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| 37873414 | GWAS meta-analysis of psoriasis identifies new susceptibility alleles impacting disease mechanisms and therapeutic targets. | medRxiv | 2023 |
| 35578897 | Cohort Profile Update: The HUNT Study, Norway. | International Journal of Epidemiology | 2023 |
| 35315439 | Characterization of the genetic architecture of infant and early childhood body mass index. | Nat Metab | 2022 |
| 36777998 | The HUNT study: A population-based cohort for genetic research. | Cell Genom | 2022 |
| 30936278 | Prediction of Ankylosing Spondylitis in the HUNT Study by a Genetic Risk Score Combining 110 Single-nucleotide Polymorphisms of Genome-wide Significance. | Journal of Rheumatology | 2020 |
| 31719661 | Ultralow amounts of DNA from long-term archived serum samples produce quality genotypes. | European Journal of Human Genetics | 2020 |
| 33339817 | Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. | Nat Commun | 2020 |
| 32603359 | Age-of-onset information helps identify 76 genetic variants associated with allergic disease. | PLoS Genet | 2020 |
| 30996050 | Temporal Changes in Cardiac Troponin I Are Associated with Risk of Cardiovascular Events in the General Population: The Nord-Trøndelag Health Study. | Clinical Chemistry | 2019 |
| 31160809 | Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2019 |
| 29273807 | Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2018 |
| 30061737 | Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. | Nat Genet | 2018 |
| 29899519 | Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes. | Nat Commun | 2018 |
| 30271950 | Coding variants in <i>RPL3L</i> and <i>MYZAP</i> increase risk of atrial fibrillation. | Commun Biol | 2018 |
| 29290336 | Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development. | Am J Hum Genet | 2018 |
| 29549330 | Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2018 |
| 29549329 | Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2018 |
| 29496193 | Relative Prognostic Value of Cardiac Troponin I and C-Reactive Protein in the General Population (from the Nord-Trøndelag Health [HUNT] Study). | American Journal of Cardiology | 2018 |
| 28146470 | Rare and low-frequency coding variants alter human adult height. | Nature | 2017 |
| 28861891 | Improving power of association tests using multiple sets of imputed genotypes from distributed reference panels. | Genet Epidemiol | 2017 |
| 28443625 | Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. | Nat Commun | 2017 |
| 29083408 | Exome-wide association study of plasma lipids in >300,000 individuals. | Nat Genet | 2017 |
| 29083406 | Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. | Nat Genet | 2017 |
| 28209224 | Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease. | J Am Coll Cardiol | 2017 |
| 27618452 | The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. | Nat Genet | 2016 |
| 26934567 | Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease. | N Engl J Med | 2016 |
| 27176717 | Blood pressure changes during 22-year of follow-up in large general population - the HUNT Study, Norway. | BMC Cardiovascular Disorders | 2016 |
| 27355579 | Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. | PLoS Genet | 2016 |
| 27453509 | Gender, High-Sensitivity Troponin I, and the Risk of Cardiovascular Events (from the Nord-Trøndelag Health Study). | American Journal of Cardiology | 2016 |
| 27618447 | Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. | Nat Genet | 2016 |
| 27754487 | Exome chip analyses in adult attention deficit hyperactivity disorder. | Transl Psychiatry | 2016 |
| 27876822 | A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. | Nat Commun | 2016 |
| 27548312 | A reference panel of 64,976 haplotypes for genotype imputation. | Nat Genet | 2016 |
| 26690388 | Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese. | Nat Commun | 2015 |
| 25673413 | Genetic studies of body mass index yield new insights for obesity biology. | Nature | 2015 |
| 25673412 | New genetic loci link adipose and insulin biology to body fat distribution. | Nature | 2015 |
| 25695851 | Impact of sex on the prognostic value of high-sensitivity cardiac troponin I in the general population: the HUNT study. | Clinical Chemistry | 2015 |
| 25740221 | Methods for association analysis and meta-analysis of rare variants in families. | Genet Epidemiol | 2015 |
| 26551672 | Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. | Nat Genet | 2015 |
| 26426971 | The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. | PLoS Genet | 2015 |
| 24507775 | Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. | Am J Hum Genet | 2014 |
| 25282103 | Defining the role of common variation in the genomic and biological architecture of adult human height. | Nat Genet | 2014 |
| 24336170 | Meta-analysis of gene-level tests for rare variant association. | Nat Genet | 2014 |
| 24728188 | No large-effect low-frequency coding variation found for myocardial infarction. | Hum Mol Genet | 2014 |
| 24593135 | Hypertension after preeclampsia and relation to the C1114G polymorphism (rs4606) in RGS2: data from the Norwegian HUNT2 study. | BMC Medical Genetics | 2014 |
| 24633158 | Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk. | Nat Genet | 2014 |
| 24941081 | Loss-of-function mutations in APOC3, triglycerides, and coronary disease. | N Engl J Med | 2014 |
| 24509480 | Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. | Nat Genet | 2014 |
| 23339167 | Single nucleotide polymorphisms in G protein signaling pathway genes in preeclampsia. | Hypertension | 2013 |
| 26105937 | PP084. Hypertension after preeclampsia in women with C1114G polymorphism in rgs2 (the regulator of g protein signaling 2). | Pregnancy Hypertension | 2013 |