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| Submitted by | Title | Working Group(s) | Name and Date of Professional Meeting | POST DATE |
|---|---|---|---|---|
| Laurie, Cecelia | Genetic association study of venous thromboembolism based on whole-genome sequencing in the Trans-Omics for Precision Medicine (TOPMed) program | Venous Thromboembolism | ASHG 2018 (October 16-20, 2018) | |
| Manichaikul, Ani | Whole Genome Sequence Analysis of Pulmonary Function and COPD in >16,000 Multi-ethnic Participants of the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program Identifies New Associated Loci | Chronic Obstructive Pulmonary Disease, Lung, PFT Lung Population Cohorts | American Society of Human Genetics (October 16-20, 2018) | |
| Manichaikul, Ani | Whole Genome Sequence Analysis of Pulmonary Function and COPD in >16,000 Multi-ethnic Participants of the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program Identifies New Associated Loci | Chronic Obstructive Pulmonary Disease, Lung, PFT Lung Population Cohorts | American Society of Human Genetics (October 16-20, 2018) | |
| He, Karen | Linkage evidence and TOPMed whole genome sequencing identify multiple genes on chromosome 1 with rare variants associated with blood pressure | Blood Pressure | ASHG (October, 2018) | |
| Brody, Jennifer | Whole-Genome Sequence Analysis of Body Mass Index in the Trans-Omics for Precision Medicine (TOPMed) Program | Anthropometry - Adiposity (includes Physical Activity) | ASHG (October 2018) | |
| Peloso, Gina | Monogenic and polygenic predictors of plasma lipid extremes from whole genome sequencing in diverse ancestries: The NHLBI TOPMed program | Lipids | ASHG (October 2018) | |
| Hu, Yao | Whole genome sequencing association analysis of red blood cell traits in a multi-ethnic population sample from the Trans-Omics for Precision Medicine (TOPMed) Project | Hematology and Hemostasis | October 17, 2018 | |
| Natarajan, Pradeep | Whole genome sequence association with plasma lipids in 28,541 individuals | Lipids | American Heart Association Scientific Sessions (November 10-12, 2018) | |
| Gagliano, Sarah | Analysis of densely imputed UK Biobank genetic data reveals disease-associated rare loss of function variation | Population Genetics | ASHG Annual Meeting (October 2018) | |
| Perry, James | An Omics Analysis, Search and Information System (OASIS) for Enabling Discovery in the TOPMed Diabetes Working Group | Diabetes | ASHG Conference (October 2018) |
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