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Author Details
Full Name
Aki S Havulinna
Affiliation
ORCID
Career Start Year
2004
Papers
183
H Index
58
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37500913
Greengenes2 unifies microbial data in a single reference tree.
Nat Biotechnol
2024
37853258
Author Correction: Greengenes2 unifies microbial data in a single reference tree.
Nat Biotechnol
2024
34643165
The validity of rheumatoid arthritis diagnoses in Finnish biobanks.
Scandinavian Journal of Rheumatology
2023
37808321
Advancing microbiome research with machine learning: key findings from the ML4Microbiome COST action.
2023
37873403
Microbiome-based risk prediction in incident heart failure: a community challenge.
medRxiv
2023
36653562
FinnGen provides genetic insights from a well-phenotyped isolated population.
Nature
2023
36829046
Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.
Nature
2023
36653560
Mono- and biallelic variant effects on disease at biobank scale.
Nature
2023
36653479
Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases.
Nat Med
2023
36653354
Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation.
Nat Commun
2023
36653343
Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.
Nat Commun
2023
36587850
The gut microbiome is a significant risk factor for future chronic lung disease.
J Allergy Clin Immunol
2023
37119735
Gut microbiome and atrial fibrillation-results from a large population-based study.
EBioMedicine
2023
36801832
Inflammatory proteomics profiling for prediction of incident atrial fibrillation.
2023
36602448
Risk prediction of atrial fibrillation and its complications in the community using hs troponin I.
2023
35100347
Gut Microbiome Composition Is Predictive of Incident Type 2 Diabetes in a Population Cohort of 5,572 Finnish Adults.
Diabetes Care
2022
36240095
Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke.
Neurology
2022
36097220
Genetic risk factors have a substantial impact on healthy life years.
Nat Med
2022
36295830
Substantial Fat Loss in Physique Competitors Is Characterized by Increased Levels of Bile Acids, Very-Long Chain Fatty Acids, and Oxylipins.
Metabolites
2022
35361620
A plasma metabolite score of three eicosanoids predicts incident type 2 diabetes: a prospective study in three independent cohorts.
BMJ Open Diabetes Research and Care
2022
35354069
Early prediction of incident liver disease using conventional risk factors and gut-microbiome-augmented gradient boosting.
Cell Metab
2022
36401251
Use of antibiotics and risk of type 2 diabetes, overweight and obesity: the Cardiovascular Risk in Young Finns Study and the national FINRISK study.
BMC Endocrine Disorders
2022
36114182
Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks.
Nat Commun
2022
35916366
Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans.
Elife
2022
34407993
Joint associations of depression, genetic susceptibility and the area of residence for coronary heart disease incidence.
J Epidemiol Community Health
2022
34784307
Comprehensive biomarker profiling of hypertension in 36â¿¿985 Finnish individuals.
Journal of Hypertension
2022
34479875
Efficient computation of Faith's phylogenetic diversity with applications in characterizing microbiomes.
Genome Res
2021
33491305
The Role of Inflammatory Cytokines as Intermediates in the Pathway from Increased Adiposity to Disease.
Obesity (Silver Spring)
2021
34081096
Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population.
JAMA Ophthalmol
2021
34020448
Associations of healthy food choices with gut microbiota profiles.
Am J Clin Nutr
2021
33909604
ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease.
PLoS Genet
2021
33798444
Association of structural variation with cardiometabolic traits in Finns.
Am J Hum Genet
2021
33526825
Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants.
Mol Psychiatry
2021
33458771
Risk prediction of atrial fibrillation in the community combining biomarkers and genetics.
Europace
2021
33773637
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies.
Lancet Neurol
2021
33611940
Polygenic Risk Scores Predict Hypertension Onset and Cardiovascular Risk.
Hypertension
2021
34099068
Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences.
Hum Genomics
2021
33661898
Changes in the fine-scale genetic structure of Finland through the 20th century.
PLoS Genet
2021
33822779
Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.
PLoS Genet
2021
33976176
Taxonomic signatures of cause-specific mortality risk in human gut microbiome.
Nat Commun
2021
33243845
Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health.
European Respiratory Journal
2021
33408166
Joint association between education and polygenic risk score for incident coronary heart disease events: a longitudinal population-based study of 26 203 men and women.
J Epidemiol Community Health
2021
33268560
Association of Circulating Metabolites in Plasma or Serum and Risk of Stroke: Meta-analysis From 7 Prospective Cohorts.
Neurology
2021
34668383
Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke.
J Am Heart Assoc
2021
34608296
Author Correction: Genetics of 35 blood and urine biomarkers in the UK Biobank.
Nat Genet
2021
31068116
The validity of heart failure diagnoses in the Finnish Hospital Discharge Register.
Scand J Public Health
2020
32066667
Genomic prediction of alcohol-related morbidity and mortality.
Translational Psychiatry
2020
32113648
Apolipoprotein A-I concentrations and risk of coronary artery disease: A Mendelian randomization study.
Atherosclerosis
2020
32154731
Polygenic Hyperlipidemias and Coronary Artery Disease Risk.
Circ Genom Precis Med
2020
32439900
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.
Nat Commun
2020
1 - 50 of 183
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