Markus Perola
#157,581
Most Influential Person Now
Finnish researcher, MD, PhD, research professor
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Markus Perolaphilosophy Degrees
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Philosophy
Markus Perola's Degrees
- Doctorate Medicine University of Helsinki
- PhD Medical Science University of Helsinki
Why Is Markus Perola Influential?
(Suggest an Edit or Addition)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: