Raghavan Madhavan

1.1k total citations
22 papers, 938 citations indexed

About

Raghavan Madhavan is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Raghavan Madhavan has authored 22 papers receiving a total of 938 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 11 papers in Cellular and Molecular Neuroscience and 8 papers in Cell Biology. Recurrent topics in Raghavan Madhavan's work include Ion channel regulation and function (8 papers), Muscle Physiology and Disorders (6 papers) and Axon Guidance and Neuronal Signaling (6 papers). Raghavan Madhavan is often cited by papers focused on Ion channel regulation and function (8 papers), Muscle Physiology and Disorders (6 papers) and Axon Guidance and Neuronal Signaling (6 papers). Raghavan Madhavan collaborates with scholars based in Hong Kong, United States and Switzerland. Raghavan Madhavan's co-authors include Robert Sealock, Harry W. Jarrett, Stanley C. Froehner, S. Rock Levinson, John H. Caldwell, Stephen Gee, H. Benjamin Peng, Morgan Sheng, Michael Wyszynski and Jerry Lin and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Raghavan Madhavan

21 papers receiving 928 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Raghavan Madhavan Hong Kong 14 773 379 197 166 132 22 938
Pompeo Macioce Italy 14 457 0.6× 122 0.3× 250 1.3× 133 0.8× 57 0.4× 27 627
Kenzo Hamano Japan 11 720 0.9× 261 0.7× 105 0.5× 101 0.6× 71 0.5× 23 1.0k
Masaji Tachikawa Japan 9 391 0.5× 197 0.5× 91 0.5× 70 0.4× 33 0.3× 13 547
Veit Witzemann Germany 12 570 0.7× 324 0.9× 78 0.4× 60 0.4× 55 0.4× 14 693
Luigi Sforna Italy 18 531 0.7× 232 0.6× 52 0.3× 127 0.8× 102 0.8× 33 829
Maureen G. Price United States 16 671 0.9× 209 0.6× 336 1.7× 39 0.2× 264 2.0× 19 947
Mariana C. Rocha United Kingdom 13 700 0.9× 227 0.6× 45 0.2× 110 0.7× 36 0.3× 24 942
Andrea M. Gomez United States 8 531 0.7× 298 0.8× 187 0.9× 71 0.4× 17 0.1× 8 863
Edwin B. George United States 13 362 0.5× 430 1.1× 101 0.5× 59 0.4× 15 0.1× 25 841
Chien-Ping Ko United States 12 459 0.6× 430 1.1× 88 0.4× 46 0.3× 19 0.1× 12 788

Countries citing papers authored by Raghavan Madhavan

Since Specialization
Citations

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

Fields of papers citing papers by Raghavan Madhavan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raghavan Madhavan

This figure shows the co-authorship network connecting the top 25 collaborators of Raghavan Madhavan. A scholar is included among the top collaborators of Raghavan Madhavan 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 Raghavan Madhavan. Raghavan Madhavan 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, Cheng, et al.. (2012). The function of p120 catenin in filopodial growth and synaptic vesicle clustering in neurons. Molecular Biology of the Cell. 23(14). 2680–2691. 5 indexed citations
3.
Madhavan, Raghavan, et al.. (2012). Differential regulation of axonal growth and neuromuscular junction assembly by HGF/c‐Met signaling. Developmental Dynamics. 241(10). 1562–1574. 7 indexed citations
4.
Meng, Min, et al.. (2012). Reciprocal Regulation of Axonal Filopodia and Outgrowth during Neuromuscular Junction Development. PLoS ONE. 7(9). e44759–e44759. 9 indexed citations
5.
Chen, Cheng, et al.. (2011). Axonal filopodial asymmetry induced by synaptic target. Molecular Biology of the Cell. 22(14). 2480–2490. 13 indexed citations
6.
Madhavan, Raghavan, et al.. (2009). The Function of Cortactin in the Clustering of Acetylcholine Receptors at the Vertebrate Neuromuscular Junction. PLoS ONE. 4(12). e8478–e8478. 28 indexed citations
7.
Geng, Lin, et al.. (2008). Transmembrane mechanisms in the assembly of the postsynaptic apparatus at the neuromuscular junction. Chemico-Biological Interactions. 175(1-3). 108–112. 10 indexed citations
8.
Madhavan, Raghavan, et al.. (2008). The function of Shp2 tyrosine phosphatase in the dispersal of acetylcholine receptor clusters. BMC Neuroscience. 9(1). 70–70. 18 indexed citations
9.
Madhavan, Raghavan, et al.. (2007). Regulation of ACh receptor clustering by the tyrosine phosphatase Shp2. Developmental Neurobiology. 67(13). 1789–1801. 14 indexed citations
10.
Madhavan, Raghavan, et al.. (2006). Involvement of p120 catenin in myopodial assembly and nerve–muscle synapse formation. Journal of Neurobiology. 66(13). 1511–1527. 10 indexed citations
11.
Madhavan, Raghavan & Haixin Peng. (2005). Molecular regulation of postsynaptic differentiation at the neuromuscular junction. IUBMB Life. 57(11). 719–730. 31 indexed citations
12.
Madhavan, Raghavan & H. Benjamin Peng. (2005). HGF induction of postsynaptic specializations at the neuromuscular junction. Journal of Neurobiology. 66(2). 134–147. 13 indexed citations
13.
Madhavan, Raghavan, et al.. (2004). Tyrosine phosphatase regulation of MuSK-dependent acetylcholine receptor clustering. Molecular and Cellular Neuroscience. 28(3). 403–416. 36 indexed citations
14.
Madhavan, Raghavan & H. Benjamin Peng. (2003). A synaptic balancing act: Local and global signaling in the clustering of ACh receptors at vertebrate neuromuscular junctions. Journal of Neurocytology. 32(5-8). 685–696. 13 indexed citations
15.
Madhavan, Raghavan. (2003). The involvement of calcineurin in acetylcholine receptor redistribution in muscle. Molecular and Cellular Neuroscience. 23(4). 587–599. 11 indexed citations
16.
Madhavan, Raghavan & Harry W. Jarrett. (1999). Phosphorylation of dystrophin and α-syntrophin by Ca2+-calmodulin dependent protein kinase II. Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 1434(2). 260–274. 28 indexed citations
17.
Gee, Stephen, Raghavan Madhavan, S. Rock Levinson, et al.. (1998). Interaction of Muscle and Brain Sodium Channels with Multiple Members of the Syntrophin Family of Dystrophin-Associated Proteins. Journal of Neuroscience. 18(1). 128–137. 297 indexed citations
18.
Madhavan, Raghavan & Harry W. Jarrett. (1995). Interactions between dystrophin glycoprotein complex proteins. Biochemistry. 34(38). 12204–12209. 25 indexed citations
19.
Madhavan, Raghavan & Harry W. Jarrett. (1994). Calmodulin-Activated Phosphorylation of Dystrophin. Biochemistry. 33(19). 5797–5804. 32 indexed citations
20.
Madhavan, Raghavan, et al.. (1992). Calmodulin specifically binds three proteins of the dystrophin-glycoprotein complex. Biochemical and Biophysical Research Communications. 185(2). 753–759. 40 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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