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Author Details
Full Name
Leo-Pekka Lyytik??inen
Affiliation
Tampere University
ORCID
Career Start Year
2009
Papers
200
H Index
61
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
38031635
Polygenic risk for schizophrenia, social dispositions, and pace of epigenetic aging: Results from the Young Finns Study.
Aging Cell
2024
38031635
Polygenic risk for schizophrenia, social dispositions, and pace of epigenetic aging: Results from the Young Finns Study.
Aging Cell
2024
37665031
Genetic risk scores associated with temperament clusters in Finnish depression patients.
Acta Neuropsychiatr
2024
38047377
Polygenic risk for schizophrenia predicting social trajectories in a general population sample.
Psychol Med
2024
37665031
Genetic risk scores associated with temperament clusters in Finnish depression patients.
Acta Neuropsychiatr
2024
38047377
Polygenic risk for schizophrenia predicting social trajectories in a general population sample.
Psychol Med
2024
36813803
Uncovering the complex genetic architecture of human plasma lipidome using machine learning methods.
Sci Rep
2023
38028628
Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.
Front Genet
2023
37770635
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.
Nat Genet
2023
36813803
Uncovering the complex genetic architecture of human plasma lipidome using machine learning methods.
Sci Rep
2023
37487461
Polygenic liabilities underlying job stress and exhaustion over a 10-year follow-up: A general population study.
Psychiatry Res
2023
38028628
Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.
Front Genet
2023
37487461
Polygenic liabilities underlying job stress and exhaustion over a 10-year follow-up: A general population study.
Psychiatry Res
2023
37770635
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.
Nat Genet
2023
35017526
C-type lectin receptor CLEC4A2 promotes tissue adaptation of macrophages and protects against atherosclerosis.
Nat Commun
2022
36050321
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.
Nat Commun
2022
35907279
High-risk ECG patterns in ST elevation myocardial infarction for mortality prediction.
J Electrocardiol
2022
35839706
The S1S2S3 electrocardiographic pattern - Prevalence and relation to cardiovascular and pulmonary diseases in the general population.
J Electrocardiol
2022
35961208
Long-term tracking and population characteristics of lipoprotein (a) in the Cardiovascular Risk in Young Finns Study.
Atherosclerosis
2022
35697829
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.
Commun Biol
2022
35505089
Magical thinking in individuals with high polygenic risk for schizophrenia but no non-affective psychoses-a general population study.
Mol Psychiatry
2022
35812313
Associations of Polymorphisms in the Peroxisome Proliferator-Activated Receptor Gamma Coactivator-1 Alpha Gene With Subsequent Coronary Heart Disease: An Individual-Level Meta-Analysis.
Front Physiol
2022
35533410
Interatrial block and P terminal force in the general population - Longitudinal changes, risk factors and prognosis.
J Electrocardiol
2022
35228283
Prevalence and long-term prognostic implications of prolonged QRS duration in left ventricular hypertrophy: a population-based observational cohort study.
BMJ Open
2022
35017526
C-type lectin receptor CLEC4A2 promotes tissue adaptation of macrophages and protects against atherosclerosis.
Nat Commun
2022
35077545
Mitochondrial genome-wide analysis of nuclear DNA methylation quantitative trait loci.
Hum Mol Genet
2022
35839706
The S1S2S3 electrocardiographic pattern - Prevalence and relation to cardiovascular and pulmonary diseases in the general population.
J Electrocardiol
2022
35505089
Magical thinking in individuals with high polygenic risk for schizophrenia but no non-affective psychoses-a general population study.
Mol Psychiatry
2022
35697829
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.
Commun Biol
2022
35533410
Interatrial block and P terminal force in the general population - Longitudinal changes, risk factors and prognosis.
J Electrocardiol
2022
35812313
Associations of Polymorphisms in the Peroxisome Proliferator-Activated Receptor Gamma Coactivator-1 Alpha Gene With Subsequent Coronary Heart Disease: An Individual-Level Meta-Analysis.
Front Physiol
2022
35907279
High-risk ECG patterns in ST elevation myocardial infarction for mortality prediction.
J Electrocardiol
2022
35961208
Long-term tracking and population characteristics of lipoprotein (a) in the Cardiovascular Risk in Young Finns Study.
Atherosclerosis
2022
36050321
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.
Nat Commun
2022
35228283
Prevalence and long-term prognostic implications of prolonged QRS duration in left ventricular hypertrophy: a population-based observational cohort study.
BMJ Open
2022
35077545
Mitochondrial genome-wide analysis of nuclear DNA methylation quantitative trait loci.
Hum Mol Genet
2022
32804416
Long-term outcome of intraventricular conduction delays in the general population.
Ann Noninvasive Electrocardiol
2021
36643994
Assessment of plasma ceramides as predictor for subclinical atherosclerosis.
Atheroscler Plus
2021
33491305
The Role of Inflammatory Cytokines as Intermediates in the Pathway from Increased Adiposity to Disease.
Obesity (Silver Spring)
2021
33911114
Adulthood blood levels of hsa-miR-29b-3p associate with preterm birth and adult metabolic and cognitive health.
Sci Rep
2021
34294131
Methylation status of nc886 epiallele reflects periconceptional conditions and is associated with glucose metabolism through nc886 RNAs.
Clin Epigenetics
2021
33859359
Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure.
Mol Psychiatry
2021
33897514
Functional Polymorphisms in Oxytocin and Dopamine Pathway Genes and the Development of Dispositional Compassion Over Time: The Young Finns Study.
Front Psychol
2021
33532862
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction.
Eur Heart J
2021
33893282
Publisher Correction: A meta-analysis of genome-wide association studies identifies multiple longevity genes.
Nat Commun
2021
34101137
Prehospital Adenosine Diphosphate Receptor Blocker Use, Culprit Artery Flow, and Mortality in STEMI: The MADDEC Study.
Clin Drug Investig
2021
33503553
Impedance plethysmography-based method in the assessment of subclinical atherosclerosis.
Atherosclerosis
2021
33436758
Examining the effect of mitochondrial DNA variants on blood pressure in two Finnish cohorts.
Sci Rep
2021
33137338
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline.
Kidney Int
2021
32975832
The prognostic significance of T-wave inversion according to ECG lead group during long-term follow-up in the general population.
Ann Noninvasive Electrocardiol
2021
1 - 50 of 400
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Collaborators
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Finnish Cardiovascular Research Center-Tampere - FCRCT, Tampere University
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Tampere University
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161
Olli T Raitakari
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Andr?? G Uitterlinden
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Jorma Viikari
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Albert V Smith
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Co-authored papers
54
Bruce M Psaty
Co-authored papers
53
Cornelia M van Duijn
University of Oxford
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Albert Hofman
Harvard T.H. Chan School of Public Health
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Eric Boerwinkle
Baylor College of Medicine
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50
Caroline Hayward
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49
Ruth J F Loos
Co-authored papers
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Alexander Teumer
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46
Jerome I Rotter
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Fernando Rivadeneira
University Medical Center Rotterdam
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45
Uwe V??lker
University Medicine
Co-authored papers
44
Annette Peters
Ludwig-Maximilians-Universitat Munchen
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42
Tõnu Esko
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Yongmei Liu
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Veikko Salomaa
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Oscar H Franco
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Pim van der Harst
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