Medha Gautam

3.1k total citations · 1 hit paper
19 papers, 2.5k citations indexed

About

Medha Gautam is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Biomedical Engineering. According to data from OpenAlex, Medha Gautam has authored 19 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 4 papers in Biomedical Engineering. Recurrent topics in Medha Gautam's work include Ion channel regulation and function (8 papers), Muscle Physiology and Disorders (5 papers) and Neurobiology and Insect Physiology Research (5 papers). Medha Gautam is often cited by papers focused on Ion channel regulation and function (8 papers), Muscle Physiology and Disorders (5 papers) and Neurobiology and Insect Physiology Research (5 papers). Medha Gautam collaborates with scholars based in United States, Australia and Bulgaria. Medha Gautam's co-authors include John P. Merlie, Peter G. Noakes, Joshua R. Sanes, Jacqueline L. Mudd, Lisa M. Moscoso, Joshua R. Sanes, Fabio Rupp, Richard H. Scheller, Gerald C. Chu and Mia C. Nichol and has published in prestigious journals such as Nature, Cell and Journal of Biological Chemistry.

In The Last Decade

Medha Gautam

19 papers receiving 2.5k citations

Hit Papers

Defective Neuromuscular S... 1996 2026 2006 2016 1996 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Medha Gautam United States 14 1.8k 990 720 371 255 19 2.5k
Fumiaki Saito Japan 22 2.3k 1.3× 864 0.9× 644 0.9× 270 0.7× 116 0.5× 54 3.0k
Nathalie Lamarche‐Vane Canada 29 1.9k 1.1× 713 0.7× 1.2k 1.7× 260 0.7× 42 0.2× 57 2.8k
Alfredo Brusco Italy 32 2.2k 1.2× 859 0.9× 188 0.3× 135 0.4× 355 1.4× 141 3.3k
Fabio Rupp United States 24 1.8k 1.0× 1.1k 1.1× 691 1.0× 172 0.5× 147 0.6× 29 3.0k
David R. Gies United States 14 1.3k 0.7× 1.2k 1.3× 334 0.5× 67 0.2× 204 0.8× 16 2.4k
Teresia Osborn United States 15 1.3k 0.7× 671 0.7× 372 0.5× 59 0.2× 311 1.2× 18 1.9k
Werner Hoch Germany 26 2.0k 1.1× 1.4k 1.4× 632 0.9× 81 0.2× 1.1k 4.4× 36 3.3k
N.V. Tomilin Russia 21 2.0k 1.1× 919 0.9× 726 1.0× 53 0.1× 112 0.4× 62 3.2k
Betty P. Liu United States 14 1.3k 0.7× 1.5k 1.6× 941 1.3× 247 0.7× 65 0.3× 14 2.9k
S. Carbonetto Canada 25 1.6k 0.9× 1.0k 1.0× 790 1.1× 886 2.4× 81 0.3× 37 2.8k

Countries citing papers authored by Medha Gautam

Since Specialization
Citations

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

Fields of papers citing papers by Medha Gautam

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Medha Gautam

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

All Works

19 of 19 papers shown
1.
Gautam, Medha, et al.. (2015). Corticotropin releasing factor receptor expression in painful human dental pulp. Archives of Oral Biology. 60(7). 1048–1053. 2 indexed citations
2.
Gautam, Medha, et al.. (2014). Physiology Education in North American Dental Schools: The Basic Science Survey Series. Journal of Dental Education. 78(6). 886–894. 8 indexed citations
3.
Gautam, Medha, et al.. (2013). Pharmacology Education in North American Dental Schools: The Basic Science Survey Series. Journal of Dental Education. 77(8). 1013–1021. 13 indexed citations
4.
Rowland, Kevin, et al.. (2011). Tooth injury increases expression of the cold sensitive TRP channel TRPA1 in trigeminal neurons. Archives of Oral Biology. 56(12). 1604–1609. 41 indexed citations
5.
Gautam, Medha, et al.. (2005). Multiple alternatively spliced transcripts of the receptor tyrosine kinase MuSK are expressed in muscle. Gene. 360(2). 83–91. 4 indexed citations
6.
Gautam, Medha, et al.. (2005). Deletion of N-terminal rapsyn domains disrupts clustering and has dominant negative effects on clustering of full-length rapsyn. Neuroscience. 131(3). 661–670. 17 indexed citations
7.
Mathias, Askale, et al.. (1999). Metabolic Stabilization of Muscle Nicotinic Acetylcholine Receptor by Rapsyn. Journal of Neuroscience. 19(6). 1998–2007. 38 indexed citations
8.
Gautam, Medha, Thomas M. DeChiara, David J. Glass, George D. Yancopoulos, & Joshua R. Sanes. (1999). Distinct phenotypes of mutant mice lacking agrin, MuSK, or rapsyn. Developmental Brain Research. 114(2). 171–178. 74 indexed citations
9.
Fuhrer, Christian, Medha Gautam, Janice E. Sugiyama, & Zach W. Hall. (1999). Roles of Rapsyn and Agrin in Interaction of Postsynaptic Proteins with Acetylcholine Receptors. Journal of Neuroscience. 19(15). 6405–6416. 85 indexed citations
10.
Sanes, Joshua R., Elizabeth D. Apel, Medha Gautam, et al.. (1998). Agrin Receptors at the Skeletal Neuromuscular Junction. Annals of the New York Academy of Sciences. 841(1). 1–13. 26 indexed citations
11.
Gautam, Medha, Peter G. Noakes, Lisa M. Moscoso, et al.. (1996). Defective Neuromuscular Synaptogenesis in Agrin-Deficient Mutant Mice. Cell. 85(4). 525–535. 768 indexed citations breakdown →
12.
Durkin, Marian E., Medha Gautam, Frosty Loechel, et al.. (1996). Structural Organization of the Human and Mouse Laminin β2 Chain Genes, and Alternative Splicing at the 5′ End of the Human Transcript. Journal of Biological Chemistry. 271(23). 13407–13416. 24 indexed citations
13.
Moscoso, Lisa M., Gerald C. Chu, Medha Gautam, et al.. (1995). Synapse-Associated Expression of an Acetylcholine Receptor-Inducing Protein, ARIA/Heregulin, and Its Putative Receptors, ErbB2 and ErbB3, in Developing Mammalian Muscle. Developmental Biology. 172(1). 158–169. 160 indexed citations
14.
Gautam, Medha, Peter G. Noakes, Jacqueline L. Mudd, et al.. (1995). Failure of postsynaptic specialization to develop at neuromuscular junctions of rapsyn-deficient mice. Nature. 377(6546). 232–236. 450 indexed citations
15.
Noakes, Peter G., Medha Gautam, Jacqueline L. Mudd, Joshua R. Sanes, & John P. Merlie. (1995). Aberrant differentiation of neuromuscular junctions in mice lacking s-laminin/laminin β2. Nature. 374(6519). 258–262. 377 indexed citations
16.
Noakes, Peter G., Jeffrey H. Miner, Medha Gautam, et al.. (1995). The renal glomerulus of mice lacking s–laminin/laminin β2: nephrosis despite molecular compensation by laminin β1. Nature Genetics. 10(4). 400–406. 314 indexed citations
17.
Gautam, Medha, Jacqueline L. Mudd, Neal G. Copeland, et al.. (1994). Characterization and Mapping of the Rapsn Gene Encoding the 43-kDa Acetylcholine Receptor-Associated Protein. Genomics. 24(2). 366–369. 6 indexed citations
18.
Gautam, Medha & Mark A. Tanouye. (1990). Alteration of potassium channel gating: Molecular analysis of the drosophila Sh5 mutation. Neuron. 5(1). 67–73. 26 indexed citations
19.
Ramaswami, Mani, Medha Gautam, Alexander Kamb, et al.. (1990). Human potassium channel genes: Molecular cloning and functional expression. Molecular and Cellular Neuroscience. 1(3). 214–223. 67 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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