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Author Details

Gudmar Thorleifsson
deCODE genetics/Amgen Inc.
1991
279
130
PMIDPaper TitleJournal TitlePublished Year
36376028Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement.Ann Rheum Dis2023
36376028Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement.Ann Rheum Dis2023
36239377Cartilage 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 Rheumatol2023
37606673Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.JAMA2023
37932435Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis.Nat Genet2023
37794188Large-scale plasma proteomics comparisons through genetics and disease associations.Nature2023
37714134Complex effects of sequence variants on lipid levels and coronary artery disease.Cell2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
37402774Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis.Commun Biol2023
37210288Genome-wide Association Study of Bladder Cancer Reveals New Biological and Translational Insights.Eur Urol2023
37012456Genetic effects on the timing of parturition and links to fetal birth weight.Nat Genet2023
36747475Genetic variants associated with syncope implicate neural and autonomic processes.Eur Heart J2023
36931692Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect.Ann Rheum Dis2023
37430141Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria.Commun Biol2023
37294764Sequence variants affecting voice pitch in humans.Sci Adv2023
37714134Complex effects of sequence variants on lipid levels and coronary artery disease.Cell2023
37794188Large-scale plasma proteomics comparisons through genetics and disease associations.Nature2023
37932435Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis.Nat Genet2023
37606673Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.JAMA2023
37210288Genome-wide Association Study of Bladder Cancer Reveals New Biological and Translational Insights.Eur Urol2023
37012456Genetic effects on the timing of parturition and links to fetal birth weight.Nat Genet2023
37402774Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis.Commun Biol2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
37430141Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria.Commun Biol2023
37294764Sequence variants affecting voice pitch in humans.Sci Adv2023
36747475Genetic variants associated with syncope implicate neural and autonomic processes.Eur Heart J2023
36931692Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect.Ann Rheum Dis2023
36239377Cartilage 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 Rheumatol2023
35104449Genetic Associations and Architecture of Asthma-COPD Overlap.Chest2022
35551307Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.Nat Genet2022
35859178The sequences of 150,119 genomes in the UK Biobank.Nature2022
35470158Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset.Ann Rheum Dis2022
36415660Thirty novel sequence variants impacting human intracranial volume.Brain Commun2022
36513657Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk.Nat Commun2022
35013207Functional dissection of inherited non-coding variation influencing multiple myeloma risk.Nat Commun2022
35007327Genome-wide association study on 13â¿¿167 individuals identifies regulators of blood CD34+cell levels.Blood2022
35104449Genetic Associations and Architecture of Asthma-COPD Overlap.Chest2022
35220425Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes.Hum Mol Genet2022
35551307Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.Nat Genet2022
35470158Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset.Ann Rheum Dis2022
35859178The sequences of 150,119 genomes in the UK Biobank.Nature2022
36513657Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk.Nat Commun2022
36415660Thirty novel sequence variants impacting human intracranial volume.Brain Commun2022
35013207Functional dissection of inherited non-coding variation influencing multiple myeloma risk.Nat Commun2022
35220425Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes.Hum Mol Genet2022
35007327Genome-wide association study on 13â¿¿167 individuals identifies regulators of blood CD34+cell levels.Blood2022
33167008Increased absorption of phytosterols is the simplest and most plausible explanation for coronary artery disease risk not accounted for by non-HDL cholesterol in high cholesterol absorbers.Eur Heart J2021
33580673Genetic 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
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Collaborators

Kari Stefansson
University of Iceland
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Unnur Thorsteinsdottir
University of Iceland
Co-authored papers 230
Daniel F Gudbjartsson
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Patrick Sulem
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Augustine Kong
Co-authored papers 94
Valgerdur Steinthorsdottir
Co-authored papers 77
Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers 71
Hilma Holm
Co-authored papers 64
Tim D Spector
King's College London
Co-authored papers 63
Cornelia M van Duijn
University of Oxford
Co-authored papers 62
Gisli Masson
Co-authored papers 61
Albert Hofman
Harvard T.H. Chan School of Public Health
Co-authored papers 59
Lambertus A Kiemeney
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Mark I McCarthy
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Michael Boehnke
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Andres Metspalu
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Cecilia M Lindgren
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Veikko Salomaa
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Ruth J F Loos
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Erik Ingelsson
Stanford University School of Medicine
Co-authored papers 44
Solveig Gretarsdottir
Co-authored papers 44
Karen L Mohlke
Co-authored papers 43
Leif Groop
Co-authored papers 43
Markku Laakso
Co-authored papers 43
Tõnu Esko
Co-authored papers 42
Anna Helgadottir
Co-authored papers 41
Release 1.2