Adalbjorg Jonasdottir

Reykjavik, Iceland

Last Updated: 09/26/2026

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Found 36 publications

Actionable Genotypes and Their Association with Life Span in Iceland.

Actionable Genotypes and Their Association with Life Span in Iceland.

Journal: The New England journal of medicine

Published: November 08, 2023

Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura.

Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura.

Journal: Nature genetics

Published: December 02, 2022

A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndrome.

A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndrome.

Journal: European journal of human genetics : EJHG

Published: September 20, 2022

Genetic architecture of band neutrophil fraction in Iceland.

Genetic architecture of band neutrophil fraction in Iceland.

Journal: Communications biology

Published: October 10, 2021

Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene.

Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene.

Journal: Nature communications

Published: August 25, 2021

Sequence variants in malignant hyperthermia genes in Iceland: classification and actionable findings in a population database.

Sequence variants in malignant hyperthermia genes in Iceland: classification and actionable findings in a population database.

Journal: European journal of human genetics : EJHG

Published: January 26, 2021

The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis.

The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis.

Journal: Communications biology

Published: August 06, 2020

Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits.

Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits.

Journal: Nature genetics

Published: November 18, 2019

Differences between germline genomes of monozygotic twins.

Differences between germline genomes of monozygotic twins.

Journal: Nature genetics

Published: October 07, 2019

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

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

Journal: Communications biology

Published: April 08, 2019

Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes.

Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes.

Journal: Journal of the American College of Cardiology

Published: December 20, 2018

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

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

Journal: Nature communications

Published: December 03, 2018

Showing 1-12 of 36

Last Updated: 09/26/2026