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Xianqin Zhang

Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation
2014 · Xianqin Zhang, Dusan Bogunovic, et al. · Nature · 574
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Mutation in Nuclear Pore Component NUP155 Leads to Atrial Fibrillation and Early Sudden Cardiac Death
2008 · Xianqin Zhang, Shenghan Chen, et al. · Cell · 285
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MicroRNA-34a targets epithelial to mesenchymal transition-inducing transcription factors (EMT-TFs) and inhibits breast cancer cell migration and invasion
2017 · Saber Imani, Chunli Wei, et al. · Oncotarget · 125
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Identification of a New Co-factor, MOG1, Required for the Full Function of Cardiac Sodium Channel Nav1.5
2008 · Ling Wu, Sandro L. Yong, et al. · Journal of Biological Chemistry · 100
Novel HSF4 Mutation Causes Congenital Total White Cataract in a Chinese Family
2006 · Tie Ke, Qing K. Wang, et al. · American Journal of Ophthalmology · 54
Genetic identification and molecular modeling characterization reveal a novelPROM1mutation in Stargardt4-like macular dystrophy
2017 · Saber Imani, Jingliang Cheng, et al. · Oncotarget · 51
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Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family
2005 · Qiufen Wang, Mugen Liu, et al. · Journal of Molecular Medicine · 50
Potential Genes Associated with COVID-19 and Comorbidity
2022 · Shanshan Feng, Fuqiang Song, et al. · International Journal of Medical Sciences · 44
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A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formation
2020 · Dazhi Zhang, Lixia Zhu, et al. · Journal of Assisted Reproduction and Genetics · 42
Novel mutations in ZP1 and ZP2 cause primary infertility due to empty follicle syndrome and abnormal zona pellucida
2020 · Geng Luo, Lixia Zhu, et al. · Journal of Assisted Reproduction and Genetics · 41
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A novel DSPPmutation is associated with type II dentinogenesis Imperfecta in a chinese family
2007 · Xianqin Zhang, Lanying Chen, et al. · BMC Medical Genetics · 40
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Tsga10 is essential for arrangement of mitochondrial sheath and male fertility in mice
2020 · Geng Luo, Meiqi Hou, et al. · Andrology · 39
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Novel homozygous mutations in PATL2 lead to female infertility with oocyte maturation arrest
2020 · Zhenxing Liu, Lixia Zhu, et al. · Journal of Assisted Reproduction and Genetics · 39
Novel compound heterozygous mutations in WEE2 causes female infertility and fertilization failure
2019 · Xiaopei Zhou, Lixia Zhu, et al. · Journal of Assisted Reproduction and Genetics · 38
Bacterial metabolites directly modulate farnesoid X receptor activity
2015 · Xianqin Zhang, Toshifumi Osaka, et al. · Nutrition & Metabolism · 36
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A novel RAB7 mutation in a Chinese family with Charcot–Marie–Tooth type 2B disease
2013 · Xing Wang, Chunmao Han, et al. · Gene · 36
Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2mutations
2008 · Xianqin Zhang, Shenghan Chen, et al. · BMC Medical Genetics · 24
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TUBB8 Mutations Cause Female Infertility with Large Polar Body Oocyte and Fertilization Failure
2021 · Zhenxing Liu, Qingsong Xi, et al. · Reproductive Sciences · 23
A novel donor splice-site mutation of major intrinsic protein gene associated with congenital cataract in a Chinese family.
2013 · Lu Zeng, Wenqiang Liu, et al. · Europe PMC (PubMed Central) · 23
A Mettl16/m6A/mybl2b/Igf2bp1 axis ensures cell cycle progression of embryonic hematopoietic stem and progenitor cells
2024 · Yunqiao Han, Kui Sun, et al. · The EMBO Journal · 21
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Novel mutations in ZP2 and ZP3 cause female infertility in three patients
2022 · Weimin Jia, Qingsong Xi, et al. · Journal of Assisted Reproduction and Genetics · 21
Deficiency of SCAMP5 leads to pediatric epilepsy and dysregulation of neurotransmitter release in the brain
2020 · Dazhi Zhang, Chao Yuan, et al. · Human Genetics · 21
Genetic analysis of Penthorum chinense Pursh by improved RAPD and ISSR in China
2017 · Zhiqiang Mei, Xianqin Zhang, et al. · Electronic Journal of Biotechnology · 21
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A novel homozygous mutation in ACTL7A leads to male infertility
2022 · Xiaopei Zhou, Qingsong Xi, et al. · Molecular Genetics and Genomics · 20
Actl7a deficiency in mice leads to male infertility and fertilization failure
2022 · Xiaopei Zhou, Zhenxing Liu, et al. · Biochemical and Biophysical Research Communications · 17
Works count: 56
Citation count: 1,954
H-index: 21
I10-index: 31
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