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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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Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu

International journal of epidemiology, 2015-08, Vol.44 (4), p.1137-1147

2015

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A cross-disorder dosage sensitivity map of the human genome

Cell, 2022-08, Vol.185 (16), p.3041-3055.e25

2022

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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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Educational Attainment and Personality Are Genetically Intertwined

Psychological science, 2017-11, Vol.28 (11), p.1631-1639

2017

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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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Variants near CHRNA3/5 and APOE have age- and sex-related effects on human lifespan

Nature communications, 2016-03, Vol.7 (1), p.11174-11174, Article 11174

2016

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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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Biomarker profiling by nuclear magnetic resonance spectroscopy for the prediction of all-cause mortality: an observational study of 17,345 persons

PLoS medicine, 2014-02, Vol.11 (2), p.e1001606-e1001606

2014

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Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants

European journal of human genetics : EJHG, 2021-03, Vol.29 (3), p.471-481

2021

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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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Pathogenic implications for autoimmune mechanisms derived by comparative eQTL analysis of CD4+ versus CD8+ T cells

PLoS genetics, 2017-03, Vol.13 (3), p.e1006643-e1006643

2017

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Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood

Nature communications, 2018-06, Vol.9 (1), p.2282-12, Article 2282

2018

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Genetic signature to provide robust risk assessment of psoriatic arthritis development in psoriasis patients

Nature communications, 2018-10, Vol.9 (1), p.4178-10, Article 4178

2018

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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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Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratification

BMC cancer, 2019-06, Vol.19 (1), p.557-9, Article 557

2019

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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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Improved polygenic prediction by Bayesian multiple regression on summary statistics

Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu

A cross-disorder dosage sensitivity map of the human genome

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

Educational Attainment and Personality Are Genetically Intertwined

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

Variants near CHRNA3/5 and APOE have age- and sex-related effects on human lifespan

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

Biomarker profiling by nuclear magnetic resonance spectroscopy for the prediction of all-cause mortality: an observational study of 17,345 persons

Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants

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

Pathogenic implications for autoimmune mechanisms derived by comparative eQTL analysis of CD4+ versus CD8+ T cells

Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood

Genetic signature to provide robust risk assessment of psoriatic arthritis development in psoriasis patients

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

Polygenic prediction of breast cancer: comparison of genetic predictors and implications for risk stratification

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

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