Müller M - Search Results

1

Estimating the single nucleotide polymorphism genotype misclassification from routine double measurements in a large epidemiologic sample.

Heid IM, Lamina C, Küchenhoff H, Fischer G, Klopp N, Kolz M, Grallert H, Vollmert C, Wagner S, Huth C, Müller J, Müller M, Hunt SC, Peters A, Paulweber B, Wichmann HE, Kronenberg F, Illig T. Heid IM, et al. Among authors: muller m, muller j. Am J Epidemiol. 2008 Oct 15;168(8):878-89. doi: 10.1093/aje/kwn208. Epub 2008 Sep 12. Am J Epidemiol. 2008. PMID: 18791193 Free PMC article.

2

Quantifying the contribution of genetic variants for survival phenotypes.

Müller M, Döring A, Küchenhoff H, Lamina C, Malzahn D, Bickeböller H, Vollmert C, Klopp N, Meisinger C, Heinrich J, Kronenberg F, Wichmann HE, Heid IM. Müller M, et al. Genet Epidemiol. 2008 Sep;32(6):574-85. doi: 10.1002/gepi.20333. Genet Epidemiol. 2008. PMID: 18428429

3

Association between variations in the TLR4 gene and incident type 2 diabetes is modified by the ratio of total cholesterol to HDL-cholesterol.

Kolz M, Baumert J, Müller M, Khuseyinova N, Klopp N, Thorand B, Meisinger C, Herder C, Koenig W, Illig T. Kolz M, et al. Among authors: muller m. BMC Med Genet. 2008 Feb 25;9:9. doi: 10.1186/1471-2350-9-9. BMC Med Genet. 2008. PMID: 18298826 Free PMC article.

4

Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions.

Heid IM, Boes E, Müller M, Kollerits B, Lamina C, Coassin S, Gieger C, Döring A, Klopp N, Frikke-Schmidt R, Tybjaerg-Hansen A, Brandstätter A, Luchner A, Meitinger T, Wichmann HE, Kronenberg F. Heid IM, et al. Among authors: muller m. Circ Cardiovasc Genet. 2008 Oct;1(1):10-20. doi: 10.1161/CIRCGENETICS.108.776708. Circ Cardiovasc Genet. 2008. PMID: 20031538

5

DNA variants, plasma levels and variability of C-reactive protein in myocardial infarction survivors: results from the AIRGENE study.

Kolz M, Koenig W, Müller M, Andreani M, Greven S, Illig T, Khuseyinova N, Panagiotakos D, Pershagen G, Salomaa V, Sunyer J, Peters A; AIRGENE Study Group. Kolz M, et al. Among authors: muller m. Eur Heart J. 2008 May;29(10):1250-8. doi: 10.1093/eurheartj/ehm442. Epub 2007 Oct 22. Eur Heart J. 2008. PMID: 17956875

6

RANTES/CCL5 gene polymorphisms, serum concentrations, and incident type 2 diabetes: results from the MONICA/KORA Augsburg case-cohort study, 1984-2002.

Herder C, Illig T, Baumert J, Müller M, Klopp N, Khuseyinova N, Meisinger C, Poschen U, Martin S, Koenig W, Thorand B. Herder C, et al. Among authors: muller m. Eur J Endocrinol. 2008 May;158(5):R1-5. doi: 10.1530/EJE-07-0686. Eur J Endocrinol. 2008. PMID: 18426815

7

Acute air pollution effects on heart rate variability are modified by SNPs involved in cardiac rhythm in individuals with diabetes or impaired glucose tolerance.

Hampel R, Breitner S, Schneider A, Zareba W, Kraus U, Cyrys J, Geruschkat U, Belcredi P, Müller M, Wichmann HE, Peters A; Cooperative Health Research in the Region of Augsburg (KORA) Study Group. Hampel R, et al. Among authors: muller m. Environ Res. 2012 Jan;112:177-85. doi: 10.1016/j.envres.2011.10.007. Epub 2011 Nov 8. Environ Res. 2012. PMID: 22071035

8

Common genetic variants of the FADS1 FADS2 gene cluster and their reconstructed haplotypes are associated with the fatty acid composition in phospholipids.

Schaeffer L, Gohlke H, Müller M, Heid IM, Palmer LJ, Kompauer I, Demmelmair H, Illig T, Koletzko B, Heinrich J. Schaeffer L, et al. Among authors: muller m. Hum Mol Genet. 2006 Jun 1;15(11):1745-56. doi: 10.1093/hmg/ddl117. Epub 2006 May 2. Hum Mol Genet. 2006. PMID: 16670158

9

Common variants at 12q15 and 12q24 are associated with infant head circumference.

Taal HR, Pourcain BS, Thiering E, Das S, Mook-Kanamori DO, Warrington NM, Kaakinen M, Kreiner-Møller E, Bradfield JP, Freathy RM, Geller F, Guxens M, Cousminer DL, Kerkhof M, Timpson NJ, Ikram MA, Beilin LJ, Bønnelykke K, Buxton JL, Charoen P, Chawes BLK, Eriksson J, Evans DM, Hofman A, Kemp JP, Kim CE, Klopp N, Lahti J, Lye SJ, McMahon G, Mentch FD, Müller M, O'Reilly PF, Prokopenko I, Rivadeneira F, Steegers EAP, Sunyer J, Tiesler C, Yaghootkar H; Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium; Breteler MMB, Debette S, Fornage M, Gudnason V, Launer LJ, van der Lugt A, Mosley TH, Seshadri S, Smith AV, Vernooij MW; Early Genetics & Lifecourse Epidemiology (EAGLE) consortium; Blakemore AI, Chiavacci RM, Feenstra B, Fernandez-Benet J, Grant SFA, Hartikainen AL, van der Heijden AJ, Iñiguez C, Lathrop M, McArdle WL, Mølgaard A, Newnham JP, Palmer LJ, Palotie A, Pouta A, Ring SM, Sovio U, Standl M, Uitterlinden AG, Wichmann HE, Vissing NH, DeCarli C, van Duijn CM, McCarthy MI, Koppelman GH, Estivill X, Hattersley AT, Melbye M, Bisgaard H, Pennell CE, Widen E, Hakonarson H, Smith GD, Heinrich J, Jarvelin MR; Early Growth Genetics (EGG) Consor… See abstract for full author list ➔ Taal HR, et al. Among authors: muller m. Nat Genet. 2012 Apr 15;44(5):532-538. doi: 10.1038/ng.2238. Nat Genet. 2012. PMID: 22504419 Free PMC article.

10

Macrophage migration inhibitory factor (MIF) and risk for coronary heart disease: results from the MONICA/KORA Augsburg case-cohort study, 1984-2002.

Herder C, Illig T, Baumert J, Müller M, Klopp N, Khuseyinova N, Meisinger C, Martin S, Thorand B, Koenig W. Herder C, et al. Among authors: muller m. Atherosclerosis. 2008 Oct;200(2):380-8. doi: 10.1016/j.atherosclerosis.2007.12.025. Epub 2008 Feb 1. Atherosclerosis. 2008. PMID: 18242614

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