David Catcheside

4.1k total citations
85 papers, 1.3k citations indexed

About

David Catcheside is a scholar working on Molecular Biology, Plant Science and Cell Biology. According to data from OpenAlex, David Catcheside has authored 85 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 27 papers in Plant Science and 14 papers in Cell Biology. Recurrent topics in David Catcheside's work include Fungal and yeast genetics research (27 papers), Photosynthetic Processes and Mechanisms (25 papers) and DNA Repair Mechanisms (20 papers). David Catcheside is often cited by papers focused on Fungal and yeast genetics research (27 papers), Photosynthetic Processes and Mechanisms (25 papers) and DNA Repair Mechanisms (20 papers). David Catcheside collaborates with scholars based in Australia, United States and United Kingdom. David Catcheside's co-authors include John Ralph, P. Jane Yeadon, Frederick J. Bowring, Santo Ragusa, Max E. Tate, H. Wallwork, Amanda J. Able, Colin H. Doy, Frank Kempken and David R. Rank and has published in prestigious journals such as Science, PLoS ONE and Water Research.

In The Last Decade

David Catcheside

80 papers receiving 1.2k 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 Catcheside Australia 20 597 500 223 156 154 85 1.3k
Susana Castro‐Sowinski Uruguay 23 448 0.8× 633 1.3× 140 0.6× 66 0.4× 82 0.5× 59 1.5k
M. Mergeay Belgium 15 499 0.8× 484 1.0× 231 1.0× 98 0.6× 24 0.2× 24 1.4k
Amjad Hussain China 22 710 1.2× 1.1k 2.2× 84 0.4× 43 0.3× 47 0.3× 65 1.8k
László Márton Hungary 26 1.3k 2.2× 1.4k 2.8× 78 0.3× 69 0.4× 67 0.4× 83 2.2k
Anthony J. Travis United Kingdom 20 507 0.8× 672 1.3× 88 0.4× 93 0.6× 26 0.2× 44 1.4k
J. Balandreau France 24 420 0.7× 1.6k 3.1× 102 0.5× 49 0.3× 82 0.5× 45 2.0k
Qun Zhu China 22 771 1.3× 927 1.9× 75 0.3× 396 2.5× 43 0.3× 45 1.8k
Dananjeyan Balachandar India 24 293 0.5× 833 1.7× 89 0.4× 71 0.5× 89 0.6× 118 1.4k
Gabriel Castrillo United Kingdom 24 927 1.6× 3.2k 6.5× 113 0.5× 241 1.5× 209 1.4× 36 3.8k
Katsuji Ueki Japan 22 575 1.0× 532 1.1× 147 0.7× 199 1.3× 106 0.7× 61 1.3k

Countries citing papers authored by David Catcheside

Since Specialization
Citations

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

Fields of papers citing papers by David Catcheside

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Catcheside

This figure shows the co-authorship network connecting the top 25 collaborators of David Catcheside. A scholar is included among the top collaborators of David Catcheside 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 Catcheside. David Catcheside 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.
Burgoyne, L.A., et al.. (2017). Arbitrarily Primed PCR for Comparison of Meta Genomes and Extracting Useful Loci from Them. Methods in molecular biology. 1620. 267–280. 2 indexed citations
2.
Yeadon, P. Jane, Frederick J. Bowring, & David Catcheside. (2016). Meiotic Recombination in Neurospora crassa Proceeds by Two Pathways with Extensive Holliday Junction Migration. PLoS ONE. 11(1). e0147815–e0147815. 3 indexed citations
3.
Peluso, Paul, P. Jane Yeadon, Charles Yu, et al.. (2014). Long-read, whole-genome shotgun sequence data for five model organisms. Scientific Data. 1(1). 140045–140045. 113 indexed citations
4.
Bowring, Frederick J., P. Jane Yeadon, & David Catcheside. (2012). Use of fluorescent protein to analyse recombination at three loci in Neurospora crassa. Fungal Genetics and Biology. 49(8). 619–625. 3 indexed citations
5.
Chen, Tong, et al.. (2011). A Rapid Wire‐Based Sampling Method for DNA Profiling*. Journal of Forensic Sciences. 57(2). 472–477. 2 indexed citations
6.
Bowring, Frederick J., et al.. (2006). Chromosome pairing and meiotic recombination in Neurospora crassa spo11 mutants. Current Genetics. 50(2). 115–123. 24 indexed citations
7.
Yeadon, P. Jane, et al.. (2004). Sequence heterology and gene conversion at his-3 of Neurospora crassa. Current Genetics. 45(5). 289–301. 4 indexed citations
8.
Ma, Li‐Jun, et al.. (2003). Guest, a transposable element belonging to the Tc1/mariner superfamily is an ancient invader of Neurospora genomes. Fungal Genetics and Biology. 41(1). 52–61. 10 indexed citations
9.
Catcheside, David, P. Jane Yeadon, Frederick J. Bowring, et al.. (2003). Diversification of exogenous genes in vivo in Neurospora. Applied Microbiology and Biotechnology. 62(5-6). 544–549. 6 indexed citations
10.
Windhofer, Frank, et al.. (2002). Ds-like Restless Deletion Derivatives Occur in Tolypocladium inflatum and Two Foreign Hosts, Neurospora crassa and Penicillium chrysogenum. Fungal Genetics and Biology. 35(2). 171–182. 19 indexed citations
11.
Bok, Jin-Woo, Teruo Sone, Lorelei Silverman‐Gavrila, et al.. (2001). Structure and Function Analysis of the Calcium-Related Gene spray in Neurospora crassa. Fungal Genetics and Biology. 32(3). 145–158. 25 indexed citations
12.
Windhofer, Frank, David Catcheside, & Frank Kempken. (2000). Methylation of the foreign transposon Restless in vegetative mycelia of Neurospora crassa. Current Genetics. 37(3). 194–199. 14 indexed citations
13.
Bowring, Frederick J. & David Catcheside. (1999). Recombinational landscape across a 650-kb contig on the right arm of linkage group V in Neurospora crassa. Current Genetics. 36(5). 270–274. 7 indexed citations
14.
Yeadon, P. Jane & David Catcheside. (1999). Polymorphism around cog extends into adjacent structural genes. Current Genetics. 35(6). 631–637. 11 indexed citations
15.
Catcheside, David, et al.. (1998). Analysis of conversion tracts associated with recombination events at the am locus of Neurospora crassa. Current Genetics. 34(1). 43–49. 9 indexed citations
16.
Bowring, Frederick J. & David Catcheside. (1996). Gene Conversion Alone Accounts for More Than 90% of Recombination Events at the am Locus of Neurospora crassa. Genetics. 143(1). 129–136. 28 indexed citations
17.
Yeadon, P. Jane & David Catcheside. (1995). Guest: a 98 bp inverted repeat transposable element in Neurospora crassa. Molecular and General Genetics MGG. 247(1). 105–109. 51 indexed citations
18.
Bowring, Frederick J. & David Catcheside. (1995). The orientation of gene maps by recombination of flanking markers for the am locus of Neurospora crassa. Current Genetics. 29(1). 27–33. 5 indexed citations
19.
Bowring, Frederick J. & David Catcheside. (1991). The initiation site for recombination cog is at the 3′ end of the his-3 gene in Neurospora crassa. Molecular and General Genetics MGG. 229(2). 273–277. 16 indexed citations
20.
Berry, Anne M., James C. Paton, Eric M. Glare, David Hansman, & David Catcheside. (1988). Cloning and expression of the pneumococcal neuraminidase gene in Escherichia coli. Gene. 71(2). 299–305. 32 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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