Francis Rajamohan

2.7k total citations
38 papers, 1.6k citations indexed

About

Francis Rajamohan is a scholar working on Molecular Biology, Immunology and Insect Science. According to data from OpenAlex, Francis Rajamohan has authored 38 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 11 papers in Immunology and 11 papers in Insect Science. Recurrent topics in Francis Rajamohan's work include Insect Resistance and Genetics (13 papers), Insect and Pesticide Research (11 papers) and Transgenic Plants and Applications (10 papers). Francis Rajamohan is often cited by papers focused on Insect Resistance and Genetics (13 papers), Insect and Pesticide Research (11 papers) and Transgenic Plants and Applications (10 papers). Francis Rajamohan collaborates with scholars based in United States, India and United Kingdom. Francis Rajamohan's co-authors include Donald H. Dean, Fatih M. Uckun, Fred Gould, Mi Kyong Lee, Michael K. Lee, April Curtiss, T.K. Venkatachalam, Algimantas P. Valaitis, Igor Kurinov and Hong Lü and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Applied and Environmental Microbiology.

In The Last Decade

Francis Rajamohan

38 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Francis Rajamohan United States 21 1.1k 631 456 265 207 38 1.6k
Martin Geiser Switzerland 25 1.4k 1.3× 174 0.3× 214 0.5× 123 0.5× 95 0.5× 34 2.0k
Carol S. Ringelberg United States 24 1.7k 1.6× 85 0.1× 1.1k 2.4× 88 0.3× 52 0.3× 33 2.6k
Jian Xu China 19 942 0.9× 121 0.2× 415 0.9× 172 0.6× 94 0.5× 100 1.6k
Markus Hartl Austria 23 1.2k 1.2× 149 0.2× 507 1.1× 160 0.6× 34 0.2× 52 1.9k
Hideki Inoue Japan 16 1.1k 1.0× 90 0.1× 114 0.3× 191 0.7× 30 0.1× 31 2.1k
Hui‐Wen Wu China 22 879 0.8× 140 0.2× 1.0k 2.2× 68 0.3× 123 0.6× 63 1.7k
Ryno J. Naudé South Africa 19 594 0.6× 55 0.1× 123 0.3× 128 0.5× 117 0.6× 92 1.3k
Ricardo Aparício Brazil 20 738 0.7× 71 0.1× 135 0.3× 84 0.3× 77 0.4× 61 1.3k
Isabelle Riezman Switzerland 18 1.2k 1.1× 72 0.1× 153 0.3× 77 0.3× 26 0.1× 22 1.6k
Dong Yang United States 24 1.1k 1.0× 39 0.1× 141 0.3× 64 0.2× 283 1.4× 94 1.9k

Countries citing papers authored by Francis Rajamohan

Since Specialization
Citations

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

Fields of papers citing papers by Francis Rajamohan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francis Rajamohan

This figure shows the co-authorship network connecting the top 25 collaborators of Francis Rajamohan. A scholar is included among the top collaborators of Francis Rajamohan 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 Francis Rajamohan. Francis Rajamohan 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.
Rajamohan, Francis, Allan R. Reyes, Meihua Tu, et al.. (2020). Crystal structure of human lysosomal acid lipase and its implications in cholesteryl ester storage disease. Journal of Lipid Research. 61(8). 1192–1202. 11 indexed citations
2.
Kurumbail, Ravi G., Graham M. West, Venkatasubramanian Dharmarajan, et al.. (2018). Biophysical Interactions of Direct AMPK Activators. Methods in molecular biology. 1732. 29–55. 1 indexed citations
3.
Caspers, Nicole, Seungil Han, Francis Rajamohan, et al.. (2016). Development of a high-throughput crystal structure-determination platform for JAK1 using a novel metal-chelator soaking system. Acta Crystallographica Section F Structural Biology Communications. 72(11). 840–845. 6 indexed citations
4.
Schwaid, Adam G., Allan R. Reyes, Shawn Cabral, et al.. (2016). Development of a selective activity-based probe for glycosylated LIPA. Bioorganic & Medicinal Chemistry Letters. 26(8). 1993–1996. 3 indexed citations
5.
Rajamohan, Francis, Allan R. Reyes, Lise R. Hoth, et al.. (2015). Expression and functional characterization of human lysosomal acid lipase gene (LIPA) mutation responsible for cholesteryl ester storage disease (CESD) phenotype. Protein Expression and Purification. 110. 22–29. 11 indexed citations
6.
Landgraf, Rachelle R., Devrishi Goswami, Francis Rajamohan, et al.. (2013). Activation of AMP-Activated Protein Kinase Revealed by Hydrogen/Deuterium Exchange Mass Spectrometry. Structure. 21(11). 1942–1953. 34 indexed citations
7.
Rajamohan, Francis, Eric S. Marr, Allan R. Reyes, et al.. (2011). Structure-guided Inhibitor Design for Human Acetyl-coenzyme A Carboxylase by Interspecies Active Site Conversion. Journal of Biological Chemistry. 286(48). 41510–41519. 5 indexed citations
8.
Geoghegan, Kieran F., Xidong Feng, Jeanne S. Chang, et al.. (2010). Initiation of translation at an upstream non-AUG codon accounting for N-terminally extended minor forms of recombinant proteins expressed in insect cells. Protein Expression and Purification. 76(1). 72–78. 4 indexed citations
9.
Rajamohan, Francis, Melissa S. Harris, Richard K. Frisbie, et al.. (2010). Escherichia coli expression, purification and characterization of functional full-length recombinant α2β2γ3 heterotrimeric complex of human AMP-activated protein kinase. Protein Expression and Purification. 73(2). 189–197. 21 indexed citations
10.
Yang, Rongze, Soohyun Park, William J. Reagan, et al.. (2008). Alanine aminotransferase isoenzymes: Molecular cloning and quantitative analysis of tissue expression in rats and serum elevation in liver toxicity #. Hepatology. 49(2). 598–607. 124 indexed citations
11.
Lippa, Blaise, Gonghua Pan, Matthew S. Corbett, et al.. (2008). Synthesis and structure based optimization of novel Akt inhibitors. Bioorganic & Medicinal Chemistry Letters. 18(11). 3359–3363. 64 indexed citations
12.
Rajamohan, Francis, et al.. (2000). Expression of Biologically Active Recombinant Pokeweed Antiviral Protein in Methylotrophic Yeast Pichia pastoris. Protein Expression and Purification. 18(2). 193–201. 13 indexed citations
13.
Rajamohan, Francis, et al.. (2000). Identification of the Functional Site in the Mosquito Larvicidal Binary Toxin of Bacillus sphaericus 1593M by Site-Directed Mutagenesis. Biochemical and Biophysical Research Communications. 276(3). 1048–1055. 18 indexed citations
15.
Rajamohan, Francis, Igor Kurinov, T.K. Venkatachalam, & Fatih M. Uckun. (1999). Deguanylation of Human Immunodeficiency Virus (HIV-1) RNA by Recombinant Pokeweed Antiviral Protein. Biochemical and Biophysical Research Communications. 263(2). 419–424. 32 indexed citations
16.
Kurinov, Igor, Francis Rajamohan, T.K. Venkatachalam, & Fatih M. Uckun. (1999). X‐ray crystallographic analysis of the structural basis for the interaction of pokeweed antiviral protein with guanine residues of ribosomal RNA. Protein Science. 8(11). 2399–2405. 19 indexed citations
17.
Rajamohan, Francis, et al.. (1999). High-Level Expression and Purification of Biologically Active Recombinant Pokeweed Antiviral Protein. Protein Expression and Purification. 16(2). 359–368. 30 indexed citations
18.
Rajamohan, Francis, et al.. (1996). Role of Domain II, Loop 2 Residues of Bacillus thuringiensis CryIAb δ-Endotoxin in Reversible and Irreversible Binding to Manduca sexta and Heliothis virescens. Journal of Biological Chemistry. 271(5). 2390–2396. 58 indexed citations
19.
20.
Valaitis, Algimantas P., Mi Kyong Lee, Francis Rajamohan, & Donald H. Dean. (1995). Brush border membrane aminopeptidase-n in the midgut of the gypsy moth serves as the receptor for the CryIA(c) δ-endotoxin of Bacillus thuringiensis. Insect Biochemistry and Molecular Biology. 25(10). 1143–1151. 102 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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