Publikationen von Carina Quast

Gruenewald, L.; Landaas, E. T.; Geissler, J.; Weber, H.; Quast, C.; Röh, S.; Schartner, C.; Lesch, K.-P.; Romanos, M.; Kittel-Schneider, S. et al.; Binder, E. B.; Reif, A.: Functional Impact of An ADHD-Associated DIRAS2 Promoter Polymorphism. NEUROPSYCHOPHARMACOLOGY 41 (13), S. 3025 - 3031 (2016)

Gruenewald, L.; Landaas, E. T.; Geissler, J.; Weber, H.; Quast, C.; Röh, S.; Schartner, C.; Lesch, K.-P.; Romanos, M.; Kittel-Schneider, S. et al.; Binder, E.; Reif, A.: Functional Impact of An ADHD-Associated DIRAS2 Promoter Polymorphism. NEUROPSYCHOPHARMACOLOGY 41 (13), S. 3025 - 3031 (2016)

Quast, C.; Reif, A.; Brückl, T.; Pfister, H.; Weber, H.; Mattheisen, M.; Cichon, S.; Lang, T.; Hamm, A.; Fehm, L. et al.; Stroehle, A.; Arolt, V.; Domschke, K.; Kircher, T.; Wittchen, H.-U.; Pauli, P.; Gerlach, A. L.; Alpers, G. W.; Deckert, J.; Rupprecht, R.; Binder, E. B.; Erhardt, A.: GENDER-SPECIFIC ASSOCIATION OF VARIANTS IN THE AKR1C1 GENE WITH DIMENSIONAL ANXIETY IN PATIENTS WITH PANIC DISORDER: ADDITIONAL EVIDENCE FOR THE IMPORTANCE OF NEUROSTEROIDS IN ANXIETY? DEPRESSION AND ANXIETY 31 (10), S. 843 - 850 (2014)

Labermaier, C.; Kohl, C.; Hartmann, J.; Devigny, C.; Altmann, A.; Weber, P.; Arloth, J.; Quast, C.; Wagner, K. V.; Scharf, S. H. et al.; Czibere, L.; Widner-Andrä, R.; Brenndörfer, J.; Landgraf, R.; Hausch, F.; Jones, K. A.; Mueller, M. B.; Uhr, M.; Holsboer, F.; Binder, E. B.; Schmidt, M. V.: A Polymorphism in the Crhr1 Gene Determines Stress Vulnerability in Male Mice. ENDOCRINOLOGY 155 (7), S. 2500 - 2510 (2014)

Schneider, M.; Engel, A.; Fasching, P. A.; Haeberle, L.; Binder, E. B.; Voigt, F.; Grimm, J.; Faschingbauer, F.; Eichler, A.; Dammer, U. et al.; Rebhan, D.; Amann, M.; Raabe, E.; Goecke, T. W.; Quast, C.; Beckmann, M.; Kornhuber, J.; Seifert, A.; Burghaus, S.: Genetic Variants in the Genes of the Stress Hormone Signalling Pathway and Depressive Symptoms during and after Pregnancy. BIOMED RESEARCH INTERNATIONAL, 469278 (2014)

Quast, C.; Cuboni, S.; Bader, D.; Altmann, A.; Weber, P.; Arloth, J.; Röh, S.; Brückl, T.; Ising, M.; Kopczak, A. et al.; Erhardt, A.; Hausch, F.; Lucae, S.; Binder, E. B.: Functional Coding Variants in SLC6A15, a Possible Risk Gene for Major Depression. PLOS ONE 8 (7), e68645 (2013)

Altmann, A.; Quast, C.; Weber, P.: Detecting Rare Variants for Psychiatric Disorders Using Next Generation Sequencing: A Methods Primer. CURRENT PSYCHIATRY REPORTS 15 (1), 4 (2013)

Mehta, D.; Quast, C.; Fasching, P. A.; Seifert, A.; Voigt, F.; Beckmann, M. W.; Faschingbauer, F.; Burger, P.; Ekici, A. B.; Kornhuber, J. et al.; Binder, E. B.; Goecke, T. W.: The 5-HTTLPR polymorphism modulates the influence on environmental stressors on peripartum depression symptoms. Journal of Affective Disorders 136 (3), S. 1192 - 1197 (2012)

Altmann, A.; Weber, P.; Quast, C.; Rex-Haffner, M.; Binder, E. B.; Müller-Myhsok, B.: vipR: variant identification in pooled DNA using R. Bioinformatics 27 (13), S. I77 - I84 (2011)

Quast, C.; Altmann, A.; Weber, P.; Rex-Haffner, M.; Erhardt, A.; Müller-Myhsok, B.; Binder, E. B.: Screening for rare variants in TMEM132D: a candidate gene from genome-wide association studies in anxiety disorders. European Neuropsychopharmacology 21 (Suppl. 1), S. S6 - S7 (2011)

Quast, C.: Genetic and functional characterization of candidate genes for complex psychiatric diseases using next-generation sequencing and cellular uptake assays. Dissertation, Ludwig-Maximilians-Universität München, München (2014)