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Qinjun Wei
Basic Medical Sciences
Nanjing Medical University
Jiangsu
Language: Chinese, English
Tumor
Molecular
Mechanism
Development
Genetic
Disease
Pathogenesis
Research
Biology
Biochemistry
Areas of Focus
- Molecular mechanisms of tumor development
- Molecular pathogenesis of genetic diseases
Work Experience
- 1997 to Present - Nanjing Medical University - School of Basic Medical Sciences
Academic Background & Achievements
- 1992-09 to 1997-06 Bachelor of Medicine: Nanjing Medical University
- 2003-09 to 2008-06 Master of Genetics: Nanjing Medical University
- 2017-09 to 2021-06 PhD in Biochemistry and Molecular Biology: Nanjing Medical University
- Hosted 1 National Natural Science Foundation project
- Published 15 papers, 9 indexed by SCI
- Granted 3 patents
Publications
- Mutations in OSBPL2 cause hearing loss associated with primary cilia defects via sonic hedgehog signaling., Shi H, Wang H, Zhang C, Lu Y, Yao J, Chen Z, Xing G, Wei Q, Cao X., 2022
- OSBPL2 Is Required for the Binding of COPB1 to ATGL and the Regulation of Lipid Droplet Lipolysis., Wang T, Wei Q, Liang L, Tang X, Yao J, Lu Y, Qu Y, Chen Z, Xing G, Cao X., 2020
- Identification of a novel MYO6 mutation associated with autosomal dominant non-syndromic hearing loss in a Chinese family by whole-exome sequencing., Tian T, Lu Y, Yao J, Cao X, Wei Q, Li Q., 2018
- Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss., Wei Q, Zhu H, Qian X, Chen Z, Yao J, Lu Y, Cao X, Xing G., 2014
- A novel compound heterozygous mutation in the GJB2 gene causing non-syndromic hearing loss in a family., Wei Q, Liu Y, Wang S, Liu T, Lu Y, Xing G, Cao X., 2014
- Identification and characterization of microRNAs expressed in human breast cancer T-47D cells in response to prolactin treatment by Solexa deep-sequencing technology., Wei Q, He W, Yao J, Guo L, Lu Y, Cao X., 2013
- Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of China., Wei Q, Wang S, Yao J, Lu Y, Chen Z, Xing G, Cao X., 2013
- Maternally transmitted aminoglycoside-induced and non-syndromic hearing loss caused by the 1494C > T mutation in the mitochondrial 12S rRNA gene in two Chinese families., Wei Q, Xu D, Chen Z, Li H, Lu Y, Liu C, Bu X, Xing G, Cao X., 2013
- Molecular screening of patients with nonsyndromic hearing loss from Nanjing city of China., Lu Y, Dai D, Chen Z, Cao X, Bu X, Wei Q, Xing G., 2011
- Gene silencing of hPRLR mRNA by RNA interference in human breast cancer cells., Wei Q, Lu Y, Pan M, Shu Y, Cao X., 2008
Awards
- 2006: Second Prize of Chinese Medical Association Award (5th place)
- 2010: Second Prize of Jiangsu Health Department Medical New Technology Introduction Award (3rd place)
- 2013: Yangtze River Teaching Award, Excellence Award, Nanjing Medical University
