Publikationen von Jakob C. Mueller

Hanus, P.; Goebel, B.; Dingel, J.; Weindl, J.; Zech, J.; Dawy, Z.; Hagenauer, J.; Mueller, J. C.: Information and communication theory in molecular biology. Electrical Engineering 90 (2), S. 161 - 173 (2007)

Koch, W.; Hoppmann, P.; Michou, E.; Jung, V.; Pfeufer, A.; Mueller, J. C.; Gieger, C.; Wichmann, H. E.; Meitinger, T.; Schoemig, A. et al.; Kastrati, A.: Association of variants in the BAT1-NFKB1L1-LTA genomic region with protection against myocardial infarction in Europeans. Human Molecular Genetics 16 (15), S. 1821 - 1827 (2007)

Koch, W.; Hoppmann, P.; Mueller, J. C.; Schoemig, A.; Kastrati, A.: No association of polymorphisms in the gene encoding 5-lipoxygenase-activating protein and myocardial infarction in a large central European population. Genetics in Medicine 9 (2), S. 123 - 129 (2007)

Koch, W.; Latz, W.; Eichinger, M.; Ganser, C.; Biele, J.; Mueller, J. C.; Schoemig, A.; Kastrati, A.: Association of a fibrinogen gene haplotype with myocardial infarction. European Heart Journal 28, S. 875 - 876 (2007)

Laws, S. M.; Friedrich, P.; Diehl-Schmid, J.; Mueller, J. C.; Eisele, T.; Bäuml, J.; Förstl, H.; Kurz, A.; Riemenschneider, M.: Fine mapping of the MAPT locus using quantitative trait analysis identifies possible causal variants in Alzheimer’s disease. Molecular Psychiatry 12, S. 510 - 517 (2007)

Maetzler, W.; Berg, D.; Schalamberidze, N.; Melms, A.; Schott, K.; Mueller, J. C.; Liaw, L.; Gasser, T.; Nitsch, C.: Osteopontin is elevated in Parkinson’s disease and its absence leads to reduced neurodegeneration in the MPTP model. Neurobiology of Disease 25 (3), S. 473 - 482 (2007)

Mueller, J. C.; Riemenschneider, M.; Schoepfer-Wendels, A.; Gohlke, H.; Konta, L.; Friedrich, P.; Illig, T.; Laws, S. M.; Förstl, H.; Kurz, A.: Weak independent association signals between IDE polymorphisms, Alzheimer’s disease and cognitive measures. Neurobiology of Aging 28 (5), S. 727 - 734 (2007)

Riemenschneider, M.; Schoepfer-Wendels, A.; Friedrich, P.; Konta, L.; Laws, S. M.; Mueller, J. C.; Kurz, A.; Forstl, H.: No association of Vacuolar protein sorting 26 polymorphisms with Alzheimer’s disease. Neurobiology of Aging 28 (6), S. 883 - 884 (2007)

Sarkis, M.; Goebel, B.; Dawy, Z.; Hagenauer, J.; Hanus, P.; Mueller, J. C.: Gene mapping of complex diseases: A comparison of methods from statistics, information theory, and signal processing. IEEE Signal Processing Magazine 24 (1), S. 83 - 90 (2007)

Sedlacek, K.; Neureuther, K.; Mueller, J. C.; Stark, K.; Fischer, M.; Baessler, A.; Reinhard, W.; Broeckel, U.; Lieb, W.; Erdmann, J. et al.; Schunkert, H.; Riegger, G.; Illig, T.; Meitinger, T.; Hengstenberg, C.: Lymphotoxin-alpha and galectin-2 SNPs are not associated with myocardial infarction in two different German populations. Journal of Molecular Medicine-JMM 85 (9), S. 997 - 1004 (2007)

Vollmert, C.; Hahn, S.; Lamina, C.; Huth, C.; Kolz, M.; Schöpfer-Wendels, A.; Mann, K.; Bongardt, F.; Mueller, J. C.; Kronenberg, F. et al.; Wichmann, H. E.; Herder, C.; Holle, R.; Löwel, H.; Illig, T.; Janssen, O. E.; Meisinger, C.; John, J.: Calpain-10 variants and haplotypes are associated with polycystic ovary syndrome in Caucasians. American Journal of Physiology-Endocrinology and Metabolism 292 (3), S. E836 - E844 (2007)

Weindl, J.; Hanus, P.; Dawy, Z.; Zech, J.; Hagenauer, J.; Mueller, J. C.: Modeling DNA-binding of Escherichia coli sigma(70) exhibits a characteristic energy landscape around strong promoters. Nucleic Acids Research (London) 35 (20), S. 7003 - 7010 (2007)

Dawy, Z.; Goebel, B.; Hagenauer, J.; Meitinger, T.; Andreoli, C.; Mueller, J. C.: Gene mapping and marker clustering using Shannon’s mutual information. IEEE ACM Transactions on Computational Biology and Bioinformatics 3 (1), S. 47 - 56 (2006)

Fernández-Santiago, R.; Sharma, M.; Mueller, J. C.; Gohlke, H.; Illig, T.; Anneser, J.; Münch, C.; Ludolph, A.; Kamm, C.; Gasser, T.: Association between the vascular endothelial growth factor (VEGF) gene and amyotrophic lateral sclerosis (ALS): Possible gender-dependent effect. Neurology 66 (12), S. 1929 - 1931 (2006)

Griebeler, E. M.; Mueller, J. C.; Seitz, A.: Spatial genetic patterns generated by two admixing genetic lineages: A simulation study. Conservation Genetics Resources 7 (5), S. 753 - 766 (2006)

Heid, I. M.; Wagner, S. A.; Gohlke, H.; Iglseder, B.; Mueller, J. C.; Cip, P.; Ladurner, G.; Reiter, R.; Stadlmayr, A.; Mackevics, V. et al.; Illig, T.; Kronenberg, F.; Paulweber, B.: Genetic architecture of the APM1 gene and its influence on adiponectin plasma levels and parameters of the metabolic syndrome in 1727 healthy Caucasians. Diabetes 55 (2), S. 375 - 384 (2006)

Kamm, C.; Asmus, F.; Mueller, J.; Mayer, P.; Sharma, M.; Muller, U. J.; Beckert, S.; Ehling, R.; Illig, T.; Wichmann, H. E. et al.; Poewe, W.; Mueller, J. C.; Gasser, T.: Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia. Neurology 67 (10), S. 1857 - 1859 (2006)

Koch, W.; Hoppmann, P.; Mueller, J. C.; Schomig, A.; Kastrati, A.: Association of transforming growth factor-beta1 gene polymorphisms with myocardial infarction in patients with angiographically proven coronary heart disease. Arteriosclerosis, Thrombosis, and Vascular Biology: an Official Journal of the American Heart Association 26 (5), S. 1114 - 1119 (2006)

Pichler, I.; Mueller, J. C.; Stefanov, S. A.; de Grandi, A.; Volpato, C. B.; Pinggera, G. K.; Mayr, A.; Ogriseg, M.; Ploner, F.; Meitinger, T. et al.; Pramstaller, P. P.: Genetic structure in contemporary South Tyrolean isolated populations revealed by the analysis of Y chromosome, mtDNA and Alu polymorphisms. Human Biology 78 (4), S. 441 - 464 (2006)

Riemenschneider, M.; Konta, L.; Friedrich, P.; Schwarz, S.; Taddei, K.; Neff, F.; Padovani, A.; Kölsch, H.; Laws, S. M.; Klopp, N. et al.; Bickeboller, H.; Wagenpfeil, S.; Mueller, J. C.; Rosenberger, A.; Diehl-Schmid, J.; Archetti, S.; Lautenschlager, N.; Borroni, B.; Müller, U.; Illig, T.; Heun, R.; Egensperger, R.; Schlegel, J.; Forstl, H.; Martins, R. N.; Kurz, A.: A functional polymorphism within plasminogen activator urokinase (PLAU) is associated with Alzheimer’s disease. Human Molecular Genetics 15 (16), S. 2446 - 2456 (2006)