Doruk Beyter
Reykjavik, Iceland
Last Updated: 09/26/2026
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Found 23 publications
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
Variants at the Interleukin 1 Gene Locus and Pericarditis.
Journal: JAMA cardiology
Published: December 27, 2023
Gene-based burden tests of rare germline variants identify six cancer susceptibility genes.
Journal: Nature genetics
Published: August 15, 2023
A comparison of methods for detecting DNA methylation from long-read sequencing of human genomes.
Journal: Genome biology
Published: July 28, 2023
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
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.
Journal: Nature communications
Published: July 14, 2022
Sequence variants affecting the genome-wide rate of germline microsatellite mutations.
Journal: Nature communications
Published: June 10, 2022
The correlation between CpG methylation and gene expression is driven by sequence variants.
Journal: Nature genetics
Published: April 13, 2022
Last Updated: 09/26/2026