Einträge von Grosche, Sarah auf dem Publikationsserver

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.

Bouzigon, Emmanuelle, Ferreira, Manuel A. R. , Vonk, Judith M. , Baurecht, Hansjörg, Marenholz, Ingo , Tian, Chao, Hoffman, Joshua D., Helmer, Quinta, Tillander, Annika , Ullemar, Vilhelmina, Lu, Yi, Grosche, Sarah, Rüschendorf, Franz , Granell, Raquel, Brumpton, Ben M., Fritsche, Lars G. , Bhatta, Laxmi, Gabrielsen, Maiken E., Nielsen, Jonas B., Zhou, Wei, Hveem, Kristian, Langhammer, Arnulf, Holmen, Oddgeir L. , Løset, Mari, Abecasis, Gonçalo R., Willer, Cristen J., Emami, Nima C., Cavazos, Taylor B., Witte, John S., Szwajda, Agnieszka, Hinds, David A., Hübner, Norbert, Weidinger, Stephan , Magnusson, Patrik K. E., Jorgenson, Eric, Karlsson, Robert, Paternoster, Lavinia, Boomsma, Dorret I., Almqvist, Catarina, Lee, Young-Ae und Koppelman, Gerard H. (2020) Age-of-onset information helps identify 76 genetic variants associated with allergic disease. PLOS Genetics 16 (6), e1008725. Volltext nicht vorhanden.

Mucha, Sören, Baurecht, Hansjörg, Novak, Natalija, Rodríguez, Elke, Bej, Saptarshi, Mayr, Gabriele, Emmert, Hila , Stölzl, Dora, Gerdes, Sascha , Jung, Eun Suk, Degenhardt, Frauke, Hübenthal, Matthias, Ellinghaus, Eva , Kässens, Jan Christian, Wienbrandt, Lars , Lieb, Wolfgang, Müller-Nurasyid, Martina, Hotze, Melanie, Dand, Nick , Grosche, Sarah, Marenholz, Ingo, Arnold, Andreas, Homuth, Georg, Schmidt, Carsten O., Wehkamp, Ulrike, Nöthen, Markus M., Hoffmann, Per, Paternoster, Lavinia, Standl, Marie, Bønnelykke, Klaus, Ahluwalia, Tarunveer S., Bisgaard, Hans , Peters, Annette , Gieger, Christian, Waldenberger, Melanie , Schulz, Holger, Strauch, Konstantin, Werfel, Thomas, Lee, Young-Ae, Wolfien, Markus , Rosenstiel, Philip , Wolkenhauer, Olaf, Schreiber, Stefan, Franke, Andre, Weidinger, Stephan und Ellinghaus, David (2020) Protein-coding variants contribute to the risk of atopic dermatitis and skin-specific gene expression. Journal of Allergy and Clinical Immunology 145 (4), S. 1208-1218. Volltext nicht vorhanden.