Einträge von Blankenberg, Stefan 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.

Gregson, John M., Freitag, Daniel F., Surendran, Praveen, Stitziel, Nathan O., Chowdhury, Rajiv, Burgess, Stephen , Kaptoge, Stephen, Gao, Pei , Staley, James R., Willeit, Peter, Nielsen, Sune F., Caslake, Muriel, Trompet, Stella, Polfus, Linda M., Kuulasmaa, Kari, Kontto, Jukka , Perola, Markus, Blankenberg, Stefan, Veronesi, Giovanni , Gianfagna, Francesco , Männistö, Satu, Kimura, Akinori, Lin, Honghuang , Reilly, Dermot F., Gorski, Mathias, Mijatovic, Vladan, Munroe, Patricia B., Ehret, Georg B., Thompson, Alex, Uria-Nickelsen, Maria, Malarstig, Anders, Dehghan, Abbas , Vogt, Thomas F., Sasaoka, Taishi, Takeuchi, Fumihiko, Kato, Norihiro, Yamada, Yoshiji, Kee, Frank, Müller-Nurasyid, Martina, Ferrières, Jean , Arveiler, Dominique, Amouyel, Philippe , Salomaa, Veikko, Boerwinkle, Eric, Thompson, Simon G., Ford, Ian, Wouter Jukema, J., Sattar, Naveed, Packard, Chris J., Shafi Majumder, Abdulla al, Alam, Dewan S., Deloukas, Panos, Schunkert, Heribert, Samani, Nilesh J., Kathiresan, Sekar, Nordestgaard, Børge G., Saleheen, Danish, Howson, Joanna M. M. , Di Angelantonio, Emanuele, Butterworth, Adam S. und Danesh, John (2017) Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles. European Journal of Preventive Cardiology 24 (5), S. 492-504. Volltext nicht vorhanden.