Author details

Full Name

Hilma Holm

Affiliation

ORCID

Career Start Year

2002

Papers

134

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
36269625	Genomic risk scores, biomolecules, and clinical conditions to predict atrial fibrillation: time to integrate what we can measure.	European Heart Journal	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
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
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
37400429	Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.	Nat Commun	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
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
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
37294764	Sequence variants affecting voice pitch in humans.	Sci Adv	2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
36658437	Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism.	Nat Genet	2023
35121750	Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene.	Nat Commun	2022
35859178	The sequences of 150,119 genomes in the UK Biobank.	Nature	2022
36415660	Thirty novel sequence variants impacting human intracranial volume.	Brain Commun	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
35121750	Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene.	Nat Commun	2022
34480422	The genomics of heart failure: design and rationale of the HERMES consortium.	ESC Heart Fail	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
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
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
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
34145379	Predicting the probability of death using proteomics.	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
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
34131116	Molecular benchmarks of a SARS-CoV-2 epidemic.	Nat Commun	2021
34131116	Molecular benchmarks of a SARS-CoV-2 epidemic.	Nat Commun	2021
34580418	Genetic variants associated with platelet count are predictive of human disease and physiological markers.	Commun Biol	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
34407635	Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland.	Arterioscler Thromb Vasc Biol	2021
34857953	Large-scale integration of the plasma proteome with genetics and disease.	Nat Genet	2021
34620984	A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo.	Commun Biol	2021
34480422	The genomics of heart failure: design and rationale of the HERMES consortium.	ESC Heart Fail	2021
32871063	Humoral Immune Response to SARS-CoV-2 in Iceland.	N Engl J Med	2020
31746962	Association of Genetically Predicted Lipid Levels With the Extent of Coronary Atherosclerosis in Icelandic Adults.	JAMA Cardiol	2020
32009622	[Lipoprotein(a) and risk of cardiovascular disease].	Laeknabladid	2020
32702746	Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease.	Eur Heart J	2020