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Preprints

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

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

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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

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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

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

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

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Cell specific eQTL analysis without sorting cells

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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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

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metaCCA: Summary statistics-based multivariate meta-analysis of genome-wide association studies using canonical correlation analysis

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Genome-wide association study identifies 17 new loci influencing concentrations of circulating cytokines and growth factors

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Genomic prediction of coronary heart disease

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

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

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Refining fine-mapping: effect sizes and regional heritability

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

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

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

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

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

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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

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

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Metabolomic consequences of genetic inhibition of PCSK9 compared with statin treatment

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Metabolic profiling of alcohol consumption in 9778 young adults

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

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

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A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

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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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Common variant burden contributes significantly to the familial aggregation of migraine in 1,589 families

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Elevated alpha-1 antitrypsin is a major component of GlycA-associated risk for future morbidity and mortality

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Direct estimation of HDL-mediated cholesterol efflux capacity from serum

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

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

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

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

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

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