| Dysregulated m6A modification promotes lipogenesis and development of non-alcoholic fatty liver disease and hepatocellular carcinoma Y Yang, J Cai, X Yang, K Wang, K Sun, Z Yang, L Zhang, L Yang, C Gu, ... Molecular Therapy 30 (6), 2342-2353, 2022 | 91 | 2022 |
| Catenin α 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/β-catenin signaling X Zhu, M Yang, P Zhao, S Li, L Zhang, L Huang, Y Huang, P Fei, Y Yang, ... The Journal of clinical investigation 131 (6), 2021 | 53 | 2021 |
| Exome sequencing revealed Notch ligand JAG1 as a novel candidate gene for familial exudative vitreoretinopathy L Zhang, X Zhang, H Xu, L Huang, S Zhang, W Liu, Y Yang, P Fei, S Li, ... Genetics in Medicine 22 (1), 77-84, 2020 | 47 | 2020 |
| ER complex proteins are required for rhodopsin biosynthesis and photoreceptor survival in Drosophila and mice L Xiong, L Zhang, Y Yang, N Li, W Lai, F Wang, X Zhu, T Wang Cell Death & Differentiation 27 (2), 646-661, 2020 | 37 | 2020 |
| A splicing mutation in aryl hydrocarbon receptor associated with retinitis pigmentosa Y Zhou, S Li, L Huang, Y Yang, L Zhang, M Yang, W Liu, K Ramasamy, ... Human molecular genetics 27 (14), 2563-2572, 2018 | 31 | 2018 |
| Disruption of Tmem30a results in cerebellar ataxia and degeneration of Purkinje cells Y Yang, K Sun, W Liu, L Zhang, K Peng, S Zhang, S Li, M Yang, Z Jiang, ... Cell death & disease 9 (9), 899, 2018 | 28 | 2018 |
| Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosa L Zhang, Z Sun, P Zhao, L Huang, M Xu, Y Yang, X Chen, F Lu, X Zhang, ... Human molecular genetics 27 (23), 4157-4168, 2018 | 27 | 2018 |
| Tmem30a deficiency leads to retinal rod bipolar cell degeneration Y Yang, W Liu, K Sun, L Jiang, X Zhu Journal of neurochemistry 148 (3), 400-412, 2019 | 26 | 2019 |
| Loss of Tmem30a leads to photoreceptor degeneration L Zhang, Y Yang, S Li, S Zhang, X Zhu, Z Tai, MU Yang, Y Liu, X Guo, ... Scientific reports 7 (1), 9296, 2017 | 25 | 2017 |
| Hepatic Tmem30a deficiency causes intrahepatic cholestasis by impairing expression and localization of bile salt transporters L Liu, L Zhang, L Zhang, F Yang, X Zhu, Z Lu, Y Yang, H Lu, L Feng, ... The American Journal of Pathology 187 (12), 2775-2787, 2017 | 24 | 2017 |
| CTNND1 variants cause familial exudative vitreoretinopathy through the Wnt/cadherin axis M Yang, S Li, L Huang, R Zhao, E Dai, X Jiang, Y He, J Lu, L Peng, W Liu, ... JCI insight 7 (14), 2022 | 22 | 2022 |
| Variants in the Wnt co-receptor LRP6 are associated with familial exudative vitreoretinopathy. S Li, M Yang, Y He, X Jiang, R Zhao, W Liu, L Huang, Y Shi, X Li, K Sun, ... Journal of Genetics and Genomics= Yi Chuan xue bao 49 (6), 590-594, 2021 | 22 | 2021 |
| Tmem30a plays critical roles in ensuring the survival of hematopoietic cells and leukemia cells in mice N Li, Y Yang, C Liang, Q Qiu, C Pan, M Li, S Yang, L Chen, X Zhu, Y Hu The American Journal of Pathology 188 (6), 1457-1468, 2018 | 22 | 2018 |
| The phosphatidylserine flippase β-subunit Tmem30a is essential for normal insulin maturation and secretion Y Yang, K Sun, W Liu, X Li, W Tian, P Shuai, X Zhu Molecular Therapy 29 (9), 2854-2872, 2021 | 21 | 2021 |
| The ER membrane protein complex subunit Emc3 controls angiogenesis via the FZD4/WNT signaling axis M Yang, S Li, W Liu, X Li, Y He, Y Yang, K Sun, L Zhang, W Tian, L Duan, ... Science China Life Sciences 64 (11), 1868-1883, 2021 | 20 | 2021 |
| Deletion of the Impg2 gene causes the degeneration of rod and cone cells in mice H Xu, C Qu, L Gan, K Sun, J Tan, X Liu, Z Jiang, W Tian, W Liu, S Zhang, ... Human Molecular Genetics 29 (10), 1624-1634, 2020 | 19 | 2020 |
| TMEM30A deficiency in endothelial cells impairs cell proliferation and angiogenesis S Zhang, W Liu, Y Yang, K Sun, S Li, H Xu, M Yang, L Zhang, X Zhu Journal of Cell Science 132 (7), jcs225052, 2019 | 19 | 2019 |
| Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative Vitreoretinopathy L Zhang, Y Yang, S Li, Z Tai, L Huang, Y Liu, X Zhu, Y Di, C Qu, Z Jiang, ... Genetic Testing and Molecular Biomarkers 20 (7), 346-351, 2016 | 18 | 2016 |
| Loss of phosphatidylserine flippase β-subunit Tmem30a in podocytes leads to albuminuria and glomerulosclerosis W Liu, L Peng, W Tian, Y Li, P Zhang, K Sun, Y Yang, X Li, G Li, X Zhu Disease Models & Mechanisms 14 (6), dmm048777, 2021 | 14 | 2021 |
| Loss of Wtap results in cerebellar ataxia and degeneration of Purkinje cells Y Yang, G Huang, X Jiang, X Li, K Sun, Y Shi, Z Yang, X Zhu Journal of Genetics and Genomics 49 (9), 847-858, 2022 | 12 | 2022 |
