List of works - Anna Helgadottir

A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy

scientific article published on 16 April 2019

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

scientific article published on 27 March 2013

Coding variants in and increase risk of atrial fibrillation

scientific article published on 12 June 2018

Diversity in non-repetitive human sequences not found in the reference genome

scientific article

Genes contributing to risk for common forms of stroke

scientific article

Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

scientific article published on 25 November 2020

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 variants associated with platelet count are predictive of human disease and physiological markers

scientific article published on 27 September 2021

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

scientific article published on 7 March 2018

Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

scientific article published on 09 January 2020

Genome-wide association meta-analysis yields 20 loci associated with gallstone disease

scientific article published in Nature Communications

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

Increased absorption of phytosterols is the simplest and most plausible explanation for coronary artery disease risk not accounted for by non-HDL cholesterol in high cholesterol absorbers

scientific article published on 09 November 2020

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

scientific article published on January 2013

Many sequence variants affecting diversity of adult human height

scientific article published in May 2008

Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis

scientific article published on 23 April 2020

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

scientific article

The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease

scientific article

Time course analysis of gene expression identifies multiple genes with differential expression in patients with in-stent restenosis ⬇️

scientific article published on February 28, 2011

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

List of works by Anna Helgadottir

A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy

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

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

Coding variants in and increase risk of atrial fibrillation

Diversity in non-repetitive human sequences not found in the reference genome

Genes contributing to risk for common forms of stroke

Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women

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

Genetic variants associated with platelet count are predictive of human disease and physiological markers

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

Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

Genome-wide association meta-analysis yields 20 loci associated with gallstone disease

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

Increased absorption of phytosterols is the simplest and most plausible explanation for coronary artery disease risk not accounted for by non-HDL cholesterol in high cholesterol absorbers

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

Many sequence variants affecting diversity of adult human height

Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease

Time course analysis of gene expression identifies multiple genes with differential expression in patients with in-stent restenosis ⬇️

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