Sigurjon A. Gudjonsson

Reykjavik, Iceland

Last Updated: 09/26/2026

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Found 62 publications

Sequence Diversity Lost in Early Pregnancy.

Sequence Diversity Lost in Early Pregnancy.

Journal: Obstetrical & gynecological survey
Published: November 25, 2025

A meta-analysis identifies driver genes and characterizes the molecular epidemiology of colorectal cancer.

A meta-analysis identifies driver genes and characterizes the molecular epidemiology of colorectal cancer.

Journal: Scientific reports
Published: October 02, 2025

Observational and Mendelian randomization studies of plasma sclerostin levels do not provide evidence of cardiovascular adverse effects of sclerostin inhibition.

Observational and Mendelian randomization studies of plasma sclerostin levels do not provide evidence of cardiovascular adverse effects of sclerostin inhibition.

Journal: Human molecular genetics
Published: March 10, 2025

African-ancestry-specific variant IKKβ p.Glu502Lys confers high lupus risk.

African-ancestry-specific variant IKKβ p.Glu502Lys confers high lupus risk.

Journal: Nature genetics
Published: August 17, 2024

Sequence diversity lost in early pregnancy.

Sequence diversity lost in early pregnancy.

Journal: Nature
Published: July 16, 2024

Complete human recombination maps.

Complete human recombination maps.

Journal: Nature
Published: June 06, 2024

Author Correction: Large-scale plasma proteomics comparisons through genetics and disease associations.

Author Correction: Large-scale plasma proteomics comparisons through genetics and disease associations.

Journal: Nature
Published: May 22, 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

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

Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease.

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

Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.

Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.

Journal: Nature communications
Published: July 03, 2023

Sequence variants affecting voice pitch in humans.

Sequence variants affecting voice pitch in humans.

Journal: Science advances
Published: June 09, 2023
Showing 1-12 of 62

Last Updated: 09/26/2026