Paul D. Shirk

2.4k total citations · 1 hit paper
60 papers, 1.7k citations indexed

About

Paul D. Shirk is a scholar working on Molecular Biology, Insect Science and Genetics. According to data from OpenAlex, Paul D. Shirk has authored 60 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 31 papers in Insect Science and 29 papers in Genetics. Recurrent topics in Paul D. Shirk's work include Insect Resistance and Genetics (24 papers), Insect and Arachnid Ecology and Behavior (21 papers) and Neurobiology and Insect Physiology Research (18 papers). Paul D. Shirk is often cited by papers focused on Insect Resistance and Genetics (24 papers), Insect and Arachnid Ecology and Behavior (21 papers) and Neurobiology and Insect Physiology Research (18 papers). Paul D. Shirk collaborates with scholars based in United States, Israel and Poland. Paul D. Shirk's co-authors include Norbert H. Haunerland, Herbert Röller, Corinne Royer, Toshio Kanda, Toshiki Tamura, Bernard Mauchamp, Pierre Couble, Jean‐Claude Prudhomme, Natuo Kômoto and Malcolm J. Fraser and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Biotechnology and PLoS ONE.

In The Last Decade

Paul D. Shirk

60 papers receiving 1.6k citations

Hit Papers

Germline transformation of the silkworm Bombyx mori L. us... 2000 2026 2008 2017 2000 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
Paul D. Shirk United States 19 874 788 601 503 339 60 1.7k
Bernard Mauchamp France 20 947 1.1× 741 0.9× 481 0.8× 603 1.2× 568 1.7× 59 1.8k
Anjiang Tan China 27 1.1k 1.3× 864 1.1× 475 0.8× 557 1.1× 234 0.7× 36 1.8k
Keiko Kadono‐Okuda Japan 27 1.2k 1.4× 1.1k 1.4× 402 0.7× 591 1.2× 386 1.1× 63 2.2k
Shuichiro Tomita Japan 20 874 1.0× 483 0.6× 303 0.5× 407 0.8× 139 0.4× 40 1.4k
Marian R. Goldsmith United States 28 1.5k 1.8× 1.3k 1.6× 799 1.3× 523 1.0× 705 2.1× 53 2.7k
Makoto Kiuchi Japan 23 598 0.7× 850 1.1× 505 0.8× 1.0k 2.1× 149 0.4× 69 1.7k
Keiro Uchino Japan 30 1.4k 1.6× 1.1k 1.4× 554 0.9× 730 1.5× 807 2.4× 73 2.4k
Takaaki Daimon Japan 29 1.6k 1.8× 1.2k 1.6× 727 1.2× 812 1.6× 296 0.9× 71 2.7k
Toshio Kanda Japan 15 806 0.9× 522 0.7× 444 0.7× 325 0.6× 550 1.6× 29 1.4k
Susumu Izumi Japan 26 1.1k 1.3× 618 0.8× 476 0.8× 642 1.3× 349 1.0× 60 1.9k

Countries citing papers authored by Paul D. Shirk

Since Specialization
Citations

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

Fields of papers citing papers by Paul D. Shirk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paul D. Shirk. 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 Paul D. Shirk. The network helps show where Paul D. Shirk may publish in the future.

Co-authorship network of co-authors of Paul D. Shirk

This figure shows the co-authorship network connecting the top 25 collaborators of Paul D. Shirk. A scholar is included among the top collaborators of Paul D. Shirk 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 Paul D. Shirk. Paul D. Shirk 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.
Shirk, Paul D., et al.. (2022). Gene editing of the ABC Transporter/White locus using CRISPR/Cas9-mediated mutagenesis in the Indian Meal Moth. Journal of Insect Physiology. 145. 104471–104471. 10 indexed citations
2.
Christensen, Shawn A., et al.. (2022). RNAi-induced knockdown of white gene in the southern green stink bug (Nezara viridula L.). Scientific Reports. 12(1). 10396–10396. 5 indexed citations
3.
Wu, Ke, et al.. (2018). CRISPR/Cas9 mediated knockout of the abdominal-A homeotic gene in fall armyworm moth (Spodoptera frugiperda). PLoS ONE. 13(12). e0208647–e0208647. 40 indexed citations
4.
5.
Dafoe, Nicole J., James D. Thomas, Paul D. Shirk, et al.. (2013). European Corn Borer (Ostrinia nubilalis) Induced Responses Enhance Susceptibility in Maize. PLoS ONE. 8(9). e73394–e73394. 48 indexed citations
6.
Shirk, Paul D., et al.. (2012). Predator-Prey Relationships on Apiaceae at an Organic Farm. Environmental Entomology. 41(3). 487–496. 10 indexed citations
7.
Shapiro, Jeffrey P., Paul D. Shirk, Karen Kelley, Tamera M. Lewis, & David Horton. (2010). Identity of Two Sympatric Species ofOrius(Hemiptera: Heteroptera: Anthocoridae). Journal of Insect Science. 10(189). 1–17. 16 indexed citations
8.
Shapiro, Jeffrey P., Stuart R. Reitz, & Paul D. Shirk. (2009). Nutritional Manipulation of Adult Female <I>Orius pumilio</I> (Hemiptera: Anthocoridae) Enhances Initial Predatory Performance. Journal of Economic Entomology. 102(2). 500–506. 7 indexed citations
9.
Bossin, Hervé, et al.. (2006). Somatic transformation efficiencies and expression patterns using the Jc DNV and piggyBac transposon gene vectors in insects. Insect Molecular Biology. 16(1). 37–47. 12 indexed citations
10.
Shirk, Paul D., et al.. (2004). Development of the larval ovary in the moth, Plodia interpunctella. Journal of Insect Physiology. 50(11). 1045–1051. 3 indexed citations
11.
Yun, Chi‐Young, et al.. (2003). Fat body expressed yolk protein genes in Hyphantria cunea are related to the YP4 follicular epithelium yolk protein subunit gene of pyralid moths. Insect Molecular Biology. 12(4). 383–392. 6 indexed citations
12.
Tamura, Toshiki, Chantal Thibert, Corinne Royer, et al.. (2000). Germline transformation of the silkworm Bombyx mori L. using a piggyBac transposon-derived vector. Nature Biotechnology. 18(1). 81–84. 624 indexed citations breakdown →
13.
Perera, Omaththage P. & Paul D. Shirk. (1999). cDNA of YP4, a follicular epithelium yolk protein subunit, in the moth,Plodia interpunctella. Archives of Insect Biochemistry and Physiology. 40(3). 157–164. 6 indexed citations
14.
Shirk, Paul D., et al.. (1998). α-Crystallin protein cognates in eggs of the moth, Plodia interpunctella: possible chaperones for the follicular epithelium yolk protein. Insect Biochemistry and Molecular Biology. 28(3). 151–161. 17 indexed citations
15.
Shirk, Paul D. & Grażyna Zimowska. (1997). An α-crystallin protein cognate in germ cells of the moth, Plodia interpunctella. Insect Biochemistry and Molecular Biology. 27(2). 149–157. 4 indexed citations
16.
Haunerland, Norbert H. & Paul D. Shirk. (1995). Regional and Functional Differentiation in the Insect Fact Body. Annual Review of Entomology. 40(1). 121–145. 105 indexed citations
17.
Shirk, Paul D., et al.. (1994). Yolk sphere formation is initiated in oocytes before development of patency in follicles of the moth,Plodia interpunctella. Development Genes and Evolution. 203(4). 215–226. 14 indexed citations
18.
Zimowska, Grażyna, Donald L. Silhacek, Eli Shaaya, & Paul D. Shirk. (1991). Immuno‐Fluorescent analysis of follicular growth and development in whole ovaries of the Indianmeal moth. Journal of Morphology. 209(2). 215–228. 14 indexed citations
19.
Shirk, Paul D., Paul Roberts, & Chee Hark Harn. (1988). Synthesis and secretion of salivary gland proteins in Drosophila gibberosa during larval and prepupal development. Development Genes and Evolution. 197(2). 66–74. 12 indexed citations
20.
Shirk, Paul D., G. Bhaskaran, & Herbert Röller. (1980). The transfer of juvenile hormone from male to female during mating in the Cecropia silkmoth. Cellular and Molecular Life Sciences. 36(6). 682–683. 49 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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