Guanghong Wu

1.2k total citations
17 papers, 558 citations indexed

About

Guanghong Wu is a scholar working on Nephrology, Molecular Biology and Genetics. According to data from OpenAlex, Guanghong Wu has authored 17 papers receiving a total of 558 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Nephrology, 9 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Guanghong Wu's work include Renal Diseases and Glomerulopathies (13 papers), Genetic and Kidney Cyst Diseases (3 papers) and Renal and related cancers (3 papers). Guanghong Wu is often cited by papers focused on Renal Diseases and Glomerulopathies (13 papers), Genetic and Kidney Cyst Diseases (3 papers) and Renal and related cancers (3 papers). Guanghong Wu collaborates with scholars based in United States, Ireland and United Kingdom. Guanghong Wu's co-authors include Rasheed Gbadegesin, Gentzon Hall, Michelle P. Winn, Alison Homstad, Peter Lavin, David N. Howell, Peter J. Conlon, Matthew A. Sparks, Ruiji Jiang and Andrew F. Malone and has published in prestigious journals such as Journal of Clinical Oncology, Scientific Reports and Biochemical and Biophysical Research Communications.

In The Last Decade

Guanghong Wu

17 papers receiving 556 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Guanghong Wu United States 11 358 277 102 79 78 17 558
Alison Homstad United States 6 287 0.8× 187 0.7× 82 0.8× 76 1.0× 64 0.8× 8 406
Yoshimi Nozu Japan 14 156 0.4× 412 1.5× 41 0.4× 227 2.9× 146 1.9× 21 600
Xue Jun Fu Japan 16 147 0.4× 434 1.6× 45 0.4× 282 3.6× 147 1.9× 22 661
Saori Miwa Japan 9 102 0.3× 265 1.0× 18 0.2× 85 1.1× 44 0.6× 12 462
Irini Tossidou Germany 16 374 1.0× 270 1.0× 28 0.3× 18 0.2× 113 1.4× 18 620
Eva M. Pastor‐Arroyo Switzerland 12 182 0.5× 156 0.6× 32 0.3× 8 0.1× 112 1.4× 15 456
K Shirato Japan 14 80 0.2× 92 0.3× 36 0.4× 29 0.4× 11 0.1× 28 414
Barry Robert United States 11 112 0.3× 439 1.6× 26 0.3× 77 1.0× 50 0.6× 12 627
H Nihei Japan 10 160 0.4× 242 0.9× 28 0.3× 4 0.1× 29 0.4× 17 428
Hyoe Inomata Japan 9 57 0.2× 285 1.0× 26 0.3× 29 0.4× 45 0.6× 11 625

Countries citing papers authored by Guanghong Wu

Since Specialization
Citations

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

Fields of papers citing papers by Guanghong Wu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Guanghong Wu. 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 Guanghong Wu. The network helps show where Guanghong Wu may publish in the future.

Co-authorship network of co-authors of Guanghong Wu

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

All Works

17 of 17 papers shown
1.
2.
Lane, Brandon M., Guanghong Wu, Mohamed Shalaby, et al.. (2021). Steroid-sensitive nephrotic syndrome candidate gene CLVS1 regulates podocyte oxidative stress and endocytosis. JCI Insight. 7(2). 16 indexed citations
3.
Hall, Gentzon, Gloria Michelle Ducasa, Brandon M. Lane, et al.. (2019). FO068The LMX1βR246Q Mutation Induces Podocyte Injury Through Dysregulation of Cholesterol Transport Gene Expression. Nephrology Dialysis Transplantation. 34(Supplement_1). 1 indexed citations
4.
Hall, Gentzon, Brandon M. Lane, Kamal Khan, et al.. (2018). The Human FSGS-Causing ANLN R431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes. Journal of the American Society of Nephrology. 29(8). 2110–2122. 43 indexed citations
5.
Esezobor, Christopher Imokhuede, Guanghong Wu, Brandon M. Lane, et al.. (2018). Genetic Testing for Steroid-Resistant-Nephrotic Syndrome in an Outbred Population. Frontiers in Pediatrics. 6. 307–307. 22 indexed citations
6.
Hall, Gentzon, Brandon M. Lane, Guanghong Wu, et al.. (2017). Dysregulation of WTI (−KTS) is Associated with the Kidney-Specific Effects of the LMX1B R246Q Mutation. Scientific Reports. 7(1). 39933–39933. 7 indexed citations
7.
Homstad, Alison, Gentzon Hall, Guanghong Wu, et al.. (2015). Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux. Pediatric Nephrology. 31(2). 247–253. 11 indexed citations
8.
Malone, Andrew F., Paul J. Phelan, Gentzon Hall, et al.. (2014). Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis. Kidney International. 86(6). 1253–1259. 153 indexed citations
9.
Hall, Gentzon, Rasheed Gbadegesin, Peter Lavin, et al.. (2014). A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS. Journal of the American Society of Nephrology. 26(4). 831–843. 41 indexed citations
10.
Hall, Gentzon, J. G. Rowell, Rasheed Gbadegesin, et al.. (2014). Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity. American Journal of Physiology-Renal Physiology. 306(12). F1442–F1450. 29 indexed citations
11.
Lavin, Peter, Elizabeth Finch, Jarrett Burch, et al.. (2011). TRPC6 Enhances Angiotensin II-induced Albuminuria. Journal of the American Society of Nephrology. 22(3). 526–535. 111 indexed citations
12.
Gbadegesin, Rasheed, Peter Lavin, Gentzon Hall, et al.. (2011). Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis. Kidney International. 81(1). 94–99. 55 indexed citations
13.
Hall, Gentzon, Guanghong Wu, & Michelle P. Winn. (2011). 112 Ang II Induces FAK Activation and Podocyte Migration Via a TRPC6-Dependent Mechanism. American Journal of Kidney Diseases. 57(4). B44–B44. 1 indexed citations
14.
Gbadegesin, Rasheed, Peter Lavin, Bartlomiej Bartkowiak, et al.. (2010). A New Locus for Familial FSGS on Chromosome 2P. Journal of the American Society of Nephrology. 21(8). 1390–1397. 4 indexed citations
15.
Gbadegesin, Rasheed, Bartlomiej Bartkowiak, Peter Lavin, et al.. (2008). Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS. Pediatric Nephrology. 24(2). 281–285. 19 indexed citations
16.
Puranam, Kasturi L., Guanghong Wu, Warren J. Strittmatter, & James R. Burke. (2006). Polyglutamine expansion inhibits respiration by increasing reactive oxygen species in isolated mitochondria. Biochemical and Biophysical Research Communications. 341(2). 607–613. 36 indexed citations
17.
Rich, Jeremy N., Qin Shi, Anita B. Hjelmeland, et al.. (2006). A novel low molecular weight inhibitor of focal adhesion kinase and insulin-like growth factor-1 receptor, TAE226, inhibits glioma growth. Journal of Clinical Oncology. 24(18_suppl). 11505–11505. 2 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Alison Homstad Breakdown of academic impact, for papers by Yoshimi Nozu Breakdown of academic impact, for papers by Xue Jun Fu Breakdown of academic impact, for papers by Saori Miwa Breakdown of academic impact, for papers by Irini Tossidou Breakdown of academic impact, for papers by Eva M. Pastor‐Arroyo Breakdown of academic impact, for papers by K Shirato Breakdown of academic impact, for papers by Barry Robert Breakdown of academic impact, for papers by H Nihei Breakdown of academic impact, for papers by Hyoe Inomata
Rankless by CCL
2026