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Author: Alex P Reiner

  • Most recently observed institution: Fred Hutchinson Cancer Research Center, Public Health Sciences Division

Rankings

  • All-time downloads: 10,036 (rank: 8,142 (tie) out of 395,662)
  • Categories:
    • epidemiology: 3,279 (rank: 162 (tie) out of 9,545)
    • genetics: 6,295 (rank: 2,801 out of 36,261)
    • genomics: 462 (rank: 29,416 (tie) out of 42,049)

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Preprints

An epigenetic biomarker of aging for lifespan and healthspan

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

genetics more details view paper
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GWAS of epigenetic ageing rates in blood reveals a critical role for TERT

genetics more details view paper
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Efficient variant set mixed model association tests for continuous and binary traits in large-scale whole genome sequencing studies

genetics more details view paper
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Atrial Fibrillation Genetic Risk Differentiates Cardioembolic Stroke from other Stroke Subtypes

genetics more details view paper
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HUGIn: Hi-C Unifying Genomic Interrogator

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Genome-Wide Control of Population Structure and Relatedness in Genetic Association Studies via Linear Mixed Models with Orthogonally Partitioned Structure

genetics more details view paper
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Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

genetics more details view paper
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Genome-wide association studies identify 137 loci for DNA methylation biomarkers of ageing

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Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile

genomics more details view paper
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Multi-ethnic genome-wide association study of decomposed cardioelectric phenotypes illustrates strategies to identify and characterize evidence of shared genetic effects for complex traits

epidemiology more details view paper
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Role of Rare and Low Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels

epidemiology more details view paper
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A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

genetics more details view paper
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