Publikationen von Jakob C. Mueller
Alle Typen
Zeitschriftenartikel (113)
51.
Zeitschriftenartikel
5 (3), S. 448 - 460 (2008)
Fine-scale genetic mapping using independent component analysis. IEEE ACM Transactions on Computational Biology and Bioinformatics 52.
Zeitschriftenartikel
9, 190 (2008)
Local conservation scores without a priori assumptions on neutral substitution rates. BMC Bioinformatics 53.
Zeitschriftenartikel
22 (5), S. 1327 - 1334 (2008)
Genetic variability in the SNCA gene influences alpha-synuclein levels in the blood and brain. The FASEB Journal 54.
Zeitschriftenartikel
28 (4), S. 758 - 763 (2008)
Fibrinogen genes and myocardial infarction. A haplotype analysis. Arteriosclerosis, Thrombosis, and Vascular Biology: an Official Journal of the American Heart Association 55.
Zeitschriftenartikel
40 (12), S. 1386 - 1387 (2008)
Lack of support for association between common variation in TNFSF4 and myocardial infarction in a German population. Nature Genetics 56.
Zeitschriftenartikel
29 (8), S. 1276 - 1278 (2008)
Genetic analysis of MAPT haplotype diversity in frontotemporal dementia. Neurobiology of Aging 57.
Zeitschriftenartikel
99 (2), S. 174 - 176 (2008)
Biogenic trace amine-associated receptors (TAARs) are encoded in avian genomes: Evidence and possible implications. Journal of Heredity 58.
Zeitschriftenartikel
49 (6), S. 1108 - 1109 (2008)
A functional polymorphism in the SCN1A gene is not associated with carbamazepine dosages in Austrian patients with epilepsy. Epilepsia 59.
Zeitschriftenartikel
274 (1619), S. 1685 - 1691 (2007)
Drd4 gene polymorphisms are associated with personality variation in a passerine bird. Proceedings of the Royal Society B: Biological Sciences 60.
Zeitschriftenartikel
16 (19), S. 4039 - 4050 (2007)
Genetic variation and differentiation in captive and wild zebra finches (Taeniopygia guttata). Molecular Ecology 61.
Zeitschriftenartikel
90 (2), S. 161 - 173 (2007)
Information and communication theory in molecular biology. Electrical Engineering 62.
Zeitschriftenartikel
16 (15), S. 1821 - 1827 (2007)
Association of variants in the BAT1-NFKB1L1-LTA genomic region with protection against myocardial infarction in Europeans. Human Molecular Genetics 63.
Zeitschriftenartikel
9 (2), S. 123 - 129 (2007)
No association of polymorphisms in the gene encoding 5-lipoxygenase-activating protein and myocardial infarction in a large central European population. Genetics in Medicine 64.
Zeitschriftenartikel
28, S. 875 - 876 (2007)
Association of a fibrinogen gene haplotype with myocardial infarction. European Heart Journal 65.
Zeitschriftenartikel
12, S. 510 - 517 (2007)
Fine mapping of the MAPT locus using quantitative trait analysis identifies possible causal variants in Alzheimer’s disease. Molecular Psychiatry 66.
Zeitschriftenartikel
25 (3), S. 473 - 482 (2007)
Osteopontin is elevated in Parkinson’s disease and its absence leads to reduced neurodegeneration in the MPTP model. Neurobiology of Disease 67.
Zeitschriftenartikel
28 (5), S. 727 - 734 (2007)
Weak independent association signals between IDE polymorphisms, Alzheimer’s disease and cognitive measures. Neurobiology of Aging 68.
Zeitschriftenartikel
28 (6), S. 883 - 884 (2007)
No association of Vacuolar protein sorting 26 polymorphisms with Alzheimer’s disease. Neurobiology of Aging 69.
Zeitschriftenartikel
24 (1), S. 83 - 90 (2007)
Gene mapping of complex diseases: A comparison of methods from statistics, information theory, and signal processing. IEEE Signal Processing Magazine 70.
Zeitschriftenartikel
85 (9), S. 997 - 1004 (2007)
Lymphotoxin-alpha and galectin-2 SNPs are not associated with myocardial infarction in two different German populations. Journal of Molecular Medicine-JMM 71.
Zeitschriftenartikel
292 (3), S. E836 - E844 (2007)
Calpain-10 variants and haplotypes are associated with polycystic ovary syndrome in Caucasians. American Journal of Physiology-Endocrinology and Metabolism 72.
Zeitschriftenartikel
35 (20), S. 7003 - 7010 (2007)
Modeling DNA-binding of Escherichia coli sigma(70) exhibits a characteristic energy landscape around strong promoters. Nucleic Acids Research (London) 73.
Zeitschriftenartikel
3 (1), S. 47 - 56 (2006)
Gene mapping and marker clustering using Shannon’s mutual information. IEEE ACM Transactions on Computational Biology and Bioinformatics 74.
Zeitschriftenartikel
66 (12), S. 1929 - 1931 (2006)
Association between the vascular endothelial growth factor (VEGF) gene and amyotrophic lateral sclerosis (ALS): Possible gender-dependent effect. Neurology 75.
Zeitschriftenartikel
7 (5), S. 753 - 766 (2006)
Spatial genetic patterns generated by two admixing genetic lineages: A simulation study. Conservation Genetics Resources 76.
Zeitschriftenartikel
55 (2), S. 375 - 384 (2006)
Genetic architecture of the APM1 gene and its influence on adiponectin plasma levels and parameters of the metabolic syndrome in 1727 healthy Caucasians. Diabetes 77.
Zeitschriftenartikel
67 (10), S. 1857 - 1859 (2006)
Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia. Neurology 78.
Zeitschriftenartikel
26 (5), S. 1114 - 1119 (2006)
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 79.
Zeitschriftenartikel
78 (4), S. 441 - 464 (2006)
Genetic structure in contemporary South Tyrolean isolated populations revealed by the analysis of Y chromosome, mtDNA and Alu polymorphisms. Human Biology 80.
Zeitschriftenartikel
15 (16), S. 2446 - 2456 (2006)
A functional polymorphism within plasminogen activator urokinase (PLAU) is associated with Alzheimer’s disease. Human Molecular Genetics 81.
Zeitschriftenartikel
67 (11), S. 2080 - 2082 (2006)
Comprehensive association analysis of the NOS2A gene with Parkinson disease. Neurology 82.
Zeitschriftenartikel
43 (7), S. 557 - 562 (2006)
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 83.
Zeitschriftenartikel
6 (2), S. 487 - 489 (2006)
Molecular markers for systematic identification and population genetics of the invasive Ponto-Caspian freshwater gammarid Dikerogammarus villosus (Crustacea, Amphipoda). Molecular Ecology Notes 84.
Zeitschriftenartikel
58 (6), S. 905 - 908 (2005)
Common variants of LRRK2 (PARK8) are not associated with sporadic Parkinson's disease. Annals of Neurology 85.
Zeitschriftenartikel
43 (2), S. 167 - 172 (2005)
TaqMan assays for genotyping of single nucleotide polymorphisms present at a disease susceptibility locus on chromosome 6. Clinical Chemistry and Laboratory Medicine 86.
Zeitschriftenartikel
112 (14), S. 2138 - 2142 (2005)
No replication of association between estrogen receptor alpha gene polymorphisms and susceptibility to myocardial infarction in a large Caucasian patient sample. Circulation 87.
Zeitschriftenartikel
67, S. 127 - 131 (2005)
Genetic diversity in German and European populations: Looking for substructures and genetic patterns. Gesundheitswesen 88.
Zeitschriftenartikel
36 (4), S. 731 - 736 (2005)
The ALOX5AP gene and the PDE4D gene in a Central-European population of stroke patients. Stroke 89.
Zeitschriftenartikel
57 (4), S. 535 - 541 (2005)
Multiple regions of alpha-synuclein are associated with Parkinson's disease. Annals of Neurology 90.
Zeitschriftenartikel
76 (3), S. 387 - 398 (2005)
Linkage disequilibrium patterns and tagSNP transferability among European populations. The American Journal of Human Genetics 91.
Zeitschriftenartikel
96 (6), S. 693 - 701 (2005)
Common variants in myocardial ion channel genes modify the QT interval in the general population: Results from the KORA study. Circulation Research 92.
Zeitschriftenartikel
32 (Suppl. 1), S. D459 - D462 (2004)
MitoP2, an integrated database on mitochondrial proteins in yeast and man. Nucleic Acids Research (London) 93.
Zeitschriftenartikel
36 (12), S. 1319 - 1325 (2004)
Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment. Nature Genetics 94.
Zeitschriftenartikel
5 (4), S. 355 - 364 (2004)
Linkage disequilibrium for different scales and applications. Briefings in Bioinformatics 95.
Zeitschriftenartikel
20 (5), S. 786 - 787 (2004)
Plotting haplotype-specific linkage disequilibrium patterns by extended haplotype homozygosity. Bioinformatics 96.
Zeitschriftenartikel
3 (6), S. 315 - 325 (2004)
Mechanisms for multiple intracellular localisation of human mitochondrial proteins. Mitochondrion 97.
Zeitschriftenartikel
39 (3), S. 356 - 358 (2003)
Molecular genetic diagnostics of some Daphnia species (Crustacea, Cladocera) from the Volga River. Russian Journal of Genetics 98.
Zeitschriftenartikel
40 (11), S. 1123 - 1131 (2002)
TaqMan systems for genotyping of disease-related polymorphisms present in the gene encoding Apolipoprotein E. Clinical Chemistry and Laboratory Medicine 99.
Zeitschriftenartikel
269 (1496), S. 1139 - 1142 (2002)
Canal construction destroys barrier between major European invasion lineages of the zebra mussel. Proceedings of the Royal Society B: Biological Sciences 100.
Zeitschriftenartikel
47 (11), S. 2039 - 2048 (2002)
Genetic and morphological differentiation of Dikerogammarus invaders and their invasion history in Central Europe. Freshwater Biology