Einträge von Wichter, Thomas auf dem Publikationsserver

Garnier, Sophie , Harakalova, Magdalena, Weiss, Stefan , Mokry, Michal, Regitz-Zagrosek, Vera , Hengstenberg, Christian, Cappola, Thomas P., Isnard, Richard, Arbustini, Eloisa , Cook, Stuart A., van Setten, Jessica, Calis, Jorg J. A., Hakonarson, Hakon, Morley, Michael P., Stark, Klaus, Prasad, Sanjay K., Li, Jin, O'Regan, Declan P. , Grasso, Maurizia, Müller-Nurasyid, Martina, Meitinger, Thomas, Empana, Jean-Philippe, Strauch, Konstantin, Waldenberger, Melanie, Marguiles, Kenneth B., Seidman, Christine E., Kararigas, Georgios , Meder, Benjamin, Haas, Jan, Boutouyrie, Pierre, Lacolley, Patrick, Jouven, Xavier, Erdmann, Jeanette , Blankenberg, Stefan, Wichter, Thomas, Ruppert, Volker, Tavazzi, Luigi, Dubourg, Olivier, Roizes, Gérard, Dorent, Richard, de Groote, Pascal, Fauchier, Laurent, Trochu, Jean-Noël, Aupetit, Jean-François, Bilinska, Zofia T., Germain, Marine, Völker, Uwe, Hemerich, Daiane, Raji, Ibticem, Bacq-Daian, Delphine, Proust, Carole, Remior, Paloma, Gomez-Bueno, Manuel , Lehnert, Kristin, Maas, Renee, Olaso, Robert, Saripella, Ganapathi Varma, Felix, Stephan B., McGinn, Steven, Duboscq-Bidot, Laëtitia, van Mil, Alain , Besse, Céline, Fontaine, Vincent, Blanché, Hélène, Ader, Flavie, Keating, Brendan, Curjol, Angélique, Boland, Anne, Komajda, Michel, Cambien, François, Deleuze, Jean-Francois, Dörr, Marcus, Asselbergs, Folkert W. , Villard, Eric, Trégouët, David-Alexandre und Charron, Philippe (2021) Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23. European Heart Journal 42 (20), S. 2000-2011. Volltext nicht vorhanden.

Friedrich, Felix W. , Wilding, Brendan R., Reischmann, Silke, Crocini, Claudia , Lang, Patrick, Charron, Philippe , Müller, Oliver J., McGrath, Meagan J., Vollert, Ingra, Hansen, Arne, Linke, Wolfgang A., Hengstenberg, Christian, Bonne, Gisèle , Morner, Stellan, Wichter, Thomas, Madeira, Hugo , Arbustini, Eloisa , Eschenhagen, Thomas, Mitchell, Christina A. , Isnard, Richard und Carrier, Lucie (2012) Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy. Human Molecular Genetics 21 (14), S. 3237-3254. Volltext nicht vorhanden.

Villard, Eric, Perret, Claire, Gary, Françoise, Proust, Carole, Dilanian, Gilles, Hengstenberg, Christian, Ruppert, Volker, Arbustini, Eloisa , Wichter, Thomas, Germain, Marine, Dubourg, Olivier, Tavazzi, Luigi, Aumont, Marie-Claude, DeGroote, Pascal, Fauchier, Laurent, Trochu, Jean-Noël, Gibelin, Pierre, Aupetit, Jean-François, Stark, Klaus , Erdmann, Jeanette , Hetzer, Roland, Roberts, Angharad M., Barton, Paul J.R. , Regitz-Zagrosek, Vera, Aslam, Uzma, Duboscq-Bidot, Laëtitia, Meyborg, Matthias, Maisch, Bernhard, Madeira, Hugo , Waldenström, Anders , Galve, Enrique, Cleland, John G. , Dorent, Richard, Roizes, Gerard, Zeller, Tanja, Blankenberg, Stefan, Goodall, Alison H. , Cook, Stuart , Tregouet, David A. , Tiret, Laurence, Isnard, Richard , Komajda, Michel, Charron, Philippe und Cambien, François (2011) A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. European Heart Journal 32 (9), S. 1065-1076. Volltext nicht vorhanden.

Gibson, Greg , Stark, Klaus, Esslinger, Ulrike B., Reinhard, Wibke , Petrov, George, Winkler, Thomas, Komajda, Michel , Isnard, Richard , Charron, Philippe, Villard, Eric, Cambien, François, Tiret, Laurence, Aumont, Marie-Claude, Dubourg, Olivier, Trochu, Jean-Noël, Fauchier, Laurent, DeGroote, Pascal, Richter, Anette, Maisch, Bernhard, Wichter, Thomas, Zollbrecht, Christa, Grassl, Martina, Schunkert, Heribert, Linsel-Nitschke, Patrick , Erdmann, Jeanette, Baumert, Jens, Illig, Thomas, Klopp, Norman, Wichmann, H.-Erich , Meisinger, Christa, Koenig, Wolfgang, Lichtner, Peter , Meitinger, Thomas, Schillert, Arne, König, Inke R., Hetzer, Roland, Heid, Iris M., Regitz-Zagrosek, Vera und Hengstenberg, Christian (2010) Genetic Association Study Identifies HSPB7 as a Risk Gene for Idiopathic Dilated Cardiomyopathy. PLoS Genetics 6 (10), e1001167. Volltext nicht vorhanden.