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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 70,458 bioRxiv papers from 307,648 authors.

Author: Veikko Salomaa

Rankings

  • All-time downloads: 49,748 (rank: 304 out of 307,648)
  • Categories:
    • bioinformatics: 1,483 (rank: 5,772 (tie) out of 26,816)
    • epidemiology: 2,510 (rank: 299 out of 9,540)
    • genetics: 32,898 (rank: 115 out of 30,523)
    • genomics: 11,463 (rank: 947 out of 34,830)
    • systems biology: 1,394 (rank: 1,426 (tie) out of 9,259)

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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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    • In genetics: 174 out of 3,906
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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

genetics more details view paper
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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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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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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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    • In genetics: 257 out of 3,906
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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
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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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    • In genomics: 903 out of 4,710
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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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    • In genetics: 454 out of 3,906
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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: 485 out of 3,906
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    • Site-wide: 1,969 out of 70,458
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    • Site-wide: 1,875 out of 70,458

Genomic prediction of coronary heart disease

genomics more details view paper
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    • In genomics: 1,151 out of 4,710
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Refining fine-mapping: effect sizes and regional heritability

genetics more details view paper
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    • In genetics: 570 out of 3,906
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    • Site-wide: 16,763 out of 70,458

Exome sequencing identifies high-impact trait-associated alleles enriched in Finns

genomics more details view paper
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    • In genomics: 1,253 out of 4,710
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    • Site-wide: 28,428 out of 70,458

Haplotype sharing provides insights into fine-scale population history and disease in Finland

genetics more details view paper
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    • In genetics: 661 out of 3,906
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    • Site-wide: 54,326 out of 70,458

Genetics of human plasma lipidome: Understanding lipid metabolism and its link to diseases beyond traditional lipids

genetics more details view paper
  • Downloaded 942 times
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    • In genetics: 680 out of 3,906
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    • Site-wide: 23,491 out of 70,458

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

genetics more details view paper
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    • In genetics: 683 out of 3,906
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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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    • In systems biology: 276 out of 1,943
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    • Site-wide: 5,951 out of 70,458

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: 737 out of 3,906
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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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    • In epidemiology: 120 out of 1,556
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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: 19,300 out of 70,458

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

genetics more details view paper
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    • In genetics: 929 out of 3,906
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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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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: 235 out of 1,556
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    • Site-wide: 61,341 out of 70,458

Metabolic profiling of alcohol consumption in 9778 young adults

systems biology more details view paper
  • Downloaded 503 times
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    • In systems biology: 659 out of 1,943
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    • Site-wide: 64,775 out of 70,458

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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A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

genetics more details view paper
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    • Site-wide: 40,515 out of 70,458

Systems medicine links microbial inflammatory response with glycoprotein-associated mortality risk

genomics 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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Polygenic risk score of alcohol consumption predicts alcohol-related morbidity and all-cause mortality

genomics 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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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

genetics 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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    • Site-wide: 53,884 out of 70,458

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

genetics more details view paper
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    • Site-wide: 15,147 out of 70,458

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: 68,062 out of 70,458
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    • Site-wide: 61,192 out of 70,458

Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns

genetics more details view paper
  • Downloaded 302 times
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    • In genetics: 2,358 out of 3,906
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    • Site-wide: 55,941 out of 70,458
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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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    • Site-wide: 56,266 out of 70,458

Genetic variation in apolipoprotein A-I concentrations and risk of coronary artery disease

epidemiology more details view paper
  • Downloaded 234 times
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    • In epidemiology: 867 out of 1,556
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    • Site-wide: 60,711 out of 70,458

An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease

genetics more details view paper
  • Downloaded 230 times
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    • In genetics: 2,829 out of 3,906
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    • Site-wide: 7,719 out of 70,458
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    • Site-wide: 631 out of 70,458

Coronary artery disease risk and lipidomic profiles are similar in familial and population-ascertained hyperlipidemias

epidemiology more details view paper
  • Downloaded 198 times
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    • Site-wide: 66,969 out of 70,458

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

genomics more details view paper
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