|
| 37684520 | A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndrome. | Eur J Hum Genet | 2024 |
| 37684520 | A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndrome. | Eur J Hum Genet | 2024 |
| 36239377 | Cartilage Acidic Protein 1 in Plasma Associates With Prevalent Osteoarthritis and Predicts Future Risk as Well as Progression to Joint Replacements: Results From the UK Biobank Resource. | Arthritis Rheumatol | 2023 |
| 36239377 | Cartilage Acidic Protein 1 in Plasma Associates With Prevalent Osteoarthritis and Predicts Future Risk as Well as Progression to Joint Replacements: Results From the UK Biobank Resource. | Arthritis Rheumatol | 2023 |
| 37606673 | Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events. | JAMA | 2023 |
| 37937776 | Actionable Genotypes and Their Association with Life Span in Iceland. | N Engl J Med | 2023 |
| 37596405 | Histopathology and levels of proteins in plasma associate with survival after colorectal cancer diagnosis. | Br J Cancer | 2023 |
| 37932435 | Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis. | Nat Genet | 2023 |
| 37794188 | Large-scale plasma proteomics comparisons through genetics and disease associations. | Nature | 2023 |
| 37414856 | Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study. | Commun Med (Lond) | 2023 |
| 37034649 | Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. | medRxiv | 2023 |
| 37400429 | Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality. | Nat Commun | 2023 |
| 37012456 | Genetic effects on the timing of parturition and links to fetal birth weight. | Nat Genet | 2023 |
| 37386006 | Sequence variants affecting the genome-wide rate of germline microsatellite mutations. | Nat Commun | 2023 |
| 36747475 | Genetic variants associated with syncope implicate neural and autonomic processes. | Eur Heart J | 2023 |
| 36931692 | Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect. | Ann Rheum Dis | 2023 |
| 37430141 | Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria. | Commun Biol | 2023 |
| 37301908 | Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality. | Nat Commun | 2023 |
| 37294764 | Sequence variants affecting voice pitch in humans. | Sci Adv | 2023 |
| 37038246 | Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study. | Eur Heart J | 2023 |
| 36658437 | Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism. | Nat Genet | 2023 |
| 37596405 | Histopathology and levels of proteins in plasma associate with survival after colorectal cancer diagnosis. | Br J Cancer | 2023 |
| 37794188 | Large-scale plasma proteomics comparisons through genetics and disease associations. | Nature | 2023 |
| 37937776 | Actionable Genotypes and Their Association with Life Span in Iceland. | N Engl J Med | 2023 |
| 37932435 | Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis. | Nat Genet | 2023 |
| 37606673 | Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events. | JAMA | 2023 |
| 37414856 | Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study. | Commun Med (Lond) | 2023 |
| 37386006 | Sequence variants affecting the genome-wide rate of germline microsatellite mutations. | Nat Commun | 2023 |
| 37012456 | Genetic effects on the timing of parturition and links to fetal birth weight. | Nat Genet | 2023 |
| 37038246 | Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study. | Eur Heart J | 2023 |
| 37400429 | Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality. | Nat Commun | 2023 |
| 37301908 | Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality. | Nat Commun | 2023 |
| 37034649 | Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. | medRxiv | 2023 |
| 37430141 | Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria. | Commun Biol | 2023 |
| 37294764 | Sequence variants affecting voice pitch in humans. | Sci Adv | 2023 |
| 36747475 | Genetic variants associated with syncope implicate neural and autonomic processes. | Eur Heart J | 2023 |
| 36931692 | Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect. | Ann Rheum Dis | 2023 |
| 36658437 | Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism. | Nat Genet | 2023 |
| 34936471 | Response by Björnsson et al to Letter Regarding Article, "Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland". | Arterioscler Thromb Vasc Biol | 2022 |
| 36171188 | Effect of booster vaccination against Delta and Omicron SARS-CoV-2 variants in Iceland. | Nat Commun | 2022 |
| 35650273 | Genetic architecture of band neutrophil fraction in Iceland. | Commun Biol | 2022 |
| 35697829 | Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals. | Commun Biol | 2022 |
| 35751511 | Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci. | Eur Heart J | 2022 |
| 36280732 | Multiomics study of nonalcoholic fatty liver disease. | Nat Genet | 2022 |
| 35551307 | Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. | Nat Genet | 2022 |
| 36125206 | Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles: a Mendelian randomization analysis. | Eur J Prev Cardiol | 2022 |
| 35859178 | The sequences of 150,119 genomes in the UK Biobank. | Nature | 2022 |
| 35470158 | Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset. | Ann Rheum Dis | 2022 |
| 36415660 | Thirty novel sequence variants impacting human intracranial volume. | Brain Commun | 2022 |
| 36513657 | Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk. | Nat Commun | 2022 |