Martina Müller

发表

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Ayellet V. Segrè, Cameron D. Palmer, P. Elliott, 2010, Nature.

Independent Susceptibility Markers for Atrial Fibrillation on Chromosome 4q25

Eric Boerwinkle, Annette Peters, John Barnard, 2010, Circulation.

Common variants at ten loci modulate the QT interval duration in the QTSCD Study

Christian Gieger, Thomas Meitinger, Raimund Erbel, 2009, Nature Genetics.

Genome-wide association study of PR interval

Christian Gieger, Thomas Meitinger, Jan A. Kors, 2010, Nature Genetics.

Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis

Erika Salvi, Mohamad Saad, Eric Hachulla, 2011, PLoS genetics.

Variants in the 3′ untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner

Yolan J. Reckman, A. Tijsen, Y. Pinto, 2011, European heart journal.

Chromosome 7p11.2 (EGFR) variation influences glioma risk.

Melissa Bondy, Andre Franke, Anthony Swerdlow, 2011, Human molecular genetics.

Genome-wide association analysis identifies multiple loci related to resting heart rate.

Christian Gieger, Thomas Meitinger, Henry Völzke, 2010, Human molecular genetics.

European lactase persistence genotype shows evidence of association with increase in body mass index

C. Gieger, M. McCarthy, T. Lehtimäki, 2009, Human molecular genetics.

Identification of twelve novel mutations in patients with classic and variant forms of maple syrup urine disease

Martina Müller, M. Henneke, J. Gärtner, 2003, Human mutation.

Bmc Medical Genetics Association between Variations in the Tlr4 Gene and Incident Type 2 Diabetes Is Modified by the Ratio of Total Cholesterol to Hdl-cholesterol

C. Meisinger, N. Klopp, T. Illig, 2022 .

Genome-Wide Association Studies of the PR Interval in African Americans

Kathleen F. Kerr, Jared W. Magnani, Susan Redline, 2011, PLoS genetics.

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

Jingyuan Fu, Thomas Meitinger, Jan A. Kors, 2010, Nature Genetics.

Association of Early Repolarization Pattern on ECG with Risk of Cardiac and All-Cause Mortality: A Population-Based Prospective Cohort Study (MONICA/KORA)

A. Peters, C. Hengstenberg, H. Wichmann, 2010, PLoS medicine.

Genome-Wide Association Analysis of High-Density Lipoprotein Cholesterol in the Population-Based KORA Study Sheds New Light on Intergenic Regions

C. Gieger, F. Kronenberg, T. Meitinger, 2008, Circulation. Cardiovascular genetics.

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

C. Meisinger, N. Klopp, T. Illig, 2008, European journal of endocrinology.

A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3.

C. Gieger, R. Vasan, H. Völzke, 2011, Human molecular genetics.

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

L. Palmer, H. Gohlke, T. Illig, 2006, Human molecular genetics.

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

A. Peters, H. Wichmann, W. Zareba, 2012, Environmental research.

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

C. Meisinger, N. Klopp, T. Illig, 2008, Atherosclerosis.

MicroRNAs in cardiac diseases : The devil is in the details

Yolan J. Reckman, E. Creemers, H. Tan, 2013 .

DNA variants, plasma levels and variability of interleukin-6 in myocardial infarction survivors: results from the AIRGENE study.

A. Peters, B. Jacquemin, W. Koenig, 2009, Thrombosis research.

American Journal of Epidemiology Practice of Epidemiology Estimating the Single Nucleotide Polymorphism Genotype Misclassification from Routine Double Measurements in a Large Epidemiologic Sample

F. Kronenberg, A. Peters, H. Wichmann, 2022 .

Common genetic polymorphisms and haplotypes of fibrinogen alpha, beta, and gamma chains affect fibrinogen levels and the response to proinflammatory stimulation in myocardial infarction survivors: the AIRGENE study.

A. Peters, V. Salomaa, S. Greven, 2008, Journal of the American College of Cardiology.

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

A. Peters, V. Salomaa, S. Greven, 2008, European heart journal.

No association of two functional polymorphisms in human ALOX15 with myocardial infarction.

F. Kronenberg, C. Meisinger, A. Peters, 2009, Atherosclerosis.

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

Aad van der Lugt, Xavier Estivill, Sudha Seshadri, 2012, Nature Genetics.

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

C. Meisinger, N. Klopp, T. Illig, 2008, European journal of endocrinology.

V. Salomaa, S. Greven, B. Jacquemin, 2008, Journal of the American College of Cardiology.