Author details

Full Name

Anna Helgadottir

Affiliation

ORCID

Career Start Year

1997

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37038246	Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study.	Eur Heart J	2023
37606673	Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.	JAMA	2023
37937776	Actionable Genotypes and Their Association with Life Span in Iceland.	N Engl J Med	2023
37932435	Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis.	Nat Genet	2023
37714134	Complex effects of sequence variants on lipid levels and coronary artery disease.	Cell	2023
37414856	Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study.	Commun Med (Lond)	2023
36747475	Genetic variants associated with syncope implicate neural and autonomic processes.	Eur Heart J	2023
34936471	Response by BjÃ¶rnsson et al to Letter Regarding Article, "Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland".	Arterioscler Thromb Vasc Biol	2022
36280732	Multiomics study of nonalcoholic fatty liver disease.	Nat Genet	2022
36125206	Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles: a Mendelian randomization analysis.	Eur J Prev Cardiol	2022
34480422	The genomics of heart failure: design and rationale of the HERMES consortium.	ESC Heart Fail	2021
36282123	Genetic insight into sick sinus syndrome.	Eur Heart J	2021
33580673	Genetic insight into sick sinus syndrome.	Eur Heart J	2021
34282336	Distinction between the effects of parental and fetal genomes on fetal growth.	Nat Genet	2021
33727701	Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2021
33315477	Lifelong Reduction in LDL (Low-Density Lipoprotein) Cholesterol due to a Gain-of-Function Mutation in <i>LDLR</i>.	Circ Genom Precis Med	2021
33167008	Increased 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 J	2021
34580418	Genetic variants associated with platelet count are predictive of human disease and physiological markers.	Commun Biol	2021
34407635	Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland.	Arterioscler Thromb Vasc Biol	2021
33230300	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2020
31746962	Association of Genetically Predicted Lipid Levels With the Extent of Coronary Atherosclerosis in Icelandic Adults.	JAMA Cardiol	2020
32327693	Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis.	Commun Biol	2020
32702746	Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease.	Eur Heart J	2020
30992453	A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy.	Nat Commun	2019
31641117	Sequence variants with large effects on cardiac electrophysiology and disease.	Nat Commun	2019
31865966	Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes.	J Am Coll Cardiol	2019
30476138	Sequence variants associating with urinary biomarkers.	Hum Mol Genet	2019
29590334	A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta.	Eur Heart J	2018
30271901	A rare missense variant in <i>NR1H4</i> associates with lower cholesterol levels.	Commun Biol	2018
30504769	Genome-wide association meta-analysis yields 20 loci associated with gallstone disease.	Nat Commun	2018
30354339	Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac Death.	Circ Genom Precis Med	2018
30349119	Insights into imprinting from parent-of-origin phased methylomes and transcriptomes.	Nat Genet	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
28250455	Diversity in non-repetitive human sequences not found in the reference genome.	Nat Genet	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
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
25882067	Common sequence variants associated with coronary artery disease correlate with the extent of coronary atherosclerosis.	Arterioscler Thromb Vasc Biol	2015
23535823	A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm.	Hum Mol Genet	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
22898070	Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism.	J Am Coll Cardiol	2012