TCMSP: a database of systems pharmacology for drug discovery from herbal medicines J Ru, P Li, J Wang, W Zhou, B Li, C Huang, P Li, Z Guo, W Tao, Y Yang, ... Journal of cheminformatics 6, 1-6, 2014 | 3699 | 2014 |
Expansion of GGC repeat in GIPC1 is associated with oculopharyngodistal myopathy J Deng, J Yu, P Li, X Luan, L Cao, J Zhao, M Yu, W Zhang, H Lv, Z Xie, ... The American Journal of Human Genetics 106 (6), 793-804, 2020 | 111 | 2020 |
Long-read sequencing identified repeat expansions in the 5′ UTR of the NOTCH2NLC gene from Chinese patients with neuronal intranuclear inclusion disease J Deng, M Gu, Y Miao, S Yao, M Zhu, P Fang, X Yu, P Li, Y Su, J Huang, ... Journal of medical genetics 56 (11), 758-764, 2019 | 108 | 2019 |
The GGC repeat expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy type 3 J Yu, J Deng, X Guo, J Shan, X Luan, L Cao, J Zhao, M Yu, W Zhang, H Lv, ... Brain 144 (6), 1819-1832, 2021 | 93 | 2021 |
Single-cell RNA-seq analysis of mouse preimplantation embryos by third-generation sequencing X Fan, D Tang, Y Liao, P Li, Y Zhang, M Wang, F Liang, X Wang, Y Gao, ... PLoS Biology 18 (12), e3001017, 2020 | 63 | 2020 |
Single-molecule optical mapping enables quantitative measurement of D4Z4 repeats in facioscapulohumeral muscular dystrophy (FSHD) KW Yi Dai, Pidong Li, Zhiqiang Wang, Fan Liang, Fan Yang, Li Fang, Yu Huang ... Journal of medical genetics, jmedgenet-2019-106268, 2019 | 62* | 2019 |
Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease J Deng, B Zhou, J Yu, X Han, J Fu, X Li, X Xie, M Zhu, Y Zheng, X Guo, ... Journal of medical genetics 59 (5), 462-469, 2022 | 40 | 2022 |
Insights from systems pharmacology into cardiovascular drug discovery and therapy P Li, Y Fu, J Ru, C Huang, J Du, C Zheng, X Chen, P Li, A Lu, L Yang, ... BMC systems biology 8, 1-13, 2014 | 24 | 2014 |
GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathy J Yu, X Luan, M Yu, W Zhang, H Lv, L Cao, L Meng, M Zhu, B Zhou, X Wu, ... Annals of Clinical and Translational Neurology 8 (6), 1330-1342, 2021 | 23 | 2021 |
Rapid prenatal diagnosis of Facioscapulohumeral Muscular Dystrophy 1 by combined Bionano optical mapping and karyomapping Y Zheng, L Kong, H Xu, Y Lu, X Zhao, Y Yang, G Yu, P Li, F Liang, H Jin, ... Prenatal Diagnosis 40 (3), 317-323, 2020 | 23 | 2020 |
Drug-symptom networking: Linking drug-likeness screening to drug discovery X Xu, C Zhang, PD Li, FL Zhang, K Gao, JX Chen, HC Shang Pharmacological research 103, 105-113, 2016 | 13 | 2016 |
Identification and characterization of two DMD pedigrees with large inversion mutations based on a long-read sequencing pipeline C Geng, C Zhang, P Li, Y Tong, B Zhu, J He, Y Zhao, F Yao, LY Cui, ... European Journal of Human Genetics 31 (5), 504-511, 2023 | 9 | 2023 |
Study of complex structural variations of X-linked deafness-2 based on single-molecule sequencing Y Jiang, L Wu, S Huang, P Li, B Gao, Y Yuan, S Zhang, G Yu, Y Gao, ... Bioscience Reports 41 (6), BSR20203740, 2021 | 7 | 2021 |
Systematic effects of mRNA secondary structure on gene expression and molecular function in budding yeast X Wang, P Li, RN Gutenkunst BioRxiv, 138792, 2017 | 5 | 2017 |
Amniotes co-opt intrinsic genetic instability to protect germ-line genome integrity YH Sun, H Cui, C Song, JT Shen, X Zhuo, RH Wang, X Yu, R Ndamba, ... Nature communications 14 (1), 812, 2023 | 4 | 2023 |
Noncarrier embryo selection and transfer in preimplantation genetic testing cycles for reciprocal translocation by Oxford Nanopore Technologies M Gao, L Wang, P Xu, H Xie, X Liu, S Huang, Y Zou, J Li, Y Wang, P Li, ... Journal of genetics and genomics= Yi chuan xue bao 47 (11), 718-721, 2020 | 3 | 2020 |
Expansion of 5’UTR CGG repeat in RILPL1 is associated with oculopharyngodistal myopathy X Yang, D Zhang, P Li, J Niu, D Xu, X Guo, Z Wang, Y Zhao, H Ren, ... medRxiv, 2021.09. 18.21263669, 2021 | 2 | 2021 |
A large pedigree study confirmed the CGG repeat expansion of RILPL1 Is associated with oculopharyngodistal myopathy X Yang, D Zhang, S Shen, P Li, M Li, J Niu, D Ma, D Xu, S Li, X Guo, ... BMC Medical Genomics 16 (1), 253, 2023 | | 2023 |
Detection of Complex Structural Variations of X-Linked Deafness-2 (DFNX2) by Single-Molecule Sequencing Y Jiang, S Huang, J Zha, B Gao, Y Yuan, L Wu, S Zhang, Y Liang, P Li, ... Available at SSRN 3464402, 2019 | | 2019 |