Hui Jiao
Tianjin University(CN)Beijing Chao-Yang Hospital, Capital Medical University(CN)Beijing Children’s Hospital(CN)
Publications by Year
Research Areas
Muscle Physiology and Disorders, Neurogenetic and Muscular Disorders Research, RNA modifications and cancer, RNA Research and Splicing, Mitochondrial Function and Pathology
Most-Cited Works
- → Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients(2014)74 cited
- → Congenital muscular dystrophies in China(2019)51 cited
- → FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies(2016)20 cited
- → Analysis of phenotype, enzyme activity and genotype of Chinese patients with POMT1 mutation(2016)19 cited
- → Novel copy number variation of POMGNT1 associated with muscle-eye-brain disease detected by next-generation sequencing(2017)16 cited
- → A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy(2015)11 cited
- → Novel POMGnT1 mutations cause muscle-eye-brain disease in Chinese patients