Publikationen von Jakob C. Mueller

Schulte, C.; Sharma, M.; Mueller, J. C.; Lichtner, P.; Prestel, J.; Berg, D.; Gasser, T.: Comprehensive association analysis of the NOS2A gene with Parkinson disease. Neurology 67 (11), S. 2080 - 2082 (2006)

Sharma, M.; Mueller, 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.; Muller-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)

Wattier, R. Α.; Beguet, J.; Gaillard, M.; Mueller, J. C.; Bollache, L.; Perrot-Minnot, M.-J.: Molecular markers for systematic identification and population genetics of the invasive Ponto-Caspian freshwater gammarid Dikerogammarus villosus (Crustacea, Amphipoda). Molecular Ecology Notes 6 (2), S. 487 - 489 (2006)

Biskup, S.; Mueller, J. C.; Sharma, M.; Lichtner, P.; Zimprich, A.; Berg, D.; Wüllner, U.; Illig, T.; Meitinger, T.; Gasser, T.: Common variants of LRRK2 (PARK8) are not associated with sporadic Parkinson's disease. Annals of Neurology 58 (6), S. 905 - 908 (2005)

Koch, W.; Hoppmann, P.; Michou, E.; Jung, V.; Pfeufer, A.; Mueller, J. C.; Meitinger, T.; Schomig, A.; Kastrati, A.: TaqMan assays for genotyping of single nucleotide polymorphisms present at a disease susceptibility locus on chromosome 6. Clinical Chemistry and Laboratory Medicine 43 (2), S. 167 - 172 (2005)

Koch, W.; Hoppmann, P.; Pfeufer, A.; Mueller, J. C.; Schömig, A.; Kastrati, A.: No replication of association between estrogen receptor alpha gene polymorphisms and susceptibility to myocardial infarction in a large Caucasian patient sample. Circulation 112 (14), S. 2138 - 2142 (2005)

Lamina, C.; Steffens, M.; Mueller, J. C.; Löhmussaar, E.; Meitinger, T.; Wichmann, H. E.: Genetic diversity in German and European populations: Looking for substructures and genetic patterns. Gesundheitswesen 67, S. 127 - 131 (2005)

Löhmussaar, E.; Gschwendtner, A.; Mueller, J. C.; Org, T.; Wichmann, E.; Hamann, G.; Meitinger, T.; Dichgans, M.: The ALOX5AP gene and the PDE4D gene in a Central-European population of stroke patients. Stroke 36 (4), S. 731 - 736 (2005)

Mueller, J. C.; Fuchs, J.; Hofer, A.; Zimprich, A.; Lichtner, P.; Illig, T.; Berg, D.; Wüllner, U.; Meitinger, T.; Gasser, T.: Multiple regions of alpha-synuclein are associated with Parkinson's disease. Annals of Neurology 57 (4), S. 535 - 541 (2005)

Mueller, J. C.; Löhmussaar, E.; Mägi, R.; Remm, M.; Bettecken, T.; Lichtner, P.; Biskup, S.; Illig, T.; Pfeufer, A.; Luedemann, J. et al.; Schreiber, S.; Pramstaller, P.; Pichler, I.; Romeo, G.; Gaddi, A.; Testa, A.; Wichmann, H. E.; Metspalu, A.; Meitinger, T.: Linkage disequilibrium patterns and tagSNP transferability among European populations. The American Journal of Human Genetics 76 (3), S. 387 - 398 (2005)

Pfeufer, A.; Jalilzadeh, S.; Perz, S.; Mueller, J. C.; Hinterseer, M.; Illig, T.; Akyol, M.; Huth, C.; Schöpfer-Wendels, A.; Kuch, B. et al.; Steinbeck, G.; Holle, R.; Näbauer, M.; Wichmann, H.-E.; Meitinger, T.; Kääb, S.: Common variants in myocardial ion channel genes modify the QT interval in the general population: Results from the KORA study. Circulation Research 96 (6), S. 693 - 701 (2005)

Andreoli, C.; Prokisch, H.; Hörtnagel, K.; Mueller, J. C.; Münsterkötter, M.; Scharfe, C.; Meitinger, T.: MitoP2, an integrated database on mitochondrial proteins in yeast and man. Nucleic Acids Research (London) 32 (Suppl. 1), S. D459 - D462 (2004)

Binder, E. B.; Salyakina, D.; Lichtner, P.; Wochnik, G. M.; Ising, M.; Pütz, B.; Papiol, S.; Seaman, S.; Lucae, S.; Kohli, M. A. et al.; Nickel, T.; Künzel, H. E.; Fuchs, B.; Majer, M.; Pfennig, A.; Kern, N.; Brunner, J.; Modell, S.; Baghai, T.; Deiml, T.; Zill, P.; Bondy, B.; Rupprecht, R.; Messer, T.; Köhnlein, O.; Dabitz, H.; Brückl, T.; Müller, N.; Pfister, H.; Lieb, R.; Mueller, J. C.; Lõhmussaar, E.; Strom, T. M.; Bettecken, T.; Meitinger, T.; Uhr, M.; Rein, T.; Holsboer, F.; Muller-Myhsok, B.: Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment. Nature Genetics 36 (12), S. 1319 - 1325 (2004)

Mueller, J. C.: Linkage disequilibrium for different scales and applications. Briefings in Bioinformatics 5 (4), S. 355 - 364 (2004)

Mueller, J. C.; Andreoli, C.: Plotting haplotype-specific linkage disequilibrium patterns by extended haplotype homozygosity. Bioinformatics 20 (5), S. 786 - 787 (2004)

Mueller, J. C.; Andreoli, C.; Prokisch, H.; Meitinger, T.: Mechanisms for multiple intracellular localisation of human mitochondrial proteins. Mitochondrion 3 (6), S. 315 - 325 (2004)

Bychek, E. A.; Mueller, J. C.: Molecular genetic diagnostics of some Daphnia species (Crustacea, Cladocera) from the Volga River. Russian Journal of Genetics 39 (3), S. 356 - 358 (2003)

Koch, W.; Ehrenhaft, A.; Griesser, K.; Pfeufer, A.; Mueller, J. C.; Schömig, A.; Kastrati, A.: TaqMan systems for genotyping of disease-related polymorphisms present in the gene encoding Apolipoprotein E. Clinical Chemistry and Laboratory Medicine 40 (11), S. 1123 - 1131 (2002)

Mueller, J. C.; Hidde, D.; Seitz, A.: Canal construction destroys barrier between major European invasion lineages of the zebra mussel. Proceedings of the Royal Society B: Biological Sciences 269 (1496), S. 1139 - 1142 (2002)

Mueller, J. C.; Schramm, S.; Seitz, A.: Genetic and morphological differentiation of Dikerogammarus invaders and their invasion history in Central Europe. Freshwater Biology 47 (11), S. 2039 - 2048 (2002)