Professor | Hongfeng Zhang | Asia Growth Partners

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Name	Hongfeng Zhang
Contact Information	hongfeng_zhang@xmu.edu.cn
Language ability	Chinese, English
Province	Fujian

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Name

Hongfeng Zhang

Contact Information

hongfeng_zhang@xmu.edu.cn

Language ability

Chinese, English

Province

Fujian

University/Lab Affiliation and Title	Xiamen University
Faculty	Medical
Academic Background & Achievements	2013-2016 Doctorate in Neurobiology: Peking University 2010-2013 Master's in Pharmacology: Central South University 2006-2010 Bachelor's in Biological Sciences: Northwest A&F University
Work Experience	2019-present - Xiamen University School of Medicine - Assistant Professor 2016-2019 - Xiamen University School of Medicine - Postdoctoral Researcher
Awards	2018: Neuroscience Bulletin Outstanding Paper Special Award (First Author) 2015: Hunan Province Physiology Society Outstanding Paper First Prize (First Author)

University/Lab Affiliation and Title

Xiamen University

Faculty

Medical

Academic Background & Achievements

2013-2016 Doctorate in Neurobiology: Peking University
2010-2013 Master's in Pharmacology: Central South University
2006-2010 Bachelor's in Biological Sciences: Northwest A&F University

Work Experience

2019-present - Xiamen University School of Medicine - Assistant Professor
2016-2019 - Xiamen University School of Medicine - Postdoctoral Researcher

Awards

2018: Neuroscience Bulletin Outstanding Paper Special Award (First Author)
2015: Hunan Province Physiology Society Outstanding Paper First Prize (First Author)

Areas of Focus	Genetic cerebellar ataxia Down syndrome (Trisomy 21)
Publications	SNX14 deficiency-induced defective axonal mitochondrial transport in Purkinje cells underlies cerebellar ataxia and can be reversed by valproate., Zhang HF, Hong Y, Yang W, Wang R, Yao T, Wang J, Liu K, Yuan H, Xu C, Zhou Y, Li G, Zhang L, Luo H, Zhang X, Du D, Sun H, Zheng Q, Zhang Y-W, Zhao Y, Zhou Y, Xu H, Wang X., 2021 Novel KCNJ10 Compound Heterozygous Mutations Causing EAST/SeSAME-Like Syndrome Compromise Potassium Channel Function., Zhang HF, Zhu L, Wang F, Wang R, Hong Y, Chen Y, Zhu B, Gao Y, Luo H, Zhang X, Sun H, Zhou Y, Yao Y, Wang X., 2019 Neonatal Oxytocin Treatment Ameliorates Autistic-Like Behaviors and Oxytocin Deficiency in Valproic Acid-Induced Rat Model of Autism., Dai YC, Zhang HF, Schon M, Boeckers TM, Han, SP, Han JS, Zhang R., 2018 The Retromer Complex and Sorting Nexins in Neurodegenerative Diseases., Zhang HF, Huang T, Hong Y, Yang W, Zhang X, Luo H, Xu H, Wang X., 2018 Genes Related to Oxytocin and Arginine-Vasopressin Pathways: Associations with Autism Spectrum Disorders., Zhang R, Zhang HF, Han JS, Han SP., 2017 Plasma Oxytocin and Arginine-Vasopressin Levels in Children with Autism Spectrum Disorder in China: Associations with Symptoms., Zhang HF, Dai YC, Wu J, Jia MX, Zhang JS, Shou XJ, Han SP, Zhang R, Han JS., 2016 Trisomy 21-induced dysregulation of microglial homeostasis in Alzheimer’s brains is mediated by USP25., Zheng Q, Li G, Wang S, Zhou Y, Liu K, Gao Y, Zhou Y, Zheng L, Zhu L, Deng Q, Wu M, Di A, Zhang L, Zhao Y, Zhang HF, Sun H, Dong C, Xu H, Wang X., 2021 The deubiquitinase USP6 affects memory and synaptic plasticity through modulating NMDA receptor stability., Zeng F, Ma X, Zhu L, Xu Q, Zeng Y, Gao Y, Li G, Guo T, Zhang H, Tang X, Wang Z, Ye Z, Zheng L, Zhang HF, Zheng Q, Li K, Lu J, Qi X, Luo H, Zhang X, Wang Z, Zhou Y, Yao Y, Ke R, Zhou Y, Liu Y, Sun H, Huang T, Shao Z, Xu H, Wang X., 2019

Areas of Focus

Genetic cerebellar ataxia
Down syndrome (Trisomy 21)

Publications

SNX14 deficiency-induced defective axonal mitochondrial transport in Purkinje cells underlies cerebellar ataxia and can be reversed by valproate., Zhang HF, Hong Y, Yang W, Wang R, Yao T, Wang J, Liu K, Yuan H, Xu C, Zhou Y, Li G, Zhang L, Luo H, Zhang X, Du D, Sun H, Zheng Q, Zhang Y-W, Zhao Y, Zhou Y, Xu H, Wang X., 2021
Novel KCNJ10 Compound Heterozygous Mutations Causing EAST/SeSAME-Like Syndrome Compromise Potassium Channel Function., Zhang HF, Zhu L, Wang F, Wang R, Hong Y, Chen Y, Zhu B, Gao Y, Luo H, Zhang X, Sun H, Zhou Y, Yao Y, Wang X., 2019
Neonatal Oxytocin Treatment Ameliorates Autistic-Like Behaviors and Oxytocin Deficiency in Valproic Acid-Induced Rat Model of Autism., Dai YC, Zhang HF, Schon M, Boeckers TM, Han, SP, Han JS, Zhang R., 2018
The Retromer Complex and Sorting Nexins in Neurodegenerative Diseases., Zhang HF, Huang T, Hong Y, Yang W, Zhang X, Luo H, Xu H, Wang X., 2018
Genes Related to Oxytocin and Arginine-Vasopressin Pathways: Associations with Autism Spectrum Disorders., Zhang R, Zhang HF, Han JS, Han SP., 2017
Plasma Oxytocin and Arginine-Vasopressin Levels in Children with Autism Spectrum Disorder in China: Associations with Symptoms., Zhang HF, Dai YC, Wu J, Jia MX, Zhang JS, Shou XJ, Han SP, Zhang R, Han JS., 2016
Trisomy 21-induced dysregulation of microglial homeostasis in Alzheimer’s brains is mediated by USP25., Zheng Q, Li G, Wang S, Zhou Y, Liu K, Gao Y, Zhou Y, Zheng L, Zhu L, Deng Q, Wu M, Di A, Zhang L, Zhao Y, Zhang HF, Sun H, Dong C, Xu H, Wang X., 2021
The deubiquitinase USP6 affects memory and synaptic plasticity through modulating NMDA receptor stability., Zeng F, Ma X, Zhu L, Xu Q, Zeng Y, Gao Y, Li G, Guo T, Zhang H, Tang X, Wang Z, Ye Z, Zheng L, Zhang HF, Zheng Q, Li K, Lu J, Qi X, Luo H, Zhang X, Wang Z, Zhou Y, Yao Y, Ke R, Zhou Y, Liu Y, Sun H, Huang T, Shao Z, Xu H, Wang X., 2019

Genetics Cerebellar Ataxia Down Syndrome Trisomy 21 Neurodegenerative Disorders Mechanisms Therapies Children

Pingping Jiang - Zhejiang University

Yicheng Xie - Zhejiang University

Huan Ma - Zhejiang University

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