Author: Annette Peters

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Preprints

DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning

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Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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Connecting genetic risk to disease endpoints through the human blood plasma proteome

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Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

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Epigenome-wide association meta-analysis of DNA methylation with coffee and tea consumption

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Characterization of missing values in untargeted MS-based metabolomics data and evaluation of missing data handling strategies

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An epigenome-wide association study of educational attainment (n = 10,767)

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Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

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Genome-wide association studies identify 137 loci for DNA methylation biomarkers of ageing

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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

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Discovering patterns of pleiotropy in genome-wide association studies

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Arrhythmic gut microbiome signatures for risk profiling of Type-2 Diabetes

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Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

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Alcohol consumption is associated with widespread changes in blood DNA methylation: analysis of cross-sectional and longitudinal data

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Network reconstruction for trans acting genetic loci using multi-omics data and prior information

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Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile

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The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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Cis-epistasis at the LPA locus and risk of coronary artery disease

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Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced disease

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Evaluation of the causal effect of fibrinogen on incident coronary heart disease via Mendelian randomization

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A genome-wide analysis of DNA methylation identifies a novel association signal for Lp(a) concentrations in the LPA promoter

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Renal and Renal Sinus Fat Volumes as Quantified by Magnetic Resonance Imaging in Subjects with Prediabetes, Diabetes, and Normal Glucose Tolerance.

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Investigation of an LPA KIV-2 nonsense mutation in 11,000 individuals: the importance of linkage disequilibrium structure in LPA genetics.

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Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

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