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Author Details

Gudmundur Thorgeirsson
1978
175
55
PMIDPaper TitleJournal TitlePublished Year
36658437Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism.Nat Genet2023
37606673Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.JAMA2023
37936531Proteomic prediction of incident heart failure and its main subtypes.2023
37714134Complex effects of sequence variants on lipid levels and coronary artery disease.Cell2023
37414856Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study.Commun Med (Lond)2023
37449562Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland.J Am Heart Assoc2023
36747475Genetic variants associated with syncope implicate neural and autonomic processes.Eur Heart J2023
37294764Sequence variants affecting voice pitch in humans.Sci Adv2023
37038246Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study.Eur Heart J2023
35103619[Hypertension Management in Primary Care in the Capital Area of Iceland].Laeknabladid2022
35751511Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci.Eur Heart J2022
36280732Multiomics study of nonalcoholic fatty liver disease.Nat Genet2022
36125206Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles: a Mendelian randomization analysis.Eur J Prev Cardiol2022
35315156Acetylsalicylic acid use is associated with improved survival in bacteremic pneumococcal pneumonia: A long-term nationwide study.Journal of Internal Medicine2022
34936471Response by Björnsson et al to Letter Regarding Article, "Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland".Arterioscler Thromb Vasc Biol2022
34480422The genomics of heart failure: design and rationale of the HERMES consortium.ESC Heart Fail2021
36282123Genetic insight into sick sinus syndrome.Eur Heart J2021
34282336Distinction between the effects of parental and fetal genomes on fetal growth.Nat Genet2021
34108613The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis.Commun Biol2021
34145379Predicting the probability of death using proteomics.Commun Biol2021
33982893The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large-Scale Proteomics Scan in Iceland.Arthritis Rheumatol2021
33315477Lifelong Reduction in LDL (Low-Density Lipoprotein) Cholesterol due to a Gain-of-Function Mutation in <i>LDLR</i>.Circ Genom Precis Med2021
34580418Genetic variants associated with platelet count are predictive of human disease and physiological markers.Commun Biol2021
34407635Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland.Arterioscler Thromb Vasc Biol2021
33230300Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.Nat Genet2020
31746962Association of Genetically Predicted Lipid Levels With the Extent of Coronary Atherosclerosis in Icelandic Adults.JAMA Cardiol2020
32702746Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease.Eur Heart J2020
33035477Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming.Curr Biol2020
30992453A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy.Nat Commun2019
31641117Sequence variants with large effects on cardiac electrophysiology and disease.Nat Commun2019
31865966Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes.J Am Coll Cardiol2019
30445559Prevalence and prognosis of ischaemic and non-ischaemic myocardial fibrosis in older adults.Eur Heart J2019
30971390Stress related disorders and risk of cardiovascular disease: population based, sibling controlled cohort study.BMJ, The2019
30894546Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density.Nat Commun2019
29596577Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease.Eur Heart J2018
30354339Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac Death.Circ Genom Precis Med2018
30304454Association of Unrecognized Myocardial Infarction With Long-term Outcomes in Community-Dwelling Older Adults: The ICELAND MI Study.JAMA Cardiol2018
30271901A rare missense variant in <i>NR1H4</i> associates with lower cholesterol levels.Commun Biol2018
29511194Genome-wide analysis yields new loci associating with aortic valve stenosis.Nat Commun2018
28078921Regional differences in mortality, hospital discharges and primary care contacts for cardiovascular disease.Scandinavian Journal of Public Health2017
29020384Fibrosis as measured by the biomarker, tissue inhibitor metalloproteinase-1, predicts mortality in Age Gene Environment Susceptibility-Reykjavik (AGES-Reykjavik) Study.Eur Heart J2017
28596592Sequence variant at 4q25 near PITX2 associates with appendicitis.Sci Rep2017
28497765[Acute myocardial infarction among Icelanders forty years old and younger 2005-2009. Comparison with a study carried out 1980-1984].Laeknabladid2017
28805102Favourable long-term outcome after coronary artery bypass grafting in a nationwide cohort.Scand Cardiovasc J2017
28366010Prevalence of heart failure in the elderly and future projections: the AGES-Reykjavík study.Scand Cardiovasc J2017
28398513A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease.Hum Mol Genet2017
29044038[Heart failure among elderly Icelanders: Incidence, prevalence, underlying diseases and long-term survival].Laeknabladid2017
28262628[Private hospitals and public[Editorial]].Laeknabladid2017
28250455Diversity in non-repetitive human sequences not found in the reference genome.Nat Genet2017
27742809A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.Eur Heart J2017
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