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Author Details

Samuli Ripatti
1997
285
90
PMIDPaper TitleJournal TitlePublished Year
36071625Marital status and genetic liability independently predict coronary heart disease incidence.Scand J Public Health2024
37419095Response to Li and Hopper.2023
37848354Novel Finnish-enriched variants causing severe hypercholesterolemia and their clinical impact on coronary artery disease.2023
37743161Effect of biological sex on human circulating lipidome: An overview of the literature.2023
37907536Genome-wide association analysis of plasma lipidome identifies 495 genetic associations.Nat Commun2023
36653562FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
37285119Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy.JAMA Cardiol2023
36829046Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
36653479Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases.Nat Med2023
36653477Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population.2023
36653354Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation.Nat Commun2023
36653343Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.Nat Commun2023
37211520Corrigendum to Childhood adversities are associated with shorter leukocyte telomere length at adult age in a population-based study [Psychoneuroendocrinology (2021) 130 105276].2023
36564914Association between genetic risk of alcohol consumption and alcohol-related morbidity and mortality under different alcohol policy conditions: Evidence from the Finnish alcohol price reduction of 2004.2023
37425837Metabolome-wide Mendelian randomization characterizes heterogeneous and shared causal effects of metabolites on human health.medRxiv2023
37425750Longitudinal multi-omics study reveals common etiology underlying association between plasma proteome and BMI trajectories in adolescent and young adult twins.2023
34411351Effects of PNPLA3 I148M on hepatic lipid and very-low-density lipoprotein metabolism in humans.Journal of Internal Medicine2022
35591975Genome-wide risk prediction of common diseases across ancestries in one million people.Cell Genom2022
36040803Postprandial metabolism of apolipoproteins B48, B100, C-III, and E in humans with APOC3 loss-of-function mutations.JCI insight2022
36347255Systematic comparison of family history and polygenic risk across 24 common diseases.American Journal of Human Genetics2022
35862124Increased Risk of Preeclampsia in Women With a Genetic Predisposition to Elevated Blood Pressure.Hypertension2022
36193934Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids.J Am Heart Assoc2022
35474963Multiparametric platform for profiling lipid trafficking in human leukocytes.Cell Rep Methods2022
35354965Polygenic scores in biomedical research.Nat Rev Genet2022
36055244Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk.Am J Hum Genet2022
35978133Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis.Commun Biol2022
37118290Immune system-wide Mendelian randomization and triangulation analyses support autoimmunity as a modifiable component in dementia-causing diseases.Nat Aging2022
36600884Effectiveness and feasibility of cardiovascular disease personalized prevention on high polygenic risk score subjects: a randomized controlled pilot study.2022
34407993Joint associations of depression, genetic susceptibility and the area of residence for coronary heart disease incidence.J Epidemiol Community Health2022
35301180A genome-wide association study of outcome from traumatic brain injury.EBioMedicine2022
34856119Multiomics and digital monitoring during lifestyle changes reveal independent dimensions of human biology and health.Cell Syst2022
34559723Polygenic Score for Physical Activity Is Associated with Multiple Common Diseases.Medicine and Science in Sports and Exercise2022
35130028How Communicating Polygenic and Clinical Risk for Atherosclerotic Cardiovascular Disease Impacts Health Behavior: an Observational Follow-up Study.Circulation. Genomic and precision medicine2022
34648375Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families.Cephalalgia2022
35104449Genetic Associations and Architecture of Asthma-COPD Overlap.Chest2022
35197564Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes.Communications Biology2022
29799308Genetic Influences on Patient-Oriented Outcomes in Traumatic Brain Injury: A Living Systematic Review of Non-Apolipoprotein E Single-Nucleotide Polymorphisms.J Neurotrauma2021
32064741Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.Addict Biol2021
32346736The relation of severe malocclusion to patients' mental and behavioral disorders, growth, and speech problems.European Journal of Orthodontics2021
32157176Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent.Mol Psychiatry2021
33491305The Role of Inflammatory Cytokines as Intermediates in the Pathway from Increased Adiposity to Disease.Obesity (Silver Spring)2021
33909604ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease.PLoS Genet2021
33798444Association of structural variation with cardiometabolic traits in Finns.Am J Hum Genet2021
34232692Clinical Conditions and Their Impact on Utility of Genetic Scores for Prediction of Acute Coronary Syndrome.Circ Genom Precis Med2021
33741697Accuracy of 1-Hour Plasma Glucose During the Oral Glucose Tolerance Test in Diagnosis of Type 2 Diabetes in Adults: A Meta-analysis.Diabetes Care2021
33846329Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.Nat Commun2021
33526825Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants.Mol Psychiatry2021
34051657Childhood adversities are associated with shorter leukocyte telomere length at adult age in a population-based study.Psychoneuroendocrinology2021
33730874Genome-Wide Association Study and Identification of a Protective Missense Variant on Lipoprotein(a) Concentration: Protective Missense Variant on Lipoprotein(a) Concentration-Brief Report.Arteriosclerosis, Thrombosis, and Vascular Biology2021
33661898Changes in the fine-scale genetic structure of Finland through the 20th century.PLoS Genet2021
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Co-authored papers 136
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Finnish Cardiovascular Research Center-Tampere - FCRCT, Tampere University
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Tampere University
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German Research Center for Cardiovascular Disease (DZHK)
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University of Oxford
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King's College London
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Erasmus University Medical Center
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Stanford University School of Medicine
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Harvard T.H. Chan School of Public Health
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