| Mapping transcriptomic vector fields of single cells X Qiu, Y Zhang, JD Martin-Rufino, C Weng, S Hosseinzadeh, D Yang, ... Cell 185 (4), 690-711. e45, 2022 | 195 | 2022 |
| Single-cell heterogeneity analysis and CRISPR screen identify key β-cell-specific disease genes Z Fang, C Weng, H Li, R Tao, W Mai, X Liu, L Lu, S Lai, Q Duan, C Alvarez, ... Cell reports 26 (11), 3132-3144. e7, 2019 | 101 | 2019 |
| Single-cell lineage analysis reveals extensive multimodal transcriptional control during directed beta-cell differentiation C Weng, J Xi, H Li, J Cui, A Gu, S Lai, K Leskov, L Ke, F Jin, Y Li Nature metabolism 2 (12), 1443-1458, 2020 | 44 | 2020 |
| Massively parallel base editing to map variant effects in human hematopoiesis JD Martin-Rufino, N Castano, M Pang, EI Grody, S Joubran, A Caulier, ... Cell 186 (11), 2456-2474. e24, 2023 | 35 | 2023 |
| Chemical screening identifies enhancers of mutant oligodendrocyte survival and unmasks a distinct pathological phase in Pelizaeus-Merzbacher disease MS Elitt, HE Shick, M Madhavan, KC Allan, BLL Clayton, C Weng, ... Stem Cell Reports 11 (3), 711-726, 2018 | 34 | 2018 |
| Binding interaction between a queen pheromone component HOB and pheromone binding protein ASP1 of Apis cerana C Weng, Y Fu, H Jiang, S Zhuang, H Li International journal of biological macromolecules 72, 430-436, 2015 | 31 | 2015 |
| Variant to function mapping at single-cell resolution through network propagation F Yu, LD Cato, C Weng, LA Liggett, S Jeon, K Xu, CWK Chiang, ... Nature Biotechnology 40 (11), 1644-1653, 2022 | 30 | 2022 |
| A de novo mosaic mutation of PHEX in a boy with hypophosphatemic rickets C Weng, J Chen, L Sun, ZW Zhou, X Feng, JH Sun, LP Lu, P Yu, M Qi Journal of human genetics 61 (3), 223-227, 2016 | 19 | 2016 |
| Identification of eight novel mutations and transcript analysis of two splicing mutations in Chinese newborns with MCC deficiency L Yang, J Yang, T Zhang, C Weng, F Hong, F Tong, R Yang, X Yin, P Yu, ... Clinical genetics 88 (5), 484-488, 2015 | 19 | 2015 |
| Inferring gene regulation from stochastic transcriptional variation across single cells at steady state A Gupta, JD Martin-Rufino, TR Jones, V Subramanian, X Qiu, EI Grody, ... Proceedings of the National Academy of Sciences 119 (34), e2207392119, 2022 | 18 | 2022 |
| Myt transcription factors prevent stress-response gene overactivation to enable postnatal pancreatic β cell proliferation, function, and survival R Hu, E Walker, C Huang, Y Xu, C Weng, GE Erickson, A Coldren, X Yang, ... Developmental cell 53 (4), 390-405. e10, 2020 | 13 | 2020 |
| Spateo: multidimensional spatiotemporal modeling of single-cell spatial transcriptomics X Qiu, DY Zhu, J Yao, Z Jing, L Zuo, M Wang, KH Min, H Pan, S Wang, ... BioRxiv, 2022.12. 07.519417, 2022 | 11 | 2022 |
| Deciphering cell states and genealogies of human hematopoiesis C Weng, F Yu, D Yang, M Poeschla, LA Liggett, MG Jones, X Qiu, ... Springer Science and Business Media LLC, 2024 | 10 | 2024 |
| TWO‐SIGMA: A novel two‐component single cell model‐based association method for single‐cell RNA‐seq data E Van Buren, M Hu, C Weng, F Jin, Y Li, D Wu, Y Li Genetic epidemiology 45 (2), 142-153, 2021 | 10 | 2021 |
| Two EDA gene mutations in chinese patients with hypohidrotic ectodermal dysplasia X Feng, C Weng, T Wei, J Sun, F Huang, P Yu, M Qi Journal of the European Academy of Dermatology and Venereology 32 (8), e324-e326, 2018 | 8 | 2018 |
| The R900S mutation in CACNA1S associated with hypokalemic periodic paralysis Q Ke, F He, L Lu, P Yu, Y Jiang, C Weng, H Huang, X Yi, M Qi Neuromuscular Disorders 25 (12), 955-958, 2015 | 7 | 2015 |
| Prokaryotic expression and ligand binding characteristics of pheromone binding protein ASP1 in the Chinese honeybee (Apis cerana cerana). C Weng, LY Zhang, L Zhao, YX Fu, C Luo, HL Li Acta Entomologica Sinica 56 (10), 1110-1116, 2013 | 7 | 2013 |
| Systematic investigation of mitochondrial transfer between cancer cells and T cells at single-cell resolution H Zhang, X Yu, J Ye, H Li, J Hu, Y Tan, Y Fang, E Akbay, F Yu, C Weng, ... Cancer Cell 41 (10), 1788-1802. e10, 2023 | 5 | 2023 |
| Single cell multiomic analysis reveals diabetes-associated β-cell heterogeneity driven by HNF1A C Weng, A Gu, S Zhang, L Lu, L Ke, P Gao, X Liu, Y Wang, P Hu, ... Nature Communications 14 (1), 5400, 2023 | 5 | 2023 |
| Identification and functional characterization of a hemizygous novel intronic variant in OCRL gene causes Lowe syndrome J Sun, Z Zhou, C Weng, C Wang, J Chen, X Feng, P Yu, M Qi Clinical and Experimental Nephrology 24, 657-665, 2020 | 1 | 2020 |
