lee, Phil H; Turley, Patrick; Grenier-Boley, Benjamin; Chouraki, Vincent; Kamatani, Yoichiro; Berr, Claudine; ... (2018). Analysis of shared heritability in common disorders of the brain. Science, 360(6395) American Association for the Advancement of Science 10.1126/science.aap8757
Treutlein, Jens; Frank, Josef; Streit, Fabian; Reinbold, Céline; Juraeva, Dilafruz; Degenhardt, Franziska; Rietschel, Liz; Witt, Stephanie; Forstner, Andreas; Ridinger, Monika; Strohmaier, Jana; Wodarz, Norbert; Dukal, Helene; Foo, Jerome; Hoffmann, Per; Herms, Stefan; Heilmann-Heimbach, Stefanie; Soyka, Michael; Maier, Wolfgang; Gaebel, Wolfgang; ... (2017). Genetic contribution to alcohol dependence: Investigation of a heterogeneous german sample of individuals with alcohol dependence, chronic alcoholic pancreatitis, and alcohol-related cirrhosis. Genes, 8(7), p. 183. MDPI 10.3390/genes8070183
Reinthaler, Eva M; Lal, Dennis; Lebon, Sebastien; Hildebrand, Michael S; Dahl, Hans-Henrik M; Regan, Brigid M; Feucht, Martha; Steinböck, Hannelore; Neophytou, Birgit; Ronen, Gabriel M; Roche, Laurian; Gruber-Sedlmayr, Ursula; Geldner, Julia; Haberlandt, Edda; Hoffmann, Per; Herms, Stefan; Gieger, Christian; Waldenberger, Melanie; Franke, Andre; Wittig, Michael; ... (2014). 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy. Human molecular genetics, 23(22), pp. 6069-6080. Oxford University Press 10.1093/hmg/ddu306
Arking, Dan E; Pulit, Sara L; Crotti, Lia; van der Harst, Pim; Munroe, Patricia B; Koopmann, Tamara T; Sotoodehnia, Nona; Rossin, Elizabeth J; Morley, Michael; Wang, Xinchen; Johnson, Andrew D; Lundby, Alicia; Gudbjartsson, Daníel F; Noseworthy, Peter A; Eijgelsheim, Mark; Bradford, Yuki; Tarasov, Kirill V; Dörr, Marcus; Müller-Nurasyid, Martina; Lahtinen, Annukka M; ... (2014). Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nature genetics, 46(8), pp. 826-836. Nature America 10.1038/ng.3014
Lemke, Johannes; Lal, Dennis; Reinthaler, Eva M; Steiner, Isabelle; Nothnagel, Michael; Alber, Michael; Geider, Kirsten; Laube, Bodo; Schwake, Michael; Finsterwalder, Katrin; Franke, Andre; Schilhabel, Markus; Jähn, Johanna A; Muhle, Hiltrud; Boor, Rainer; Van Paesschen, Wim; Caraballo, Roberto; Fejerman, Natalio; Weckhuysen, Sarah; De Jonghe, Peter; ... (2013). Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes. Nature genetics, 45(9), pp. 1067-1072. Nature America 10.1038/ng.2728
Albayrak, Özgür; Pütter, Carolin; Volckmar, Anna-Lena; Cichon, Sven; Hoffmann, Per; Nöthen, Markus M.; Jöckel, Karl-Heinz; Schreiber, Stefan; Wichmann, H-Erich; Faraone, Stephen V.; Neale, Benjamin M.; Herpertz-Dahlmann, Beate; Lehmkuhl, Gerd; Sinzig, Judith; Renner, Tobias J.; Romanos, Marcel; Warnke, Andreas; Lesch, Klaus-Peter; Reif, Andreas; Schimmelmann, Benno G.; ... (2013). Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder. American journal of medical genetics. Part B - Neuropsychiatric genetics, 162B(4), pp. 295-305. Hoboken, N.J.: Wiley-Liss 10.1002/ajmg.b.32144
Nokhbehsaim, Marjan; Eick, Sigrun; Nogueira, Andressa Vilas Boas; Hoffmann, Per; Herms, Stefan; Fröhlich, Holger; Jepsen, Søren; Jäger, Andreas; Cirelli, Joni Augusto; Deschner, James (2013). Stimulation of MMP-1 and CCL2 by NAMPT in PDL cells. Mediators of inflammation, 2013, p. 437123. Hindawi Publishing Corp. 10.1155/2013/437123
