Jayashree Aiyar

3.3k total citations · 1 hit paper
30 papers, 2.4k citations indexed

About

Jayashree Aiyar is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Organic Chemistry. According to data from OpenAlex, Jayashree Aiyar has authored 30 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 8 papers in Cardiology and Cardiovascular Medicine and 5 papers in Organic Chemistry. Recurrent topics in Jayashree Aiyar's work include Ion channel regulation and function (20 papers), Nicotinic Acetylcholine Receptors Study (12 papers) and Cardiac electrophysiology and arrhythmias (7 papers). Jayashree Aiyar is often cited by papers focused on Ion channel regulation and function (20 papers), Nicotinic Acetylcholine Receptors Study (12 papers) and Cardiac electrophysiology and arrhythmias (7 papers). Jayashree Aiyar collaborates with scholars based in United States, India and Netherlands. Jayashree Aiyar's co-authors include K. George Chandy, George A. Gutman, Stephan Grissmer, Douglas C. Hanson, A. N. Nguyen, Robert J. Mather, Naomi J. Logsdon, Michael J. Karmilowicz, D. D. Auperin and Edward P. Christian and has published in prestigious journals such as Journal of Biological Chemistry, Neuron and Journal of Neuroscience.

In The Last Decade

Jayashree Aiyar

29 papers receiving 2.3k citations

Hit Papers

Pharmacological characterization of five cloned voltage-g... 1994 2026 2004 2015 1994 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jayashree Aiyar United States 17 2.0k 877 814 256 229 30 2.4k
Neil A. Castle United States 25 2.1k 1.0× 927 1.1× 972 1.2× 185 0.7× 322 1.4× 40 2.6k
Robert S. Slaughter United States 27 1.9k 0.9× 739 0.8× 668 0.8× 198 0.8× 202 0.9× 43 2.3k
William A. Schmalhofer United States 21 1.5k 0.7× 581 0.7× 567 0.7× 233 0.9× 211 0.9× 32 1.9k
Eitan Reuveny Israel 30 3.0k 1.5× 1.6k 1.8× 836 1.0× 112 0.4× 183 0.8× 52 3.5k
Eric Guillemare France 21 3.4k 1.7× 1.8k 2.0× 2.3k 2.8× 156 0.6× 148 0.6× 27 4.0k
Julio A. Copello United States 22 1.9k 1.0× 701 0.8× 1.2k 1.5× 124 0.5× 173 0.8× 54 2.5k
Patrick Bois France 25 1.2k 0.6× 494 0.6× 960 1.2× 80 0.3× 118 0.5× 80 1.9k
H G Knaus Austria 13 1.8k 0.9× 923 1.1× 400 0.5× 58 0.2× 113 0.5× 17 1.9k
Stefan McDonough United States 24 1.3k 0.6× 634 0.7× 154 0.2× 249 1.0× 265 1.2× 34 1.7k
Andrea Brüggemann Germany 31 1.9k 0.9× 975 1.1× 993 1.2× 57 0.2× 188 0.8× 52 2.4k

Countries citing papers authored by Jayashree Aiyar

Since Specialization
Citations

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

Fields of papers citing papers by Jayashree Aiyar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jayashree Aiyar

This figure shows the co-authorship network connecting the top 25 collaborators of Jayashree Aiyar. A scholar is included among the top collaborators of Jayashree Aiyar 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 Jayashree Aiyar. Jayashree Aiyar 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.
Prasad, Pramada, Jayashree Aiyar, Saurabh Joshi, et al.. (2023). An ultrastructural and genomic study on the SARS-CoV-2 variant B.1.210 circulating during the first wave of COVID-19 pandemic in India. Indian Journal of Medical Microbiology. 41. 45–52. 1 indexed citations
2.
Kalindjian, S. Barret, Christopher A. Hewson, Venkateshappa Chandregowda, et al.. (2016). A New Series of Orally Bioavailable Chemokine Receptor 9 (CCR9) Antagonists; Possible Agents for the Treatment of Inflammatory Bowel Disease. Journal of Medicinal Chemistry. 59(7). 3098–3111. 14 indexed citations
3.
Mammen, Mathai, et al.. (2011). Muscarinic receptor subtypes and signalling involved in the attenuation of isoprenaline-induced rat urinary bladder relaxation. Naunyn-Schmiedeberg s Archives of Pharmacology. 384(6). 555–563. 16 indexed citations
5.
Urban, M.O., Ke Ren, Ki‐Tae Park, et al.. (2005). Comparison of the Antinociceptive Profiles of Gabapentin and 3-Methylgabapentin in Rat Models of Acute and Persistent Pain: Implications for Mechanism of Action. Journal of Pharmacology and Experimental Therapeutics. 313(3). 1209–1216. 60 indexed citations
6.
Lim, Jongwon, Nicholas Stock, Richard Pracitto, et al.. (2004). N-Acridin-9-yl-butane-1,4-diamine derivatives: high-affinity ligands of the α2δ subunit of voltage gated calcium channels. Bioorganic & Medicinal Chemistry Letters. 14(8). 1913–1916. 10 indexed citations
7.
Lebsack, Alec D., Janet L. Gunzner, Bowei Wang, et al.. (2004). Identification and synthesis of [1,2,4]triazolo[3,4-a]phthalazine derivatives as high-affinity ligands to the α2δ-1 subunit of voltage gated calcium channel. Bioorganic & Medicinal Chemistry Letters. 14(10). 2463–2467. 29 indexed citations
8.
Williams, Mark E., Bill Burton, Arturo Urrutia, et al.. (2004). Ric-3 Promotes Functional Expression of the Nicotinic Acetylcholine Receptor α7 Subunit in Mammalian Cells. Journal of Biological Chemistry. 280(2). 1257–1263. 134 indexed citations
9.
Hu, Tao, Brian A. Stearns, Brian T. Campbell, et al.. (2004). Synthesis and biological evaluation of 6-aryl-6 H -pyrrolo[3,4- d ]pyridazine derivatives as high-affinity ligands of the α 2 δ subunit of voltage-gated calcium channels. Bioorganic & Medicinal Chemistry Letters. 14(9). 2031–2034. 13 indexed citations
10.
Rauer, Heiko, Mark D. Lanigan, Michael W. Pennington, et al.. (2000). Structure-guided Transformation of Charybdotoxin Yields an Analog That Selectively Targets Ca2+-activated over Voltage-gated K+ Channels. Journal of Biological Chemistry. 275(2). 1201–1208. 100 indexed citations
11.
Aiyar, Jayashree. (1999). . Perspectives in Drug Discovery and Design. 15/16. 257–280. 8 indexed citations
12.
Jäger, Heike, et al.. (1998). Regulation of mammalian Shaker‐related K+ channels: evidence for non‐conducting closed and non‐conducting inactivated states. The Journal of Physiology. 506(2). 291–301. 42 indexed citations
13.
Logsdon, Naomi J., Jiesheng Kang, James Togo, Edward P. Christian, & Jayashree Aiyar. (1997). A Novel Gene, hKCa4, Encodes the Calcium-activated Potassium Channel in Human T Lymphocytes. Journal of Biological Chemistry. 272(52). 32723–32726. 253 indexed citations
14.
Spencer, Robert H., Yuri Sokolov, Huilin Li, et al.. (1997). Purification, Visualization, and Biophysical Characterization of Kv1.3 Tetramers. Journal of Biological Chemistry. 272(4). 2389–2395. 49 indexed citations
15.
Wymore, Randy S., et al.. (1996). Characterization of the Transcription Unit of Mouse Kv1.4, a Voltage-gated Potassium Channel Gene. Journal of Biological Chemistry. 271(26). 15629–15634. 30 indexed citations
16.
Aiyar, Jayashree, Jane M. Withka, James P. Rizzi, et al.. (1995). Topology of the pore-region of a K+ channel revealed by the NMR-derived structures of scorpion toxins. Neuron. 15(5). 1169–1181. 221 indexed citations
17.
Grissmer, Stephan, A. N. Nguyen, Jayashree Aiyar, et al.. (1994). Pharmacological characterization of five cloned voltage-gated K+ channels, types Kv1.1, 1.2, 1.3, 1.5, and 3.1, stably expressed in mammalian cell lines.. Molecular Pharmacology. 45(6). 1227–1234. 692 indexed citations breakdown →
19.
Aiyar, Jayashree, A. N. Nguyen, K. George Chandy, & Stephan Grissmer. (1994). The P-region and S6 of Kv3.1 contribute to the formation of the ion conduction pathway. Biophysical Journal. 67(6). 2261–2264. 42 indexed citations
20.
Aiyar, Jayashree, M. K. Bhan, Nita Bhandari, et al.. (1990). Rotavirus-Specific Antibody Response in Saliva of Infants with Rotavirus Diarrhea. The Journal of Infectious Diseases. 162(6). 1383–1384. 15 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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