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Distinct epigenomic patterns are associated with haploinsufficiency and predict risk genes of developmental disorders X Han, S Chen, E Flynn, S Wu, D Wintner, Y Shen Nature communications 9 (1), 2138, 2018 | 38 | 2018 |
Population-scale analysis of common and rare genetic variation associated with hearing loss in adults K Praveen, L Dobbyn, L Gurski, AH Ayer, J Staples, S Mishra, Y Bai, ... Communications biology 5 (1), 540, 2022 | 13 | 2022 |
A deep catalog of protein-coding variation in 985,830 individuals KY Sun, X Bai, S Chen, S Bao, M Kapoor, C Zhang, J Backman, T Joseph, ... bioRxiv, 2023 | 6 | 2023 |
Dissecting Autism Genetic Risk Using Single-cell RNA-seq Data YS Siying Chen, Xueya Zhou, Eve Byington, Samuel L Bruce, Haicang Zhang bioRxiv, 2020 | 4* | 2020 |
A deep catalogue of protein-coding variation in 983,578 individuals KY Sun, X Bai, S Chen, S Bao, C Zhang, M Kapoor, J Backman, T Joseph, ... Nature, 1-3, 2024 | | 2024 |
Integration of Functional Genomic Data in Genetic Analysis S Chen Columbia University, 2021 | | 2021 |