Guðmundur Þorgeirsson

deCODE Genetics (Iceland) — IS

Biochemistry, Genetics and Molecular Biology · Life Sciences

62h-index28.8kcitations183works31.32yr avg
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Research Topics

Genetic Associations and Epidemiology(33), Lipoproteins and Cardiovascular Health(25), Cardiovascular Function and Risk Factors(21), Cardiac Imaging and Diagnostics(15), RNA modifications and cancer(12)

Publications169 total

Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy
Nature Genetics·2024· 45 citedOpen Access
Variants at the Interleukin 1 Gene Locus and Pericarditis
JAMA Cardiology·2023· 22 citedOpen Access
Proteomic Prediction of Incident Heart Failure and Its Main Subtypes
European Journal of Heart Failure·2023· 12 citedOpen Access
Genome-wide association analysis reveals insights into the molecular etiology underlying dilated cardiomyopathy
2023· 6 citedOpen Access
Complex effects of sequence variants on lipid levels and coronary artery disease
Cell·2023· 19 cited
Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events
JAMA·2023· 91 citedOpen Access
Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland
Journal of the American Heart Association·2023· 4 citedOpen Access
Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study
Communications Medicine·2023· 3 citedOpen Access
Sequence variants affecting voice pitch in humans
Science Advances·2023· 18 citedOpen Access
GWAS Summary Statistics from a Global Meta-Analysis of Aortic Stenosis
Zenodo (CERN European Organization for Nuclear Research)·2023Open Access
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study
European Heart Journal·2023· 104 citedOpen Access
Genetic variants associated with syncope implicate neural and autonomic processes
European Heart Journal·2023· 17 citedOpen Access
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism
Nature Genetics·2023· 149 cited
GWAS Summary Statistics from a Global Meta-Analysis of Aortic Stenosis
Zenodo (CERN European Organization for Nuclear Research)·2023· 2 citedOpen Access
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Nature Genetics·2022· 633 citedOpen Access
Multiomics study of nonalcoholic fatty liver disease
Nature Genetics·2022· 212 citedOpen Access
Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles: a Mendelian randomization analysis
European Journal of Preventive Cardiology·2022· 30 citedOpen Access
HLA alleles, disease severity, and age associate with T-cell responses following infection with SARS-CoV-2
Communications Biology·2022· 12 citedOpen Access
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci
European Heart Journal·2022· 17 citedOpen Access
Symptoms, physical measures and cognitive tests after SARS-CoV-2 infection in a large population-based case-control study
Research Square (Research Square)·2022Open Access
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Frequent Co-authors

Guðmar Þorleifsson(25), Unnur Þorsteinsdóttir(25), Kāri Stefánsson(24), Daníel F. Guðbjartsson(23), Sólveig Grétarsdóttir(20), Hilma Hólm(19), Anna Helgadóttir(18), Augustine Kong(16), Davíð O. Arnar(14), Jeffrey R. Gulcher(12), Patrick Sulem(11), Vilmundur Guðnason(11), Einar Már Valdimarsson(10), Valgerður Steinthórsdóttir(10), Allan I. Levey(9), Ísleifur Ólafsson(9), Andrei Manolescu(8), Gísli Másson(8), Muredach P. Reilly(8), Daniel J. Rader(8)