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List of works by Annette Peters
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A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
A randomization-based causal inference framework for uncovering environmental exposure effects on human gut microbiota
Alcohol consumption is associated with widespread changes in blood DNA methylation: analysis of cross-sectional and longitudinal data
An integrative analysis of clinical and epigenetic biomarkers of mortality
Association analysis between an epigenetic alcohol risk score and blood pressure
Better ageing with personalized lifestyle support from a health coach using a digital app – a population-based intervention study in Germany
Breaking the Norm: Population-Scale Normative Modeling of Brain Structure in Depression and Anxiety
CODI: Enhancing machine learning-based molecular profiling through contextual out-of-distribution integration
Circulating interleukin-6 levels and incident ischemic stroke: a systematic review and meta-analysis of population-based cohort studies
Circulating metabolites modulated by diet are causally associated with depression
DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases
Determinants of ascending aortic morphology: Cross-sectional deep learning-based analysis on 25,073 non-contrast-enhanced MRI of NAKO
Development and validation of DNA Methylation scores in two European cohorts augment 10-year risk prediction of type 2 diabetes
Distribution and associated factors of hepatic iron – a population-based imaging study
Epigenetic scores for the circulating proteome as tools for disease prediction
Genetic Contributions to Early and Late Onset Ischemic Stroke
Genome-wide analysis in over 1 million individuals reveals over 2,000 independent genetic signals for blood pressure
Implicating genes, pleiotropy and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Individual bioenergetic capacity as a potential source of resilience to Alzheimer’s disease
Mendelian Randomization evaluation of causal effects of fibrinogen on incident coronary heart disease
Methylation status of VTRNA2-1/nc886 is stable across human populations, monozygotic twin pairs and in majority of somatic tissues
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction
Proteogenomic integration reveals CXCL10 as a potentially downstream causal mediator for IL-6 signaling on atherosclerosis
Proteomic Signatures as Biomarkers of Atherosclerosis Burden
Stroke genetics informs drug discovery and risk prediction across ancestries
The mediating role of epigenetic clocks underlying educational inequalities in mortality: a multi-cohort study