Markus Perola

Q: What Schools Are Affiliated With Markus Perola

Markus Perola is affiliated with the following schools: Tampere University, University of Tartu, University of California, Los Angeles, Massachusetts General Hospital, University of Helsinki

Markus Perola's AcademicInfluence.com Rankings

Markus Perola

Philosophy

#8957

World Rank

#12444

Historical Rank

Logic

#5962

World Rank

#7428

Historical Rank

philosophy Degrees

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Philosophy

Markus Perola's Degrees

Doctorate Medicine University of Helsinki
PhD Medical Science University of Helsinki

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Markus Perola's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (2010) (3485)
Discovery and Refinement of Loci Associated with Lipid Levels (2013) (2475)
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (2010) (2087)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (2010) (2011)
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study (2012) (2002)
Hundreds of variants clustered in genomic loci and biological pathways affect human height (2010) (1961)
Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk (2011) (1928)
Defining the role of common variation in the genomic and biological architecture of adult human height (2014) (1805)
Systematic identification of trans eQTLs as putative drivers of known disease associations (2013) (1593)
A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease (2015) (1567)
Large-scale association analysis identifies new risk loci for coronary artery disease (2012) (1507)
New genetic loci link adipose and insulin biology to body fat distribution (2014) (1227)
Genome-wide association study identifies eight loci associated with blood pressure (2009) (1225)
Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index (2010) (1179)
Genome-wide association study identifies 74 loci associated with educational attainment (2016) (1114)
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts (2009) (909)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) (897)
GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (2013) (803)
Common variants associated with plasma triglycerides and risk for coronary artery disease (2013) (767)
Identification of seven loci affecting mean telomere length and their association with disease (2013) (761)
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) (758)
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance (2012) (756)
Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans (2015) (724)
Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior (2010) (688)
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations (2012) (678)
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (659)
Heritability of adult body height: a comparative study of twin cohorts in eight countries. (2003) (644)
Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations (2009) (617)
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) (568)
Genome-wide association study identifies multiple loci influencing human serum metabolite levels (2012) (552)
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium (2009) (551)
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2015) (532)
A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses (2010) (531)
Rare and low-frequency coding variants alter human adult height (2016) (511)
Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels (2011) (476)
Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase. (1998) (473)
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA (2016) (471)
Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals (2012) (459)
Mapping the human genetic architecture of COVID-19 (2021) (455)
Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis (2018) (451)
The transcriptional landscape of age in human peripheral blood (2015) (450)
Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease (2016) (434)
Exome-wide association study of plasma lipids in >300,000 individuals (2017) (428)
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk (2017) (428)
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (421)
The prevalence of metabolic syndrome and metabolically healthy obesity in Europe: a collaborative analysis of ten large cohort studies (2014) (419)
Metabolite profiling and cardiovascular event risk: a prospective study of 3 population-based cohorts. (2015) (401)
Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism. (2000) (391)
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function (2016) (388)
Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits (2013) (365)
Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) (348)
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals (2016) (347)
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile (2011) (313)
Sequence variants at CHRNB 3 – CHRNA 6 and CYP 2 A 6 affect smoking behavior (2010) (312)
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. (2016) (309)
Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis (2012) (302)
The impact of low-frequency and rare variants on lipid levels (2015) (300)
Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders (2013) (299)
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) (294)
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure (2020) (288)
Biomarker Profiling by Nuclear Magnetic Resonance Spectroscopy for the Prediction of All-Cause Mortality: An Observational Study of 17,345 Persons (2014) (284)
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression (2021) (284)
Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited (2011) (273)
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu. (2015) (273)
Metabonomic, transcriptomic, and genomic variation of a population cohort (2010) (271)
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization (2014) (260)
A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) (252)
Genome-wide analysis identifies 12 loci influencing human reproductive behavior (2016) (250)
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk (2016) (242)
Genomic prediction of coronary heart disease (2016) (241)
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension (2016) (234)
Dual origins of Finns revealed by Y chromosome haplotype variation. (1998) (223)
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. (2018) (221)
Genetically determined height and coronary artery disease. (2015) (220)
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. (2017) (212)
The Three-Factor Eating Questionnaire, body mass index, and responses to sweet and salty fatty foods: a twin study of genetic and environmental associations. (2008) (210)
Genome-Wide Screen for Metabolic Syndrome Susceptibility Loci Reveals Strong Lipid Gene Contribution But No Evidence for Common Genetic Basis for Clustering of Metabolic Syndrome Traits (2012) (204)
The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis (2013) (199)
Genetic evidence of assortative mating in humans (2017) (199)
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure underpinning obesity (2017) (193)
Sweet taste preferences are partly genetically determined: identification of a trait locus on chromosome 16. (2007) (187)
Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study. (2009) (187)
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study (2011) (185)
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland. (2000) (184)
A metabolic view on menopause and ageing (2014) (184)
Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers (2020) (182)
Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertension. (1999) (177)
Cohort Profile: The National FINRISK Study. (2018) (177)
Combined Genome Scans for Body Stature in 6,602 European Twins: Evidence for Common Caucasian Loci (2007) (175)
Age-dependent association of apolipoprotein E genotype with coronary and aortic atherosclerosis in middle-aged men: an autopsy study. (1999) (175)
Novel Loci for Metabolic Networks and Multi-Tissue Expression Studies Reveal Genes for Atherosclerosis (2012) (174)
Genome‐wide linkage analysis for human longevity: Genetics of Healthy Aging Study (2013) (174)
Association of serum cotinine level with a cluster of three nicotinic acetylcholine receptor genes (CHRNA3/CHRNA5/CHRNB4) on chromosome 15. (2009) (173)
Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1 (2011) (172)
Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation (2018) (171)
DataSHIELD: taking the analysis to the data, not the data to the analysis (2014) (170)
Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humans. (2007) (167)
Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels. (1999) (164)
Meta‐Analysis of Genome‐wide Linkage Studies in BMI and Obesity (2007) (159)
The Biomarker GlycA Is Associated with Chronic Inflammation and Predicts Long-Term Risk of Severe Infection. (2015) (156)
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis (2017) (156)
Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies (2010) (154)
Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (153)
Metabolomic Profiling of Statin Use and Genetic Inhibition of HMG-CoA Reductase (2016) (151)
FTO genetic variants, dietary intake and body mass index: insights from 177,330 individuals. (2014) (151)
Promoter polymorphism of the CD14 endotoxin receptor gene as a risk factor for alcoholic liver disease (2001) (149)
An Immune Response Network Associated with Blood Lipid Levels (2010) (148)
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels (2016) (147)
Food Neophobia in Young Adults: Genetic Architecture and Relation to Personality, Pleasantness and Use Frequency of Foods, and Body Mass Index—A Twin Study (2011) (146)
Toward a roadmap in global biobanking for health (2012) (146)
Directional dominance on stature and cognition in diverse human populations (2015) (144)
Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances (2018) (144)
Gender Differences in Genetic Risk Profiles for Cardiovascular Disease (2008) (143)
The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories. (2003) (141)
Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits (2018) (139)
A metabolic profile of all-cause mortality risk identified in an observational study of 44,168 individuals (2019) (139)
Genome‐wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings (2000) (139)
The Molecular Genetic Architecture of Self-Employment (2013) (137)
Food neophobia shows heritable variation in humans (2007) (137)
MORGAM (an international pooling of cardiovascular cohorts). (2004) (136)
The functional -374 T/A RAGE gene polymorphism is associated with proteinuria and cardiovascular disease in type 1 diabetic patients. (2003) (135)
Association of branched-chain amino acids and other circulating metabolites with risk of incident dementia and Alzheimer’s disease: A prospective study in eight cohorts (2018) (134)
Heritability and risk factors of uterine fibroids--the Finnish Twin Cohort study. (2000) (132)
Association of FXIII Val34Leu with decreased risk of myocardial infarction in Finnish males. (1999) (131)
Adiposity as a cause of cardiovascular disease: a Mendelian randomization study. (2015) (128)
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (127)
Array-based multiplex analysis of candidate genes reveals two independent and additive genetic risk factors for myocardial infarction in the Finnish population. (1998) (125)
Midlife sleep characteristics associated with late life cognitive function. (2013) (124)
Metabolic profiling of pregnancy: cross-sectional and longitudinal evidence (2016) (121)
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney (2017) (121)
Polymorphisms within the tumor necrosis factor locus and prevalence of coronary artery disease in middle-aged men. (2001) (117)
Neolithic dairy farming at the extreme of agriculture in northern Europe (2014) (116)
Data harmonization and federated analysis of population-based studies: the BioSHaRE project (2013) (116)
Geographical structure and differential natural selection among North European populations. (2009) (114)
Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studies (2018) (113)
Coronary Artery Complicated Lesion Area Is Related to Functional Polymorphism of Matrix Metalloproteinase 9 Gene: An Autopsy Study (2001) (112)
Lessons from studying monogenic disease for common disease. (2006) (110)
Susceptibility of low-density lipoprotein particles to aggregate depends on particle lipidome, is modifiable, and associates with future cardiovascular deaths (2018) (110)
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits (2017) (110)
Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups. (2001) (109)
Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families. (2002) (107)
Cell Specific eQTL Analysis without Sorting Cells (2014) (105)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2011) (104)
Variation in the alpha2B-adrenoceptorgene as a risk factor for prehospitalfatal myocardial infarction and sudden cardiac death (2003) (101)
Same genetic components underlie different measures of sweet taste preference. (2007) (100)
Comprehensive catalog of European biobanks (2011) (99)
Habitual sleep duration is associated with BMI and macronutrient intake and may be modified by CLOCK genetic variants. (2015) (98)
Coronary artery wall atherosclerosis in relation to the estrogen receptor 1 gene polymorphism: an autopsy study (2002) (97)
Genetic architecture of human plasma lipidome and its link to cardiovascular disease (2019) (96)
Variation in the selenoprotein S gene locus is associated with coronary heart disease and ischemic stroke in two independent Finnish cohorts (2007) (96)
The co-occurrence of mtDNA mutations on different oxidative phosphorylation subunits, not detected by haplogroup analysis, affects human longevity and is population specific (2013) (95)
The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts (2009) (95)
Left ventricular size, mass, and function in relation to angiotensin-converting enzyme gene polymorphism in humans. (1994) (94)
Metabolite Profiling and Cardiovascular Event RiskCLINICAL PERSPECTIVE (2015) (94)
A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease (2016) (92)
Evaluation of O2PLS in Omics data integration (2016) (91)
Glycoprotein IIIa Pl(A) polymorphism associates with progression of coronary artery disease and with myocardial infarction in an autopsy series of middle-aged men who died suddenly. (1999) (91)
IgG Glycome in Colorectal Cancer (2016) (90)
Eight blood pressure loci identified by genome-wide association study of 34,433 people of European ancestry (2009) (88)
Genetic and environmental contributions to food use patterns of young adult twins (2008) (88)
Detailed metabolic and genetic characterization reveals new associations for 30 known lipid loci. (2012) (88)
Gene × dietary pattern interactions in obesity: analysis of up to 68 317 adults of European ancestry (2015) (87)
Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q. (2004) (86)
Evidence of susceptibility loci on 4q32 and 16p12 for bipolar disorder. (2003) (86)
Platelet glycoprotein Ibalpha HPA-2 Met/VNTR B haplotype as a genetic predictor of myocardial infarction and sudden cardiac death. (2001) (85)
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos (2014) (83)
Sex hormone-binding globulin associations with circulating lipids and metabolites and the risk for type 2 diabetes: observational and causal effect estimates. (2015) (82)
An MDL Method for Finding Haplotype Blocks and for Estimating the Strength of Haplotype Block Boundaries (2002) (82)
BBMRI-ERIC as a resource for pharmaceutical and life science industries: the development of biobank-based Expert Centres (2014) (81)
Evidence of Inbreeding Depression on Human Height (2012) (81)
Circulating metabolites and the risk of type 2 diabetes: a prospective study of 11,896 young adults from four Finnish cohorts (2018) (80)
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals (2022) (80)
Risks of Light and Moderate Alcohol Use in Fatty Liver Disease: Follow‐Up of Population Cohorts (2020) (79)
Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease (2017) (78)
Dissecting a population genome for targeted screening of disease mutations. (2001) (78)
Platelet membrane collagen receptor glycoprotein VI polymorphism is associated with coronary thrombosis and fatal myocardial infarction in middle-aged men. (2004) (77)
Metabolic profiling of alcohol consumption in 9778 young adults (2016) (76)
Meta-analysis of genome-wide scans for hypertension and blood pressure in Caucasians shows evidence of susceptibility regions on chromosomes 2 and 3. (2004) (75)
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length (2020) (74)
Fine-Scale Genetic Structure in Finland (2017) (73)
Risk Alleles of USF1 Gene Predict Cardiovascular Disease of Women in Two Prospective Studies (2006) (72)
Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation (2015) (72)
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci (2019) (72)
Increased plasma N-glycome complexity is associated with higher risk of type 2 diabetes (2017) (71)
Cohort Profile: the Corogene study. (2012) (69)
Associations of autozygosity with a broad range of human phenotypes (2019) (68)
PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION (2018) (67)
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women (2020) (67)
High Risk Population Isolate Reveals Low Frequency Variants Predisposing to Intracranial Aneurysms (2014) (66)
Interleukin-6 Signaling Effects on Ischemic Stroke and Other Cardiovascular Outcomes (2019) (66)
European lactase persistence genotype shows evidence of association with increase in body mass index (2009) (65)
Phenotype expression in familial combined hyperlipidemia. (1997) (65)
Midlife cardiovascular risk factors and late cognitive impairment (2013) (63)
Identifying flavor preference subgroups. Genetic basis and related eating behavior traits (2014) (62)
Age- and Sex-Specific Causal Effects of Adiposity on Cardiovascular Risk Factors (2015) (62)
Glycoprotein IIIa PlA1/A2 polymorphism and sudden cardiac death (2000) (62)
Low galactosylation of IgG associates with higher risk for future diagnosis of rheumatoid arthritis during 10 years of follow-up. (2018) (62)
Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection (2021) (61)
Chronic disease research in Europe and the need for integrated population cohorts (2017) (61)
OSBPL10, a novel candidate gene for high triglyceride trait in dyslipidemic Finnish subjects, regulates cellular lipid metabolism (2009) (60)
Glycosylation of immunoglobulin G is regulated by a large network of genes pleiotropic with inflammatory diseases (2020) (60)
An epigenome-wide association study meta-analysis of educational attainment (2017) (60)
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape (2016) (59)
USF1 deficiency activates brown adipose tissue and improves cardiometabolic health (2016) (59)
Effects of hormonal contraception on systemic metabolism: cross-sectional and longitudinal evidence (2016) (59)
Associations between interleukin‐1 (IL‐1) gene variations or IL‐1 receptor antagonist levels and the development of type 2 diabetes (2011) (58)
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2020) (58)
Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland. (2019) (58)
Linkage of nicotine dependence and smoking behavior on 10q, 7q and 11p in twins with homogeneous genetic background (2008) (58)
Genetic Relationship between Schizophrenia and Nicotine Dependence (2016) (58)
Chromosome X-Wide Association Study Identifies Loci for Fasting Insulin and Height and Evidence for Incomplete Dosage Compensation (2014) (57)
Variation in the alpha2B-adrenoceptor gene as a risk factor for prehospital fatal myocardial infarction and sudden cardiac death. (2003) (57)
Haplotype sharing provides insights into fine-scale population history and disease in Finland (2017) (56)
No evidence of linkage between familial combined hyperlipidemia and genes encoding lipolytic enzymes in Finnish families. (1997) (56)
Common Genetic Variants, QT Interval, and Sudden Cardiac Death in a Finnish Population-Based Study (2011) (54)
Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium (2018) (54)
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (53)
The role of polygenic risk and susceptibility genes in breast cancer over the course of life (2020) (53)
Common Variants Show Predicted Polygenic Effects on Height in the Tails of the Distribution, Except in Extremely Short Individuals (2011) (53)
C-reactive protein-associated genetic variants and cancer risk: findings from FINRISK 1992, FINRISK 1997 and Health 2000 studies. (2011) (53)
Common Genetic Variants Associated with Sudden Cardiac Death: The FinSCDgen Study (2012) (52)
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits (2017) (52)
The GPIIIa (beta3 integrin) PlA polymorphism in the early development of coronary atherosclerosis. (2001) (50)
Genetic Variants in SGLT1, Glucose Tolerance, and Cardiometabolic Risk (2018) (49)
Early perivenular fibrogenesis--precirrhotic lesions among moderate alcohol consumers and chronic alcoholics. (1995) (49)
Genetic Association and Interaction Analysis of USF1 and APOA5 on Lipid Levels and Atherosclerosis (2010) (48)
Appetitive traits as behavioural pathways in genetic susceptibility to obesity: a population-based cross-sectional study (2015) (48)
Plasma N-Glycans as Emerging Biomarkers of Cardiometabolic Risk: A Prospective Investigation in the EPIC-Potsdam Cohort Study (2020) (48)
Experimental and Human Evidence for Lipocalin‐2 (Neutrophil Gelatinase‐Associated Lipocalin [NGAL]) in the Development of Cardiac Hypertrophy and Heart Failure (2017) (48)
Genome‐wide association study of sleep duration in the Finnish population (2014) (48)
Design, recruitment, logistics, and data management of the GEHA (Genetics of Healthy Ageing) project (2011) (48)
The prevalence of metabolic syndrome and metabolically healthy obesity in Europe (2014) (48)
Self‐Ratings of Olfactory Function Reflect Odor Annoyance Rather than Olfactory Acuity (2008) (46)
Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use (2019) (45)
Gene-Environment Interactions of Circadian-Related Genes for Cardiometabolic Traits (2015) (45)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (45)
Intertumoral heterogeneity in patient-specific drug sensitivities in treatment-naïve glioblastoma (2019) (45)
Plasma N-glycans in colorectal cancer risk (2018) (44)
The Use of Genome-Wide eQTL Associations in Lymphoblastoid Cell Lines to Identify Novel Genetic Pathways Involved in Complex Traits (2011) (44)
ACE gene and physical activity, blood pressure, and hypertension: a population study in Finland. (2002) (43)
Glutathione-S-transferase GST M1 "null" genotype and the risk of alcoholic liver disease. (1996) (43)
Plasminogen Activator Inhibitor-1 (PAI-1) 4G/5G Polymorphism, Coronary Thrombosis, and Myocardial Infarction in Middle-aged Finnish Men who Died Suddenly (2000) (43)
Coronary artery calcification is related to functional polymorphism of matrix metalloproteinase 3: the Helsinki Sudden Death Study. (2002) (42)
Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions (2017) (41)
Metabolic signatures of birthweight in 18 288 adolescents and adults (2016) (41)
Meta-analysis on blood transcriptomic studies identifies consistently coexpressed protein–protein interaction modules as robust markers of human aging (2013) (41)
Polymorphism in the cytochrome P450 2E1 gene and the risk of alcoholic liver disease. (1997) (41)
Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2 (2016) (41)
Genetic Determinants of Circulating Interleukin-1 Receptor Antagonist Levels and Their Association With Glycemic Traits (2014) (40)
Metabolomic Consequences of Genetic Inhibition of PCSK9 Compared With Statin Treatment (2018) (40)
Association of the endothelial nitric oxide synthase gene polymorphism with risk of coronary artery disease and myocardial infarction in middle-aged men (2002) (40)
Genetics in an isolated population like Finland: a different basis for genomic medicine? (2017) (39)
Midlife alcohol consumption and later risk of cognitive impairment: a twin follow-up study. (2010) (39)
Myeloperoxidase Gene Variation as a Determinant of Atherosclerosis Progression in the Abdominal and Thoracic Aorta: An Autopsy Study (2003) (39)
The Effects of Intensive Weight Reduction on Body Composition and Serum Hormones in Female Fitness Competitors (2017) (39)
AUTOGSCAN: powerful tools for automated genome-wide linkage and linkage disequilibrium analysis. (2005) (38)
Matrix metalloproteinase3 and 9 gene promoter polymorphisms: joint action of two loci as a risk factor for coronary artery complicated plaques. (2005) (38)
Association of variation in the interleukin-1 gene family with diabetes and glucose homeostasis. (2009) (38)
Glycoprotein IIIa Pl(A1/A2) polymorphism and sudden cardiac death. (2000) (38)
Environmental Effects Exceed Genetic Effects on Perceived Intensity and Pleasantness of Several Odors: A Three-Population Twin Study (2008) (37)
Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study (2016) (37)
Radiographic Assessment of Dental Health in Middle-aged Men Following Sudden Cardiac Death (2006) (36)
Food neophobia associates with poorer dietary quality, metabolic risk factors, and increased disease outcome risk in population-based cohorts in a metabolomics study. (2019) (36)
Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns (2018) (36)
Cortical ¹¹C-PIB uptake is associated with age, APOE genotype, and gender in "healthy aging". (2014) (35)
Glutathione S-transferase-M1 'null' genotype and alcohol-induced disorders of human spermatogenesis. (1996) (35)
Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture (2013) (35)
A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol (2011) (34)
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. (2016) (34)
Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure (2012) (34)
Abuse of alcohol in sudden out-of-hospital deaths in Finland. (1994) (34)
Genetic contribution to sour taste preference (2012) (34)
Genetic component of identification, intensity and pleasantness of odours: a Finnish family study (2007) (34)
Mortality Rate Increases Steeply With Nonadherence to Statin Therapy in Patients With Acute Coronary Syndrome (2012) (34)
Apolipoprotein A-I concentrations and risk of coronary artery disease: A Mendelian randomization study. (2020) (34)
Bipolar disorder susceptibility region on Xq24–q27.1 in Finnish families (2002) (33)
An interaction map of circulating metabolites, immune gene networks, and their genetic regulation (2016) (33)
Heritability of Adult Body Height: A Comparative Study of Twin Cohorts in Eight Countries (2003) (33)
Association Analysis of Allelic Variants of USF1 in Coronary Atherosclerosis (2008) (33)
Genetics of Maximal Walking Speed and Skeletal Muscle Characteristics in Older Women (2008) (32)
Ageing with elegans: a research proposal to map healthspan pathways (2016) (32)
Genome-wide meta-analysis of common variant differences between men and women (2012) (31)
Genetic predisposition to obesity, restrained eating and changes in body weight: a population-based prospective study (2018) (31)
Combined Effects of Thrombosis Pathway Gene Variants Predict Cardiovascular Events (2007) (31)
Shared genetic background for regulation of mood and sleep: association of GRIA3 with sleep duration in healthy Finnish women. (2011) (31)
Family history and perceived risk of diabetes, cardiovascular disease, cancer, and depression. (2016) (30)
Heritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE Consortium. (2016) (29)
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour (2021) (29)
Quality of dietary fat and genetic risk of type 2 diabetes: individual participant data meta-analysis (2019) (29)
Geographic variation and bias in polygenic scores of complex diseases and traits in Finland (2018) (28)
Disentangling the genetics of lean mass. (2019) (28)
Biomarker Glycoprotein Acetyls Is Associated With the Risk of a Wide Spectrum of Incident Diseases and Stratifies Mortality Risk in Angiography Patients (2018) (28)
TRIB1 constitutes a molecular link between regulation of sleep and lipid metabolism in humans (2012) (28)
Low-Expression Variant of Fatty Acid–Binding Protein 4 Favors Reduced Manifestations of Atherosclerotic Disease and Increased Plaque Stability (2014) (28)
Evaluation of HapMap data in six populations of European descent (2008) (27)
A Genome-Wide Association Study of Monozygotic Twin-Pairs Suggests a Locus Related to Variability of Serum High-Density Lipoprotein Cholesterol (2012) (27)
Polymorphisms in the nephrin gene and diabetic nephropathy in type 1 diabetic patients. (2003) (27)
A first update on mapping the human genetic architecture of COVID-19 (2022) (27)
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) (26)
Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (26)
Locus for quantitative HDL-cholesterol on chromosome 10q in Finnish families with dyslipidemia Published, JLR Papers in Press, July 16, 2004. DOI 10.1194/jlr.M400141-JLR200 (2004) (26)
Associations of Vitamin D Receptor, Calcium-Sensing Receptor and Parathyroid Hormone Gene Polymorphisms with Calcium Homeostasis and Peripheral Bone Density in Adult Finns (2009) (26)
Lipoprotein signatures of cholesteryl ester transfer protein and HMG-CoA reductase inhibition (2018) (26)
A male-specific quantitative trait locus on 1p21 controlling human stature (2005) (26)
USF1 gene variants contribute to metabolic traits in men in a longitudinal 32-year follow-up study (2008) (26)
Angiotensin‐converting enzyme genotypes in the high‐ and low‐risk area for coronary heart disease in Finland (1995) (25)
Taxonomic signatures of cause-specific mortality risk in human gut microbiome (2021) (25)
ADAM8 and its single nucleotide polymorphism 2662 T/G are associated with advanced atherosclerosis and fatal myocardial infarction: Tampere vascular study (2009) (24)
An epigenome-wide association study of metabolic syndrome and its components (2020) (24)
Genome-wide linkage screen for stature and body mass index in 3.032 families: evidence for sex- and population-specific genetic effects (2009) (24)
Familial idiopathic normal pressure hydrocephalus (2015) (24)
Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci (2009) (24)
A distinctive DNA methylation pattern in insufficient sleep (2019) (24)
Taxonomic Signatures of Long-Term Mortality Risk in Human Gut Microbiota (2020) (24)
Substantial fat mass loss reduces low-grade inflammation and induces positive alteration in cardiometabolic factors in normal-weight individuals (2019) (24)
Genetic Risk Scores Predict Recurrence of Acute Coronary Syndrome (2016) (23)
Protective Low-Frequency Variants for Preeclampsia in the Fms Related Tyrosine Kinase 1 Gene in the Finnish Population (2017) (23)
Molecular Pathways Mediating Immunosuppression in Response to Prolonged Intensive Physical Training, Low-Energy Availability, and Intensive Weight Loss (2019) (23)
The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice (2021) (23)
Identification, Heritability, and Relation With Gene Expression of Novel DNA Methylation Loci for Blood Pressure (2020) (23)
FinnGen provides genetic insights from a well-phenotyped isolated population (2023) (22)
Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles (2016) (22)
Minimum description length block finder, a method to identify haplotype blocks and to compare the strength of block boundaries. (2003) (21)
Evaluating whole genome amplification via multiply-primed rolling circle amplification for SNP genotyping of samples with low DNA yield. (2005) (21)
Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using Metabolomics (2019) (20)
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2017) (20)
Multivariate genome-wide association analysis of a cytokine network reveals variants with widespread immune, haematological and cardiometabolic pleiotropy (2019) (20)
Metabolomic Consequences of Genetic Inhibition of PCSK9 Compared With Statin Treatment (2018) (20)
Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116)) (2010) (20)
Genetic and Environmental Contributions to Perceived Intensity and Pleasantness of Androstenone Odor: An International Twin Study (2008) (19)
Combined Effects of Alcohol and Metabolic Disorders in Patients With Chronic Liver Disease. (2020) (19)
Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs (2008) (19)
Evaluation of HLA-DRB1 imputation using a Finnish dataset. (2014) (19)
Transnational access to large prospective cohorts in Europe: Current trends and unmet needs. (2019) (19)
Genome-Wide Meta-Analysis of Sciatica in Finnish Population (2016) (19)
Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population (2013) (19)
Genetic Variants Contributing to Circulating Matrix Metalloproteinase 8 Levels and Their Association With Cardiovascular Diseases: A Genome-Wide Analysis (2017) (19)
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus (2018) (18)
Associations of nicotine intake measures with CHRN genes in Finnish smokers. (2011) (18)
Serum lipopolysaccharides predict advanced liver disease in the general population (2019) (18)
Interactions of Functional Apolipoprotein E Gene Promoter Polymorphisms With Smoking on Aortic Atherosclerosis (2008) (18)
Thyroid cancer and co-occurring RET mutations in Hirschsprung disease. (2013) (18)
Genetic variation of the interleukin-1 family and nongenetic factors determining the interleukin-1 receptor antagonist phenotypes. (2010) (18)
Thrombomodulin Gene Polymorphisms and Haplotypes and the Risk of Cardiovascular Events: A Prospective Follow-Up Study (2006) (18)
The GPIIIa Pl(A) polymorphism in the progression of abdominal aortic atherosclerosis. (1999) (18)
Long-extension PCR to detect deleted mitochondrial DNA molecules is compromized by technical artefacts. (1999) (17)
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (17)
Association of Circulating Metabolites in Plasma or Serum and Risk of Stroke (2020) (17)
Platelet Glycoprotein Ib&agr; HPA-2 Met/VNTR B Haplotype as a Genetic Predictor of Myocardial Infarction and Sudden Cardiac Death (2001) (17)
Feasibility study of using high-throughput drug sensitivity testing to target recurrent glioblastoma stem cells for individualized treatment (2019) (17)
Affective responses to sweet products and sweet solution in British and Finnish adults (2017) (17)
Metabolic profiling of angiopoietin-like protein 3 and 4 inhibition: a drug-target Mendelian randomization analysis (2020) (16)
CRP gene variation affects early development of Alzheimer's disease-related plaques (2011) (16)
Genome-wide association meta-analysis of fish and EPA+DHA consumption in 17 US and European cohorts (2017) (16)
The hepatic lipase gene C‐480T polymorphism in the development of early coronary atherosclerosis: the Helsinki Sudden Death Study (2007) (16)
Birthplace predicts risk for prehospital sudden cardiac death in middle-aged men who migrated to metropolitan area: The Helsinki Sudden Death Study (2009) (16)
Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies (2016) (16)
Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population (2017) (16)
Elevated serum alpha-1 antitrypsin is a major component of GlycA-associated risk for future morbidity and mortality (2019) (16)
Bayesian Variable Selection in Searching for Additive and Dominant Effects in Genome-Wide Data (2012) (15)
Genetics of Human Stature: Lessons from Genome-Wide Association Studies (2011) (14)
Characterization of the metabolic profile associated with serum 25-hydroxyvitamin D: a cross-sectional analysis in population-based data (2016) (14)
Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease (2019) (14)
Narcolepsy risk loci are enriched in immune cells and suggest autoimmune modulation of the T cell receptor repertoire (2018) (14)
Astringency Perception and Heritability Among Young Finnish Twins (2011) (14)
Genetic and lifestyle risk factors for advanced liver disease among men and women (2020) (14)
Genetic analysis of over one million people identifies 535 novel loci for blood pressure (2017) (14)
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2 p 14 and 16 q 12 . 1 (2017) (13)
Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant. (2019) (13)
Direct estimation of HDL-mediated cholesterol efflux capacity from serum (2018) (13)
The Role of Inflammatory Cytokines as Intermediates in the Pathway from Increased Adiposity to Disease (2021) (12)
Metabolic biomarkers for peripheral artery disease compared with coronary artery disease: Lipoprotein and metabolite profiling of 31,657 individuals from five prospective cohorts (2020) (12)
Platelet collagen receptor GPIa (C807T/HPA-5) haplotype is not associated with an increased risk of fatal coronary events in middle-aged men. (2002) (12)
Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood (2018) (12)
Age-dependent association between hepatic lipase gene C-480T polymorphism and the risk of pre-hospital sudden cardiac death: the Helsinki Sudden Death Study. (2007) (12)
Genetic polymorphism of the C-reactive protein (CRP) gene and a deep infection focus determine maximal serum CRP level in Staphylococcus aureus bacteremia (2010) (12)
Testing genetic susceptibility loci for alcoholic heart muscle disease. (2001) (11)
A Dynamic Aspartate‐to‐Alanine Aminotransferase Ratio Provides Valid Predictions of Incident Severe Liver Disease (2021) (11)
Genetic Variation on the BAT1-NFKBIL1-LTA Region of Major Histocompatibility Complex Class III Associates with Periodontitis (2014) (11)
A common variant near the KCNJ2 gene is associated with T-peak to T-end interval. (2012) (11)
Meta-analysis of five genome-wide linkage studies for body mass index reveals significant evidence for linkage to chromosome 8p (2005) (11)
Refining Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Genetic Loci by Integrating Summary Data From Genome-wide Association, Gene Expression, and DNA Methylation Studies (2020) (11)
Genome-wide association approaches for identifying loci for human height genes. (2011) (11)
Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population (2015) (11)
Meta-analysis of five genome-wide linkage studies for body mass index reveals significant evidence for linkage to chromosome 8p (2005) (10)
Polymorphism in the cytochrome P450 2E1 gene and alcohol-induced disorders of human spermatogenesis. (1996) (10)
Role of Academic Biobanks in Public-Private Partnerships in the European Biobanking and BioMolecular Resources Research Infrastructure Community. (2019) (10)
A Functional variant of the iNOS gene flanking region is associated with LAD coronary artery disease: an autopsy study (2003) (10)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (10)
Genome-Wide Association Study of Peripheral Artery Disease (2021) (9)
A cross-omics integrative study of metabolic signatures of chronic obstructive pulmonary disease (2020) (9)
Dopamine D3 receptor gene polymorphisms, blood pressure and nephropathy in type 1 diabetic patients. (2004) (9)
Correction: Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1 (2011) (9)
Utility 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 study (2001) (9)
Correction: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (9)
DNA extraction yield is associated with several phenotypic characteristics: results from two large population surveys (2004) (9)
Smoking-dependent association between paraoxonase 1 M/L55 genotype and coronary atherosclerosis in males: an autopsy study. (2003) (9)
Development and validation of a model to predict incident chronic liver disease in the general population: the CLivD score. (2022) (9)
Data-driven multivariate population subgrouping via lipoprotein phenotypes versus apolipoprotein B in the risk assessment of coronary heart disease. (2019) (9)
Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (8)
Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome (2016) (8)
Erratum to: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits : (Nature Genetics, (2018), 50, 10, (1412-1425), 10.1038/s41588-018-0205-x) (2018) (8)
Birthplace 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 (2010) (8)
Plasma N-glycome shows continuous deterioration as the diagnosis of insulin resistance approaches (2021) (8)
Platelet GPIbα, GPIV and vWF polymorphisms and fatal pre-hospital MI among middle-aged men (2008) (8)
Low MMP-8/TIMP-1 reflects left ventricle impairment in takotsubo cardiomyopathy and high TIMP-1 may help to differentiate it from acute coronary syndrome (2017) (8)
Systems medicine links microbial inflammatory response with glycoprotein-associated mortality risk (2015) (7)
Incidence of liver‐related morbidity and mortality in a population cohort of non‐alcoholic fatty liver disease (2021) (7)
A Web Portal for Communicating Polygenic Risk Score Results for Health Care Use—The P5 Study (2021) (7)
Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2016) (7)
Neuregulin signaling pathway in smoking behavior (2017) (7)
Spline Methods for the Comparison of Physical and Genetic Maps (2003) (7)
Molecular genetics of hypertension and related traits (1999) (6)
Platelet Glycoprotein Iba HPA-2 Met/VNTR B Haplotype as a Genetic Predictor of Myocardial Infarction and Sudden Cardiac Death (2001) (6)
Waist and hip circumference are independently associated with risk of liver disease in population-based studies. (2021) (6)
Effects of dexmedetomidine, propofol, sevoflurane and S-ketamine on the human metabolome (2021) (6)
MixFit: Methodology for Computing Ancestry-Related Genetic Scores at the Individual Level and Its Application to the Estonian and Finnish Population Studies (2017) (6)
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (6)
Effect of remdesivir post hospitalization for COVID-19 infection from the randomized SOLIDARITY Finland trial (2022) (6)
A polymorphism in the protein kinase C gene PRKCB is associated with &agr;2-adrenoceptor-mediated vasoconstriction (2013) (6)
Immunoglobulin G N-Glycosylation Signatures in Incident Type 2 Diabetes and Cardiovascular Disease (2022) (5)
Food neophobia in young adults. Genetic architecture and relation to personality, BMI, and pleasantness and use frequency of foods (2010) (5)
Genome-wide association and Mendelian randomization analysis prioritizes bioactive metabolites with putative causal effects on common diseases (2020) (5)
Correction to: Increased plasma N-glycome complexity is associated with higher risk of type 2 diabetes (2018) (5)
Age-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 (2013) (5)
Changes in the fine-scale genetic structure of Finland through the 20th century (2021) (5)
On the Combination of Omics Data for Prediction of Binary Outcomes (2016) (5)
THU-251-Metabolic risk factors for advanced liver disease among alcohol risk users in the general population (2019) (5)
Dysfunction of complement receptors CR3 (CD11b/18) and CR4 (CD11c/18) in pre‐eclampsia: a genetic and functional study (2021) (5)
Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants (2021) (5)
Erratum to “Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studies” [Alzheimer’s & Dementia 2018;14:707-22.] (2019) (5)
Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure (2019) (5)
The Detection of Metabolite-Mediated Gene Module Co-Expression Using Multivariate Linear Models (2016) (4)
Mendelian randomisation analysis of clustered causal effects of body mass on cardiometabolic biomarkers (2018) (4)
Metabolic Biomarker Discovery for Risk of Peripheral Artery Disease Compared With Coronary Artery Disease: Lipoprotein and Metabolite Profiling of 31 657 Individuals From 5 Prospective Cohorts (2021) (4)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (4)
Platelet GPIbalpha, GPIV and vWF polymorphisms and fatal pre-hospital MI among middle-aged men. (2008) (4)
Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke (2021) (4)
Pharmacoepigenetics of hypertension: genome-wide methylation analysis of responsiveness to four classes of antihypertensive drugs using a double-blind crossover study design (2022) (4)
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells (2020) (4)
Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals (2022) (4)
Associations of increased physical performance and change in body composition with molecular pathways of heart disease and diabetes risk. (2019) (4)
Common Variation in the b -Carotene 15,15 0 -Monooxygenase 1 Gene Affects Circulating Levels of Carotenoids: A Genome-wide Association Study (2009) (4)
Supplementary Material 5 (2014) (3)
An epigenome-wide association study of educational attainment (n = 10,767) (2017) (3)
Association of paraoxonase-1 M55L genotype and alcohol consumption with coronary atherosclerosis: the Helsinki Sudden Death Study. (2004) (3)
The genomics of heart failure: design and rationale of the HERMES consortium (2021) (3)
BMI is positively associated with accelerated epigenetic aging in twin pairs discordant for body mass index (2021) (3)
Resistance Training Induces Antiatherogenic Effects on Metabolomic Pathways. (2019) (3)
A data-driven medication score predicts 10-year mortality among aging adults (2020) (3)
Diabetes is associated with familial idiopathic normal pressure hydrocephalus: a case–control comparison with family members (2020) (3)
Genome scans provide evidence for low HDL-C loci on 8q23, 16q24.1-24.2 and 20q13.11 in Finnish families (2002) (3)
Dopamine D 3 receptor gene polymorphisms , blood pressure and nephropathy in type 1 diabetic patients (2004) (3)
Identification of healthspan-promoting genes in Caenorhabditis elegans based on a human GWAS study (2022) (3)
Supplementary Material 7 (2014) (3)
Genetic and observational evidence: No independent role for cholesterol efflux over static high‐density lipoprotein concentration measures in coronary heart disease risk assessment (2022) (3)
Sequential double cross-validation for assessment of added predictive ability in high-dimensional omic applications (2016) (3)
Supplementary Material 6 (2014) (3)
An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease (2020) (3)
Sequential double cross-validation for augmented prediction assessment in high-dimensional omic applications (2016) (3)
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (3)
Supplementary Material 3 (2015) (3)
LBP-01-In NAFLD, alcohol drinking habits and genetics predict progression to advanced liver disease: follow-up of population surveys (2019) (3)
The rs2516839 variation of USF1 gene is associated with 4‐year mortality of nonagenarian women: The Vitality 90+ study (2018) (2)
Genetics of Platelet Glycoprotein Receptors: Risk of Thrombotic Events and Pharmacogenetic Implications (2005) (2)
Elevated alpha-1 antitrypsin is a major component of GlycA-associated risk for future morbidity and mortality (2018) (2)
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation (2019) (2)
AUTOGSCAN: Powerful Tools for Automated Genome-Wide Linkage and Linkage Disequilibrium Analysis (2005) (2)
Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers (2020) (2)
22nd European Congress on Obesity (ECO2015), Prague, Czech Republic, May 6-9, 2015: Abstracts (2015) (2)
Effects of hormonal contraception on systemic metabolism (2)
Mitochondrial bioenergetic pathways in blood leukocyte transcriptome decrease after intensive weight loss but are rescued following weight regain in female physique athletes (2021) (2)
Evaluating Robustness and Geographic Differences in Polygenic Risk in Finland (2017) (2)
Insomnia does not mediate or modify the association between MTNR1B risk variant rs10830963 and glucose levels (2016) (2)
Genetic causal beliefs about morbidity: associations with health behaviors and health outcome beliefs about behavior changes between 1982–2002 in the Finnish population (2015) (2)
Genome-wide analysis of nuclear magnetic resonance metabolites revealed parent-of-origin effect on triglycerides in medium very low-density lipoprotein in PTPRD gene. (2018) (2)
The landscape of incident disease risk for the biomarker GlycA and its mortality stratification in angiography patients (2018) (2)
Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney (2017) (2)
COMPREHENSIVE BIOMARKER PROFILING OF HYPERTENSION IN 36,985 FINNISH INDIVIDUALS. (2022) (2)
Genetics of vaccination-related narcolepsy (2017) (2)
Meta-analysis on blood transcriptomic studies identifies consistently co-expressed PPI modules as robust markers of human ageing (2014) (2)
Circulating metabolic biomarkers are consistently associated with type 2 diabetes risk in Asian and European populations. (2022) (2)
Genome-wide physical activity interactions in adiposity (2017) (1)
Large scale trans-ethnic meta-analyses identify novel rare and common variants associated with blood pressure and hypertension (2016) (1)
Comprehensive biomarker profiling of hypertension in 36 985 Finnish individuals (2021) (1)
University of Groningen A Genome-Wide Screen for Interactions Reveals a New Locus on 4 p 15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol (2011) (1)
Cross-sectionally calculated metabolic ageing does not relate to longitudinal metabolic changes - support for stratified ageing models. (2023) (1)
Abdominal obesity is key when evaluating interactions between alcohol use and obesity for liver disease (2022) (1)
Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus (2020) (1)
Comparison of various strategies to define the optimal target population for liver fibrosis screening: A population‐based cohort study (2022) (1)
1192Salt intake and the risk of heart failure (2017) (1)
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution (2019) (1)
An interaction map of circulating metabolites, immune gene networks, and their genetic regulation (2017) (1)
Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population (2023) (1)
Discovery and Refinement Supplementary (2015) (1)
Supplementary Material 9 (2013) (1)
Supplementary Material 15 (2013) (1)
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2020) (1)
Correction: Lipoprotein signatures of cholesteryl ester transfer protein and HMG-CoA reductase inhibition (2020) (1)
Rare mutations in factor H predispose to severe preeclampsia (2018) (1)
Causal Effects of Adiposity on Cardiovascular Risk Factors (2015) (1)
Glycoprotein IIIa PlA 1 / A 2 Polymorphism and Sudden Cardiac Death (2016) (1)
Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability (2021) (1)
Genome-wide search for QTLs for apolipoprotein A-I level in elderly Swedish DZ twins: evidence of female-specific locus on 15q11–13 (2008) (1)
Supplementary Material 4 (2015) (1)
Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen (2022) (1)
The role of adiposity in cardiometabolic traits (2013) (1)
Metabolic signatures of birth weight in 18 288 adolescents and adults (2016) (1)
Substantial Fat Loss in Physique Competitors Is Characterized by Increased Levels of Bile Acids, Very-Long Chain Fatty Acids, and Oxylipins (2022) (1)
Genetic variation in apolipoprotein A-I concentrations and risk of coronary artery disease (2019) (1)
Low serum vitamin D level associated with incident advanced liver disease in the general population – a prospective study (2021) (1)
Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries (2022) (1)
Psychosocial Effects of Receiving Genome-Wide Polygenic Risk Information Concerning Type 2 Diabetes and Coronary Heart Disease: A Randomized Controlled Trial (2022) (1)
Reply to Letter by Tellier et al., ‘Scientific refutation of ESHG statement on embryo selection’ (2022) (1)
CYP2B6 and OPRM1 Receptor Polymorphisms at Methadone Clinics And Novel OPRM1 Haplotypes: A Cross-Sectional Study. (2016) (1)
Atlas of plasma NMR biomarkers for health and disease in 118,461 individuals from the UK Biobank (2023) (1)
North European populations Geographical structure and differential natural selection among Material Supplemental (2009) (1)
[Genetics of multifactorial diseases]. (2010) (1)
Plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphism in the development of coronary thrombosis, coronary stenosis and myocardial infarction in middle-aged Finnish men who died suddenly (2000) (0)
USF1 regulates sleep and circadian traits in humans (2013) (0)
Variations in the Thrombomodulin Gene Predispose for Cardiovascular Events Such as Stroke and Coronary Heart Disease in a Finnish Case-cohort Study Finrisk (2004) (0)
Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation (vol 25, pg 1859, 2018) (2020) (0)
Circulating metabolic biomarkers consistently predict incident type 2 diabetes in Asian and European populations - a plasma metabolomics analysis of four ethnic groups (2021) (0)
Genome-Wide Screen for Common and Rare Copy Number Variation in Metabolic Syndrome (2010) (0)
Nationwide health, socio-economic and genetic predictors of COVID-19 vaccination status in Finland. (2023) (0)
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure (2020) (0)
Genome-wide Linkage Analyses of Lipidprofile Biomarkers in the Genomeutwin Cohort: Results from Pooled Data and Meta-analysis (2007) (0)
A RISK LOCUS FOR NON-ST-ELEVATION MYOCARDIAL INFARCTION ON CHROMOSOME 1P13.3 IS ALSO ASSOCIATED WITH PERIPHERAL ARTERY DISEASE IN PATIENTS WITH ACUTE CORONARY SYNDROME (2017) (0)
Source code for the article Taxonomic Signatures of Long-Term Mortality Risk in Human Gut Microbiota (2020) (0)
Delft University of Technology Evaluation of O 2 PLS in Omics data integration (2017) (0)
1P-0228 A quantitative trait locus on chromosome 10p11 influences variation in plasma HDL-C levels in Finnish dyslipidemic families (2003) (0)
Haplotype analysis of rs9275224, rs2856717, rs9275424, and rs9275596 at the HLA-DQB1/DRB1 locus. (2012) (0)
Combined Linkage Scan of Body Mass Index in European-originated Twin Cohorts (2007) (0)
Diabetes is associated with familial idiopathic normal pressure hydrocephalus: a case–control comparison with family members (2020) (0)
ACTR-79. ESTABLISHMENT OF CLINICAL PROTOCOL TARGETING CANCER STEM CELLS IN RECURRENT GLIOBLASTOMA USING HIGH-THROUGHPUT DRUG SCREENING (2017) (0)
OP-EHEA200971 1..10 (2020) (0)
M72 GENETICS OF VACCINATION RELATED NARCOLEPSY (2019) (0)
Erratum: Meta-analysis of five genome-wide linkage studies for body mass index reveals significant evidence for linkage to chromosome 8p (International Journal of Obesity (2005) 29 (413-419) DOI: 10.1038/sj.ijo.0802817) (2005) (0)
Finemapping of a QTL for body height on the human X chromosome in a Finnish twin cohort. (2007) (0)
Cardiac Arrest and Pulmonary Edema Variation in the Alpha 2 B-Adrenoceptor Gene as a Risk Factor for Prehospital Fatal Myocardial Infarction and Sudden Cardiac Death (2016) (0)
Editorial: Can population health be personalized? Estonia and Finland as examples (2022) (0)
A multivariate linear model for investigating the association between gene-module co-expression and a continuous covariate (2019) (0)
Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice (2022) (0)
Subject Index Vol. 76, Suppl. 3, 2011 (2011) (0)
Advances in modeling of the bovine estrous cycle: Synchronization with PGF2 (2022) (0)
Abstract P195: Lipoprotein and Metabolite Biomarkers for Coronary and Peripheral Artery Disease: Blood Biomarker Profiling of 32,000 Individuals From Five Prospective Studies (2020) (0)
Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice (2022) (0)
A common haplotype of thrombomodulin gene predisposes to cardiovascular events in a prospective follow-up study (2005) (0)
P5362Metabolomic signature of incident type 2 diabetes: evidence from NMR in over 18,000 individuals (2017) (0)
TRAFFIC FATALITIES AND ALCOHOLIC LIVER DISEASE IN FINLAND - A COMPARATIVE STUDY OF THE YEARS 1982-1985 AND 1989-1990 (1993) (0)
Shox, a Candidate Gene for Body Height (2004) (0)
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (0)
HDL-Mediated Cholesterol Efflux Associates with Incident Kidney Disease. (2021) (0)
GENETIC VARIATIONS IN CLASSES I AND III OF MHC ASSOCIATE WITH ACUTE CORONARY SYNDROME IN FINNISH POPULATION (2017) (0)
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals (2018) (0)
SAT-271-Genetic risk factors for advanced alcoholic and non-alcoholic liver disease in the general population (2019) (0)
NEXT GENERATION SEQUENCING OF BTNL2 REVEALS NOVEL ASSOCIATIONS WITH ACUTE CORONARY SYNDROME IN FINNISH POPULATION (2018) (0)
GENETIC ASSOCIATION OF COMPLEMENT RECEPTORS TO PREECLAMPSIA REVEALED BY TARGETED EXOMIC SEQUENCING (2017) (0)
Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2019) (0)
Combined Analysis of Genome Scans from Six Twin Cohorts to Locate Quantitative Trait Loci for Body Mass Index and Stature in the Genomeutwin Project (2004) (0)
On Inferior Power of Recently Developed Family-Based Association Analysis Methods for Next-Generation Sequencing Studies of Rare-Variants (2016) (0)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2019) (0)
Genetics in an isolated population like Finland: a different basis for genomic medicine? (2017) (0)
Mendelian randomisation analysis of clustered causal effects of body mass on cardiometabolic biomarkers (2018) (0)
UNCORRECTED PROOF 1 Design, recruitment, logistics, and data management of the GEHA (Genetics of 2 Healthy Ageing) project (2011) (0)
A distinctive DNA methylation pattern in insufficient sleep (2019) (0)
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA Kettunen (0)
Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2017) (0)
PO5-124 THE HEPATIC LIPASE GENE C-480T POLYMORPHISM IN THE EARLY DEVELOPMENT OF CORONARY ATHEROSCLEROSIS: THE HELSINKI SUDDEN DEATH STUDY (2007) (0)
Genome-Wide Screen for Metabolic Syndrome Loci (2010) (0)
Conserved Haplotype in SGLT1 and Risk for Dietary Hyperglycemia (2018) (0)
Circulating oxylipin and bile acid profiles of dexmedetomidine, propofol, sevoflurane, and S-ketamine: a randomised controlled trial using tandem mass spectrometry (2022) (0)
Supplementary Material (nature09270-s1) (2012) (0)
BAT1-NFKBIL1-LTA OF MHC CLASS III IS A PREDISPOSING GENE REGION TO PERIODONTITIS (2014) (0)
[DNA chips--a new diagnostic revolution?]. (1998) (0)
LB-OR-6 TRANSCRIPT PROFILES FROM MUSCLE AND FAT EXPOSE MOLECULAR MECHANISM BEHIND USF1 ASSOCIATED DYSLIPIDEMIA WITH ALLELE- SPECIFIC EFFECTS ON THE VESSEL WALL (2007) (0)
USF1 GENE IS INVOLVED IN THE REGULATION OF HUMAN LONGEVITY (2008) (0)
The low-expression variant of fatty acid-binding protein 4 favors reduced manifestations of atherosclerotic disease and increased plaque stability (2014) (0)
Complicated dental root canal treatment and risk of prehospital sudden cardiac death (2013) (0)
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits (2017) (0)
The power of many (2010) (0)
1126. Effect of Remdesivir on Recovery, Quality of Life, and Long-COVID Symptoms One Year after Hospitalization for COVID-19 Infection: A Randomized Controlled SOLIDARITY Finland Trial (2022) (0)
Economic 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 risk (2022) (0)
Finland's largest next generation biobank provides valuable resources for genomics research (2019) (0)
Evaluation of O2PLS in Omics data integration (2016) (0)
A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) (0)
Quality Issues in the Centralized Sample Handling and Storage Unit in Genomeutwin (2004) (0)
eQTLGen Consortium (2018). Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. (2018) (0)
Genetic Relationship between Schizophrenia and Nicotine Dependence (2016) (0)
The Effects Of Intensive Weight Loss On Metabolome In Female Fitness Competitors: 2486 Board #1 June 1 1 (2018) (0)
Family disease history and perceived risk for Type 2 diabetes, cardiovascular disease, cancer and depression (2015) (0)
W01.124 Chromosome 10Q11 associated with HDL-C levels in finnish dyslipidemic families (2004) (0)
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2018) (0)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
W07-P-004 Hepatic lipase gene C-480T polymorphism and age modulate the risk of acute myocardial infarction and sudden cardiac death the Helsinki sudden death study (2005) (0)
4P-1124 Co-operative polymorphisms of matrix metalloproteinase 3 and 9 and area of coronary artery lesions related to risk of acute coronary events (2003) (0)
Epigenetic fingerprint of stress in a Finnish shift-working occupational cohort (2015) (0)
EVALUATION OF IMPUTATION METHODS FOR CLASSICAL HLA-DRB1 USING A FINNISH DATASET (2014) (0)
Association between mitochondrial DNA haplogroups J and K, serum branched-chain amino acids and lowered capability for endurance exercise (2022) (0)
Abdominal obesity and alcohol use modify the impact of genetic risk for incident advanced liver disease in the general population (2023) (0)
INSULIN RESISTANCE AND GENETIC RISK PREDICT LIVER-RELATED OUTCOMES AND DEATH IN NON-ALCOHOLIC FATTY LIVER DISEASE (2019) (0)
Association of Interleukin 1 (IL-1) Gene Variation with IL-1 Receptor Antagonist and Inflammation Marker Phenotypes in European Myocardial Infarction Survivors and Health Population Samples (2009) (0)
Fine-Scale Genetic Structure in Finland Kerminen , Sini 2017-10 (0)
Abstract 14425: Exome Sequencing Reveals a Low Frequency Variant in BMPER in a Pedigree With Recurrence of Left Ventricular Outflow Tract Obstruction Defects (2016) (0)
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits (2018) (0)
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity (2018) (0)
APOE GENOTYPE-BY-SMOKING INTERACTIONS AND EARLY ATHEROSCLEROTIC LESIONS (2008) (0)
Reaching for Precision Healthcare in Finland via Use of Genomic Data (2022) (0)
Obesity and alcohol intake modify the impact of genetic variants on the risk for incident liver disease in the general population (2020) (0)
ACE gene, physical activity, and physical fitness (2002) (0)
Genomics as a personalized medicine approach in disease risk prediction-P5.fi FinHealth (2019) (0)
METABOLIC PROFILING OF HYPERTENSION IN 36,985 FINNISH INDIVIDUALS (2021) (0)
Genome-wide linkage analysis for longevity in European nonagenarian siblings: Genetics of Healthy Ageing Study (GEHA). (2011) (0)
Genetic risk factors for advanced alcoholic and non-alcoholic liver disease in the general population (2019) (0)
No association between three polymorphisms in the dopamine D3 receptor gene and diabetic nephropathy in type 1 diabetic patients (2002) (0)
Increased Complexity of Plasma N-glycome is Associated with Higher Risk of Type 2 Diabetes Development (2018) (0)
Genome wide association analysis in human height of European-originated monozygotic female twins. (2008) (0)
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus (2018) (0)
Morgam: An International Project Pooling Cohort Studies of Cardiovascular Disease (2004) (0)
Publisher Correction: Identification of 371 genetic variants for age at first sex and birth linked to externalising behavior (2021) (0)
Metabolic profiling of pregnancy (0)
Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (2021) (0)
Longitudinal profiling of metabolic ageing trends in two population cohorts of young adults. (2022) (0)
Risk Haplotype Predisposes to Acute Coronary Syndrome (2016) (0)
Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata (2023) (0)
Polygenic risk information for coronary artery disease-P5.fi FinHealth (2019) (0)
Title Amerindian-specific regions under positive selection harbour new lipid variants in Latinos Permalink (2014) (0)
Correction to: Reply to Letter by Tellier et al., ‘Scientific refutation of ESHG statement on embryo selection’ (2022) (0)
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes (2018) (0)
CNV Association with Neurodevelopmental Phenotypes in Finnish Population Cohort (2019) (0)
COHORT PROFILE Cohort Profile: The Corogene study (2012) (0)
Abstract 5095: Association of Genetic Variation in the IL-1 Gene with Diabetes and Glucose Homeostasis (2008) (0)
DDIS-13. IDENTIFICATION OF INDIVIDUALIZED THERAPY OPTIONS IN PATIENTS WITH GLIOBLASTOMA BY HIGH-THROUGHPUT DRUG SCREENING (2016) (0)
Edinburgh Research Explorer Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (2018) (0)
Risk perceptions for Type 2 diabetes and coronary heart disease after receiving risk information - participants of P5 FinHealth study (2019) (0)
Plasma N-glycans in colorectal cancer risk (2018) (0)
Genome-wide physical activity interactions in adiposity A meta-analysis of 200,452 adults Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults (2017) (0)
Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population Salo (0)
Attribution of diabetes to the development of severe liver disease in the general population (2022) (0)
ETIOLOGY OF NIGHTMARES: ENVIRONMENTAL AND GENETIC CORRELATES (2013) (0)
Major histocompatibility complex risk haplotype predisposes to acute coronary syndrome (2015) (0)
Evaluating Whole Genome Amplification via Multiply-Primed Rolling Circle Amplification for SNP Genotyping of Samples With Low DNA Yield (2005) (0)
Intertumoral heterogeneity in patient-specific drug sensitivities in treatment-naïve glioblastoma (2019) (0)
GENOMEUTWIN: an integrated project of eight twin cohorts for studies on complex traits (2004) (0)
064Genetic association of complement receptors to preeclampsia revealed by targeted exomic sequencing (2017) (0)
Genomic Prediction of Type 2 Diabetes and Coronary Heart Disease Following Diabetes (2017) (0)
Association between arterial hypertension and liver outcomes using polygenic risk scores: a population-based study (2022) (0)
[Genes and hypertension]. (2000) (0)
Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes (2022) (0)
Combined Analysis of Genome Scans from Four Twin Cohorts to Locate Quantitative Trait Loci for Body Mass Index and Stature in the Genomeutwin Project - Session: Molecular Genetics and Twin Studies (2004) (0)
Ageing with elegans: a research proposal to map healthspan pathways (2016) (0)
Longitudinal metabolomics of increasing body-mass index and waist-hip ratio reveals two dynamic patterns of obesity pandemic. (2023) (0)
Insulin Resistance and Genetic Risk Predict Liver‐Related Outcomes and Death in Nonalcoholic Fatty Liver Disease (2019) (0)

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What Schools Are Affiliated With Markus Perola?

Markus Perola is affiliated with the following schools: