Jason Ellul

3.0k total citations
15 papers, 829 citations indexed

About

Jason Ellul is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Jason Ellul has authored 15 papers receiving a total of 829 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Cancer Research and 4 papers in Genetics. Recurrent topics in Jason Ellul's work include Cancer Genomics and Diagnostics (6 papers), Genomics and Rare Diseases (3 papers) and Genomics and Phylogenetic Studies (3 papers). Jason Ellul is often cited by papers focused on Cancer Genomics and Diagnostics (6 papers), Genomics and Rare Diseases (3 papers) and Genomics and Phylogenetic Studies (3 papers). Jason Ellul collaborates with scholars based in Australia, United States and United Kingdom. Jason Ellul's co-authors include Jason Li, Grant A. McArthur, David M. Thomas, Stephen B. Fox, Andrew Fellowes, Ross D. Hannan, Stephen Q. Wong, Elaine Sanij, Alexander Dobrovic and Ravikiran Vedururu and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Investigation and PLoS ONE.

In The Last Decade

Jason Ellul

15 papers receiving 821 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jason Ellul Australia 14 476 301 225 186 139 15 829
Anne Reiman United Kingdom 12 564 1.2× 367 1.2× 303 1.3× 278 1.5× 177 1.3× 18 901
Peiyong Guan Singapore 13 560 1.2× 308 1.0× 167 0.7× 102 0.5× 130 0.9× 26 897
Beate Betz Germany 16 610 1.3× 224 0.7× 187 0.8× 243 1.3× 167 1.2× 25 928
Hendrik F. van Essen Netherlands 13 326 0.7× 276 0.9× 278 1.2× 153 0.8× 200 1.4× 22 775
Sally M. Hunter Australia 14 413 0.9× 248 0.8× 199 0.9× 151 0.8× 154 1.1× 20 852
Keisuke Kurose Japan 14 634 1.3× 310 1.0× 312 1.4× 96 0.5× 191 1.4× 30 1.0k
Nicolas Goardon France 16 470 1.0× 223 0.7× 160 0.7× 245 1.3× 114 0.8× 29 905
Narinder Tamber United Kingdom 13 533 1.1× 456 1.5× 459 2.0× 125 0.7× 197 1.4× 13 1.1k
Arisa Ueki Japan 19 386 0.8× 341 1.1× 213 0.9× 113 0.6× 191 1.4× 66 870
Chiara Battelli United States 9 504 1.1× 264 0.9× 210 0.9× 300 1.6× 141 1.0× 17 837

Countries citing papers authored by Jason Ellul

Since Specialization
Citations

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

Fields of papers citing papers by Jason Ellul

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jason Ellul

This figure shows the co-authorship network connecting the top 25 collaborators of Jason Ellul. A scholar is included among the top collaborators of Jason Ellul 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 Jason Ellul. Jason Ellul is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

15 of 15 papers shown
1.
Markham, John, Georgina L. Ryland, Huei San Leong, et al.. (2019). CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencing. Scientific Reports. 9(1). 6426–6426. 19 indexed citations
2.
Doig, Kenneth, Andrew Fellowes, Anthony Bell, et al.. (2017). PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories. Genome Medicine. 9(1). 38–38. 19 indexed citations
3.
Doig, Kenneth, Jason Ellul, Andrew Fellowes, et al.. (2017). Canary: an atomic pipeline for clinical amplicon assays. BMC Bioinformatics. 18(1). 555–555. 2 indexed citations
4.
Wong, Stephen Q., Andrew Fellowes, Jason Ellul, et al.. (2015). Assessing the clinical value of targeted massively parallel sequencing in a longitudinal, prospective population-based study of cancer patients. British Journal of Cancer. 112(8). 1411–1420. 40 indexed citations
5.
Doggett, Karen, Nezaket Türkel, Lee Willoughby, et al.. (2015). BTB-Zinc Finger Oncogenes Are Required for Ras and Notch-Driven Tumorigenesis in Drosophila. PLoS ONE. 10(7). e0132987–e0132987. 28 indexed citations
6.
Sanij, Elaine, Jeannine Diesch, Gretchen Poortinga, et al.. (2014). A novel role for the Pol I transcription factor UBTF in maintaining genome stability through the regulation of highly transcribed Pol II genes. Genome Research. 25(2). 201–212. 45 indexed citations
7.
Wong, Stephen Q., Jason Li, Angela Tan, et al.. (2014). Sequence artefacts in a prospective series of formalin-fixed tumours tested for mutations in hotspot regions by massively parallel sequencing. BMC Medical Genomics. 7(1). 23–23. 192 indexed citations
8.
Li, Jason, Maria Doyle, Isaam Saeed, et al.. (2014). Bioinformatics Pipelines for Targeted Resequencing and Whole-Exome Sequencing of Human and Mouse Genomes: A Virtual Appliance Approach for Instant Deployment. PLoS ONE. 9(4). e95217–e95217. 18 indexed citations
9.
Diesch, Jeannine, Elaine Sanij, Omer Gilan, et al.. (2014). Widespread FRA1-Dependent Control of Mesenchymal Transdifferentiation Programs in Colorectal Cancer Cells. PLoS ONE. 9(3). e88950–e88950. 67 indexed citations
10.
Matthews, Geoffrey M., Marcus Lefebure, Maria Doyle, et al.. (2013). Preclinical screening of histone deacetylase inhibitors combined with ABT-737, rhTRAIL/MD5-1 or 5-azacytidine using syngeneic Vk*MYC multiple myeloma. Cell Death and Disease. 4(9). e798–e798. 41 indexed citations
11.
Türkel, Nezaket, Jessica E. Bolden, Karen Doggett, et al.. (2013). The BTB-zinc Finger Transcription Factor Abrupt Acts as an Epithelial Oncogene in Drosophila melanogaster through Maintaining a Progenitor-like Cell State. PLoS Genetics. 9(7). e1003627–e1003627. 28 indexed citations
12.
Kansara, Maya, Huei San Leong, Puiyi Pang, et al.. (2013). Immune response to RB1-regulated senescence limits radiation-induced osteosarcoma formation. Journal of Clinical Investigation. 123(12). 5351–5360. 64 indexed citations
13.
Thompson, Ella R., Maria Doyle, Georgina L. Ryland, et al.. (2012). Exome Sequencing Identifies Rare Deleterious Mutations in DNA Repair Genes FANCC and BLM as Potential Breast Cancer Susceptibility Alleles. PLoS Genetics. 8(9). e1002894–e1002894. 147 indexed citations
14.
Brettingham‐Moore, Kate H., Cuong Duong, Danielle Greenawalt, et al.. (2011). Pretreatment Transcriptional Profiling for Predicting Response to Neoadjuvant Chemoradiotherapy in Rectal Adenocarcinoma. Clinical Cancer Research. 17(9). 3039–3047. 43 indexed citations
15.
Poortinga, Gretchen, Meaghan Wall, Elaine Sanij, et al.. (2010). c-MYC coordinately regulates ribosomal gene chromatin remodeling and Pol I availability during granulocyte differentiation. Nucleic Acids Research. 39(8). 3267–3281. 76 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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