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Author: Matti Pirinen

Rankings

  • All-time downloads: 20,466 (rank: 2,841 out of 397,872)
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    • bioinformatics: 3,957 (rank: 2,489 (tie) out of 33,918)
    • genetics: 13,339 (rank: 850 out of 36,495)
    • genomics: 3,170 (rank: 6,319 (tie) out of 42,235)

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Preprints

Bayesian model comparison for rare variant association studies of multiple phenotypes

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Assessing allele specific expression across multiple tissues from RNA-seq read data

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Functionally-informed fine-mapping and polygenic localization of complex trait heritability

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

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Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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

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Refining fine-mapping: effect sizes and regional heritability

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FINEMAP: Efficient variable selection using summary data from genome-wide association studies

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

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

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

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Bayesian meta-analysis across genome-wide association studies of diverse phenotypes

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

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    • Site-wide: 56,976 out of 93,215

MetaPhat: Detecting and decomposing multivariate associations from univariate genome-wide association statistics

bioinformatics more details view paper
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    • Site-wide: 25,799 out of 93,215

biMM: Efficient estimation of genetic variances and covariances for cohorts with high-dimensional phenotype measurements

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

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

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Polygenic Hyperlipidemias and Coronary Artery Disease Risk

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    • Site-wide: 87,854 out of 93,215

High-resolution population-specific recombination rates and their effect on phasing and genotype imputation

genomics more details view paper
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    • In genomics: 5,004 out of 5,870
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    • Site-wide: 23,454 out of 93,215

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