Markus Perola
Reproducibility track record
1
assessed papers
90/100
mean reproducibility
1
reproduced (C1–C2)
0
flagged
171
total citations
flag rate:
0%
(0/1)
The share of this author’s assessed papers carrying a ⚑ flag. A concentration is a prompt for expert review — never, on its own, a determination about the person.
Authorship role
first author: 0
last author: 0
Topics
Funders
—
Frequent co-authors
Mathieu Platteel 1David Melzer 1Thomas Meitinger 1Jingyuan Fu 1Tōnu Esko 1Astrid Petersmann 1Bernett Lee 1Fernando Rivadeneira 1Michael Roden 1Johannes Kettunen 1
Institutions
University Medical Center Groningen 1University of Groningen 1University of Tartu 1Boston Children's Hospital 1Broad Institute 1Harvard University 1
Geography (author institutions)
NL 1EE 1US 1DE 1FI 1GB 1
Co-author network
Collaborators, sized by shared output and coloured by their own reproducibility (green = high, red = low). Click a node to open their card. A pattern is a prompt for review, never a determination.
How this author’s assessed papers reproduced — the outcome of reproduction attempts, not a judgement of the person. Coverage is partial and grows over time.
Assessed papers (1)
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Cell Specific eQTL Analysis without Sorting Cells.
2015 L1 90/100
Complete publication record (835)
Request a reproduction →1 assessed by us (1 reproduced) · 834 not yet assessed — every PubMed paper on record, linked below.
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Obesity rise plateaus in developed nations and accelerates in developing nations ↗Nature · 2026 · PMID 42129527not yet assessed
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Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes ↗Nature Genetics · 2025 · PMID 40038546not yet assessed
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Electronic health records reveal variations in the use of blood units by hour and medical specialty ↗Vox Sanguinis · 2025 · PMID 40268495not yet assessed
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Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty ↗Nature Aging · 2025 · PMID 40764432not yet assessed
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Low prevalence of CWH43 variants among Finnish and Norwegian idiopathic normal pressure hydrocephalus patients: a cohort-based observational study ↗Fluids and Barriers of the CNS · 2025 · PMID 39948543not yet assessed
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Evidence-based criteria for identifying at-risk individuals requiring liver disease screening ↗Hepatology Communications · 2025 · PMID 40116748not yet assessed
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Effects of parental autoimmune diseases on type 1 diabetes in offspring can be partially explained by HLA and non-HLA polymorphisms ↗Cell Genomics · 2025 · PMID 40286789not yet assessed
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Alzheimer and cardiovascular genetic scores and cognition: the FINGER randomized controlled trial ↗Brain · 2025 · PMID 40747850not yet assessed
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Developing risk prediction models for type 2 diabetes and assessing the role of circulating metabolic biomarkers in five independent Finnish cohorts with over 22,000 individuals ↗Journal of Clinical Epidemiology · 2025 · PMID 40975243not yet assessed
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Genetic association of preeclampsia to von Willebrand factor and its size-regulator ADAMTS13 ↗Research Square · 2025 · PMID 40671815not yet assessed
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not yet assessed
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Association between genetic proxies for neuroticism and labour market outcomes ↗European Psychiatry · 2025not yet assessed
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Polygenic risk for depression and career performance ↗European Psychiatry · 2025not yet assessed
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Federated Analysis of Cross-European Health Data: Improving CVD prediction with Machine Learning ↗European Journal of Public Health · 2025not yet assessed
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Genome-wide characterization of circulating metabolic biomarkers ↗Nature · 2024 · PMID 38448586not yet assessed
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Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction ↗Nature Genetics · 2024 · PMID 38839884not yet assessed
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Metabolomic and genomic prediction of common diseases in 700,217 participants in three national biobanks ↗Nature Communications · 2024 · PMID 39572536not yet assessed
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Comprehensive Inherited Risk Estimation for Risk-Based Breast Cancer Screening in Women ↗Journal of Clinical Oncology · 2024 · PMID 38422475not yet assessed
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Risk Variants Associated With Normal Pressure Hydrocephalus ↗Neurology · 2024 · PMID 39141892not yet assessed
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ALT levels, alcohol use, and metabolic risk factors have prognostic relevance for liver-related outcomes in the general population ↗JHEP Reports · 2024 · PMID 39430577not yet assessed
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Markers of imminent myocardial infarction ↗Nature Cardiovascular Research · 2024 · PMID 39196201not yet assessed
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X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements ↗Nature Communications · 2024 · PMID 38233393not yet assessed
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Patterns of reproductive health in inflammatory rheumatic diseases and other immune-mediated diseases: a nationwide registry study ↗Lara D. Veeken · 2024 · PMID 38503536not yet assessed
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The PROPHET project paves the way for personalized prevention in the future healthcare ↗European Journal of Cancer Prevention · 2024 · PMID 38598497not yet assessed
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Genetic Susceptibility to Acute Viral Bronchiolitis ↗The Journal of Infectious Diseases · 2024 · PMID 39299705not yet assessed
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Value of Pharmacogenetic Testing Assessed with Real‐World Drug Utilization and Genotype Data ↗Clinical Pharmacology & Therapeutics · 2024 · PMID 39365028not yet assessed
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Deep learning-based prediction of one-year mortality in Finland is an accurate but unfair aging marker ↗Nature Aging · 2024 · PMID 38914859not yet assessed
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Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia ↗Genes and Immunity · 2024 · PMID 39690307not yet assessed
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Divergent trends in the incidence and mortality of acute myocardial ischaemic syndrome, especially in women. Evidence from Finland in 1996–2021 ↗Annals of Medicine · 2024 · PMID 39600115not yet assessed
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Effects of fat loss and low energy availability on the serum cardiometabolic profile of physique athletes ↗Scandinavian Journal of Medicine and Science in Sports · 2024 · PMID 38268074not yet assessed
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Prioritization of Kidney Cell Types Highlights Myofibroblast Cells in Regulating Human Blood Pressure ↗Kidney International Reports · 2024 · PMID 38899223not yet assessed
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A metabolic profile of xenon and metabolite associations with 6-month mortality after out-of-hospital cardiac arrest: A post-hoc study of the randomised Xe-Hypotheca trial ↗PLoS ONE · 2024 · PMID 38833442not yet assessed
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Rare variants in genes coding for components of the terminal pathway of the complement system in preeclampsia ↗Research Square · 2024 · PMID 38645143not yet assessed
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Effects of parental autoimmune diseases on type 1 diabetes in offspring can be partially explained by HLA and non-HLA polymorphisms ↗medRxiv · 2024not yet assessed
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Short- and long-term effects of imatinib in patients hospitalised for COVID-19 infection: A randomised controlled trial ↗medRxiv · 2024not yet assessed
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TOP-308 Steatotic liver disease subclasses have prognostic relevance for liver-related outcomes in the general population ↗Journal of Hepatology · 2024not yet assessed
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Real-World Comparative Effectiveness of SARS-CoV-2 Primary Vaccination Campaigns Against SARS-CoV-2 Infections: A Federated Observational Study Emulating a Target Trial in Three Nations ↗SSRN Electronic Journal · 2024not yet assessed
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Health Impact Assessment in Personalized Prevention: three applications on pharmacogenomic testing ↗European Journal of Public Health · 2024not yet assessed
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Electronic health records reveal variations in the use of blood units by hour and medical specialty ↗medRxiv · 2024not yet assessed
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not yet assessed
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Towards modeling evolving longitudinal health trajectories with a transformer-based deep learning model ↗arXiv (Cornell University) · 2024not yet assessed
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FinnGen provides genetic insights from a well-phenotyped isolated population ↗Nature · 2023 · PMID 36653562not yet assessed
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Atlas of plasma NMR biomarkers for health and disease in 118,461 individuals from the UK Biobank ↗Nature Communications · 2023 · PMID 36737450not yet assessed
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Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy ↗JAMA Cardiology · 2023 · PMID 37285119not yet assessed
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A second update on mapping the human genetic architecture of COVID-19 ↗Nature · 2023 · PMID 37674002not yet assessed
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Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy ↗Nature Communications · 2023 · PMID 37188663not yet assessed
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OTTERS: a powerful TWAS framework leveraging summary-level reference data ↗Nature Communications · 2023 · PMID 36882394not yet assessed
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Nationwide health, socio-economic and genetic predictors of COVID-19 vaccination status in Finland ↗Nature Human Behaviour · 2023 · PMID 37081098not yet assessed
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Risk factors for severe respiratory syncytial virus infection during the first year of life: development and validation of a clinical prediction model ↗The Lancet Digital Health · 2023 · PMID 37890904not yet assessed
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Genetic insights into resting heart rate and its role in cardiovascular disease ↗Nature Communications · 2023 · PMID 37532724not yet assessed
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Data Resource Profile: Nationwide registry data for high-throughput epidemiology and machine learning (FinRegistry) ↗International Journal of Epidemiology · 2023 · PMID 37365732not yet assessed
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Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity ↗Stroke · 2023 · PMID 36655558not yet assessed
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The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections ↗EBioMedicine · 2023 · PMID 37301713not yet assessed
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Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study ↗Stroke · 2023 · PMID 37212139not yet assessed
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Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata ↗Nature Communications · 2023 · PMID 36726022not yet assessed
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Identification of complement factor H variants that predispose to pre‐eclampsia: A genetic and functional study ↗BJOG An International Journal of Obstetrics & Gynaecology · 2023 · PMID 37156755not yet assessed
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Waist-hip ratio is superior to BMI in predicting liver-related outcomes and synergizes with harmful alcohol use ↗Communications Medicine · 2023 · PMID 37674006not yet assessed
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Major Genetic Risk Factors for Dupuytren's Disease Are Inherited From Neandertals ↗Molecular Biology and Evolution · 2023 · PMID 37315093not yet assessed
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Cross-sectionally Calculated Metabolic Aging Does Not Relate to Longitudinal Metabolic Changes—Support for Stratified Aging Models ↗The Journal of Clinical Endocrinology & Metabolism · 2023 · PMID 36658689not yet assessed
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Longitudinal metabolomics of increasing body-mass index and waist-hip ratio reveals two dynamic patterns of obesity pandemic ↗International Journal of Obesity · 2023 · PMID 36823293not yet assessed
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Abdominal obesity and alcohol use modify the impact of genetic risk for incident advanced liver disease in the general population ↗Liver International · 2023 · PMID 36843445not yet assessed
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Persistent organic pollutants associate with liver disease in a Finnish general population sample ↗Liver International · 2023 · PMID 37312647not yet assessed
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NTHL1 is a recessive cancer susceptibility gene ↗Scientific Reports · 2023 · PMID 38036545not yet assessed
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A FinnGen pilot clinical recall study for Alzheimer’s disease ↗Scientific Reports · 2023 · PMID 37537264not yet assessed
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Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population ↗Nature · 2023 · PMID 36829046not yet assessed
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Metabolomic and genomic prediction of common diseases in 477,706 participants in three national biobanks ↗medRxiv · 2023not yet assessed
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Mapping the aetiological foundations of the heart failure spectrum using human genetics ↗medRxiv · 2023not yet assessed
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not yet assessed
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not yet assessed
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not yet assessed
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Divergent trends in the incidence and mortality of coronary events, especially in women. Evidence from Finland in 1996-2021 ↗medRxiv · 2023not yet assessed
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Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women ↗RePEc: Research Papers in Economics · 2023not yet assessed
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not yet assessed
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not yet assessed
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Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population ↗Circulation Genomic and Precision Medicine · 2023 · PMID 37577800not yet assessed
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not yet assessed
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Recalling Biobank Participants to Clinical Study of Alzheimer’s Disease – FinnGen Pilot Study ↗Alzheimer s & Dementia · 2023not yet assessed
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Remdesivir and three other drugs for hospitalised patients with COVID-19: final results of the WHO Solidarity randomised trial and updated meta-analyses ↗The Lancet · 2022 · PMID 35512728not yet assessed
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Whole-genome sequencing reveals host factors underlying critical COVID-19 ↗Nature · 2022 · PMID 35255492not yet assessed
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A first update on mapping the human genetic architecture of COVID-19 ↗Nature · 2022 · PMID 35922517not yet assessed
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BMI is positively associated with accelerated epigenetic aging in twin pairs discordant for body mass index ↗Journal of Internal Medicine · 2022 · PMID 35699258not yet assessed
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Development and validation of a model to predict incident chronic liver disease in the general population: The CLivD score ↗Journal of Hepatology · 2022 · PMID 35271949not yet assessed
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Immunoglobulin G N-Glycosylation Signatures in Incident Type 2 Diabetes and Cardiovascular Disease ↗Diabetes Care · 2022 · PMID 36174116not yet assessed
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Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes ↗Communications Biology · 2022 · PMID 35197564not yet assessed
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Circulating Metabolic Biomarkers Are Consistently Associated With Type 2 Diabetes Risk in Asian and European Populations ↗The Journal of Clinical Endocrinology & Metabolism · 2022 · PMID 35390150not yet assessed
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Longitudinal profiling of metabolic ageing trends in two population cohorts of young adults ↗International Journal of Epidemiology · 2022 · PMID 35441226not yet assessed
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Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals ↗Communications Biology · 2022 · PMID 35697829not yet assessed
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Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations ↗Journal of Thrombosis and Haemostasis · 2022 · PMID 35285134not yet assessed
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Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis ↗Communications Biology · 2022 · PMID 35978133not yet assessed
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Pharmacoepigenetics of hypertension: genome-wide methylation analysis of responsiveness to four classes of antihypertensive drugs using a double-blind crossover study design ↗Epigenetics · 2022 · PMID 35213289not yet assessed
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Understanding the complex genetic architecture connecting rheumatoid arthritis, osteoporosis and inflammation: discovering causal pathways ↗Human Molecular Genetics · 2022 · PMID 35349660not yet assessed
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Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen ↗BMJ Open · 2022 · PMID 36198465not yet assessed
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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 ↗Frontiers in Genetics · 2022 · PMID 36186460not yet assessed
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Psychosocial Effects of Receiving Genome-Wide Polygenic Risk Information Concerning Type 2 Diabetes and Coronary Heart Disease: A Randomized Controlled Trial ↗Frontiers in Genetics · 2022 · PMID 35706448not yet assessed
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Association between arterial hypertension and liver outcomes using polygenic risk scores: a population-based study ↗Scientific Reports · 2022 · PMID 36114231not yet assessed
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Comparison of various strategies to define the optimal target population for liver fibrosis screening: A population‐based cohort study ↗United European Gastroenterology Journal · 2022 · PMID 36318497not yet assessed
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Identification of healthspan-promoting genes in Caenorhabditis elegans based on a human GWAS study ↗Biogerontology · 2022 · PMID 35748965not yet assessed
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Genetic and observational evidence: No independent role for cholesterol efflux over static high‐density lipoprotein concentration measures in coronary heart disease risk assessment ↗Journal of Internal Medicine · 2022 · PMID 35289444not yet assessed
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Reaching for Precision Healthcare in Finland via Use of Genomic Data ↗Frontiers in Genetics · 2022 · PMID 35559047not yet assessed
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Substantial Fat Loss in Physique Competitors Is Characterized by Increased Levels of Bile Acids, Very-Long Chain Fatty Acids, and Oxylipins ↗Metabolites · 2022 · PMID 36295830not yet assessed
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Attribution of diabetes to the development of severe liver disease in the general population ↗Liver International · 2022 · PMID 35574998not yet assessed
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Circulating oxylipin and bile acid profiles of dexmedetomidine, propofol, sevoflurane, and S-ketamine: a randomised controlled trial using tandem mass spectrometry ↗BJA Open · 2022 · PMID 37588789not yet assessed
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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 ↗Open Forum Infectious Diseases · 2022not yet assessed
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Abdominal obesity is key when evaluating interactions between alcohol use and obesity for liver disease ↗Journal of Hepatology · 2022not yet assessed
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FinnGen: Unique genetic insights from combining isolated population and national health register data ↗medRxiv · 2022not yet assessed
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Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries ↗Nature · 2022 · PMID 36376532not yet assessed
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Atlas of plasma nuclear magnetic resonance biomarkers for health and disease in 118,461 individuals from the UK Biobank ↗medRxiv · 2022not yet assessed
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Immunoglobulin G N-glycosylation signatures in incident type 2 diabetes and cardiovascular disease ↗2022not yet assessed
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Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice ↗European Journal of Human Genetics · 2022not yet assessed
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Genome-wide characterization of circulating metabolic biomarkers reveals substantial pleiotropy and novel disease pathways ↗medRxiv · 2022not yet assessed
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Health, socioeconomic and genetic predictors of COVID-19 vaccination uptake: a nationwide machine-learning study ↗medRxiv · 2022not yet assessed
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Reply to Letter by Tellier et al., ‘Scientific refutation of ESHG statement on embryo selection’ ↗European Journal of Human Genetics · 2022 · PMID 36450798not yet assessed
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Association between mitochondrial DNA haplogroups J and K, serum branched-chain amino acids and lowered capability for endurance exercise ↗BMC Sports Science Medicine and Rehabilitation · 2022 · PMID 35619160not yet assessed
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COMPREHENSIVE BIOMARKER PROFILING OF HYPERTENSION IN 36,985 FINNISH INDIVIDUALS ↗Journal of Hypertension · 2022not yet assessed
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Immunoglobulin G N-glycosylation signatures in incident type 2 diabetes and cardiovascular disease ↗2022not yet assessed
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Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice ↗European Journal of Human Genetics · 2022 · PMID 35982123not yet assessed
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Editorial: Can population health be personalized? Estonia and Finland as examples ↗Frontiers in Genetics · 2022 · PMID 36353106not yet assessed
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Correction to: Reply to Letter by Tellier et al., ‘Scientific refutation of ESHG statement on embryo selection’ ↗European Journal of Human Genetics · 2022 · PMID 36536147not yet assessed
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Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression ↗Nature Genetics · 2021 · PMID 34475573not yet assessed
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Mapping the human genetic architecture of COVID-19 ↗Nature · 2021 · PMID 34237774not yet assessed
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Taxonomic signatures of cause-specific mortality risk in human gut microbiome ↗Nature Communications · 2021 · PMID 33976176not yet assessed
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Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour ↗Nature Human Behaviour · 2021 · PMID 34211149not yet assessed
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The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice ↗European Journal of Human Genetics · 2021 · PMID 34916614not yet assessed
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Genome-Wide Association Study of Peripheral Artery Disease ↗Circulation Genomic and Precision Medicine · 2021 · PMID 34601942not yet assessed
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The Role of Inflammatory Cytokines as Intermediates in the Pathway from Increased Adiposity to Disease ↗Obesity · 2021 · PMID 33491305not yet assessed
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Cardiovascular Risk Factors and MRI Markers of Cerebral Small Vessel Disease ↗Neurology · 2021 · PMID 34845052not yet assessed
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Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices ↗Nature Communications · 2021 · PMID 33846329not yet assessed
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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 CohortsUniversity of Oulu Repository (University of Oulu) · 2021not yet assessed
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A Dynamic Aspartate‐to‐Alanine Aminotransferase Ratio Provides Valid Predictions of Incident Severe Liver Disease ↗Hepatology Communications · 2021 · PMID 34141987not yet assessed
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Plasma N-glycome shows continuous deterioration as the diagnosis of insulin resistance approaches ↗BMJ Open Diabetes Research & Care · 2021 · PMID 34518155not yet assessed
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Association of Circulating Metabolites in Plasma or Serum and Risk of Stroke: Meta-analysis From 7 Prospective Cohorts. ↗PubMed · 2021 · PMID 33268560not yet assessed
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Incidence of liver‐related morbidity and mortality in a population cohort of non‐alcoholic fatty liver disease ↗Liver International · 2021 · PMID 34219352not yet assessed
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Effects of dexmedetomidine, propofol, sevoflurane and S-ketamine on the human metabolome ↗European Journal of Anaesthesiology · 2021 · PMID 34534172not yet assessed
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A Web Portal for Communicating Polygenic Risk Score Results for Health Care Use—The P5 Study ↗Frontiers in Genetics · 2021 · PMID 34777479not yet assessed
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Comprehensive biomarker profiling of hypertension in 36 985 Finnish individuals ↗Journal of Hypertension · 2021 · PMID 34784307not yet assessed
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Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants ↗Molecular Psychiatry · 2021 · PMID 33526825not yet assessed
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The Genomics of Heart Failure: Design and Rationale of the HERMES Consortium ↗ESC Heart Failure · 2021 · PMID 34480422not yet assessed
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Dysfunction of complement receptors CR3 (CD11b/18) and CR4 (CD11c/18) in pre‐eclampsia: a genetic and functional study ↗BJOG An International Journal of Obstetrics & Gynaecology · 2021 · PMID 33539617not yet assessed
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Changes in the fine-scale genetic structure of Finland through the 20th century ↗PLoS Genetics · 2021 · PMID 33661898not yet assessed
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Waist and hip circumference are independently associated with the risk of liver disease in population‐based studies ↗Liver International · 2021 · PMID 34510711not yet assessed
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Mitochondrial bioenergetic pathways in blood leukocyte transcriptome decrease after intensive weight loss but are rescued following weight regain in female physique athletes ↗The FASEB Journal · 2021 · PMID 33710692not yet assessed
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Low serum vitamin D level associated with incident advanced liver disease in the general population – a prospective study ↗Scandinavian Journal of Gastroenterology · 2021 · PMID 33478287not yet assessed
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HDL-Mediated Cholesterol Efflux Associates with Incident Kidney Disease ↗Clinical Chemistry · 2021 · PMID 33723592not yet assessed
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Regulating the unknown: A guide to regulating genomics for health policy-makers2021not yet assessed
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Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expressionFigshare · 2021not yet assessed
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Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability ↗Nature Communications · 2021 · PMID 33558525not yet assessed
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Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals ↗Nature Genetics · 2021 · PMID 33727701not yet assessed
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not yet assessed
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A Web Portal for Communicating Polygenic Risk Score Results for Health Care Use-The P5 StudySTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2021not yet assessed
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Dysfunction of complement receptors CR3 (CD11b/18) and CR4 (CD11c/18) in pre-eclampsia: a genetic and functional studySTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2021not yet assessed
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METABOLIC PROFILING OF HYPERTENSION IN 36,985 FINNISH INDIVIDUALS ↗Journal of the American College of Cardiology · 2021not yet assessed
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Chromosome Xq23 Is Associated with Lower Atherogenic Lipid Concentrations and Favorable Cardiometabolic IndicesDigital Commons@Becker (Washington University School of Medicine) · 2021not yet assessed
-
Mitochondrial bioenergetic pathways in blood leukocyte transcriptome decrease after intensive weight loss but are rescued following weight regain in female physique athletesSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2021not yet assessed
-
METABOLIC PROFILING OF HYPERTENSION IN 36,985 FINNISH INDIVIDUALSSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2021not yet assessed
-
Incidence of liver-related morbidity and mortality in a population cohort of non-alcoholic fatty liver diseaseSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2021not yet assessed
-
Publisher Correction: Identification of 371 genetic variants for age at first sex and birth linked to externalising behavior ↗Nature Human Behaviour · 2021 · PMID 34321615not yet assessed
-
HDL-Mediated Cholesterol Efflux Associates with Incident Kidney DiseaseSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2021not yet assessed
-
A Dynamic Aspartate-to-Alanine Aminotransferase Ratio Provides Valid Predictions of Incident Severe Liver DiseaseSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2021not yet assessed
-
Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variantsDigital Commons@Becker (Washington University School of Medicine) · 2021not yet assessed
-
Low serum vitamin D level associated with incident advanced liver disease in the general population - a prospective studySTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2021not yet assessed
-
Waist and hip circumference are independently associated with the risk of liver disease in population-based studiesSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2021not yet assessed
-
Plasma N-glycome shows continuous deterioration as the diagnosis of insulin resistance approachesSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2021not yet assessed
-
The Role of Inflammatory Cytokines as Intermediates in the Pathway from Increased Adiposity to DiseaseSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2021not yet assessed
-
Genome-Wide Association Study of Peripheral Artery DiseaseOxford University Research Archive (ORA) (University of Oxford) · 2021not yet assessed
-
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 ↗Journal of the American Heart Association · 2021 · PMID 34845932not yet assessed
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Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke ↗Journal of the American Heart Association · 2021 · PMID 34668383not yet assessed
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Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure ↗Nature Communications · 2020 · PMID 31919418not yet assessed
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Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals ↗Nature Genetics · 2020 · PMID 33230300not yet assessed
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Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women ↗Nature Communications · 2020 · PMID 33239696not yet assessed
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Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length ↗The American Journal of Human Genetics · 2020 · PMID 32109421not yet assessed
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The role of polygenic risk and susceptibility genes in breast cancer over the course of life ↗Nature Communications · 2020 · PMID 33318493not yet assessed
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Interleukin-6 Signaling Effects on Ischemic Stroke and Other Cardiovascular Outcomes ↗Circulation Genomic and Precision Medicine · 2020 · PMID 32397738not yet assessed
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Glycosylation of immunoglobulin G is regulated by a large network of genes pleiotropic with inflammatory diseases ↗Science Advances · 2020 · PMID 32128391not yet assessed
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Metabolic profiling of angiopoietin-like protein 3 and 4 inhibition: a drug-target Mendelian randomization analysis ↗European Heart Journal · 2020 · PMID 33351885not yet assessed
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Plasma <i>N</i>-Glycans as Emerging Biomarkers of Cardiometabolic Risk: A Prospective Investigation in the EPIC-Potsdam Cohort Study ↗Diabetes Care · 2020 · PMID 31915204not yet assessed
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Identification, Heritability, and Relation With Gene Expression of Novel DNA Methylation Loci for Blood Pressure ↗Hypertension · 2020 · PMID 32520614not yet assessed
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Apolipoprotein A-I concentrations and risk of coronary artery disease: A Mendelian randomization study ↗Atherosclerosis · 2020 · PMID 32113648not yet assessed
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Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma ↗PLoS Genetics · 2020 · PMID 32369491not yet assessed
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An epigenome-wide association study of metabolic syndrome and its components ↗Scientific Reports · 2020 · PMID 33239708not yet assessed
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not yet assessed
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A cross-omics integrative study of metabolic signatures of chronic obstructive pulmonary disease ↗BMC Pulmonary Medicine · 2020 · PMID 32677943not yet assessed
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A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease ↗UNC Libraries · 2020not yet assessed
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Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus ↗Circulation Genomic and Precision Medicine · 2020 · PMID 33321069not yet assessed
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Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels ↗UNC Libraries · 2020not yet assessed
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Diabetes is associated with familial idiopathic normal pressure hydrocephalus: a case–control comparison with family members ↗Fluids and Barriers of the CNS · 2020 · PMID 32933532not yet assessed
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A data-driven medication score predicts 10-year mortality among aging adults ↗Scientific Reports · 2020 · PMID 32978407not yet assessed
-
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape ↗UNC Libraries · 2020not yet assessed
-
Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulationUEF eRepo (University of Eastern Finland) · 2020not yet assessed
-
Genetic Predisposition to Coronary Artery Disease in Type 2 diabetes2020not yet assessed
-
not yet assessed
-
Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus ↗EUR Research Repository (Erasmus University Rotterdam) · 2020not yet assessed
-
not yet assessed
-
not yet assessed
-
not yet assessed
-
Plasma N-Glycans as Emerging Biomarkers of Cardiometabolic Risk: A Prospective Investigation in the EPIC-Potsdam Cohort StudySTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2020not yet assessed
-
Risks of Light and Moderate Alcohol Use in Fatty Liver Disease: Follow-Up of Population CohortsSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2020not yet assessed
-
Correction: Lipoprotein signatures of cholesteryl ester transfer protein and HMG-CoA reductase inhibition ↗PLoS Biology · 2020 · PMID 32142508not yet assessed
-
Data-driven multivariate population subgrouping via lipoprotein phenotypes versus apolipoprotein B in the risk assessment of coronary heart diseaseSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2020not yet assessed
-
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk ↗Research at the University of Copenhagen (University of Copenhagen) · 2020not yet assessed
-
not yet assessed
-
Glycosylation of immunoglobulin G is regulated by a large network of genes pleiotropic with inflammatory diseasesUtrecht University Repository (Utrecht University) · 2020not yet assessed
-
Combined Effects of Alcohol and Metabolic Disorders in Patients With Chronic Liver DiseaseSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2020not yet assessed
-
Apolipoprotein A-I concentrations and risk of coronary artery disease: A Mendelian randomization studyTampere University Institutional Repository (Tampere University) · 2020not yet assessed
-
Identification, Heritability, and Relation With Gene Expression of Novel DNA Methylation Loci for Blood PressureUtrecht University Repository (Utrecht University) · 2020not yet assessed
-
Diabetes is associated with familial idiopathic normal pressure hydrocephalus: a case–control comparison with family members ↗Työväentutkimus Vuosikirja · 2020not yet assessed
-
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)WOS · 2020not yet assessed
-
Genetic risk factors for pre-eclampsia in the Finnish populationSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2020not yet assessed
-
Lipoprotein and Metabolite Biomarkers for Coronary and Peripheral Artery Disease: Blood Biomarker Profiling of 32,000 Individuals From Five Prospective StudiesSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2020not yet assessed
-
Metabolic profiling of angiopoietin-like protein 3 and 4 inhibition: a drug-target Mendelian randomization analysis. ↗STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2020not yet assessed
-
Regulating the unknown2020not yet assessed
-
Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucomaSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2020not yet assessed
-
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length. ↗QUT ePrints (Queensland University of Technology) · 2020not yet assessed
-
A data-driven medication score predicts 10-year mortality among aging adultsSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2020not yet assessed
-
Polygenic risk score in type 2 diabetes risk prediction: genomics to healthcareSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2020not yet assessed
-
Source code for the article Taxonomic Signatures of Long-Term Mortality Risk in Human Gut Microbiota ↗Zenodo (CERN European Organization for Nuclear Research) · 2020not yet assessed
-
A cross-omics integrative study of metabolic signatures of chronic obstructive pulmonary disease ↗Työväentutkimus Vuosikirja · 2020not yet assessed
-
Obesity and alcohol intake modify the impact of genetic variants on the risk for incident liver disease in the general population ↗Journal of Hepatology · 2020not yet assessed
-
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals ↗UNC Libraries · 2020not yet assessed
-
Correction: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults ↗UNC Libraries · 2020not yet assessed
-
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways ↗UNC Libraries · 2020not yet assessed
-
Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass ↗UNC Libraries · 2020not yet assessed
-
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ↗UNC Libraries · 2020not yet assessed
-
Additional file 1 of A cross-omics integrative study of metabolic signatures of chronic obstructive pulmonary disease ↗Figshare · 2020not yet assessed
-
A catalog of genetic loci associated with kidney function from analyses of a million individuals ↗Nature Genetics · 2019 · PMID 31152163not yet assessed
-
A metabolic profile of all-cause mortality risk identified in an observational study of 44,168 individuals ↗Nature Communications · 2019 · PMID 31431621not yet assessed
-
Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits ↗Nature Communications · 2019 · PMID 31341166not yet assessed
-
Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances ↗eLife · 2019 · PMID 30642433not yet assessed
-
Circulating metabolites and the risk of type 2 diabetes: a prospective study of 11,896 young adults from four Finnish cohorts ↗Diabetologia · 2019 · PMID 31584131not yet assessed
-
Genetic architecture of human plasma lipidome and its link to cardiovascular disease ↗Nature Communications · 2019 · PMID 31551469not yet assessed
-
Associations of autozygosity with a broad range of human phenotypes ↗Nature Communications · 2019 · PMID 31673082not yet assessed
-
Risks of Light and Moderate Alcohol Use in Fatty Liver Disease: Follow‐Up of Population Cohorts ↗Hepatology · 2019 · PMID 31323122not yet assessed
-
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci ↗Molecular Psychiatry · 2019 · PMID 30617275not yet assessed
-
Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland ↗The American Journal of Human Genetics · 2019 · PMID 31155286not yet assessed
-
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution ↗Nature Genetics · 2019 · PMID 30778226not yet assessed
-
Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns ↗Journal of Medical Genetics · 2019 · PMID 31217265not yet assessed
-
A distinctive DNA methylation pattern in insufficient sleep ↗Scientific Reports · 2019 · PMID 30718923not yet assessed
-
Lipoprotein signatures of cholesteryl ester transfer protein and HMG-CoA reductase inhibition ↗PLoS Biology · 2019 · PMID 31860674not yet assessed
-
Multivariate Genome-wide Association Analysis of a Cytokine Network Reveals Variants with Widespread Immune, Haematological, and Cardiometabolic Pleiotropy ↗The American Journal of Human Genetics · 2019 · PMID 31679650not yet assessed
-
Food neophobia associates with poorer dietary quality, metabolic risk factors, and increased disease outcome risk in population-based cohorts in a metabolomics study ↗American Journal of Clinical Nutrition · 2019 · PMID 31161197not yet assessed
-
Intertumoral heterogeneity in patient-specific drug sensitivities in treatment-naïve glioblastoma ↗BMC Cancer · 2019 · PMID 31238897not yet assessed
-
Substantial fat mass loss reduces low-grade inflammation and induces positive alteration in cardiometabolic factors in normal-weight individuals ↗Scientific Reports · 2019 · PMID 30837600not yet assessed
-
Molecular Pathways Mediating Immunosuppression in Response to Prolonged Intensive Physical Training, Low-Energy Availability, and Intensive Weight Loss ↗Frontiers in Immunology · 2019 · PMID 31134054not yet assessed
-
Quality of dietary fat and genetic risk of type 2 diabetes: individual participant data meta-analysis ↗BMJ · 2019 · PMID 31345923not yet assessed
-
Serum lipopolysaccharides predict advanced liver disease in the general population ↗JHEP Reports · 2019 · PMID 32039385not yet assessed
-
Combined Effects of Alcohol and Metabolic Disorders in Patients With Chronic Liver Disease ↗Clinical Gastroenterology and Hepatology · 2019 · PMID 31255807not yet assessed
-
Elevated serum alpha-1 antitrypsin is a major component of GlycA-associated risk for future morbidity and mortality ↗PLoS ONE · 2019 · PMID 31644575not yet assessed
-
Genetic and lifestyle risk factors for advanced liver disease among men and women ↗Journal of Gastroenterology and Hepatology · 2019 · PMID 31260143not yet assessed
-
Feasibility study of using high‐throughput drug sensitivity testing to target recurrent glioblastoma stem cells for individualized treatment ↗Clinical and Translational Medicine · 2019 · PMID 31889236not yet assessed
-
Data-driven multivariate population subgrouping via lipoprotein phenotypes versus apolipoprotein B in the risk assessment of coronary heart disease ↗Atherosclerosis · 2019 · PMID 31931463not yet assessed
-
Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using Metabolomics ↗Endocrinology · 2019 · PMID 31125048not yet assessed
-
Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease ↗Journal of the American Heart Association · 2019 · PMID 31070104not yet assessed
-
Direct Estimation of HDL-Mediated Cholesterol Efflux Capacity from Serum ↗Clinical Chemistry · 2019 · PMID 30996052not yet assessed
-
Resistance Training Induces Antiatherogenic Effects on Metabolomic Pathways ↗Medicine & Science in Sports & Exercise · 2019 · PMID 30973481not yet assessed
-
THU-251-Metabolic risk factors for advanced liver disease among alcohol risk users in the general population ↗Journal of Hepatology · 2019not yet assessed
-
LBP-01-In NAFLD, alcohol drinking habits and genetics predict progression to advanced liver disease: follow-up of population surveys ↗Journal of Hepatology · 2019not yet assessed
-
FinnGen-tutkimuksen lupauksetTyöväentutkimus Vuosikirja · 2019not yet assessed
-
Insulin Resistance and Genetic Risk Predict Liver‐Related Outcomes and Death in Nonalcoholic Fatty Liver Disease ↗Hepatology Communications · 2019 · PMID 31832576not yet assessed
-
Circulating metabolites and the risk of type 2 diabetes: a prospective study of 11,896 young adults from four Finnish cohorts ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation ↗Molecular Psychiatry · 2019not yet assessed
-
Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗Nature Genetics · 2019not yet assessed
-
Multivariate genome-wide association analysis of a cytokine network reveals variants with widespread immune, haematological and cardiometabolic pleiotropy ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Search for early pancreatic cancer blood biomarkers in five European prospective population biobanks using metabolomics ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in FinlandSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
Genetic variation in apolipoprotein A-I concentrations and risk of coronary artery disease ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Metabolic risk factors for advanced liver disease among alcohol risk users in the general populationSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
In NAFLD, alcohol drinking habits and genetics predict progression to advanced liver disease: follow-up of population surveysSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
Genetic and lifestyle risk factors for advanced liver disease among men and womenSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
Transnational access to large prospective cohorts in Europe: Current trends and unmet needsData Archiving and Networked Services (DANS) · 2019not yet assessed
-
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. ↗Archive ouverte UNIGE (University of Geneva) · 2019not yet assessed
-
A distinctive DNA methylation pattern in insufficient sleepSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
Associations of increased physical performance and change in body composition with molecular pathways of heart disease and diabetes riskSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studies (vol 14, pg 707, 2018)WOS · 2019not yet assessed
-
The rs2516839 variation of USF1 gene is associated with 4-year mortality of nonagenarian women: The Vitality 90+studySTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
A multivariate linear model for investigating the association between gene-module co-expression and a continuous covariate ↗Statistical Applications in Genetics and Molecular Biology · 2019 · PMID 30875332not yet assessed
-
Disentangling the genetics of lean massPure Amsterdam UMC · 2019not yet assessed
-
Substantial fat mass loss reduces low-grade inflammation and induces positive alteration in cardiometabolic factors in normal-weight individualsSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
GENETICS OF VACCINATION RELATED NARCOLEPSY ↗European Neuropsychopharmacology · 2019not yet assessed
-
SAT-271-Genetic risk factors for advanced alcoholic and non-alcoholic liver disease in the general population ↗Journal of Hepatology · 2019not yet assessed
-
Genetic risk factors for advanced alcoholic and non-alcoholic liver disease in the general populationSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variantSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
Rare protein-altering variants in <i>ANGPTL7</i> lower intraocular pressure and protect against glaucoma ↗bioRxiv (Cold Spring Harbor Laboratory) · 2019not yet assessed
-
Intertumoral heterogeneity in patient-specific drug sensitivities in treatment-naïve glioblastoma ↗Työväentutkimus Vuosikirja · 2019not yet assessed
-
Food neophobia associates with poorer dietary quality, metabolic risk factors, and increased disease outcome risk in population-based cohorts in a metabolomics studySTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traitsData Archiving and Networked Services (DANS) · 2019not yet assessed
-
Direct Estimation of HDL-Mediated Cholesterol Efflux Capacity from SerumSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
A metabolic profile of all-cause mortality risk identified in an observational study of 44,168 individualsData Archiving and Networked Services (DANS) · 2019not yet assessed
-
Resistance Training Induces Antiatherogenic Effects on Metabolomic PathwaysSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
Genetic architecture of human plasma lipidome and its link to cardiovascular diseaseUEF eRepo (University of Eastern Finland) · 2019not yet assessed
-
INSULIN RESISTANCE AND GENETIC RISK PREDICT LIVER-RELATED OUTCOMES AND DEATH IN NON-ALCOHOLIC FATTY LIVER DISEASESTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
CNV Association with Neurodevelopmental Phenotypes in Finnish Population CohortSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
Polygenic risk information for coronary artery disease-P5.fi FinHealthSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
Risk perceptions for Type 2 diabetes and coronary heart disease after receiving risk information - participants of P5 FinHealth studySTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
Multivariate Genome-wide Association Analysis of a Cytokine Network Reveals Variants with Widespread Immune, Haematological, and Cardiometabolic Pleiotropy. ↗STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
Lipoprotein signatures of cholesteryl ester transfer protein and HMG-CoA reductase inhibition. ↗Apollo (University of Cambridge) · 2019not yet assessed
-
Circulating metabolites and the risk of type 2 diabetes: a prospective study of 11,896 young adults from four Finnish cohortsTampere University Institutional Repository (Tampere University) · 2019not yet assessed
-
Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using MetabolomicsData Archiving and Networked Services (DANS) · 2019not yet assessed
-
Lipoprotein signatures of cholesteryl ester transfer protein and HMG-CoA reductase inhibition ↗Apollo (University of Cambridge) · 2019not yet assessed
-
A multivariate linear model for investigating the association between gene-module co-expression and a continuous covariateSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2019not yet assessed
-
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk ↗UNC Libraries · 2019not yet assessed
-
not yet assessed
-
not yet assessed
-
Additional file 1: of Intertumoral heterogeneity in patient-specific drug sensitivities in treatment-naïve glioblastoma ↗Figshare · 2019not yet assessed
-
not yet assessed
-
not yet assessed
-
Additional file 3: of Intertumoral heterogeneity in patient-specific drug sensitivities in treatment-naïve glioblastoma ↗Figshare · 2019not yet assessed
-
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes ↗Nature Communications · 2018 · PMID 30054458not yet assessed
-
Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood ↗Nature Communications · 2018 · PMID 29891976not yet assessed
-
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes ↗Nature Genetics · 2018 · PMID 29632382not yet assessed
-
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 ↗Alzheimer s & Dementia · 2018 · PMID 29519576not yet assessed
-
Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation ↗Molecular Psychiatry · 2018 · PMID 30108311not yet assessed
-
Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studies ↗Alzheimer s & Dementia · 2018 · PMID 29316447not yet assessed
-
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes ↗Diabetes · 2018 · PMID 29703844not yet assessed
-
Susceptibility of low-density lipoprotein particles to aggregate depends on particle lipidome, is modifiable, and associates with future cardiovascular deaths ↗European Heart Journal · 2018 · PMID 29982602not yet assessed
-
Metabolomic Consequences of Genetic Inhibition of PCSK9 Compared With Statin Treatment ↗Circulation · 2018 · PMID 30524137not yet assessed
-
Low galactosylation of IgG associates with higher risk for future diagnosis of rheumatoid arthritis during 10 years of follow-up ↗Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 2018 · PMID 29572115not yet assessed
-
Genetic Variants in SGLT1, Glucose Tolerance, and Cardiometabolic Risk ↗Journal of the American College of Cardiology · 2018 · PMID 30286918not yet assessed
-
Plasma N-glycans in colorectal cancer risk ↗Scientific Reports · 2018 · PMID 29872119not yet assessed
-
Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland ↗The American Journal of Human Genetics · 2018 · PMID 29706349not yet assessed
-
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 ↗Molecular Psychiatry · 2018 · PMID 29988085not yet assessed
-
Biomarker Glycoprotein Acetyls Is Associated With the Risk of a Wide Spectrum of Incident Diseases and Stratifies Mortality Risk in Angiography Patients ↗Circulation Genomic and Precision Medicine · 2018 · PMID 30571186not yet assessed
-
Disentangling the genetics of lean mass ↗American Journal of Clinical Nutrition · 2018 · PMID 30721968not yet assessed
-
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. ↗Open Access CRIS of the University of Bern · 2018not yet assessed
-
Transnational access to large prospective cohorts in Europe: Current trends and unmet needs ↗New Biotechnology · 2018 · PMID 30342241not yet assessed
-
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus ↗European Journal of Human Genetics · 2018 · PMID 29379196not yet assessed
-
Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant ↗European Journal of Medical Genetics · 2018 · PMID 30031151not yet assessed
-
Role of Academic Biobanks in Public–Private Partnerships in the European Biobanking and BioMolecular Resources Research Infrastructure Community ↗Biopreservation and Biobanking · 2018 · PMID 30499696not yet assessed
-
Mendelian randomisation analysis of clustered causal effects of body mass on cardiometabolic biomarkers ↗BMC Bioinformatics · 2018 · PMID 30066639not yet assessed
-
Sequential double cross-validation for assessment of added predictive ability in high-dimensional omic applications ↗Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) · 2018not yet assessed
-
Associations of increased physical performance and change in body composition with molecular pathways of heart disease and diabetes risk ↗American Journal of Physiology-Endocrinology and Metabolism · 2018 · PMID 30422703not yet assessed
-
Circulating Metabolites and the Risk of Type 2 Diabetes—A Prospective Study of 10,938 Young Adults from Four Finnish Cohorts ↗Diabetes · 2018not yet assessed
-
The <i>rs2516839</i> variation of <i>USF1</i> gene is associated with 4‐year mortality of nonagenarian women: The Vitality 90+ study ↗Annals of Human Genetics · 2018 · PMID 30203836not yet assessed
-
Genome-Wide Analysis of Nuclear Magnetic Resonance Metabolites Revealed Parent-of-Origin Effect on Triglycerides in Medium Very Low-Density Lipoprotein in <i>PTPRD</i> Gene ↗Biomarkers in Medicine · 2018 · PMID 29536759not yet assessed
-
Suomalaisten geenitietämys ja suhtautuminen perimästä saatavaan terveystietoonTyöväentutkimus Vuosikirja · 2018not yet assessed
-
Sequential double cross-validation for assessment of added predictive ability in high-dimensional omic applications ↗The Annals of Applied Statistics · 2018not yet assessed
-
Susceptibility of low-density lipoprotein particles to aggregate depends on particle lipidome, is modifiable, and associates with future cardiovascular deathsTampere University Institutional Repository (Tampere University) · 2018not yet assessed
-
Rare mutations in factor H predispose to severe preeclampsia ↗Molecular Immunology · 2018not yet assessed
-
Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Geographic variation and bias in polygenic scores of complex diseases and traits in Finland ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Protein-Coding Variants Implicate Novel Genes Related to Lipid Homeostasis Contributing to Body Fat Distribution ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Narcolepsy risk loci are enriched in immune cells and suggest autoimmune modulation of the T cell receptor repertoire ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗Nature Genetics · 2018 · PMID 29549329not yet assessed
-
Lipoprotein Signatures of Cholesteryl Ester Transfer Protein and HMG-CoA Reductase Inhibition ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Plasma N-glycans in colorectal cancer riskSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018not yet assessed
-
Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
The landscape of incident disease risk for the biomarker GlycA and its mortality stratification in angiography patients ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Elevated alpha-1 antitrypsin is a major component of GlycA-associated risk for future morbidity and mortality ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Low galactosylation of IgG associates with higher risk for future diagnosis of rheumatoid arthritis during 10 years of follow-upSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018not yet assessed
-
not yet assessed
-
NEXT GENERATION SEQUENCING OF BTNL2 REVEALS NOVEL ASSOCIATIONS WITH ACUTE CORONARY SYNDROME IN FINNISH POPULATIONSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018not yet assessed
-
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locusSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018not yet assessed
-
Jätetäänkö sitten myös verenpaine mittaamattaTyöväentutkimus Vuosikirja · 2018not yet assessed
-
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. ↗UWA Profiles and Research Repository (University of Western Australia) · 2018not yet assessed
-
Genomitiedon arkaluonteisuus on tiukassa elävä myyttiTyöväentutkimus Vuosikirja · 2018not yet assessed
-
Genetic predisposition to obesity, restrained eating and changes in body weight: a population-based prospective studyUCL Discovery (University College London) · 2018not yet assessed
-
The Effects Of Intensive Weight Loss On Metabolome In Female Fitness Competitors ↗Medicine & Science in Sports & Exercise · 2018not yet assessed
-
not yet assessed
-
Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studiesKölner Universitäts PublikationsServer (Universität zu Köln) · 2018not yet assessed
-
Association of branched-chain amino acids and other circulating metabolites with risk of incident dementia and Alzheimer's disease: A prospective study in eight cohortsTampere University Institutional Repository (Tampere University) · 2018not yet assessed
-
Direct estimation of HDL-mediated cholesterol efflux capacity from serum ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Cohort Profile: The National FINRISK StudySTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018not yet assessed
-
Rare mutations in factor H predispose to severe preeclampsiaSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018not yet assessed
-
Biomarker Glycoprotein Acetyls Associated With the Risk of a Wide Spectrum of Incident Diseases and Stratifies Mortality Risk in Angiography PatientsSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018not yet assessed
-
Role of Academic Biobanks in Public-Private Partnerships in the European Biobanking and BioMolecular Resources Research Infrastructure CommunitySTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018not yet assessed
-
The Effects Of Intensive Weight Loss On Metabolome In Female Fitness CompetitorsSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018not yet assessed
-
Metabolomic consequences of genetic inhibition of PCSK9 compared with statin treatment ↗bioRxiv (Cold Spring Harbor Laboratory) · 2018not yet assessed
-
Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in FinlandSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018not yet assessed
-
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci ↗Apollo (University of Cambridge) · 2018not yet assessed
-
Mendelian randomisation analysis of clustered causal effects of body mass on cardiometabolic biomarkers ↗STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018not yet assessed
-
Genome-wide analysis of nuclear magnetic resonance metabolites revealed parent-of-origin effect on triglycerides in medium very low-density lipoprotein in PTPRD geneSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018not yet assessed
-
Correction to: Increased plasma N-glycome complexity is associated with higher risk of type 2 diabetes (vol 60, pg 2352, 2017)STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018not yet assessed
-
Genetic determinants of healthy ageingSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2018not yet assessed
-
Additional file 2 of Mendelian randomisation analysis of clustered causal effects of body mass on cardiometabolic biomarkers ↗Figshare · 2018not yet assessed
-
Rare and low-frequency coding variants alter human adult height ↗Nature · 2017 · PMID 28146470not yet assessed
-
Exome-wide association study of plasma lipids in >300,000 individuals ↗Nature Genetics · 2017 · PMID 29083408not yet assessed
-
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity ↗Nature Genetics · 2017 · PMID 29273807not yet assessed
-
Genetic evidence of assortative mating in humans ↗Nature Human Behaviour · 2017not yet assessed
-
Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults ↗PLoS Genetics · 2017 · PMID 28448500not yet assessed
-
Cohort Profile: The National FINRISK Study ↗International Journal of Epidemiology · 2017 · PMID 29165699not yet assessed
-
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis ↗The Lancet Neurology · 2017 · PMID 29029846not yet assessed
-
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits ↗The American Journal of Human Genetics · 2017 · PMID 28552196not yet assessed
-
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass ↗Nature Communications · 2017 · PMID 28724990not yet assessed
-
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney ↗Hypertension · 2017 · PMID 28739976not yet assessed
-
Fine-Scale Genetic Structure in Finland ↗G3 Genes Genomes Genetics · 2017 · PMID 28983069not yet assessed
-
Rare and low-frequency coding variants alter human adult height ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2017not yet assessed
-
Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease ↗Journal of the American Heart Association · 2017 · PMID 28550093not yet assessed
-
Increased plasma N-glycome complexity is associated with higher risk of type 2 diabetes ↗Diabetologia · 2017 · PMID 28905229not yet assessed
-
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits ↗Nature Communications · 2017 · PMID 28963451not yet assessed
-
Chronic disease research in Europe and the need for integrated population cohorts ↗European Journal of Epidemiology · 2017 · PMID 28986739not yet assessed
-
Experimental and Human Evidence for Lipocalin‐2 (Neutrophil Gelatinase‐Associated Lipocalin [NGAL]) in the Development of Cardiac Hypertrophy and Heart Failure ↗Journal of the American Heart Association · 2017 · PMID 28615213not yet assessed
-
Exome-wide association study of plasma lipids in > 300,000 individualsFigshare · 2017not yet assessed
-
An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗Genome biology · 2017 · PMID 28764798not yet assessed
-
The Effects of Intensive Weight Reduction on Body Composition and Serum Hormones in Female Fitness Competitors ↗Frontiers in Physiology · 2017 · PMID 28119632not yet assessed
-
Loss of Cardioprotective Effects at the <i>ADAMTS7</i> Locus as a Result of Gene-Smoking Interactions ↗Circulation · 2017 · PMID 28461624not yet assessed
-
Genetics in an isolated population like Finland: a different basis for genomic medicine? ↗Journal of Community Genetics · 2017 · PMID 28730583not yet assessed
-
Genetic predisposition to obesity, restrained eating and changes in body weight: a population-based prospective study ↗International Journal of Obesity · 2017 · PMID 29158543not yet assessed
-
Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population ↗Circulation Cardiovascular Genetics · 2017 · PMID 29237677not yet assessed
-
Protective Low-Frequency Variants for Preeclampsia in the Fms Related Tyrosine Kinase 1 Gene in the Finnish Population ↗Hypertension · 2017 · PMID 28652462not yet assessed
-
Genetic Variants Contributing to Circulating Matrix Metalloproteinase 8 Levels and Their Association With Cardiovascular Diseases ↗Circulation Cardiovascular Genetics · 2017 · PMID 29212897not yet assessed
-
Affective responses to sweet products and sweet solution in British and Finnish adults ↗Food Quality and Preference · 2017not yet assessed
-
Genome-wide association meta-analysis of fish and EPA+DHA consumption in 17 US and European cohorts ↗PLoS ONE · 2017 · PMID 29236708not yet assessed
-
MixFit: Methodology for Computing Ancestry-Related Genetic Scores at the Individual Level and Its Application to the Estonian and Finnish Population Studies ↗PLoS ONE · 2017 · PMID 28107396not yet assessed
-
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 ↗PLoS ONE · 2017 · PMID 28278213not yet assessed
-
Neuregulin signaling pathway in smoking behavior ↗Translational Psychiatry · 2017 · PMID 28892072not yet assessed
-
Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking InteractionsEUR Research Repository (Erasmus University Rotterdam) · 2017not yet assessed
-
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (vol 8, 80, 2017)eScholarship (California Digital Library) · 2017not yet assessed
-
1192Salt intake and the risk of heart failure ↗European Heart Journal · 2017not yet assessed
-
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the KidneyUWA Profiles and Research Repository (University of Western Australia) · 2017not yet assessed
-
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. ↗Duo Research Archive (University of Oslo) · 2017not yet assessed
-
Rare and low-frequency coding variants alter human adult height ↗Apollo (University of Cambridge) · 2017not yet assessed
-
Genetic analysis of over one million people identifies 535 novel loci for blood pressure ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
Correction: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults ↗PLoS Genetics · 2017 · PMID 28832619not yet assessed
-
Correction to: Increased plasma N-glycome complexity is associated with higher risk of type 2 diabetes ↗Diabetologia · 2017 · PMID 29188337not yet assessed
-
Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass ↗Nature Communications · 2017not yet assessed
-
Genetics of vaccination-related narcolepsy ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
Haplotype sharing provides insights into fine-scale population history and disease in Finland ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (Nature Communications 8:80)STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2017not yet assessed
-
Metabolomic signature of incident type 2 diabetes: evidence from NMR in over 18,000 individualsSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2017not yet assessed
-
Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney ↗bioRxiv (Cold Spring Harbor Laboratory) · 2017not yet assessed
-
Salt intake and the risk of heart failureSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2017not yet assessed
-
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 ↗Journal of the American College of Cardiology · 2017not yet assessed
-
GENETIC VARIATIONS IN CLASSES I AND III OF MHC ASSOCIATE WITH ACUTE CORONARY SYNDROME IN FINNISH POPULATIONSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2017not yet assessed
-
Genetic association of complement receptors to preeclampsia revealed by targeted exomic sequencing ↗Molecular Immunology · 2017not yet assessed
-
P5362Metabolomic signature of incident type 2 diabetes: evidence from NMR in over 18,000 individuals ↗European Heart Journal · 2017not yet assessed
-
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. ↗eScholarship@McGill (McGill) · 2017not yet assessed
-
ACTR-79. ESTABLISHMENT OF CLINICAL PROTOCOL TARGETING CANCER STEM CELLS IN RECURRENT GLIOBLASTOMA USING HIGH-THROUGHPUT DRUG SCREENING ↗Neuro-Oncology · 2017not yet assessed
-
ESTABLISHMENT OF CLINICAL PROTOCOL TARGETING CANCER STEM CELLS IN RECURRENT GLIOBLASTOMA USING HIGH-THROUGHPUT DRUG SCREENINGSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2017not yet assessed
-
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth FactorsSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2017not yet assessed
-
Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. ↗MPG.PuRe (Max Planck Society) · 2017not yet assessed
-
Terveyden ja hyvinvoinnin laitoksen tutkimuksen nykytilan kartoitus : Selvitys 2016 - 2017STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2017not yet assessed
-
Affective responses to sweet products and sweet solution in British and Finnish adults2017not yet assessed
-
Evaluating Robustness and Geographic Differences in Polygenic Risk in FinlandSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2017not yet assessed
-
Neuregulin signaling pathway in smoking behaviorSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2017not yet assessed
-
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease (vol 374, pg 1134, 2016)Data Archiving and Networked Services (DANS) · 2017not yet assessed
-
Low MMP-8/TIMP-1 reflects left ventricle impairment in takotsubo cardiomyopathy and high TIM P-1 may help to differentiate it from acute coronary syndromeSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2017not yet assessed
-
An epigenome-wide association study meta-analysis of educational attainmentMax Planck Digital Library · 2017not yet assessed
-
Genome-wide association meta-analysis of fish and EPA plus DHA consumption in 17 US and European cohortsData Archiving and Networked Services (DANS) · 2017not yet assessed
-
Genetic Variants Contributing to Circulating Matrix Metalloproteinase 8 Levels and Their Association With Cardiovascular Diseases: A Genome-Wide AnalysisSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2017not yet assessed
-
Chronic disease research in Europe and the need for integrated population cohortsData Archiving and Networked Services (DANS) · 2017not yet assessed
-
Increased plasma N-glycome complexity is associated with higher risk of type 2 diabetesRepository of the Medical Faculty of the University of Zagreb (University of Zagreb) · 2017not yet assessed
-
Additional file 7: Table S6. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗Figshare · 2017not yet assessed
-
Additional file 8: Table S7. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗Figshare · 2017not yet assessed
-
Additional file 5: Table S4. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗Figshare · 2017not yet assessed
-
Additional file 11: Table S10. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗Figshare · 2017not yet assessed
-
Additional file 10: Table S9. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗Figshare · 2017not yet assessed
-
Additional file 1: Table S1. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗Figshare · 2017not yet assessed
-
Additional file 6: Table S5. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗Figshare · 2017not yet assessed
-
Additional file 2: Table S2. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗Figshare · 2017not yet assessed
-
Additional file 9: Table S8. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗Figshare · 2017not yet assessed
-
Additional file 3: Table S3. of An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ↗Figshare · 2017not yet assessed
-
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA ↗Nature Communications · 2016 · PMID 27005778not yet assessed
-
Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors ↗The American Journal of Human Genetics · 2016 · PMID 27989323not yet assessed
-
Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease ↗Science · 2016 · PMID 26965621not yet assessed
-
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function ↗Nature Communications · 2016 · PMID 26831199not yet assessed
-
Genome-wide analysis identifies 12 loci influencing human reproductive behavior ↗Nature Genetics · 2016 · PMID 27798627not yet assessed
-
Genomic prediction of coronary heart disease ↗European Heart Journal · 2016 · PMID 27655226not yet assessed
-
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ↗Nature Genetics · 2016 · PMID 27618447not yet assessed
-
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk ↗Nature Communications · 2016 · PMID 26833246not yet assessed
-
Metabolic profiling of pregnancy: cross-sectional and longitudinal evidence ↗BMC Medicine · 2016 · PMID 27955712not yet assessed
-
Metabolomic Profiling of Statin Use and Genetic Inhibition of HMG-CoA Reductase ↗Journal of the American College of Cardiology · 2016 · PMID 26965542not yet assessed
-
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels ↗Nature Communications · 2016 · PMID 26833098not yet assessed
-
Evaluation of O2PLS in Omics data integration ↗BMC Bioinformatics · 2016 · PMID 26822911not yet assessed
-
Metabolic profiling of alcohol consumption in 9778 young adults ↗International Journal of Epidemiology · 2016 · PMID 27494945not yet assessed
-
IgG Glycome in Colorectal Cancer ↗Clinical Cancer Research · 2016 · PMID 26831718not yet assessed
-
A genomic approach to therapeutic target validation identifies a glucose-lowering <i>GLP1R</i> variant protective for coronary heart disease ↗Science Translational Medicine · 2016 · PMID 27252175not yet assessed
-
Effects of hormonal contraception on systemic metabolism: cross-sectional and longitudinal evidence ↗International Journal of Epidemiology · 2016 · PMID 27538888not yet assessed
-
USF1 deficiency activates brown adipose tissue and improves cardiometabolic health ↗Science Translational Medicine · 2016 · PMID 26819196not yet assessed
-
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index ↗Molecular Psychiatry · 2016 · PMID 27184124not yet assessed
-
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape ↗Nature Communications · 2016 · PMID 27876822not yet assessed
-
Metabolic signatures of birthweight in 18 288 adolescents and adults ↗International Journal of Epidemiology · 2016 · PMID 27892411not yet assessed
-
Family history and perceived risk of diabetes, cardiovascular disease, cancer, and depression ↗Preventive Medicine · 2016 · PMID 27353304not yet assessed
-
Familial idiopathic normal pressure hydrocephalus ↗Journal of the Neurological Sciences · 2016 · PMID 27538594not yet assessed
-
Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2 ↗Scientific Reports · 2016 · PMID 26833182not yet assessed
-
Heritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE Consortium ↗SLEEP · 2016 · PMID 27568811not yet assessed
-
Ageing with elegans: a research proposal to map healthspan pathways ↗Biogerontology · 2016 · PMID 27040825not yet assessed
-
Genetic invalidation of Lp-PLA<sub>2</sub> as a therapeutic target: Large-scale study of five functional Lp-PLA<sub>2</sub>-lowering alleles ↗European Journal of Preventive Cardiology · 2016 · PMID 27940953not yet assessed
-
Genome-Wide Meta-Analysis of Sciatica in Finnish Population ↗PLoS ONE · 2016 · PMID 27764105not yet assessed
-
Genetic Risk Scores Predict Recurrence of Acute Coronary Syndrome ↗Circulation Cardiovascular Genetics · 2016 · PMID 26980882not yet assessed
-
Characterization of the metabolic profile associated with serum 25-hydroxyvitamin D: a cross-sectional analysis in population-based data ↗International Journal of Epidemiology · 2016 · PMID 27605587not yet assessed
-
Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome ↗Circulation Cardiovascular Genetics · 2016 · PMID 26679868not yet assessed
-
The Detection of Metabolite-Mediated Gene Module Co-Expression Using Multivariate Linear Models ↗PLoS ONE · 2016 · PMID 26918614not yet assessed
-
Genetic invalidation of Lp-PLA$_{2}$ as a therapeutic target: Large-scale study of five functional Lp-PLA$_{2}$-lowering alleles ↗Apollo (University of Cambridge) · 2016not yet assessed
-
Insomnia does not mediate or modify the association between MTNR1B risk variant rs10830963 and glucose levels ↗Diabetologia · 2016 · PMID 26912228not yet assessed
-
CYP2B6 and OPRM1 Receptor Polymorphisms at Methadone Clinics And Novel OPRM1 Haplotypes: A Cross-Sectional Study ↗Drug Metabolism Letters · 2016 · PMID 27515451not yet assessed
-
not yet assessed
-
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease ↗Apollo (University of Cambridge) · 2016not yet assessed
-
Genomic prediction of coronary heart disease ↗bioRxiv (Cold Spring Harbor Laboratory) · 2016not yet assessed
-
Metabolic profiling of alcohol consumption in 9778 young adults ↗bioRxiv (Cold Spring Harbor Laboratory) · 2016not yet assessed
-
Sequential double cross-validation for augmented prediction assessment in high-dimensional omic applicationsarXiv (Cornell University) · 2016not yet assessed
-
Genome-wide association study identifies 17 new loci influencing concentrations of circulating cytokines and growth factors ↗bioRxiv (Cold Spring Harbor Laboratory) · 2016not yet assessed
-
An interaction map of circulating metabolites, immune gene networks and their genetic regulation ↗bioRxiv (Cold Spring Harbor Laboratory) · 2016not yet assessed
-
DDIS-13. IDENTIFICATION OF INDIVIDUALIZED THERAPY OPTIONS IN PATIENTS WITH GLIOBLASTOMA BY HIGH-THROUGHPUT DRUG SCREENING ↗Neuro-Oncology · 2016not yet assessed
-
On Inferior Power of Recently Developed Family-Based Association Analysis Methods for Next-Generation Sequencing Studies of Rare-VariantsSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2016not yet assessed
-
SNPs associated for height explain about half of the height difference between two historical subpopulations in Finland日本人類遺伝学会大会プログラム・抄録集 · 2016not yet assessed
-
Metabolic and transciptomic associations of change in body fat percentage.Metabolic and transciptomic associations of change in body fat percentage日本人類遺伝学会大会プログラム・抄録集 · 2016not yet assessed
-
Genetic Risk Scores Predict Recurrence of Acute Coronary SyndromeSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2016not yet assessed
-
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels ↗University of Southern Denmark Research Portal (University of Southern Denmark) · 2016not yet assessed
-
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2016not yet assessed
-
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals ↗Archive ouverte UNIGE (University of Geneva) · 2016not yet assessed
-
Abstract 14425: Exome Sequencing Reveals a Low Frequency Variant in BMPER in a Pedigree With Recurrence of Left Ventricular Outflow Tract Obstruction DefectsCirculation · 2016not yet assessed
-
Genome-Wide Meta-Analysis of Sciatica in Finnish PopulationTampere University Institutional Repository (Tampere University) · 2016not yet assessed
-
Metabolic profiling of alcohol consumption in 9778 young adultsSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2016not yet assessed
-
Metabolomic Profiling of Statin Use and Genetic Inhibition of HMG-CoA ReductaseUCL Discovery (University College London) · 2016not yet assessed
-
Genomic prediction of coronary heart disease ↗EUR Research Repository (Erasmus University Rotterdam) · 2016not yet assessed
-
Metabolic signatures of birthweight in 18 288 adolescents and adultsSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2016not yet assessed
-
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease (vol 374, pg 1134, 2016, Correction)STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2016not yet assessed
-
Heritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE ConsortiumUtrecht University Repository (Utrecht University) · 2016not yet assessed
-
Sequential double cross-validation for assessment of added predictive\n ability in high-dimensional omic applications ↗arXiv (Cornell University) · 2016not yet assessed
-
On the combination of omics data for prediction of binary outcomes ↗arXiv (Cornell University) · 2016not yet assessed
-
Additional file 3: of Metabolic profiling of pregnancy: cross-sectional and longitudinal evidence ↗Figshare · 2016not yet assessed
-
Additional file 3: of Metabolic profiling of pregnancy: cross-sectional and longitudinal evidence ↗Figshare · 2016not yet assessed
-
Genetic studies of body mass index yield new insights for obesity biology ↗Nature · 2015 · PMID 25673413not yet assessed
-
New genetic loci link adipose and insulin biology to body fat distribution ↗Nature · 2015 · PMID 25673412not yet assessed
-
Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans ↗PLoS ONE · 2015 · PMID 25811787not yet assessed
-
Metabolite Profiling and Cardiovascular Event Risk ↗Circulation · 2015 · PMID 25573147not yet assessed
-
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study ↗PLoS Genetics · 2015 · PMID 26426971not yet assessed
-
A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery diseaseEUR Research Repository (Erasmus University Rotterdam) · 2015not yet assessed
-
The impact of low-frequency and rare variants on lipid levels ↗Nature Genetics · 2015 · PMID 25961943not yet assessed
-
The Biomarker GlycA Is Associated with Chronic Inflammation and Predicts Long-Term Risk of Severe Infection ↗Cell Systems · 2015 · PMID 27136058not yet assessed
-
Cell Specific eQTL Analysis without Sorting CellsPLoS Genetics · 2015 · PMID 25955312L1 90/100
-
Adiposity as a cause of cardiovascular disease: a Mendelian randomization study ↗International Journal of Epidemiology · 2015 · PMID 26016847not yet assessed
-
Gene × dietary pattern interactions in obesity: analysis of up to 68 317 adults of European ancestry ↗Human Molecular Genetics · 2015 · PMID 25994509not yet assessed
-
Sex hormone-binding globulin associations with circulating lipids and metabolites and the risk for type 2 diabetes: observational and causal effect estimates ↗International Journal of Epidemiology · 2015 · PMID 26050255not yet assessed
-
Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation ↗PLoS Genetics · 2015 · PMID 26132169not yet assessed
-
Age- and Sex-Specific Causal Effects of Adiposity on Cardiovascular Risk Factors ↗Diabetes · 2015 · PMID 25712996not yet assessed
-
Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population ↗PLoS ONE · 2015 · PMID 26509668not yet assessed
-
Gene x dietary pattern interactions in obesity: analysis of up to 68 317 adults of European ancestryEUR Research Repository (Erasmus University Rotterdam) · 2015not yet assessed
-
Appetitive traits as behavioural pathways in genetic susceptibility to obesity: a population-based cross-sectional study ↗Scientific Reports · 2015 · PMID 26423639not yet assessed
-
Genetic causal beliefs about morbidity: associations with health behaviors and health outcome beliefs about behavior changes between 1982–2002 in the Finnish population ↗BMC Public Health · 2015 · PMID 25884345not yet assessed
-
Systems medicine links microbial inflammatory response with glycoprotein-associated mortality risk ↗bioRxiv (Cold Spring Harbor Laboratory) · 2015not yet assessed
-
Scatter plot of age versus biomarker summary score for men and women from the Estonian Biobank cohort. ↗Figshare · 2015not yet assessed
-
Major histocompatibility complex risk haplotype predisposes to acute coronary syndromeSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2015not yet assessed
-
Epigenetic fingerprint of stress in a Finnish shift-working occupational cohortSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2015not yet assessed
-
Haplotype analysis of rs9275224, rs2856717, rs9275424, and rs9275596 at the HLA-DQB1/DRB1 locus. ↗Figshare · 2015not yet assessed
-
Family disease history and perceived risk for Type 2 diabetes, cardiovascular disease, cancer and depressionEuropean Health Psychologist · 2015not yet assessed
-
Directional dominance on stature and cognition in diverse human populations ↗Archive ouverte UNIGE (University of Geneva) · 2015not yet assessed
-
The impact of low-frequency and rare variants on lipid levelsData Archiving and Networked Services (DANS) · 2015not yet assessed
-
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization ↗BORIS (University Library Bern) · 2015not yet assessed
-
Habitual sleep duration is associated with BMI and macronutrient intake and may be modified by CLOCK genetic variants2015not yet assessed
-
Genetic causal beliefs about morbidity: associations with health behaviors and health outcome beliefs about behavior changes between 1982-2002 in the Finnish populationTampere University Institutional Repository (Tampere University) · 2015not yet assessed
-
Familial idiopathic normal pressure hydrocephalus ↗Fluids and Barriers of the CNS · 2015not yet assessed
-
Defining the role of common variation in the genomic and biological architecture of adult human height ↗Nature Genetics · 2014not yet assessed
-
The prevalence of metabolic syndrome and metabolically healthy obesity in Europe: A collaborative analysis of ten large cohort studiesDuo Research Archive (University of Oslo) · 2014not yet assessed
-
Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu ↗International Journal of Epidemiology · 2014 · PMID 24518929not yet assessed
-
Biomarker Profiling by Nuclear Magnetic Resonance Spectroscopy for the Prediction of All-Cause Mortality: An Observational Study of 17,345 Persons ↗PLoS Medicine · 2014 · PMID 24586121not yet assessed
-
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization ↗Nature Genetics · 2014 · PMID 24952745not yet assessed
-
A metabolic view on menopause and ageing ↗Nature Communications · 2014 · PMID 25144627not yet assessed
-
FTO genetic variants, dietary intake and body mass index: insights from 177 330 individuals ↗Human Molecular Genetics · 2014 · PMID 25104851not yet assessed
-
Neolithic dairy farming at the extreme of agriculture in northern Europe ↗Proceedings of the Royal Society B Biological Sciences · 2014 · PMID 25080345not yet assessed
-
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos ↗Nature Communications · 2014 · PMID 24886709not yet assessed
-
BBMRI-ERIC as a resource for pharmaceutical and life science industries: the development of biobank-based Expert Centres ↗European Journal of Human Genetics · 2014 · PMID 25407005not yet assessed
-
High Risk Population Isolate Reveals Low Frequency Variants Predisposing to Intracranial Aneurysms ↗PLoS Genetics · 2014 · PMID 24497844not yet assessed
-
Chromosome X-Wide Association Study Identifies Loci for Fasting Insulin and Height and Evidence for Incomplete Dosage Compensation ↗PLoS Genetics · 2014 · PMID 24516404not yet assessed
-
The prevalence of metabolic syndrome and metabolically healthy obesity in Europe: a collaborative analysis of ten large cohort studies ↗BMC Endocrine Disorders · 2014 · PMID 24484869not yet assessed
-
Genome‐wide association study of sleep duration in the <scp>F</scp>innish population ↗Journal of Sleep Research · 2014 · PMID 25109461not yet assessed
-
Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population ↗PLoS Genetics · 2014 · PMID 25078778not yet assessed
-
Genetic Determinants of Circulating Interleukin-1 Receptor Antagonist Levels and Their Association With Glycemic Traits ↗Diabetes · 2014 · PMID 24969107not yet assessed
-
Low-Expression Variant of Fatty Acid–Binding Protein 4 Favors Reduced Manifestations of Atherosclerotic Disease and Increased Plaque Stability ↗Circulation Cardiovascular Genetics · 2014 · PMID 25122052not yet assessed
-
Cortical 11C-PIB Uptake is Associated with Age, APOE Genotype, and Gender in “Healthy Aging” ↗Journal of Alzheimer s Disease · 2014 · PMID 24603945not yet assessed
-
Evaluation of <scp>HLA‐DRB1</scp> imputation using a Finnish dataset ↗Tissue Antigens · 2014 · PMID 24666112not yet assessed
-
Genetic Variation on the <i>BAT1-NFKBIL1-LTA</i> Region of Major Histocompatibility Complex Class III Associates with Periodontitis ↗Infection and Immunity · 2014 · PMID 24566624not yet assessed
-
The low-expression variant of fatty acid-binding protein 4 favors reduced manifestations of atherosclerotic disease and increased plaque stability ↗Atherosclerosis · 2014not yet assessed
-
Amerindian-specific regions under positive selection harbour new lipid variants in LatinoseScholarship (California Digital Library) · 2014not yet assessed
-
Cell specific eQTL analysis without sorting cells ↗bioRxiv (Cold Spring Harbor Laboratory) · 2014not yet assessed
-
Genome-wide association study of sleep duration in the Finnish populationSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2014not yet assessed
-
High Risk Population Isolate Reveals Low Frequency Variants Predisposing to Intracranial AneurysmsTampere University Institutional Repository (Tampere University) · 2014not yet assessed
-
Genetic Variation on the BAT1-NFKBIL1-LTA Region of Major Histocompatibility Complex Class III Associates with PeriodontitisSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2014not yet assessed
-
Neolithic dairy farming at the extreme of agriculture in northern EuropeExplore Bristol Research · 2014not yet assessed
-
A metabolic view on menopause and ageingRePEc: Research Papers in Economics · 2014not yet assessed
-
Discovery and refinement of loci associated with lipid levels ↗Nature Genetics · 2013 · PMID 24097068not yet assessed
-
Systematic identification of trans eQTLs as putative drivers of known disease associations ↗Nature Genetics · 2013 · PMID 24013639not yet assessed
-
Identification of seven loci affecting mean telomere length and their association with disease ↗Nature Genetics · 2013 · PMID 23535734not yet assessed
-
Common variants associated with plasma triglycerides and risk for coronary artery disease ↗Nature Genetics · 2013 · PMID 24097064not yet assessed
-
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture ↗Nature Genetics · 2013 · PMID 23563607not yet assessed
-
Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits ↗PLoS Genetics · 2013 · PMID 23754948not yet assessed
-
Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders ↗Nature Genetics · 2013 · PMID 23583979not yet assessed
-
The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis ↗PLoS Medicine · 2013 · PMID 23824655not yet assessed
-
Midlife Sleep Characteristics Associated with Late Life Cognitive Function ↗SLEEP · 2013 · PMID 24082313not yet assessed
-
Genome‐wide linkage analysis for human longevity: Genetics of Healthy Aging Study ↗Aging Cell · 2013 · PMID 23286790not yet assessed
-
The Molecular Genetic Architecture of Self-Employment ↗PLoS ONE · 2013 · PMID 23593239not yet assessed
-
Data harmonization and federated analysis of population-based studies: the BioSHaRE project ↗Emerging Themes in Epidemiology · 2013 · PMID 24257327not yet assessed
-
The co‐occurrence of mt<scp>DNA</scp> mutations on different oxidative phosphorylation subunits, not detected by haplogroup analysis, affects human longevity and is population specific ↗Aging Cell · 2013 · PMID 24341918not yet assessed
-
Midlife cardiovascular risk factors and late cognitive impairment ↗European Journal of Epidemiology · 2013 · PMID 23532744not yet assessed
-
Identifying flavor preference subgroups. Genetic basis and related eating behavior traits ↗Appetite · 2013 · PMID 24361469not yet assessed
-
Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture ↗Journal of Thrombosis and Haemostasis · 2013 · PMID 23910795not yet assessed
-
Meta‐analysis on blood transcriptomic studies identifies consistently coexpressed protein–protein interaction modules as robust markers of human aging ↗Aging Cell · 2013 · PMID 24119000not yet assessed
-
Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population ↗Annals of Medicine · 2013 · PMID 23651034not yet assessed
-
Thyroid cancer and co-occurring RET mutations in Hirschsprung disease ↗Endocrine Related Cancer · 2013 · PMID 23744765not yet assessed
-
A polymorphism in the protein kinase C gene PRKCB is associated with α2-adrenoceptor-mediated vasoconstriction ↗Pharmacogenetics and Genomics · 2013 · PMID 23337848not yet assessed
-
Genome-wide association analyses identify 18 new loci associated with serum urate concentrationsUCL Discovery (University College London) · 2013not yet assessed
-
Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits ↗Archive ouverte UNIGE (University of Geneva) · 2013not yet assessed
-
Supplementary Material 152013not yet assessed
-
A polymorphism in the protein kinase C gene PRKCB is associated with alpha(2)-adrenoceptor-mediated vasoconstrictionSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2013not yet assessed
-
Identification of seven loci affecting mean telomere length and their association with disease ↗QUT ePrints (Queensland University of Technology) · 2013not yet assessed
-
Midlife Sleep Characteristics Associated with Late Life Cognitive FunctionSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2013not yet assessed
-
Large-scale association analysis identifies new risk loci for coronary artery disease ↗Nature Genetics · 2012 · PMID 23202125not yet assessed
-
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance ↗Nature Genetics · 2012 · PMID 22581228not yet assessed
-
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations ↗Nature Genetics · 2012 · PMID 23263486not yet assessed
-
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways ↗Nature Genetics · 2012 · PMID 22885924not yet assessed
-
Genome-wide association study identifies multiple loci influencing human serum metabolite levels ↗Nature Genetics · 2012 · PMID 22286219not yet assessed
-
Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals ↗PLoS Genetics · 2012 · PMID 22479202not yet assessed
-
Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis ↗PLoS Genetics · 2012 · PMID 22737082not yet assessed
-
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 ↗Circulation Cardiovascular Genetics · 2012 · PMID 22399527not yet assessed
-
Novel Loci for Metabolic Networks and Multi-Tissue Expression Studies Reveal Genes for Atherosclerosis ↗PLoS Genetics · 2012 · PMID 22916037not yet assessed
-
Toward a roadmap in global biobanking for health ↗European Journal of Human Genetics · 2012 · PMID 22713808not yet assessed
-
Evidence of Inbreeding Depression on Human Height ↗PLoS Genetics · 2012 · PMID 22829771not yet assessed
-
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study ↗The Lancet · 2012 · PMID 22607825not yet assessed
-
Genetic contribution to sour taste preference ↗Appetite · 2012 · PMID 22245130not yet assessed
-
Genome-wide meta-analysis of common variant differences between men and women ↗Human Molecular Genetics · 2012 · PMID 22843499not yet assessed
-
Common Genetic Variants Associated with Sudden Cardiac Death: The FinSCDgen Study ↗PLoS ONE · 2012 · PMID 22844511not yet assessed
-
TRIB1 constitutes a molecular link between regulation of sleep and lipid metabolism in humans ↗Translational Psychiatry · 2012 · PMID 22832862not yet assessed
-
A Genome-Wide Association Study of Monozygotic Twin-Pairs Suggests a Locus Related to Variability of Serum High-Density Lipoprotein Cholesterol ↗Twin Research and Human Genetics · 2012 · PMID 23031429not yet assessed
-
Intracranial Aneurysm Risk Locus 5q23.2 Is Associated with Elevated Systolic Blood Pressure ↗PLoS Genetics · 2012 · PMID 22438818not yet assessed
-
Mortality Rate Increases Steeply With Nonadherence to Statin Therapy in Patients With Acute Coronary Syndrome ↗Clinical Cardiology · 2012 · PMID 22961648not yet assessed
-
Bayesian Variable Selection in Searching for Additive and Dominant Effects in Genome-Wide Data ↗PLoS ONE · 2012 · PMID 22235263not yet assessed
-
A common variant near the KCNJ2 gene is associated with T-peak to T-end interval ↗Heart Rhythm · 2012 · PMID 22342860not yet assessed
-
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 ↗Annals of Medicine · 2012 · PMID 23110590not yet assessed
-
Genome-wide association study identifies multiple loci influencing human serum metabolite levelsOxford University Research Archive (ORA) (University of Oxford) · 2012not yet assessed
-
Common Genetic Variants Associated with Sudden Cardiac Death: The FinSCDgen StudyTampere University Institutional Repository (Tampere University) · 2012not yet assessed
-
Mortality Rate Increases Steeply With Nonadherence to Statin Therapy in Patients With Acute Coronary SyndromeSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2012not yet assessed
-
Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk AnalysisInstitutional Research Information System (Università degli Studi di Brescia) · 2012not yet assessed
-
Supplementary Material (nature09270-s1)2012not yet assessed
-
TRIB1 constitutes a molecular link between regulation of sleep and lipid metabolism in humansSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2012not yet assessed
-
Novel Loci for Metabolic Networks and Multi-Tissue Expression Studies Reveal Genes for AtherosclerosisDigital Access to Scholarship at Harvard (DASH) (Harvard University) · 2012not yet assessed
-
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 TraitsUCL Discovery (University College London) · 2012not yet assessed
-
A common variant near the KCNJ2 gene is associated with T-peak to T-end intervalSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2012not yet assessed
-
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk ↗Nature · 2011 · PMID 21909115not yet assessed
-
Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels ↗Circulation · 2011 · PMID 21300955not yet assessed
-
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile ↗Nature Genetics · 2011 · PMID 21706003not yet assessed
-
Genome‐wide association study identifies a single major locus contributing to survival into old age; the <i>APOE</i> locus revisited ↗Aging Cell · 2011 · PMID 21418511not yet assessed
-
Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1 ↗PLoS Genetics · 2011 · PMID 21779176not yet assessed
-
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study ↗Human Molecular Genetics · 2011 · PMID 21378095not yet assessed
-
Detailed metabolic and genetic characterization reveals new associations for 30 known lipid loci ↗Human Molecular Genetics · 2011 · PMID 22156771not yet assessed
-
Cohort Profile: The Corogene study ↗International Journal of Epidemiology · 2011 · PMID 21642350not yet assessed
-
Common Variants Show Predicted Polygenic Effects on Height in the Tails of the Distribution, Except in Extremely Short Individuals ↗PLoS Genetics · 2011 · PMID 22242009not yet assessed
-
Design, recruitment, logistics, and data management of the GEHA (Genetics of Healthy Ageing) project ↗Experimental Gerontology · 2011 · PMID 21871552not yet assessed
-
Common Genetic Variants, QT Interval, and Sudden Cardiac Death in a Finnish Population-Based Study ↗Circulation Cardiovascular Genetics · 2011 · PMID 21511878not yet assessed
-
The Use of Genome-Wide eQTL Associations in Lymphoblastoid Cell Lines to Identify Novel Genetic Pathways Involved in Complex Traits ↗PLoS ONE · 2011 · PMID 21789213not yet assessed
-
A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol ↗PLoS Genetics · 2011 · PMID 22028671not yet assessed
-
Shared Genetic Background for Regulation of Mood and Sleep: Association of GRIA3 with Sleep Duration in Healthy Finnish Women ↗SLEEP · 2011 · PMID 21966062not yet assessed
-
Common variants at 10 genomic loci influence hemoglobin A1C levels via glycemic and nonglycemic pathways (Diabetes (2010) 59, (3229-3239))Oxford University Research Archive (ORA) (University of Oxford) · 2011not yet assessed
-
Astringency Perception and Heritability Among Young Finnish Twins ↗Chemosensory Perception · 2011not yet assessed
-
Associations of Nicotine Intake Measures With CHRN Genes in Finnish Smokers ↗Nicotine & Tobacco Research · 2011 · PMID 21498873not yet assessed
-
Meta-Analysis of Genome-Wide Association Studies in > 80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2011not yet assessed
-
CRP gene variation affects early development of Alzheimer's disease-related plaques ↗Journal of Neuroinflammation · 2011 · PMID 21831326not yet assessed
-
Genome-wide association approaches for identifying loci for human height genes ↗Best Practice & Research Clinical Endocrinology & Metabolism · 2011 · PMID 21396572not yet assessed
-
Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution ↗Nature Genetics · 2011not yet assessed
-
Correction: Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1 ↗PLoS Genetics · 2011not yet assessed
-
Genetics of Human Stature: Lessons from Genome-Wide Association Studies ↗Hormone Research in Paediatrics · 2011 · PMID 21912147not yet assessed
-
Astringency Perception and Heritability Among Young Finnish TwinsSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2011not yet assessed
-
ETIOLOGY OF NIGHTMARES: ENVIRONMENTAL AND GENETIC CORRELATESSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2011not yet assessed
-
Complicated dental root canal treatment and risk of prehospital sudden cardiac deathSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2011not yet assessed
-
Subject Index Vol. 76, Suppl. 3, 2011 ↗Hormone Research in Paediatrics · 2011not yet assessed
-
A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total CholesterolTampere University Institutional Repository (Tampere University) · 2011not yet assessed
-
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profileResearch Bank (Australian Catholic University) · 2011not yet assessed
-
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk ↗Archive ouverte UNIGE (University of Geneva) · 2011not yet assessed
-
Genome-wide association approaches for identifying loci for human height genesSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2011not yet assessed
-
Associations of Nicotine Intake Measures With CHRN Genes in Finnish SmokersSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2011not yet assessed
-
Food Neophobia in Young Adults: Genetic Architecture and Relation to Personality, Pleasantness and Use Frequency of Foods, and Body Mass Index-A Twin StudySTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2011not yet assessed
-
Common Genetic Variants, QT Interval, and Sudden Cardiac Death in a Finnish Population-Based StudySTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2011not yet assessed
-
Author Index Vol. 76, Suppl. 3, 2011 ↗Hormone Research in Paediatrics · 2011not yet assessed
-
Biological, clinical and population relevance of 95 loci for blood lipids ↗Nature · 2010 · PMID 20686565not yet assessed
-
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index ↗Nature Genetics · 2010 · PMID 20935630not yet assessed
-
Hundreds of variants clustered in genomic loci and biological pathways affect human height ↗Nature · 2010 · PMID 20881960not yet assessed
-
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution ↗Nature Genetics · 2010not yet assessed
-
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index ↗Carolina Digital Repository (University of North Carolina at Chapel Hill) · 2010not yet assessed
-
Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior ↗Nature Genetics · 2010 · PMID 20418888not yet assessed
-
A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses ↗The Lancet · 2010 · PMID 20971364not yet assessed
-
Metabonomic, transcriptomic, and genomic variation of a population cohort ↗Molecular Systems Biology · 2010 · PMID 21179014not yet assessed
-
Food Neophobia in Young Adults: Genetic Architecture and Relation to Personality, Pleasantness and Use Frequency of Foods, and Body Mass Index—A Twin Study ↗Behavior Genetics · 2010 · PMID 20953688not yet assessed
-
Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies ↗International Journal of Epidemiology · 2010 · PMID 20813861not yet assessed
-
An Immune Response Network Associated with Blood Lipid Levels ↗PLoS Genetics · 2010 · PMID 20844574not yet assessed
-
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (vol 42, pg 105, 2010)UCL Discovery (University College London) · 2010not yet assessed
-
C-reactive protein-associated genetic variants and cancer risk: Findings from FINRISK 1992, FINRISK 1997 and Health 2000 studies ↗European Journal of Cancer · 2010 · PMID 20727736not yet assessed
-
Midlife Alcohol Consumption and Later Risk of Cognitive Impairment: A Twin Follow-up Study ↗Journal of Alzheimer s Disease · 2010 · PMID 20858964not yet assessed
-
Genetic polymorphism of the C-reactive protein (CRP) gene and a deep infection focus determine maximal serum CRP level in Staphylococcus aureus bacteremia ↗European Journal of Clinical Microbiology & Infectious Diseases · 2010 · PMID 20552244not yet assessed
-
Genetic variation of the interleukin-1 family and nongenetic factors determining the interleukin-1 receptor antagonist phenotypes ↗Metabolism · 2010 · PMID 20178882not yet assessed
-
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 ↗Annals of Medicine · 2010 · PMID 20350252not yet assessed
-
Associations between interleukin-1 (IL-1) gene variations or IL-1 receptor antagonist levels and the development of type 2 diabetes ↗Journal of Internal Medicine · 2010 · PMID 21205020not yet assessed
-
Food neophobia in young adults. Genetic architecture and relation to personality, BMI, and pleasantness and use frequency of foods ↗Appetite · 2010not yet assessed
-
Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk ↗Nature Genetics · 2010not yet assessed
-
[Genetics of multifactorial diseases]. ↗PubMed · 2010 · PMID 21086688not yet assessed
-
Monitekijäisten tautien genetiikka2010not yet assessed
-
The power of many ↗New Biotechnology · 2010not yet assessed
-
Genome-Wide Screen for Common and Rare Copy Number Variation in Metabolic SyndromeSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2010not yet assessed
-
Genome-wide screen for metabolic syndrome lociSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2010not yet assessed
-
Midlife Alcohol Consumption and Later Risk of Cognitive Impairment: A Twin Follow-up StudySTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2010not yet assessed
-
European lactase persistence genotype shows evidence of association with increase in body mass indexOxford University Research Archive (ORA) (University of Oxford) · 2010not yet assessed
-
Genome-wide association study identifies eight loci associated with blood pressure ↗Nature Genetics · 2009 · PMID 19430483not yet assessed
-
Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations ↗PLoS Genetics · 2009 · PMID 19503597not yet assessed
-
Common Variation in the β-Carotene 15,15′-Monooxygenase 1 Gene Affects Circulating Levels of Carotenoids: A Genome-wide Association Study ↗The American Journal of Human Genetics · 2009 · PMID 19185284not yet assessed
-
Association of serum cotinine level with a cluster of three nicotinic acetylcholine receptor genes (CHRNA3/CHRNA5/CHRNB4) on chromosome 15 ↗Human Molecular Genetics · 2009 · PMID 19628476not yet assessed
-
European lactase persistence genotype shows evidence of association with increase in body mass index ↗Human Molecular Genetics · 2009 · PMID 20015952not yet assessed
-
OSBPL10, a novel candidate gene for high triglyceride trait in dyslipidemic Finnish subjects, regulates cellular lipid metabolism ↗Journal of Molecular Medicine · 2009 · PMID 19554302not yet assessed
-
Genetic Association and Interaction Analysis of <i>USF1</i> and <i>APOA5</i> on Lipid Levels and Atherosclerosis ↗Arteriosclerosis Thrombosis and Vascular Biology · 2009 · PMID 19910639not yet assessed
-
Association of Variation in the Interleukin-1 Gene Family with Diabetes and Glucose Homeostasis ↗The Journal of Clinical Endocrinology & Metabolism · 2009 · PMID 19820020not yet assessed
-
ADAM8 and its single nucleotide polymorphism 2662 T/G are associated with advanced atherosclerosis and fatal myocardial infarction: Tampere vascular study ↗Annals of Medicine · 2009 · PMID 19575316not yet assessed
-
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 ↗International Journal of Obesity · 2009 · PMID 19721450not yet assessed
-
Associations of Vitamin D Receptor, Calcium-Sensing Receptor and Parathyroid Hormone Gene Polymorphisms with Calcium Homeostasis and Peripheral Bone Density in Adult Finns ↗Lifestyle Genomics · 2009 · PMID 19690432not yet assessed
-
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium ↗Nature Genetics · 2009 · PMID 19820697not yet assessed
-
Geographical structure and differential natural selection among North European populations ↗Genome Research · 2009 · PMID 19265028not yet assessed
-
Association of serum cotinine level with a cluster of three nicotinic acetylcholine receptor genes (CHRNA3/CHRNA5/CHRNB4) on chromosome 15STM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2009not yet assessed
-
Association of Variation in the Interleukin-1 Gene Family with Diabetes and Glucose HomeostasisSite cant be reached · 2009not yet assessed
-
ISNN Membership Application Form ↗Lifestyle Genomics · 2009not yet assessed
-
The Three-Factor Eating Questionnaire, body mass index, and responses to sweet and salty fatty foods: a twin study of genetic and environmental associations ↗American Journal of Clinical Nutrition · 2008 · PMID 18689360not yet assessed
-
Gender Differences in Genetic Risk Profiles for Cardiovascular Disease ↗PLoS ONE · 2008 · PMID 18974842not yet assessed
-
The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts ↗Genetic Epidemiology · 2008 · PMID 18979498not yet assessed
-
Self‐Ratings of Olfactory Function Reflect Odor Annoyance Rather than Olfactory Acuity ↗The Laryngoscope · 2008 · PMID 18948833not yet assessed
-
Environmental Effects Exceed Genetic Effects on Perceived Intensity and Pleasantness of Several Odors: A Three-Population Twin Study ↗Behavior Genetics · 2008 · PMID 18543092not yet assessed
-
Association Analysis of Allelic Variants of USF1 in Coronary Atherosclerosis ↗Arteriosclerosis Thrombosis and Vascular Biology · 2008 · PMID 18276913not yet assessed
-
Genetics of Maximal Walking Speed and Skeletal Muscle Characteristics in Older Women ↗Twin Research and Human Genetics · 2008 · PMID 18498210not yet assessed
-
Evaluation of HapMap data in six populations of European descent ↗European Journal of Human Genetics · 2008 · PMID 18398430not yet assessed
-
Genome-wide linkage screen for stature and body mass index in 3.032 families: evidence for sex- and population-specific genetic effects ↗European Journal of Human Genetics · 2008 · PMID 18781184not yet assessed
-
Birthplace predicts risk for prehospital sudden cardiac death in middle-aged men who migrated to metropolitan area: The Helsinki Sudden Death Study ↗Annals of Medicine · 2008 · PMID 18615340not yet assessed
-
Genetic and Environmental Contributions to Perceived Intensity and Pleasantness of Androstenone Odor: An International Twin Study ↗Chemosensory Perception · 2008not yet assessed
-
Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs ↗European Journal of Human Genetics · 2008 · PMID 18197190not yet assessed
-
Interactions of Functional Apolipoprotein E Gene Promoter Polymorphisms With Smoking on Aortic Atherosclerosis ↗Circulation Cardiovascular Genetics · 2008 · PMID 20031552not yet assessed
-
Abstract 5095: Association of Genetic Variation in the IL-1 Gene with Diabetes and Glucose Homeostasis ↗Circulation · 2008not yet assessed
-
USF1 GENE IS INVOLVED IN THE REGULATION OF HUMAN LONGEVITY ↗Atherosclerosis Supplements · 2008not yet assessed
-
Genome-wide search for QTLs for apolipoprotein A-I level in elderly Swedish DZ twins: evidence of female-specific locus on 15q11–13 ↗European Journal of Human Genetics · 2008 · PMID 18322452not yet assessed
-
Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairsQueensland's institutional digital repository (The University of Queensland) · 2008not yet assessed
-
Genome wide association analysis in human height of European-originated monozygotic female twins.Research Portal (King's College London) · 2008not yet assessed
-
Sweet taste preferences are partly genetically determined: identification of a trait locus on chromosome 16 ↗American Journal of Clinical Nutrition · 2007 · PMID 17616763not yet assessed
-
Food neophobia shows heritable variation in humans ↗Physiology & Behavior · 2007 · PMID 17459432not yet assessed
-
Combined Genome Scans for Body Stature in 6,602 European Twins: Evidence for Common Caucasian Loci ↗PLoS Genetics · 2007 · PMID 17559308not yet assessed
-
Evidence of Still-Ongoing Convergence Evolution of the Lactase Persistence T-13910 Alleles in Humans ↗The American Journal of Human Genetics · 2007 · PMID 17701907not yet assessed
-
Meta‐Analysis of Genome‐wide Linkage Studies in BMI and Obesity ↗Obesity · 2007 · PMID 17890495not yet assessed
-
Same genetic components underlie different measures of sweet taste preference ↗American Journal of Clinical Nutrition · 2007 · PMID 18065584not yet assessed
-
Genetic and environmental contributions to food use patterns of young adult twins ↗Physiology & Behavior · 2007 · PMID 17897688not yet assessed
-
Variation in the selenoprotein S gene locus is associated with coronary heart disease and ischemic stroke in two independent Finnish cohorts ↗Human Genetics · 2007 · PMID 17641917not yet assessed
-
Linkage of nicotine dependence and smoking behavior on 10q, 7q and 11p in twins with homogeneous genetic background ↗The Pharmacogenomics Journal · 2007 · PMID 17549066not yet assessed
-
Same genetic components underlie different measures of sweet taste preference ↗American Journal of Clinical Nutrition · 2007not yet assessed
-
Genetic component of identification, intensity and pleasantness of odours: a Finnish family study ↗European Journal of Human Genetics · 2007 · PMID 17342154not yet assessed
-
Combined Effects of Thrombosis Pathway Gene Variants Predict Cardiovascular Events ↗PLoS Genetics · 2007 · PMID 17677000not yet assessed
-
USF1 gene variants contribute to metabolic traits in men in a longitudinal 32-year follow-up study ↗Diabetologia · 2007 · PMID 18097648not yet assessed
-
Platelet GPIbα, GPIV and vWF polymorphisms and fatal pre-hospital MI among middle-aged men ↗Journal of Thrombosis and Thrombolysis · 2007 · PMID 17619827not yet assessed
-
The hepatic lipase gene C‐480T polymorphism in the development of early coronary atherosclerosis: the Helsinki Sudden Death Study ↗European Journal of Clinical Investigation · 2007 · PMID 17537154not yet assessed
-
PO5-124 THE HEPATIC LIPASE GENE C-480T POLYMORPHISM IN THE EARLY DEVELOPMENT OF CORONARY ATHEROSCLEROSIS: THE HELSINKI SUDDEN DEATH STUDY ↗Atherosclerosis Supplements · 2007not yet assessed
-
Combined Linkage Scan of Body Mass Index in European-originated Twin CohortsTwin Research and Human Genetics · 2007not yet assessed
-
Food neophobia shows heritable variation in humansResearch Portal (King's College London) · 2007not yet assessed
-
Finemapping of a QTL for body height on the human X chromosome in a Finnish twin cohort.2007not yet assessed
-
Lessons from studying monogenic disease for common disease ↗Human Molecular Genetics · 2006 · PMID 16651371not yet assessed
-
Radiographic Assessment of Dental Health in Middle-aged Men Following Sudden Cardiac Death ↗Journal of Dental Research · 2006 · PMID 16373688not yet assessed
-
Risk Alleles of USF1 Gene Predict Cardiovascular Disease of Women in Two Prospective Studies ↗PLoS Genetics · 2006 · PMID 16699592not yet assessed
-
Thrombomodulin Gene Polymorphisms and Haplotypes and the Risk of Cardiovascular Events ↗Arteriosclerosis Thrombosis and Vascular Biology · 2006 · PMID 16456088not yet assessed
-
Age-dependent association between hepatic lipase gene C-480T polymorphism and the risk of pre-hospital sudden cardiac death: The Helsinki Sudden Death Study ↗Atherosclerosis · 2006 · PMID 16793047not yet assessed
-
Sydänterveyteen liittyvän perimän tutkimus KTL:ssaSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2006not yet assessed
-
Age-dependent association between hepatic lipase gene C-480T polymorphism and the risk of pre-hospital sudden cardiac deathSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2006not yet assessed
-
AUTOGSCAN: Powerful Tools for Automated Genome-Wide Linkage and Linkage Disequilibrium Analysis ↗Twin Research and Human Genetics · 2005 · PMID 15836805not yet assessed
-
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 · PMID 15685251not yet assessed
-
AUTOGSCAN: Powerful Tools for Automated Genome-Wide Linkage and Linkage Disequilibrium Analysis ↗Twin Research and Human Genetics · 2005not yet assessed
-
Combined genome scans for body stature in 6602 European twins: evidence for common Caucasian loci ↗PLoS Genetics · 2005not yet assessed
-
Evaluating Whole Genome Amplification via Multiply-Primed Rolling Circle Amplification for SNP Genotyping of Samples With Low DNA Yield ↗Twin Research and Human Genetics · 2005 · PMID 16176722not yet assessed
-
Evaluating Whole Genome Amplification via Multiply-Primed Rolling Circle Amplification for SNP Genotyping of Samples With Low DNA Yield ↗Twin Research and Human Genetics · 2005not yet assessed
-
Risk Alleles of USF1 -Gene Predict Cardiovascular Disease of Women in Two Prospective Studies ↗PLoS Genetics · 2005not yet assessed
-
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 ↗Atherosclerosis Supplements · 2005not yet assessed
-
Genetics of Platelet Glycoprotein Receptors: Risk of Thrombotic Events and Pharmacogenetic Implications ↗Clinical and Applied Thrombosis/Hemostasis · 2005 · PMID 15821818not yet assessed
-
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 · 2005not yet assessed
-
A common haplotype of thrombomodulin gene predisposes to cardiovascular events in a prospective follow-up studyCirculation · 2005not yet assessed
-
Combined Effects of Thrombosis Pathway Gene Variants Predict Cardiovascular Events ↗PLoS Genetics · 2005not yet assessed
-
Platelet membrane collagen receptor glycoprotein VI polymorphism is associated with coronary thrombosis and fatal myocardial infarction in middle-aged men ↗Atherosclerosis · 2004 · PMID 15306180not yet assessed
-
Matrix metalloproteinase 3 and 9 gene promoter polymorphisms: joint action of two loci as a risk factor for coronary artery complicated plaques ↗Atherosclerosis · 2004 · PMID 15823277not yet assessed
-
Locus for quantitative HDL-cholesterol on chromosome 10q in Finnish families with dyslipidemia ↗Journal of Lipid Research · 2004 · PMID 15258200not yet assessed
-
Dopamine D3 receptor gene polymorphisms, blood pressure and nephropathy in type 1 diabetic patients ↗Nephrology Dialysis Transplantation · 2004 · PMID 15004255not yet assessed
-
Association of paraoxonase-1 M55L genotype and alcohol consumption with coronary atherosclerosis ↗Pharmacogenetics · 2004 · PMID 15284530not yet assessed
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DNA extraction yield is associated with several phenotypic characteristics: results from two large population surveys ↗Journal of Thrombosis and Haemostasis · 2004 · PMID 15550056not yet assessed
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Suomalaiset geenit hyötykäyttöönDoria (University of Helsinki) · 2004not yet assessed
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Variations in the Thrombomodulin Gene Predispose for Cardiovascular Events Such as Stroke and Coronary Heart Disease in a Finnish Case-cohort Study FinriskTwin Research and Human Genetics · 2004not yet assessed
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Morgam: An International Project Pooling Cohort Studies of Cardiovascular DiseaseTwin Research and Human Genetics · 2004not yet assessed
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Combined Analysis of Genome Scans from Six Twin Cohorts to Locate Quantitative Trait Loci for Body Mass Index and Stature in the Genomeutwin ProjectData Archiving and Networked Services (DANS) · 2004not yet assessed
-
Quality Issues in the Centralized Sample Handling and Storage Unit in GenomeutwinTwin Research and Human Genetics · 2004not yet assessed
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GENOMEUTWIN: an integrated project of eight twin cohorts for studies on complex traitsData Archiving and Networked Services (DANS) · 2004not yet assessed
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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 StudiesTwin Research and Human Genetics · 2004not yet assessed
-
Heritability of Adult Body Height: A Comparative Study of Twin Cohorts in Eight Countries ↗Twin Research · 2003 · PMID 14624724not yet assessed
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The Functional −374 T/A RAGE Gene Polymorphism Is Associated With Proteinuria and Cardiovascular Disease in Type 1 Diabetic Patients ↗Diabetes · 2003 · PMID 12606536not yet assessed
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Variation in the alpha2B-adrenoceptorgene as a risk factor for prehospitalfatal myocardial infarction and sudden cardiac death ↗Journal of the American College of Cardiology · 2003 · PMID 12535806not yet assessed
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Heritability of Adult Body Height: A Comparative Study of Twin Cohorts in Eight Countries ↗Twin Research · 2003not yet assessed
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Evidence of susceptibility loci on 4q32 and 16p12 for bipolar disorder ↗Human Molecular Genetics · 2003 · PMID 12874110not yet assessed
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Myeloperoxidase Gene Variation as a Determinant of Atherosclerosis Progression in the Abdominal and Thoracic Aorta: An Autopsy Study ↗Laboratory Investigation · 2003 · PMID 12861032not yet assessed
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Minimum Description Length Block Finder, a Method to Identify Haplotype Blocks and to Compare the Strength of Block Boundaries ↗The American Journal of Human Genetics · 2003 · PMID 12761696not yet assessed
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Polymorphisms in the nephrin gene and diabetic nephropathy in type 1 diabetic patients ↗Kidney International · 2003 · PMID 12631336not yet assessed
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A Functional variant of the iNOS gene flanking region is associated with LAD coronary artery disease: an autopsy study ↗European Journal of Clinical Investigation · 2003 · PMID 14636285not yet assessed
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Smoking-dependent association between paraoxonase 1 M/L55 genotype and coronary atherosclerosis in males: an autopsy study ↗Atherosclerosis · 2003 · PMID 14642403not yet assessed
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Skytthe A, Spector TD, Stazi MA, Willemsen G, Kaprio J, Heritability of adult body height: a comparative study of twin cohorts in eight countriesData Archiving and Networked Services (DANS) · 2003not yet assessed
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4P-1124 Co-operative polymorphisms of matrix metalloproteinase 3 and 9 and area of coronary artery lesions related to risk of acute coronary events ↗Atherosclerosis Supplements · 2003not yet assessed
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Genome Scans Provide Evidence for Low-HDL-C Loci on Chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish Families ↗The American Journal of Human Genetics · 2002 · PMID 11891617not yet assessed
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ACE gene and physical activity, blood pressure, and hypertension: a population study in Finland ↗Journal of Applied Physiology · 2002 · PMID 12015366not yet assessed
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Association of the endothelial nitric oxide synthase gene polymorphism with risk of coronary artery disease and myocardial infarction in middle-aged men ↗Journal of Molecular Medicine · 2002 · PMID 12226742not yet assessed
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Coronary artery wall atherosclerosis in relation to the estrogen receptor 1 gene polymorphism: an autopsy study ↗Journal of Molecular Medicine · 2002 · PMID 11894143not yet assessed
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AN MDL METHOD FOR FINDING HAPLOTYPE BLOCKS AND FOR ESTIMATING THE STRENGTH OF HAPLOTYPE BLOCK BOUNDARIES ↗2002 · PMID 12603053not yet assessed
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Coronary artery calcification is related to functional polymorphism of matrix metalloproteinase 3: the Helsinki Sudden Death Study ↗Atherosclerosis · 2002 · PMID 12204805not yet assessed
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Bipolar disorder susceptibility region on Xq24–q27.1 in Finnish families ↗Molecular Psychiatry · 2002 · PMID 12082562not yet assessed
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Platelet collagen receptor GPIa (C807T/HPA-5) haplotype is not associated with an increased risk of fatal coronary events in middle-aged men ↗Atherosclerosis · 2002 · PMID 12208476not yet assessed
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Spline Methods for the Comparison of Physical and Genetic Maps ↗Journal of Computational Biology · 2002 · PMID 12162886not yet assessed
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No association between three polymorphisms in the dopamine D3 receptor gene and diabetic nephropathy in type 1 diabetic patients2002not yet assessed
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Promoter Polymorphism of the Cd14 Endotoxin Receptor Gene As A Risk Factor for Alcoholic Liver Disease ↗Hepatology · 2001 · PMID 11343243not yet assessed
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Polymorphisms within the tumor necrosis factor locus and prevalence of coronary artery disease in middle-aged men ↗Atherosclerosis · 2001 · PMID 11257271not yet assessed
-
Coronary Artery Complicated Lesion Area Is Related to Functional Polymorphism of <i>Matrix Metalloproteinase 9</i> Gene ↗Arteriosclerosis Thrombosis and Vascular Biology · 2001 · PMID 11557670not yet assessed
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Platelet Glycoprotein Ibα HPA-2 Met/VNTR B Haplotype as a Genetic Predictor of Myocardial Infarction and Sudden Cardiac Death ↗Circulation · 2001 · PMID 11514372not yet assessed
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Quantitative-Trait-Locus Analysis of Body-Mass Index and of Stature, by Combined Analysis of Genome Scans of Five Finnish Study Groups ↗The American Journal of Human Genetics · 2001 · PMID 11410840not yet assessed
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The GPIIIa (β3 integrin) PlA polymorphism in the early development of coronary atherosclerosis ↗Atherosclerosis · 2001 · PMID 11257275not yet assessed
-
Testing Genetic Susceptibility Loci for Alcoholic Heart Muscle Disease ↗Alcoholism Clinical and Experimental Research · 2001 · PMID 11696658not yet assessed
-
Testing Genetic Susceptibility Loci for Alcoholic Heart Muscle Disease ↗Alcoholism Clinical and Experimental Research · 2001not yet assessed
-
Apolipoprotein E Variation at the Sequence Haplotype Level: Implications for the Origin and Maintenance of a Major Human Polymorphism ↗The American Journal of Human Genetics · 2000 · PMID 10986041not yet assessed
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Heritability and risk factors of uterine fibroids — The Finnish Twin Cohort Study ↗Maturitas · 2000 · PMID 11099869not yet assessed
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Two Loci on Chromosomes 2 and X for Premature Coronary Heart Disease Identified in Early- and Late-Settlement Populations of Finland ↗The American Journal of Human Genetics · 2000 · PMID 11078477not yet assessed
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Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings ↗Journal of Hypertension · 2000 · PMID 11081770not yet assessed
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Glycoprotein IIIa PlA1/A2 polymorphism and sudden cardiac death ↗Journal of the American College of Cardiology · 2000 · PMID 11028489not yet assessed
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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 suddenlySTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 2000not yet assessed
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Age-Dependent Association of Apolipoprotein E Genotype With Coronary and Aortic Atherosclerosis in Middle-Aged Men ↗Circulation · 1999 · PMID 10441097not yet assessed
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Evidence for Involvement of the Type 1 Angiotensin II Receptor Locus in Essential Hypertension ↗Hypertension · 1999 · PMID 10082497not yet assessed
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Genomewide Scan for Familial Combined Hyperlipidemia Genes in Finnish Families, Suggesting Multiple Susceptibility Loci Influencing Triglyceride, Cholesterol, and Apolipoprotein B Levels ↗The American Journal of Human Genetics · 1999 · PMID 10205279not yet assessed
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Association of FXIII Val34Leu with decreased risk of myocardial infarction in Finnish males ↗Atherosclerosis · 1999 · PMID 10030380not yet assessed
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Glycoprotein IIIa Pl <sup>A</sup> Polymorphism Associates With Progression of Coronary Artery Disease and With Myocardial Infarction in an Autopsy Series of Middle-Aged Men Who Died Suddenly ↗Arteriosclerosis Thrombosis and Vascular Biology · 1999 · PMID 10521390not yet assessed
-
The GPIIIa PlA polymorphism in the progression of abdominal aortic atherosclerosis ↗Atherosclerosis · 1999 · PMID 10525125not yet assessed
-
Long-Extension PCR to Detect Deleted Mitochondrial DNA Molecules Is Compromized by Technical Artefacts ↗Biochemical and Biophysical Research Communications · 1999 · PMID 9918869not yet assessed
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Molecular genetics of hypertension and related traitsSTM:n Hallinnonalan avoin julkaisuarkisto (Julkari) · 1999not yet assessed
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Dual Origins of Finns Revealed by Y Chromosome Haplotype Variation ↗The American Journal of Human Genetics · 1998 · PMID 9545401not yet assessed
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Haplotype Structure and Population Genetic Inferences from Nucleotide-Sequence Variation in Human Lipoprotein Lipase ↗The American Journal of Human Genetics · 1998 · PMID 9683608not yet assessed
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Phenotype expression in familial combined hyperlipidemia ↗Atherosclerosis · 1997 · PMID 9298685not yet assessed
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Polymorphism in the cytochrome P450 2E1 gene and the risk of alcoholic liver disease ↗Journal of Hepatology · 1997 · PMID 9148022not yet assessed
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No Evidence of Linkage Between Familial Combined Hyperlipidemia and Genes Encoding Lipolytic Enzymes in Finnish Families ↗Arteriosclerosis Thrombosis and Vascular Biology · 1997 · PMID 9157946not yet assessed
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Glutathione <i>S</i>‐transferase‐M1 ‘null’ genotype and alcohol‐induced disorders of human spermatogenesis ↗International Journal of Andrology · 1996 · PMID 8876265not yet assessed
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Glutathione‐S‐Transferase GST M1 “Null” Genotype and the Risk of Alcoholic Liver Disease ↗Alcoholism Clinical and Experimental Research · 1996 · PMID 8947308not yet assessed
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Polymorphism in the cytochrome P450 2E1 gene and alcohol‐induced disorders of human spermatogenesis ↗International Journal of Andrology · 1996 · PMID 8985781not yet assessed
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Early perivenular fibrogenesis - precirrhotic lesions among moderate alcohol consumers and chronic alcoholics ↗Journal of Hepatology · 1995 · PMID 8583139not yet assessed
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Angiotensin‐converting enzyme genotypes in the high‐ and low‐risk area for coronary heart disease in Finland ↗Genetic Epidemiology · 1995 · PMID 8536956not yet assessed
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Abuse of Alcohol in Sudden Out‐of‐Hospital Deaths in Finland ↗Alcoholism Clinical and Experimental Research · 1994 · PMID 8048723not yet assessed
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TRAFFIC FATALITIES AND ALCOHOLIC LIVER DISEASE IN FINLAND - A COMPARATIVE STUDY OF THE YEARS 1982-1985 AND 1989-1990International Conference on Alcohol, Drugs and Traffic Safety-T92, Proceedings of the 12th Conference.Verlag TUeV Rheinland · 1993not yet assessed
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(untitled)Edinburgh Research Explorer (University of Edinburgh) ·not yet assessed
Full bibliography from OpenAlex; reproducibility verdicts matched by PMID.
Author attribution follows OpenAlex disambiguation, which is imperfect — a researcher's papers can be split across profiles or mixed with a namesake.
Merged across profiles sharing this ORCID where present. See every “Perola M” paper on PubMed ↗