Publikationen von 0000-0002-7464-3354
(ORCID: 0000-0002-7464-3354)

Grosche, Sarah, Marenholz, Ingo, Esparza-Gordillo, Jorge, Arnau-Soler, Aleix, Pairo-Castineira, Erola , Rüschendorf, Franz, Ahluwalia, Tarunveer S. , Almqvist, Catarina, Arnold, Andreas, Baurecht, Hansjörg , Bisgaard, Hans , Bønnelykke, 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., Müller-Nurasyid, Martina, Nöthen, 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, Stölzl, 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. Nature Communications 12 (1). Volltext nicht vorhanden.

Waage, Johannes, Standl, Marie, Curtin, John A., Jessen, Leon E. , Thorsen, Jonathan , Tian, Chao, Schoettler, Nathan, Flores, Carlos, Abdellaoui, Abdel, Ahluwalia, Tarunveer S. , Alves, Alexessander C., Amaral, Andre F. S. , Antó, Josep M. , Arnold, Andreas, Barreto-Luis, Amalia, Baurecht, Hansjörg , van Beijsterveldt, Catharina E. M., Bleecker, Eugene R., Bonàs-Guarch, Sílvia , Boomsma, Dorret I., Brix, Susanne, Bunyavanich, Supinda, Burchard, Esteban G., Chen, Zhanghua, Curjuric, Ivan, Custovic, Adnan , Den Dekker, Herman T., Dharmage, Shyamali C. , Dmitrieva, Julia, Duijts, Liesbeth, Ege, Markus J. , Gauderman, W. James, Georges, Michel, Gieger, Christian, Gilliland, Frank, Granell, Raquel, Gui, Hongsheng , Hansen, Torben , Heinrich, Joachim , Henderson, John, Hernandez-Pacheco, Natalia, Holt, Patrick , Imboden, Medea, Jaddoe, Vincent W. V., Jarvelin, Marjo-Riitta, Jarvis, Deborah L., Jensen, Kamilla K., Jónsdóttir, Ingileif, Kabesch, Michael , Kaprio, Jaakko , Kumar, Ashish, Lee, Young-Ae, Levin, Albert M., Li, Xingnan, Lorenzo-Diaz, Fabian, Melén, Erik, Mercader, Josep M., Meyers, Deborah A., Myers, Rachel, Nicolae, Dan L., Nohr, Ellen A., Palviainen, Teemu , Paternoster, Lavinia, Pennell, Craig E., Pershagen, Göran, Pino-Yanes, Maria , Probst-Hensch, Nicole M., Rüschendorf, Franz, Simpson, Angela, Stefansson, Kari, Sunyer, Jordi , Sveinbjornsson, Gardar, Thiering, Elisabeth, Thompson, Philip J., Torrent, Maties, Torrents, David, Tung, Joyce Y., Wang, Carol A. , Weidinger, Stephan, Weiss, Scott, Willemsen, Gonneke, Williams, L. Keoki, Ober, Carole , Hinds, David A., Ferreira, Manuel A., Bisgaard, Hans , Strachan, David P. und Bønnelykke, Klaus (2018) Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Nature Genetics 50 (8), S. 1072-1080. Volltext nicht vorhanden.