Michael J. Adang

8.4k total citations
101 papers, 6.1k citations indexed

About

Michael J. Adang is a scholar working on Molecular Biology, Insect Science and Plant Science. According to data from OpenAlex, Michael J. Adang has authored 101 papers receiving a total of 6.1k indexed citations (citations by other indexed papers that have themselves been cited), including 98 papers in Molecular Biology, 75 papers in Insect Science and 40 papers in Plant Science. Recurrent topics in Michael J. Adang's work include Insect Resistance and Genetics (94 papers), Insect and Pesticide Research (56 papers) and Entomopathogenic Microorganisms in Pest Control (27 papers). Michael J. Adang is often cited by papers focused on Insect Resistance and Genetics (94 papers), Insect and Pesticide Research (56 papers) and Entomopathogenic Microorganisms in Pest Control (27 papers). Michael J. Adang collaborates with scholars based in United States, China and Canada. Michael J. Adang's co-authors include Juan Luis Jurat‐Fuentes, Gang Hua, Sreedhara Sangadala, Mohd Amir F. Abdullah, Rebecca J. McNall, Ke Luo, Stephen F. Garczynski, Fred Gould, Luke Masson and Kemet D. Spence and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Michael J. Adang

100 papers receiving 5.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Michael J. Adang United States	50	5.7k	4.3k	2.8k	410	183	101	6.1k
Neil Crickmore United Kingdom	35	7.1k 1.2×	5.8k 1.3×	3.1k 1.1×	247 0.6×	162 0.9×	164	7.7k
Donald H. Dean United States	41	6.6k 1.2×	5.1k 1.2×	2.5k 0.9×	348 0.8×	182 1.0×	111	7.0k
Mário Soberón Mexico	50	8.7k 1.5×	6.8k 1.6×	3.9k 1.4×	245 0.6×	264 1.4×	205	9.6k
Ruud A. de Maagd Netherlands	39	4.0k 0.7×	1.9k 0.4×	3.3k 1.2×	180 0.4×	154 0.8×	98	5.4k
Juan Luis Jurat‐Fuentes United States	41	3.9k 0.7×	3.2k 0.7×	1.8k 0.7×	133 0.3×	104 0.6×	110	4.4k
Yvan Rahbé France	37	1.6k 0.3×	2.2k 0.5×	1.6k 0.6×	317 0.8×	244 1.3×	88	3.3k
Klaus Gase Germany	31	1.7k 0.3×	1.5k 0.4×	2.5k 0.9×	161 0.4×	63 0.3×	56	3.8k
Yannick Pauchet Germany	29	1.7k 0.3×	1.6k 0.4×	912 0.3×	172 0.4×	199 1.1×	61	2.6k
Brenda Oppert United States	31	1.8k 0.3×	1.3k 0.3×	730 0.3×	178 0.4×	143 0.8×	88	2.3k
Bryony C. Bonning United States	36	2.9k 0.5×	3.2k 0.7×	1.3k 0.5×	181 0.4×	223 1.2×	159	4.5k

Countries citing papers authored by Michael J. Adang

Since Specialization

Citations

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

Fields of papers citing papers by Michael J. Adang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael J. Adang. 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 Michael J. Adang. The network helps show where Michael J. Adang may publish in the future.

Co-authorship network of co-authors of Michael J. Adang

This figure shows the co-authorship network connecting the top 25 collaborators of Michael J. Adang. A scholar is included among the top collaborators of Michael J. Adang 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 Michael J. Adang. Michael J. Adang is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Hua, Gang, et al.. (2024). Scavenger Receptor C1 Mediates Toxicity of Binary Toxin from Lysinibacillus sphaericus to Ag55 Cells. Toxins. 16(8). 369–369. 1 indexed citations

Chen, Li, Michael J. Adang, & Guangmao Shen. (2024). A novel spider venom peptide from the predatory mite Neoseiulus barkeri shows lethal effect on phytophagous pests. Pesticide Biochemistry and Physiology. 202. 105963–105963.

Riaz, Muhammad, et al.. (2020). Identification of Lysinibacillus sphaericus Binary toxin binding proteins in a malarial mosquito cell line by proteomics: A novel approach towards improving mosquito control. Journal of Proteomics. 227. 103918–103918. 11 indexed citations

Romão, Tatiany Patrícia, et al.. (2017). Identification of Cry48Aa/Cry49Aa toxin ligands in the midgut of Culex quinquefasciatus larvae. Insect Biochemistry and Molecular Biology. 88. 63–70. 12 indexed citations

Zhang, Qi, Gang Hua, & Michael J. Adang. (2015). Chitosan/DsiRNA nanoparticle targeting identifies AgCad1 cadherin in Anopheles gambiae larvae as an in vivo receptor of Cry11Ba toxin of Bacillus thuringiensis subsp. jegathesan. Insect Biochemistry and Molecular Biology. 60. 33–38. 17 indexed citations

Perera, Omaththage P., Kent S. Shelby, Holly J.R. Popham, et al.. (2015). Generation of a Transcriptome in a Model Lepidopteran Pest, Heliothis virescens, Using Multiple Sequencing Strategies for Profiling Midgut Gene Expression. PLoS ONE. 10(6). e0128563–e0128563. 17 indexed citations

Zhang, Qi, et al.. (2013). Analyses of α-amylase and α-glucosidase in the malaria vector mosquito, Anopheles gambiae, as receptors of Cry11Ba toxin of Bacillus thuringiensis subsp. jegathesan. Insect Biochemistry and Molecular Biology. 43(10). 907–915. 26 indexed citations

Tetreau, Guillaume, Christopher M. Jones, Renaud Stalinski, et al.. (2012). Larval midgut modifications associated with Bti resistance in the yellow fever mosquito using proteomic and transcriptomic approaches. BMC Genomics. 13(1). 248–248. 54 indexed citations

Andacht, Tracy M., et al.. (2009). Proteomic identification of Bacillus thuringiensis subsp. israelensis toxin Cry4Ba binding proteins in midgut membranes from Aedes (Stegomyia) aegypti Linnaeus (Diptera, Culicidae) larvae. Insect Biochemistry and Molecular Biology. 39(4). 279–286. 66 indexed citations

10.

Karumbaiah, Lohitash, Brenda Oppert, Juan Luis Jurat‐Fuentes, & Michael J. Adang. (2006). Analysis of midgut proteinases from Bacillus thuringiensis-susceptible and -resistant Heliothis virescens (Lepidoptera: Noctuidae). Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology. 146(1). 139–146. 57 indexed citations

11.

Krishnamoorthy, Malini, Juan Luis Jurat‐Fuentes, Rebecca J. McNall, Tracy M. Andacht, & Michael J. Adang. (2006). Identification of novel Cry1Ac binding proteins in midgut membranes from Heliothis virescens using proteomic analyses. Insect Biochemistry and Molecular Biology. 37(3). 189–201. 90 indexed citations

12.

Griffitts, Joel S., Stuart M. Haslam, Tinglu Yang, et al.. (2005). Glycolipids as Receptors for Bacillus thuringiensis Crystal Toxin. Science. 307(5711). 922–925. 274 indexed citations

13.

Chen, Jiang, Mark R. Brown, Gang Hua, & Michael J. Adang. (2005). Comparison of the localization of Bacillus thuringiensis Cry1A δ-endotoxins and their binding proteins in larval midgut of tobacco hornworm, Manduca sexta. Cell and Tissue Research. 321(1). 123–129. 43 indexed citations

14.

Hua, Gang, Juan Luis Jurat‐Fuentes, & Michael J. Adang. (2004). Bt-R1a Extracellular Cadherin Repeat 12 Mediates Bacillus thuringiensis Cry1Ab Binding and Cytotoxicity. Journal of Biological Chemistry. 279(27). 28051–28056. 89 indexed citations

15.

Hua, Gang, Juan Luis Jurat‐Fuentes, & Michael J. Adang. (2003). Fluorescent-based assays establish Manduca sexta Bt-R1a cadherin as a receptor for multiple Bacillus thuringiensis Cry1A toxins in Drosophila S2 cells. Insect Biochemistry and Molecular Biology. 34(3). 193–202. 43 indexed citations

16.

Banks, David J., Juan Luis Jurat‐Fuentes, Donald H. Dean, & Michael J. Adang. (2001). Bacillus thuringiensis Cry1Ac and Cry1Fa δ-endotoxin binding to a novel 110 kDa aminopeptidase in Heliothis virescens is not N-acetylgalactosamine mediated. Insect Biochemistry and Molecular Biology. 31(9). 909–918. 47 indexed citations

17.

Schwartz, Jean‐Louis, et al.. (1997). Ion channels formed in planar lipid bilayers by Bacillus thuringiensis toxins in the presence of Manduca sexta midgut receptors. FEBS Letters. 412(2). 270–276. 89 indexed citations

18.

Masson, Luke, et al.. (1995). The CryIA(c) Receptor Purified from Manduca sexta Displays Multiple Specificities. Journal of Biological Chemistry. 270(35). 20309–20315. 132 indexed citations

19.

Garczynski, Stephen F. & Michael J. Adang. (1995). Bacillus thuringiensis CryIA(c) δ-endotoxin binding aminopeptidase in the Manduca sexta midgut has a glycosyl-phosphatidylinositol anchor. Insect Biochemistry and Molecular Biology. 25(4). 409–415. 71 indexed citations

20.

Murray, Elizabeth E., Thomas A. Rocheleau, Mary Eberle, et al.. (1991). Analysis of unstable RNA transcripts of insecticidal crystal protein genes of Bacillus thuringiensis in transgenic plants and electroporated protoplasts. Plant Molecular Biology. 16(6). 1035–1050. 90 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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