| Trio-based exome sequencing arrests de novo mutations in early-onset high myopia ZB Jin, J Wu, XF Huang, CY Feng, XB Cai, JY Mao, L Xiang, KC Wu, ... Proceedings of the National Academy of Sciences 114 (16), 4219-4224, 2017 | 89 | 2017 |
| An alternatively spliced heat shock transcription factor, OsHSFA2dI, functions in the heat stress‐induced unfolded protein response in rice Q Cheng, Y Zhou, Z Liu, L Zhang, G Song, Z Guo, W Wang, X Qu, Y Zhu, ... Plant Biology 17 (2), 419-429, 2015 | 88 | 2015 |
| OsPRR37 and Ghd7 are the major genes for general combining ability of DTH, PH and SPP in rice C Liu, G Song, Y Zhou, X Qu, Z Guo, Z Liu, D Jiang, D Yang Scientific reports 5 (1), 12803, 2015 | 50 | 2015 |
| Identification of de novo germline mutations and causal genes for sporadic diseases using trio‐based whole‐exome/genome sequencing ZB Jin, Z Li, Z Liu, Y Jiang, XB Cai, J Wu Biological Reviews 93 (2), 1014-1031, 2018 | 39 | 2018 |
| Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism Y Du, Z Li, Z Liu, N Zhang, R Wang, F Li, T Zhang, Y Jiang, X Zhi, Z Wang, ... Genetics in Medicine 22 (1), 170-180, 2020 | 34 | 2020 |
| Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathies Z Lin, Z Liu, X Li, F Li, Y Hu, B Chen, Z Wang, Y Liu Scientific Reports 7 (1), 258, 2017 | 28 | 2017 |
| Elevated CCL19/CCR7 Expression During the Disease Process of Primary Sjögren's Syndrome Z Liu, F Li, A Pan, H Xue, S Jiang, C Zhu, M Jin, J Fang, X Zhu, MA Brown, ... Frontiers in immunology 10, 795, 2019 | 26 | 2019 |
| Microbiota dysbiosis in primary Sjögren’s syndrome and the ameliorative effect of hydroxychloroquine X Wang, K Pang, J Wang, B Zhang, Z Liu, S Lu, X Xu, L Zhu, Z Zhou, ... Cell Reports 40 (11), 2022 | 25 | 2022 |
| Circular RNA sequencing indicates circ-IQGAP2 and circ-ZC3H6 as noninvasive biomarkers of primary Sjögren’s syndrome F Li, Z Liu, B Zhang, S Jiang, Q Wang, L Du, H Xue, Y Zhang, M Jin, X Zhu, ... Rheumatology 59 (9), 2603-2615, 2020 | 25 | 2020 |
| A SNP in OsMCA1 responding for a plant architecture defect by deactivation of bioactive GA in rice Z Liu, Q Cheng, Y Sun, H Dai, G Song, Z Guo, X Qu, D Jiang, C Liu, ... Plant molecular biology 87, 17-30, 2015 | 19 | 2015 |
| Integrative analyses of gene expression profile reveal potential crucial roles of mitotic cell cycle and microtubule cytoskeleton in pulmonary artery hypertension J Luo, H Li, Z Liu, C Li, R Wang, J Fang, S Lu, J Guo, X Zhu, X Wang BMC Medical Genomics 13, 1-14, 2020 | 18 | 2020 |
| mirDNMR: a gene-centered database of background de novo mutation rates in human Y Jiang, Z Li, Z Liu, D Chen, W Wu, Y Du, L Ji, ZB Jin, W Li, J Wu Nucleic Acids Research, gkw1044, 2016 | 18 | 2016 |
| Different experiences of two PRRT2-associated self-limited familial infantile epilepsy Q Zhao, Z Liu, Y Hu, S Fang, F Zheng, X Li, F Li, Z Lin Acta Neurologica Belgica 120, 1025-1028, 2020 | 16 | 2020 |
| Prioritized high-confidence risk genes for intellectual disability reveal molecular convergence during brain development Z Liu, N Zhang, Y Zhang, Y Du, T Zhang, Z Li, J Wu, X Wang Frontiers in Genetics 9, 349, 2018 | 14 | 2018 |
| De Novo Germline Mutations in SEMA5A Associated With Infantile Spasms Q Wang, Z Liu, Z Lin, R Zhang, Y Lu, W Su, F Li, X Xu, M Tu, Y Lou, ... Frontiers in Genetics 10, 605, 2019 | 11 | 2019 |
| A de novo pathogenic CSNK1E mutation identified by exome sequencing in family trios with epileptic encephalopathy X Chen, J Jin, Q Wang, H Xue, N Zhang, Y Du, T Zhang, B Zhang, J Wu, ... Human Mutation 40 (3), 281-287, 2019 | 8 | 2019 |
| PRRT2 variants and effectiveness of various antiepileptic drugs in self-limited familial infantile epilepsy Q Zhao, Y Hu, Z Liu, S Fang, F Zheng, X Wang, F Li, X Li, Z Lin Seizure 91, 360-368, 2021 | 7 | 2021 |
| Whole Exome Sequencing Identified a Novel Biallelic SMARCAL1 Mutation in the Extremely Rare Disease SIOD J Jin, K Wu, Z Liu, X Chen, S Jiang, Z Wang, W Li Frontiers in Genetics 10, 565, 2019 | 7 | 2019 |
| Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome Sequencing Z Liu, Z Li, X Zhi, Y Du, Z Lin, J Wu Molecular Neurobiology 55, 2483-2493, 2018 | 7 | 2018 |
| The OsSec18 complex interacts with P0(P1-P2)2 to regulate vacuolar morphology in rice endosperm cell Y Sun, T Ning, Z Liu, J Pang, D Jiang, Z Guo, G Song, D Yang BMC plant biology 15, 1-9, 2015 | 7 | 2015 |
