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Zeng Hanshi/doctor

Specialties: Clinical geneticist


Clinical Interests: Genetic and metabolic diseases,Congenital heart disease,Pediatric emergency, Common Pediatric Diseases.


Bio: He has been working in the Department of Pediatrics, Guangdong Provincial People's Hospital since 2016.


Education: He graduated from Jinan University in 2016 with a master's degree.


Professional memberships: Member of Guangdong Provincial Health Association,Member of Nanomedicine Branch of Guangdong Academy of Precision Medicine Application.


Publications:

[1] Zeng HS, Zhao ST, Deng M, et al. Inspissated bile syndrome in an infant with citrin deficiency and congenital anomalies of the biliary tract and esophagus: identification and pathogenicity analysis of a novel SLC25A13 mutation with incomplete penetrance[J]. Int J Mol Med. 2014, 34(5):1241-1248.

[2] Zhang ZH, Lin WX, Deng M, Zhao ST, Zeng HS et al. Clinical, molecular and functional investigation on an infant with Neonatal Intrahepatic Cholestasis caused by Citrin Deficiency (NICCD)[J]. PLoS One. 2014, 9: e89267.

[3] Zeng HS, Lin WX, Zhao ST, et al. SLC25A13 cDNA cloning analysis using peripheral blood lymphocytes facilitates the identification of a large deletion mutation: Molecular diagnosis of an infant with neonatal intrahepatic cholestasis caused by citrin deficiency[J]. Mol Med Report. 2016.5873. [Epub ahead of print]

[4] Zheng QQ, Zhang ZH, Zeng HS, et al. Identification of a Large SLC25A13 Deletion via Sophisticated Molecular Analyses Using Peripheral Blood Lymphocytes in an Infant with Neonatal Intrahepatic Cholestasis caused by Citrin Deficiency (NICCD): A Clinical and Molecular Study[J]. Biomed Res Int. 2016, 2016: 4124263.

[5]Wei-Xia Lin, Han-Shi Zeng, Zhan-Hui Zhang, et al. .Molecular diagnosis of pediatric patients with citrin deficiency in China: SLC25A13 mutation spectrum and the geographic distribution[J].Sci Rep. 2016 Jul 11;6:29732.

[6] Wu Y, Xia Y, Li P,... Zeng HS et al. Role of the ADCY9 gene in cardiac abnormalities of the Rubinstein-Taybi syndrome. Orphanet J Rare Dis. 2020;15(1):101. Published 2020 Apr 22. doi:10.1186/s13023-020-01378-9