| Genomic analyses implicate noncoding de novo variants in congenital heart disease F Richter, SU Morton, SW Kim, A Kitaygorodsky, LK Wasson, KM Chen, ... Nature genetics 52 (8), 769-777, 2020 | 113 | 2020 |
| Large-scale analysis of branchpoint usage across species and cell lines AJ Taggart, CL Lin, B Shrestha, C Heintzelman, S Kim, WG Fairbrother Genome research 27 (4), 639-649, 2017 | 109 | 2017 |
| Widespread intra-dependencies in the removal of introns from human transcripts SW Kim, AJ Taggart, C Heintzelman, KJ Cygan, CG Hull, J Wang, ... Nucleic Acids Research 45 (16), 9503-9513, 2017 | 48 | 2017 |
| GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm A Sharma, LK Wasson, JAL Willcox, SU Morton, JM Gorham, ... Elife 9, e53278, 2020 | 41 | 2020 |
| An ancient founder mutation located between ROBO1 and ROBO2 is responsible for increased microtia risk in Amerindigenous populations D Quiat, SW Kim, Q Zhang, SU Morton, AC Pereira, SR DePalma, ... Proceedings of the National Academy of Sciences 119 (21), e2203928119, 2022 | 5 | 2022 |
| Functional dissection of human cardiac enhancers and noncoding de novo variants in congenital heart disease F Xiao, X Zhang, SU Morton, SW Kim, Y Fan, JM Gorham, H Zhang, ... Nature Genetics, 1-11, 2024 | 1 | 2024 |
| Multiplexed Single‐Nucleus RNA Sequencing Using Lipid‐Oligo Barcodes Q Zhang, SW Kim, JM Gorham, DM DeLaughter, T Ward, CE Seidman, ... Current protocols 2 (10), e579, 2022 | 1 | 2022 |
| The unusual gene architecture of polyubiquitin is created by dual-specific splice sites C Duan, T Mooney, L Buerer, C Bowers, S Rong, SW Kim, AM Fredericks, ... Genome Biology 25 (1), 33, 2024 | | 2024 |
