Terkko Navigator / Lyytikäinen, L(eo)-P(ekka)

Interatrial block and P terminal force in the general population - Longitudinal changes, risk factors and prognosis

Magical thinking in individuals with high polygenic risk for schizophrenia but no non-affective psychoses-a general population study

Prevalence and long-term prognostic implications of prolonged QRS duration in left ventricular hypertrophy: a population-based observational cohort study

Mitochondrial genome-wide analysis of nuclear DNA methylation quantitative trait loci

C-type lectin receptor CLEC4A2 promotes tissue adaptation of macrophages and protects against atherosclerosis

The power of genetic diversity in genome-wide association studies of lipids

Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits

Genetic differential susceptibility to the parent-child relationship quality and the life span development of compassion

Methylation status of nc886 epiallele reflects periconceptional conditions and is associated with glucose metabolism through nc886 RNAs

Prehospital Adenosine Diphosphate Receptor Blocker Use, Culprit Artery Flow, and Mortality in STEMI: The MADDEC Study

Adulthood blood levels of hsa-miR-29b-3p associate with preterm birth and adult metabolic and cognitive health

Functional Polymorphisms in Oxytocin and Dopamine Pathway Genes and the Development of Dispositional Compassion Over Time: The Young Finns Study

Publisher Correction: A meta-analysis of genome-wide association studies identifies multiple longevity genes

Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

Variants associated with <em>HHIP</em> expression have sex-differential effects on lung function

Genome-wide analysis identifies novel susceptibility loci for myocardial infarction

Impedance plethysmography-based method in the assessment of subclinical atherosclerosis

The Role of Inflammatory Cytokines as Intermediates in the Pathway from Increased Adiposity to Disease

Examining the effect of mitochondrial DNA variants on blood pressure in two Finnish cohorts

Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits

Relation of intraventricular conduction delay to risk of new-onset heart failure and structural heart disease in the general population

The prognostic significance of T-wave inversion according to ECG lead group during long-term follow-up in the general population

Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity

The Polygenic and Monogenic Basis of Blood Traits and Diseases

Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

Long-term outcome of intraventricular conduction delays in the general population

Association of Factor V Leiden With Subsequent Atherothrombotic Events: A GENIUS-CHD Study of Individual Participant Data

Systemic vascular resistance predicts the development of hypertension: the cardiovascular risk in young Finns study

Serum apolipoprotein A-I concentration differs in coronary and peripheral artery disease

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci

The prevalence and prognostic significance of interatrial block in the general population

Long-term prognostic significance of the ST level and ST slope in the 12‑lead ECG in the general population

Influence of Genetic Variation in <em>PDE3A</em> on Endothelial Function and Stroke

RNA-sequencing reveals that STRN, ZNF484 and WNK1 add to the value of mitochondrial MT-COI and COX10 as markers of unstable coronary artery disease

The association between charlson comorbidity index and mortality in acute coronary syndrome - the MADDEC study

Three genetic-environmental networks for human personality

Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration

Model selection for metabolomics: predicting diagnosis of coronary artery disease using automated machine learning

Multivariate Genome-wide Association Analysis of a Cytokine Network Reveals Variants with Widespread Immune, Haematological, and Cardiometabolic Pleiotropy

Combination of low blood pressure response, low exercise capacity and slow heart rate recovery during an exercise test significantly increases mortality risk

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity

Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration

Cardiorespiratory fitness and heart rate recovery predict sudden cardiac death independent of ejection fraction

A meta-analysis of genome-wide association studies identifies multiple longevity genes

New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders