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Circulating Ceramides Predict Cardiovascular Outcomes in the Population-Based FINRISK 2002 Cohort

Arteriosclerosis, thrombosis, and vascular biology, 2016-12, Vol.36 (12), p.2424-2430

2016

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Prospects of Fine-Mapping Trait-Associated Genomic Regions by Using Summary Statistics from Genome-wide Association Studies

American journal of human genetics, 2017-10, Vol.101 (4), p.539-551

2017

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

Bioinformatics, 2016-05, Vol.32 (10), p.1493-1501

2016

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Greengenes2 unifies microbial data in a single reference tree

Nature biotechnology, 2024-05, Vol.42 (5), p.715-718

2024

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Genetics of 35 blood and urine biomarkers in the UK Biobank

Nature genetics, 2021-02, Vol.53 (2), p.185-194

2021

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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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Polygenic Risk Scores Predict Hypertension Onset and Cardiovascular Risk

Hypertension (Dallas, Tex. 1979), 2021-04, Vol.77 (4), p.1119-1127

2021

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Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors

American journal of human genetics, 2017-01, Vol.100 (1), p.40-50

2017

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Genomic prediction of coronary heart disease

European heart journal, 2016-11, Vol.37 (43), p.3267-3278

2016

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Genetic risk prediction and a 2-stage risk screening strategy for coronary heart disease

Arteriosclerosis, thrombosis, and vascular biology, 2013-09, Vol.33 (9), p.2261-2266

2013

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Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland

American journal of human genetics, 2019-06, Vol.104 (6), p.1169-1181

2019

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Twenty-five-year trends in myocardial infarction attack and mortality rates, and case-fatality, in six European populations

Heart (British Cardiac Society), 2015-09, Vol.101 (17), p.1413-1421

2015

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ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease

PLoS genetics, 2021-04, Vol.17 (4), p.e1009501-e1009501

2021

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Machine learning of human plasma lipidomes for obesity estimation in a large population cohort

PLoS biology, 2019-10, Vol.17 (10), p.e3000443

2019

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Changes in the fine-scale genetic structure of Finland through the 20th century

PLoS genetics, 2021-03, Vol.17 (3), p.e1009347-e1009347

2021

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Taxonomic signatures of cause-specific mortality risk in human gut microbiome

Nature communications, 2021-05, Vol.12 (1), p.2671-2671, Article 2671

2021

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A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses

The Lancet (British edition), 2010-10, Vol.376 (9750), p.1393-1400

2010

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Apolipoprotein A-I concentrations and risk of coronary artery disease: A Mendelian randomization study

Atherosclerosis, 2020-04, Vol.299, p.56-63

2020

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Fine-Scale Genetic Structure in Finland

G3 : genes - genomes - genetics, 2017-10, Vol.7 (10), p.3459-3468

2017

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Genetic Associations of Chronotype in the Finnish General Population

Journal of biological rhythms, 2020-10, Vol.35 (5), p.501-511

2020

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Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma

PLoS genetics, 2020-05, Vol.16 (5), p.e1008682-e1008682

2020

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Association Between the Gut Microbiota and Blood Pressure in a Population Cohort of 6953 Individuals

Journal of the American Heart Association, 2020-08, Vol.9 (15), p.e016641-e016641

2020

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Risk factors for major adverse cardiovascular events after the first acute coronary syndrome

Annals of medicine (Helsinki), 2021-01, Vol.53 (1), p.817-823

2021

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Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation

Nature communications, 2023-01, Vol.14 (1), p.83-15, Article 83

2023

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Circulating Ceramides Predict Cardiovascular Outcomes in the Population-Based FINRISK 2002 Cohort

Prospects of Fine-Mapping Trait-Associated Genomic Regions by Using Summary Statistics from Genome-wide Association Studies

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

Greengenes2 unifies microbial data in a single reference tree

Genetics of 35 blood and urine biomarkers in the UK Biobank

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

Polygenic Risk Scores Predict Hypertension Onset and Cardiovascular Risk

Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors

Genomic prediction of coronary heart disease

Genetic risk prediction and a 2-stage risk screening strategy for coronary heart disease

Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland

Twenty-five-year trends in myocardial infarction attack and mortality rates, and case-fatality, in six European populations

Metabolic signatures of adiposity in young adults: Mendelian randomization analysis and effects of weight change

ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease

Machine learning of human plasma lipidomes for obesity estimation in a large population cohort

Changes in the fine-scale genetic structure of Finland through the 20th century

Taxonomic signatures of cause-specific mortality risk in human gut microbiome

A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses

Apolipoprotein A-I concentrations and risk of coronary artery disease: A Mendelian randomization study

Fine-Scale Genetic Structure in Finland

Genetic Associations of Chronotype in the Finnish General Population

Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma

Association Between the Gut Microbiota and Blood Pressure in a Population Cohort of 6953 Individuals

Risk factors for major adverse cardiovascular events after the first acute coronary syndrome

Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation

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