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| Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program Y Hu, AM Stilp, CP McHugh, S Rao, D Jain, X Zheng, J Lane, ... The American Journal of Human Genetics 108 (5), 874-893, 2021 | 46* | 2021 |
| Leveraging base-pair mammalian constraint to understand genetic variation and human disease PF Sullivan, JRS Meadows, S Gazal, BDN Phan, X Li, DP Genereux, ... Science 380 (6643), eabn2937, 2023 | 37 | 2023 |
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| TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data L Huang, JD Rosen, Q Sun, J Chen, MM Wheeler, Y Zhou, YI Min, ... The American Journal of Human Genetics 109 (6), 1175-1181, 2022 | 29 | 2022 |
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| Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patients Q Sun, W Liu, JD Rosen, L Huang, RG Pace, H Dang, PJ Gallins, EE Blue, ... Human Genetics and Genomics Advances 3 (2), 2022 | 15 | 2022 |
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