Journal Article (27)

21.
Journal Article
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), pp. 59 - 63 (2009)
22.
Journal Article
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), p. E109 - E109 (2009)
23.
Journal Article
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), pp. 407 - 414 (2009)
24.
Journal Article
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), pp. 970 - 972 (2009)
25.
Journal Article
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), pp. 665 - 672 (2009)
26.
Journal Article
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), pp. 104 - 114 (2009)
27.
Journal Article
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), pp. 15 - 25 (2009)
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