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GWAMA: software for genome-wide association meta-analysis

BMC bioinformatics, 2010-05, Vol.11 (1), p.288-288, Article 288

2010

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Ancestry deconvolution and partial polygenic score can improve susceptibility predictions in recently admixed individuals

Nature communications, 2020-04, Vol.11 (1), p.1628-1628, Article 1628

2020

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Trans-ethnic meta-regression of genome-wide association studies accounting for ancestry increases power for discovery and improves fine-mapping resolution

Human molecular genetics, 2017-09, Vol.26 (18), p.3639-3650

2017

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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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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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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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Causal relationships between obesity and the leading causes of death in women and men

PLoS genetics, 2019-10, Vol.15 (10), p.e1008405-e1008405

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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Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores

Genetics in medicine, 2017-03, Vol.19 (3), p.322-329

2017

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Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis

Journal of allergy and clinical immunology, 2022-03, Vol.149 (3), p.1105-1112.e9

2022

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Probabilistic inference of the genetic architecture underlying functional enrichment of complex traits

Nature communications, 2021-11, Vol.12 (1), p.6972-16, Article 6972

2021

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Genome-wide association study meta-analysis supports association between MUC1 and ectopic pregnancy

Human reproduction (Oxford), 2023-12, Vol.38 (12), p.2516-2525

2023

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Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions

Genetics in medicine, 2019-06, Vol.21 (6), p.1345-1354

2019

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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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Using Genetic Variants to Assess the Relationship Between Circulating Lipids and Type 2 Diabetes

Diabetes (New York, N.Y.), 2015-07, Vol.64 (7), p.2676-2684

2015

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In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages

Nature medicine, 2019-11, Vol.25 (11), p.1699-1705

2019

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The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects

American journal of human genetics, 2021-04, Vol.108 (4), p.608-619

2021

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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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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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Genomic architecture and prediction of censored time-to-event phenotypes with a Bayesian genome-wide analysis

Nature communications, 2021-04, Vol.12 (1), p.2337-17, Article 2337

2021

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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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Global genetic diversity of human apolipoproteins and effects on cardiovascular disease risk [S]

Journal of lipid research, 2018-10, Vol.59 (10), p.1987-2000

2018

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Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse

Nature communications, 2022-06, Vol.13 (1), p.3584-3584, Article 3584

2022

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Genetic insights into the age-specific biological mechanisms governing human ovarian aging

American journal of human genetics, 2023-09, Vol.110 (9), p.1549-1563

2023

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GWAMA: software for genome-wide association meta-analysis

Ancestry deconvolution and partial polygenic score can improve susceptibility predictions in recently admixed individuals

Trans-ethnic meta-regression of genome-wide association studies accounting for ancestry increases power for discovery and improves fine-mapping resolution

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

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

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

Causal relationships between obesity and the leading causes of death in women and men

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

Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores

Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis

Probabilistic inference of the genetic architecture underlying functional enrichment of complex traits

Genome-wide association study meta-analysis supports association between MUC1 and ectopic pregnancy

Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions

Long-range regulatory effects of Neandertal DNA in modern humans

Upper Palaeolithic Siberian genome reveals dual ancestry of Native Americans

Using Genetic Variants to Assess the Relationship Between Circulating Lipids and Type 2 Diabetes

In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages

The landscape of autosomal-recessive pathogenic variants in European populations reveals phenotype-specific effects

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

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

Genomic architecture and prediction of censored time-to-event phenotypes with a Bayesian genome-wide analysis

Genetic determinants of plasma protein levels in the Estonian population

Global genetic diversity of human apolipoproteins and effects on cardiovascular disease risk [S]

Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse

Genetic insights into the age-specific biological mechanisms governing human ovarian aging

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