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10,912 results

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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
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.
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
Association of early repolarization pattern on ECG with risk of cardiac and all-cause mortality: a population-based prospective cohort study (MONICA/KORA).
Sinner MF, Reinhard W, Müller M, Beckmann BM, Martens E, Perz S, Pfeufer A, Winogradow J, Stark K, Meisinger C, Wichmann HE, Peters A, Riegger GA, Steinbeck G, Hengstenberg C, Kääb S. Sinner MF, et al. Among authors: muller m. PLoS Med. 2010 Jul 27;7(7):e1000314. doi: 10.1371/journal.pmed.1000314. PLoS Med. 2010. PMID: 20668657 Free PMC article.
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.
No association of two functional polymorphisms in human ALOX15 with myocardial infarction.
Hersberger M, Müller M, Marti-Jaun J, Heid IM, Coassin S, Young TF, Waechter V, Hengstenberg C, Meisinger C, Peters A, König W, Holmer S, Schunkert H, Klopp N, Kronenberg F, Illig T. Hersberger M, et al. Among authors: muller m. Atherosclerosis. 2009 Jul;205(1):192-6. doi: 10.1016/j.atherosclerosis.2008.11.017. Epub 2008 Nov 27. Atherosclerosis. 2009. PMID: 19131063
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