Arnor Vikingsson
Reykjavik, Iceland
Last Updated: 09/26/2026
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Found 19 publications
Congenital insensitivity to pain caused by a novel SCN9A-genotype
Journal: Laeknabladid
Published: May 27, 2026
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.
Journal: Nature medicine
Published: September 18, 2025
Missense variants in FRS3 affect body mass index in populations of diverse ancestries.
Journal: Nature communications
Published: May 22, 2024
Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.
Journal: Nature communications
Published: April 28, 2022
A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome.
Journal: Nature communications
Published: December 20, 2021
A meta-analysis uncovers the first sequence variant conferring risk of Bell's palsy.
Journal: Scientific reports
Published: August 13, 2020
A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy.
Journal: Nature communications
Published: December 03, 2018
Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood.
Journal: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
Published: September 25, 2018
Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation.
Journal: Nature communications
Published: May 31, 2016
Last Updated: 09/26/2026