Elizabeth Willott

1.7k total citations
23 papers, 1.3k citations indexed

About

Elizabeth Willott is a scholar working on Immunology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Elizabeth Willott has authored 23 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Immunology, 8 papers in Molecular Biology and 8 papers in Cellular and Molecular Neuroscience. Recurrent topics in Elizabeth Willott's work include Invertebrate Immune Response Mechanisms (11 papers), Neurobiology and Insect Physiology Research (8 papers) and Insect Resistance and Genetics (6 papers). Elizabeth Willott is often cited by papers focused on Invertebrate Immune Response Mechanisms (11 papers), Neurobiology and Insect Physiology Research (8 papers) and Insect Resistance and Genetics (6 papers). Elizabeth Willott collaborates with scholars based in United States, Germany and Russia. Elizabeth Willott's co-authors include María S. Balda, James M. Anderson, A. S. Fanning, Christina Van Itallie, Michael R. Kanost, Frank B. Ramberg, X Y Wang, M A Wells, Matthew B. Heintzelman and Tina E. Trenczek and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Archives of Biochemistry and Biophysics.

In The Last Decade

Elizabeth Willott

22 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elizabeth Willott United States 17 634 301 278 268 239 23 1.3k
Jeongsil Kim‐Ha South Korea 17 1.3k 2.1× 150 0.5× 335 1.2× 18 0.1× 210 0.9× 34 1.8k
Nicolas Matt France 13 793 1.3× 339 1.1× 480 1.7× 13 0.0× 110 0.5× 17 1.3k
J. Robert Manak United States 31 2.3k 3.6× 133 0.4× 190 0.7× 16 0.1× 205 0.9× 68 2.9k
Eugene Yujun Xu United States 21 957 1.5× 102 0.3× 63 0.2× 84 0.3× 82 0.3× 40 1.7k
Kimberly McCall United States 31 2.7k 4.3× 294 1.0× 1.0k 3.6× 30 0.1× 773 3.2× 61 3.9k
Alexander Mazo United States 33 3.2k 5.1× 51 0.2× 152 0.5× 28 0.1× 166 0.7× 62 3.6k
Paolo Edomi Italy 17 336 0.5× 37 0.1× 233 0.8× 100 0.4× 466 1.9× 37 947
Leonie M. Quinn Australia 22 1.4k 2.3× 78 0.3× 384 1.4× 10 0.0× 254 1.1× 50 1.8k
Cory J. Evans United States 17 919 1.4× 529 1.8× 1.2k 4.5× 8 0.0× 715 3.0× 19 2.0k
Tina L. Gumienny United States 16 881 1.4× 29 0.1× 369 1.3× 18 0.1× 86 0.4× 30 1.8k

Countries citing papers authored by Elizabeth Willott

Since Specialization
Citations

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

Fields of papers citing papers by Elizabeth Willott

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elizabeth Willott

This figure shows the co-authorship network connecting the top 25 collaborators of Elizabeth Willott. A scholar is included among the top collaborators of Elizabeth Willott 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 Elizabeth Willott. Elizabeth Willott 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.
Schmidtz, David & Elizabeth Willott. (2012). Private Landowners Cooperate to Sustain Wildlife Habitat: The Case of the Sabi Sand Game Reserve*. Journal of applied corporate finance. 24(2). 78–85.
2.
Willott, Elizabeth & Frank B. Ramberg. (2007). Identification and Geographical Distribution of the Mosquitoes of North America, North of Mexico. Journal of Wildlife Diseases. 43(4). 806–807. 29 indexed citations
4.
Willott, Elizabeth. (2004). Restoring Nature, Without Mosquitoes?. Restoration Ecology. 12(2). 147–153. 47 indexed citations
5.
Willott, Elizabeth, et al.. (2002). Zinc and Manduca sexta hemocyte functions. Journal of Insect Science. 2(1). 6–6. 20 indexed citations
6.
Willott, Elizabeth, et al.. (2002). Influence of calcium on Manduca sexta plasmatocyte spreading and network formation. Archives of Insect Biochemistry and Physiology. 49(4). 187–202. 16 indexed citations
7.
Willott, Elizabeth, et al.. (2002). Zinc and Manduca sexta hemocyte functions. Journal of Insect Science. 2(6). 1–9. 12 indexed citations
8.
Carrière, Yves, Timothy J. Dennehy, Brent S. Pedersen, et al.. (2001). Large-Scale Management of Insect Resistance to Transgenic Cotton in Arizona - Can Transgenic Insecticidal Crops be Sustained?. Journal of Economic Entomology. 94(2). 315–325. 79 indexed citations
9.
Wiegand, Claudia, David Michael Levin, Jeremy P. Gillespie, et al.. (2000). Monoclonal antibody MS13 identifies a plasmatocyte membrane protein and inhibits encapsulation and spreading reactions ofManduca sexta hemocytes. Archives of Insect Biochemistry and Physiology. 45(3). 95–108. 31 indexed citations
10.
Meyer-Fernandes, J.R., Humberto Lanz‐Mendoza, Kátia C. Gondim, Elizabeth Willott, & Michael A. Wells. (2000). Ectonucleotide Diphosphohydrolase Activities in Hemocytes of Larval Manduca sexta. Archives of Biochemistry and Biophysics. 382(1). 152–159. 13 indexed citations
11.
Wang, Y., Elizabeth Willott, & Michael R. Kanost. (1995). Organization and expression of the hemolin gene, a member of the immunoglobulin superfamily in an insect, Manduca sexta. Insect Molecular Biology. 4(2). 113–123. 53 indexed citations
12.
Kanost, Michael R., Sarvamangala V. Prasad, Yanling Huang, & Elizabeth Willott. (1995). Regulation of serpin gene-1 in Manduca sexta. Insect Biochemistry and Molecular Biology. 25(2). 285–291. 28 indexed citations
13.
14.
Willott, Elizabeth, et al.. (1994). Immunochemical identification of insect hemocyte populations: monoclonal antibodies distinguish four major hemocyte types in manduca sexta.. PubMed. 65(2). 417–23. 90 indexed citations
15.
Willott, Elizabeth, et al.. (1993). The tight junction protein ZO-1 is homologous to the Drosophila discs-large tumor suppressor protein of septate junctions.. Proceedings of the National Academy of Sciences. 90(16). 7834–7838. 405 indexed citations
16.
Willott, Elizabeth, et al.. (1992). Localization and differential expression of two isoforms of the tight junction protein ZO-1. American Journal of Physiology-Cell Physiology. 262(5). C1119–C1124. 148 indexed citations
17.
Willott, Elizabeth. (1989). Manduca sexta fat body during the larval-pupal transformation: A structural and biochemical study.. UA Campus Repository (The University of Arizona). 3 indexed citations
18.
Willott, Elizabeth, X Y Wang, & M A Wells. (1989). cDNA and gene sequence of Manduca sexta arylphorin, an aromatic amino acid-rich larval serum protein. Journal of Biological Chemistry. 264(32). 19052–19059. 102 indexed citations
19.
Willott, Elizabeth, et al.. (1988). Sequential structural changes in the fat body of the tobacco hornworm, Manduca sexta, during the fifth larval stadium. Tissue and Cell. 20(4). 635–643. 25 indexed citations
20.
Ryan, Robert O., et al.. (1986). Major hemolymph proteins from larvae of the black swallowtail butterfly, Papilio polyxenes. Archives of Insect Biochemistry and Physiology. 3(6). 539–550. 16 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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