Lizabeth A. Perkins

5.8k total citations · 2 hit papers
37 papers, 4.0k citations indexed

About

Lizabeth A. Perkins is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Lizabeth A. Perkins has authored 37 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 9 papers in Cell Biology and 8 papers in Cellular and Molecular Neuroscience. Recurrent topics in Lizabeth A. Perkins's work include Developmental Biology and Gene Regulation (19 papers), Neurobiology and Insect Physiology Research (8 papers) and Protein Tyrosine Phosphatases (7 papers). Lizabeth A. Perkins is often cited by papers focused on Developmental Biology and Gene Regulation (19 papers), Neurobiology and Insect Physiology Research (8 papers) and Protein Tyrosine Phosphatases (7 papers). Lizabeth A. Perkins collaborates with scholars based in United States, United Kingdom and Austria. Lizabeth A. Perkins's co-authors include Norbert Perrimon, Joseph G. Culotti, Edward M. Hedgecock, J. Nichol Thomson, Inger Kristin Larsen, Richard Binari, Michael Melnick, Matthew A. Booker, Rong Tao and Donghui Yang‐Zhou and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Lizabeth A. Perkins

37 papers receiving 4.0k citations

Hit Papers

Mutant sensory cilia in the nematode Caenorhabditis elegans 1986 2026 1999 2012 1986 2011 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
Lizabeth A. Perkins United States 28 2.8k 907 820 814 714 37 4.0k
Roger A. Hoskins United States 24 3.8k 1.4× 1.5k 1.7× 479 0.6× 1.1k 1.3× 964 1.4× 35 5.3k
Frank Schnorrer Germany 31 3.0k 1.1× 1.6k 1.7× 345 0.4× 1.2k 1.5× 546 0.8× 56 4.5k
Georg Dietzl Austria 6 2.2k 0.8× 1.6k 1.8× 286 0.3× 979 1.2× 440 0.6× 6 3.4k
Richard Binari United States 29 3.0k 1.1× 1.1k 1.2× 305 0.4× 691 0.8× 555 0.8× 40 4.5k
Yuchun He United States 14 2.3k 0.8× 1.3k 1.4× 262 0.3× 732 0.9× 592 0.8× 18 3.3k
Koen J. T. Venken United States 30 3.2k 1.2× 1.8k 2.0× 268 0.3× 906 1.1× 904 1.3× 50 4.8k
Todd Laverty United States 16 3.1k 1.1× 1.5k 1.6× 227 0.3× 708 0.9× 733 1.0× 19 4.1k
Michael J. Pankratz Germany 32 1.6k 0.6× 1.5k 1.6× 466 0.6× 219 0.3× 791 1.1× 59 3.3k
David P. Welchman United Kingdom 9 2.2k 0.8× 254 0.3× 1.7k 2.1× 576 0.7× 348 0.5× 9 3.6k
Pierre Léopold France 33 2.3k 0.8× 2.8k 3.1× 952 1.2× 1.2k 1.5× 886 1.2× 64 5.8k

Countries citing papers authored by Lizabeth A. Perkins

Since Specialization
Citations

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

Fields of papers citing papers by Lizabeth A. Perkins

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lizabeth A. Perkins. 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 Lizabeth A. Perkins. The network helps show where Lizabeth A. Perkins may publish in the future.

Co-authorship network of co-authors of Lizabeth A. Perkins

This figure shows the co-authorship network connecting the top 25 collaborators of Lizabeth A. Perkins. A scholar is included among the top collaborators of Lizabeth A. Perkins 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 Lizabeth A. Perkins. Lizabeth A. Perkins 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.
Comjean, Aram, et al.. (2015). GLAD: an Online Database of Gene List Annotation for Drosophila. PubMed. 3. 75–81. 50 indexed citations
2.
Jodoin, Jeanne N., Soline Chanet, Claudia G. Vasquez, et al.. (2015). Stable Force Balance between Epithelial Cells Arises from F-Actin Turnover. Developmental Cell. 35(6). 685–697. 77 indexed citations
3.
Sopko, Richelle, Marianna Foos, Arunachalam Vinayagam, et al.. (2014). Combining Genetic Perturbations and Proteomics to Examine Kinase-Phosphatase Networks in Drosophila Embryos. Developmental Cell. 31(1). 114–127. 50 indexed citations
4.
Yan, Dong, Ralph A. Neumüller, Michael Buckner, et al.. (2014). A Regulatory Network of Drosophila Germline Stem Cell Self-Renewal. Developmental Cell. 28(4). 459–473. 104 indexed citations
5.
Ni, Jian-Quan, Rui Zhou, B. Czech, et al.. (2011). A genome-scale shRNA resource for transgenic RNAi in Drosophila. Nature Methods. 8(5). 405–407. 605 indexed citations breakdown →
6.
James, Brian P., et al.. (2007). Nuclear Localization of the ERK MAP Kinase Mediated byDrosophilaαPS2βPS Integrin and Importin-7. Molecular Biology of the Cell. 18(10). 4190–4199. 32 indexed citations
7.
Vrailas‐Mortimer, Alysia D., Daniel R. Marenda, Maureen A. Powers, et al.. (2006). smoothened and thickveins regulate Moleskin/Importin 7-mediated MAP kinase signaling in the developing Drosophila eye. Development. 133(8). 1485–1494. 22 indexed citations
8.
Oishi, Kimihiko, Konstantin Gaengel, Ursula Weber, et al.. (2006). Transgenic Drosophila models of Noonan syndrome causing PTPN11 gain-of-function mutations. Human Molecular Genetics. 15(4). 543–553. 51 indexed citations
9.
Marenda, Daniel R., Alysia D. Vrailas‐Mortimer, Maureen A. Powers, et al.. (2005). MAP kinase subcellular localization controls both pattern and proliferation in the developing Drosophila wing. Development. 133(1). 43–51. 41 indexed citations
10.
Vincent, Stéphane D., Lizabeth A. Perkins, & Norbert Perrimon. (2001). Doublesex Surprises. Cell. 106(4). 399–402. 13 indexed citations
11.
Lorenzen, James A., Scott Baker, Fabienne Denhez, et al.. (2001). Nuclear import of activated D-ERK by DIM-7, an importin family member encoded by the gene moleskin. Development. 128(8). 1403–1414. 78 indexed citations
12.
Perrimon, Norbert & Lizabeth A. Perkins. (1997). There Must Be 50 Ways to Rule the Signal: The Case of the Drosophila EGF Receptor. Cell. 89(1). 13–16. 124 indexed citations
13.
Perkins, Lizabeth A., Michelle R. Johnson, Michael Melnick, & Norbert Perrimon. (1996). The Nonreceptor Protein Tyrosine Phosphatase Corkscrew Functions in Multiple Receptor Tyrosine Kinase Pathways inDrosophila. Developmental Biology. 180(1). 63–81. 101 indexed citations
14.
Noll, Elizabeth, Lizabeth A. Perkins, Anthony P. Mahowald, & Norbert Perrimon. (1993). Approaches to identify genes involved in Drosophila embryonic CNS development. Journal of Neurobiology. 24(6). 701–722. 2 indexed citations
15.
Perkins, Lizabeth A., Inger Kristin Larsen, & Norbert Perrimon. (1992). corkscrew encodes a putative protein tyrosine phosphatase that functions to transduce the terminal signal from the receptor tyrosine kinase torso. Cell. 70(2). 225–236. 354 indexed citations
16.
Eberl, Daniel F., Lizabeth A. Perkins, Marcy Engelstein, Arthur J. Hilliker, & Norbert Perrimon. (1992). Genetic and developmental analysis of polytene section 17 of the X chromosome of Drosophila melanogaster.. Genetics. 130(3). 569–583. 32 indexed citations
17.
Siegfried, Esther, et al.. (1990). Putative protein kinase product of the Drosophila segment-polarity gene zeste-white3. Nature. 345(6278). 825–829. 142 indexed citations
18.
Perkins, Lizabeth A., et al.. (1990). Molecular and developmental characterization of the heat shock cognate 4 gene of Drosophila melanogaster.. Molecular and Cellular Biology. 10(6). 3232–3238. 46 indexed citations
19.
Perkins, Lizabeth A., Edward M. Hedgecock, J. Nichol Thomson, & Joseph G. Culotti. (1986). Mutant sensory cilia in the nematode Caenorhabditis elegans. Developmental Biology. 117(2). 456–487. 730 indexed citations breakdown →
20.
Hedgecock, Edward M., Joseph G. Culotti, J. Nichol Thomson, & Lizabeth A. Perkins. (1985). Axonal guidance mutants of Caenorhabditis elegans identified by filling sensory neurons with fluorescein dyes. Developmental Biology. 111(1). 158–170. 371 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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