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Wen Huang
Chinese, English
Hunan
Central South University
Life Sciences
  • 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
Genetics of Fragile X Syndrome
Molecular Genetics
Neurogenetics
  • 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
Fragile X Syndrome Cgg Repeat Mutation Analysis Genetic Counseling Pediatric Genetics Neurodevelopmental Disorders Gene Expression Molecular Diagnostics Clinical Genetics Research Methodology

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