R J Trent

1.6k total citations
29 papers, 796 citations indexed

About

R J Trent is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, R J Trent has authored 29 papers receiving a total of 796 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Genetics. Recurrent topics in R J Trent's work include Hemoglobinopathies and Related Disorders (8 papers), Folate and B Vitamins Research (5 papers) and Metabolism and Genetic Disorders (4 papers). R J Trent is often cited by papers focused on Hemoglobinopathies and Related Disorders (8 papers), Folate and B Vitamins Research (5 papers) and Metabolism and Genetic Disorders (4 papers). R J Trent collaborates with scholars based in Australia, New Zealand and United States. R J Trent's co-authors include K N Mickleson, Magnus Hertzberg, Bing Yu, Tanya Boston, Brett D. Hambly, S. W. Serjeantson, John F. Prior, Douglas R. Higgs, D. J. Weatherall and Stephen Oppenheimer and has published in prestigious journals such as Nucleic Acids Research, Blood and British Journal of Haematology.

In The Last Decade

R J Trent

29 papers receiving 754 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R J Trent Australia 15 473 235 155 124 120 29 796
Stavit Shalev Israel 14 70 0.1× 172 0.7× 16 0.1× 67 0.5× 17 0.1× 29 536
B. Rafael Elejalde United States 15 467 1.0× 357 1.5× 7 0.0× 37 0.3× 10 0.1× 39 833
Dashzeveg Bayarsaihan United States 16 172 0.4× 710 3.0× 39 0.3× 26 0.2× 5 0.0× 48 1.1k
Edmond G. Lemire Canada 14 202 0.4× 240 1.0× 16 0.1× 51 0.4× 4 0.0× 42 616
Jürgen Föll Germany 11 149 0.3× 202 0.9× 82 0.5× 22 0.2× 3 0.0× 19 660
F Salamanca Mexico 15 287 0.6× 285 1.2× 31 0.2× 33 0.3× 2 0.0× 60 709
Ana Elisa C. Billerbeck Brazil 23 747 1.6× 1.1k 4.6× 19 0.1× 21 0.2× 5 0.0× 53 1.5k
LaDonna Immken United States 13 339 0.7× 372 1.6× 9 0.1× 20 0.2× 5 0.0× 21 689
Estelle Colin France 13 237 0.5× 304 1.3× 30 0.2× 62 0.5× 2 0.0× 36 546

Countries citing papers authored by R J Trent

Since Specialization
Citations

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

Fields of papers citing papers by R J Trent

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R J Trent

This figure shows the co-authorship network connecting the top 25 collaborators of R J Trent. A scholar is included among the top collaborators of R J Trent 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 R J Trent. R J Trent 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.
Morahan, Julia M., Bing Yu, R J Trent, & Roger Pamphlett. (2006). Are metallothionein genes silenced in ALS?. Toxicology Letters. 168(1). 83–87. 24 indexed citations
2.
3.
Yu, Shaoqing, A L Fimmel, David Fung, & R J Trent. (2000). Polymorphisms in the CAG repeat – a source of error in Huntington disease DNA testing. Clinical Genetics. 58(6). 469–472. 16 indexed citations
4.
McCusker, Elizabeth, Fiona Richards, David Sillence, Matthew Wilson, & R J Trent. (2000). Huntington’s disease: neurological assessment of potential gene carriers presenting for predictive DNA testing. Journal of Clinical Neuroscience. 7(1). 38–41. 15 indexed citations
5.
Yu, Bing, et al.. (1998). Elite endurance athletes and the ACE I allele - the role of genes in athletic performance. Human Genetics. 103(1). 48–50. 281 indexed citations
6.
Trent, R J. (1998). Oligonucleotides as Therapeutic Agents. Journal of Medical Genetics. 35(8). 703.2–704. 17 indexed citations
7.
Trent, R J. (1995). Handbook of prenatal diagnosis. Cambridge University Press eBooks. 1 indexed citations
8.
Serjeantson, S. W., et al.. (1994). A 3.5 kb deletion in the glycophorin C gene accounts for the Gerbich‐negative blood group in Melanesians. Immunology and Cell Biology. 72(1). 23–27. 12 indexed citations
9.
Crosbie, J., et al.. (1993). Human Gγ and Aγ globin gene constructs containing the 3′ Aγ enhancer show persistent fetal expression in transgenic mice. Transgenic Research. 2(2). 121–124. 1 indexed citations
10.
Hertzberg, Magnus, K N Mickleson, & R J Trent. (1992). Limited Genetic Diversity in Polynesians Reflected in the Highly Polymorphic 3’HVRα-Globin Gene Marker. Human Heredity. 42(3). 157–161. 13 indexed citations
11.
Lindeman, Robert W., et al.. (1991). Dinucleotide repeat polymorphism of D15S10 in the Prader-Willi chromosome region (PWCR). Nucleic Acids Research. 19(19). 5449–5449. 20 indexed citations
12.
Trent, R J. (1991). Human Prenatal Diagnosis. Pathology. 23(4). 367–367. 1 indexed citations
13.
Kearney, Alison L., et al.. (1990). Occurrence of the alpha thalassaemia-mental retardation syndrome (non-deletional type) in an Australian male.. Journal of Medical Genetics. 27(9). 577–581. 11 indexed citations
14.
Hertzberg, Magnus, Virginia L. Ferguson, H H Dahl, et al.. (1989). Phenylalanine hydroxylase gene haplotypes in Polynesians: evolutionary origins and absence of alleles associated with severe phenylketonuria.. PubMed. 44(3). 382–7. 22 indexed citations
15.
Donald, Jennifer A., et al.. (1988). Hemoglobin F production in heterocellular hereditary persistence of fetal hemoglobin and its linkage to the ? globin gene complex. Human Genetics. 80(1). 69–74. 5 indexed citations
16.
Trent, R J, et al.. (1988). Population Genetics of the Globin Genes in Polynesians. Hemoglobin. 12(5-6). 533–537. 8 indexed citations
17.
Hertzberg, Magnus, K N Mickleson, & R J Trent. (1988). Alpha-globin gene haplotypes in Polynesians: their relationships to population groups and gene rearrangements.. PubMed. 43(6). 971–7. 15 indexed citations
18.
Serjeantson, S. W., et al.. (1987). HLA-DR and -DQ DNA polymorphisms: New linkage relationships established by RFLP genomic typing in Polynesians and Melanesians. Human Immunology. 20(2). 145–153. 17 indexed citations
19.
Hill, Adrian V. S., D. K. Bowden, R J Trent, et al.. (1985). Melanesians and Polynesians share a unique alpha-thalassemia mutation.. PubMed. 37(3). 571–80. 70 indexed citations
20.
Higgs, Douglas R., et al.. (1981). THE MOLECULAR BASIS FOR THE HAEMOGLOBIN BART'S HYDROPS FETALIS SYNDROME IN CYPRUS. British Journal of Haematology. 47(1). 153–156. 24 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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