Publikationen von Bertram Mueller-Myhsok

Thoeringer, C. K.; Binder, E. B.; Salyakina, D.; Erhardt, A.; Ising, M.; Unschuld, P. G.; Kern, N.; Lucae, S.; Brueckl, T. M.; Mueller, M. B. et al.; Fuchs, B.; Puetz, B.; Lieb, R.; Uhr, M.; Holsboer, F.; Mueller-Myhsok, B.; Keck, M.: Association of a Met88Val diazepam binding inhibitor (DBI) gene polymorphism and anxiety disorders with panic attacks. Journal of Psychiatric Research 41, doi:10.1016/j.jpsychires.2006.06.001, S. 579 - 584 (2007)

Opherk, C.; Peters, N.; Holtmannspötter, M.; Gschwendtner, A.; Müller-Myhsok, B.; Dichgans, M.: Heritability of MRI lesion volume in CADASIL - Evidence for genetic modifiers. Stroke 37 (11), S. 2684 - 2689 (2006)

Bender, A.; Koch, W.; Elstner, M.; Schombacher, Y.; Bender, J.; Moeschl, M.; Gekeler, F.; Müller-Myhsok, B.; Gasser, T.; Tatsch, K. et al.; Klopstock, T.: Creatine supplementation in Parkinson disease: A placebo-controlled randomized pilot trial. Neurology 67 (7), S. 1262 - 1264 (2006)

Unschuld, P. G.; Erhardt, A.; Ising, M.; Lucae, S.; Kloiber, S.; Kohli, M.; Binder, E. B.; Müller-Myhsok, B.; Keck, M. E.; Holsboer, F.: An association candidate-gene study on genetic variations within HTR2A in patients suffering from panic disorder. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 141B (7), S. 739 - 740 (2006)

Liebetanz, K. M.; Winkelmann, J.; Trenkwalder, C.; Pütz, B.; Dichgans, M.; Gasser, T.; Müller-Myhsok, B.: RLS3: Fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity. Neurology 67 (2), S. 320 - 321 (2006)

Glas, J.; Torok, H. P.; Tonenchi, L.; Müller-Myhsok, B.; Mussack, T.; Wetzke, M.; Klein, W.; Epplen, J. T.; Griga, T.; Schiemann, U. et al.; Lohse, P.; Seiderer, J.; Schnitzler, F.; Brand, S.; Ochsenkuhn, T.; Folwaczny, M.; Folwaczny, C.: Role of the NFKB1-94ins/delATTG promoter polymorphism in IBD and potential interactions with Polymorphisms in the CARD15/NOD2, IKBL, and IL-1RN genes. Inflammatory Bowel Diseases 12 (7), S. 606 - 611 (2006)

Sharma, M.; Müller, J. C.; Zimprich, A.; Lichtner, P.; Hofer, A.; Leitner, P.; Maass, S.; Berg, D.; Dürr, A.; Bonifati, V. et al.; De Michele, G.; Oostra, B.; Brice, A.; Wood, N. W.; Müller-Myhsok, B.; Gasser, T.: The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations. Journal of Medical Genetics 43 (7), S. 557 - 562 (2006)

Barden, N.; Harvey, M.; Gagne, B.; Shink, E.; Tremblay, M.; Raymond, C.; Labbe, M.; Villeneuve, A.; Rochette, D.; Bordeleau, L. et al.; Stadler, H.; Holsboer, F.; Müller-Myhsok, B.: Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 141B (4), S. 374 - 382 (2006)

Binder, E. B.; Lucae, S.; Salyakina, D.; Lichtner, P.; Meitinger, T.; Bondy, B.; Wochnik, G.; Rein, T.; Holsboer, F.; Müller-Myhsok, B.: SNPs in FKBP5 determine a novel subtype of depression characterized by rapid response to antidepressant treatment. European Neuropsychopharmacology 16 (Suppl. 1), S. S75 - S75 (2006)

Erhardt, A.; Unschuld, P. G.; Lucae, S.; Ising, M.; Salyakina, D.; Pütz, B.; Müller-Myhsok, B.; Binder, E. B.; Holsboer, F.; Keck, M. E.: Possible genetic implications of the endo-cannabinoid system in anxiety disorders versus depressive disorders. European Neuropsychopharmacology 16 (Suppl. 1), S. S88 - S88 (2006)

Baghai, T. C.; Binder, E. B.; Schule, C.; Salyakina, D.; Eser, D.; Lucae, S.; Zwanzger, P.; Haberger, C.; Zill, P.; Ising, M. et al.; Deiml, T.; Uhr, M.; Illig, T.; Wichmann, H.-E.; Modell, S.; Nothdurfter, C.; Holsboer, F.; Müller-Myhsok, B.; Möller, H.-J.; Rupprecht, R.; Bondy, B.: Polymorphisms in the angiotensin-converting enzyme gene are associated with unipolar depression, ACE activity and hypercortisolism. Molecular Psychiatry 11, S. 1003 - 1015 (2006)

Lucae, S.; Salyakina, D.; Barden, N.; Harvey, M.; Gagné, B.; Labbé, M.; Binder, E. B.; Uhr, M.; Paez-Pereda, M.; Sillaber, I. et al.; Ising, M.; Brückl, T.; Lieb, R.; Holsboer, F.; Müller-Myhsok, B.: P2RX7, a gene coding for a purinergic ligand-gated ion channel, is associated with major depressive disorder. Human Molecular Genetics 15 (16), S. 2438 - 2445 (2006)

Winkelmann, J.; Lichtner, P.; Pütz, B.; Trenkwalder, C.; Hauk, S.; Meitinger, T.; Strom, T.; Müller-Myhsok, B.: Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome. Movement Disorders 21 (1), S. 28 - 33 (2006)

Glas, J.; Török, H. P.; Tonenchi, L.; Kapser, J.; Schiemann, U.; Müller-Myhsok, B.; Folwaczny, M.; Folwaczny, C.: Association of polymorphisms in the interleukin-18 gene in patients with Crohn's disease depending on the CARD15/NOD2 genotype. Inflammatory Bowel Diseases 11 (12), S. 1031 - 1037 (2005)

Müller-Myhsok, B.; Yan, K.; Leal, S. M.: SimPed: A simulation program to generate haplotype and genotype data for pedigree structures. Annals of Human Genetics 69, S. 771 - 771 (2005)

Seaman, S. R.; Müller-Myhsok, B.: Rapid simulation of p-values for product methods and multiple-testing adjustment in association studies. Annals of Human Genetics 69, S. 772 - 773 (2005)

Torok, H. P.; Glas, J.; Tonenchi, L.; Lohse, P.; Müller-Myhsok, B.; Limbersky, O.; Neugebauer, C.; Schnitzler, F.; Seiderer, J.; Tillack, C. et al.; Brand, S.; Brunnler, G.; Jagiello, P.; Epplen, J. T.; Griga, T.; Klein, W.; Schiemann, U.; Folwaczny, M.; Ochsenkuhn, T.; Folwaczny, C.: Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease. Gut 54 (10), S. 1421 - 1427 (2005)

Barden, N.; Harvey, M.; Gagne, B.; Raymond, C.; Labbe, M.; Müller-Myhsok, B.; Binder, E.; Holsboer, F.: A glutamine to arginine mutation in the C-terminal domain of P2RX7 determines the risk for mood disorders. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 138B (1), S. 82 - 82 (2005)

Erhardt, A.; Seaman, S. R.; Lucae, S.; Unschuld, P. G.; Kern, N.; Welt, T.; Ising, M.; Salyakina, D.; Pütz, B.; Lieb, R. et al.; Binder, E.; Müller-Myhsok, B.; Holsboer, F.; Keck, M. E.: Genetic implications of the endocannabinoid system in anxiety disorders versus depressive disorders: Is there any evidence for the continuum hypothesis? American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 138B (1), S. 44 - 44 (2005)

Horstmann, S.; Ising, M.; Lucae, S.; Kloiber, S.; Dose, T.; Salyakina, D.; Pütz, B.; Uhr, M.; Müller-Myhsok, B.; Holsboer, F.: The cortisol and ACTH response in the combined Dex/CRH test of acutely depressed patients varies significantly between 5-HT2A receptor genotypes. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 138B (1), S. 48 - 48 (2005)