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| Submitted by | Title | Working Group(s) | Name and Date of Professional Meeting | POST DATE |
|---|---|---|---|---|
| Liu, Dajiang | Near-optimal trans-ethnic association and fine mapping of smoking associated genes integrating GWAS and TOPMed sequence data of 1.3 million individuals | Smoking | the American Society of Human Genetics annual meeting | |
| Reiner, Alex | Prospective Association of TET2 Mediated Clonal Hematopoiesis and Heart Failure and tis subtypes in Post Menopausal Women | Heart Failure - Cardiac Function - Morphology, Hematology and Hemostasis | AHA Epi Council March 6, 2020 | |
| Hsu, Yi-Hsiang | A large-scale whole genome sequencing to identify less common and rare variants associated with osteoporosis and fracture: The NHLBI TopMed Study | Bone Mineralization | American Society of Human Genetics (October 2019) | |
| Minster, Ryan L | Identification of susceptibility loci for reproductive traits in Samoan women | Reproductive Health | ASHG (Oct 18, 2019) | |
| Minster, Ryan L | A novel variant in CETP is associated with higher HDL-cholesterol in people of Polynesian ancestry | Lipids | ASHG (Oct 16, 2019) | |
| Jaiswal, Sidd | Clonal hematopoiesis of indeterminate potential and epigenetic age acceleration | Atherosclerosis - Clinical and Subclinical, Epigenetics, Hematology and Hemostasis, Longevity and Healthy Aging | ASHG Conference October 14-19, 2019 | |
| Manning, Alisa | Understanding the genetic basis of type 2 diabetes risk: whole genome sequence analysis of glycemic traits from the NHBLI’s TOPMed Program | Diabetes | American Society of Human Genetics Conference (October 18, 2019) | |
| Manning, Alisa | Understanding the genetic basis of type 2 diabetes risk: whole genome sequence analysis of glycemic traits from the NHBLI’s TOPMed Program | Diabetes | American Society of Human Genetics Conference (October 18, 2019) | |
| Russell, Emily | Evidence of natural selection in Samoans is associated with BMI and the immune system | Population Genetics | ASHG Conference (October 18, 2019) | |
| Zhu, Xiaofeng | Targeted genome sequencing identifies multiple rare variants in Caveolin-1 (CAV1) associated with obstructive sleep apnea trait | Sleep Traits | ASHG 2019 |
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