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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 3
2022
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
2021
Grosche, Sarah; Marenholz, Ingo; Esparza-Gordillo, Jorge; Arnau-Soler, Aleix; Pairo-Castineira, Erola; Rüschendorf, Norbert; Strauch, Konstantin; Szwajda, Agnieszka; Tenesa, Albert; Thompson, Philip J.; Ullemar, Vilhelmina; Visconti, Alessia; Vonk, Judith M.; Wang, Carol A.; Weidinger, Stephan; Wielscher, Matthias; Worth, Catherine L.; Xu, Chen-Jian; Lee, Young-Ae; Müller-Nurasyid, Martina und Strauch, Konstantin
(2021):
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4.
In: Nature Communications, Bd. 12, 6618
[PDF, 1MB]
Grosche, Sarah; Marenholz, Ingo; Esparza-Gordillo, Jorge; Arnau-Soler, Aleix; Pairo-Castineira, Erola; Rueschendorf, Franz; Ahluwalia, Tarunveer S.; Almqvist, Catarina; Arnold, Andreas; Baurecht, Hansjoerg; Bisgaard, Hans; Bonnelykke, Klaus; Brown, Sara J.; Bustamante, Mariona; Curtin, John A.; Custovic, Adnan; Dharmage, Shyamali C.; Esplugues, Ana; Falchi, Mario; Fernandez-Orth, Dietmar; Ferreira, Manuel A. R.; Franke, Andre; Gerdes, Sascha; Gieger, Christian; Hakonarson, Hakon; Holt, Patrick G.; Homuth, Georg; Hubner, Norbert; Hysi, Pirro G.; Jarvelin, Marjo-Riitta; Karlsson, Robert; Koppelman, Gerard H.; Lau, Susanne; Lutz, Manuel; Magnusson, Patrik K. E.; Marks, Guy B.; Mueller-Nurasyid, Martina; Noethen, Markus M.; Paternoster, Lavinia; Pennell, Craig E.; Peters, Annette; Rawlik, Konrad; Robertson, Colin F.; Rodriguez, Elke; Sebert, Sylvain; Simpson, Angela; Sleiman, Patrick M. A.; Standl, Marie; Stoelzl, Dora; Strauch, Konstantin; Szwajda, Agnieszka; Tenesa, Albert; Thompson, Philip J.; Ullemar, Vilhelmina; Visconti, Alessia; Vonk, Judith M.; Wang, Carol A.; Weidinger, Stephan; Wielscher, Matthias; Worth, Catherine L.; Xu, Chen-Jian und Lee, Young-Ae
(2021):
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4.
In: Nature Communications, Bd. 12, Nr. 1, 6618