Astros T. Skuladottir

Reykjavik, Iceland

Last Updated: 09/26/2026

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Found 26 publications

The genetic architecture of fibromyalgia across 2.5 million individuals.

The genetic architecture of fibromyalgia across 2.5 million individuals.

Journal: medRxiv : the preprint server for health sciences

Published: September 26, 2025

The genetic architecture of fibromyalgia across 2.5 million individuals.

The genetic architecture of fibromyalgia across 2.5 million individuals.

Journal: Nature medicine

Published: September 18, 2025

Genome-wide association study of borderline personality disorder identifies 11 loci and highlights shared risk with mental and somatic disorders.

Genome-wide association study of borderline personality disorder identifies 11 loci and highlights shared risk with mental and somatic disorders.

Journal: medRxiv : the preprint server for health sciences

Published: August 20, 2025

Variant in a Taste Receptor Locus Tied to Changes in the Use of Insomnia Medication.

Variant in a Taste Receptor Locus Tied to Changes in the Use of Insomnia Medication.

Journal: Biological psychiatry global open science

Published: August 19, 2025

An Icelandic pangenome reference.

An Icelandic pangenome reference.

Journal: Nature

Published: March 12, 2025

Genome-wide association analyses of borderline personality disorder identify 11 loci and highlight shared risk with mental and somatic disorders.

Genome-wide association analyses of borderline personality disorder identify 11 loci and highlight shared risk with mental and somatic disorders.

Journal: Nature genetics

Published: November 21, 2024

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy.

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy.

Journal: American journal of human genetics

Published: August 18, 2024

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy.

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy.

Journal: medRxiv : the preprint server for health sciences

Published: July 15, 2024

Homozygosity for R47H in TREM2 and the Risk of Alzheimer's Disease.

Homozygosity for R47H in TREM2 and the Risk of Alzheimer's Disease.

Journal: The New England journal of medicine

Published: June 20, 2024

Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease.

Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease.

Journal: NPJ Parkinson's disease

Published: January 29, 2024

Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder.

Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder.

Journal: Nature genetics

Published: January 18, 2024

GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis.

GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis.

Journal: Communications biology

Published: December 04, 2023

Showing 1-12 of 26

Last Updated: 09/26/2026