Mueller JC - Search Results

1

Lymphotoxin-alpha and galectin-2 SNPs are not associated with myocardial infarction in two different German populations.

Sedlacek K, Neureuther K, Mueller JC, Stark K, Fischer M, Baessler A, Reinhard W, Broeckel U, Lieb W, Erdmann J, Schunkert H, Riegger G, Illig T, Meitinger T, Hengstenberg C. Sedlacek K, et al. Among authors: mueller jc. J Mol Med (Berl). 2007 Sep;85(9):997-1004. doi: 10.1007/s00109-007-0211-4. Epub 2007 May 12. J Mol Med (Berl). 2007. PMID: 17497114

2

Multiple regions of alpha-synuclein are associated with Parkinson's disease.

Mueller JC, Fuchs J, Hofer A, Zimprich A, Lichtner P, Illig T, Berg D, Wüllner U, Meitinger T, Gasser T. Mueller JC, et al. Ann Neurol. 2005 Apr;57(4):535-41. doi: 10.1002/ana.20438. Ann Neurol. 2005. PMID: 15786467

3

Common variants of LRRK2 are not associated with sporadic Parkinson's disease.

Biskup S, Mueller JC, Sharma M, Lichtner P, Zimprich A, Berg D, Wüllner U, Illig T, Meitinger T, Gasser T. Biskup S, et al. Among authors: mueller jc. Ann Neurol. 2005 Dec;58(6):905-8. doi: 10.1002/ana.20664. Ann Neurol. 2005. PMID: 16254973

4

Association of variants in the BAT1-NFKBIL1-LTA genomic region with protection against myocardial infarction in Europeans.

Koch W, Hoppmann P, Michou E, Jung V, Pfeufer A, Mueller JC, Gieger C, Wichmann HE, Meitinger T, Schömig A, Kastrati A. Koch W, et al. Among authors: mueller jc. Hum Mol Genet. 2007 Aug 1;16(15):1821-7. doi: 10.1093/hmg/ddm130. Epub 2007 May 21. Hum Mol Genet. 2007. PMID: 17517687

5

The transcription factor PITX3 is associated with sporadic Parkinson's disease.

Fuchs J, Mueller JC, Lichtner P, Schulte C, Munz M, Berg D, Wüllner U, Illig T, Sharma M, Gasser T. Fuchs J, et al. Among authors: mueller jc. Neurobiol Aging. 2009 May;30(5):731-8. doi: 10.1016/j.neurobiolaging.2007.08.014. Epub 2007 Oct 1. Neurobiol Aging. 2009. PMID: 17905480

6

Linkage disequilibrium patterns and tagSNP transferability among European populations.

Mueller JC, Lõhmussaar E, Mägi R, Remm M, Bettecken T, Lichtner P, Biskup S, Illig T, Pfeufer A, Luedemann J, Schreiber S, Pramstaller P, Pichler I, Romeo G, Gaddi A, Testa A, Wichmann HE, Metspalu A, Meitinger T. Mueller JC, et al. Am J Hum Genet. 2005 Mar;76(3):387-98. doi: 10.1086/427925. Epub 2005 Jan 6. Am J Hum Genet. 2005. PMID: 15637659 Free PMC article.

7

Common variants in myocardial ion channel genes modify the QT interval in the general population: results from the KORA study.

Pfeufer A, Jalilzadeh S, Perz S, Mueller JC, Hinterseer M, Illig T, Akyol M, Huth C, Schöpfer-Wendels A, Kuch B, Steinbeck G, Holle R, Näbauer M, Wichmann HE, Meitinger T, Kääb S. Pfeufer A, et al. Among authors: mueller jc. Circ Res. 2005 Apr 1;96(6):693-701. doi: 10.1161/01.RES.0000161077.53751.e6. Epub 2005 Mar 3. Circ Res. 2005. PMID: 15746444

8

Genetic architecture of the APM1 gene and its influence on adiponectin plasma levels and parameters of the metabolic syndrome in 1,727 healthy Caucasians.

Heid IM, Wagner SA, Gohlke H, Iglseder B, Mueller JC, Cip P, Ladurner G, Reiter R, Stadlmayr A, Mackevics V, Illig T, Kronenberg F, Paulweber B. Heid IM, et al. Among authors: mueller jc. Diabetes. 2006 Feb;55(2):375-84. doi: 10.2337/diabetes.55.02.06.db05-0747. Diabetes. 2006. PMID: 16443770

9

ALOX5AP gene and the PDE4D gene in a central European population of stroke patients.

Lõhmussaar E, Gschwendtner A, Mueller JC, Org T, Wichmann E, Hamann G, Meitinger T, Dichgans M. Lõhmussaar E, et al. Among authors: mueller jc. Stroke. 2005 Apr;36(4):731-6. doi: 10.1161/01.STR.0000157587.59821.87. Epub 2005 Feb 24. Stroke. 2005. PMID: 15731479

10

Possible gender-dependent association of vascular endothelial growth factor (VEGF) gene and ALS.

Fernández-Santiago R, Sharma M, Mueller JC, Gohlke H, Illig T, Anneser J, Münch C, Ludolph A, Kamm C, Gasser T. Fernández-Santiago R, et al. Among authors: mueller jc. Neurology. 2006 Jun 27;66(12):1929-31. doi: 10.1212/01.wnl.0000219756.71928.25. Neurology. 2006. PMID: 16801663 Clinical Trial.

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