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Pidong Li
Pidong Li
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在 nwafu.edu.cn 的电子邮件经过验证
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引用次数
年份
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
36992014
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
1112020
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
1082019
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
932021
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
632020
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
402022
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
242014
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
232021
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
232020
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
132016
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
92023
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
72021
Systematic effects of mRNA secondary structure on gene expression and molecular function in budding yeast
X Wang, P Li, RN Gutenkunst
BioRxiv, 138792, 2017
52017
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
42023
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
32020
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
22021
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
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