Author: Allan Linneberg

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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: 3,725
  • In genomics: 418
• Year to date:
  • Site-wide: 60,960
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  • Site-wide: 48,016

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

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  • Site-wide: 5,300
  • In genomics: 593
• Year to date:
  • Site-wide: 57,049
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  • Site-wide: 43,189

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

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  • Site-wide: 5,730
  • In genetics: 267
• Year to date:
  • Site-wide: 5,184
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  • Site-wide: 5,563

The Polygenic and Monogenic Basis of Blood Traits and Diseases

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  • Site-wide: 7,434
  • In genetic and genomic medicine: 25
• Year to date:
  • Site-wide: 22,560
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  • Site-wide: 19,931

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

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  • Site-wide: 8,456
  • In genetics: 396
• Year to date:
  • Site-wide: 90,038
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  • Site-wide: 96,550

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

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  • Site-wide: 9,939
  • In genetics: 472
• Year to date:
  • Site-wide: 66,135
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  • Site-wide: 48,322

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

• Downloaded 1,655 times
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  • Site-wide: 9,990
  • In genetics: 477
• Year to date:
  • Site-wide: 72,996
• Since beginning of last month:
  • Site-wide: 61,536

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

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  • Site-wide: 12,536
  • In genetics: 615
• Year to date:
  • Site-wide: 79,592
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  • Site-wide: 54,769

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: 14,098
  • In genetics: 689
• Year to date:
  • Site-wide: 90,132
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  • Site-wide: 128,891

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

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  • Site-wide: 18,793
  • In genetic and genomic medicine: 69
• Year to date:
  • Site-wide: 8,328
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  • Site-wide: 11,014

Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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  • Site-wide: 25,518
  • In genetics: 1,229
• Year to date:
  • Site-wide: 20,709
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  • Site-wide: 12,812

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

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  • Site-wide: 28,437
  • In genetic and genomic medicine: 91
• Year to date:
  • Site-wide: 28,635
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  • Site-wide: 25,228

The Trans-Ancestral Genomic Architecture of Glycaemic Traits

• Downloaded 794 times
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  • Site-wide: 29,255
  • In genetics: 1,418
• Year to date:
  • Site-wide: 15,105
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  • Site-wide: 12,478

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: 39,923
  • In genetics: 1,896
• Year to date:
  • Site-wide: 5,061
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  • Site-wide: 14,153

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

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  • Site-wide: 44,935
  • In genetics: 2,104
• Year to date:
  • Site-wide: 73,156
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  • Site-wide: 118,163

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

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  • Site-wide: 56,112
  • In genetics: 2,598
• Year to date:
  • Site-wide: 119,440
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  • Site-wide: 133,547

Explaining Deep Neural Networks for Knowledge Discovery in Electrocardiogram Analysis

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  • Site-wide: 93,036
  • In cardiovascular medicine: 166
• Year to date:
  • Site-wide: 7,879
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  • Site-wide: 12,349

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

• Downloaded 266 times
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  • Site-wide: 93,059
  • In genetics: 4,172
• Year to date:
  • Site-wide: 107,397
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  • Site-wide: 124,863

DEVELOPING AND VALIDATING COVID-19 ADVERSE OUTCOME RISK PREDICTION MODELS FROM A BI-NATIONAL EUROPEAN COHORT OF 5594 PATIENTS.

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  • Site-wide: 105,372
  • In infectious diseases: 3,948
• Year to date:
  • Site-wide: 40,891
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  • Site-wide: 52,298