Pidong Li

发表

Drug-symptom networking: Linking drug-likeness screening to drug discovery.

Jianxin Chen, Xue Xu, Chao Zhang, 2016, Pharmacological research.

Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy.

Y. Liang, H. Lv, Wei Zhang, 2020, American journal of human genetics.

Single-cell RNA-seq analysis of mouse preimplantation embryos by third-generation sequencing

F. Tang, Lu Wen, Fan Liang, 2020, PLoS biology.

Long-read sequencing identified repeat expansions in the 5′UTR of the NOTCH2NLC gene from Chinese patients with neuronal intranuclear inclusion disease

Zhaoxia Wang, Yun Yuan, Yining Huang, 2019, Journal of Medical Genetics.

Identification and characterization of two DMD pedigrees with large inversion mutations based on a long-read sequencing pipeline.

Fan Liang, Pidong Li, Depeng Wang, 2022, European journal of human genetics : EJHG.

Noncarrier embryo selection and transfer in preimplantation genetic testing cycles for reciprocal translocation by Oxford Nanopore Technologies.

Pidong Li, Zijiang Chen, Yuan Gao, 2020, Journal of genetics and genomics = Yi chuan xue bao.

TCMSP: a database of systems pharmacology for drug discovery from herbal medicines

Wei Zhou, Peng Li, Ling Yang, 2014, Journal of Cheminformatics.

Amniotes co-opt intrinsic genetic instability to protect germ-line genome integrity

O. Gokcumen, Fan Liang, Ying Wang, 2023, Nature Communications.

Study of complex structural variations of X-linked deafness-2 based on single-molecule sequencing

Lihua Wu, Pidong Li, Guoliang Yu, 2021, Bioscience reports.

GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathy

H. Lv, Wei Zhang, Zhaoxia Wang, 2021, Annals of clinical and translational neurology.

Systematic effects of mRNA secondary structure on gene expression and molecular function in budding yeast

R. Gutenkunst, Pidong Li, Xia Wang, 2017, bioRxiv.

The GGC repeat expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy type 3

H. Lv, Wei Zhang, Zhaoxia Wang, 2021, Brain : a journal of neurology.

Rapid prenatal diagnosis of Facioscapulohumeral Muscular Dystrophy 1 by combined Bionano optical mapping and karyomapping

Fan Liang, X. Kong, Pidong Li, 2019, Prenatal diagnosis.

Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease

Wei Zhang, Zhaoxia Wang, Jing Liu, 2021, Journal of Medical Genetics.

Single-molecule optical mapping enables quantitative measurement of D4Z4 repeats in facioscapulohumeral muscular dystrophy (FSHD)

L. Cui, Fan Liang, Kai Wang, 2019, Journal of Medical Genetics.

Insights from systems pharmacology into cardiovascular drug discovery and therapy

Peng Li, Chao Huang, Ling Yang, 2014, BMC Systems Biology.

Single-molecule optical mapping enables accurate molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD)

L. Cui, Fan Liang, Kai Wang, 2018, bioRxiv.

Drug-symptom networking: Linking drug-likeness screening to drug discovery.

Jianxin Chen, Xue Xu, Chao Zhang, 2016, Pharmacological research.