Professor | Wen Huang | Asia Growth Partners

Name	Wen Huang
Language ability	Chinese, English
Province	Hunan

Name

Wen Huang

Language ability

Chinese, English

Province

Hunan

University/Lab Affiliation and Title	Central South University
Faculty	Life Sciences
Academic Background & Achievements	2017.2-2018.2 Postdoctoral Fellow at National Children's Medical Center, USA; Supervisor: Zhe Han 2006.9–2010.6 PhD in Genetics, Hunan Normal University 2003.9–2006.6 Master's in Developmental Biology, Hunan Normal University 1999.9–2003.6 Bachelor's in Biological Sciences, Hunan Normal University

University/Lab Affiliation and Title

Central South University

Faculty

Life Sciences

Academic Background & Achievements

2017.2-2018.2 Postdoctoral Fellow at National Children's Medical Center, USA; Supervisor: Zhe Han
2006.9–2010.6 PhD in Genetics, Hunan Normal University
2003.9–2006.6 Master's in Developmental Biology, Hunan Normal University
1999.9–2003.6 Bachelor's in Biological Sciences, Hunan Normal University

Areas of Focus	Genetics of Fragile X Syndrome
Publications	Correlation between FMR1 expression and clinical phenotype in discordant dichorionic–diamniotic monozygotic twin sisters with the fragile x mutation, Wen Huang et al., 2014 Distribution of fragile X mental retardation 1 CGG Repeat and Flanking Haplotypes in a Large Chinese Population, Wen Huang et al., 2015 Mutational Analyses of the FMR1 Gene in Chinese Pediatric Population of Fragile X Suspects: Low Tolerance for Point Mutation, Wen Huang et al., 2015 A novel deletion to normal size in the sperm of a fragile X full mutation male, Wen Huang et al., 2014 Amyotrophic Lateral Sclerosis-associated GGGGCC repeat expansion promotes Tau phosphorylation and toxicity, Wen Huang et al., 2019

Areas of Focus

Genetics of Fragile X Syndrome

Publications

Correlation between FMR1 expression and clinical phenotype in discordant dichorionic–diamniotic monozygotic twin sisters with the fragile x mutation, Wen Huang et al., 2014
Distribution of fragile X mental retardation 1 CGG Repeat and Flanking Haplotypes in a Large Chinese Population, Wen Huang et al., 2015
Mutational Analyses of the FMR1 Gene in Chinese Pediatric Population of Fragile X Suspects: Low Tolerance for Point Mutation, Wen Huang et al., 2015
A novel deletion to normal size in the sperm of a fragile X full mutation male, Wen Huang et al., 2014
Amyotrophic Lateral Sclerosis-associated GGGGCC repeat expansion promotes Tau phosphorylation and toxicity, Wen Huang et al., 2019

Genetics Fragile X Syndrome Cgg Repeat Mutation Analysis Clinical Phenotype Twin Studies Neurogenetics Molecular Genetics Genomic Medicine Pediatric Genetics

Wen Huang - Central South University

Tan Jieqiong - Central South University

Xiangzong Meng - Shanghai Normal University

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