Items where Author is "Mangold, Elisabeth"

2015

Paternoster, Lavinia and Standl, Marie and Waage, Johannes and Baurecht, Hansjörg and Hotze, Melanie and Strachan, David P. and Curtin, John A. and Bønnelykke, Klaus and Tian, Chao and Takahashi, Atsushi and Esparza-Gordillo, Jorge and Alves, Alexessander Couto and Thyssen, Jacob P. and den Dekker, Herman T. and Ferreira, Manuel A. and Altmaier, Elisabeth and Sleiman, Patrick M. and Xiao, Feng Li and Gonzalez, Juan R. and Marenholz, Ingo and Kalb, Birgit and Pino-Yanes, Maria and Xu, Cheng Jian and Carstensen, Lisbeth and Groen-Blokhuis, Maria M. and Venturini, Cristina and Pennell, Craig E. and Barton, Sheila J. and Levin, Arbet M. and Curjuric, Ivan and Bustamante, Mariona and Kreiner-Møller, Eskil and Lockett, Gabrielle A. and Bacelis, Jonas and Bunyavanich, Supinda and Myers, Rachel A. and Matanovic, Anja and Kumar, Ashish and Tung, Joyce Y and Hirota, Tomomitsu and Kubo, Michiaki and McArdle, Wendy L. and Henderson, A. John and Kemp, John P. and Zheng, Jie and Smith, George Davey and Rüschendorf, Franz and Bauerfeind, Anja and Lee-Kirsch, Min Ae and Arnold, Andreas and Homuth, Georg and Schmidt, Carsten O. and Mangold, Elisabeth and Cichon, Sven and Keil, Thomas and Rodríguez, Elke and Peters, Annette and Franke, Andre and Lieb, Wolfgang and Novak, Natalija and Fölster-Holst, Regina and Horikoshi, Momoko and Pekkanen, Juha and Sebert, Sylvain and Husemoen, Lise L. and Grarup, Niels and de Jongste, Johan C. and Rivadeneira, Fernando and Hofman, Albert and Jaddoe, Vincent W. V. and Pasmans, Suzanne G. M. A. and Elbert, Niels J. and Uitterlinden, André G. and Marks, Guy B. and Thompson, Philip J. and Matheson, Melanie C. and Robertson, Colin F. and Australian Asthma Genetics, Consortium (AAGC) and Ried, Janina S. and Li, Jin and Zuo, Xian Bo and Zheng, Xiao Dong and Yin, Xian Yong Yin and Sun, Liang Dan and McAleer, Maeve A. and O'Regan, Grainne M. and Fahy, Caoimhe M. R. and Campbell, Linda E. and Macek, Milan and Kurek, Michael and Hu, Donglei and Eng, Celeste and Postma, Dirkje S. and Feenstra, Bjarke and Geller, Frank and Hottenga, Jouke Jan and Middeldorp, Christel M. and Hysi, Pirro and Bataille, Veronique and Spector, Tim and Tiesler, Carla M. T. and Thiering, Elisabeth and Pahukasahasram, Badri and Yang, James J. and Imboden, Madea and Huntsman, Scott and Vilor-Tejedor, Natàlia and Relton, Caroline L. and Myhre, Ronny and Nystad, Wenche and Custovic, Adnan and Weiss, Scott T. and Meyers, Deborah A. and Soderhall, Cilla and Melén, Erik and Ober, Carole and Raby, Benjamin A. and Simpson, Angela and Jacobsson, Bo and Holloway, John W. and Bisgaard, Hans and Sunyer, Jordi and Probst-Hensch, Nicole M. and Williams, L. Keoki and Godfrey, Keith M. and Wang, Carol A. and Boomsma, Dorret I. and Melbye, Mads and Koppelman, Gerard H. and Jarvis, Deborah and McLean, W. H. Irwin and Irvine, Alan D. and Zhang, Xue Jun and Hakonarson, Hakon and Gieger, Christian and Burchard, Esteban G. and Martin, Nicholas G. and Duijts, Liesbeth and Linneberg, Allan and Jarvelin, Marjo-Riitta and Noethen, Markus M. and Lau, Susanne and Hübner, Norbert and Lee, Young-Ae and Tamari, Mayum and Hinds, David A. and Glass, Daniel and Brown, Sara J. and Heinrich, Joachim and Evans, David M. and Weidinger, Stephan and EArly Genetics, and Lifecourse Epidemiology (EAGLE) Eczema Consortium, . (2015) Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis. Nature Genetics, 47 (12). pp. 1449-1456.

2014

Hammer, Christian and Degenhardt, Franziska and Priebe, Lutz and Stutz, Adrian M. and Heilmann, Stefanie and Waszak, Sebastian M. and Schlattl, Andreas and Mangold, Elisabeth and Hoffmann, Per and MooDS Consortium, and Nöthen, Markus M. and Rietschel, Marcella and Rappold, Gudrun and Korbel, Jan O. and Cichon, Sven and Niesler, Beate. (2014) A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders. Bipolar disorders, 16 (7). pp. 764-768.

2002

Friedl, Waltraut and Uhlhaas, Siegfried and Schulmann, Karsten and Stolte, Manfred and Loff, Steffan and Back, Walter and Mangold, Elisabeth and Stern, Martin and Knaebel, Hanns-Peter and Sutter, Christian and Weber, Ruthild G. and Pistorius, Steffen and Burger, Bettina and Propping, Peter. (2002) Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers. Human genetics, 111 (1). pp. 108-111.

Burger, Bettina and Uhlhaas, Siegfried and Mangold, Elisabeth and Propping, Peter and Friedl, Waltraut and Jenne, Dieter and Dockter, Gerhard and Back, Walter. (2002) Novel de novo mutation of MADH4/SMAD4 in a patient with juvenile polyposis. American Journal of Medical Genetics, 110 (3). pp. 289-291.