Xianqin Zhang - Concepedia

Concepedia

Author

Xianqin Zhang

Huazhong University of Science and Technology ORCID

Also Known As

XIANQIN ZHANG, Xian-Qin ZHANG, Xianqin Zhang

56

Publications

1.8K

Citations

20

H-Index

58

Concepts

All Affiliations

Huazhong University of Science and Technology Tongji Hospital Cleveland Clinic Lerner College of Medicine Case Western Reserve University Southwest Medical University

XZ

About

Xianqin Zhang is an author at Huazhong University of Science and Technology specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	15	1.2K
2	Public Health	7	7	176
3	Cell Biology	2	2	576
4	Immunology	2	2	550
5	Social Sciences	1	1	20

Xianqin Zhang

×

31

Publications

1.8K

Citations

20

H-Index

	Year	Citations
Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation Xianqin Zhang, Dusan Bogunovic, Béatrice Payelle‐Brogard, Nature InflammationCytokineImmunologyChronic InflammationInnate Immunity	2014	539
Mutation in Nuclear Pore Component NUP155 Leads to Atrial Fibrillation and Early Sudden Cardiac Death Xianqin Zhang, Shenghan Chen, Shin Yoo, Cell Cardiac MuscleCardiomyopathyGeneticsMolecular BiologyAtrial Fibrillation	2008	274
MicroRNA-34a targets epithelial to mesenchymal transition-inducing transcription factors (EMT-TFs) and inhibits breast cancer cell migration and invasion Saber İmani, Chunli Wei, Jingliang Cheng, Oncotarget	2017	120
Identification of a New Co-factor, MOG1, Required for the Full Function of Cardiac Sodium Channel Nav1.5 Ling Wu, Sandro L. Yong, Chun‐Po Steve Fan, Journal of Biological Chemistry	2008	93
Genetic identification and molecular modeling characterization reveal a novel<i>PROM1</i>mutation in Stargardt4-like macular dystrophy Saber İmani, Jingliang Cheng, Marzieh Dehghan Shasaltaneh, Oncotarget	2017	53
Novel HSF4 Mutation Causes Congenital Total White Cataract in a Chinese Family Tie Ke, Qing K. Wang, Binchu Ji, American Journal of Ophthalmology Chinese FamilyGenetic DisorderGeneticsGenetic EpidemiologyPathology	2006	51
Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family Qiufen Wang, Mugen Liu, Chunsheng Xu, Journal of Molecular Medicine Chinese FamilyMolecular NeuroscienceGeneticsPhysiologyNovel Cacna1s Mutation	2005	50
Potential Genes Associated with COVID-19 and Comorbidity Shanshan Feng, Fu-Qiang Song, Wenqiong Guo, International Journal of Medical Sciences	2022	42
<i>Tsga10</i> is essential for arrangement of mitochondrial sheath and male fertility in mice Geng Luo, Meiqi Hou, Bo Wang, Andrology	2020	41
A novel DSPPmutation is associated with type II dentinogenesis Imperfecta in a chinese family Xianqin Zhang, Lanying Chen, Jingyu Liu, BMC Medical Genetics	2007	40

Page 1