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Improved polygenic prediction by Bayesian multiple regression on summary statistics

Nature communications, 2019-11, Vol.10 (1), p.5086-11, Article 5086

2019

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Systematic identification of trans eQTLs as putative drivers of known disease associations

Nature genetics, 2013-10, Vol.45 (10), p.1238-1243

2013

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Genome-wide association study identifies five risk loci for pernicious anemia

Nature communications, 2021-06, Vol.12 (1), p.3761-3761, Article 3761

2021

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Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel

European journal of human genetics : EJHG, 2017-06, Vol.25 (7), p.869-876

2017

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Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes

Nature communications, 2018-07, Vol.9 (1), p.2941-14, Article 2941

2018

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Impact of the gut microbiota and associated metabolites on cardiometabolic traits, chronic diseases and human longevity: a Mendelian randomization study

Journal of translational medicine, 2023-01, Vol.21 (1), p.60-60, Article 60

2023

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Long-range regulatory effects of Neandertal DNA in modern humans

Genetics (Austin), 2023-03, Vol.223 (3)

2023

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GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk

Nature communications, 2017-11, Vol.8 (1), p.1584-10, Article 1584

2017

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Analytical strategies to include the X‐chromosome in variance heterogeneity analyses: Evidence for trait‐specific polygenic variance structure

Genetic epidemiology, 2019-10, Vol.43 (7), p.815-830

2019

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Genetic determinants of plasma protein levels in the Estonian population

Scientific reports, 2024-04, Vol.14 (1), p.7694-7694, Article 7694

2024

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Using genetic variation to disentangle the complex relationship between food intake and health outcomes

PLoS genetics, 2022-06, Vol.18 (6), p.e1010162

2022

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Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records

European journal of human genetics : EJHG, 2019-03, Vol.27 (3), p.442-454

2019

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Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

Nature communications, 2022-06, Vol.13 (1), p.3200-3200, Article 3200

2022

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Stratification of Type 2 Diabetes by Age of Diagnosis in the UK Biobank Reveals Subgroup-Specific Genetic Associations and Causal Risk Profiles

Diabetes (New York, N.Y.), 2021-08, Vol.70 (8), p.1816-1825

2021

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Within-trait heterogeneity in age group differences in personality domains and facets: implications for the development and coherence of personality traits

PloS one, 2015-03, Vol.10 (3), p.e0119667-e0119667

2015

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Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia

Genetics in medicine, 2019-05, Vol.21 (5), p.1173-1180

2019

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Replicability and Robustness of Genome-Wide-Association Studies for Behavioral Traits

Psychological science, 2014-11, Vol.25 (11), p.1975-1986

2014

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Cell Specific eQTL Analysis without Sorting Cells

PLoS genetics, 2015-05, Vol.11 (5), p.e1005223

2015

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Altered Gene Expression Associated with microRNA Binding Site Polymorphisms

PloS one, 2015, Vol.10 (10), p.e0141351-e0141351

2015

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Differences in local population history at the finest level: the case of the Estonian population

European journal of human genetics : EJHG, 2020-11, Vol.28 (11), p.1580-1591

2020

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An exploratory phenome wide association study linking asthma and liver disease genetic variants to electronic health records from the Estonian Biobank

PloS one, 2019-04, Vol.14 (4), p.e0215026

2019

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MixFit: Methodology for Computing Ancestry-Related Genetic Scores at the Individual Level and Its Application to the Estonian and Finnish Population Studies

PloS one, 2017-01, Vol.12 (1), p.e0170325-e0170325

2017

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Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration

JAMA ophthalmology, 2023-05, Vol.141 (5), p.449

2023

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Comparison of variation in frequency for SNPs associated with asthma or liver disease between Estonia, HapMap populations and the 1000 genome project populations

International journal of immunogenetics, 2019-04, Vol.46 (2), p.49-58

2019

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Improved polygenic prediction by Bayesian multiple regression on summary statistics

Systematic identification of trans eQTLs as putative drivers of known disease associations

Genome-wide association study identifies five risk loci for pernicious anemia

Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel

Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes

Impact of the gut microbiota and associated metabolites on cardiometabolic traits, chronic diseases and human longevity: a Mendelian randomization study

Long-range regulatory effects of Neandertal DNA in modern humans

GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk

Analytical strategies to include the X‐chromosome in variance heterogeneity analyses: Evidence for trait‐specific polygenic variance structure

Genetic determinants of plasma protein levels in the Estonian population

Using genetic variation to disentangle the complex relationship between food intake and health outcomes

Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records

Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci

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

Stratification of Type 2 Diabetes by Age of Diagnosis in the UK Biobank Reveals Subgroup-Specific Genetic Associations and Causal Risk Profiles

Within-trait heterogeneity in age group differences in personality domains and facets: implications for the development and coherence of personality traits

Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia

Replicability and Robustness of Genome-Wide-Association Studies for Behavioral Traits

Cell Specific eQTL Analysis without Sorting Cells

Altered Gene Expression Associated with microRNA Binding Site Polymorphisms

Differences in local population history at the finest level: the case of the Estonian population

An exploratory phenome wide association study linking asthma and liver disease genetic variants to electronic health records from the Estonian Biobank

MixFit: Methodology for Computing Ancestry-Related Genetic Scores at the Individual Level and Its Application to the Estonian and Finnish Population Studies

Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration

Comparison of variation in frequency for SNPs associated with asthma or liver disease between Estonia, HapMap populations and the 1000 genome project populations

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