Kristjan S. Moore

Reykjavik, Iceland

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 23 publications

An Icelandic pangenome reference.

An Icelandic pangenome reference.

Journal: Nature

Published: March 12, 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

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

Missense variants in FRS3 affect body mass index in populations of diverse ancestries.

Missense variants in FRS3 affect body mass index in populations of diverse ancestries.

Journal: Nature communications

Published: May 22, 2024

Corroborating written history with ancient DNA: The case of the Well-man described in an Old Norse saga.

Corroborating written history with ancient DNA: The case of the Well-man described in an Old Norse saga.

Journal: iScience

Published: February 02, 2024

Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency.

Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency.

Journal: Nature genetics

Published: February 01, 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

The rate and nature of mitochondrial DNA mutations in human pedigrees.

The rate and nature of mitochondrial DNA mutations in human pedigrees.

Journal: Cell

Published: August 26, 2023

Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.

Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.

Journal: JAMA

Published: August 22, 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

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

Showing 1-12 of 23

Last Updated: 09/26/2026