Hugh D. Campbell

2.9k total citations
43 papers, 2.5k citations indexed

About

Hugh D. Campbell is a scholar working on Molecular Biology, Cell Biology and Immunology. According to data from OpenAlex, Hugh D. Campbell has authored 43 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 10 papers in Cell Biology and 7 papers in Immunology. Recurrent topics in Hugh D. Campbell's work include Cellular Mechanics and Interactions (6 papers), Immune Cell Function and Interaction (5 papers) and RNA Research and Splicing (4 papers). Hugh D. Campbell is often cited by papers focused on Cellular Mechanics and Interactions (6 papers), Immune Cell Function and Interaction (5 papers) and RNA Research and Splicing (4 papers). Hugh D. Campbell collaborates with scholars based in Australia, United States and United Kingdom. Hugh D. Campbell's co-authors include Ian G. Young, S. Ymer, Charles Claudianos, M. C. Fung, Anthony Jaworowski, Donna Cohén, R. M. Johnson, Andrew J. Hapel, Colin J. Sanderson and William Q. J. Tucker and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Hugh D. Campbell

43 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hugh D. Campbell Australia 27 1.2k 724 350 346 265 43 2.5k
Christine A. Kozak United States 30 1.9k 1.5× 651 0.9× 315 0.9× 696 2.0× 171 0.6× 65 2.9k
Juhani Saarinen Finland 25 1.1k 0.9× 682 0.9× 319 0.9× 120 0.3× 139 0.5× 37 2.4k
Nicholas Harris United States 23 1.5k 1.2× 1.4k 1.9× 133 0.4× 246 0.7× 278 1.0× 37 3.5k
Jane Clifford Azizkhan United States 28 2.3k 1.9× 534 0.7× 263 0.8× 539 1.6× 135 0.5× 44 3.5k
Akio Matsuda Japan 33 2.0k 1.6× 810 1.1× 238 0.7× 239 0.7× 409 1.5× 111 3.7k
Susana González Spain 20 3.2k 2.6× 547 0.8× 185 0.5× 223 0.6× 489 1.8× 30 4.2k
Christopher C. Rider United Kingdom 27 1.3k 1.1× 285 0.4× 568 1.6× 149 0.4× 113 0.4× 63 2.3k
James F. Crish United States 29 1.4k 1.1× 350 0.5× 817 2.3× 180 0.5× 138 0.5× 50 2.7k
Walker Wharton United States 27 1.9k 1.5× 365 0.5× 242 0.7× 222 0.6× 216 0.8× 74 3.5k
François Amalric France 42 3.6k 2.9× 750 1.0× 498 1.4× 380 1.1× 144 0.5× 76 4.7k

Countries citing papers authored by Hugh D. Campbell

Since Specialization
Citations

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

Fields of papers citing papers by Hugh D. Campbell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hugh D. Campbell

This figure shows the co-authorship network connecting the top 25 collaborators of Hugh D. Campbell. A scholar is included among the top collaborators of Hugh D. Campbell 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 Hugh D. Campbell. Hugh D. Campbell 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.
Ali, Radiya G., Tamsin E. M. Jones, Damian Adams, et al.. (2011). Mouse strains for the ubiquitous or conditional overexpression of the Flii gene. genesis. 49(8). 681–688. 15 indexed citations
2.
Adams, Damian, Nadira Ruzehaji, Xanthe L. Strudwick, et al.. (2009). Attenuation of Flightless I, an actin-remodelling protein, improves burn injury repair via modulation of transforming growth factor (TGF)-β1 and TGF-β3. British Journal of Dermatology. 161(2). 326–336. 42 indexed citations
3.
Adams, Damian, Xanthe L. Strudwick, Zlatko Kopecki, et al.. (2007). Gender specific effects on the actin-remodelling protein Flightless I and TGF-β1 contribute to impaired wound healing in aged skin. The International Journal of Biochemistry & Cell Biology. 40(8). 1555–1569. 26 indexed citations
4.
Young, Ian G., et al.. (2006). Expression and evolution of the mammalian brain gene Ttyh1. Journal of Neurochemistry. 100(3). 693–707. 30 indexed citations
5.
Archer, Stuart K., Charles Claudianos, & Hugh D. Campbell. (2005). Evolution of the gelsolin family of actin-binding proteins as novel transcriptional coactivators. BioEssays. 27(4). 388–396. 53 indexed citations
6.
Campbell, Hugh D., Ian S. McLennan, Leise A. Berven, et al.. (2002). Fliih, a Gelsolin-Related Cytoskeletal Regulator Essential for Early Mammalian Embryonic Development. Molecular and Cellular Biology. 22(10). 3518–3526. 75 indexed citations
7.
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9.
Campbell, Hugh D., et al.. (1997). The HumanPIN1Peptidyl-Prolylcis/transIsomerase Gene Maps to Human Chromosome 19p13 and the Closely RelatedPIN1LGene to 1p31. Genomics. 44(2). 157–162. 16 indexed citations
10.
Campbell, Hugh D., et al.. (1997). Genomic Structure, Evolution, and Expression of HumanFLII,a Gelsolin and Leucine-Rich-Repeat Family Member: Overlap withLLGL. Genomics. 42(1). 46–54. 34 indexed citations
11.
Campbell, Hugh D., Graham C. Webb, & Ian G. Young. (1997). A human homologue of the Drosophila melanogaster sluggish-A (proline oxidase) gene maps to 22q11.2, and is a candidate gene for type-I hyperprolinaemia. Human Genetics. 101(1). 69–74. 26 indexed citations
12.
Campbell, Hugh D., et al.. (1992). The evolution of protein domains and the organizational complexities of metazoans. Current Opinion in Genetics & Development. 2(6). 902–906. 13 indexed citations
13.
Webb, Graham C., et al.. (1989). The genes for interleukins 3 and 5 map to the same locus on mouse chromosome 11. Cytogenetic and Genome Research. 50(2-3). 107–110. 23 indexed citations
14.
Ymer, S., William Q. J. Tucker, Hugh D. Campbell, & Ian G. Young. (1986). Nudeotide sequence of the intracisternal A-particle genome Inserted 5′ to the lnterleukin-3 gene of the leukaemia cell line WEHI-3B. Nucleic Acids Research. 14(14). 5901–5918. 53 indexed citations
15.
Campbell, Hugh D. & Ian G. Young. (1983). Stereospecificity and requirements for activity of the respiratory NADH dehydrogenase of Escherichia coli. Biochemistry. 22(25). 5754–5760. 7 indexed citations
16.
Jaworowski, Anthony, et al.. (1981). Characterization of the respiratory NADH dehydrogenase of Escherichia coli and reconstitution of NADH oxidase in ndh mutant membrane vesicles. Biochemistry. 20(12). 3621–3628. 84 indexed citations
17.
Shaw, Denis C., et al.. (1981). In vitro synthesis of the respiratory dehydrogenase of Escherichia coli. Role of UUG as initiation codon. Biochemistry. 20(14). 4178–4185. 33 indexed citations
18.
Jaworowski, Anthony, et al.. (1981). Genetic identification and purification of the respiratory NADH dehydrogenase of Escherichia coli. Biochemistry. 20(7). 2041–2047. 59 indexed citations
19.
Hamilton, Susan E., Hugh D. Campbell, John de Jersey, & Burt Zerner. (1975). Carboxylesterases (EC 3.1.1). The source of variations in substrate specificity and properties of pig liver carboxylesterase. Biochemical and Biophysical Research Communications. 63(4). 1146–1150. 5 indexed citations
20.
Campbell, Hugh D. & Burt Zerner. (1973). A low-molecular-weight acid phosphatase which contains iron. Biochemical and Biophysical Research Communications. 54(4). 1498–1503. 48 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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