Author: Harald Grallert

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Preprints

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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Cell specific eQTL analysis without sorting cells

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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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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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

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Genome-wide methylation data mirror ancestry information

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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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Genetic architecture of early childhood growth phenotypes gives insights into their link with later obesity

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

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

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The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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Novel DNA methylation sites of glucose and insulin homeostasis: an integrative cross-omics analysis

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Maternal and fetal genetic contribution to gestational weight gain

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