Author: Niels Grarup

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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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Human pancreatic islet 3D chromatin architecture provides insights into the genetics of type 2 diabetes

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

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Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

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

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A Comprehensive Reanalysis Of Publicly Available GWAS Datasets Reveals An X Chromosome Rare Regulatory Variant Associated With High Risk For Type 2 Diabetes.

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Trans-ethnic and ancestry-specific blood-cell genetics in 746,667 individuals from 5 global populations

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Selection on the FADS region in Europeans

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A common allele in FGF21 associated with preference for sugar consumption lowers body fat in the lower body and increases blood pressure

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Extreme distribution of deleterious variation in a historically small and isolated population-insights from the Greenlandic Inuit

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Estimating narrow-sense heritability from genome-wide data in admixed populations

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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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Meta-analysis of exome array data identifies six novel genetic loci for lung function

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Exome-wide association study on Albuminuria identifies a novel rare variant in CUBN and additional genes, in 33,985 Europeans with and without diabetes

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