Tie Ke

1.8k total citations
35 papers, 913 citations indexed

About

Tie Ke is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology. According to data from OpenAlex, Tie Ke has authored 35 papers receiving a total of 913 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 8 papers in Cardiology and Cardiovascular Medicine and 4 papers in Cell Biology. Recurrent topics in Tie Ke's work include Cardiac electrophysiology and arrhythmias (7 papers), Connexins and lens biology (7 papers) and Ion channel regulation and function (6 papers). Tie Ke is often cited by papers focused on Cardiac electrophysiology and arrhythmias (7 papers), Connexins and lens biology (7 papers) and Ion channel regulation and function (6 papers). Tie Ke collaborates with scholars based in China, United States and Germany. Tie Ke's co-authors include Qing K. Wang, Qiuyun Chen, Xianqin Zhang, Mugen Liu, Sandro L. Yong, Shin Yoo, Zhaohui Tang, C Oberti, Lejin Wang and Shenghan Chen and has published in prestigious journals such as Cell, Journal of Biological Chemistry and The FASEB Journal.

In The Last Decade

Tie Ke

34 papers receiving 907 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Tie Ke China 16 704 258 117 89 64 35 913
Belaïd Sekkali Belgium 15 603 0.9× 145 0.6× 111 0.9× 48 0.5× 36 0.6× 21 854
Steve Catarino Portugal 15 656 0.9× 101 0.4× 40 0.3× 106 1.2× 20 0.3× 24 805
Elżbieta Ciara Poland 17 647 0.9× 48 0.2× 278 2.4× 50 0.6× 27 0.4× 88 1.1k
Patrick G. Burgon Canada 20 748 1.1× 418 1.6× 127 1.1× 60 0.7× 42 0.7× 36 1.2k
Jiaxiang Qu United States 9 431 0.6× 281 1.1× 64 0.5× 20 0.2× 28 0.4× 11 660
Almundher Al‐Maawali Oman 14 312 0.4× 65 0.3× 142 1.2× 47 0.5× 62 1.0× 55 605
David Merrick United States 9 506 0.7× 82 0.3× 388 3.3× 47 0.5× 19 0.3× 14 925
Harry Holzmüller Germany 10 324 0.5× 48 0.2× 115 1.0× 91 1.0× 79 1.2× 11 595
Danila Ivanov Switzerland 11 465 0.7× 56 0.2× 36 0.3× 56 0.6× 57 0.9× 14 722
Gaynor Miller United Kingdom 15 380 0.5× 162 0.6× 77 0.7× 42 0.5× 57 0.9× 20 700

Countries citing papers authored by Tie Ke

Since Specialization
Citations

This map shows the geographic impact of Tie Ke's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Tie Ke with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tie Ke more than expected).

Fields of papers citing papers by Tie Ke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tie Ke. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Tie Ke. The network helps show where Tie Ke may publish in the future.

Co-authorship network of co-authors of Tie Ke

This figure shows the co-authorship network connecting the top 25 collaborators of Tie Ke. A scholar is included among the top collaborators of Tie Ke based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Tie Ke. Tie Ke is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Chen, Fang, Pengxia Wang, Yu Dong, et al.. (2022). Genome-Wide Association Study for Idiopathic Ventricular Tachyarrhythmias Identifies Key Role of CCR7 and PKN2 in Calcium Homeostasis and Cardiac Rhythm Maintenance. Circulation Genomic and Precision Medicine. 15(5). e003603–e003603. 5 indexed citations
3.
Zhao, Miao, Lina Liang, Qixue Song, et al.. (2022). Mog1 deficiency promotes cardiac contractile dysfunction and isoproterenol-induced arrhythmias associated with cardiac fibrosis and Cx43 remodeling. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1868(9). 166429–166429. 3 indexed citations
4.
Zhao, Yuanyuan, Mengchen Zhou, Mengru Wang, et al.. (2022). KCNMA1 promotes obesity-related hypertension: Integrated analysis based on genome-wide association studies. Genes & Diseases. 10(1). 58–61. 1 indexed citations
5.
Bai, Xuemei, Quan Zhuang, Yu Dong, et al.. (2021). Mechanistic insights into the interaction of cardiac sodium channel Nav1.5 with MOG1 and a new molecular mechanism for Brugada syndrome. Heart Rhythm. 19(3). 478–489. 8 indexed citations
6.
Luo, Chunyan, Fan Wang, Xiang Ren, et al.. (2017). Identification of a molecular signaling gene-gene regulatory network between GWAS susceptibility genes ADTRP and MIA3/TANGO1 for coronary artery disease. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1863(6). 1640–1653. 28 indexed citations
7.
Ke, Tie, Miao Zhao, Qing K. Wang, et al.. (2016). Alpha-actin-2 mutations in Chinese patients with a non-syndromatic thoracic aortic aneurysm. BMC Medical Genetics. 17(1). 45–45. 8 indexed citations
8.
Zhan, Ting, et al.. (2014). Increased expression of RRM2 by human papillomavirus E7 oncoprotein promotes angiogenesis in cervical cancer. British Journal of Cancer. 110(4). 1034–1044. 84 indexed citations
9.
Cui, Xiukun, Lei Wang, Jing Zhang, et al.. (2013). HSF4 regulates DLAD expression and promotes lens de-nucleation. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1832(8). 1167–1172. 41 indexed citations
10.
Cui, Xiukun, Jing Zhang, Lei Wang, et al.. (2012). HSF4 is involved in DNA damage repair through regulation of Rad51. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822(8). 1308–1315. 26 indexed citations
11.
Yang, Guohua, Shan Zhong, Xianrong Zhang, et al.. (2010). Molecular genetic analysis of autosomal dominant late-onset cataract in a Chinese Family. Journal of Huazhong University of Science and Technology [Medical Sciences]. 30(6). 792–797. 2 indexed citations
12.
Fan, Chun‐Po Steve, Ping Ouyang, Ayse Anil Timur, et al.. (2009). Novel Roles of GATA1 in Regulation of Angiogenic Factor AGGF1 and Endothelial Cell Function. Journal of Biological Chemistry. 284(35). 23331–23343. 48 indexed citations
13.
Ke, Tie, et al.. (2009). Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family. Journal of Human Genetics. 54(11). 660–664. 35 indexed citations
14.
Ke, Tie, et al.. (2008). [Two variants in MYOC and CYP1B1 genes in a Chinese family with primary angle-closure glaucoma].. PubMed. 25(5). 493–6. 14 indexed citations
15.
Li, Hui, Chang Li, Qiulun Lu, et al.. (2008). Cataract mutation P20S of αB-crystallin impairs chaperone activity of αA-crystallin and induces apoptosis of human lens epithelial cells. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1782(5). 303–309. 29 indexed citations
16.
Wu, Ling, Sandro L. Yong, Chun‐Po Steve Fan, et al.. (2008). Identification of a New Co-factor, MOG1, Required for the Full Function of Cardiac Sodium Channel Nav1.5. Journal of Biological Chemistry. 283(11). 6968–6978. 68 indexed citations
17.
Zhang, Xianqin, Shenghan Chen, Shin Yoo, et al.. (2008). Mutation in Nuclear Pore Component NUP155 Leads to Atrial Fibrillation and Early Sudden Cardiac Death. Cell. 135(6). 1017–1027. 210 indexed citations
18.
Ke, Tie, Qing K. Wang, Xu Wang, et al.. (2006). Novel HSF4 Mutation Causes Congenital Total White Cataract in a Chinese Family. American Journal of Ophthalmology. 142(2). 298–303.e2. 46 indexed citations
19.
Huang, Changzheng, Qinbo Yang, Tie Ke, et al.. (2006). A novel de novo frame-shift mutation of the EDA gene in a Chinese Han family with hypohidrotic ectodermal dysplasia. Journal of Human Genetics. 51(12). 1133–1137. 18 indexed citations
20.
Wang, Qiufen, Mugen Liu, Chunsheng Xu, et al.. (2005). Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family. Journal of Molecular Medicine. 83(3). 203–208. 42 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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