David B. Guiliano

2.5k total citations
35 papers, 1.6k citations indexed

About

David B. Guiliano is a scholar working on Infectious Diseases, Molecular Biology and Insect Science. According to data from OpenAlex, David B. Guiliano has authored 35 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Infectious Diseases, 11 papers in Molecular Biology and 10 papers in Insect Science. Recurrent topics in David B. Guiliano's work include Parasitic Diseases Research and Treatment (14 papers), Insect symbiosis and bacterial influences (8 papers) and Parasite Biology and Host Interactions (8 papers). David B. Guiliano is often cited by papers focused on Parasitic Diseases Research and Treatment (14 papers), Insect symbiosis and bacterial influences (8 papers) and Parasite Biology and Host Interactions (8 papers). David B. Guiliano collaborates with scholars based in United Kingdom, United States and Indonesia. David B. Guiliano's co-authors include Mark Blaxter, John Parkinson, Judith E. Allen, Sara Lustigman, Steven A. Williams, Jennifer Daub, P’ng Loke, Meera G. Nair, Yelena Oksov and Alan L. Scott and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and The Journal of Infectious Diseases.

In The Last Decade

David B. Guiliano

35 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
David B. Guiliano United Kingdom 21 539 420 382 376 314 35 1.6k
Antony P. Page United Kingdom 26 783 1.5× 247 0.6× 233 0.6× 492 1.3× 184 0.6× 56 1.8k
Tellervo Huima United States 20 397 0.7× 355 0.8× 236 0.6× 213 0.6× 122 0.4× 31 1.4k
William F. Gregory United Kingdom 23 359 0.7× 688 1.6× 477 1.2× 797 2.1× 294 0.9× 36 1.7k
Tatsuyuki Mimori Japan 27 564 1.0× 157 0.4× 125 0.3× 296 0.8× 236 0.8× 85 2.2k
G. F. J. NEWLANDS United Kingdom 28 349 0.6× 222 0.5× 511 1.3× 708 1.9× 59 0.2× 58 2.2k
Juan F. Quintana United Kingdom 13 759 1.4× 236 0.6× 366 1.0× 464 1.2× 197 0.6× 25 1.6k
Matthew A. Field Australia 24 722 1.3× 348 0.8× 249 0.7× 228 0.6× 39 0.1× 71 1.8k
Robert J. Pryor United States 12 1.3k 2.3× 162 0.4× 271 0.7× 78 0.2× 66 0.2× 13 2.3k
Jean-Marc Reichhart France 7 830 1.5× 212 0.5× 58 0.2× 132 0.4× 852 2.7× 7 3.6k
Elena Rydkina United States 18 417 0.8× 658 1.6× 22 0.1× 937 2.5× 215 0.7× 30 1.8k

Countries citing papers authored by David B. Guiliano

Since Specialization
Citations

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

Fields of papers citing papers by David B. Guiliano

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David B. Guiliano. 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 David B. Guiliano. The network helps show where David B. Guiliano may publish in the future.

Co-authorship network of co-authors of David B. Guiliano

This figure shows the co-authorship network connecting the top 25 collaborators of David B. Guiliano. A scholar is included among the top collaborators of David B. Guiliano 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 David B. Guiliano. David B. Guiliano 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.
Guiliano, David B., et al.. (2023). Bioengineering of Antibody Fragments: Challenges and Opportunities. Bioengineering. 10(2). 122–122. 31 indexed citations
2.
Oksov, Yelena, et al.. (2020). Vaccination with novel low-molecular weight proteins secreted from Trichinella spiralis inhibits establishment of infection. PLoS neglected tropical diseases. 14(11). e0008842–e0008842. 6 indexed citations
3.
Awwad, Sahar, et al.. (2020). Dual-acting therapeutic proteins for intraocular use. Drug Discovery Today. 26(1). 44–55. 2 indexed citations
4.
Fasken, Milo B., Shonna M. McBride, Emily G. Kuiper, et al.. (2014). Functional Heterologous Protein Expression by Genetically Engineered Probiotic Yeast Saccharomyces boulardii. PLoS ONE. 9(11). e112660–e112660. 43 indexed citations
5.
Guiliano, David B. & Antony N. Antoniou. (2012). Measuring Synthesis and Degradation of MHC Class I Molecules. Methods in molecular biology. 1988. 93–108. 4 indexed citations
6.
Antoniou, Antony N., et al.. (2011). The Oxidative Folding and Misfolding of Human Leukocyte Antigen-B27. Antioxidants and Redox Signaling. 15(3). 669–684. 8 indexed citations
7.
Guiliano, David B., Yelena Oksov, Sara Lustigman, Kleoniki Gounaris, & Murray E. Selkirk. (2008). Characterisation of novel protein families secreted by muscle stage larvae of Trichinella spiralis. International Journal for Parasitology. 39(5). 515–524. 15 indexed citations
8.
Guiliano, David B. & Mark Blaxter. (2006). Operon Conservation and the Evolution of trans-Splicing in the Phylum Nematoda. PLoS Genetics. 2(11). e198–e198. 62 indexed citations
9.
Ford, Louise, David B. Guiliano, Yelena Oksov, et al.. (2005). Characterization of a Novel Filarial Serine Protease Inhibitor, Ov-SPI-1, from Onchocerca volvulus, with Potential Multifunctional Roles during Development of the Parasite. Journal of Biological Chemistry. 280(49). 40845–40856. 60 indexed citations
10.
Guiliano, David B., Xiqiang Hong, James H. McKerrow, et al.. (2004). A gene family of cathepsin L-like proteases of filarial nematodes are associated with larval molting and cuticle and eggshell remodeling. Molecular and Biochemical Parasitology. 136(2). 227–242. 85 indexed citations
11.
Lamb, Tracey J., Laëtitia Le Goff, Agnes Kurniawan, et al.. (2004). Most of the Response Elicited against Wolbachia Surface Protein in Filarial Nematode Infection Is Due to the Infective Larval Stage. The Journal of Infectious Diseases. 189(1). 120–127. 22 indexed citations
12.
Guiliano, David B., et al.. (2002). Conservation of long-range synteny and microsynteny between the genomes of two distantly related nematodes. Genome biology. 3(10). RESEARCH0057–RESEARCH0057. 55 indexed citations
13.
Blaxter, Mark, et al.. (2002). The Brugia malayi genome project: expressed sequence tags and gene discovery. Transactions of the Royal Society of Tropical Medicine and Hygiene. 96(1). 7–17. 66 indexed citations
14.
Ware, Jennifer, Laurie S. Moran, Jeremy M. Foster, et al.. (2002). Sequencing and analysis of a 63 kb bacterial artificial chromosome insert from the Wolbachia endosymbiont of the human filarial parasite Brugia malayi. International Journal for Parasitology. 32(2). 159–166. 7 indexed citations
15.
Loke, P’ng, Meera G. Nair, John Parkinson, et al.. (2002). IL-4 dependent alternatively-activated macrophages have a distinctive in vivo gene expression phenotype. BMC Immunology. 3(1). 7–7. 275 indexed citations
16.
Parkinson, John, Claire Whitton, David B. Guiliano, Jennifer Daub, & Mark Blaxter. (2001). 200 000 nematode expressed sequence tags on the Net. Trends in Parasitology. 17(8). 394–396. 36 indexed citations
17.
Lizotte‐Waniewski, Michelle, Wilson Tawe, David B. Guiliano, et al.. (2000). Identification of Potential Vaccine and Drug Target Candidates by Expressed Sequence Tag Analysis and Immunoscreening ofOnchocerca volvulusLarval cDNA Libraries. Infection and Immunity. 68(6). 3491–3501. 79 indexed citations
18.
Williams, Steven A., Michelle Lizotte‐Waniewski, Jeremy M. Foster, et al.. (2000). The filarial genome project: analysis of the nuclear, mitochondrial and endosymbiont genomes of Brugia malayi. International Journal for Parasitology. 30(4). 411–419. 75 indexed citations
19.
Blaxter, Mark, Nithyakalyani Raghavan, Inca Ghosh, et al.. (1996). Genes expressed in Brugia malayi infective third stage larvae. Molecular and Biochemical Parasitology. 77(1). 77–93. 99 indexed citations
20.
Blaxter, Mark, Jennifer Daub, David B. Guiliano, et al.. (1995). The Filarial Genome Project. Parasitology Today. 11. 811–812. 11 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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