Jie Qiao

ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 8

Top Venues

Clinical and translational medicine

Molecular genetics & genomic medicine

The Journal of clinical endocrinology and metabolism

Orphanet journal of rare diseases

Shanghai Jiao Tong University School of Medicine (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Shanghai Jiao Tong University School of Medicine Sep 01 2003 - Jun 30 2006

China

PHD :: Dept of Internal Medicine, Ruijin Hospital

Publications

Wenjiao Zhu, Yuanping Shi, Changrun Zhang, Yajie Peng, Yueyue Wan, Yue Xu, Xuemeng Liu, Bing Han, Shuangxia Zhao, Yanping Kuang, Huaidong Song, Jie Qiao
In-frame deletion of SMC5 related with the phenotype of primordial dwarfism, chromosomal instability and insulin resistance. Clinical and translational medicine 13 (1) (2023)
Wenjiao Zhu, Yuanping Shi, Changrun Zhang, Yajie Peng, Yueyue Wan, Yue Xu, Xuemeng Liu, Bing Han, Shuangxia Zhao, Yanping Kuang, Huaidong Song, Jie Qiao
In-frame deletion of SMC5 related with the phenotype of primordial dwarfism, chromosomal instability and insulin resistance. Clinical and translational medicine 13 (1) (2023)
Wenjiao Zhu, Yuanping Shi, Changrun Zhang, Yajie Peng, Yueyue Wan, Yue Xu, Xuemeng Liu, Bing Han, Shuangxia Zhao, Yanping Kuang, Huaidong Song, Jie Qiao
In-frame deletion of SMC5 related with the phenotype of primordial dwarfism, chromosomal instability and insulin resistance. Clinical and translational medicine 13 (1) (2023)
Wenjiao Zhu, Yuanping Shi, Changrun Zhang, Yajie Peng, Yueyue Wan, Yue Xu, Xuemeng Liu, Bing Han, Shuangxia Zhao, Yanping Kuang, Huaidong Song, Jie Qiao
In-frame deletion of SMC5 related with the phenotype of primordial dwarfism, chromosomal instability and insulin resistance. Clinical and translational medicine 13 (1) (2023)
Yue Xu, Shutian Jiang, Zheng Yan, Yao Niu, Wenhua Du, Bingli Liu, Bing Han, Xuemeng Liu, Shuangxia Zhao, Huaidong Song, Yanping Kuang, Jie Qiao
Phenotypic Heterogeneity and Fertility Potential of Patients With 17-Hydroxylase/17,20-lyase Deficiency. The Journal of clinical endocrinology and metabolism 107 (6) (2022)
Hui Zhu, Haijun Yao, Yue Xu, Yan Chen, Bing Han, Nan Wang, Hao Wang, Qiang Zhang, Wenjiao Zhu, Yuanping Shi, Hua Sun, Shuangxia Zhao, Huaidong Song, Yang Liu, Jie Qiao
Phenotypic and biochemical characteristics and molecular basis in 36 Chinese patients with androgen receptor variants. Orphanet journal of rare diseases 16 (1) (2021)
Bing Han, Tong Cheng, Hui Zhu, Jie Yu, Wen-Jiao Zhu, Huai-Dong Song, Haijun Yao, Jie Qiao
Genetic Analysis of 25 Patients with 5α-Reductase Deficiency in Chinese Population. BioMed research international 2020 (2020)
Hao Wang, Hui Zhu, Nan Wang, Tong Cheng, Bing Han, Shuangxia Zhao, Huaidong Song, Kaixiang Cheng, Yang Liu, Jie Qiao
Somatic mosaicism of androgen receptor gene in an androgen insensitivity syndrome patient conceived through assisted reproduction technique. Molecular genetics & genomic medicine 7 (10) (2019)

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Publication Activity (10 Years)

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Jie Qiao