Author details

Full Name

Erna V Ivarsdottir

Affiliation

ORCID

Career Start Year

2017

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37294764	Sequence variants affecting voice pitch in humans.	Sci Adv	2023
37606673	Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.	JAMA	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
37430141	Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria.	Commun Biol	2023
35121750	Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene.	Nat Commun	2022
35650273	Genetic architecture of band neutrophil fraction in Iceland.	Commun Biol	2022
34620984	A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo.	Commun Biol	2021
36282123	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
33580673	Genetic insight into sick sinus syndrome.	Eur Heart J	2021
34108613	The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis.	Commun Biol	2021
34145379	Predicting the probability of death using proteomics.	Commun Biol	2021
33982893	The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large-Scale Proteomics Scan in Iceland.	Arthritis Rheumatol	2021
32581359	FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease.	Nature	2020
31959851	Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis.	Nat Commun	2020
32327693	Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis.	Commun Biol	2020
33035477	Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming.	Curr Biol	2020
32871063	Humoral Immune Response to SARS-CoV-2 in Iceland.	N Engl J Med	2020
30992453	A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy.	Nat Commun	2019
30476138	Sequence variants associating with urinary biomarkers.	Hum Mol Genet	2019
31053729	GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures.	Nat Commun	2019
30894546	Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density.	Nat Commun	2019
30271932	A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin.	Commun Biol	2018
30271950	Coding variants in <i>RPL3L</i> and <i>MYZAP</i> increase risk of atrial fibrillation.	Commun Biol	2018
30361506	A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease.	Nat Commun	2018
28783164	Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritability.	Nat Genet	2017