Elisabeth C. Walcott

1.3k total citations
19 papers, 1.1k citations indexed

About

Elisabeth C. Walcott is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cognitive Neuroscience. According to data from OpenAlex, Elisabeth C. Walcott has authored 19 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 3 papers in Cognitive Neuroscience. Recurrent topics in Elisabeth C. Walcott's work include Neuroscience and Neuropharmacology Research (4 papers), Neural dynamics and brain function (3 papers) and Insect and Pesticide Research (3 papers). Elisabeth C. Walcott is often cited by papers focused on Neuroscience and Neuropharmacology Research (4 papers), Neural dynamics and brain function (3 papers) and Insect and Pesticide Research (3 papers). Elisabeth C. Walcott collaborates with scholars based in United States, Australia and Japan. Elisabeth C. Walcott's co-authors include Niraj S. Desai, Frank C. Hoppensteadt, Eugene M. Izhikevich, Kathryn L. Crossin, Marina Tsatmali, Helen P. Makarenkova, Takayuki Saito, Toru Miyamoto, Izuru YAMAMOTO and K Sumikawa and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Elisabeth C. Walcott

19 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elisabeth C. Walcott United States 11 442 363 323 151 124 19 1.1k
Deborah J. Baro United States 23 217 0.5× 856 2.4× 636 2.0× 58 0.4× 64 0.5× 46 1.4k
Vatsala Thirumalai India 17 372 0.8× 623 1.7× 219 0.7× 59 0.4× 16 0.1× 26 991
Hailing Su United States 23 438 1.0× 1.3k 3.5× 1.0k 3.2× 38 0.3× 85 0.7× 32 1.9k
Jakob Wolfart Germany 13 379 0.9× 841 2.3× 549 1.7× 39 0.3× 22 0.2× 15 1.1k
Nathan E. Schoppa United States 22 373 0.8× 2.0k 5.6× 1.1k 3.6× 42 0.3× 37 0.3× 34 2.8k
Marco Beato United Kingdom 28 326 0.7× 1.0k 2.8× 982 3.0× 29 0.2× 37 0.3× 44 1.8k
Alberto E. Pereda United States 16 360 0.8× 768 2.1× 644 2.0× 117 0.8× 5 0.0× 24 1.4k
Adrian Mason United Kingdom 11 440 1.0× 586 1.6× 187 0.6× 53 0.4× 11 0.1× 16 831
Simon J. Mitchell United Kingdom 11 649 1.5× 954 2.6× 368 1.1× 33 0.2× 12 0.1× 14 1.3k
Mingpo Yang China 13 400 0.9× 656 1.8× 390 1.2× 46 0.3× 5 0.0× 18 955

Countries citing papers authored by Elisabeth C. Walcott

Since Specialization
Citations

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

Fields of papers citing papers by Elisabeth C. Walcott

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elisabeth C. Walcott. 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 Elisabeth C. Walcott. The network helps show where Elisabeth C. Walcott may publish in the future.

Co-authorship network of co-authors of Elisabeth C. Walcott

This figure shows the co-authorship network connecting the top 25 collaborators of Elisabeth C. Walcott. A scholar is included among the top collaborators of Elisabeth C. Walcott 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 Elisabeth C. Walcott. Elisabeth C. Walcott 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.
Owens, Geoffrey C. & Elisabeth C. Walcott. (2012). Extensive Fusion of Mitochondria in Spinal Cord Motor Neurons. PLoS ONE. 7(6). e38435–e38435. 9 indexed citations
2.
Walcott, Elisabeth C., Emily A. Higgins, & Niraj S. Desai. (2011). Synaptic and Intrinsic Balancing during Postnatal Development in Rat Pups Exposed to Valproic Acidin Utero. Journal of Neuroscience. 31(37). 13097–13109. 36 indexed citations
3.
Meech, Robyn, Christopher Woolley, Marietta Barro, et al.. (2010). The Homeobox Transcription Factor Barx2 Regulates Plasticity of Young Primary Myofibers. PLoS ONE. 5(7). e11612–e11612. 29 indexed citations
4.
Desai, Niraj S. & Elisabeth C. Walcott. (2006). Synaptic Bombardment Modulates Muscarinic Effects in Forelimb Motor Cortex. Journal of Neuroscience. 26(8). 2215–2226. 27 indexed citations
5.
Tsatmali, Marina, Elisabeth C. Walcott, Helen P. Makarenkova, & Kathryn L. Crossin. (2006). Reactive oxygen species modulate the differentiation of neurons in clonal cortical cultures. Molecular and Cellular Neuroscience. 33(4). 345–357. 93 indexed citations
6.
Tsatmali, Marina, Elisabeth C. Walcott, & Kathryn L. Crossin. (2005). Newborn neurons acquire high levels of reactive oxygen species and increased mitochondrial proteins upon differentiation from progenitors. Brain Research. 1040(1-2). 137–150. 115 indexed citations
7.
Salbaum, J. Michael, et al.. (2004). Chlorotoxin-mediated disinhibition of noradrenergic locus coeruleus neurons using a conditional transgenic approach. Brain Research. 1016(1). 20–32. 7 indexed citations
8.
Izhikevich, Eugene M., Niraj S. Desai, Elisabeth C. Walcott, & Frank C. Hoppensteadt. (2003). Bursts as a unit of neural information: selective communication via resonance. Trends in Neurosciences. 26(3). 161–167. 475 indexed citations
9.
Stonehouse, Anthony H., Megumi Adachi, Elisabeth C. Walcott, & Frederick S. Jones. (2003). Caffeine Regulates Neuronal Expression of the Dopamine 2 Receptor Gene. Molecular Pharmacology. 64(6). 1463–1473. 26 indexed citations
10.
Walcott, Elisabeth C. & Ronald B. Langdon. (2002). Synaptically driven spikes and long-term potentiation in neocortical layer 2/3. Neuroscience. 112(4). 815–826. 9 indexed citations
11.
Walcott, Elisabeth C. & Ronald B. Langdon. (2001). Short-term plasticity of extrinsic excitatory inputs to neocortical layer 1. Experimental Brain Research. 136(2). 143–151. 5 indexed citations
12.
YAMAMOTO, Izuru, Motohiro Tomizawa, Takayuki Saito, et al.. (1998). Structural factors contributing to insecticidal and selective actions of neonicotinoids. Archives of Insect Biochemistry and Physiology. 37(1). 24–32. 121 indexed citations
13.
Walcott, Elisabeth C., et al.. (1997). N-Glycosylation at the conserved sites ensures the expression of properly folded functional ACh receptors. Molecular Brain Research. 45(2). 219–229. 61 indexed citations
14.
Walcott, Elisabeth C. & Katumi Sumikawa. (1996). A conserved disulfide loop facilitates conformational maturation in the subunits of the acetylcholine receptor. Molecular Brain Research. 41(1-2). 289–300. 5 indexed citations
15.
Walcott, Elisabeth C. & Barbara Tate. (1996). Entrainment of Aged, Dysrhythmic Rats to a Restricted Feeding Schedule. Physiology & Behavior. 60(5). 1205–1208. 18 indexed citations
16.
Tate, Barbara, et al.. (1992). Disruption of circadian regulation by brain grafts that overexpress Alzheimer beta/A4 amyloid.. Proceedings of the National Academy of Sciences. 89(15). 7090–7094. 42 indexed citations
17.
Majocha, Ronald E., et al.. (1990). of Amino Terminal and A4 (β-Amyloid) Antigens in Alzheimer Plaques: Evidence for Coordinated Processing of the Amyloid Precursor Protein. Journal of Geriatric Psychiatry and Neurology. 3(3). 139–145. 2 indexed citations
18.
Majocha, Ronald E., et al.. (1989). INVESTIGATION INTO THE PROCESSING OF THE AMYLOID PRECURSOR PROTEIN USING SITE-SPECIFIC ANTIBODIES. Journal of Neuropathology & Experimental Neurology. 48(3). 335–335. 1 indexed citations
19.
Stopa, Edward G., et al.. (1989). HUMAN SUPRACHIASMATIC NUCLEI IN ALZHEIMERʼS DISEASE. Journal of Neuropathology & Experimental Neurology. 48(3). 327–327. 1 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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