Last Updated: 09/26/2026
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Found 10 publications
Genealogy based trait association with LOCATER boosts power at loci with allelic heterogeneity.
Journal: medRxiv : the preprint server for health sciences
Published: November 26, 2025
Genealogy-based trait association with LOCATER boosts power at loci with allelic heterogeneity.
Journal: Genome research
Published: December 30, 2024
Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification.
Journal: Nature cardiovascular research
Published: May 31, 2024
Rare variant contribution to the heritability of coronary artery disease.
Journal: Nature communications
Published: February 07, 2024
Instrumental variable and colocalization analyses identify endotrophin and HTRA1 as potential therapeutic targets for coronary artery disease.
Journal: iScience
Published: October 10, 2023
Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci.
Journal: Nature communications
Published: August 13, 2021
Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences.
Journal: Human genomics
Published: March 23, 2021
Association of structural variation with cardiometabolic traits in Finns.
Journal: American journal of human genetics
Published: December 12, 2020
SVEP1 is a human coronary artery disease locus that promotes atherosclerosis.
Journal: Science translational medicine
Published: July 27, 2020
Capitalizing on Insights from Human Genetics to Identify Novel Therapeutic Targets for Coronary Artery Disease.
Journal: Annual review of medicine
Published: October 26, 2018
Showing 1-10 of 10
Last Updated: 09/26/2026