Search Results - Hartmann, A. M.
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Contribution of rare and potentially functionally relevant sequence variants in schizophrenia risk-Locus Xq28,distal by Claus, Isabelle (Author) , Sivalingam, S. (Author) , Koller, A. C. (Author) , Weiß, A. (Author) , Mathey, C. M. (Author) , Sindermann, L. (Author) , Klein, D. (Author) , Henschel, L. (Author) , Ludwig, K. U. (Author) , Hoffmann, P. (Author) , Heimbach, A. (Author) , Heilmann-Heimbach, S. (Author) , Vedder, H. (Author) , Kammerer-Ciernioch, J. (Author) , Stürmer, T. (Author) , Streit, Fabian (Author) , Maaser-Hecker, A. (Author) , Nenadić, I. (Author) , Baune, B. T. (Author) , Hartmann, A. M. (Author) , Konte, B. (Author) , Giegling, I. (Author) , Heilbronner, U. (Author) , Wagner, M. (Author) , Philipsen, A. (Author) , Schmidt, B. (Author) , Rujescu, D. (Author) , Buness, A. (Author) , Schulze, T. G. (Author) , Rietschel, Marcella (Author) , Forstner, A. J. (Author) , Nöthen, M. M. (Author) , Degenhardt, F. (Author) ,
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Analysis of genetic diversity in patients with major psychiatric disorders versus healthy controls: a molecular-genetic study of 1698 subjects genotyped for 100 candidate genes (54... by Stassen, Hans H. (Author) , Bachmann, Silke (Author) , Bridler, R. (Author) , Cattapan, K. (Author) , Hartmann, A. M. (Author) , Rujescu, Dan (Author) , Seifritz, E. (Author) , Weisbrod, Matthias (Author) , Scharfetter, Christian (Author) ,
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Genetic determinants of antidepressant and antipsychotic drug response by Stassen, Hans H. (Author) , Bachmann, S. (Author) , Bridler, R. (Author) , Cattapan-Ludewig, Katja (Author) , Hartmann, A. M. (Author) , Rujescu, Dan (Author) , Seifritz, Erich (Author) , Weisbrod, Matthias (Author) , Scharfetter, Christian (Author) ,
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4
Risk gene variants for nicotine dependence in the CHRNA5-CHRNA3-CHRNB4 cluster are associated with cognitive performance by Winterer, Georg (Author)
Other Authors: “…Hartmann, A. M.…”
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Related Subjects
Adult
Case-Control Studies
Chromosomes, Human, X
Cohort Studies
European People
Female
Genetic Loci
Genetic Predisposition to Disease
Genetic Variation
Germany
Humans
Male
Polymorphism, Single Nucleotide
Risk Factors
Schizophrenia
X‐chromosome
burden analysis
copy number variation
rare variants
schizophrenia