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282 peer-reviewed articles • 49,195 peer-reviewed citations • Sorted by year • Download PDF (PDF by citations)
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1Value of Pharmacogenetic Testing Assessed with Real‐World Drug Utilization and Genotype Data4.79Citations (PDF)
2Evidence-based criteria for identifying at-risk individuals requiring liver disease screening4.54Citations (PDF)
3The impact of supplementing traditional risk information with polygenic risk score concerning type 2 diabetes and coronary heart disease on health behavior: a randomized controlled trial1.13Citations (PDF)
4Schizophrenia genetic risk and labour market outcomes in the Finnish general population: Are schizophrenia-related traits penalised or rewarded?
Comprehensive Psychiatry, 2025, 140, 152600
4.03Citations (PDF)
5Patterns of reproductive health in inflammatory rheumatic diseases and other immune-mediated diseases: a nationwide registry study
Rheumatology, 2024, 63, 2701-2710
1.912Citations (PDF)
6Deep learning-based prediction of one-year mortality in Finland is an accurate but unfair aging marker
Nature Aging, 2024, 4, 1014-1027
14.59Citations (PDF)
7Attention-Deficit/Hyperactivity Disorder Diagnoses in Finland During the COVID-19 Pandemic
JAMA Network Open, 2024, 7, e2418204
6.632Citations (PDF)
8ALT levels, alcohol use, and metabolic risk factors have prognostic relevance for liver-related outcomes in the general population
JHEP Reports, 2024, 6, 101172
4.517Citations (PDF)
9Divergent trends in the incidence and mortality of acute myocardial ischaemic syndrome, especially in women. Evidence from Finland in 1996–2021
Annals of Medicine, 2024, 56,
3.83Citations (PDF)
10Cross-sectionally Calculated Metabolic Aging Does Not Relate to Longitudinal Metabolic Changes—Support for Stratified Aging Models4.015Citations (PDF)
11Longitudinal metabolomics of increasing body-mass index and waist-hip ratio reveals two dynamic patterns of obesity pandemic3.013Citations (PDF)
12Data Resource Profile: Nationwide registry data for high-throughput epidemiology and machine learning (FinRegistry)4.926Citations (PDF)
13Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population2.90Citations (PDF)
14Waist-hip ratio is superior to BMI in predicting liver-related outcomes and synergizes with harmful alcohol use4.520Citations (PDF)
15Comprehensive biomarker profiling of hypertension in 36 985 Finnish individuals
Journal of Hypertension, 2022, 40, 579-587
2.120Citations (PDF)
16Longitudinal profiling of metabolic ageing trends in two population cohorts of young adults4.924Citations (PDF)
17Pharmacoepigenetics of hypertension: genome-wide methylation analysis of responsiveness to four classes of antihypertensive drugs using a double-blind crossover study design
Epigenetics, 2022, 17, 1432-1445
3.017Citations (PDF)
18Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes4.438Citations (PDF)
19Development and validation of a model to predict incident chronic liver disease in the general population: The CLivD score
Journal of Hepatology, 2022, 77, 302-311
4.271Citations (PDF)
20Circulating Metabolic Biomarkers Are Consistently Associated With Type 2 Diabetes Risk in Asian and European Populations4.025Citations (PDF)
21Association between mitochondrial DNA haplogroups J and K, serum branched-chain amino acids and lowered capability for endurance exercise2.20Citations (PDF)
22Psychosocial Effects of Receiving Genome-Wide Polygenic Risk Information Concerning Type 2 Diabetes and Coronary Heart Disease: A Randomized Controlled Trial2.313Citations (PDF)
23BMI is positively associated with accelerated epigenetic aging in twin pairs discordant for body mass index
Journal of Internal Medicine, 2022, 292, 627-640
7.375Citations (PDF)
24Abdominal obesity is key when evaluating interactions between alcohol use and obesity for liver disease
Journal of Hepatology, 2022, 77, S80-S81
4.21Citations (PDF)
25Economic evaluation of using polygenic risk score to guide risk screening and interventions for the prevention of type 2 diabetes in individuals with high overall baseline risk2.313Citations (PDF)
26Repurposed Antiviral Drugs for Covid-19 — Interim WHO Solidarity Trial Results34.52,315Citations (PDF)
27Association of Circulating Metabolites in Plasma or Serum and Risk of Stroke
Neurology, 2021, 96,
1.043Citations (PDF)
28Metabolic profiling of angiopoietin-like protein 3 and 4 inhibition: a drug-target Mendelian randomization analysis
European Heart Journal, 2021, 42, 1160-1169
2.270Citations (PDF)
29Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability13.7141Citations (PDF)
30Mitochondrial bioenergetic pathways in blood leukocyte transcriptome decrease after intensive weight loss but are rescued following weight regain in female physique athletes
FASEB Journal, 2021, 35,
0.67Citations (PDF)
31HDL-Mediated Cholesterol Efflux Associates with Incident Kidney Disease
Clinical Chemistry, 2021, 67, 689-691
1.11Citations (PDF)
32Changes in the fine-scale genetic structure of Finland through the 20th century
PLoS Genetics, 2021, 17, e1009347
3.216Citations (PDF)
33Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
JAMA Ophthalmology, 2021, 139, 762
6.19Citations (PDF)
34The Role of Inflammatory Cytokines as Intermediates in the Pathway from Increased Adiposity to Disease
Obesity, 2021, 29, 428-437
4.062Citations (PDF)
35Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke4.024Citations (PDF)
36Genome-Wide Association Study of Peripheral Artery Disease2.981Citations (PDF)
37A Web Portal for Communicating Polygenic Risk Score Results for Health Care Use—The P5 Study2.318Citations (PDF)
38Metabolic Biomarker Discovery for Risk of Peripheral Artery Disease Compared With Coronary Artery Disease: Lipoprotein and Metabolite Profiling of 31 657 Individuals From 5 Prospective Cohorts4.059Citations (PDF)
39Risks of Light and Moderate Alcohol Use in Fatty Liver Disease: Follow‐Up of Population Cohorts
Hepatology, 2020, 71, 835-848
10.1163Citations (PDF)
40Data-driven multivariate population subgrouping via lipoprotein phenotypes versus apolipoprotein B in the risk assessment of coronary heart disease
Atherosclerosis, 2020, 294, 10-15
1.514Citations (PDF)
41Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Nature Genetics, 2020, 52, 1314-1332
25.2180Citations (PDF)
42Obesity and alcohol intake modify the impact of genetic variants on the risk for incident liver disease in the general population
Journal of Hepatology, 2020, 73, S162-S163
4.20Citations (PDF)
43Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus2.910Citations (PDF)
44An epigenome-wide association study of metabolic syndrome and its components
Scientific Reports, 2020, 10,
3.443Citations (PDF)
45Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma
PLoS Genetics, 2020, 16, e1008682
3.248Citations (PDF)
46Identification, Heritability, and Relation With Gene Expression of Novel DNA Methylation Loci for Blood Pressure
Hypertension, 2020, 76, 195-205
6.663Citations (PDF)
47Glycosylation of immunoglobulin G is regulated by a large network of genes pleiotropic with inflammatory diseases
Science Advances, 2020, 6,
10.9129Citations (PDF)
48Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length6.5170Citations (PDF)
49Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant1.618Citations (PDF)
50A metabolic profile of all-cause mortality risk identified in an observational study of 44,168 individuals13.7331Citations (PDF)
51Intertumoral heterogeneity in patient-specific drug sensitivities in treatment-naïve glioblastoma
BMC Cancer, 2019, 19,
2.979Citations (PDF)
52Multivariate Genome-wide Association Analysis of a Cytokine Network Reveals Variants with Widespread Immune, Haematological, and Cardiometabolic Pleiotropy6.542Citations (PDF)
53Elevated serum alpha-1 antitrypsin is a major component of GlycA-associated risk for future morbidity and mortality
PLoS ONE, 2019, 14, e0223692
2.319Citations (PDF)
54Circulating metabolites and the risk of type 2 diabetes: a prospective study of 11,896 young adults from four Finnish cohorts
Diabetologia, 2019, 62, 2298-2309
7.5229Citations (PDF)
55Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland6.5114Citations (PDF)
56Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using Metabolomics
Endocrinology, 2019, 160, 1731-1742
2.526Citations (PDF)
57Food neophobia associates with poorer dietary quality, metabolic risk factors, and increased disease outcome risk in population-based cohorts in a metabolomics study4.771Citations (PDF)
58Direct Estimation of HDL-Mediated Cholesterol Efflux Capacity from Serum
Clinical Chemistry, 2019, 65, 1042-1050
1.119Citations (PDF)
59A multivariate linear model for investigating the association between gene-module co-expression and a continuous covariate0.40Citations (PDF)
60Substantial fat mass loss reduces low-grade inflammation and induces positive alteration in cardiometabolic factors in normal-weight individuals3.449Citations (PDF)
61A distinctive DNA methylation pattern in insufficient sleep3.456Citations (PDF)
62Feasibility study of using high‐throughput drug sensitivity testing to target recurrent glioblastoma stem cells for individualized treatment5.530Citations (PDF)
63Serum lipopolysaccharides predict advanced liver disease in the general population
JHEP Reports, 2019, 1, 345-352
4.541Citations (PDF)
64Resistance Training Induces Antiatherogenic Effects on Metabolomic Pathways0.89Citations (PDF)
65Transnational access to large prospective cohorts in Europe: Current trends and unmet needs
New Biotechnology, 2019, 49, 98-103
4.625Citations (PDF)
66Role of Academic Biobanks in Public–Private Partnerships in the European Biobanking and BioMolecular Resources Research Infrastructure Community1.411Citations (PDF)
67Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
Molecular Psychiatry, 2019, 25, 2392-2409
7.8111Citations (PDF)
68Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland6.568Citations (PDF)
69Cohort Profile: The National FINRISK Study4.9295Citations (PDF)
70Low galactosylation of IgG associates with higher risk for future diagnosis of rheumatoid arthritis during 10 years of follow-up4.185Citations (PDF)
71Sequential double cross-validation for assessment of added predictive ability in high-dimensional omic applications1.23Citations (PDF)
72Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders6.5430Citations (PDF)
73Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Nature Genetics, 2018, 50, 1412-1425
25.21,365Citations (PDF)
74Mendelian randomisation analysis of clustered causal effects of body mass on cardiometabolic biomarkers
BMC Bioinformatics, 2018, 19,
3.02Citations (PDF)
75Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation
Molecular Psychiatry, 2018, 25, 1859-1875
7.8234Citations (PDF)
76Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles2.035Citations (PDF)
77Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions
Circulation, 2017, 135, 2336-2353
18.062Citations (PDF)
78Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease4.0111Citations (PDF)
79Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits6.5176Citations (PDF)
80Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors6.5617Citations (PDF)
81Exome-wide association study of plasma lipids in >300,000 individuals
Nature Genetics, 2017, 49, 1758-1766
25.2555Citations (PDF)
82CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits13.789Citations (PDF)
83Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
Lancet Neurology, The, 2017, 16, 898-907
17.9243Citations (PDF)
84Genetics in an isolated population like Finland: a different basis for genomic medicine?1.146Citations (PDF)
85Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney
Hypertension, 2017, 70,
6.6146Citations (PDF)
86Affective responses to sweet products and sweet solution in British and Finnish adults
Food Quality and Preference, 2017, 62, 128-136
4.322Citations (PDF)
87Large meta-analysis of genome-wide association studies identifies five loci for lean body mass13.7179Citations (PDF)
88Protective Low-Frequency Variants for Preeclampsia in the Fms Related Tyrosine Kinase 1 Gene in the Finnish Population
Hypertension, 2017, 70, 365-371
6.640Citations (PDF)
89Fine-Scale Genetic Structure in Finland
G3: Genes, Genomes, Genetics, 2017, 7, 3459-3468
1.9114Citations (PDF)
90The Effects of Intensive Weight Reduction on Body Composition and Serum Hormones in Female Fitness Competitors2.859Citations (PDF)
91An interaction map of circulating metabolites, immune gene networks, and their genetic regulation
Genome Biology, 2017, 18,
8.160Citations (PDF)
92Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Nature Genetics, 2017, 50, 26-41
25.2399Citations (PDF)
93Genetic Variants Contributing to Circulating Matrix Metalloproteinase 8 Levels and Their Association With Cardiovascular Diseases3.831Citations (PDF)
94Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults
PLoS Genetics, 2017, 13, e1006528
3.2188Citations (PDF)
95MixFit: Methodology for Computing Ancestry-Related Genetic Scores at the Individual Level and Its Application to the Estonian and Finnish Population Studies
PLoS ONE, 2017, 12, e0170325
2.39Citations (PDF)
96Low MMP-8/TIMP-1 reflects left ventricle impairment in takotsubo cardiomyopathy and high TIMP-1 may help to differentiate it from acute coronary syndrome
PLoS ONE, 2017, 12, e0173371
2.310Citations (PDF)
97Family history and perceived risk of diabetes, cardiovascular disease, cancer, and depression
Preventive Medicine, 2016, 90, 177-183
2.839Citations (PDF)
98Genetic Risk Scores Predict Recurrence of Acute Coronary Syndrome3.826Citations (PDF)
99Insomnia does not mediate or modify the association between MTNR1B risk variant rs10830963 and glucose levels
Diabetologia, 2016, 59, 1070-1072
7.53Citations (PDF)
100Genomic prediction of coronary heart disease
European Heart Journal, 2016, 37, 3267-3278
2.2330Citations (PDF)
101A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape13.792Citations (PDF)
102A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease12.5114Citations (PDF)
103Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA13.7771Citations (PDF)
104Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.23.443Citations (PDF)
105Heritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE Consortium
Sleep, 2016, 39, 1859-1869
0.942Citations (PDF)
106Metabolic profiling of pregnancy: cross-sectional and longitudinal evidence
BMC Medicine, 2016, 14,
7.1175Citations (PDF)
107USF1 deficiency activates brown adipose tissue and improves cardiometabolic health12.573Citations (PDF)
108Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome3.87Citations (PDF)
109Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease
Science, 2016, 351, 1166-1171
36.2523Citations (PDF)
110New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk13.7285Citations (PDF)
111Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels13.7177Citations (PDF)
112Metabolomic Profiling of Statin Use and Genetic Inhibition of HMG-CoA Reductase2.3195Citations (PDF)
113The Detection of Metabolite-Mediated Gene Module Co-Expression Using Multivariate Linear Models
PLoS ONE, 2016, 11, e0150257
2.37Citations (PDF)
114Genome-Wide Meta-Analysis of Sciatica in Finnish Population
PLoS ONE, 2016, 11, e0163877
2.328Citations (PDF)
115Appetitive traits as behavioural pathways in genetic susceptibility to obesity: a population-based cross-sectional study3.459Citations (PDF)
116The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
PLoS Genetics, 2015, 11, e1005378
3.2405Citations (PDF)
117Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation
PLoS Genetics, 2015, 11, e1005230
3.285Citations (PDF)
118Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population
PLoS ONE, 2015, 10, e0140576
2.36Citations (PDF)
119Adiposity as a cause of cardiovascular disease: a Mendelian randomization study4.9140Citations (PDF)
120Sex hormone-binding globulin associations with circulating lipids and metabolites and the risk for type 2 diabetes: observational and causal effect estimates4.9100Citations (PDF)
121Genetic causal beliefs about morbidity: associations with health behaviors and health outcome beliefs about behavior changes between 1982–2002 in the Finnish population
BMC Public Health, 2015, 15,
3.13Citations (PDF)
122Gene × dietary pattern interactions in obesity: analysis of up to 68 317 adults of European ancestry
Human Molecular Genetics, 2015, 24, 4728-4738
2.996Citations (PDF)
123New genetic loci link adipose and insulin biology to body fat distribution
Nature, 2015, 518, 187-196
37.91,599Citations (PDF)
124Genetic studies of body mass index yield new insights for obesity biology
Nature, 2015, 518, 197-206
37.94,562Citations (PDF)
125Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu4.9468Citations (PDF)
126Metabolite Profiling and Cardiovascular Event Risk
Circulation, 2015, 131, 774-785
18.0666Citations (PDF)
127Age- and Sex-Specific Causal Effects of Adiposity on Cardiovascular Risk Factors
Diabetes, 2015, 64, 1841-1852
4.272Citations (PDF)
128Cell Specific eQTL Analysis without Sorting Cells
PLoS Genetics, 2015, 11, e1005223
3.2129Citations (PDF)
129The impact of low-frequency and rare variants on lipid levels
Nature Genetics, 2015, 47, 589-597
25.2348Citations (PDF)
130Genetically Determined Height and Coronary Artery Disease
New England Journal of Medicine, 2015, 372, 1608-1618
34.5250Citations (PDF)
131A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
Nature Genetics, 2015, 47, 1121-1130
25.22,547Citations (PDF)
132Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans
PLoS ONE, 2015, 10, e0119752
2.373Citations (PDF)
133Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population
PLoS Genetics, 2014, 10, e1004494
3.2396Citations (PDF)
134Chromosome X-Wide Association Study Identifies Loci for Fasting Insulin and Height and Evidence for Incomplete Dosage Compensation
PLoS Genetics, 2014, 10, e1004127
3.277Citations (PDF)
135High Risk Population Isolate Reveals Low Frequency Variants Predisposing to Intracranial Aneurysms
PLoS Genetics, 2014, 10, e1004134
3.258Citations (PDF)
136Amerindian-specific regions under positive selection harbour new lipid variants in Latinos13.799Citations (PDF)
137Genetic Determinants of Circulating Interleukin-1 Receptor Antagonist Levels and Their Association With Glycemic Traits
Diabetes, 2014, 63, 4343-4359
4.244Citations (PDF)
138FTO genetic variants, dietary intake and body mass index: insights from 177 330 individuals
Human Molecular Genetics, 2014, 23, 6961-6972
2.9154Citations (PDF)
139Meta‐analysis on blood transcriptomic studies identifies consistently coexpressed protein–protein interaction modules as robust markers of human aging
Aging Cell, 2014, 13, 216-225
6.846Citations (PDF)
140Neolithic dairy farming at the extreme of agriculture in northern Europe2.4102Citations (PDF)
141DataSHIELD: taking the analysis to the data, not the data to the analysis4.9267Citations (PDF)
142Biomarker Profiling by Nuclear Magnetic Resonance Spectroscopy for the Prediction of All-Cause Mortality: An Observational Study of 17,345 Persons
PLoS Medicine, 2014, 11, e1001606
8.0346Citations (PDF)
143Identifying flavor preference subgroups. Genetic basis and related eating behavior traits
Appetite, 2014, 75, 1-10
2.874Citations (PDF)
144Genome‐wide association study of sleep duration in the Finnish population
Journal of Sleep Research, 2014, 23, 609-618
3.849Citations (PDF)
145A metabolic view on menopause and ageing13.7258Citations (PDF)
146Low-Expression Variant of Fatty Acid–Binding Protein 4 Favors Reduced Manifestations of Atherosclerotic Disease and Increased Plaque Stability3.837Citations (PDF)
147Defining the role of common variation in the genomic and biological architecture of adult human height
Nature Genetics, 2014, 46, 1173-1186
25.21,987Citations (PDF)
148Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
Nature Genetics, 2014, 46, 826-836
25.2327Citations (PDF)
149Cortical 11C-PIB Uptake is Associated with Age, APOE Genotype, and Gender in “Healthy Aging”2.633Citations (PDF)
150BBMRI-ERIC as a resource for pharmaceutical and life science industries: the development of biobank-based Expert Centres3.082Citations (PDF)
151Discovery and refinement of loci associated with lipid levels
Nature Genetics, 2013, 45, 1274-1283
25.23,055Citations (PDF)
152Common variants associated with plasma triglycerides and risk for coronary artery disease
Nature Genetics, 2013, 45, 1345-1352
25.2854Citations (PDF)
153Age-dependent interaction of apolipoprotein E gene with eastern birthplace in Finland affects severity of coronary atherosclerosis and risk of fatal myocardial infarction—Helsinki Sudden Death Study
Annals of Medicine, 2013, 45, 213-219
3.84Citations (PDF)
154Midlife cardiovascular risk factors and late cognitive impairment5.361Citations (PDF)
155Systematic identification of trans eQTLs as putative drivers of known disease associations
Nature Genetics, 2013, 45, 1238-1243
25.21,696Citations (PDF)
156Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
Nature Genetics, 2013, 45, 501-512
25.2660Citations (PDF)
157Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population
Annals of Medicine, 2013, 45, 328-335
3.821Citations (PDF)
158Data harmonization and federated analysis of population-based studies: the BioSHaRE project3.1133Citations (PDF)
159Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits
PLoS Genetics, 2013, 9, e1003500
3.2425Citations (PDF)
160The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis
PLoS Medicine, 2013, 10, e1001474
8.0196Citations (PDF)
161Midlife Sleep Characteristics Associated with Late Life Cognitive Function
Sleep, 2013, 36, 1533-1541
0.9164Citations (PDF)
162A polymorphism in the protein kinase C gene PRKCB is associated with α2-adrenoceptor-mediated vasoconstriction1.25Citations (PDF)
163The Molecular Genetic Architecture of Self-Employment
PLoS ONE, 2013, 8, e60542
2.345Citations (PDF)
164Novel Loci for Metabolic Networks and Multi-Tissue Expression Studies Reveal Genes for Atherosclerosis
PLoS Genetics, 2012, 8, e1002907
3.2182Citations (PDF)
165Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways
Nature Genetics, 2012, 44, 991-1005
25.2811Citations (PDF)
166Cohort Profile: The Corogene study4.962Citations (PDF)
167A common variant near the KCNJ2 gene is associated with T-peak to T-end interval
Heart Rhythm, 2012, 9, 1099-1103
2.78Citations (PDF)
168Genome-wide association study identifies multiple loci influencing human serum metabolite levels
Nature Genetics, 2012, 44, 269-276
25.2554Citations (PDF)
169Detailed metabolic and genetic characterization reveals new associations for 30 known lipid loci
Human Molecular Genetics, 2012, 21, 1444-1455
2.999Citations (PDF)
170Genetic contribution to sour taste preference
Appetite, 2012, 58, 687-694
2.840Citations (PDF)
171Mortality Rate Increases Steeply With Nonadherence to Statin Therapy in Patients With Acute Coronary Syndrome2.035Citations (PDF)
172A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
Nature Genetics, 2012, 44, 659-669
25.2838Citations (PDF)
173Large-scale association analysis identifies new risk loci for coronary artery disease
Nature Genetics, 2012, 45, 25-33
25.21,579Citations (PDF)
174Bayesian Variable Selection in Searching for Additive and Dominant Effects in Genome-Wide Data
PLoS ONE, 2012, 7, e29115
2.312Citations (PDF)
175Common Genetic Variants Associated with Sudden Cardiac Death: The FinSCDgen Study
PLoS ONE, 2012, 7, e41675
2.339Citations (PDF)
176Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels
Circulation, 2011, 123, 731-738
18.0495Citations (PDF)
177Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile
Nature Genetics, 2011, 43, 753-760
25.2316Citations (PDF)
178Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Nature, 2011, 478, 103-109
37.92,015Citations (PDF)
179Comprehensive catalog of European biobanks
Nature Biotechnology, 2011, 29, 795-797
29.886Citations (PDF)
180C-reactive protein-associated genetic variants and cancer risk: Findings from FINRISK 1992, FINRISK 1997 and Health 2000 studies
European Journal of Cancer, 2011, 47, 404-412
4.950Citations (PDF)
181Genome-wide association approaches for identifying loci for human height genes5.110Citations (PDF)
182Shared Genetic Background for Regulation of Mood and Sleep: Association of GRIA3 with Sleep Duration in Healthy Finnish Women
Sleep, 2011, 34, 1309-1316
0.928Citations (PDF)
183Astringency Perception and Heritability Among Young Finnish Twins
Chemosensory Perception, 2011, 4, 134-144
0.318Citations (PDF)
184CRP gene variation affects early development of Alzheimer's disease-related plaques9.015Citations (PDF)
185Associations of Nicotine Intake Measures With CHRN Genes in Finnish Smokers2.317Citations (PDF)
186Common Genetic Variants, QT Interval, and Sudden Cardiac Death in a Finnish Population-Based Study3.852Citations (PDF)
187A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol
PLoS Genetics, 2011, 7, e1002333
3.231Citations (PDF)
188Midlife Alcohol Consumption and Later Risk of Cognitive Impairment: A Twin Follow-up Study2.633Citations (PDF)
189Genetic polymorphism of the C-reactive protein (CRP) gene and a deep infection focus determine maximal serum CRP level in Staphylococcus aureus bacteremia2.616Citations (PDF)
190Genetic variation of the interleukin-1 family and nongenetic factors determining the interleukin-1 receptor antagonist phenotypes9.117Citations (PDF)
191Biological, clinical and population relevance of 95 loci for blood lipids
Nature, 2010, 466, 707-713
37.93,482Citations (PDF)
192Hundreds of variants clustered in genomic loci and biological pathways affect human height
Nature, 2010, 467, 832-838
37.91,892Citations (PDF)
193Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior
Nature Genetics, 2010, 42, 448-453
25.2678Citations (PDF)
194Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
Nature Genetics, 2010, 42, 949-960
25.2906Citations (PDF)
195Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Nature Genetics, 2010, 42, 937-948
25.22,805Citations (PDF)
196Genetic Association and Interaction Analysis of USF1 and APOA5 on Lipid Levels and Atherosclerosis6.044Citations (PDF)
197European lactase persistence genotype shows evidence of association with increase in body mass index
Human Molecular Genetics, 2010, 19, 1129-1136
2.960Citations (PDF)
198Common Variants at 10 Genomic Loci Influence Hemoglobin A1C Levels via Glycemic and Nonglycemic Pathways
Diabetes, 2010, 59, 3229-3239
4.2430Citations (PDF)
199An Immune Response Network Associated with Blood Lipid Levels
PLoS Genetics, 2010, 6, e1001113
3.2120Citations (PDF)
200Birthplace in area with high coronary heart disease mortality predicts the severity of coronary atherosclerosis among middle-aged Finnish men who had migrated to capital area: The Helsinki Sudden Death Study
Annals of Medicine, 2010, 42, 286-295
3.84Citations (PDF)
201New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Nature Genetics, 2010, 42, 105-116
25.22,123Citations (PDF)
202A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses
Lancet, The, 2010, 376, 1393-1400
62.1534Citations (PDF)
203Metabonomic, transcriptomic, and genomic variation of a population cohort6.7247Citations (PDF)
204Food Neophobia in Young Adults: Genetic Architecture and Relation to Personality, Pleasantness and Use Frequency of Foods, and Body Mass Index—A Twin Study
Behavior Genetics, 2010, 41, 512-521
1.3163Citations (PDF)
205ADAM8 and its single nucleotide polymorphism 2662 T/G are associated with advanced atherosclerosis and fatal myocardial infarction: Tampere vascular study
Annals of Medicine, 2009, 41, 497-507
3.822Citations (PDF)
206Birthplace predicts risk for prehospital sudden cardiac death in middle-aged men who migrated to metropolitan area: The Helsinki Sudden Death Study
Annals of Medicine, 2009, 41, 57-65
3.811Citations (PDF)
207Association of Variation in the Interleukin-1 Gene Family with Diabetes and Glucose Homeostasis4.038Citations (PDF)
208Association of serum cotinine level with a cluster of three nicotinic acetylcholine receptor genes (CHRNA3/CHRNA5/CHRNB4) on chromosome 15
Human Molecular Genetics, 2009, 18, 4007-4012
2.9155Citations (PDF)
209OSBPL10, a novel candidate gene for high triglyceride trait in dyslipidemic Finnish subjects, regulates cellular lipid metabolism3.760Citations (PDF)
210Genome-wide association study identifies eight loci associated with blood pressure
Nature Genetics, 2009, 41, 666-676
25.21,158Citations (PDF)
211A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
Nature Genetics, 2009, 41, 1182-1190
25.2509Citations (PDF)
212Genetic and Environmental Contributions to Perceived Intensity and Pleasantness of Androstenone Odor: An International Twin Study
Chemosensory Perception, 2008, 1, 34-42
0.322Citations (PDF)
213Environmental Effects Exceed Genetic Effects on Perceived Intensity and Pleasantness of Several Odors: A Three-Population Twin Study
Behavior Genetics, 2008, 38, 484-492
1.338Citations (PDF)
214Genome-wide search for QTLs for apolipoprotein A-I level in elderly Swedish DZ twins: evidence of female-specific locus on 15q11–133.00Citations (PDF)
215Evaluation of HapMap data in six populations of European descent3.021Citations (PDF)
216Self‐Ratings of Olfactory Function Reflect Odor Annoyance Rather than Olfactory Acuity
Laryngoscope, 2008, 118, 2212-2217
1.451Citations (PDF)
217Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs3.013Citations (PDF)
218Genetic and environmental contributions to food use patterns of young adult twins
Physiology and Behavior, 2008, 93, 235-242
2.291Citations (PDF)
219Association Analysis of Allelic Variants of USF1 in Coronary Atherosclerosis6.027Citations (PDF)
220Interactions of Functional Apolipoprotein E Gene Promoter Polymorphisms With Smoking on Aortic Atherosclerosis3.812Citations (PDF)
221The Three-Factor Eating Questionnaire, body mass index, and responses to sweet and salty fatty foods: a twin study of genetic and environmental associations4.7187Citations (PDF)
222Gender Differences in Genetic Risk Profiles for Cardiovascular Disease
PLoS ONE, 2008, 3, e3615
2.388Citations (PDF)
223Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
Nature Genetics, 2008, 41, 47-55
25.2794Citations (PDF)
224Genome-wide linkage screen for stature and body mass index in 3.032 families: evidence for sex- and population-specific genetic effects3.016Citations (PDF)
225Combined Genome Scans for Body Stature in 6,602 European Twins: Evidence for Common Caucasian Loci
PLoS Genetics, 2007, 3, e97
3.2153Citations (PDF)
226Combined Effects of Thrombosis Pathway Gene Variants Predict Cardiovascular Events
PLoS Genetics, 2007, 3, e120
3.226Citations (PDF)
227Sweet taste preferences are partly genetically determined: identification of a trait locus on chromosome 164.7178Citations (PDF)
228Same genetic components underlie different measures of sweet taste preference4.7107Citations (PDF)
229Food neophobia shows heritable variation in humans
Physiology and Behavior, 2007, 91, 573-578
2.2157Citations (PDF)
230Age-dependent association between hepatic lipase gene C-480T polymorphism and the risk of pre-hospital sudden cardiac death: The Helsinki Sudden Death Study
Atherosclerosis, 2007, 192, 421-427
1.512Citations (PDF)
231Genetic component of identification, intensity and pleasantness of odours: a Finnish family study3.040Citations (PDF)
232Variation in the selenoprotein S gene locus is associated with coronary heart disease and ischemic stroke in two independent Finnish cohorts
Human Genetics, 2007, 122, 355-365
2.9102Citations (PDF)
233Platelet GPIbα, GPIV and vWF polymorphisms and fatal pre-hospital MI among middle-aged men1.99Citations (PDF)
234Same genetic components underlie different measures of sweet taste preference4.749Citations (PDF)
235Risk Alleles of USF1 Gene Predict Cardiovascular Disease of Women in Two Prospective Studies
PLoS Genetics, 2006, 2, e69
3.251Citations (PDF)
236Lessons from studying monogenic disease for common disease
Human Molecular Genetics, 2006, 15, R67-R74
2.988Citations (PDF)
237Genetics of Platelet Glycoprotein Receptors: Risk of Thrombotic Events and Pharmacogenetic Implications1.70Citations (PDF)
238Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q
Human Molecular Genetics, 2004, 13, 1693-1702
2.974Citations (PDF)
239Dopamine D3 receptor gene polymorphisms, blood pressure and nephropathy in type 1 diabetic patients0.811Citations (PDF)
240MORGAM (an international pooling of cardiovascular cohorts)4.9116Citations (PDF)
241Platelet membrane collagen receptor glycoprotein VI polymorphism is associated with coronary thrombosis and fatal myocardial infarction in middle-aged men
Atherosclerosis, 2004, 176, 95-99
1.564Citations (PDF)
242Association of paraoxonase-1 M55L genotype and alcohol consumption with coronary atherosclerosis6.74Citations (PDF)
243Polymorphisms in the nephrin gene and diabetic nephropathy in type 1 diabetic patients
Kidney International, 2003, 63, 1205-1210
5.320Citations (PDF)
244A Functional variant of the iNOS gene flanking region is associated with LAD coronary artery disease: an autopsy study3.08Citations (PDF)
245Myeloperoxidase Gene Variation as a Determinant of Atherosclerosis Progression in the Abdominal and Thoracic Aorta: An Autopsy Study
Laboratory Investigation, 2003, 83, 919-925
3.235Citations (PDF)
246Variation in the alpha2B-adrenoceptorgene as a risk factor for prehospitalfatal myocardial infarction and sudden cardiac death2.399Citations (PDF)
247Smoking-dependent association between paraoxonase 1 M/L55 genotype and coronary atherosclerosis in males: an autopsy study
Atherosclerosis, 2003, 171, 31-37
1.58Citations (PDF)
248The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories
Human Molecular Genetics, 2003, 12, 51-59
2.9114Citations (PDF)
249Evidence of susceptibility loci on 4q32 and 16p12 for bipolar disorder
Human Molecular Genetics, 2003, 12, 1907-1915
2.970Citations (PDF)
250Spline Methods for the Comparison of Physical and Genetic Maps1.57Citations (PDF)
251Platelet collagen receptor GPIa (C807T/HPA-5) haplotype is not associated with an increased risk of fatal coronary events in middle-aged men
Atherosclerosis, 2002, 165, 111-118
1.511Citations (PDF)
252ACE gene and physical activity, blood pressure, and hypertension: a population study in Finland
Journal of Applied Physiology, 2002, 92, 2508-2512
2.835Citations (PDF)
253Coronary artery wall atherosclerosis in relation to the estrogen receptor 1 gene polymorphism: an autopsy study3.791Citations (PDF)
254Association of the endothelial nitric oxide synthase gene polymorphism with risk of coronary artery disease and myocardial infarction in middle-aged men3.726Citations (PDF)
255Polymorphisms within the tumor necrosis factor locus and prevalence of coronary artery disease in middle-aged men
Atherosclerosis, 2001, 154, 691-697
1.5110Citations (PDF)
256The GPIIIa (β3 integrin) PlA polymorphism in the early development of coronary atherosclerosis
Atherosclerosis, 2001, 154, 721-727
1.543Citations (PDF)
257Promoter polymorphism of the CD14 endotoxin receptor gene as a risk factor for alcoholic liver disease
Hepatology, 2001, 33, 1148-1153
10.1130Citations (PDF)
258Utility of the Arg/Gln polymorphism of the factor VII (FVII) gene, serum lipid levels and body mass index in the prediction of the FVII:C and FVII:Ag in North Karelia; a cross-sectional and prospective study1.08Citations (PDF)
259Testing Genetic Susceptibility Loci for Alcoholic Heart Muscle Disease2.511Citations (PDF)
260Dissecting a population genome for targeted screening of disease mutations
Human Molecular Genetics, 2001, 10, 2961-2972
2.955Citations (PDF)
261Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings
Journal of Hypertension, 2000, 18, 1579-1585
2.1104Citations (PDF)
262Heritability and risk factors of uterine fibroids — The Finnish Twin Cohort Study
Maturitas, 2000, 37, 15-26
2.9134Citations (PDF)
263Apolipoprotein E Variation at the Sequence Haplotype Level: Implications for the Origin and Maintenance of a Major Human Polymorphism6.5414Citations (PDF)
264Glycoprotein IIIa PlA1/A2 polymorphism and sudden cardiac death2.361Citations (PDF)
265Association of FXIII Val34Leu with decreased risk of myocardial infarction in Finnish males
Atherosclerosis, 1999, 142, 295-300
1.5123Citations (PDF)
266The GPIIIa PlA polymorphism in the progression of abdominal aortic atherosclerosis
Atherosclerosis, 1999, 147, 55-60
1.514Citations (PDF)
267Long-Extension PCR to Detect Deleted Mitochondrial DNA Molecules Is Compromized by Technical Artefacts2.116Citations (PDF)
268Dual Origins of Finns Revealed by Y Chromosome Haplotype Variation6.5165Citations (PDF)
269Haplotype Structure and Population Genetic Inferences from Nucleotide-Sequence Variation in Human Lipoprotein Lipase6.5440Citations (PDF)
270Array-based multiplex analysis of candidate genes reveals two independent and additive genetic risk factors for myocardial infarction in the Finnish population
Human Molecular Genetics, 1998, 7, 1453-1462
2.9101Citations (PDF)
271Polymorphism in the cytochrome P450 2E1 gene and the risk of alcoholic liver disease
Journal of Hepatology, 1997, 26, 55-61
4.244Citations (PDF)
272Angiotensin-converting enzyme genotypes in the high- and low-risk area for coronary heart disease in Finland
Genetic Epidemiology, 1995, 12, 391-399
3.120Citations (PDF)
273Early perivenular fibrogenesis - precirrhotic lesions among moderate alcohol consumers and chronic alcoholics
Journal of Hepatology, 1995, 23, 524-531
4.259Citations (PDF)
274Abuse of Alcohol in Sudden Out-of-Hospital Deaths in Finland2.531Citations (PDF)
275Alzheimer and cardiovascular genetic scores and cognition: the FINGER randomized controlled trial
Brain, 0, 149, 644-652
8.41Citations (PDF)
276Towards modeling evolving longitudinal health trajectories with a transformer-based deep learning model
Annals of Epidemiology, 0, 111, 30-43
1.73Citations (PDF)
277Genetic predisposition for morningness-eveningness and economic disadvantage: Evidence from Finland over 25 years
Sleep Medicine, 0, 136, 106811
1.64Citations (PDF)
278Developing risk prediction models for type 2 diabetes and assessing the role of circulating metabolic biomarkers in five independent Finnish cohorts with over 22,000 individuals3.61Citations (PDF)
279Real-world comparative effectiveness of SARS-CoV-2 primary vaccination campaigns against SARS-CoV-2 infections: a federated observational study emulating a target trial in three nations0.30Citations (PDF)
280The proteomic profile of leisure time physical activity across two decades: implications for future cardiovascular risk and mortality2.01Citations (PDF)
281Polygenic Risks for Mood Disorders and Economic Well‐being: Study of Finnish Cohorts4.00Citations (PDF)
282Supplementing Disease Risk Information for Type 2 Diabetes and Coronary Heart Disease with Polygenic Risk Scores: Testing a Health Action Process Approach–Inspired Path Model to Predict Health Behavior1.30Citations (PDF)