 | Up a level |
2019
Maaser, Anna, Strohmaier, Jana 
ORCID: 0000-0002-4364-1487, Ludwig, Kerstin U., Degenhardt, Franziska, Streit, Fabian ORCID: 0000-0003-1080-4339, Schenk, L. M., Koller, A. C., Fischer, Sarah ORCID: 0000-0001-6227-3950, Thiele, Holger ORCID: 0000-0002-0169-998X, Nuernberg, Peter, Guzman-Parra, Jose ORCID: 0000-0002-1463-6435, Orozco Diaz, G., Auburger, G., Albus, Margot, Borrmann-Hassenbach, M., Jose Gonzalez, M., Gil Flores, S., Cabaleiro Fabeiro, F. J., del Rio Noriega, F., Perez Perez, F., Haro Gonzalez, J., Rivas, F., Mayoral, F., Herms, Stefan ORCID: 0000-0002-2786-8200, Hoffmann, Per ORCID: 0000-0002-6573-983X, Cichon, Sven ORCID: 0000-0002-9475-086X, Rietschel, Marcella ORCID: 0000-0002-5236-6149, Noethen, Markus M. and Forstner, Andreas J. ORCID: 0000-0002-1876-6368
(2019).
Exome sequencing of multiply affected bipolar disorder families and follow-up resequencing implicate rare variants in neuronal genes contributing to disease etiology.
European Neuropsychopharmacology, 29 (3).
S. 836- 837.
Elsevier.
ISSN 0924-977X