|
| 37350734 | Genetic, sociodemographic, lifestyle, and clinical risk factors of recurrent coronary artery disease events: a population-based cohort study. | Eur Heart J | 2023 |
| 37601974 | Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries. | Cell Genom | 2023 |
| 37798380 | Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. | Nat Genet | 2023 |
| 37790435 | Complexities of cerebral small vessel disease, blood pressure, and dementia relationship: new insights from genetics. | medRxiv | 2023 |
| 36580301 | Sex-Specific Survival Bias and Interaction Modeling in Coronary Artery Disease Risk Prediction. | | 2023 |
| 37124606 | Genetic predisposition may not improve prediction of cardiac surgery-associated acute kidney injury. | Front Genet | 2023 |
| 37308786 | Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program. | Nat Genet | 2023 |
| 37235137 | Genetic variants in HFE are associated with non-alcoholic fatty liver disease in lean individuals. | | 2023 |
| 35130028 | How Communicating Polygenic and Clinical Risk for Atherosclerotic Cardiovascular Disease Impacts Health Behavior: an Observational Follow-up Study. | Circulation. Genomic and precision medicine | 2022 |
| 35974141 | Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning. | Mol Psychiatry | 2022 |
| 35978133 | Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis. | Commun Biol | 2022 |
| 36777998 | The HUNT study: A population-based cohort for genetic research. | Cell Genom | 2022 |
| 34916535 | Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer. | Nat Commun | 2021 |
| 33909604 | ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease. | PLoS Genet | 2021 |
| 33961016 | Genome-wide association study of cardiac troponin I in the general population. | Hum Mol Genet | 2021 |
| 34265237 | Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm. | Am J Hum Genet | 2021 |
| 33604704 | Translating genetic association of lipid levels for biological and clinical application. | Cardiovascular Drugs and Therapy | 2021 |
| 33249422 | High-resolution population-specific recombination rates and their effect on phasing and genotype imputation. | European Journal of Human Genetics | 2021 |
| 34746691 | Type 2 diabetes sex-specific effects associated with E167K coding variant in . | iScience | 2021 |
| 33339817 | Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. | Nat Commun | 2020 |
| 32056457 | Mitochondrial genome-wide association study of migraine - the HUNT Study. | Cephalalgia | 2020 |
| 32154731 | Polygenic Hyperlipidemias and Coronary Artery Disease Risk. | Circ Genom Precis Med | 2020 |
| 34317346 | A Novel Variant in Gene Causes Extremely Low LDL-C Without Known Adverse Effects. | JACC: Case Reports | 2020 |
| 32769997 | GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer. | Nat Commun | 2020 |
| 33087929 | Exome sequencing and characterization of 49,960 individuals in the UK Biobank. | Nature | 2020 |
| 32517536 | Use of a Polygenic Risk Score Improves Prediction of Myocardial Injury After Non-Cardiac Surgery. | Circulation. Genomic and precision medicine | 2020 |
| 31155286 | Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland. | Am J Hum Genet | 2019 |
| 30645169 | Variation in Serum PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9), Cardiovascular Disease Risk, and an Investigation of Potential Unanticipated Effects of PCSK9 Inhibition. | Circ Genom Precis Med | 2019 |
| 29532581 | Genome-wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway. | Addiction Biology | 2019 |
| 30804560 | New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. | Nat Genet | 2019 |
| 31015462 | Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. | Nat Commun | 2019 |
| 29683540 | Blood pressure levels in the acute phase after intracerebral hemorrhage are associated with mortality in young adults. | European Journal of Neurology | 2018 |
| 30608196 | Risk Factors for Early-Onset Ischemic Stroke: A Case-Control Study. | Journal of the American Heart Association | 2018 |
| 29973585 | Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries. | Nat Commun | 2018 |
| 30061737 | Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. | Nat Genet | 2018 |
| 30140049 | Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries. | Nat Commun | 2018 |
| 30140000 | Deep-coverage whole genome sequences and blood lipids among 16,324 individuals. | Nat Commun | 2018 |
| 30189203 | Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families. | Neuron | 2018 |
| 29290336 | Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development. | Am J Hum Genet | 2018 |
| 29547983 | Electronic health records: the next wave of complex disease genetics. | Human Molecular Genetics | 2018 |
| 29731251 | Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families. | Neuron | 2018 |
| 28166213 | Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. | Nat Genet | 2017 |
| 27840886 | The Value of FLG Null Mutations in Predicting Treatment Response in Atopic Dermatitis: An Observational Study in Finnish Patients. | Acta Dermato-Venereologica | 2017 |
| 27529662 | Post-thrombolytic blood pressure and symptomatic intracerebral hemorrhage. | European Journal of Neurology | 2016 |
| 27227539 | The Contribution of GWAS Loci in Familial Dyslipidemias. | PLoS Genet | 2016 |
| 27217509 | Acute-Phase Blood Pressure Levels Correlate With a High Risk of Recurrent Strokes in Young-Onset Ischemic Stroke. | Stroke | 2016 |
| 27036123 | Meta-analysis of 49â¿¿549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels. | J Med Genet | 2016 |
| 26819196 | USF1 deficiency activates brown adipose tissue and improves cardiometabolic health. | Sci Transl Med | 2016 |
| 26030606 | Targeted resequencing of the pericentromere of chromosome 2 linked to constitutional delay of growth and puberty. | PLoS One | 2015 |
| 25828238 | Trends in Door-to-Thrombolysis Time in the Safe Implementation of Stroke Thrombolysis Registry: Effect of Center Volume and Duration of Registry Membership. | Stroke | 2015 |