Dao‐Hong Lin

2.8k total citations
81 papers, 2.3k citations indexed

About

Dao‐Hong Lin is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Dao‐Hong Lin has authored 81 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Molecular Biology, 24 papers in Pulmonary and Respiratory Medicine and 13 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Dao‐Hong Lin's work include Ion Transport and Channel Regulation (53 papers), Ion channel regulation and function (42 papers) and Electrolyte and hormonal disorders (17 papers). Dao‐Hong Lin is often cited by papers focused on Ion Transport and Channel Regulation (53 papers), Ion channel regulation and function (42 papers) and Electrolyte and hormonal disorders (17 papers). Dao‐Hong Lin collaborates with scholars based in United States, China and Switzerland. Dao‐Hong Lin's co-authors include Wen‐Hui Wang, Xiao‐Tong Su, Peng Yue, Chengbiao Zhang, Gerhard Giebisch, Hyacinth Sterling, Peng Sun, Peng Wu, Zhong‐Xiuzi Gao and Yuan Wei and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The Journal of Immunology.

In The Last Decade

Dao‐Hong Lin

80 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dao‐Hong Lin United States	30	1.8k	668	488	416	284	81	2.3k
Dominique Loffing‐Cueni Switzerland	29	2.2k 1.2×	1.0k 1.5×	604 1.2×	782 1.9×	182 0.6×	53	3.2k
Hassane Amlal United States	32	1.8k 1.0×	658 1.0×	237 0.5×	411 1.0×	161 0.6×	65	2.7k
Nikola Jeck Germany	23	1.7k 0.9×	504 0.8×	407 0.8×	178 0.4×	353 1.2×	38	2.1k
John J Gildea United States	30	1.6k 0.9×	253 0.4×	294 0.6×	467 1.1×	586 2.1×	80	2.5k
Tengis S. Pavlov United States	23	791 0.4×	192 0.3×	204 0.4×	331 0.8×	194 0.7×	53	1.4k
May Bloch-Faure France	22	1.1k 0.6×	376 0.6×	260 0.5×	542 1.3×	630 2.2×	29	2.1k
Vladislav Levchenko United States	25	941 0.5×	223 0.3×	228 0.5×	305 0.7×	230 0.8×	82	1.7k
Daria V. Ilatovskaya United States	28	1.1k 0.6×	247 0.4×	260 0.5×	343 0.8×	418 1.5×	93	2.2k
Chao-Ling Yang United States	27	2.8k 1.6×	1.1k 1.7×	1.0k 2.1×	730 1.8×	278 1.0×	35	3.5k
J. P. Bonvalet France	33	1.9k 1.0×	864 1.3×	234 0.5×	1.5k 3.7×	391 1.4×	76	3.3k

Countries citing papers authored by Dao‐Hong Lin

Since Specialization

Citations

This map shows the geographic impact of Dao‐Hong Lin'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 Dao‐Hong Lin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dao‐Hong Lin more than expected).

Fields of papers citing papers by Dao‐Hong Lin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dao‐Hong Lin. 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 Dao‐Hong Lin. The network helps show where Dao‐Hong Lin may publish in the future.

Co-authorship network of co-authors of Dao‐Hong Lin

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

All Works

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20 of 20 papers shown

Su, Xiao‐Tong, Susan B. Gurley, Jacqueline Emathinger, et al.. (2023). Role of Angiotensin II Type 1a Receptor (AT1aR) of Renal Tubules in Regulating Inwardly Rectifying Potassium Channels 4.2 (Kir4.2), Kir4.1, and Epithelial Na ⁺ Channel (ENaC). Hypertension. 81(1). 126–137. 3 indexed citations

Ferdaus, Mohammed Z., Anindit Mukherjee, Jonathan W. Nelson, et al.. (2019). Mg ²⁺ restriction downregulates NCC through NEDD4-2 and prevents its activation by hypokalemia. American Journal of Physiology-Renal Physiology. 317(4). F825–F838. 22 indexed citations

Wu, Peng, Zhong‐Xiuzi Gao, Dandan Zhang, et al.. (2019). Deletion of Kir5.1 Impairs Renal Ability to Excrete Potassium during Increased Dietary Potassium Intake. Journal of the American Society of Nephrology. 30(8). 1425–1438. 42 indexed citations

Wu, Peng, Zhong‐Xiuzi Gao, Xiao‐Tong Su, et al.. (2018). Kir4.1/Kir5.1 Activity Is Essential for Dietary Sodium Intake–Induced Modulation of Na-Cl Cotransporter. Journal of the American Society of Nephrology. 30(2). 216–227. 31 indexed citations

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

Waldman, Maayan, Lars Bellner, Luca Vanella, et al.. (2016). Epoxyeicosatrienoic Acids Regulate Adipocyte Differentiation of Mouse 3T3 Cells, Via PGC-1α Activation, Which Is Required for HO-1 Expression and Increased Mitochondrial Function. Stem Cells and Development. 25(14). 1084–1094. 70 indexed citations

Halilovic, Adna, et al.. (2013). HO-2 knockdown delays wound healing in Human Corneal Epithelial (HCE) cells by altering the signaling of EGFR and FAK mediated pathway. Investigative Ophthalmology & Visual Science. 54(15). 2572–2572. 29 indexed citations

Lin, Dao‐Hong, Adna Halilovic, Peng Yue, et al.. (2013). Inhibition of miR-205 Impairs the Wound-Healing Process in Human Corneal Epithelial Cells by Targeting KIR4.1 (KCNJ10). Investigative Ophthalmology & Visual Science. 54(9). 6167–6167. 39 indexed citations

Yue, Peng, Chengbiao Zhang, Dao‐Hong Lin, Peng Sun, & Wen‐Hui Wang. (2013). WNK4 inhibits Ca2+-activated big-conductance potassium channels (BK) via mitogen-activated protein kinase-dependent pathway. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1833(10). 2101–2110. 28 indexed citations

10.

Zhang, Chengbiao, Lijun Wang, Kemeng Wang, et al.. (2013). Src Family Protein Tyrosine Kinase Regulates the Basolateral K Channel in the Distal Convoluted Tubule (DCT) by Phosphorylation of KCNJ10 Protein. Journal of Biological Chemistry. 288(36). 26135–26146. 47 indexed citations

11.

Sun, Peng, Dao‐Hong Lin, Peng Yue, et al.. (2010). High Potassium Intake Enhances the Inhibitory Effect of 11,12-EET on ENaC. Journal of the American Society of Nephrology. 21(10). 1667–1677. 23 indexed citations

12.

Yue, Peng, et al.. (2010). Angiotensin II diminishes the effect of SGK1 on the WNK4-mediated inhibition of ROMK1 channels. Kidney International. 79(4). 423–431. 39 indexed citations

13.

Lin, Dao‐Hong, Peng Yue, Peng Sun, et al.. (2009). POSH Stimulates the Ubiquitination and the Clathrin-independent Endocytosis of ROMK1 Channels. Journal of Biological Chemistry. 284(43). 29614–29624. 26 indexed citations

14.

Wang, Zhiqin, Kesheng Wang, Jie Yang, et al.. (2009). The Novel Lipopolysaccharide-Binding Protein CRISPLD2 Is a Critical Serum Protein to Regulate Endotoxin Function. The Journal of Immunology. 183(10). 6646–6656. 49 indexed citations

15.

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

16.

Zhang, Xin, Dao‐Hong Lin, Yan Jin, et al.. (2007). Inhibitor of growth 4 (ING4) is up-regulated by a low K intake and suppresses renal outer medullary K channels (ROMK) by MAPK stimulation. Proceedings of the National Academy of Sciences. 104(22). 9517–9522. 8 indexed citations

17.

Babilonia, Elisa, Zhijian Wang, Peng Sun, et al.. (2006). Mitogen-Activated Protein Kinases Inhibit the ROMK (Kir 1.1)-Like Small Conductance K Channels in the Cortical Collecting Duct. Journal of the American Society of Nephrology. 17(10). 2687–2696. 41 indexed citations

18.

Wei, Yuan, Dao‐Hong Lin, Rowena Kemp, et al.. (2004). Arachidonic Acid Inhibits Epithelial Na Channel Via Cytochrome P450 (CYP) Epoxygenase-dependent Metabolic Pathways. The Journal of General Physiology. 124(6). 719–727. 85 indexed citations

19.

Sterling, Hyacinth, Dao‐Hong Lin, Yu-Jung Chen, et al.. (2004). PKC expression is regulated by dietary K intake and mediates internalization of SK channels in the CCD. American Journal of Physiology-Renal Physiology. 286(6). F1072–F1078. 18 indexed citations

20.

Lin, Dao‐Hong, Hyacinth Sterling, Baofeng Yang, et al.. (2004). Protein tyrosine kinase is expressed and regulates ROMK1 location in the cortical collecting duct. American Journal of Physiology-Renal Physiology. 286(5). F881–F892. 54 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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