Anzahl der Publikationen: 5
2022
Le Floch, Edith; Cosentino, Teresa; Larsen, Casper K.; Beuschlein, Felix ORCID: https://orcid.org/0000-0001-7826-3984; Reincke, Martin ORCID: https://orcid.org/0000-0002-9817-9875; Amar, Laurence; Rossi, Gian-Paolo; De Sousa, Kelly; Baron, Stéphanie; Chantalat, Sophie; Saintpierre, Benjamin; Lenzini, Livia; Frouin, Arthur; Giscos-Douriez, Isabelle; Ferey, Matthis; Abdellatif, Alaa B.; Meatchi, Tchao; Empana, Jean-Philippe; Jouven, Xavier; Gieger, Christian ORCID: https://orcid.org/0000-0001-6986-9554; Waldenberger, Melanie ORCID: https://orcid.org/0000-0003-0583-5093; Peters, Annette ORCID: https://orcid.org/0000-0001-6645-0985; Cusi, Daniele; Salvi, Erika ORCID: https://orcid.org/0000-0002-2724-2291; Meneton, Pierre; Touvier, Mathilde; Deschasaux, Mélanie; Druesne-Pecollo, Nathalie; Boulkroun, Sheerazed ORCID: https://orcid.org/0000-0002-8796-7534; Fernandes-Rosa, Fabio L. ORCID: https://orcid.org/0000-0002-0162-0792; Deleuze, Jean-François ORCID: https://orcid.org/0000-0002-5358-4463; Jeunemaitre, Xavier ORCID: https://orcid.org/0000-0001-5925-381X und Zennaro, Maria-Christina ORCID: https://orcid.org/0000-0001-5449-9191
(2022):
Identification of risk loci for primary aldosteronism in genome-wide association studies.
In: Nature Communications, Bd. 13, Nr. 1, 5198
[PDF, 3MB]
2021
Garnier, Sophie; Harakalova, Magdalena; Weiss, Stefan; Mokry, Michal; Regitz-Zagrosek, Vera; Hengstenberg, Christian; Cappola, Thomas P.; Isnard, Richard; Arbustini, Eloisa; Cook, Stuart A.; Setten, Jessica van; 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, Gerard; Dorent, Richard; Groote, Pascal de; Fauchier, Laurent; Trochu, Jean-Noel; Aupetit, Jean-Francois; 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, Laetitia; Mil, Alain van; Besse, Celine; Fontaine, Vincent; Blanche, Helene; Ader, Flavie; Keating, Brendan; Curjol, Angelique; Boland, Anne; Komajda, Michel; Cambien, Francois; Deleuze, Jean-Francois; Dörr, Marcus; Asselbergs, Folkert W.; Villard, Eric; Tregoueet, 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.
In: European Heart Journal, Bd. 42, Nr. 20: S. 2000-2011
2018
Ashar, Foram N.; Mitchell, Rebecca N.; Albert, Christine M.; Newton-Cheh, Christopher; Brody, Jennifer A.; Müller-Nurasyid, Martina; Moes, Anna; Meitinger, Thomas; Mak, Angel; Huikuri, Heikki; Junttila, M. Juhani; Goyette, Philippe; Pulit, Sara L.; Pazoki, Raha; Tanck, MichaelW.; Blom, Marieke T.; Zhao, XiaoQing; Havulinna, Aki S.; Jabbari, Reza; Glinge, Charlotte; Tragante, Vinicius; Escher, Stefan A.; Chakravarti, Aravinda; Ehret, Georg; Coresh, Josef; Li, Man; Prineas, Ronald J.; Franco, Oscar H.; Kwok, Pui-Yan; Lumley, Thomas; Dumas, Florence; McKnight, Barbara; Rotter, Jerome I.; Lemaitre, Rozenn N.; Heckbert, Susan R.; O'Donnell, Christopher J.; Hwang, Shih-Jen; Tardif, Jean-Claude; VanDenburgh, Martin; Uitterlinden, Andre G.; Hofman, Albert; Stricker, Bruno H. C.; Bakker, Paul I. W. de; Franks, Paul W.; Jansson, Jan-Hakan; Asselbergs, Folkert W.; Halushka, Marc K.; Maleszewski, Joseph J.; Tfelt-Hansen, Jacob; Engstrom, Thomas; Salomaa, Veikko; Virmani, Renu; Kolodgie, Frank; Wilde, Arthur A. M.; Tan, Hanno L.; Bezzina, Connie R.; Eijgelsheim, Mark; Rioux, John D.; Jouven, Xavier; Kääb, Stefan; Psaty, Bruce M.; Siscovick, David S.; Arking, Dan E. und Sotoodehnia, Nona
(2018):
A comprehensive evaluation of the genetic architecture of sudden cardiac arrest.
In: European Heart Journal, Bd. 39, Nr. 44: S. 3961-3969
2017
Nolte, Ilja M.; Munoz, M. Loretto; Tragante, Vinicius; Amare, Azmeraw T.; Jansen, Rick; Väz, Ahmad; Heyde, Benedikt von der; Avery, Christy L.; Bis, Joshua C.; Dierckx, Bram; Dongen, Jenny van; Gogarten, Stephanie M.; Goyette, Philippe; Hernesniemi, Jussi; Huikari, Ville; Hwang, Shih-Jen; Jaju, Deepali; Kerr, Kathleen F.; Kluttig, Alexander; Krijthe, Bouwe P.; Kumar, Jitender; Laan, Sander W. van der; Lyytikainen, Leo-Pekka; Maihofer, Adam X.; Minassian, Arpi; Most, Peter J. van der; Müller-Nurasyid, Martina; Nivard, Michel; Salvi, Erika; Stewart, James D.; Thayer, Julian F.; Verweij, Niek; Wong, Andrew; Zabaneh, Delilah; Zafarmand, Mohammad H.; Abdellaoui, Abdel; Albarwani, Sulayma; Albert, Christine; Alonso, Alvaro; Ashar, Foram; Auvinen, Juha; Axelsson, Tomas; Baker, Dewleen G.; Bakker, Paul I. W. de; Barcella, Matteo; Bayoumi, Riad; Bieringa, Rob J.; Boomsma, Dorret; Boucher, Gabrielle; Britton, Annie R.; Christophersen, Ingrid E.; Dietrich, Andrea; Ehret, George B.; Ellinor, Patrick T.; Eskola, Markku; Felix, Janine F.; Floras, John S.; Franco, Oscar H.; Friberg, Peter; Gademan, Maaike G. J.; Geyer, Mark A.; Giedraitis, Vilmantas; Hartman, Catharina A.; Hemerich, Daiane; Hofman, Albert; Hottenga, Jouke-Jan; Huikuri, Heikki; Hutri-Kähönen, Nina; Jouven, Xavier; Junttila, Juhani; Juonala, Markus; Kiviniemi, Antti M.; Kors, Jan A.; Kumari, Meena; Kuznetsova, Tatiana; Laurie, Cathy C.; Lefrandt, Joop D.; Li, Yong; Li, Yun; Liao, Duanping; Limacher, Marian C.; Lin, Henry J.; Lindgren, Cecilia M.; Lubitz, Steven A.; Mahajan, Anubha; McKnight, Barbara; zu Schwabedissen, Henriette Meyer; Milaneschi, Yuri; Mononen, Nina; Morris, Andrew P.; Nalls, Mike A.; Navis, Gerjan; Neijts, Melanie; Nikus, Kjell; North, Kari E.; O'Connor, Daniel T.; Ormel, Johan; Perz, Siegfried; Peters, Annette; Psaty, Bruce M.; Raitakari, Olli T.; Risbrough, Victoria B.; Sinner, Moritz F.; Siscovick, David; Smit, Johannes H.; Smith, Nicholas L.; Soliman, Elsayed Z.; Sotoodehnia, Nona; Stässen, Jan A.; Stein, Phyllis K.; Stilp, Adrienne M.; Stolarz-Skrzypek, Katarzyna; Strauch, Konstantin; Sundstrom, Johan; Swenne, Cees A.; Syvanen, Ann-Christine; Tardif, Jean-Claude; Taylor, Kent D.; Teumer, Alexander; Thornton, Timothy A.; Tinker, Lesley E.; Uitterlinden, Andre G.; Setten, Jessica van; Voss, Andreas; Waldenberger, Melanie; Wilhelmsen, Kirk C.; Willemsen, Gonneke; Wong, Quenna; Zhang, Zhu-Ming; Zonderman, Alan B.; Cusi, Daniele; Evans, Michele K.; Greiser, Halina K.; Harst, Pim van der; Hassan, Mohammad; Ingelsson, Erik; Jarvelin, Marjo-Riitta; Kääb, Stefan; Kähönen, Mika; Kivimaki, Mika; Kooperberg, Charles; Kuh, Diana; Lehtimaki, Terho; Lind, Lars; Nievergelt, Caroline M.; O'Donnell, Chris J.; Oldehinkel, Albertine J.; Penninx, Brenda; Reiner, Alexander P.; Riese, Harriette; Roon, Arie M. van; Rioux, John D.; Rotter, Jerome I.; Sofer, Tamar; Stricker, Bruno H.; Tiemeier, Henning; Vrijkotte, Tanja G. M.; Asselbergs, Folkert W.; Brundel, Bianca J. J. M.; Heckbert, Susan R.; Whitsel, Eric A.; Höd, Marcel den; Snieder, Harold und Geus, Eco J. C. de
(2017):
Genetic loci associated with heart rate variability and their effects on cardiac disease risk.
In: Nature Communications, Bd. 8, 15805
[PDF, 605kB]
Esslinger, Ulrike; Garnier, Sophie; Korniat, Agathe; Proust, Carole; Kararigas, Georgios; Müller-Nurasyid, Martina; Empana, Jean-Philippe; Morley, Michael P.; Perret, Claire; Stark, Klaus; Bick, Alexander G.; Prasad, Sanjay K.; Kriebel, Jennifer; Li, Jin; Tiret, Laurence; Strauch, Konstantin; O'Regan, Declan P.; Marguiles, Kenneth B.; Seidman, Jonathan G.; Boutouyrie, Pierre; Lacolley, Patrick; Jouven, Xavier; Hengstenberg, Christian; Komajda, Michel; Hakonarson, Hakon; Isnard, Richard; Arbustini, Eloisa; Grallert, Harald; Cook, Stuart A.; Seidman, Christine E.; Regitz-Zagrosek, Vera; Cappola, Thomas P.; Charron, Philippe; Cambien, Francois und Villard, Eric
(2017):
Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.
In: PLOS One
12(3), e0172995
[PDF, 1MB]
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