Wenjuan Qiu

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 11

Top Venues

Orphanet journal of rare diseases

Human mutation

Journal of medical genetics

Molecular genetics & genomic medicine

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

Publications

Ruifang Wang, Xiaomei Luo, Yu Sun, Lili Liang, Aiping Mao, Deyun Lu, Kaichuang Zhang, Yi Yang, Yuning Sun, Manqing Sun, Lianshu Han, Huiwen Zhang, Xuefan Gu, Wenjuan Qiu, Yong-Guo Yu
Long-read sequencing solves complex structure of CYP21A2 in a large 21-hydroxylase deficiency cohort. The Journal of clinical endocrinology and metabolism (2024)
Taozi Du, Yu Xia, Chengkai Sun, Zhuwen Gong, Lili Liang, Zizhen Gong, Ruifang Wang, Deyun Lu, Kaichuang Zhang, Yi Yang, Yuning Sun, Manqing Sun, Yu Sun, Bing Xiao, Wenjuan Qiu
Clinical, genetic profile and therapy evaluation of 11 Chinese pediatric patients with Fanconi-Bickel syndrome. Orphanet journal of rare diseases 19 (1) (2024)
Taozi Du, Yu Xia, Chengkai Sun, Zhuwen Gong, Lili Liang, Zizhen Gong, Ruifang Wang, Deyun Lu, Kaichuang Zhang, Yi Yang, Yuning Sun, Manqing Sun, Yu Sun, Bing Xiao, Wenjuan Qiu
Clinical, genetic profile and therapy evaluation of 11 Chinese pediatric patients with Fanconi-Bickel syndrome. Orphanet journal of rare diseases 19 (1) (2024)
Taozi Du, Yu Xia, Chengkai Sun, Zhuwen Gong, Lili Liang, Zizhen Gong, Ruifang Wang, Deyun Lu, Kaichuang Zhang, Yi Yang, Yuning Sun, Manqing Sun, Yu Sun, Bing Xiao, Wenjuan Qiu
Clinical, genetic profile and therapy evaluation of 11 Chinese pediatric patients with Fanconi-Bickel syndrome. Orphanet journal of rare diseases 19 (1) (2024)
Ying Duan, Wanqi Zheng, Yu Xia, Huiwen Zhang, Lili Liang, Ruifang Wang, Yi Yang, Kaichuang Zhang, Deyun Lu, Yuning Sun, Lian-Shu Han, Yong-Guo Yu, Xuefan Gu, Yu Sun, Bing Xiao, Wenjuan Qiu
Genetic and phenotypic spectrum of non-21-hydroxylase-deficiency primary adrenal insufficiency in childhood: data from 111 Chinese patients. Journal of medical genetics (2023)
Lili Liang, Shiying Ling, Yue Yu, Ruixue Shuai, Wenjuan Qiu, Huiwen Zhang, Linghua Shen, Shengnan Wu, Haiyan Wei, Yongxing Chen, Chiju Yang, Peng Xu, Xigui Chen, Hui Zou, Jizhen Feng, Tingting Niu, Haili Hu, Zhuwen Gong, Ting Chen, Xia Zhan, Xuefan Gu, Lian-Shu Han
Evaluation of the clinical, biochemical, genotype and prognosis of mut -type methylmalonic acidemia in 365 Chinese cases. Journal of medical genetics (2023)
Wanqi Zheng, Ying Duan, Yu Xia, Lili Liang, Zhuwen Gong, Ruifang Wang, Deyun Lu, Kaichuang Zhang, Yi Yang, Yuning Sun, Huiwen Zhang, Lianshu Han, Zizhen Gong, Bing Xiao, Wenjuan Qiu
Clinical and genetic characteristics of 42 Chinese paediatric patients with X-linked adrenal hypoplasia congenita. Orphanet journal of rare diseases 18 (1) (2023)
Yu Sun, Jing Peng, Desheng Liang, Xiantao Ye, Na Xu, Linlin Chen, Dan Yan, Huiwen Zhang, Bing Xiao, Wenjuan Qiu, Yiping Shen, Nan Pang, Yingdi Liu, Chen Liang, Zailong Qin, Jingsi Luo, Fei Chen, Jingmin Wang, Zhixin Zhang, Haiyan Wei, Juan Du, Huifang Yan, Ruoyu Duan, Junyu Wang, Yu Zhang, Bingtao Hao, Kun Sun, Lingqian Wu, Yong-Guo Yu
Genome sequencing demonstrates high diagnostic yield in children with undiagnosed global developmental delay/intellectual disability: A prospective study. Human mutation 43 (5) (2022)
Xiaomei Luo, Ying Duan, Di Fang, Yu Sun, Bing Xiao, Huiwen Zhang, Lian-Shu Han, Lili Liang, Zhuwen Gong, Xuefan Gu, Yong-Guo Yu, Wenjuan Qiu
Diagnosis and follow-up of glycogen storage disease (GSD) type VI from the largest GSD center in China. Human mutation 43 (5) (2022)
Yue Yu, Ruixue Shuai, Lili Liang, Wenjuan Qiu, Linghua Shen, Shengnan Wu, Haiyan Wei, Yongxing Chen, Chiju Yang, Peng Xu, Xigui Chen, Hui Zou, Jizhen Feng, Tingting Niu, Haili Hu, Jun Ye, Huiwen Zhang, Deyun Lu, Zhuwen Gong, Xia Zhan, Wenjun Ji, Xuefan Gu, Lian-Shu Han
Different mutations in the MMUT gene are associated with the effect of vitamin B12 in a cohort of 266 Chinese patients with mut-type methylmalonic acidemia: A retrospective study. Molecular genetics & genomic medicine 9 (11) (2021)
Lili Liang, Jun Ye, Lianshu Han, Wenjuan Qiu, Huiwen Zhang, Yong-Guo Yu, Tianwen Zhu, Feng Xu, Xia Zhan, Peizhong Bao, Wenjun Ji, Xuefan Gu
Examining the blood amino acid status in pretherapeutic patients with hyperphenylalaninemia. Journal of clinical laboratory analysis 34 (3) (2019)

Wenjuan Qiu.css-eqlu8i{font-size:small;padding-left:4px;}

Publication Activity (10 Years)

Top Topics

Top Venues

Wenjuan Qiu