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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
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
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