Chao Chun Zou (Chaochun Zou, C-C Zou, Chao-Chun Zou, Zou Chao-Chun)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 37

Top Topics

Mass Spectrometry

Recombinant Human

Endoplasmic Reticulum

Top Venues

Orphanet journal of rare diseases

Molecular genetics & genomic medicine

Endocrine connections

Clinical genetics

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

Publications

Wei Tang, Ke-Mi Wu, Qiong Zhou, Yan-Fei Tang, Jun-Fen Fu, Guan-Ping Dong, Chao Chun Zou
Genotype and phenotype in patients with ACAN gene variants: Three cases and literature review. Molecular genetics & genomic medicine 12 (4) (2024)
Qing Zhou, Li Yong Zhang, Mei Feng Dai, Zhen Li, Chao Chun Zou, Hui Liu
Thyroid-stimulating hormone induces insulin resistance in adipocytes via endoplasmic reticulum stress. Endocrine connections 13 (8) (2024)
Qing Zhou, Li Yong Zhang, Mei Feng Dai, Zhen Li, Chao Chun Zou, Hui Liu
Thyroid-stimulating hormone induces insulin resistance in adipocytes via endoplasmic reticulum stress. Endocrine connections 13 (8) (2024)
Shujiong Mao, Lili Yang, Ying Gao, Chao Chun Zou
Genotype-phenotype correlation in Prader-Willi syndrome: A large-sample analysis in China. Clinical genetics 105 (4) (2024)
Jing-Wen Li, Yan-Jie Qian, Shao-Jia Mao, Yun-Qi Chao, Yi-Fang Qin, Chen-Xi Hu, Zheng-Lan Li, Chao Chun Zou
Clinical features associated with maternal uniparental disomy for chromosome 6. Molecular cytogenetics 17 (1) (2024)
Jing-Wen Li, Yan-Jie Qian, Shao-Jia Mao, Yun-Qi Chao, Yi-Fang Qin, Chen-Xi Hu, Zheng-Lan Li, Chao Chun Zou
Clinical features associated with maternal uniparental disomy for chromosome 6. Molecular cytogenetics 17 (1) (2024)
Xuefei Chen, Chao Chun Zou
Further delineation of phenotype and genotype of Kenny-Caffey syndrome type 2 (phenotype and genotype of KCS type 2). Molecular genetics & genomic medicine 12 (4) (2024)
Shujiong Mao, Lili Yang, Ying Gao, Chao Chun Zou
Genotype-phenotype correlation in Prader-Willi syndrome: A large-sample analysis in China. Clinical genetics 105 (4) (2024)
Jing-Wen Li, Shao-Jia Mao, Yun-Qi Chao, Chen-Xi Hu, Yan-Jie Qian, Yang-Li Dai, Ke Huang, Zheng Shen, Chao Chun Zou
Application of tandem mass spectrometry in the screening and diagnosis of mucopolysaccharidoses. Orphanet journal of rare diseases 19 (1) (2024)
Shujiong Mao, Lili Yang, Ying Gao, Chao Chun Zou
Genotype-phenotype correlation in Prader-Willi syndrome: A large-sample analysis in China. Clinical genetics 105 (4) (2024)
Qing Zhou, Li Yong Zhang, Mei Feng Dai, Zhen Li, Chao Chun Zou, Hui Liu
Thyroid-stimulating hormone induces insulin resistance in adipocytes via endoplasmic reticulum stress. Endocrine connections 13 (8) (2024)
Xuefei Chen, Chao Chun Zou
Further delineation of phenotype and genotype of Kenny-Caffey syndrome type 2 (phenotype and genotype of KCS type 2). Molecular genetics & genomic medicine 12 (4) (2024)
Qing Zhou, Li Yong Zhang, Mei Feng Dai, Zhen Li, Chao Chun Zou, Hui Liu
Thyroid-stimulating hormone induces insulin resistance in adipocytes via endoplasmic reticulum stress. Endocrine connections 13 (8) (2024)
Shujiong Mao, Lili Yang, Ying Gao, Chao Chun Zou
Genotype-phenotype correlation in Prader-Willi syndrome: A large-sample analysis in China. Clinical genetics (2024)
Wei Tang, Ke-Mi Wu, Qiong Zhou, Yan-Fei Tang, Jun-Fen Fu, Guan-Ping Dong, Chao Chun Zou
Genotype and phenotype in patients with ACAN gene variants: Three cases and literature review. Molecular genetics & genomic medicine 12 (4) (2024)
Jing-Wen Li, Shao-Jia Mao, Yun-Qi Chao, Chen-Xi Hu, Yan-Jie Qian, Yang-Li Dai, Ke Huang, Zheng Shen, Chao Chun Zou
Application of tandem mass spectrometry in the screening and diagnosis of mucopolysaccharidoses. Orphanet journal of rare diseases 19 (1) (2024)
Xiaoying Wang, Wenbo Weng, Yifei Cui, Chao Chun Zou
Sitagliptin Alleviates Obesity in Immature Mice by Inhibiting Oxidative Stress and Inflammation. Reproductive sciences (Thousand Oaks, Calif.) (2024)
Jing-Wen Li, Shao-Jia Mao, Yun-Qi Chao, Chen-Xi Hu, Yan-Jie Qian, Yang-Li Dai, Ke Huang, Zheng Shen, Chao Chun Zou
Application of tandem mass spectrometry in the screening and diagnosis of mucopolysaccharidoses. Orphanet journal of rare diseases 19 (1) (2024)
Jing-Wen Li, Yan-Jie Qian, Shao-Jia Mao, Yun-Qi Chao, Yi-Fang Qin, Chen-Xi Hu, Zheng-Lan Li, Chao Chun Zou
Clinical features associated with maternal uniparental disomy for chromosome 6. Molecular cytogenetics 17 (1) (2024)
Wei Tang, Ke-Mi Wu, Qiong Zhou, Yan-Fei Tang, Jun-Fen Fu, Guan-Ping Dong, Chao Chun Zou
Genotype and phenotype in patients with ACAN gene variants: Three cases and literature review. Molecular genetics & genomic medicine 12 (4) (2024)
Ying Gao, Li-Li Yang, Yang-Li Dai, Zheng Shen, Qiong Zhou, Chao Chun Zou
Effects of early recombinant human growth hormone treatment in young Chinese children with Prader-Willi syndrome. Orphanet journal of rare diseases 18 (1) (2023)
Ying Gao, Li-Li Yang, Yang-Li Dai, Zheng Shen, Qiong Zhou, Chao Chun Zou
Effects of early recombinant human growth hormone treatment in young Chinese children with Prader-Willi syndrome. Orphanet journal of rare diseases 18 (1) (2023)
Ying Gao, Li-Li Yang, Yang-Li Dai, Zheng Shen, Qiong Zhou, Chao Chun Zou
Effects of early recombinant human growth hormone treatment in young Chinese children with Prader-Willi syndrome. Orphanet journal of rare diseases 18 (1) (2023)
M-L Zhong, Y-Q Cai, Y-F Tang, Y-L Dai, Y-H Jiang, Y Ni, Chao Chun Zou
Gut microbiota, a potential cause of higher insulin sensitivity in children with Prader-Willi syndrome. Journal of endocrinological investigation (2023)
Ying Gao, Li-Li Yang, Yang-Li Dai, Zheng Shen, Qiong Zhou, Chao Chun Zou
Effects of early recombinant human growth hormone treatment in young Chinese children with Prader-Willi syndrome. Orphanet journal of rare diseases 18 (1) (2023)
Qing Zhou, Bin Liang, Qing-Xian Fu, Hui Liu, Chao Chun Zou
Different AHO phenotype in a Chinese family with a novel GNAS missense variant: a case report. Italian journal of pediatrics 48 (1) (2022)
Yanjie Qian, Fangling Xia, Yiming Zuo, Mianling Zhong, Lili Yang, Yonghui Jiang, Chao Chun Zou
Do patients with Prader-Willi syndrome have favorable glucose metabolism? Orphanet journal of rare diseases 17 (1) (2022)
Qiong Zhou, Wenbin Sheng, Suhong Yang, Chao Chun Zou
The Clinical and Genetic Characteristics in Children with Idiopathic Hypogonadotropin Hypogonadism. Journal of oncology 2022 (2022)
Dan Huang, Jia Zhao, Fang-Ling Xia, Chao Chun Zou
Recombinant Human Growth Hormone Therapy for Childhood Trichorhinophalangeal Syndrome Type I: A Case Report. Children (Basel, Switzerland) 9 (10) (2022)
Yumei Zu, Hui Wang, Weijia Lin, Chao Chun Zou
Hereditary nonspherocytic hemolytic anemia caused by glucose-6-phosphate isomerase (GPI) deficiency in a Chinese patient: a case report. BMC pediatrics 22 (1) (2022)
Yanjie Qian, Xiaoying Wang, Wei Tang, Chao Chun Zou
Microdeletion of 4p16.2 in Children: A Case Report and Literature Review. Case reports in genetics 2022 (2022)
Dai Yang-Li, Luo Fei-Hong, Zhang Hui-Wen, Ma Ming-Sheng, Luo Xiao-Ping, Liu Li, Wang Yi, Zhou Qing, Jiang Yong-Hui, Chao Chun Zou, null null, null null
Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China. Orphanet journal of rare diseases 17 (1) (2022)
Yunqi Chao, Yifang Qin, Xinyi Zou, Xiangzhi Wang, Chenxi Hu, Fangling Xia, Chao Chun Zou
Promising therapeutic aspects in human genetic imprinting disorders. Clinical epigenetics 14 (1) (2022)
Yunqi Chao, Yonghui Jiang, Mianling Zhong, Kaiyan Wei, Chenxi Hu, Yifang Qin, Yiming Zuo, Lili Yang, Zheng Shen, Chao Chun Zou
Regulatory roles and mechanisms of alternative RNA splicing in adipogenesis and human metabolic health. Cell & bioscience 11 (1) (2021)
Mian-Ling Zhong, Ye-Mei Song, Chao Chun Zou
6q25.1-q25.3 Microdeletion in a Chinese Girl Journal of clinical research in pediatric endocrinology 13 (1) (2020)
Shu-Jiong Mao, Jian Shen, Fang Xu, Chao Chun Zou
Quality of life in caregivers of young children with Prader-Willi syndrome. World journal of pediatrics : WJP 15 (5) (2019)
Xin-Yi Zou, Yun-Qi Chao, Lin-Hui Zeng, Chao Chun Zou
Prader-Willi Syndrome Coincident with DiGeorge Syndrome. Indian journal of pediatrics 87 (6) (2019)