Wen-Hui Wang

1.0k total citations · 1 hit paper
11 papers, 793 citations indexed

About

Wen-Hui Wang is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Wen-Hui Wang has authored 11 papers receiving a total of 793 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 2 papers in Cardiology and Cardiovascular Medicine and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Wen-Hui Wang's work include Ion Transport and Channel Regulation (7 papers), Ion channel regulation and function (5 papers) and Nitric Oxide and Endothelin Effects (2 papers). Wen-Hui Wang is often cited by papers focused on Ion Transport and Channel Regulation (7 papers), Ion channel regulation and function (5 papers) and Nitric Oxide and Endothelin Effects (2 papers). Wen-Hui Wang collaborates with scholars based in United States, China and France. Wen-Hui Wang's co-authors include David H. Ellison, Chao-Ling Yang, James A. McCormick, Xiao‐Tong Su, Andrew S. Terker, Dao‐Hong Lin, Catherina A. Cuevas, Chong Zhang, Hae J. Park and David Cohen and has published in prestigious journals such as Journal of Biological Chemistry, Cell Metabolism and Kidney International.

In The Last Decade

Wen-Hui Wang

11 papers receiving 788 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Potassium Modulates Electrolyte Balance and Blood Pressure through Effects on Distal Cell Voltage and Chloride

2015 348 citations Andrew S. Terker, Chong Zhang et al. Cell Metabolism profile →

Peers

Wen-Hui Wang

MB

PRM

ND

EDM

NEPHR

Rebecca Lazelle United States

Antonio Morey Molina Spain

María Chávez‐Canales Mexico

Nicole Schulz Switzerland

Iva Dostanic‐Larson United States

Bernadette Wallendorff Canada

A. Gairard France

Denisha Spires United States

Stephanie M. Busque Switzerland

Lucília M. A. Lessa Brazil

Rebecca Lazelle United States

Wen-Hui Wang

415 ×0.7

MB

230 ×0.7

PRM

198 ×0.7

ND

141 ×0.9

EDM

112 ×0.8

NEPHR

Citations per year, relative to Wen-Hui Wang Wen-Hui Wang (= 1×) peers Rebecca Lazelle

Countries citing papers authored by Wen-Hui Wang

Since Specialization

Citations

This map shows the geographic impact of Wen-Hui Wang'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 Wen-Hui Wang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wen-Hui Wang more than expected).

Fields of papers citing papers by Wen-Hui Wang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wen-Hui Wang. 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 Wen-Hui Wang. The network helps show where Wen-Hui Wang may publish in the future.

Co-authorship network of co-authors of Wen-Hui Wang

This figure shows the co-authorship network connecting the top 25 collaborators of Wen-Hui Wang. A scholar is included among the top collaborators of Wen-Hui Wang 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 Wen-Hui Wang. Wen-Hui Wang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

1.

Su, Xiao‐Tong, et al.. (2020). Distal convoluted tubule Cl⁻concentration is modulated via K⁺channels and transporters. American Journal of Physiology-Renal Physiology. 319(3). F534–F540. 39 indexed citations

2.

Zhang, Xiaoyu, Jing Guo, Xin Wan, et al.. (2020). Biochemical and antigenic characterization of the structural proteins and their post-translational modifications in purified SARS-CoV-2 virions of an inactivated vaccine candidate. Emerging Microbes & Infections. 9(1). 2653–2662. 13 indexed citations

3.

Su, Xiao‐Tong, David H. Ellison, & Wen-Hui Wang. (2019). Kir4.1/Kir5.1 in the DCT plays a role in the regulation of renal K⁺excretion. American Journal of Physiology-Renal Physiology. 316(3). F582–F586. 44 indexed citations

4.

Cuevas, Catherina A., Xiao‐Tong Su, Peng Wu, et al.. (2018). Potassium intake modulates the thiazide-sensitive sodium-chloride cotransporter (NCC) activity via the Kir4.1 potassium channel. Kidney International. 93(4). 893–902. 114 indexed citations

5.

Wu, Peng, Zhong‐Xiuzi Gao, Xiao‐Tong Su, et al.. (2018). Role of WNK4 and kidney-specific WNK1 in mediating the effect of high dietary K⁺ intake on ROMK channel in the distal convoluted tubule. American Journal of Physiology-Renal Physiology. 315(2). F223–F230. 19 indexed citations

6.

García, Víctor, Ankit Gilani, Frank Fan Zhang, et al.. (2017). The Blood Pressure–Lowering Effect of 20-HETE Blockade in Cyp4a14(−/−) Mice Is Associated with Natriuresis. Journal of Pharmacology and Experimental Therapeutics. 363(3). 412–418. 12 indexed citations

7.

Cuevas, Catherina A., Xiao‐Tong Su, Andrew S. Terker, et al.. (2017). Potassium Sensing by Renal Distal Tubules Requires Kir4.1. Journal of the American Society of Nephrology. 28(6). 1814–1825. 132 indexed citations

8.

Terker, Andrew S., Chong Zhang, James A. McCormick, et al.. (2015). Potassium Modulates Electrolyte Balance and Blood Pressure through Effects on Distal Cell Voltage and Chloride. Cell Metabolism. 21(1). 39–50. 348 indexed citations breakdown →

9.

Lin, Dao‐Hong, Erik-Jan Kamsteeg, Yan Zhang, et al.. (2008). Expression of Tetraspan Protein CD63 Activates Protein-tyrosine Kinase (PTK) and Enhances the PTK-induced Inhibition of ROMK Channels. Journal of Biological Chemistry. 283(12). 7674–7681. 21 indexed citations

10.

Lin, Dao‐Hong, Hyacinth Sterling, Kenneth M. Lerea, et al.. (2002). K depletion increases protein tyrosine kinase-mediated phosphorylation of ROMK. American Journal of Physiology-Renal Physiology. 283(4). F671–F677. 39 indexed citations

11.

Ali, Shariq, Yuan Wei, Kenneth M. Lerea, et al.. (2001). PKA-Induced Stimulation of ROMK1 Channel Activity is Governed by Both Tethering and Non-Tethering Domains of an A Kinase Anchor Protein. Cellular Physiology and Biochemistry. 11(3). 135–142. 12 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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