Items where Author is "Meier, Sandra"

2015

Basmanav, F. Buket and Forstner, Andreas J. and Fier, Heide and Herms, Stefan and Meier, Sandra and Degenhardt, Franziska and Hoffmann, Per and Barth, Sandra and Fricker, Nadine and Strohmaier, Jana and Witt, Stephanie H. and Ludwig, Michael and Schmael, Christine and Moebus, Susanne and Maier, Wolfgang and Mössner, Rainald and Rujescu, Dan and Rietschel, Marcella and Lange, Christoph and Nöthen, Markus M. and Cichon, Sven. (2015) Investigation of the Role of TCF4 Rare Sequence Variants in Schizophrenia. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 168B (5). pp. 354-362.

2014

Muhleisen, Thomas W. and Leber, Markus and Schulze, Thomas G. and Strohmaier, Jana and Degenhardt, Franziska and Treutlein, Jens and Mattheisen, Manuel and Forstner, Andreas J. and Schumacher, Johannes and Breuer, René and Meier, Sandra and Herms, Stefan and Hoffmann, Per and Lacour, André and Witt, Stephanie H. and Reif, Andreas and Müller-Myhsok, Bertram and Lucae, Susanne and Maier, Wolfgang and Schwarz, Markus and Vedder, Helmut and Kammerer-Ciernioch, Jutta and Pfennig, Andrea and Bauer, Michael and Hautzinger, Martin and Moebus, Susanne and Priebe, Lutz and Czerski, Piotr M. and Hauser, Joanna and Lissowska, Jolanta and Szeszenia-Dabrowska, Neonila and Brennan, Paul and McKay, James and Wright, Adam and Mitchell, Philip B and Fullerton, Janice M. and Schofield, Peter R. and Montgomery, Grant W. and Medland, Sarah E. and Gordon, Scott D. and Martin, Nicolas G. and Krasnow, Valery and Chuchalin, Alexander and Babadjanova, Gulja and Pantelejeva, Galina and Abramova, Lilia I. and Tiganov, Alexander S. and Polonikov, Alexey and Khusnutdinova, Elza and Alda, Martin and Grof, Paul and Rouleau, Guy A. and Turecki, Gustavo and Laprise, Catherine and Rivas, Fabio and Mayoral, Fermin and Kogevinas, Manolis and Grigoroiu-Serbanescu, Maria and Propping, Peter and Becker, Tim and Rietschel, Marcella and Nöthen, Markus M. and Cichon, Sven. (2014) Genome-wide association study reveals two new risk loci for bipolar disorder. Nat Commun, 5. p. 3339.

Juraeva, Dilafruz and Haenisch, Britta and Zapatka, Marc and Frank, Josef and Group Investigators, and Psych-Gems Scz Working Group, and Witt, Stephanie H. and Muhleisen, Thomas W. and Treutlein, Jens and Strohmaier, Jana and Meier, Sandra and Degenhardt, Franziska and Giegling, Ina and Ripke, Stephan and Leber, Markus and Lange, Christoph and Schulze, Thomas G. and Mössner, Rainald and Nenadic, Igor and Sauer, Heinrich and Rujescu, Dan and Maier, Wolfgang and Borglum, Anders and Ophoff, Roel A. and Cichon, Sven and Nöthen, Markus M. and Rietschel, Marcella and Mattheisen, Manuel and Brors, Benedikt. (2014) Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia. PLoS Genetics, 10 (6). e1004345.