Anzahl der Publikationen: 4
Zeitschriftenartikel
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
de Winther, Menno P. J.; Back, Magnus; Evans, Paul; Gomez, Delphine; Goncalves, Isabel; Jorgensen, Helle F.; Koenen, Rory R.; Lutgens, Esther; Norata, Giuseppe Danilo; Osto, Elena; Dib, Lea; Simons, Michael; Stellos, Konstantinos; Yla-Herttuala, Seppo; Winkels, Holger; Bochaton-Piallat, Marie-Luce und Monaco, Claudia
(2022):
Translational opportunities of single-cell biology in atherosclerosis.
In: European Heart Journal, Bd. 44, Nr. 14: S. 1216-1230
Tapper, William; Jones, Amy V.; Kralovics, Robert; Harutyunyan, Ashot S.; Zoi, Katerina; Leung, William; Godfrey, Anna L.; Guglielmelli, Paola; Callaway, Alison; Ward, Daniel; Aranaz, Paula; White, Helen E.; Waghorn, Katherine; Lin, Feng; Chase, Andrew; Baxter, E. Joanna; Maclean, Cathy; Nangalia, Jyoti; Chen, Edwin; Evans, Paul; Short, Michael; Jack, Andrew; Wallis, Louise; Oscier, David; Duncombe, Andrew S.; Schuh, Anna; Mead, Adam J.; Griffiths, Michael; Ewing, Joanne; Gale, Rosemary E.; Schnittger, Susanne; Haferlach, Torsten; Stegelmann, Frank; Döhner, Konstanze; Grallert, Harald; Strauch, Konstantin; Tanaka, Toshiko; Bandinelli, Stefania; Giannopoulos, Andreas; Pieri, Lisa; Mannarelli, Carmela; Gisslinger, Heinz; Barosi, Giovanni; Cazzola, Mario; Reiter, Andreas; Harrison, Claire; Campbell, Peter; Green, Anthony R.; Vannucchi, Alessandro und Cross, Nicholas C. P.
(2015):
Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms.
In: Nature Communications, Bd. 6, 6691
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