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Anzahl der Publikationen: 6
Zeitschriftenartikel
Marchetti, Claudia; Ataseven, Beyhan 
ORCID: https://orcid.org/0000-0002-2823-7590; Cassani, Chiara; Sassu, Carolina Maria; Congedo, Luigi; D'Indinosante, Marco; Cappuccio, Serena; Rhiem, Kerstin; Hahnen, Eric; Lucci Cordisco, Emanuela; Arbustini, Eloisa; Harter, Philipp; Minucci, Angelo ORCID: https://orcid.org/0000-0002-0833-4334; Scambia, Giovanni ORCID: https://orcid.org/0000-0003-2758-1063 und Fagotti, Anna ORCID: https://orcid.org/0000-0001-5579-335X
(2022):
Ovarian cancer onset across different BRCA mutation types: a view to a more tailored approach forBRCAmutated patients.
In: International Journal of Gynecologic Cancer, Bd. 33, Nr. 2: S. 257-262
ORCID: https://orcid.org/0000-0002-2823-7590; Cassani, Chiara; Sassu, Carolina Maria; Congedo, Luigi; D'Indinosante, Marco; Cappuccio, Serena; Rhiem, Kerstin; Hahnen, Eric; Lucci Cordisco, Emanuela; Arbustini, Eloisa; Harter, Philipp; Minucci, Angelo ORCID: https://orcid.org/0000-0002-0833-4334; Scambia, Giovanni ORCID: https://orcid.org/0000-0003-2758-1063 und Fagotti, Anna ORCID: https://orcid.org/0000-0001-5579-335X
(2022):
Ovarian cancer onset across different BRCA mutation types: a view to a more tailored approach forBRCAmutated patients.
In: International Journal of Gynecologic Cancer, Bd. 33, Nr. 2: S. 257-262
Arbustini, Eloisa; Behr, Elijah R.; Carrier, Lucie; Duijn, Cornelia van; Evans, Paul; Favalli, Valentina; Harst, Pim van der; Haugaa, Kristina Hermann; Jondeau, Guillaume; Kääb, Stefan; Kaski, Juan Pablo; Kavousi, Maryam; Loeys, Bart; Pantazis, Antonis; Pinto, Yigal; Schunkert, Heribert; Di Toro, Alessandro; Thum, Thomas; Urtis, Mario; Waltenberger, Johannes und Elliott, Perry
(2022):
Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics.
In: European Heart Journal, Bd. 43, Nr. 20: S. 1901-1916
Garnier, Sophie; Harakalova, Magdalena; Weiss, Stefan; Mokry, Michal; Regitz-Zagrosek, Vera; Hengstenberg, Christian; Cappola, Thomas P.; Isnard, Richard; Arbustini, Eloisa; Cook, Stuart A.; Meitinger, Thomas; Charron, Philippe; Müller-Nurasyid, Martina und Strauch, Konstantin
(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
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
Martens, Leonie; Ruehle, Frank; Witten, Anika; Meder, Benjamin; Katus, Hugo A.; Arbustini, Eloisa; Hasenfuss, Gerd; Sinner, Moritz F.; Kaeaeb, Stefan; Pankuweit, Sabine; Angermann, Christiane; Bornberg-Bauer, Erich und Stoll, Monika
(2021):
A genetic variant alters the secondary structure of the lncRNA H19 and is associated with dilated cardiomyopathy.
In: Rna Biology, Bd. 18: S. 409-415
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]