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Title Working Group(s) Name and Date of Professional Meeting POST DATE
Whole genome sequence analysis of long non-coding RNAs for plasma lipid traits Lipids CHARGE Seattle Conference (Oct 12-14, 2022)
Systematic Integration of Multi-omics Data for Coronary Artery Disease and Subclinical Atherosclerosis Atherosclerosis - Clinical and Subclinical ASHG Conference (Oct. 24-28, 2022) and CHARGE Seattle Conference (Oct. 13-14, 2022)
Rare protein-truncating DNA variants in APOB or PCSK9, low-density lipoprotein cholesterol, and risk of coronary artery disease Lipids ASHG Meeting (October 2022)
Whole Genome Sequencing Analyses of 87,652 Individuals Reveal Rare Variants in Promoter of HMGA1 Associated with Height Anthropometry - Adiposity (includes Physical Activity) American Society of Human Genetics Annual Meeting (October 25-29, 2022)
Somatic mutations in chronic lung disease are associated with reduced lung function Lung ASHG 10/26/2022
Whole genome sequence analysis of long non-coding RNAs for plasma lipid traits Lipids ASHG (October 27, 2022)
Cross-cohort eQTL fine-mapping utilizing TOPMed whole genome sequencing identifies tens of thousands of independent eQTLs signals and thousands of eQTLs colocalizing with complex trait-associated variants Multi-Omics ASHG 2022 Annual Meeting (Oct. 25 - 29, 2022)
A Cox proportional hazards whole genome sequencing study of ischemic stroke risk in a Brazilian sickle cell population ASHG Oct 25-29, 2022
Whole Genome Sequencing Analyses of 45,090 Individuals Reveal Rare Coding and Noncoding Variants Associated with Kidney Function Kidney Function ASHG 2022 (Oct 25-Oct 29)
Predicted nasal epithelial transcriptome-wide association study in African-ancestry populations Asthma ASHG October 2022
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