Publications of B. Müller-Myhsok

Ludwig, K. U.; Roeske, D.; Herms, S.; Schumacher, J.; Warnke, A.; Plume, E.; Neuhoff, N.; Bruder, J.; Remschmidt, H.; Schulte-Korne, G. et al.; Müller-Myhsok, B.; Nöthen, M. M.; Hoffmann, P.: Variation in GRIN2B Contributes to Weak Performance in Verbal Short-Term Memory in Children With Dyslexia. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 153B (2), pp. 503 - 511 (2010)

Horstmann, S.; Lucae, S.; Menke, A.; Hennings, J. M.; Ising, M.; Roeske, D.; Müller-Myhsok, B.; Holsboer, F.; Binder, E. B.: Polymorphisms in GRIK4, HTR2A, and FKBP5 Show Interactive Effects in Predicting Remission to Antidepressant Treatment. Neuropsychopharmacology 35 (3), pp. 727 - 740 (2010)

Pfeufer, A.; van Noord, C.; Marciante, K. D.; Arking, D. E.; Larson, M. G.; Smith, A. V.; Tarasov, K. V.; Müller, M.; Sotoodehnia, N.; Sinner, M. F. et al.; Verwoert, G. C.; Li, M.; Kao, W. H. L.; Kottgen, A.; Coresh, J.; Bis, J. C.; Psaty, B. M.; Rice, K.; Rotter, J. I.; Rivadeneira, F.; Hofman, A.; Kors, J. A.; Stricker, B. H. C.; Uitterlinden, A. G.; van Duijn, C. M.; Beckmann, B. M.; Sauter, W.; Gieger, C.; Lubitz, S. A.; Newton-Cheh, C.; Wang, T. J.; Magnani, J. W.; Schnabel, R. B.; Chung, M. K.; Barnard, J.; Smith, J. D.; Van Wagoner, D. R.; Vasan, R. S.; Aspelund, T.; Eiriksdottir, G.; Harris, T. B.; Launer, L. J.; Najjar, S. S.; Lakatta, E.; Schlessinger, D.; Uda, M.; Abecasis, G. R.; Müller-Myhsok, B.; Ehret, G. B.; Boerwinkle, E.; Chakravarti, A.; Soliman, E. Z.; Lunetta, K. L.; Perz, S.; Wichmann, H. E.; Meitinger, T.; Levy, D.; Gudnason, V.; Ellinor, P. T.; Sanna, S.; Kaab, S.; Witteman, J. C. M.; Alonso, A.; Benjamin, E. J.; Heckbert, S. R.: Genome-wide association study of PR interval. Nature Genetics 42 (2), pp. 153 - 159 (2010)

Wolf, C.; Gramer, E.; Müller-Myhsok, B.; Pasutto, F.; Gramer, G.; Wissinger, B.; Weisschuh, N.: Lysyl Oxidase-like 1 Gene Polymorphisms in German Patients With Normal Tension Glaucoma, Pigmentary Glaucoma and Exfoliation Glaucoma. Journal of Glaucoma 19 (2), pp. 136 - 141 (2010)

Kleensang, A.; Franke, D.; Alcais, A.; Abel, L.; Müller-Myhsok, B.; Ziegler, A.: An Extensive Comparison of Quantitative Trait Loci Mapping Methods. Human Heredity 69 (3), pp. 202 - 211 (2010)

Lucae, S.; Ising, M.; Horstmann, S.; Baune, B. T.; Arolt, V.; Müller-Myhsok, B.; Holsboer, F.; Domschke, K.: HTR2A gene variation is involved in antidepressant treatment response. European Neuropsychopharmacology 20 (1), pp. 65 - 68 (2010)

Wolf, C.; Gramer, E.; Müller-Myhsok, B.; Pasutto, F.; Wissinger, B.; Weisschuh, N.: Mitochondrial haplogroup U is associated with a reduced risk to develop exfoliation glaucoma in the German population. BMC Genetics 11 (8), 8 (2010)

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)