Hoffmann, P

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Number of items: 3.

Journal Article

Treutlein, J; Strohmaier, J; Frank, J; Witt, SH; Rietschel, L; Forstner, AJ; Lang, M; Degenhardt, F; Dukal, H; Herms, S; Streit, F; Hoffmann, P; Cichon, S; Nöthen, MM; Rietschel, M (2017). Association between neuropeptide Y receptor Y2 promoter variant rs6857715 and major depressive disorder. Psychiatric genetics, 27(1), pp. 34-37. Lippincott Williams & Wilkins 10.1097/YPG.0000000000000149

Jarick, I; Volckmar, A-L; Pütter, C; Pechlivanis, S; Nguyen, T T; Dauvermann, M R; Beck, S; Albayrak, O; Scherag, S; Gilsbach, S; Cichon, S; Hoffmann, P; Degenhardt, F; Nöthen, M M; Schreiber, S; Wichmann, H-E; Jöckel, K-H; Heinrich, J; Tiesler, C M T; Faraone, S V; ... (2014). Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. Molecular psychiatry, 19(1), pp. 115-121. Basingstoke: Nature Publishing Group 10.1038/mp.2012.161

Conference or Workshop Item

Marcu, I C; Hoffmann, P; Jaconi, M; Ullrich, N D (2012). Functional characterization of stem cell-derived cardiomyocytes. In: Conference Proceedings of ICGEB/CVR Symposium.

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