Rare coding variant analysis for human diseases across biobanks and ancestries
Jurgens SJ, Wang X, Choi SH, Weng LC, Koyama S, Pirruccello JP, Nguyen T, Smadbeck P, Jang D, Chaffin M, Walsh R, Roselli C, Elliott AL, Wijdeveld LFJM, Biddinger KJ, Kany S, Rämö JT, Natarajan P, Aragam KG, Flannick J, Burtt NP, Bezzina CR, Lubitz SA, Lunetta KL, Ellinor PT. Nat Genet. 2024 Sep;56(9):1811-1820. doi: 10.1038/s41588-024-01894-5. Epub 2024 Aug 29. PMID: 39210047.