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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 62,747 bioRxiv papers from 278,434 authors.

Author: Veikko Salomaa

Rankings

  • All-time downloads: 46,456 (rank: 298 out of 278,434)
  • Categories:
    • bioinformatics: 1,460 (rank: 5,208 (tie) out of 24,395)
    • epidemiology: 2,372 (rank: 307 out of 9,529)
    • genetics: 30,822 (rank: 119 out of 27,725)
    • genomics: 10,566 (rank: 932 out of 31,945)
    • systems biology: 1,236 (rank: 1,364 (tie) out of 8,440)

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Preprints

A reference panel of 64,976 haplotypes for genotype imputation

genetics more details view paper
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    • In genetics: 55 out of 3,562
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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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    • In genetics: 95 out of 3,562
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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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    • Site-wide: 13,420 out of 62,747
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    • Site-wide: 26,734 out of 62,747

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

genetics more details view paper
  • Downloaded 2,358 times
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    • In genetics: 161 out of 3,562
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    • Site-wide: 38,656 out of 62,747
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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

genetics more details view paper
  • Downloaded 2,184 times
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    • In genetics: 184 out of 3,562
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    • Site-wide: 42,903 out of 62,747

Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

genomics more details view paper
  • Downloaded 1,970 times
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    • In genomics: 485 out of 4,316
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    • Site-wide: 38,222 out of 62,747

Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum

genetics more details view paper
  • Downloaded 1,854 times
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    • Site-wide: 21,557 out of 62,747

Cell specific eQTL analysis without sorting cells

genetics more details view paper
  • Downloaded 1,734 times
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    • In genetics: 254 out of 3,562
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    • Site-wide: 19,408 out of 62,747
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    • Site-wide: 14,538 out of 62,747

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

genetics more details view paper
  • Downloaded 1,659 times
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    • In genetics: 270 out of 3,562
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    • Site-wide: 22,472 out of 62,747
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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
  • Downloaded 1,601 times
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    • In genetics: 286 out of 3,562
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    • Site-wide: 48,814 out of 62,747

Polygenic and clinical risk scores and their impact on age at onset of cardiometabolic diseases and common cancers

genomics more details view paper
  • Downloaded 1,530 times
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    • In genomics: 664 out of 4,316
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    • Site-wide: 679 out of 62,747
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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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    • In bioinformatics: 764 out of 6,251
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    • Site-wide: 50,502 out of 62,747

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
  • Downloaded 1,276 times
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    • In genomics: 839 out of 4,316
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    • Site-wide: 37,660 out of 62,747

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

genetics more details view paper
  • Downloaded 1,108 times
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    • In genetics: 488 out of 3,562
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    • Site-wide: 3,360 out of 62,747
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    • Site-wide: 15,294 out of 62,747

Genomic prediction of coronary heart disease

genomics more details view paper
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    • In genomics: 1,061 out of 4,316
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    • Site-wide: 55,446 out of 62,747
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    • Site-wide: 57,999 out of 62,747

Refining fine-mapping: effect sizes and regional heritability

genetics more details view paper
  • Downloaded 993 times
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    • In genetics: 560 out of 3,562
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    • Site-wide: 12,734 out of 62,747

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

genomics more details view paper
  • Downloaded 958 times
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    • Site-wide: 7,572 out of 62,747
    • In genomics: 1,201 out of 4,316
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    • Site-wide: 4,096 out of 62,747
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    • Site-wide: 21,052 out of 62,747

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

genetics more details view paper
  • Downloaded 938 times
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    • In genetics: 610 out of 3,562
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    • Site-wide: 37,704 out of 62,747
  • Since beginning of last month:
    • Site-wide: 43,765 out of 62,747

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

genetics more details view paper
  • Downloaded 887 times
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    • Site-wide: 8,586 out of 62,747
    • In genetics: 642 out of 3,562
  • Year to date:
    • Site-wide: 15,849 out of 62,747
  • Since beginning of last month:
    • Site-wide: 30,255 out of 62,747

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

genetics more details view paper
  • Downloaded 865 times
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    • In genetics: 667 out of 3,562
  • Year to date:
    • Site-wide: 4,465 out of 62,747
  • Since beginning of last month:
    • Site-wide: 4,695 out of 62,747

Geographic variation and bias in polygenic scores of complex diseases and traits in Finland

genetics more details view paper
  • Downloaded 829 times
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    • In genetics: 706 out of 3,562
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    • Site-wide: 4,957 out of 62,747
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    • Site-wide: 18,695 out of 62,747

Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

genetics more details view paper
  • Downloaded 808 times
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    • In genetics: 728 out of 3,562
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    • Site-wide: 2,955 out of 62,747

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
  • Downloaded 760 times
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    • In epidemiology: 119 out of 1,556
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    • Site-wide: 8,786 out of 62,747

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: 316 out of 1,783
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    • Site-wide: 5,214 out of 62,747

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

genetics more details view paper
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    • In genetics: 859 out of 3,562
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    • Site-wide: 34,231 out of 62,747

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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    • In genomics: 1,728 out of 4,316
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    • Site-wide: 2,842 out of 62,747
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    • Site-wide: 9,879 out of 62,747

An interaction map of circulating metabolites, immune gene networks and their genetic regulation

genomics more details view paper
  • Downloaded 663 times
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    • Site-wide: 13,174 out of 62,747
    • In genomics: 1,784 out of 4,316
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    • Site-wide: 57,381 out of 62,747
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    • Site-wide: 53,225 out of 62,747

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

genomics more details view paper
  • Downloaded 616 times
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    • Site-wide: 14,552 out of 62,747
    • In genomics: 1,902 out of 4,316
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    • Site-wide: 60,596 out of 62,747

Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

genomics more details view paper
  • Downloaded 588 times
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    • Site-wide: 15,553 out of 62,747
    • In genomics: 1,971 out of 4,316
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    • Site-wide: 41,584 out of 62,747
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    • Site-wide: 45,656 out of 62,747

Metabolomic consequences of genetic inhibition of PCSK9 compared with statin treatment

epidemiology more details view paper
  • Downloaded 549 times
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    • Site-wide: 17,060 out of 62,747
    • In epidemiology: 208 out of 1,556
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    • Site-wide: 25,875 out of 62,747
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    • Site-wide: 56,723 out of 62,747

Metabolic profiling of alcohol consumption in 9778 young adults

systems biology more details view paper
  • Downloaded 488 times
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    • Site-wide: 19,771 out of 62,747
    • In systems biology: 598 out of 1,783
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    • Site-wide: 57,411 out of 62,747

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

genetics more details view paper
  • Downloaded 468 times
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    • Site-wide: 39,592 out of 62,747

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

genomics more details view paper
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    • Site-wide: 58,159 out of 62,747

A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

genetics more details view paper
  • Downloaded 425 times
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    • In genetics: 1,537 out of 3,562
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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
  • Downloaded 399 times
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    • Site-wide: 58,517 out of 62,747

Direct estimation of HDL-mediated cholesterol efflux capacity from serum

epidemiology more details view paper
  • Downloaded 350 times
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    • Site-wide: 28,459 out of 62,747
    • In epidemiology: 421 out of 1,556
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    • Site-wide: 43,652 out of 62,747

Advantages of genotype imputation with ethnically matched reference panel for rare variant association analyses

genomics more details view paper
  • Downloaded 346 times
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    • Site-wide: 9,043 out of 62,747
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    • Site-wide: 21,826 out of 62,747

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

genomics more details view paper
  • Downloaded 330 times
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    • Site-wide: 30,225 out of 62,747
    • In genomics: 2,972 out of 4,316
  • Year to date:
    • Site-wide: 9,782 out of 62,747
  • Since beginning of last month:
    • Site-wide: 17,377 out of 62,747

The landscape of incident disease risk for the biomarker GlycA and its mortality stratification in angiography patients

epidemiology more details view paper
  • Downloaded 316 times
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    • Site-wide: 31,400 out of 62,747
    • In epidemiology: 488 out of 1,556
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    • Site-wide: 43,120 out of 62,747
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    • Site-wide: 50,374 out of 62,747

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

genetics more details view paper
  • Downloaded 284 times
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    • Site-wide: 34,493 out of 62,747
    • In genetics: 2,159 out of 3,562
  • Year to date:
    • Site-wide: 23,655 out of 62,747
  • Since beginning of last month:
    • Site-wide: 45,638 out of 62,747

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

genetics more details view paper
  • Downloaded 264 times
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    • Site-wide: 13,760 out of 62,747
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    • Site-wide: 10,514 out of 62,747

Lipoprotein Signatures of Cholesteryl Ester Transfer Protein and HMG-CoA Reductase Inhibition

genetics more details view paper
  • Downloaded 250 times
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    • Site-wide: 38,018 out of 62,747
    • In genetics: 2,341 out of 3,562
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    • Site-wide: 44,059 out of 62,747
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    • Site-wide: 45,449 out of 62,747

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

epidemiology more details view paper
  • Downloaded 211 times
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    • Site-wide: 42,678 out of 62,747
    • In epidemiology: 785 out of 1,556
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    • Site-wide: 18,610 out of 62,747
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    • Site-wide: 37,496 out of 62,747

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

epidemiology more details view paper
  • Downloaded 186 times
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    • Site-wide: 45,778 out of 62,747
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  • Year to date:
    • Site-wide: 47,729 out of 62,747
  • Since beginning of last month:
    • Site-wide: 49,074 out of 62,747

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

genomics more details view paper
  • Downloaded 107 times
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    • Site-wide: 56,183 out of 62,747
    • In genomics: 4,103 out of 4,316
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    • Site-wide: 38,076 out of 62,747
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    • Site-wide: 22,758 out of 62,747

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