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Author Details

Kari Stefansson
University of Iceland
1980
763
185
PMIDPaper TitleJournal TitlePublished Year
37334623Multi-polygenic scores in psychiatry: From disorder specific to transdiagnostic perspectives.Am J Med Genet B Neuropsychiatr Genet2024
37946686Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD.Am J Med Genet B Neuropsychiatr Genet2024
38007706Polygenic risk scores associate with blood pressure traits across the lifespan.Eur J Prev Cardiol2024
38007706Polygenic risk scores associate with blood pressure traits across the lifespan.Eur J Prev Cardiol2024
37962958Spliceosome malfunction causes neurodevelopmental disorders with overlapping features.J Clin Invest2024
38052102Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity.Hum Reprod2024
37684520A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndrome.Eur J Hum Genet2024
37334623Multi-polygenic scores in psychiatry: From disorder specific to transdiagnostic perspectives.Am J Med Genet B Neuropsychiatr Genet2024
37326842Genome-wide investigation of persistence with methotrexate treatment in early rheumatoid arthritis.Rheumatology (Oxford)2024
37962958Spliceosome malfunction causes neurodevelopmental disorders with overlapping features.J Clin Invest2024
38007706Polygenic risk scores associate with blood pressure traits across the lifespan.Eur J Prev Cardiol2024
38007706Polygenic risk scores associate with blood pressure traits across the lifespan.Eur J Prev Cardiol2024
37946686Predicting ADHD in alcohol dependence using polygenic risk scores for ADHD.Am J Med Genet B Neuropsychiatr Genet2024
38052102Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity.Hum Reprod2024
37684520A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndrome.Eur J Hum Genet2024
37326842Genome-wide investigation of persistence with methotrexate treatment in early rheumatoid arthritis.Rheumatology (Oxford)2024
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
37606673Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.JAMA2023
37753640Combining Polygenic and Proteomic Risk Scores With Clinical Risk Factors to Improve Performance for Diagnosing Absence of Coronary Artery Disease in Patients With de novo Chest Pain.Circ Genom Precis Med2023
37753640Combining Polygenic and Proteomic Risk Scores With Clinical Risk Factors to Improve Performance for Diagnosing Absence of Coronary Artery Disease in Patients With de novo Chest Pain.Circ Genom Precis Med2023
37937776Actionable Genotypes and Their Association with Life Span in Iceland.N Engl J Med2023
37937776Actionable Genotypes and Their Association with Life Span in Iceland.N Engl J Med2023
37596405Histopathology and levels of proteins in plasma associate with survival after colorectal cancer diagnosis.Br J Cancer2023
37932435Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis.Nat Genet2023
37919453An atlas of genetic determinants of forearm fracture.Nat Genet2023
37714134Complex effects of sequence variants on lipid levels and coronary artery disease.Cell2023
37414752Characterizing the evolution and phenotypic impact of ampliconic Y chromosome regions.Nat Commun2023
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
37464041Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses.Nat Med2023
37012456Genetic effects on the timing of parturition and links to fetal birth weight.Nat Genet2023
37449562Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland.J Am Heart Assoc2023
37244984DanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals.BMC Genom Data2023
36931692Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect.Ann Rheum Dis2023
37301908Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.Nat Commun2023
36608656The genetic history of Scandinavia from the Roman Iron Age to the present.Cell2023
36926036Four missense genetic variants in <i>CUBN</i> are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans.Front Endocrinol (Lausanne)2023
37038246Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study.Eur Heart J2023
37038246Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study.Eur Heart J2023
37503126Understanding the genetic complexity of puberty timing across the allele frequency spectrum.medRxiv2023
37486023Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor.Ann Neurol2023
37919453An atlas of genetic determinants of forearm fracture.Nat Genet2023
37596405Histopathology and levels of proteins in plasma associate with survival after colorectal cancer diagnosis.Br J Cancer2023
37753640Combining Polygenic and Proteomic Risk Scores With Clinical Risk Factors to Improve Performance for Diagnosing Absence of Coronary Artery Disease in Patients With de novo Chest Pain.Circ Genom Precis Med2023
37753640Combining Polygenic and Proteomic Risk Scores With Clinical Risk Factors to Improve Performance for Diagnosing Absence of Coronary Artery Disease in Patients With de novo Chest Pain.Circ Genom Precis Med2023
37714134Complex effects of sequence variants on lipid levels and coronary artery disease.Cell2023
37486023Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor.Ann Neurol2023
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Collaborators

Unnur Thorsteinsdottir
University of Iceland
Co-authored papers 333
Gudmar Thorleifsson
deCODE genetics/Amgen Inc.
Co-authored papers 260
Daniel F Gudbjartsson
Co-authored papers 254
Patrick Sulem
Co-authored papers 200
Augustine Kong
Co-authored papers 171
Hreinn Stefansson
Co-authored papers 156
Gisli Masson
Co-authored papers 110
Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers 101
Lambertus A Kiemeney
Co-authored papers 98
Agnar Helgason
University of Iceland
Co-authored papers 94
Tim D Spector
King's College London
Co-authored papers 93
Cornelia M van Duijn
University of Oxford
Co-authored papers 91
Valgerdur Steinthorsdottir
Co-authored papers 89
Hilma Holm
Co-authored papers 85
Albert Hofman
Harvard T.H. Chan School of Public Health
Co-authored papers 80
Nicholas J Wareham
Co-authored papers 71
Andres Metspalu
Co-authored papers 69
Dorret I Boomsma
Co-authored papers 67
Tõnu Esko
Co-authored papers 66
Fernando Rivadeneira
University Medical Center Rotterdam
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Vilmundur Gudnason
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Caroline Hayward
Co-authored papers 64
Christian Gieger
German Research Center for Cardiovascular Disease (DZHK)
Co-authored papers 63
Nicholas G Martin
Co-authored papers 62
Olafur Th Magnusson
Co-authored papers 62
Mark I McCarthy
Co-authored papers 62
Graham R Walters
Co-authored papers 62
Panos Deloukas
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 61
Veikko Salomaa
Co-authored papers 60
Anna Helgadottir
Co-authored papers 58
Release 1.2