Author details

Full Name

Daniel F Gudbjartsson

Affiliation

ORCID

Career Start Year

2000

Papers

286

H Index

102

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
38052102	Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity.	Hum Reprod	2024
38007706	Polygenic risk scores associate with blood pressure traits across the lifespan.	Eur J Prev Cardiol	2024
36658437	Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism.	Nat Genet	2023
36239377	Cartilage Acidic Protein 1 in Plasma Associates With Prevalent Osteoarthritis and Predicts Future Risk as Well as Progression to Joint Replacements: Results From the UK Biobank Resource.	Arthritis Rheumatol	2023
37606673	Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.	JAMA	2023
37753640	Combining Polygenic and Proteomic Risk Scores With Clinical Risk Factors to Improve Performance for Diagnosing Absence of Coronary Artery Disease in Patients With de novo Chest Pain.	Circ Genom Precis Med	2023
37937776	Actionable Genotypes and Their Association with Life Span in Iceland.	N Engl J Med	2023
37596405	Histopathology and levels of proteins in plasma associate with survival after colorectal cancer diagnosis.	Br J Cancer	2023
37932435	Genetics and epidemiology of mutational barcode-defined clonal hematopoiesis.	Nat Genet	2023
37794188	Large-scale plasma proteomics comparisons through genetics and disease associations.	Nature	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
37400429	Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.	Nat Commun	2023
37012456	Genetic effects on the timing of parturition and links to fetal birth weight.	Nat Genet	2023
37449562	Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland.	J Am Heart Assoc	2023
37386006	Sequence variants affecting the genome-wide rate of germline microsatellite mutations.	Nat Commun	2023
36747475	Genetic variants associated with syncope implicate neural and autonomic processes.	Eur Heart J	2023
37244984	DanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals.	BMC Genom Data	2023
36931692	Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect.	Ann Rheum Dis	2023
37430141	Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria.	Commun Biol	2023
37301908	Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.	Nat Commun	2023
37294764	Sequence variants affecting voice pitch in humans.	Sci Adv	2023
37038246	Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study.	Eur Heart J	2023
37503126	Understanding the genetic complexity of puberty timing across the allele frequency spectrum.	medRxiv	2023
37486023	Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor.	Ann Neurol	2023
35121750	Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene.	Nat Commun	2022
36171188	Effect of booster vaccination against Delta and Omicron SARS-CoV-2 variants in Iceland.	Nat Commun	2022
35650273	Genetic architecture of band neutrophil fraction in Iceland.	Commun Biol	2022
35697829	Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.	Commun Biol	2022
35751511	Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci.	Eur Heart J	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
35859178	The sequences of 150,119 genomes in the UK Biobank.	Nature	2022
35474271	GWAS of Hematuria.	Clin J Am Soc Nephrol	2022
35470158	Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset.	Ann Rheum Dis	2022
36415660	Thirty novel sequence variants impacting human intracranial volume.	Brain Commun	2022
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	2022
35182757	Reconstruction of a large-scale outbreak of SARS-CoV-2 infection in Iceland informs vaccination strategies.	Clin Microbiol Infect	2022
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
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
36070241	Cohort profile: Copenhagen Hospital Biobank - Cardiovascular Disease Cohort (CHB-CVDC): Construction of a large-scale genetic cohort to facilitate a better understanding of heart diseases.	BMJ Open	2021
33972781	Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits.	Nat Genet	2021
33707627	Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiency.	Eur J Hum Genet	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
34108613	The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis.	Commun Biol	2021
33727701	Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	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