Gudmundur L. Norddahl
Reykjavik, Iceland
Last Updated: 09/26/2026
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Found 68 publications
Sequence Diversity Lost in Early Pregnancy.
Journal: Obstetrical & gynecological survey
Published: November 25, 2025
African-ancestry-specific variant IKKβ p.Glu502Lys confers high lupus risk.
Journal: Nature genetics
Published: August 17, 2024
Homozygosity for R47H in TREM2 and the Risk of Alzheimer's Disease.
Journal: The New England journal of medicine
Published: June 20, 2024
Missense variants in FRS3 affect body mass index in populations of diverse ancestries.
Journal: Nature communications
Published: May 22, 2024
A partial loss-of-function variant in STAT6 protects against type 2 asthma.
Journal: The Journal of allergy and clinical immunology
Published: February 29, 2024
A genome-wide association meta-analysis links hidradenitis suppurativa to common and rare sequence variants causing disruption of the Notch and Wnt/β-catenin signaling pathways.
Journal: Journal of the American Academy of Dermatology
Published: February 16, 2024
Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder.
Journal: Nature genetics
Published: January 18, 2024
Sequence variants influencing the regulation of serum IgG subclass levels.
Journal: Nature communications
Published: December 01, 2023
Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease.
Journal: Nature communications
Published: September 15, 2023
Last Updated: 09/26/2026