Publications
2019 (1)
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Dietz C, Müller M, Reinhold AK, Karch L, Schwab B, Forer L, Vlckova E, Brede EM, Jakubietz R, Üçeyler N, Meffert R, Bednarik J, Kress M, Sommer C, Dimova V, Birklein F, Rittner HL:
What is normal trauma healing and what is complex regional pain syndrome I? An analysis of clinical and experimental biomarkers.
Pain
160:2278-2289, 2019. PMID:
31095096
Journal Article
2009 (1)
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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:
No association of two functional polymorphisms in human ALOX15 with myocardial infarction.
Atherosclerosis
205:192-196, 2009. PMID:
19131063
Journal Article
2008 (3)
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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:
Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions.
Circ. Cardiovasc. Genet.
1:Oct.20, 2008. PMID:
20031538
Journal Article
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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:
Estimating the single nucleotide polymorphism genotype misclassification from routine double measurements in a large epidemiologic sample.
Am. J. Epidemiol.
168:878-889, 2008. PMID:
18791193
Journal Article
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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:
Quantifying the contribution of genetic variants for survival phenotypes.
Genet. Epidemiol.
32:574-585, 2008. PMID:
18428429
Journal Article
