Publications Bertram Müller-Myhsok

Unschuld, P. G.; Ising, M.; Specht, M.; Erhardt, A.; Ripke, S.; Heck, A.; Kloiber, S.; Straub, V.; Brueckl, T.; Müller-Myhsok, B. et al.; Holsboer, F.; Binder, E. B.: Polymorphisms in the GAD2 Gene-Region Are Associated With Susceptibility for Unipolar Depression and With a Risk Factor for Anxiety Disorders. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 150B (8), pp. 1100 - 1109 (2009)

Ising, M.; Lucae, S.; Binder, E. B.; Bettecken, T.; Uhr, M.; Ripke, S.; Kohli, M. A.; Hennings, J.; Horstmann, S.; Kloiber, S. et al.; Menke, A.; Bondy, B.; Rupprecht, R.; Domschke, K.; Baune, B. T.; Arolt, V.; Rush, A. J.; Holsboer, F.; Müller-Myhsok, B.: Pharmacogenetics of antidepressant treatment outcome - Results from a genome-wide multilocus analysis including clinical predictors. Annals of Human Genetics 73, pp. 665 - 666 (2009)

Yehuda, R.; Cai, G. Q.; Golier, J. A.; Sarapas, C.; Galea, S.; Ising, M.; Rein, T.; Schmeidler, J.; Müller-Myhsok, B.; Holsboer, F. et al.; Buxbaum, J. D.: Gene Expression Patterns Associated with Posttraumatic Stress Disorder Following Exposure to the World Trade Center Attacks. Biological Psychiatry 66 (7), pp. 708 - 711 (2009)

Wolf, C.; Gramer, E.; Müller-Myhsok, B.; Pasutto, F.; Reinthal, E.; Wissinger, B.; Weisschuh, N.: Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study. BMC Medical Genetics 10, doi:10.1186/1471-2350-10-91, p. 91 - 91 (2009)

Ditzen, C.; Varadarajulu, J.; Czibere, L.; Gonik, M.; Bunck, M.; Teplytska, L.; Müller-Myhsok, B.; Holsboer, F.; Landgraf, R.; Turck, C. W.: Proteomic genotyping in a mouse model of trait anxiety exposes disease relevant pathways. Pharmacopsychiatry 42 (5), pp. 215 - 216 (2009)

Ising, M.; Lucae, S.; Binder, E. B.; Bettecken, T.; Uhr, M.; Ripke, S.; Kohli, M. A.; Hennings, J. M.; Horstmann, S.; Kloiber, S. et al.; Menke, A.; Bondy, B.; Rupprecht, R.; Domschke, K.; Baune, B. T.; Arolt, V.; Rush, A. J.; Holsboer, F.; Müller-Myhsok, B.: A Genomewide Association Study Points to Multiple Loci That Predict Antidepressant Drug Treatment Outcome in Depression. Archives of General Psychiatry 66 (9), pp. 966 - 975 (2009)

Ising, M.; Lucae, S.; Binder, E. B.; Bettecken, T.; Uhr, M.; Ripke, S.; Kohli, M. A.; Hennings, J. M.; Horstmann, S.; Kloiber, S. et al.; Menke, A.; Bondy, B.; Rupprecht, R.; Domschke, K.; Baune, B. T.; Arolt, V.; Rush, A. J.; Holsboer, F.; Müller-Myhsok, B.: A genome-wide association study points to multiple loci predicting antidepressant treatment outcome in depression. Pharmacopsychiatry 42 (5), p. 224 - 224 (2009)

Kloiber, S.; Kohli, M. A.; Brückl, T.; Ripke, S.; Ising, M.; Uhr, M.; Menke, A.; Unschuld, P. G.; Horstmann, S.; Salyakina, D. et al.; Müller-Myhsok, B.; Binder, E. B.; Holsboer, F.; Lucae, S.: Polymorphisms in tryptophan hydroxylase 2 leading to decreased serotonergic activity contribute to elevated risk for metabolic syndrome in depression. Pharmacopsychiatry 42 (5), p. 226 - 226 (2009)

Lucae, S.; Kohli, M. A.; Schmidt, M. V.; Sämann, P. G.; Demirkan, A.; Hek, K.; Salyakina, D.; Ripke, S.; Roeske, D.; van Duijn, C. M. et al.; Uhr, M.; Bettecken, V.; Holsboer, F.; Müller-Myhsok, B.; Binder, E. B.: The neuronal transporter gene SLC6A15 confers risk to major depression. Pharmacopsychiatry 42 (5), p. 230 - 230 (2009)

Unschuld, P. G.; Ising, M.; Roeske, D.; Erhardt, A.; Specht, M.; Ripke, S.; Uhr, M.; Kloiber, S.; Müller-Myhsok, B.; Holsboer, F. et al.; Binder, E. B.: Polymorphisms in the gene encoding the neuropeptide galanin are associated with HPA-axis dysregulation and symptome severity in major-depressive- and anxiety-disorder patients. Pharmacopsychiatry 42 (5), p. 244 - 244 (2009)

Wegerer, M.; Adena, S.; Binder, E. B.; Huber, J.; Sailer, U.; Bettecken, T.; Müller-Myhsok, B.; Modell, S.; Holsboer, F.; Ising, M.: Polymorphisms within the 4-aminobutyrate aminotransferase gene are associated with long-latency somatosensory potentials in families vulnerable for affective disorders. Pharmacopsychiatry 42 (5), p. 246 - 246 (2009)

Ludwig, K. U.; Mattheisen, M.; Mühleisen, T. W.; Roeske, D.; Schmäl, C.; Breuer, R.; Schulte-Körne, G.; Müller-Myhsok, B.; Nöthen, M. M.; Hoffmann, P. et al.; Rietschel, M.; Cichon, S.: Supporting evidence for LRRTM1 imprinting effects in schizophrenia. Molecular Psychiatry 14 (8), pp. 743 - 745 (2009)

Glas, J. N.; Stallhofer, J.; Ripke, S.; Wetzke, M.; Pfennig, S.; Klein, W.; Epplen, J. T.; Griga, T.; Schiemann, U.; Lacher, M. et al.; Koletzko, S.; Folwaczny, M.; Lohse, P.; Göke, B.; Ochsenkühn, T.; Müller-Myhsok, B.; Brand, S.: Novel Genetic Risk Markers for Ulcerative Colitis in the IL2/IL21 Region Are in Epistasis With IL23R and Suggest a Common Genetic Background for Ulcerative Colitis and Celiac Disease. American Journal of Gastroenterology 104 (7), pp. 1737 - 1744 (2009)

Torok, P.; Glas, J.; Endres, I.; Tonenchi, L.; Teshome, M. Y.; Wetzke, M.; Klein, W.; Lohse, P.; Ochsenkühn, O.; Folwaczny, M. et al.; Goke, B.; Folwaczny, C.; Müller-Myhsok, B.; Brand, S.: Epistasis Between Toll-Like Receptor-9 Polymorphisms and Variants in NOD2 and IL23R Modulates Susceptibility to Crohn's Disease. American Journal of Gastroenterology 104 (7), pp. 1723 - 1733 (2009)

Heck, A.; Lieb, R.; Ellgas, A.; Pfister, H.; Lucae, S.; Roeske, D.; Pütz, B.; Müller-Myhsok, B.; Uhr, M.; Holsboer, F. et al.; Ising, M.: Investigation of 17 candidate genes for personality traits confirms effects of the HTR2A gene on novelty seeking. Genes Brain and Behavior 8 (4), pp. 464 - 472 (2009)

Thoeringer, C. K.; Ripke, S.; Unschuld, P. G.; Lucae, S.; Ising, M.; Bettecken, T.; Uhr, M.; Keck, M. E.; Mueller-Myhsok, B.; Holsboer, F. et al.; Binder, E. B.; Erhardt, A.: The GABA transporter 1 (SLC6A1): a novel candidate gene for anxiety disorders. Journal of Neural Transmission 116 (6), pp. 649 - 657 (2009)

Gschwendtner, A.; Bevan, S.; Cole, J. W.; Plourde, A.; Matarin, M.; Ross-Adams, H.; Meitinger, T.; Wichmann, E.; Mitchell, B. D.; Furie, K. et al.; Slowik, A.; Rich, S. S.; Syme, P. D.; MacLeod, M. J.; Meschia, J. F.; Rosand, J.; Kittner, S. J.; Markus, H. S.; Müller-Myhsok, B.; Dichgans, M.: Sequence Variants on Chromosome 9p21.3 Confer Risk for Atherosclerotic Stroke. Annals of Neurology 65 (5), pp. 531 - 539 (2009)

Hoffmann, K.; Planitz, C.; Rüschendorf, F.; Müller-Myhsok, B.; Stassen, H. H.; Lucke, B.; Mattheisen, M.; Stumvoll, M.; Bochmann, R.; Zschornacki, M. et al.; Wienker, T. F.; Nürnberg, P.; Reis, A.; Luft, F. C.; Lindner, T. H.: A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany. Journal of Hypertension 27 (5), pp. 983 - 990 (2009)

Kemlink, D.; Polo, O.; Frauscher, B.; Gschliesser, V.; Hogl, B.; Poewe, W.; Vodicka, P.; Vavrova, J.; Sonka, K.; Nevsimalova, S. et al.; Schormair, B.; Lichtner, P.; Silander, K.; Peltonen, L.; Gieger, C.; Wichmann, H. E.; Zimprich, A.; Roeske, D.; Müller-Myhsok, B.; Meitinger, T.; Winkelmann, J.: Replication of restless legs syndrome loci in three European populations. Journal of Medical Genetics 46 (5), pp. 315 - 318 (2009)

Bunck, M.; Czibere, L.; Horvath, C.; Graf, C.; Frank, E.; Kessler, M. S.; Murgatroyd, C.; Müller-Myhsok, B.; Gonik, M.; Weber, P. et al.; Pütz, B.; Muigg, P.; Panhuysen, M.; Singewald, N.; Bettecken, T.; Deussing, J. M.; Holsboer, F.; Spengler, D.; Landgraf, R.: A Hypomorphic Vasopressin Allele Prevents Anxiety-Related Behavior. PLoS ONE 4 (4), doi: 10.1371/journal.pone.0005129 (2009)