Author details

Full Name

Valgerdur Steinthorsdottir

Affiliation

ORCID

Career Start Year

1989

Papers

106

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36926036	Four missense genetic variants in <i>CUBN</i> are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans.	Front Endocrinol (Lausanne)	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
37414856	Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study.	Commun Med (Lond)	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
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
36747475	Genetic variants associated with syncope implicate neural and autonomic processes.	Eur Heart J	2023
37301908	Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.	Nat Commun	2023
35220425	Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes.	Hum Mol Genet	2022
36280732	Multiomics study of nonalcoholic fatty liver disease.	Nat Genet	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	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
34857953	Large-scale integration of the plasma proteome with genetics and disease.	Nat Genet	2021
34282336	Distinction between the effects of parental and fetal genomes on fetal growth.	Nat Genet	2021
33602785	Loss-of-Function Variants in the Tumor-Suppressor Gene <i>PTPN14</i> Confer Increased Cancer Risk.	Cancer Res	2021
34407635	Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland.	Arterioscler Thromb Vasc Biol	2021
32702746	Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease.	Eur Heart J	2020
32184442	Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank.	Commun Biol	2020
30992453	A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy.	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
31160809	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2019
29273807	Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
30297969	Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.	Nat Genet	2018
30194396	Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.	Nat Commun	2018
29899519	Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.	Nat Commun	2018
29549330	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29511194	Genome-wide analysis yields new loci associating with aortic valve stenosis.	Nat Commun	2018
29549329	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29632382	Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.	Nat Genet	2018
28146470	Rare and low-frequency coding variants alter human adult height.	Nature	2017
28900119	Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry.	Sci Rep	2017
28628106	Variants in the fetal genome near FLT1 are associated with risk of preeclampsia.	Nat Genet	2017
28537267	Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism.	Nat Commun	2017
28783164	Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritability.	Nat Genet	2017
28566273	An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.	Diabetes	2017
27876822	A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape.	Nat Commun	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
27355579	Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.	PLoS Genet	2016
27453397	Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis.	Nat Commun	2016
26327206	A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease.	PLoS Genet	2015
25673413	Genetic studies of body mass index yield new insights for obesity biology.	Nature	2015
25673412	New genetic loci link adipose and insulin biology to body fat distribution.	Nature	2015
25605810	Association analysis of 29,956 individuals confirms that a low-frequency variant at CCND2 halves the risk of type 2 diabetes by enhancing insulin secretion.	Diabetes	2015
25961943	The impact of low-frequency and rare variants on lipid levels.	Nat Genet	2015
26132169	Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation.	PLoS Genet	2015
26551672	Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.	Nat Genet	2015
26426971	The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.	PLoS Genet	2015