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Wen Huang
Life Science
Central South University
Hunan
Language: Chinese, English
Fragile X Syndrome
Cgg Repeat
Mutation Analysis
Genetic Counseling
Pediatric Genetics
Neurodevelopmental Disorders
Gene Expression
Molecular Diagnostics
Clinical Genetics
Research Methodology
Areas of Focus
- Genetics of Fragile X Syndrome
- Molecular Genetics
- Neurogenetics
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
Publications
- Correlation between FMR1 expression and clinical phenotype in discordant dichorionic–diamniotic monozygotic twin sisters with the fragile x mutation, Wen Huang, 2014
- Distribution of fragile X mental retardation 1 CGG Repeat and Flanking Haplotypes in a Large Chinese Population, Wen Huang, 2015
- Mutational Analyses of the FMR1 Gene in Chinese Pediatric Population of Fragile X Suspects: Low Tolerance for Point Mutation, Wen Huang, 2015
- A novel deletion to normal size in the sperm of a fragile X full mutation male, Wen Huang, 2014
- Amyotrophic Lateral Sclerosis-associated GGGGCC repeat expansion promotes Tau phosphorylation and toxicity, Wen Huang, 2019
