List of works - Solveig Gretarsdottir

A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease

scientific article published on September 2015

A drastic reduction in the life span of cystatin C L68Q carriers due to life-style changes during the last two centuries

scientific article

A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation

scientific article

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

scientific article

A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm

scientific article published on 27 March 2013

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

scientific article

ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma

scientific article

Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1

scientific article

Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism

scientific article published in August 2012

Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.

scientific article published in July 2017

European bone mineral density loci are also associated with BMD in East-Asian populations

scientific article (publication date: 7 October 2010)

Genes contributing to risk for common forms of stroke

scientific article

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies

scientific article published on 5 October 2012

Genetic variation at 16q24.2 is associated with small vessel stroke

scientific article

Genome-wide analysis yields new loci associating with aortic valve stenosis

scientific article published on 7 March 2018

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

scientific journal article

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

scientific article

Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity

scientific article

Ischemic stroke is associated with the ABO locus: the EuroCLOT study

scientific article published on January 2013

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

scientific article

Large-scale whole-genome sequencing of the Icelandic population

scientific article

Localization of a susceptibility gene for common forms of stroke to 5q12

scientific article

Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci ⬇️

scientific article

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

scientific article published on 12 March 2018

Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

scientific article published in 2022

New common variants affecting susceptibility to basal cell carcinoma

scientific article

New sequence variants associated with bone mineral density

scientific article

Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

scientific article published on 01 July 2019

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

scientific article

The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis

scientific article (publication date: 2013)

Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease

scientific article

Variants conferring risk of atrial fibrillation on chromosome 4q25.

scientific article

Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease

scientific article

Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis

scientific article published on 20 March 2017

List of works by Solveig Gretarsdottir

A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease

A drastic reduction in the life span of cystatin C L68Q carriers due to life-style changes during the last two centuries

A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma

Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1

Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism

Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.

European bone mineral density loci are also associated with BMD in East-Asian populations

Genes contributing to risk for common forms of stroke

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies

Genetic variation at 16q24.2 is associated with small vessel stroke

Genome-wide analysis yields new loci associating with aortic valve stenosis

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity

Ischemic stroke is associated with the ABO locus: the EuroCLOT study

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

Large-scale whole-genome sequencing of the Icelandic population

Localization of a susceptibility gene for common forms of stroke to 5q12

Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci ⬇️

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

New common variants affecting susceptibility to basal cell carcinoma

New sequence variants associated with bone mineral density

Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis

Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease

Variants conferring risk of atrial fibrillation on chromosome 4q25.

Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease

Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis