Lili Liang

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 6

Top Topics

Gene Expression

Peritoneal Dialysis

Intellectual Disability

Top Venues

Journal of medical genetics

Molecular genetics & genomic medicine

Metabolic brain disease

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

Publications

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)
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)
Sha Hong, Tianwen Zhu, Simin Zheng, Xia Zhan, Feng Xu, Xuefan Gu, Lili Liang
Gene expression profiles in the brain of phenylketonuria mouse model reversed by the low phenylalanine diet therapy. Metabolic brain disease 36 (8) (2021)
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)