Area of research
Genetics · Surgery
Research interest
Research interests include Genetic Associations and Epidemiology, Lipoproteins and Cardiovascular Health, Cancer, Lipids, and Metabolism, and Diabetes, Cardiovascular Risks, and Lipoproteins.
The impact of common and rare genetic variants on bradyarrhythmia development
Cardiomyopathy-Associated Gene Variants in Atrial Fibrillation
A deep learning digital biomarker to detect hypertension and stratify cardiovascular risk from the electrocardiogram
Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma
Electrocardiogram-Based Artificial Intelligence to Identify Coronary Artery Disease
Pathogenic Cardiomyopathy-Associated Gene Variants and Prognosis in Atrial Fibrillation
Associations of “Weekend Warrior” Physical Activity With Incident Disease and Cardiometabolic Health
Rare coding variant analysis for human diseases across biobanks and ancestries
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience
Cardiovascular Significance and Genetics of Epicardial and Pericardial Adiposity
Genetic testing in early-onset atrial fibrillation
Deep learning of left atrial structure and function provides link to atrial fibrillation risk
Noninvasive assessment of organ-specific and shared pathways in multi-organ fibrosis using T1 mapping
Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank
Rare Genetic Variants in <i>LDLR</i> , <i>APOB</i> , and <i>PCSK9</i> Are Associated With Aortic Stenosis
Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias
FinnGen provides genetic insights from a well-phenotyped isolated population
Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population
Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases
The Genetic Determinants of Aortic Distention
Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
Effects of TM6SF2 E167K on hepatic lipid and very low-density lipoprotein metabolism in humans
Genetic architecture of human plasma lipidome and its link to cardiovascular disease
The Contribution of GWAS Loci in Familial Dyslipidemias