Publications Bertram Müller-Myhsok

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), pp. 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, p. 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, pp. 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), pp. 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), p. 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), p. 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), p. 48 - 48 (2005)

Kern, N.; Erhardt, A.; Pfennig, A.; Lucae, S.; Ising, M.; Salyakina, D.; Pütz, B.; Müller-Myhsok, B.; Uhr, M.; Holsboer, F. et al.; Binder, E. B.; Keck, M. E.: Syndromal panic attacks are possibly associated with polymorphisms in the angiotensin converting enzyme (ACE) gene. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 138B (1), p. 45 - 45 (2005)

Erhardt, A.; Seaman, S. R.; Lucae, S.; Kern, N.; Unschuld, P. G.; Welt, T.; Ising, M.; Salyakina, D.; Pütz, B.; Lieb, R. et al.; Binder, E. B.; 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? Pharmacopsychiatry 38 (5), p. 240 - 240 (2005)

Salyakina, D.; Binder, E. B.; Ising, M.; Uhr, M.; Lucae, S.; Müller-Myhsok, B.: Within- and Inter-gene interactions in FKBP5 and GR genes and its association with early response. Pharmacopsychiatry 38 (5), p. 274 - 274 (2005)

Seaman, S. R.; Müller-Myhsok, B.: On rapid simulation of P values in association studies - Reply to Lin. American Journal of Human Genetics 77 (3), pp. 514 - 515 (2005)

Unschuld, P. G.; Ising, M.; Erhardt, A.; Lucae, S.; Welt, T.; Kloiber, S.; Kern, N.; Salyakina, D.; Binder, E. B.; Brückl, T. et al.; Uhr, M.; Müller-Myhsok, B.; Holsboer, F.; Keck, M. E.: Polymorphisms in the serotonin receptor gene HTR2A modulate disease severity and susceptibility for anxiety disorders but not depression and are associated with specific personality traits. Pharmacopsychiatry 38 (5), p. 282 - 282 (2005)

Müller-Myhsok, B.: The usefulness of single nucleotide polymorphisms (SNPs) for genetic epidemiological investigation of complex psychiatric diseases. Progress in Neuro-Psychopharmacology & Biological Psychiatry 29 (6), pp. 1017 - 1020 (2005)

Klopstock, T.; Elstner, M.; Lücking, C. B.; Müller-Myhsok, B.; Gasser, T.; Botz, E.; Lichtner, P.; Hörtnagel, K.: Mutations in the pantothenate kinase gene PANK2 are not associated with Parkinson disease. Neuroscience Letters 379 (3), pp. 195 - 198 (2005)

Seaman, S. R.; Müller-Myhsok, B.: Rapid simulation of P values for product methods and multiple-testing adjustment in association studies. American Journal of Human Genetics 76 (3), pp. 399 - 408 (2005)

Asmus, F.; Schoenian, S.; Lichtner, P.; Munz, M.; Mayer, P.; Müller-Myhsok, B.; Zimprich, A.; Remschmidt, H.; Hebebrand, J.; Bandmann, O. et al.; Gasser, T.: Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndrome. Neurogenetics 6 (1), pp. 55 - 56 (2005)

Prestel, J.; Sharma, M.; Leitner, P.; Zimprich, A.; Vaughan, J. R.; Dürr, A.; Bonifati, V.; De Michele, G.; Hanagasi, H. A.; Farrer, M. et al.; Hofer, A.; Asmus, F.; Volpe, G.; Meco, G.; Brice, A.; Wood, N. W.; Müller-Myhsok, B.; Gasser, T.: PARK11 is not linked with Parkinson's disease in European families. European Journal of Human Genetics 13 (2), pp. 193 - 197 (2005)

Leal, S. M.; Yan, K.; Müller-Myhsok, B.: SimPed: A simulation program to generate haplotype and genotype data for pedigree structures. Human Heredity 60 (2), pp. 119 - 122 (2005)

Salyakina, D.; Seaman, S. R.; Browning, B. L.; Dudbridge, F.; Müller-Myhsok, B.: Evaluation of Nyholt`s Procedure for Multiple Testing Correction. Human Heredity 60, pp. 19 - 25 (2005)

Ziegler, A.; König, I. R.; Deimel, W.; Plume, E.; Nöthen, M. M.; Propping, P.; Kleensang, A.; Müller-Myhsok, B.; Warnke, A.; Remschmidt, H. et al.; Schulte-Körne, G.: Developmental dyslexia - Recurrence risk estimates from a German bi-center study using the single proband sib pair design. Human Heredity 59 (3), pp. 136 - 143 (2005)