Last Updated: 09/26/2026
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Found 142 publications
Integrating multi-ancestry common and rare variant mapping accelerates therapeutic target discovery.
Integrating multi-ancestry common and rare variant mapping accelerates therapeutic target discovery.
Journal: medRxiv : the preprint server for health sciences
Published: July 17, 2026
Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMed.
Journal: Science (New York, N.Y.)
Published: July 16, 2026
A Common CD36 Variant and the Genetic Landscape of Dilated Cardiomyopathy in Individuals of African Ancestry.
Journal: medRxiv : the preprint server for health sciences
Published: June 05, 2026
GWAS Meta-analysis Identifies Novel Associated Loci and Points to Causal Tissues in Central Serous Chorioretinopathy.
Journal: medRxiv : the preprint server for health sciences
Published: June 04, 2026
Whole genome sequencing analysis of over 3500 individuals dementia-free over 85 years old.
Journal: Journal of Alzheimer's disease : JAD
Published: April 23, 2026
Genetically Mediated Differences in LDL Cholesterol and Risk of Venous Thromboembolism.
Journal: Journal of the American College of Cardiology
Published: April 06, 2026
Proton-activated chloride channel 1 is essential for innate host defense against bacterial sepsis.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 06, 2026
The Impact of Structural Variation on Alzheimer's Disease in the Alzheimer's Disease Sequencing Project.
Journal: Research square
Published: February 06, 2026
Proton-Activated Chloride Channel 1 (PACC1) is essential for innate host defense against bacterial sepsis.
Journal: bioRxiv : the preprint server for biology
Published: January 09, 2026
Physical Activity and Cardiovascular Outcomes in Phenotype-Negative Cardiomyopathy Variant Carriers.
Physical Activity and Cardiovascular Outcomes in Phenotype-Negative Cardiomyopathy Variant Carriers.
Journal: JAMA cardiology
Published: November 08, 2025
Last Updated: 09/26/2026