Anzahl der Einträge: 2.
2021
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.
2018
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.
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