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V. Tragante · SciRah

Researcher profile · Semantic Scholar

V. Tragante

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V. Tragante — researcher profile on SciRah

h-index: 44
Works: 117
Citations: 7,317

Most-cited papers

Large-scale integration of the plasma proteome with genetics and disease
E. Ferkingstad, P. Sulem, Bjarni A Atlason, G. Sveinbjornsson +36 more
2021Nature Genetics1,452 citations
Semantic Scholar
The sequences of 150,119 genomes in the UK Biobank
B. Halldórsson, H. Eggertsson, K. Moore, Hannes Hauswedell +52 more
2021Nature395 citations Open access
Semantic Scholar
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
P. Surendran, F. Drenos, R. Young, H. Warren +206 more
2016Nature Genetics280 citations Open access
Semantic Scholar
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women
V. Steinthorsdottir, R. McGinnis, Nicholas O. Williams, L. Stefánsdóttir +71 more
2020Nature Communications173 citations Open access
Semantic Scholar
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
P. Surendran, E. Feofanova, N. Lahrouchi, I. Ntalla +278 more
2020Nature Genetics145 citations Open access
Semantic Scholar
A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis
S. Bell, A. Rigas, Magnus K. Magnusson, E. Ferkingstad +57 more
2021Communications Biology142 citations Open access
Semantic Scholar
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
Nicola Barban, R. Jansen, R. de Vlaming, A. Vaez +250 more
2016Nature Genetics137 citations Open access
Semantic Scholar
Genetic loci associated with heart rate variability and their effects on cardiac disease risk
I. Nolte, M. Muñoz, V. Tragante, A. Amare +160 more
2017Nature Communications133 citations Open access
Semantic Scholar
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease
S. Saevarsdottir, T. Olafsdottir, Erna V. Ivarsdottir, G. Halldorsson +42 more
2020Nature131 citations
Semantic Scholar
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism
J. Ghouse, V. Tragante, G. Ahlberg, S. Rand +32 more
2023Nature Genetics120 citations
Semantic Scholar
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
A. Erzurumluoglu, Meng-Zhen Liu, V. Jackson, D. Barnes +171 more
2019Molecular Psychiatry117 citations Open access
Semantic Scholar
52 Genetic Loci Influencing Myocardial Mass
P. van der Harst, J. van Setten, N. Verweij, Georg Vogler +155 more
2017115 citations
Semantic Scholar
Genome-wide analysis yields new loci associating with aortic valve stenosis
A. Helgadóttir, G. Thorleifsson, S. Gretarsdottir, O. Stefansson +42 more
2017Nature Communications114 citations Open access
Semantic Scholar
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
Ragnar P. Kristjansson, Stefania Benonisdottir, O. Davidsson, A. Oddsson +36 more
2019Nature Genetics108 citations
Semantic Scholar
Cystatin C and Cardiovascular Disease
S. W. van der Laan, T. Fall, A. Soumaré, A. Teumer +68 more
2016Journal of the American College of Cardiology102 citations Open access
Semantic Scholar
Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association study
S. Zewinger, M. Kleber, V. Tragante, R. McCubrey +100 more
2017The Lancet Diabetes and Endocrinology93 citations Open access
Semantic Scholar
Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis
T. Olafsdottir, Fannar Theódórs, Kristbjorg Bjarnadottir, U. Bjornsdottir +31 more
2020Nature Communications90 citations Open access
Semantic Scholar
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits
T. Rafnar, Bjarni Gunnarsson, O. Stefansson, P. Sulem +33 more
2018Nature Communications90 citations Open access
Semantic Scholar
Genetically determined NLRP3 inflammasome activation associates with systemic inflammation and cardiovascular mortality.
Stefan J. Schunk, M. Kleber, W. März, S. Pang +64 more
2021European Heart Journal87 citations Open access
Semantic Scholar
Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease
A. Helgadóttir, G. Thorleifsson, Kristjan F. Alexandersson, V. Tragante +39 more
2020European Heart Journal84 citations Open access
Semantic Scholar
Distinction between the effects of parental and fetal genomes on fetal growth
Thorhildur Juliusdottir, V. Steinthorsdottir, L. Stefánsdóttir, G. Sveinbjornsson +18 more
2021Nature Genetics82 citations
Semantic Scholar
A comprehensive evaluation of the genetic architecture of sudden cardiac arrest
Foram N. Ashar, Rebecca N. Mitchell, C. Albert, C. Newton-Cheh +60 more
2018European Heart Journal78 citations Open access
Semantic Scholar
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
J. Ghouse, G. Sveinbjornsson, Marijana Vujković, A. Seidelin +47 more
2024Nature Genetics67 citations Open access
Semantic Scholar
Exome chip meta-analysis fine maps causal variants and elucidates the genetic architecture of rare coding variants in smoking and alcohol use.
D. Brazel, Yu Jiang, Jordan M. Hughey, Valérie Turcot +174 more
2018Biological Psychiatry66 citations Open access
Semantic Scholar
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA
J. Gudmundsson, J. K. Sigurdsson, L. Stefánsdóttir, B. Agnarsson +24 more
2018Nature Communications66 citations Open access
Semantic Scholar
Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation
Rosa B. Thorolfsdottir, G. Sveinbjornsson, P. Sulem, J. Nielsen +31 more
2018Communications Biology65 citations Open access
Semantic Scholar
Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis
S. Stacey, F. Zink, G. Halldorsson, L. Stefánsdóttir +27 more
2023Nature Genetics60 citations Open access
Semantic Scholar
The correlation between CpG methylation and gene expression is driven by sequence variants
Olafur A. Stefansson, Brynja D. Sigurpálsdóttir, S. Rognvaldsson, G. Halldorsson +28 more
2024Nature Genetics56 citations Open access
Semantic Scholar
New Blood Pressure Associated Loci Identified in Meta-Analyses of 475,000 Individuals
A. Kraja, J. Cook, H. Warren, P. Surendran +138 more
2017Circulation: Cardiovascular Genetics54 citations Open access
Semantic Scholar
Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies
Y. Li, J. van Setten, S. Verma, Yontao Lu +62 more
2015Genome Medicine54 citations Open access
Semantic Scholar
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis
Erna V. Ivarsdottir, H. Hólm, Stefania Benonisdottir, T. Ólafsdóttir +24 more
2021Communications Biology52 citations Open access
Semantic Scholar
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura
G. Bjornsdottir, M. A. Chalmer, L. Stefánsdóttir, A. Skuladóttir +90 more
2023Nature Genetics51 citations Open access
Semantic Scholar
Genetic insight into sick sinus syndrome
Rosa B. Thorolfsdottir, G. Sveinbjornsson, Hildur M. Aegisdottir, Stefania Benonisdottir +51 more
2021European Heart Journal51 citations Open access
Semantic Scholar
Assessing thyroid cancer risk using polygenic risk scores
S. Liyanarachchi, J. Gudmundsson, E. Ferkingstad, Huiling He +17 more
2020Proceedings of the National Academy of Sciences of the United States of America49 citations Open access
Semantic Scholar
Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targets
Harri Lempiäinen, Ingrid Brænne, T. Michoel, V. Tragante +31 more
2018Scientific Reports49 citations Open access
Semantic Scholar
Sequence variants associating with urinary biomarkers
Stefania Benonisdottir, Ragnar P. Kristjansson, A. Oddsson, V. Steinthorsdottir +34 more
2018Human Molecular Genetics38 citations Open access
Semantic Scholar
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis
Gudjon R. Oskarsson, A. Oddsson, M. K. Magnusson, Ragnar P. Kristjansson +34 more
2020Communications Biology37 citations Open access
Semantic Scholar
Association of Genetically Predicted Lipid Levels With the Extent of Coronary Atherosclerosis in Icelandic Adults
E. Björnsson, G. Thorleifsson, A. Helgadóttir, Thórarinn Guðnason +14 more
2019JAMA cardiology37 citations Open access
Semantic Scholar
Variants at the Interleukin 1 Gene Locus and Pericarditis.
Rosa B. Thorolfsdottir, Andrea B. Jonsdottir, G. Sveinbjornsson, Hildur M. Aegisdottir +42 more
2023JAMA cardiology34 citations Open access
Semantic Scholar
Sequence variants with large effects on cardiac electrophysiology and disease
Kristjan Norland, G. Sveinbjornsson, Rosa B. Thorolfsdottir, O. Davidsson +19 more
2019Nature Communications34 citations Open access
Semantic Scholar
Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming.
Rosa S. Gisladottir, Erna V. Ivarsdottir, A. Helgason, L. Jonsson +24 more
2020Current Biology33 citations Open access
Semantic Scholar
Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank
T. Ólafsdóttir, G. Thorleifsson, P. Sulem, O. Stefansson +27 more
2020Communications Biology31 citations Open access
Semantic Scholar
The Impact of Selection Bias on Estimation of Subsequent Event Risk
Yi-Juan Hu, A. Schmidt, F. Dudbridge, M. Holmes +169 more
2017Circulation: Cardiovascular Genetics28 citations Open access
Semantic Scholar
52 Genetic Loci Influencing Myocardial Mass
P. van der Harst, J. van Setten, N. Verweij, Georg Vogler +156 more
2016Journal of the American College of Cardiology27 citations Open access
Semantic Scholar
Association of Chromosome 9p21 with Subsequent Coronary Heart Disease Events: A GENIUS-CHD Study of Individual Participant Data
R. Patel, A. Schmidt, V. Tragante, R. McCubrey +163 more
2019Circulation Genomic and Precision Medicine26 citations Open access
Semantic Scholar
Integrated genomics and protein interaction analyses implicate postsynaptic signaling in schizophrenia
D. Schijven, D. Kofink, V. Tragante, Marloes Verkerke +6 more
2017bioRxiv26 citations Open access
Semantic Scholar
rs41291957 controls miR‐143 and miR‐145 expression and impacts coronary artery disease risk
I. F. Hall, M. Climent, Chiara Viviani-Anselmi, Laura Papa +8 more
2021EMBO Molecular Medicine24 citations Open access
Semantic Scholar
Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles - A Mendelian randomization analysis.
A. Helgadóttir, G. Thorleifsson, Audunn S. Snaebjarnarson, L. Stefánsdóttir +33 more
2022European Journal of Preventive Cardiology23 citations Open access
Semantic Scholar
Eleven genomic loci affect plasma levels of chronic inflammation marker soluble urokinase-type plasminogen activator receptor
Joseph Dowsett, E. Ferkingstad, L. J. H. Rasmussen, L. Thørner +36 more
2021Communications Biology22 citations Open access
Semantic Scholar
Subsequent Event Risk in Individuals with Established Coronary Heart Disease: Design and Rationale of the GENIUS-CHD Consortium
Riyaz S. Patel, V. Tragante, A. Schmidt, R. McCubrey +177 more
2019Circulation Genomic and Precision Medicine20 citations Open access
Semantic Scholar

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