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: 4,777
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  • Site-wide: 109,472
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  • Site-wide: 143,780

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

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  • Site-wide: 5,364
  • In genetics: 212
• Year to date:
  • Site-wide: 5,483
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  • Site-wide: 27,518

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

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  • Site-wide: 6,522
  • In genomics: 653
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The Polygenic and Monogenic Basis of Blood Traits and Diseases

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  • Site-wide: 9,003
  • In genetic and genomic medicine: 44
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  • Site-wide: 43,756
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  • Site-wide: 118,943

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

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  • Site-wide: 10,737
  • In genetics: 455
• Year to date:
  • Site-wide: 131,789
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  • Site-wide: 158,990

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

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  • Site-wide: 11,874
  • In genetic and genomic medicine: 54
• Year to date:
  • Site-wide: 5,826
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  • Site-wide: 5,711

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

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  • Site-wide: 11,958
  • In genetics: 509
• Year to date:
  • Site-wide: 79,631
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  • Site-wide: 132,578

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

• Downloaded 1,735 times
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  • Site-wide: 12,358
  • In genetics: 525
• Year to date:
  • Site-wide: 103,718
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  • Site-wide: 124,118

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

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  • Site-wide: 16,062
  • In genetics: 707
• Year to date:
  • Site-wide: 134,121
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  • Site-wide: 161,173

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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  • Site-wide: 18,174
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• Year to date:
  • Site-wide: 147,997
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  • Site-wide: 140,879

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: 19,762
  • In genetics: 878
• Year to date:
  • Site-wide: 5,392
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  • Site-wide: 13,090

The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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  • Site-wide: 21,885
  • In genetics: 956
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  • Site-wide: 13,348
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  • Site-wide: 80,528

Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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  • Site-wide: 25,554
  • In genetics: 1,121
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  • Site-wide: 30,207
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  • Site-wide: 65,273

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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  • Site-wide: 26,771
  • In genetics: 1,177
• Year to date:
  • Site-wide: 89,202
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  • Site-wide: 90,011

Selection on the FADS region in Europeans

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  • Site-wide: 29,178
  • In genetics: 1,283
• Year to date:
  • Site-wide: 158,139
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  • Site-wide: 148,440

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

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  • Site-wide: 29,831
  • In genetic and genomic medicine: 139
• Year to date:
  • Site-wide: 42,643
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  • Site-wide: 106,214

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

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  • Site-wide: 30,969
  • In genetics: 1,360
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  • Site-wide: 59,132
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  • Site-wide: 44,993

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

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  • Site-wide: 35,630
  • In genetics: 1,556
• Year to date:
  • Site-wide: 146,957
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  • Site-wide: 146,562

DeepFake electrocardiograms: the beginning of the end for privacy issues in medicine

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  • Site-wide: 40,957
  • In cardiovascular medicine: 71
• Year to date:
  • Site-wide: 7,985
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  • Site-wide: 11,666

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

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  • Site-wide: 57,154
  • In genetics: 2,417
• Year to date:
  • Site-wide: 137,992
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  • Site-wide: 158,034

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

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  • Site-wide: 68,644
  • In genetics: 2,917
• Year to date:
  • Site-wide: 143,981
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  • Site-wide: 95,592

Explaining Deep Neural Networks for Knowledge Discovery in Electrocardiogram Analysis

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  • Site-wide: 83,180
  • In cardiovascular medicine: 174
• Year to date:
  • Site-wide: 19,303
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  • Site-wide: 86,353

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: 117,674
  • In genetics: 4,784
• Year to date:
  • Site-wide: 156,715
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  • Site-wide: 154,696

Genome-Wide Association Meta-Analysis Using a Recessive Model Illuminates Genetic Architecture of Type 2 Diabetes

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  • Site-wide: 122,845
  • In endocrinology: 118
• Year to date:
  • Site-wide: 38,704
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  • Site-wide: 55,866

Genetic analyses of the QT interval and its components in over 250K individuals identifies new loci and pathways affecting ventricular depolarization and repolarization

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  • Site-wide: 161,006
  • In genetic and genomic medicine: 1,036
• Year to date:
  • Site-wide: 118,852
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  • Site-wide: 19,182