Chao-Ling Yang

4.4k total citations · 1 hit paper
35 papers, 3.5k citations indexed

About

Chao-Ling Yang is a scholar working on Molecular Biology, Nutrition and Dietetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Chao-Ling Yang has authored 35 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 14 papers in Nutrition and Dietetics and 13 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Chao-Ling Yang's work include Ion Transport and Channel Regulation (33 papers), Ion channel regulation and function (13 papers) and Magnesium in Health and Disease (11 papers). Chao-Ling Yang is often cited by papers focused on Ion Transport and Channel Regulation (33 papers), Ion channel regulation and function (13 papers) and Magnesium in Health and Disease (11 papers). Chao-Ling Yang collaborates with scholars based in United States, Germany and China. Chao-Ling Yang's co-authors include David H. Ellison, James A. McCormick, Andrew S. Terker, Peter S. Aronson, Rose Mitchell, Jordan Angell, Arohan R. Subramanya, Xiaoman Zhu, Chong Zhang and Gerhard Giebisch and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Chao-Ling Yang

35 papers receiving 3.5k citations

Hit Papers

Potassium Modulates Electrolyte Balance and Blood Pressur... 2015 2026 2018 2022 2015 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chao-Ling Yang United States 27 2.8k 1.1k 1.0k 730 513 35 3.5k
Dominique Loffing‐Cueni Switzerland 29 2.2k 0.8× 1.0k 0.9× 604 0.6× 782 1.1× 412 0.8× 53 3.2k
David B. Simon United States 18 4.2k 1.5× 1.4k 1.2× 1.3k 1.2× 997 1.4× 1.0k 2.0× 33 5.6k
Oleh Pochynyuk United States 36 2.1k 0.7× 644 0.6× 445 0.4× 589 0.8× 219 0.4× 89 2.8k
Shyama Masilamani United States 22 2.0k 0.7× 1.1k 1.0× 351 0.3× 855 1.2× 305 0.6× 34 2.4k
Hassane Amlal United States 32 1.8k 0.6× 658 0.6× 237 0.2× 411 0.6× 554 1.1× 65 2.7k
Dao‐Hong Lin United States 30 1.8k 0.6× 668 0.6× 488 0.5× 416 0.6× 161 0.3× 81 2.3k
Ignacio Gíménez Spain 22 1.7k 0.6× 493 0.4× 382 0.4× 256 0.4× 192 0.4× 69 2.3k
Kerstin Richter Germany 20 1.4k 0.5× 443 0.4× 258 0.3× 612 0.8× 350 0.7× 32 2.4k
Olivier Bonny Switzerland 32 1.2k 0.4× 615 0.5× 354 0.3× 364 0.5× 1.0k 2.0× 101 3.0k
Birgitte Mønster Christensen Denmark 26 2.1k 0.7× 1.3k 1.2× 218 0.2× 272 0.4× 261 0.5× 43 2.6k

Countries citing papers authored by Chao-Ling Yang

Since Specialization
Citations

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

Fields of papers citing papers by Chao-Ling Yang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chao-Ling Yang. 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 Chao-Ling Yang. The network helps show where Chao-Ling Yang may publish in the future.

Co-authorship network of co-authors of Chao-Ling Yang

This figure shows the co-authorship network connecting the top 25 collaborators of Chao-Ling Yang. A scholar is included among the top collaborators of Chao-Ling Yang 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 Chao-Ling Yang. Chao-Ling Yang 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.
Mukherjee, Anindit, et al.. (2021). Roles of WNK4 and SPAK in K+-mediated dephosphorylation of the NaCl cotransporter. American Journal of Physiology-Renal Physiology. 320(5). F719–F733. 17 indexed citations
2.
Su, Xiao‐Tong, et al.. (2020). Distal convoluted tubule Clconcentration is modulated via K+channels and transporters. American Journal of Physiology-Renal Physiology. 319(3). F534–F540. 39 indexed citations
3.
Su, Xiao‐Tong, Chao-Ling Yang, & David H. Ellison. (2020). Kidney Is Essential for Blood Pressure Modulation by Dietary Potassium. Current Cardiology Reports. 22(10). 124–124. 8 indexed citations
4.
Swanson, Elizabeth A., Jonathan W. Nelson, Sophia Jeng, et al.. (2019). Salt-sensitive transcriptome of isolated kidney distal tubule cells. Physiological Genomics. 51(4). 125–135. 9 indexed citations
5.
Cornelius, Ryan J., Chao-Ling Yang, & David H. Ellison. (2019). Hypertension-causing cullin 3 mutations disrupt COP9 signalosome binding. American Journal of Physiology-Renal Physiology. 318(1). F204–F208. 12 indexed citations
6.
Cornelius, Ryan J., Catherina A. Cuevas, Jonathan W. Nelson, et al.. (2018). Renal COP9 Signalosome Deficiency Alters CUL3-KLHL3-WNK Signaling Pathway. Journal of the American Society of Nephrology. 29(11). 2627–2640. 20 indexed citations
7.
Cornelius, Ryan J., Chong Zhang, Kayla J. Erspamer, et al.. (2018). Dual gain and loss of cullin 3 function mediates familial hyperkalemic hypertension. American Journal of Physiology-Renal Physiology. 315(4). F1006–F1018. 17 indexed citations
8.
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
9.
Gama, Alejandro Rodríguez, Silvana Bazúa‐Valenti, Norma Vázquez, et al.. (2018). C-terminally truncated, kidney-specific variants of the WNK4 kinase lack several sites that regulate its activity. Journal of Biological Chemistry. 293(31). 12209–12221. 14 indexed citations
10.
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 →
11.
Zhang, Chong, Nicholas P. Meermeier, Andrew S. Terker, et al.. (2015). Degradation by Cullin 3 and effect on WNK kinases suggest a role of KLHL2 in the pathogenesis of Familial Hyperkalemic Hypertension. Biochemical and Biophysical Research Communications. 469(1). 44–48. 16 indexed citations
12.
Terker, Andrew S., Chong Zhang, Kayla J. Erspamer, et al.. (2015). Unique chloride-sensing properties of WNK4 permit the distal nephron to modulate potassium homeostasis. Kidney International. 89(1). 127–134. 203 indexed citations
13.
McCormick, James A., Chao-Ling Yang, Chong Zhang, et al.. (2014). Hyperkalemic hypertension–associated cullin 3 promotes WNK signaling by degrading KLHL3. Journal of Clinical Investigation. 124(11). 4723–4736. 112 indexed citations
14.
Picard, Nicolas, Chao-Ling Yang, R. Lance Miller, et al.. (2013). Protein Phosphatase 1 Inhibitor-1 Deficiency Reduces Phosphorylation of Renal NaCl Cotransporter and Causes Arterial Hypotension. Journal of the American Society of Nephrology. 25(3). 511–522. 65 indexed citations
15.
Hoorn, Ewout J., Stephen B. Walsh, James A. McCormick, et al.. (2011). The calcineurin inhibitor tacrolimus activates the renal sodium chloride cotransporter to cause hypertension. Nature Medicine. 17(10). 1304–1309. 275 indexed citations
16.
Rozansky, David J., Arohan R. Subramanya, Shaunessy Rogers, et al.. (2009). Aldosterone mediates activation of the thiazide-sensitive Na-Cl cotransporter through an SGK1 and WNK4 signaling pathway. Journal of Clinical Investigation. 119(9). 2601–2612. 119 indexed citations
17.
Yang, Chao-Ling, Xuehong Liu, Alexander Paliege, et al.. (2006). WNK1 and WNK4 modulate CFTR activity. Biochemical and Biophysical Research Communications. 353(3). 535–540. 44 indexed citations
18.
Yang, Chao-Ling, Xiaoman Zhu, Juan Wang, Arohan R. Subramanya, & David H. Ellison. (2005). Mechanisms of WNK1 and WNK4 interaction in the regulation of thiazide-sensitive NaCl cotransport. Journal of Clinical Investigation. 115(5). 1379–1387. 139 indexed citations
19.
Subramanya, Arohan R., Chao-Ling Yang, Xiaoman Zhu, & David H. Ellison. (2005). Dominant-negative regulation of WNK1 by its kidney-specific kinase-defective isoform. American Journal of Physiology-Renal Physiology. 290(3). F619–F624. 91 indexed citations
20.
Yang, Chao-Ling, Jordan Angell, Rose Mitchell, & David H. Ellison. (2003). WNK kinases regulate thiazide-sensitive Na-Cl cotransport. Journal of Clinical Investigation. 111(7). 1039–1045. 351 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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