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Number of items: 7.

Journal Article

Gaertner, Vincent D., Michel, Sven, Curtin, John A., Pulkkinen, Ville, Acevedo, Nathalie, Soderhall, Cilla, von Berg, Andrea, Bufe, Albrecht, Laub, Otto, Rietschel, Ernst, Heinzmann, Andrea, Simma, Burkhard, Vogelberg, Christian, Pershagen, Goeran, Melen, Erik, Simpson, Angela ORCID: 0000-0003-2733-6666, Custovic, Adnan ORCID: 0000-0001-5218-7071, Kere, Juha ORCID: 0000-0003-1974-0271 and Kabesch, Michael (2019). Nocturnal asthma is affected by genetic interactions between RORA and NPSR1. Pediatr. Pulmonol., 54 (6). S. 847 - 858. HOBOKEN: WILEY. ISSN 1099-0496

Michel, Sven, Liang, Liming, Depner, Martin, Klopp, Norman, Ruether, Andreas, Kumar, Ashish ORCID: 0000-0002-7075-5930, Schedel, Michaela ORCID: 0000-0001-8465-2986, Vogelberg, Christian, von Mutius, Erika ORCID: 0000-0002-8893-4515, von Berg, Andrea, Bufe, Albrecht ORCID: 0000-0001-7335-9362, Rietschel, Ernst, Heinzmann, Andrea, Laub, Otto, Simma, Burkhard, Frischer, Thomas, Genuneit, Jon, Gut, Ivo G., Schreiber, Stefan, Lathrop, Mark, Illig, Thomas and Kabesch, Michael (2010). Unifying Candidate Gene and GWAS Approaches in Asthma. PLoS One, 5 (11). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1932-6203

Schedel, Michaela ORCID: 0000-0001-8465-2986, Michel, Sven, Gaertner, Vincent D., Toncheva, Antoaneta A., Depner, Martin, Binia, Aristea ORCID: 0000-0002-8327-049X, Schieck, Maximilian ORCID: 0000-0001-5878-0546, Rieger, Marie T., Klopp, Norman, von Berg, Andrea, Bufe, Albrecht ORCID: 0000-0001-7335-9362, Laub, Otto, Rietschel, Ernst, Heinzmann, Andrea, Simma, Burkard, Vogelberg, Christian, Genuneit, Jon, Illig, Thomas and Kabesch, Michael (2015). Polymorphisms related to ORMDL3 are associated with asthma susceptibility, alterations in transcriptional regulation of ORMDL3, and changes in T(H)2 cytokine levels. J. Allergy Clin. Immunol., 136 (4). S. 893 - 918. NEW YORK: MOSBY-ELSEVIER. ISSN 1097-6825

Schieck, Maximilian ORCID: 0000-0001-5878-0546, Michel, Sven, Suttner, Kathrin, Illig, Thomas, Zeilinger, Sonja, Franke, Andre ORCID: 0000-0003-1530-5811, Vogelberg, Christian, von Berg, Andrea, Bufe, Albrecht ORCID: 0000-0001-7335-9362, Heinzmann, Andrea, Laub, Otto, Rietschel, Ernst, Simma, Burkhard, Frischer, Thomas, Genuneit, Jon, Kerzel, Sebastian and Kabesch, Michael (2014). Genetic variation in T(H)17 pathway genes, childhood asthma, and total serum IgE levels. J. Allergy Clin. Immunol., 133 (3). S. 888 - 893. NEW YORK: MOSBY-ELSEVIER. ISSN 1097-6825

Schieck, Maximilian ORCID: 0000-0001-5878-0546, Schouten, Jan P., Michel, Sven, Suttner, Kathrin, Toncheva, Antoaneta A., Gaertner, Vincent D., Illig, Thomas, Lipinski, Simone ORCID: 0000-0002-9322-7372, Franke, Andre ORCID: 0000-0003-1530-5811, Klintschar, Michael, Kalayci, Omer, Sahiner, Umit M., Birben, Esra, Melen, Erik, Pershagen, Goeran, Freidin, Maxim B., Ogorodova, Ludmila M., Granell, Raquel ORCID: 0000-0002-4890-4012, Henderson, John, Brunekreef, Bert, Smit, Henriette A., Vogelberg, Christian, von Berg, Andrea, Bufe, Albrecht, Heinzmann, Andrea, Laub, Otto, Rietschel, Ernst, Simma, Burkhard, Genuneit, Jon, Jonigk, Danny, Postma, Dirkje S., Koppelman, Gerard H., Vonk, Judith M., Timens, Wim ORCID: 0000-0002-4146-6363, Boezen, H. Marike and Kabesch, Michael (2016). Doublesex and mab-3 related transcription factor 1 (DMRT1) is a sex-specific genetic determinant of childhood-onset asthma and is expressed in testis and macrophages. J. Allergy Clin. Immunol., 138 (2). S. 421 - 432. NEW YORK: MOSBY-ELSEVIER. ISSN 1097-6825

Toncheva, Antoaneta A., Suttner, Kathrin, Michel, Sven, Klopp, Norman, Illig, Thomas, Balschun, Tobias, Vogelberg, Christian, von Berg, Andrea, Bufe, Albrecht ORCID: 0000-0001-7335-9362, Heinzmann, Andrea, Laub, Otto, Rietschel, Ernst, Simma, Burkhard, Frischer, Thomas, Genuneit, Jon, von Mutius, Erika ORCID: 0000-0002-8893-4515 and Kabesch, Michael (2012). Genetic variants in Protocadherin-1, bronchial hyper-responsiveness, and asthma subphenotypes in German children. Pediatr. Allergy Immunol., 23 (7). S. 636 - 642. HOBOKEN: WILEY-BLACKWELL. ISSN 0905-6157

Wallmeier, Julia, Frank, Diana, Shoemark, Amelia, Noethe-Menchen, Tabea, Cindric, Sandra, Olbrich, Heike, Loges, Niki T., Aprea, Isabella, Dougherty, Gerard W., Pennekamp, Petra, Kaiser, Thomas ORCID: 0000-0002-6699-0014, Mitchison, Hannah M., Hogg, Claire, Carr, Siobhan B., Zariwala, Maimoona A., Ferkol, Thomas, Leigh, Margaret W., Davis, Stephanie D., Atkinson, Jeffrey, Dutcher, Susan K., Knowles, Michael R., Thiele, Holger, Altmueller, Janine, Krenz, Henrike, Woeste, Marius, Brentrup, Angela, Ahrens, Frank, Vogelberg, Christian, Morris-Rosendahl, Deborah J. and Omran, Heymut (2019). De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry. Am. J. Hum. Genet., 105 (5). S. 1030 - 1040. CAMBRIDGE: CELL PRESS. ISSN 1537-6605

This list was generated on Tue Oct 26 07:08:10 2021 CEST.