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Anzahl der Publikationen: 5
Zeitschriftenartikel
Reichart, Daniel; Lindberg, Eric L.; Maatz, Henrike; Miranda, Antonio M. A.; Viveiros, Anissa; Shvetsov, Nikolay; Gaertner, Anna; Nadelmann, Emily R.; Lee, Michael; Kanemaru, Kazumasa; Ruiz-Orera, Jorge; Strohmenger, Viktoria; DeLaughter, Daniel M.; Patone, Giannino; Zhang, Hao; Woehler, Andrew; Lippert, Christoph; Kim, Yuri; Adami, Eleonora; Gorham, Joshua M.; Barnett, Sam N.; Brown, Kemar; Buchan, Rachel J.; Chowdhury, Rasheda A.; Constantinou, Chrystalla; Cranley, James; Felkin, Leanne E.; Fox, Henrik; Ghauri, Ahla; Gummert, Jan; Kanda, Masatoshi; Li, Ruoyan; Mach, Lukas; McDonough, Barbara; Samari, Sara; Shahriaran, Farnoush; Yapp, Clarence; Stanasiuk, Caroline; Theotokis, Pantazis I.; Theis, Fabian J.; Bogaerdt, Antoon van der; Wakimoto, Hiroko; Ware, James S.; Worth, Catherine L.; Barton, Paul J. R.; Lee, Young-Ae; Teichmann, Sarah A.; Milting, Hendrik; Noseda, Michela; Oudit, Gavin Y.; Heinig, Matthias; Seidman, Jonathan G.; Hubner, Norbert und Seidman, Christine E.
(2022):
Pathogenic variants damage cell composition and single-cell transcription in cardiomyopathies.
In: Science, Bd. 377, Nr. 6606, eabo1984
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
Kamitaki, Nolan 
ORCID: https://orcid.org/0000-0003-0614-0189; Sekar, Aswin; Handsaker, Robert E. ORCID: https://orcid.org/0000-0002-3128-3547; Rivera, Heather de; Tooley, Katherine; Morris, David L. ORCID: https://orcid.org/0000-0002-1754-8932; Taylor, Kimberly E.; Whelan, Christopher W. ORCID: https://orcid.org/0000-0001-8446-8468; Tombleson, Philip; Loohuis, Loes M. Olde ORCID: https://orcid.org/0000-0002-3327-7837; Boehnke, Michael ORCID: https://orcid.org/0000-0002-6442-7754; Kimberly, Robert P.; Kaufman, Kenneth M.; Harley, John B.; Langefeld, Carl D.; Seidman, Christine E. ORCID: https://orcid.org/0000-0001-6380-1209; Pato, Michele T.; Pato, Carlos N.; Ophoff, Roel A. ORCID: https://orcid.org/0000-0002-8287-6457; Graham, Robert R.; Criswell, Lindsey A.; Vyse, Timothy J. ORCID: https://orcid.org/0000-0003-1123-1464 und McCarroll, Steven A.
(2020):
Complement genes contribute sex-biased vulnerability in diverse disorders.
In: Nature, Bd. 582, Nr. 7813: S. 577-581
ORCID: https://orcid.org/0000-0003-0614-0189; Sekar, Aswin; Handsaker, Robert E. ORCID: https://orcid.org/0000-0002-3128-3547; Rivera, Heather de; Tooley, Katherine; Morris, David L. ORCID: https://orcid.org/0000-0002-1754-8932; Taylor, Kimberly E.; Whelan, Christopher W. ORCID: https://orcid.org/0000-0001-8446-8468; Tombleson, Philip; Loohuis, Loes M. Olde ORCID: https://orcid.org/0000-0002-3327-7837; Boehnke, Michael ORCID: https://orcid.org/0000-0002-6442-7754; Kimberly, Robert P.; Kaufman, Kenneth M.; Harley, John B.; Langefeld, Carl D.; Seidman, Christine E. ORCID: https://orcid.org/0000-0001-6380-1209; Pato, Michele T.; Pato, Carlos N.; Ophoff, Roel A. ORCID: https://orcid.org/0000-0002-8287-6457; Graham, Robert R.; Criswell, Lindsey A.; Vyse, Timothy J. ORCID: https://orcid.org/0000-0003-1123-1464 und McCarroll, Steven A.
(2020):
Complement genes contribute sex-biased vulnerability in diverse disorders.
In: Nature, Bd. 582, Nr. 7813: S. 577-581
Hulsmans, Maarten; Clauss, Sebastian; Xiao, Ling; Aguirre, Aaron D.; King, Kevin R.; Hanley, Alan; Hucker, William J.; Wuelfers, Eike M.; Seemann, Gunnar; Courties, Gabriel; Iwamoto, Yoshiko; Sun, Yuan; Savol, Andrej J.; Sager, Hendrik B.; Lavine, Kory J.; Fishbein, Gregory A.; Capen, Diane E.; Silva, Nicolas da; Miquerol, Lucile; Wakimoto, Hiroko; Seidman, Christine E.; Seidman, Jonathan G.; Sadreyev, Ruslan I.; Naxerova, Kamila; Mitchell, Richard N.; Brown, Dennis; Libby, Peter; Weissleder, Ralph; Swirski, Filip K.; Kohl, Peter; Vinegoni, Claudio; Milan, David J.; Ellinor, Patrick T. und Nahrendorf, Matthias
(2017):
Macrophages Facilitate Electrical Conduction in the Heart.
In: Cell, Bd. 169, Nr. 3: S. 510-522
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]
In: PLOS One 12(3), e0172995 [PDF, 1MB]