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Rxivist combines preprints from bioRxiv with data from Twitter to help you find the papers being discussed in your field. Currently indexing 65,454 bioRxiv papers from 289,944 authors.

Author: Veikko Salomaa

Rankings

  • All-time downloads: 47,467 (rank: 305 out of 289,944)
  • Categories:
    • bioinformatics: 1,466 (rank: 5,376 (tie) out of 25,248)
    • epidemiology: 2,427 (rank: 297 (tie) out of 9,548)
    • genetics: 31,333 (rank: 119 out of 28,782)
    • genomics: 10,941 (rank: 917 out of 33,034)
    • systems biology: 1,300 (rank: 1,384 (tie) out of 8,800)

Downloads per author, site-wide

Preprints

A reference panel of 64,976 haplotypes for genotype imputation

genetics more details view paper
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Phenome-wide association studies (PheWAS) across large "real-world data" population cohorts support drug target validation

genetics more details view paper
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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

genetics more details view paper
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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

genetics more details view paper
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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

genetics more details view paper
  • Downloaded 2,193 times
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Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

genomics more details view paper
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Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

genetics more details view paper
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Cell specific eQTL analysis without sorting cells

genetics more details view paper
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Polygenic and clinical risk scores and their impact on age at onset of cardiometabolic diseases and common cancers

genomics more details view paper
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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

genetics more details view paper
  • Downloaded 1,668 times
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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

genetics more details view paper
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metaCCA: Summary statistics-based multivariate meta-analysis of genome-wide association studies using canonical correlation analysis

bioinformatics more details view paper
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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
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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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Genomic prediction of coronary heart disease

genomics more details view paper
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Refining fine-mapping: effect sizes and regional heritability

genetics more details view paper
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    • In genetics: 550 out of 3,699
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Exome sequencing identifies high-impact trait-associated alleles enriched in Finns

genomics more details view paper
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Haplotype sharing provides insights into fine-scale population history and disease in Finland

genetics more details view paper
  • Downloaded 952 times
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    • In genetics: 626 out of 3,699
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Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

genetics more details view paper
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    • In genetics: 642 out of 3,699
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    • Site-wide: 2,733 out of 65,454

Narrow-sense heritability estimation of complex traits using identity-by-descent information.

genetics more details view paper
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Genetics of human plasma lipidome: Understanding lipid metabolism and its link to diseases beyond traditional lipids

genetics more details view paper
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Geographic variation and bias in polygenic scores of complex diseases and traits in Finland

genetics more details view paper
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    • In genetics: 725 out of 3,699
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Elevated alpha-1 antitrypsin is a major component of GlycA-associated risk for future morbidity and mortality

systems biology more details view paper
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Circulating metabolites and the risk of type 2 diabetes: a prospective study of 11,896 young adults from four Finnish cohorts

epidemiology more details view paper
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Multivariate genome-wide association analysis of a cytokine network reveals variants with widespread immune, haematological and cardiometabolic pleiotropy

genomics more details view paper
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    • Site-wide: 7,505 out of 65,454

The rate of false polymorphisms introduced when imputing genotypes from global imputation panels

genetics more details view paper
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    • In genetics: 893 out of 3,699
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An interaction map of circulating metabolites, immune gene networks and their genetic regulation

genomics more details view paper
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    • Site-wide: 62,284 out of 65,454

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

genomics more details view paper
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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

genomics more details view paper
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Metabolomic consequences of genetic inhibition of PCSK9 compared with statin treatment

epidemiology more details view paper
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    • In epidemiology: 216 out of 1,556
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    • Site-wide: 63,677 out of 65,454

Metabolic profiling of alcohol consumption in 9778 young adults

systems biology more details view paper
  • Downloaded 493 times
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    • In systems biology: 619 out of 1,836
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    • Site-wide: 60,477 out of 65,454

Contribution of rare and common variants to intellectual disability in a high-risk population sub-isolate of Northern Finland

genetics more details view paper
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Systems medicine links microbial inflammatory response with glycoprotein-associated mortality risk

genomics more details view paper
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A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

genetics more details view paper
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Whole genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom

genetics more details view paper
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Advantages of genotype imputation with ethnically matched reference panel for rare variant association analyses

genomics more details view paper
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Direct estimation of HDL-mediated cholesterol efflux capacity from serum

epidemiology more details view paper
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Polygenic risk score of alcohol consumption predicts alcohol-related morbidity and all-cause mortality

genomics more details view paper
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The landscape of incident disease risk for the biomarker GlycA and its mortality stratification in angiography patients

epidemiology more details view paper
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    • Site-wide: 36,618 out of 65,454

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

genetics more details view paper
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Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns

genetics more details view paper
  • Downloaded 288 times
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Lipoprotein Signatures of Cholesteryl Ester Transfer Protein and HMG-CoA Reductase Inhibition

genetics more details view paper
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Genetic variation in apolipoprotein A-I concentrations and risk of coronary artery disease

epidemiology more details view paper
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Coronary artery disease risk and lipidomic profiles are similar in familial and population-ascertained hyperlipidemias

epidemiology more details view paper
  • Downloaded 192 times
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    • Site-wide: 54,458 out of 65,454

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

genomics more details view paper
  • Downloaded 120 times
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    • In genomics: 4,212 out of 4,464
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