Publikationen von B. Müller-Myhsok

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), S. 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), S. 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), S. 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), S. 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), S. 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), S. 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)

Dahdouh, F.; Anthoni, H.; Tapia-Paez, I.; Peyrard-Janvid, M.; Schulte-Körne, G.; Warnke, A.; Remschmidt, H.; Ziegler, A.; Kere, J.; Müller-Myhsok, B. et al.; Nöthen, M. M.; Schumacher, J.; Zucchelli, M.: Further evidence for DYX1C1 as a susceptibility factor for dyslexia. Psychiatric Genetics 19 (2), S. 59 - 63 (2009)

Dichgans, M.; Bevan, S.; Cole, J. W.; Plourde, A.; Matarin, M.; Ross-Adams, H.; Meitinger, T.; Wichmann, E.; Mitchel, B. D.; Furie, K. et al.; Rich, S. S.; MacLeod, M. J.; Meschia, J.; Rosand, J.; Kittner, S. J.; Markus, H. S.; Müller-Myhsok, B.; Gschwendtner, A.: Sequence Variants on Chromosome 9p21 Confer Risk of Large Vessel Stroke. Stroke 40 (4), S. E109 - E109 (2009)

Pfeufer, A.; Sanna, S.; Arking, D. E.; Müller, M.; Gateva, V.; Fuchsberger, C.; Ehret, G. B.; Orru, M.; Pattaro, C.; Köttgen, A. et al.; Perz, S.; Usala, G.; Barbalic, M.; Li, M.; Pütz, B.; Scuteri, A.; Prineas, R. J.; Sinner, M. F.; Gieger, C.; Najjar, S. S.; Kao, W. H. L.; Mühleisen, T. W.; Dei, M.; Happle, C.; Möhlenkamp, S.; Crisponi, L.; Erbel, R.; Jöckel, K. H.; Naitza, S.; Steinbeck, G.; Marroni, F.; Hicks, A. A.; Lakatta, E.; Müller-Myhsok, B.; Pramstaller, P. P.; Wichmann, H. E.; Schlessinger, D.; Boerwinkle, E.; Meitinger, T.; Uda, M.; Coresh, J.; Kaab, S.; Abecasis, G. R.; Chakravarti, A.: Common variants at ten loci modulate the QT interval duration in the QTSCD Study. Nature Genetics 41 (4), S. 407 - 414 (2009)

Freilinger, T.; Bevan, S.; Ripke, S.; Gschwendtner, A.; Lichtner, P.; Müller-Myhsok, B.; Wichmann, H. E.; Markus, H. S.; Meitinger, T.; Dichgans, M.: Genetic Variation in the Lymphotoxin-Alpha Pathway and the Risk of Ischemic Stroke in European Populations. Stroke 40 (3), S. 970 - 972 (2009)

Glas, J.; Seiderer, J.; Pasciuto, G.; Tillack, C.; Diegelmann, J.; Pfennig, S.; Konrad, A.; Schmechel, S.; Wetzke, M.; Torok, H. P. et al.; Stallhofer, J.; Jürgens, M.; Griga, T.; Klein, W.; Epplen, J. T.; Schiemann, U.; Mussack, T.; Lohse, P.; Göke, B.; Ochsenkühn, T.; Folwaczny, M.; Müller-Myhsok, B.; Brand, S.: rs224136 on Chromosome 10q21.1 and Variants in PHOX2B, NCF4, and FAM92B Are Not Major Genetic Risk Factors for Susceptibility to Crohn's Disease in the German Population. American Journal of Gastroenterology 104 (3), S. 665 - 672 (2009)

Heck, A.; Lieb, R.; Ellgas, A.; Pfister, H.; Lucae, S.; Erhardt, A.; Himmerich, H.; Horstmann, S.; Kloiber, S.; Ripke, S. et al.; Müller-Myhsok, B.; Bettecken, T.; Uhr, M.; Holsboer, F.; Ising, M.: Polymorphisms in the Angiotensin-Converting Enzyme Gene Region Predict Coping Styles in Healthy Adults and Depressed Patients. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 150B (1), S. 104 - 114 (2009)

Gusareva, E. S.; Havelkova, H.; Blazkova, H.; Kosarova, M.; Kucera, P.; Kral, V.; Salyakina, D.; Müller-Myhsok, B.; Lipoldova, M.: Mouse to human comparative genetics reveals a novel immunoglobulin E-controlling locus on Hsa8q12. Immunogenetics 61 (1), S. 15 - 25 (2009)

Kemlink, D.; Vavrova, J.; Högl, B.; Frauscher, B.; Polo, O.; Silander, K.; Müller-Myhsok, B.; Winkelmann, J.: Independent replication of association of restless legs syndrome to MEIS1, BTBD9 and MAP2K5/LBXCOR1 in the European population. Journal of Sleep Research 17 (Suppl. 1), S. 26 - 26 (2008)

Ludwig, K. U.; Schumacher, J.; Schulte-Körne, G.; König, I. R.; Warnke, A.; Plume, E.; Anthoni, H.; Peyrard-Janvid, M.; Meng, H.; Ziegler, A. et al.; Remschmidt, H.; Kere, J.; Gruen, J. R.; Mueller-Myhsok, B.; Nöthen, M. M.; Hoffmann, P.: Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample. Psychiatric Genetics 18 (6), S. 310 - 312 (2008)

Ludwig, K. U.; Roeske, D.; Schumacher, J.; Schulte-Körne, G.; König, I. R.; Warnke, A.; Plume, E.; Ziegler, A.; Remschmidt, H.; Müller-Myhsok, B. et al.; Nöthen, M. M.; Hoffmann, P.: Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample. Journal of Neural Transmission 115 (11), S. 1587 - 1589 (2008)

Keck, M. E.; Kern, N.; Erhardt, A.; Unschuld, P. G.; Ising, M.; Salyakina, D.; Müller, M. B.; Knorr, C. C.; Lieb, R.; Hohoff, C. et al.; Krakowitzky, P.; Maier, W.; Bandelow, B.; Fritze, J.; Deckert, J.; Holsboer, F.; Müller-Myhsok, B.; Binder, E. B.: Combined Effects of Exonic Polymorphisms in CRHR1 and AVPR1B Genes in a Case/Control Study for Panic Disorder. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 147B (7), S. 1196 - 1204 (2008)

Heck, A.; Lieb, R.; Unschuld, P.; Ellgas, A.; Pfister, H.; Lucae, S.; Erhardt, A.; Himmerich, H.; Horstmann, S.; Kloiber, S. et al.; Ripke, S.; Müller-Myhsok, B.; Bettecken, T.; Uhr, M.; Holsboer, F.; Ising, M.: Evidence for associations between PDE4D polymorphisms and a subtype of neuroticism. Molecular Psychiatry 13 (9), S. 831 - 832 (2008)

Müller-Myhsok, B.: Genome-wide linkage and genome-wide association - Can they be reconciled? Annals of Human Genetics 72, S. 687 - 687 (2008)