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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  • Site-wide: 93,792

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

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  • Site-wide: 60,971

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

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  • Site-wide: 6,133
  • In genetics: 309
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The Polygenic and Monogenic Basis of Blood Traits and Diseases

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  • In genetic and genomic medicine: 17
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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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  • In genetics: 368
• Year to date:
  • Site-wide: 49,978
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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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  • Site-wide: 8,921
  • In genetics: 454
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  • Site-wide: 43,070
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PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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

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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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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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  • In genetics: 1,053
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  • Site-wide: 53,317
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  • Site-wide: 63,544

Trans-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

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  • Site-wide: 23,325
  • In genetic and genomic medicine: 61
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  • Site-wide: 10,097
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  • Site-wide: 5,799

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

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  • In genetics: 1,285
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  • Site-wide: 52,661

Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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  • In genetics: 1,372
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  • Site-wide: 21,319
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Estimating narrow-sense heritability from genome-wide data in admixed populations

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Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

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  • Site-wide: 29,030
  • In genetic and genomic medicine: 73
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  • Site-wide: 16,947

The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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  • Site-wide: 34,275
  • In genetics: 1,717
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  • Site-wide: 20,390
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  • Site-wide: 11,222

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

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  • Site-wide: 42,552
  • In genetics: 2,090
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  • Site-wide: 74,702
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  • Site-wide: 79,041

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

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  • Site-wide: 50,708
  • In genetics: 2,460
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  • Site-wide: 113,283

Rare coding variants in 35 genes associate with circulating lipid levels: a multi-ancestry analysis of 170,000 exomes

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  • Site-wide: 51,523
  • In genetics: 2,496
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  • Site-wide: 658
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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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  • Site-wide: 85,308
  • In genetics: 3,966
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Explaining Deep Neural Networks for Knowledge Discovery in Electrocardiogram Analysis

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  • Site-wide: 122,760
  • In cardiovascular medicine: 318
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  • Site-wide: 4,782
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