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Author

Qingping Zhang

Observed names: Qing-Ping Zhang, QingPing Zhang, Zhang, Qingping
Institutions: Qinghai University, Qinghai University Affiliated Hospital, Zhongnan Hospital of Wuhan University, Peking University First Hospital, Second Affiliated Hospital of Zhejiang University, Zhejiang University
Observed institutions: Qinghai University, Harbin Medical University, Sun Yat-sen University, The University of Texas at San Antonio Health Science Center, Shenzhen University, Anhui University of Traditional Chinese Medicine, Qinghai University Affiliated Hospital, Shenzhen Sixth People's Hospital, Third Affiliated Hospital of Harbin Medical University, Guangxi University of Chinese Medicine, Zhongnan Hospital of Wuhan University, First Affiliated Hospital of Xi'an Jiaotong University, Peking University First Hospital, Shenzhen University Health Science Center, Shanghai Institute of Quality Inspection and Technical Research, Second Affiliated Hospital of Zhejiang University, Tongji Hospital, Huazhong University of Science and Technology, Zhejiang University, Xi'an Jiaotong University
ORCID: 0000-0003-1819-4475
Observed ORCIDs: 0000-0003-1819-4475, 0000-0003-3202-4368
OpenAlex ID: A5101618624
Modeling Rett Syndrome Using TALEN-Edited MECP2 Mutant Cynomolgus Monkeys
2017 · Yongchang Chen, Juehua Yu, et al. · Cell · 200
Tamoxifen-Bound Estrogen Receptor (ER) Strongly Interacts with the Nuclear Matrix Protein HET/SAF-B, a Novel Inhibitor of ER-Mediated Transactivation
2000 · Steffi Oesterreich, Qingping Zhang, et al. · Molecular Endocrinology · 107
Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome
2019 · Jiaping Wang, Yongxin Wen, et al. · Seizure · 43
Rett and Rett‐like syndrome: Expanding the genetic spectrum to KIF1A and GRIN1 gene
2019 · Jiaping Wang, Qingping Zhang, et al. · Molecular Genetics & Genomic Medicine · 42
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Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese patients
2014 · Ying Zhao, Xiaoying Zhang, et al. · BMC Medical Genetics · 41
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Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort
2018 · Qingping Zhang, Xiaoxu Yang, et al. · Genetics in Medicine · 34
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Selenium nanoparticles reduce glucose metabolism and promote apoptosis of glioma cells through reactive oxygen species-dependent manner
2019 · Binchu Xu, Qingping Zhang, et al. · Neuroreport · 31
Pluronic block copolymers: Novel functions in ultrasound-mediated gene transfer and against cell damage
2005 · Yun-Chao Chen, Hai-Dong Liang, et al. · Ultrasound in Medicine & Biology · 30
Tenascin C Promotes Glioma Cell Malignant Behavior and Inhibits Chemosensitivity to Paclitaxel via Activation of the PI3K/AKT Signaling Pathway
2021 · Qingping Zhang, Binchu Xu, et al. · Journal of Molecular Neuroscience · 28
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Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation
2018 · Jiaping Wang, Qingping Zhang, et al. · BMC Medical Genetics · 27
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The genetic and clinical characteristics of aromatic L-amino acid decarboxylase deficiency in mainland China
2020 · Yongxin Wen, Jiaping Wang, et al. · Journal of Human Genetics · 26
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Microbial Community Succession and Its Correlation with Quality Characteristics during Gray Sufu Fermentation
2023 · Lei Zhao, Yang Liu, et al. · Foods · 22
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Familial cases and male cases with MECP2 mutations
2017 · Qingping Zhang, Ying Zhao, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 22
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CACNA1A Gene Variants in Eight Chinese Patients With a Wide Range of Phenotypes
2020 · Linxia Zhang, Yongxin Wen, et al. · Frontiers in Pediatrics · 21
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Electroacupuncture improves cognitive impairment in diabetic cognitive dysfunction rats by regulating the mitochondrial autophagy pathway
2022 · Xia Ge, Ling Wang, et al. · The Journal of Physiological Sciences · 18
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Clinical and Genetic Heterogeneity in a Cohort of Chinese Children With Dopa-Responsive Dystonia
2020 · Yan Chen, Xinhua Bao, et al. · Frontiers in Pediatrics · 17
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Circ_0048856 competes with ABCC1 for miR-193a-5p/miR-98-5p binding sites to promote the cisplatin resistance and tumorigenesis in lung cancer
2022 · Lingxi Liu, Qingping Zhang, et al. · Journal of Chemotherapy · 13
Both subthalamic and pallidal deep brain stimulation are effective for GNAO1-associated dystonia: three case reports and a literature review
2022 · Ye Liu, Qingping Zhang, et al. · Therapeutic Advances in Neurological Disorders · 12
MECP2 duplication syndrome in a Chinese family
2015 · Qingping Zhang, Ying Zhao, et al. · BMC Medical Genetics · 11
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MECP2 germline mosaicism plays an important part in the inheritance of Rett syndrome: a study of MECP2 germline mosaicism in males
2023 · Yongxin Wen, Jiaping Wang, et al. · BMC Medicine · 10
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MECP2 mutation spectrum and its clinical characteristics in a Chinese cohort
2020 · Yongxin Wen, Jiaping Wang, et al. · Clinical Genetics · 10
Targeting of MALT1 May Improve Functional Recovery and Attenuate Microglia M1 Polarization-Mediated Neuroinflammation During Spinal Cord Injury
2023 · Qingping Zhang, Shitao Zhang, et al. · Molecular Neurobiology · 8
CADD-engineered peptide protacs efficiently target PCSK9 for hypercholesterolemia in vivo
2025 · Gang Fan, Weiming Guo, et al. · Metabolism · 5
Correction: Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort
2019 · Qingping Zhang, Xiaoxu Yang, et al. · Genetics in Medicine · 5
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[Clinical and genetic features of five patients with Allan-Herndon-Dudley syndrome].
2018 · Jiaping Wang, Qingping Zhang, et al. · PubMed · 5
Works count: 55
Citation count: 802
H-index: 16
I10-index: 21
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