Author details

Full Name

Solveig Gretarsdottir

Affiliation

ORCID

Career Start Year

1992

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36658437	Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism.	Nat Genet	2023
37606673	Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.	JAMA	2023
37932435	Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis.	Nat Genet	2023
36747475	Genetic variants associated with syncope implicate neural and autonomic processes.	Eur Heart J	2023
34407635	Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland.	Arterioscler Thromb Vasc Biol	2021
31746962	Association of Genetically Predicted Lipid Levels With the Extent of Coronary Atherosclerosis in Icelandic Adults.	JAMA Cardiol	2020
31865966	Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes.	J Am Coll Cardiol	2019
31641117	Sequence variants with large effects on cardiac electrophysiology and disease.	Nat Commun	2019
29590334	A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta.	Eur Heart J	2018
30271950	Coding variants in <i>RPL3L</i> and <i>MYZAP</i> increase risk of atrial fibrillation.	Commun Biol	2018
29511194	Genome-wide analysis yields new loci associating with aortic valve stenosis.	Nat Commun	2018
29596577	Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease.	Eur Heart J	2018
27742809	A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.	Eur Heart J	2017
28747754	Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.	Nat Genet	2017
28398513	A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease.	Hum Mol Genet	2017
28319091	Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.	Nat Genet	2017
29050564	A Missense Variant in PLEC Increases RiskÂ of Atrial Fibrillation.	J Am Coll Cardiol	2017
27899403	Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci.	Circ Res	2017
27997041	Genetic variation at 16q24.2 is associated with small vessel stroke.	Ann Neurol	2017
26952864	A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences.	Mol Psychiatry	2016
27192541	Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease.	N Engl J Med	2016
27135400	Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease.	Nat Genet	2016
26327206	A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease.	PLoS Genet	2015
25807286	Large-scale whole-genome sequencing of the Icelandic population.	Nat Genet	2015
25031287	Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12.	Neurology	2014
24262325	Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.	Stroke	2014
23535823	A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm.	Hum Mol Genet	2013
24046328	A variant in LDLR is associated with abdominal aortic aneurysm.	Circ Cardiovasc Genet	2013
23824655	The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis.	PLoS Med	2013
23381943	Ischemic stroke is associated with the ABO locus: the EuroCLOT study.	Ann Neurol	2013
23041239	Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.	Lancet Neurol	2012
22306652	Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.	Nat Genet	2012
22941190	Common variants at 6p21.1 are associated with large artery atherosclerotic stroke.	Nat Genet	2012
22898070	Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism.	J Am Coll Cardiol	2012
22055160	Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1.	Am J Hum Genet	2011
21378990	Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.	Nat Genet	2011
21378987	A rare variant in MYH6 is associated with high risk of sick sinus syndrome.	Nat Genet	2011
20418888	Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior.	Nat Genet	2010
20949110	European bone mineral density loci are also associated with BMD in East-Asian populations.	PLoS One	2010
20622881	Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm.	Nat Genet	2010
19597491	A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.	Nat Genet	2009
19079262	New sequence variants associated with bone mineral density.	Nat Genet	2009
19079260	Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.	Nat Genet	2009
19578363	New common variants affecting susceptibility to basal cell carcinoma.	Nat Genet	2009
18991354	Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke.	Ann Neurol	2008
18344981	Genetics of gene expression and its effect on disease.	Nature	2008
18566660	A drastic reduction in the life span of cystatin C L68Q carriers due to life-style changes during the last two centuries.	PLoS Genet	2008
18325076	Genetic profile of ischemic cerebrovascular disease and carotid stenosis.	Acta Neurologica Scandinavica	2008
18176561	The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm.	Nat Genet	2008
18488027	ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.	Nat Genet	2008