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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: Samuli Ripatti

Rankings

  • All-time downloads: 46,974 (rank: 307 out of 289,944)
  • Categories:
    • bioinformatics: 1,748 (rank: 4,428 (tie) out of 25,248)
    • epidemiology: 192 (rank: 6,309 (tie) out of 9,548)
    • genetics: 28,213 (rank: 145 out of 28,782)
    • genomics: 16,075 (rank: 423 out of 33,034)
    • systems biology: 746 (rank: 2,776 (tie) out of 8,800)

Downloads per author, site-wide

Preprints

Unraveling the polygenic architecture of complex traits using blood eQTL meta-analysis

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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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Genetics of 38 blood and urine biomarkers in the UK Biobank

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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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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Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

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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Genome-wide association study identifies 48 common genetic variants associated with handedness.

genetics more details view paper
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FINEMAP: Efficient variable selection using summary data from genome-wide association studies

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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Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy

genomics more details view paper
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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
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    • In genetics: 626 out of 3,699
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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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Towards a molecular systems model of coronary artery disease

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

genetics more details view paper
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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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Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation

genetics more details view paper
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biMM: Efficient estimation of genetic variances and covariances for cohorts with high-dimensional phenotype measurements

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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CCR5-del32 is not deleterious in the homozygous state in humans

genetics more details view paper
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    • In genetics: 1,726 out of 3,699
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    • Site-wide: 446 out of 65,454

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

genomics more details view paper
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    • Site-wide: 26,834 out of 65,454

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

genomics more details view paper
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MetaPhat: Detecting and decomposing multivariate associations from univariate genome-wide association statistics

bioinformatics 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
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Polygenic Hyperlipidemias and Coronary Artery Disease Risk

genomics more details view paper
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