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Publications
| Submitting Author | Title | Journal Name | Publication Date Sort ascending | PMID | Associated proposal ID(s) |
|---|---|---|---|---|---|
| Willer, Cristen | Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease | Nature Communications | 33339817 | 6213 | |
| O'Connor, Tim | De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population | Proceedings of the National Academy of Sciences of the United States of America | 31964835 | 6274 | |
| O'Connor, Tim | Evolutionary History of Modern Samoans | Proceedings of the National Academy of Sciences | 32291332 | 5164 | |
| Quick, Corbin | Sequencing and Imputation in GWAS: Cost-Effective Strategies to Increase Power and Genomic Coverage Across Diverse Populations | Genetic Epidemiology | 32519380 | 1205 | |
| Browning, Brian | Estimating the Genome-wide Mutation Rate with Three-Way Identity by Descent | American Journal of Human Genetics | 31587867 | ||
| Khera, Amit | Rare Genetic Variants Associated With Sudden Cardiac Death in Adults | Journal of the American College of Cardiology | 31727422 | 2568 | |
| Cho, Michael | A flexible and nearly optimal sequential testing approach to randomized testing: QUICK-STOP. | Genetic Epidemiology | 31713269 | ||
| Geng, Xin | An Exome-Wide Sequencing Study of the GOLDN Cohort Reveals Novel Associations of Coding Variants and Fasting Plasma Lipids. | Frontiers in Genetics | 30863429 | 2275 | |
| Khera, Amit V. | Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction. | Circulation | 30586733 | 1440 | |
| Auer, Paul | Allelic heterogeneity at the CRP locus identified by whole-genome sequencing in multi-ancestry cohorts | American Journal of Human Genetics | 31883642 | 6684 |
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