Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

E. Ferkingstad · SciRah

Researcher profile · Semantic Scholar

E. Ferkingstad

Share profile

E. Ferkingstad — researcher profile on SciRah

h-index: 21
Works: 41
Citations: 3,377

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
Large-scale plasma proteomics comparisons through genetics and disease associations
Grimur Hjorleifsson Eldjarn, E. Ferkingstad, S. Lund, H. Helgason +29 more
2023Nature506 citations Open access
Semantic Scholar
Multiomics study of nonalcoholic fatty liver disease
G. Sveinbjornsson, M. Ulfarsson, Rosa B. Thorolfsdottir, B. A. Jónsson +42 more
2022Nature Genetics207 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 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
Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.
H. Helgason, Thjodbjorg Eiriksdottir, M. Ulfarsson, A. Choudhary +31 more
2023Journal of the American Medical Association (JAMA)100 citations Open access
Semantic Scholar
Genome-wide association meta-analysis yields 20 loci associated with gallstone disease
E. Ferkingstad, A. Oddsson, S. Gretarsdottir, Stefania Benonisdottir +28 more
2018Nature Communications92 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
Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset
S. Saevarsdottir, L. Stefánsdóttir, P. Sulem, G. Thorleifsson +74 more
2022Annals of the Rheumatic Diseases80 citations Open access
Semantic Scholar
Dynamic path analysis—a new approach to analyzing time-dependent covariates
J. Fosen, E. Ferkingstad, Ø. Borgan, O. Aalen
2006Lifetime Data Analysis69 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
Cluster Headache Genomewide Association Study and Meta‐Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor
B. Winsvold, A. V. Harder, C. Ran, M. A. Chalmer +89 more
2023Annals of Neurology59 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
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
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology
G. Bjornsdottir, L. Stefánsdóttir, G. Thorleifsson, P. Sulem +42 more
2022Nature Communications48 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
Predicting the probability of death using proteomics
Thjodbjorg Eiriksdottir, Steinthor Ardal, B. A. Jónsson, S. Lund +15 more
2021Communications Biology29 citations Open access
Semantic Scholar
Deciphering the genetics and mechanisms of predisposition to multiple myeloma
M. Went, Laura Duran-Lozano, G. Halldorsson, A. Gunnell +46 more
2024Nature Communications22 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
A genome-wide association meta-analysis links hidradenitis suppurativa to common and rare sequence variants causing disruption of the Notch and Wnt/β-catenin signaling pathways.
R. Andersen, L. Stefánsdóttir, P. Riis, Gh Halldorsson +39 more
2024Journal of American Academy of Dermatology21 citations Open access
Semantic Scholar
Complex effects of sequence variants on lipid levels and coronary artery disease.
Audunn S. Snaebjarnarson, A. Helgadóttir, G. Arnadottir, Erna V. Ivarsdottir +29 more
2023Cell21 citations Open access
Semantic Scholar
Sequence variants affecting voice pitch in humans
Rosa S. Gisladottir, Agnar Helgason, B. Halldórsson, H. Helgason +29 more
2023Science Advances19 citations Open access
Semantic Scholar
A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome
A. Skuladóttir, G. Bjornsdottir, E. Ferkingstad, G. Einarsson +45 more
2022Nature Communications19 citations Open access
Semantic Scholar
Genetic variants associated with syncope implicate neural and autonomic processes.
Hildur M. Aegisdottir, Rosa B. Thorolfsdottir, G. Sveinbjornsson, O. Stefansson +41 more
2023European Heart Journal16 citations Open access
Semantic Scholar
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
A. Oddsson, P. Sulem, G. Sveinbjornsson, G. Arnadottir +76 more
2023Nature Communications15 citations Open access
Semantic Scholar
Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease
S. Saevarsdottir, Kristbjorg Bjarnadottir, Thorsteinn Markusson, J. Berglund +37 more
2024Nature Communications14 citations Open access
Semantic Scholar
Author Correction: Large-scale plasma proteomics comparisons through genetics and disease associations
Grimur Hjorleifsson Eldjarn, E. Ferkingstad, S. Lund, H. Helgason +29 more
2024Nature10 citations Open access
Semantic Scholar
Novel loci and biomedical consequences of iron homoeostasis variation
E. Allara, Steven Bell, Rebecca F Smith, S. Keene +68 more
2024Communications Biology9 citations Open access
Semantic Scholar
Thirty novel sequence variants impacting human intracranial volume
M. S. Nawaz, G. Einarsson, Mariana Bustamante, Rosa S. Gisladottir +23 more
2022Brain Communications6 citations Open access
Semantic Scholar
Uncovering drug targets for cluster headache through proteome-wide Mendelian randomization analysis
Zhong-Hua Xiong, Zhi Guo, Lei Zhao, Dong Qiu +61 more
2025The Journal of Headache and Pain5 citations Open access
Semantic Scholar
Genome-Wide Association Study of Accessory Atrioventricular Pathways.
Hildur M. Aegisdottir, L. Andreasen, Rosa B. Thorolfsdottir, G. Sveinbjornsson +39 more
2024JAMA cardiology4 citations Open access
Semantic Scholar
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria
Ragnar P. Kristjansson, Gudjon R. Oskarsson, A. Skuladóttir, A. Oddsson +33 more
2023Communications Biology4 citations Open access
Semantic Scholar
Large-scale comparison of immunoassay- and aptamer-based plasma proteomics through genetics and disease
Grimur Hjorleifsson Eldjarn, E. Ferkingstad, S. Lund, H. Helgason +28 more
2022bioRxiv2 citations Open access
Semantic Scholar
Genetic architecture of band neutrophil fraction in Iceland
Gudjon R. Oskarsson, M. K. Magnusson, A. Oddsson, B. Jensson +30 more
2022Communications Biology2 citations Open access
Semantic Scholar
Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology
G. Bjornsdottir, L. Stefánsdóttir, G. Thorleifsson, P. Sulem +42 more
2022Nature Communications2 citations Open access
Semantic Scholar
GWAS of amiodarone-induced thyroid dysfunction: Applications for genotype-guided risk stratification
S. Rand, J. Bundgaard, V. Tragante, S. Rognvaldsson +33 more
2026medRxiv0 citations
Semantic Scholar
Resistant hypertension variants link to hyperaldosteronism and potassium levels
V. Tragante, P. Sulem, G. Thorleifsson, M. Frigge +42 more
2026HYPERTENSION0 citations Open access
Semantic Scholar
Observational and Mendelian randomization studies of plasma sclerostin levels do not provide evidence of cardiovascular adverse effects of sclerostin inhibition.
Rosa B. Thorolfsdottir, G. Sveinbjornsson, Grimur Hjorleifsson Eldjarn, Hildur M. Aegisdottir +36 more
2025Human Molecular Genetics0 citations
Semantic Scholar
Correction: Uncovering drug targets for cluster headache through proteome-wide Mendelian randomization analysis
Zhong-Hua Xiong, Zhi Guo, Lei Zhao, Dong Qiu +101 more
2025The Journal of Headache and Pain0 citations Open access
Semantic Scholar
Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
A. Oddsson, P. Sulem, G. Sveinbjornsson, G. Arnadottir +76 more
2023Nature Communications0 citations Open access
Semantic Scholar
A genome-wide meta-analysis identifies 53 sequence variants associating with carpal tunnel syndrome
A. Skuladóttir, G. Bjornsdottir, E. Ferkingstad, G. Einarsson +26 more
20220 citations Open access
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

D. Gudbjartsson×39
Invite
D. Gudbjartsson — researcher profile on SciRah
K. Stefánsson×39
Invite
K. Stefánsson — researcher profile on SciRah
P. Sulem×34
Invite
P. Sulem — researcher profile on SciRah
U. Thorsteinsdóttir×29
Invite
U. Thorsteinsdóttir — researcher profile on SciRah

I. Jónsdóttir

×27

Invite

I. Jónsdóttir — researcher profile on SciRah

Invite

H. Hólm — researcher profile on SciRah

G. Thorleifsson×26

Invite

G. Thorleifsson — researcher profile on SciRah

G. Halldorsson×24

Invite

G. Halldorsson — researcher profile on SciRah

H. Stefánsson×23

Invite

H. Stefánsson — researcher profile on SciRah

C. Erikstrup×23

Invite

C. Erikstrup — researcher profile on SciRah

G. Sveinbjornsson×22

Invite

G. Sveinbjornsson — researcher profile on SciRah

Invite

A. Oddsson — researcher profile on SciRah