Publications of the Max Planck Research Group of Development and Evolution of Cognition

51.

Journal Article

Dawy, Z.; Sarkis, M.; Hagenauer, J.; Mueller, J. C.: Fine-scale genetic mapping using independent component analysis. IEEE ACM Transactions on Computational Biology and Bioinformatics 5 (3), pp. 448 - 460 (2008)

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52.

Journal Article

Dingel, J.; Hanus, P.; Leonardi, N.; Hagenauer, J.; Zech, J.; Mueller, J. C.: Local conservation scores without a priori assumptions on neutral substitution rates. BMC Bioinformatics 9, 190 (2008)

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53.

Journal Article

Fuchs, J.; Tichopad, A.; Golub, Y.; Munz, M.; Schweitzer, K. J.; Wolf, B.; Berg, D.; Mueller, J. C.; Gasser, T.: Genetic variability in the SNCA gene influences alpha-synuclein levels in the blood and brain. The FASEB Journal 22 (5), pp. 1327 - 1334 (2008)

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54.

Journal Article

Koch, W.; Hoppmann, P.; Biele, J.; Mueller, J. C.; Schoemig, A.; Kastrati, A.: Fibrinogen genes and myocardial infarction. A haplotype analysis. Arteriosclerosis, Thrombosis, and Vascular Biology: an Official Journal of the American Heart Association 28 (4), pp. 758 - 763 (2008)

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55.

Journal Article

Koch, W.; Hoppmann, P.; Mueller, J. C.; Schoemig, A.; Kastrati, A.: Lack of support for association between common variation in TNFSF4 and myocardial infarction in a German population. Nature Genetics 40 (12), pp. 1386 - 1387 (2008)

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56.

Journal Article

Laws, S. M.; Friedrich, P.; Diehl-Schmid, J.; Mueller, J. C.; Ibach, B.; Bauml, J.; Eisele, T.; Forstl, H.; Kurz, A.; Riemenschneider, M.: Genetic analysis of MAPT haplotype diversity in frontotemporal dementia. Neurobiology of Aging 29 (8), pp. 1276 - 1278 (2008)

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57.

Journal Article

Mueller, J. C.; Steiger, S. S.; Fidler, A. E.; Kempenaers, B.: Biogenic trace amine-associated receptors (TAARs) are encoded in avian genomes: Evidence and possible implications. Journal of Heredity 99 (2), pp. 174 - 176 (2008)

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58.

Journal Article

Zimprich, F.; Stogmann, E.; Bonelli, S.; Baumgartner, C.; Mueller, J. C.; Meitinger, T.; Zimprich, A.; Strom, T. M.: A functional polymorphism in the SCN1A gene is not associated with carbamazepine dosages in Austrian patients with epilepsy. Epilepsia 49 (6), pp. 1108 - 1109 (2008)

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59.

Journal Article

Fidler, A. E.; van Oers, K.; Drent, P. J.; Kuhn, S.; Mueller, J. C.; Kempenaers, B.: Drd4 gene polymorphisms are associated with personality variation in a passerine bird. Proceedings of the Royal Society B: Biological Sciences 274 (1619), pp. 1685 - 1691 (2007)

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60.

Journal Article

Forstmeier, W.; Segelbacher, G.; Mueller, J. C.; Kempenaers, B.: Genetic variation and differentiation in captive and wild zebra finches (Taeniopygia guttata). Molecular Ecology 16 (19), pp. 4039 - 4050 (2007)

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61.

Journal Article

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), pp. 161 - 173 (2007)

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62.

Journal Article

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), pp. 1821 - 1827 (2007)

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63.

Journal Article

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), pp. 123 - 129 (2007)

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64.

Journal Article

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, pp. 875 - 876 (2007)

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65.

Journal Article

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, pp. 510 - 517 (2007)

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66.

Journal Article

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), pp. 473 - 482 (2007)

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67.

Journal Article

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), pp. 727 - 734 (2007)

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68.

Journal Article

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), pp. 883 - 884 (2007)

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69.

Journal Article

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), pp. 83 - 90 (2007)

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70.

Journal Article

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), pp. 997 - 1004 (2007)

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71.

Journal Article

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), pp. E836 - E844 (2007)

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72.

Journal Article

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), pp. 7003 - 7010 (2007)

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73.

Journal Article

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), pp. 47 - 56 (2006)

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74.

Journal Article

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), pp. 1929 - 1931 (2006)

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75.

Journal Article

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), pp. 753 - 766 (2006)

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76.

Journal Article

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), pp. 375 - 384 (2006)

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77.

Journal Article

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), pp. 1857 - 1859 (2006)

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78.

Journal Article

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), pp. 1114 - 1119 (2006)

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79.

Journal Article

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), pp. 441 - 464 (2006)

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80.

Journal Article

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), pp. 2446 - 2456 (2006)

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81.

Journal Article

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), pp. 2080 - 2082 (2006)

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82.

Journal Article

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), pp. 557 - 562 (2006)

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83.

Journal Article

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), pp. 487 - 489 (2006)

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84.

Journal Article

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), pp. 905 - 908 (2005)

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85.

Journal Article

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), pp. 167 - 172 (2005)

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86.

Journal Article

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), pp. 2138 - 2142 (2005)

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87.

Journal Article

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, pp. 127 - 131 (2005)

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88.

Journal Article

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), pp. 731 - 736 (2005)

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89.

Journal Article

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), pp. 535 - 541 (2005)

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90.

Journal Article

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), pp. 387 - 398 (2005)

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91.

Journal Article

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), pp. 693 - 701 (2005)

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92.

Journal Article

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), pp. D459 - D462 (2004)

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93.

Journal Article

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), pp. 1319 - 1325 (2004)

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94.

Journal Article

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

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95.

Journal Article

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

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96.

Journal Article

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

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97.

Journal Article

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), pp. 356 - 358 (2003)

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98.

Journal Article

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), pp. 1123 - 1131 (2002)

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99.

Journal Article

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), pp. 1139 - 1142 (2002)

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100.

Journal Article

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), pp. 2039 - 2048 (2002)

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Publications of Jakob C. Mueller

Journal Article (113)