Publications by authors named "Haofeng Ning"

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Clinical Genetic Study of Mosaic Pseudoisodicentric X Chromosome Patient.
Hua-Cheng Wang, Xiu-Jing Huang, Hao-Feng Ning, Yan-Chou Ye, Xiao-Nan Wang

Clin Lab· November 2025

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Prenatal diagnosis of Prader-Willi syndrome via maternal UPD15 with placental mosaicism: incidental discovery of fetal DMD carrier status.
Yanchou Ye, Yiman Fu, Zhechao Zhang, Haofeng Ning, Fangchao Tao

Front Genet· November 2025

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[Analysis of EEF1A2 gene variant in a child with Global developmental delay].
Haofeng Ning, Yuqiong Chai, Wanzhen Huang, Ya'nan Wang

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· November 2024

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[Analysis of ACADVL gene variant in a Chinese pedigree affected with Very-long-chain acl-CoA dehydrogenase deficiency].
Haofeng Ning, Yuqiong Chai, Jieqiong Wang, Ya'nan Wang

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· October 2024

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[Analysis of PAH gene variants and prenatal diagnosis for 43 Chinese pedigrees affected with Phenylketonuria].
Yuqiong Chai, Haofeng Ning, Junke Xia, Ya'nan Wang, Xiangdong Kong

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· June 2024

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Genetic analysis of 37 cases with primary periodic paralysis in Chinese patients.
Xuechao Zhao, Haofeng Ning, Lina Liu, Chaofeng Zhu, Yinghui Zhang

Orphanet J Rare Dis· April 2024

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Genetic analysis and identification of novel variations in Chinese patients with pediatric epilepsy by whole-exome sequencing.
Xuechao Zhao, Haofeng Ning, Yanhong Wang, Ganye Zhao, Shiyue Mei, Ning Liu

Neurol Sci· July 2022

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Oxidized low-density lipoprotein-induced p62/SQSTM1 accumulation in THP-1-derived macrophages promotes IL-18 secretion and cell death.
Haofeng Ning, Dan Liu, Xiaochen Yu, Xiuru Guan

Exp Ther Med· December 2017

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The roles of p62/SQSTM1 on regulation of matrix metalloproteinase-9 gene expression in response to oxLDL in atherosclerosis.
Feng Zhou, Dan Liu, Hao-feng Ning, Xiao-chen Yu, Xiu-ru Guan

Biochem Biophys Res Commun· April 2016

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