Research Interests

• As a chief physician as well as master’s supervisor, I’m working at Xinhua Hospital, Shanghai Institute of Pediatric Medicine, Shanghai Jiao Tong University School of Medicine.

• I’m mainly engaged in the screening, clinical management, and prenatal diagnosis of pediatric endocrine genetic diseases, including methylmalonic acidemia, phenylketonuria, primary carnitine deficiency, dwarfism, precocious puberty and hypothyroidism. Meanwhile, I have conducted systematic clinical and basic research on methylmalonic acidemia, propionic acidemia, glutaric acidemia type I, and primary carnitine deficiency.

• In addition, I’m a member of the Pediatric Branch and Endocrine Genetic Metabolism Group of the Chinese Medical Association; a member of the quality control expert group of the newborn screening laboratory of the National Health Care