Professor | Qinjun Wei | Asia Growth Partners

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Name	Qinjun Wei
Contact Information	wqj@njmu.edu.cn
Language ability	Chinese, English
Province	Jiangsu

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Name

Qinjun Wei

Contact Information

wqj@njmu.edu.cn

Language ability

Chinese, English

Province

Jiangsu

University/Lab Affiliation and Title	Nanjing Medical University
Faculty	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
Work Experience	1997 to Present - Nanjing Medical University - School of Basic Medical Sciences
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

University/Lab Affiliation and Title

Nanjing Medical University

Faculty

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

Work Experience

1997 to Present - Nanjing Medical University - School of Basic Medical Sciences

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

Areas of Focus	Molecular mechanisms of tumor development Molecular pathogenesis of genetic diseases
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

Areas of Focus

Molecular mechanisms of tumor development
Molecular pathogenesis of genetic diseases

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

Tumor Molecular Mechanism Development Genetic Disease Pathogenesis Research Biology Biochemistry

Kong Wei - Peking University

Xunde Xian - Peking University

Li-Bin Wang - Peking University

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