Jing Peng

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 15

Top Topics

Acinetobacter Baumannii

Autism Spectrum Disorder

Top Venues

Annals of neurology

Molecular neurobiology

Italian journal of pediatrics

Molecular genetics & genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Donglei Liao, Saying Zhu, Lifen Yang, Ciliu Zhang, Fang He, Fei Yin, Jing Peng
Clinical characteristics and long-term outcome of CASPR2 antibody-associated autoimmune encephalitis in children. Italian journal of pediatrics 50 (1) (2024)
Changning Xie, Miriam Kessi, Fei Yin, Jing Peng
Roles of KCNA2 in Neurological Diseases: from Physiology to Pathology. Molecular neurobiology (2024)
Hailan He, Xiaoshuang Cao, Fang He, Wen Zhang, Xiaole Wang, Pan Peng, Changning Xie, Fei Yin, Dengfeng Li, Jia-Da Li, Minghui Wang, Malte Klüssendorf, Thomas J Jentsch, Tobias Stauber, Jing Peng
Mutations in CLCN6 as a Novel Genetic Cause of Neuronal Ceroid Lipofuscinosis in a Murine Model. Annals of neurology 96 (3) (2024)
Donglei Liao, Saying Zhu, Lifen Yang, Ciliu Zhang, Fang He, Fei Yin, Jing Peng
Clinical characteristics and long-term outcome of CASPR2 antibody-associated autoimmune encephalitis in children. Italian journal of pediatrics 50 (1) (2024)
Donglei Liao, Saying Zhu, Lifen Yang, Ciliu Zhang, Fang He, Fei Yin, Jing Peng
Clinical characteristics and long-term outcome of CASPR2 antibody-associated autoimmune encephalitis in children. Italian journal of pediatrics 50 (1) (2024)
Hailan He, Xiaoshuang Cao, Fang He, Wen Zhang, Xiaole Wang, Pan Peng, Changning Xie, Fei Yin, Dengfeng Li, Jia-Da Li, Minghui Wang, Malte Klüssendorf, Thomas J Jentsch, Tobias Stauber, Jing Peng
Mutations in CLCN6 as a Novel Genetic Cause of Neuronal Ceroid Lipofuscinosis in a Murine Model. Annals of neurology 96 (3) (2024)
Hailan He, Xiaoshuang Cao, Fang He, Wen Zhang, Xiaole Wang, Pan Peng, Changning Xie, Fei Yin, Dengfeng Li, Jia-Da Li, Minghui Wang, Malte Klüssendorf, Thomas J Jentsch, Tobias Stauber, Jing Peng
Mutations in CLCN6 as a Novel Genetic Cause of Neuronal Ceroid Lipofuscinosis. Annals of neurology (2024)
Tenghui Wu, Ciliu Zhang, Fang He, Li Yang, Fei Yin, Jing Peng
Large heterozygous deletion and uniparental disomy masquerading as homozygosity in CHKB gene. Molecular genetics & genomic medicine (2023)
Hailan He, Huiwen Zhang, Hui Chen, Fang He, Fei Yin, Tobias Stauber, Xiaomin Zou, Jing Peng
Functional analysis of two SLC9A6 frameshift variants in lymphoblastoid cells from patients with Christianson syndrome. CNS neuroscience & therapeutics (2023)
Zou Pan, Chen Chen, Fei Yin, Jing Peng
Genotypic and phenotypic spectra of NBEA-related neurodevelopmental disorder with epilepsy: a case series and literature review. World journal of pediatrics : WJP 18 (9) (2022)
Hui Xiao, Hailan He, Tenghui Wu, Xiaoyuan Ni, Fangyun Liu, Fei Yin, Jing Peng
Functional Investigation of TUBB4A Variants Associated with Different Clinical Phenotypes. Molecular neurobiology 59 (8) (2022)
Wen Zhang, Fanghua Ye, Juan Xiong, Fang He, Li Yang, Fei Yin, Jing Peng, Xiaole Wang
Silencing of miR-132-3p protects against neuronal injury following status epilepticus by inhibiting IL-1β-induced reactive astrocyte (A1) polarization. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 36 (10) (2022)
Hailan He, Xiaoshuang Cao, Fei Yin, Tenghui Wu, Tobias Stauber, Jing Peng
West Syndrome Caused By a Chloride/Proton Exchange-Uncoupling CLCN6 Mutation Related to Autophagic-Lysosomal Dysfunction. Molecular neurobiology 58 (6) (2021)
Hailan He, Raul E Guzman, Dezhi Cao, Juan Sierra-Marquez, Fei Yin, Christoph Fahlke, Jing Peng, Tobias Stauber
The molecular and phenotypic spectrum of CLCN4-related epilepsy. Epilepsia 62 (6) (2021)
Tenghui Wu, Fei Yin, Shiqi Guang, Fang He, Li Yang, Jing Peng
The Glycosylphosphatidylinositol biosynthesis pathway in human diseases. Orphanet journal of rare diseases 15 (1) (2020)