David Eccles

12.0k total citations
34 papers, 633 citations indexed

About

David Eccles is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, David Eccles has authored 34 papers receiving a total of 633 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in David Eccles's work include Genomics and Phylogenetic Studies (5 papers), Metabolism and Genetic Disorders (4 papers) and Genetic Associations and Epidemiology (3 papers). David Eccles is often cited by papers focused on Genomics and Phylogenetic Studies (5 papers), Metabolism and Genetic Disorders (4 papers) and Genetic Associations and Epidemiology (3 papers). David Eccles collaborates with scholars based in New Zealand, Australia and United States. David Eccles's co-authors include Rod A. Lea, Lyn R. Griffiths, Donia Macartney‐Coxson, Miles C. Benton, A.C. Johnstone, Richard S. Stubbs, Eric P. Hoffman, Brennan Harmon, Mark Hayes and Geoffrey K. Chambers and has published in prestigious journals such as The Journal of Experimental Medicine, PLoS ONE and Scientific Reports.

In The Last Decade

David Eccles

32 papers receiving 627 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 Eccles New Zealand 12 350 136 105 70 57 34 633
Kate Hall United Kingdom 13 417 1.2× 85 0.6× 59 0.6× 124 1.8× 120 2.1× 28 840
Rachael P. Norris United States 14 733 2.1× 109 0.8× 53 0.5× 139 2.0× 28 0.5× 21 1.3k
Jingwei Wang China 11 410 1.2× 131 1.0× 130 1.2× 56 0.8× 14 0.2× 25 908
Xiya Zhang China 11 1.1k 3.1× 282 2.1× 163 1.6× 49 0.7× 85 1.5× 48 1.4k
Stefano Castellana Italy 16 616 1.8× 259 1.9× 38 0.4× 63 0.9× 32 0.6× 73 952
Julian Gutekunst Germany 13 480 1.4× 125 0.9× 63 0.6× 145 2.1× 31 0.5× 17 924
Claire C. Morgan United Kingdom 14 335 1.0× 106 0.8× 188 1.8× 55 0.8× 57 1.0× 16 877
Valérie Bernard France 15 281 0.8× 274 2.0× 37 0.4× 50 0.7× 18 0.3× 39 1.0k
Thomas C. R. Miller United States 19 654 1.9× 220 1.6× 24 0.2× 64 0.9× 38 0.7× 35 1.1k
R. Brent Calder United States 13 580 1.7× 99 0.7× 155 1.5× 63 0.9× 23 0.4× 17 905

Countries citing papers authored by David Eccles

Since Specialization
Citations

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

Fields of papers citing papers by David Eccles

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Eccles

This figure shows the co-authorship network connecting the top 25 collaborators of David Eccles. A scholar is included among the top collaborators of David Eccles 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 Eccles. David Eccles 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.
Herst, Patries M., David Eccles, Alfonso Schmidt, et al.. (2024). Residual OXPHOS is required to drive primary and metastatic lung tumours in an orthotopic breast cancer model. Frontiers in Oncology. 14. 1362786–1362786. 2 indexed citations
2.
Herst, Patries M., et al.. (2022). Bioenergetic and Metabolic Adaptation in Tumor Progression and Metastasis. Frontiers in Oncology. 12. 857686–857686. 12 indexed citations
3.
Koepfli, Klaus‐Peter, Stephanie J. Galla, David Eccles, et al.. (2021). Expanding the conservation genomics toolbox: Incorporating structural variants to enhance genomic studies for species of conservation concern. Molecular Ecology. 30(23). 5949–5965. 31 indexed citations
4.
Grasso, Carole, David Eccles, Štěpána Boukalová, et al.. (2020). Mitochondrial DNA Affects the Expression of Nuclear Genes Involved in Immune and Stress Responses in a Breast Cancer Model. Frontiers in Physiology. 11. 543962–543962. 7 indexed citations
5.
Smith, Alexander, et al.. (2020). A semi-automated technique for adenoma quantification in the ApcMin mouse using FeatureCounter. Scientific Reports. 10(1). 3064–3064. 2 indexed citations
6.
Harvey, Nicholas R., Cassie L. Albury, Shani Stuart, et al.. (2019). Ion torrent high throughput mitochondrial genome sequencing (HTMGS). PLoS ONE. 14(11). e0224847–e0224847. 11 indexed citations
7.
Schalamun, Miriam, David Kainer, David Eccles, et al.. (2018). Harnessing the MinION: An example of how to establish long‐read sequencing in a laboratory using challenging plant tissue from Eucalyptus pauciflora. Molecular Ecology Resources. 19(1). 77–89. 51 indexed citations
8.
Albury, Cassie L., Neven Maksemous, Robert A. Smith, et al.. (2018). Exome Sequencing Diagnoses X-Linked Moesin-Associated Immunodeficiency in a Primary Immunodeficiency Case. Frontiers in Immunology. 9. 420–420. 23 indexed citations
9.
Eccles, David, Jodie Chandler, Mali Camberis, et al.. (2018). De novo assembly of the complex genome of Nippostrongylus brasiliensis using MinION long reads. BMC Biology. 16(1). 6–6. 21 indexed citations
10.
Matovinovic, Elizabeth, Pik Fang Kho, Rod A. Lea, et al.. (2017). Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate.. PubMed. 23. 660–665. 2 indexed citations
11.
Connor, Lisa M., Shiau‐Choot Tang, Kerry L. Hilligan, et al.. (2016). Th2 responses are primed by skin dendritic cells with distinct transcriptional profiles. The Journal of Experimental Medicine. 214(1). 125–142. 57 indexed citations
12.
Benton, Miles C., Rod A. Lea, Donia Macartney‐Coxson, et al.. (2015). A Phenomic Scan of the Norfolk Island Genetic Isolate Identifies a Major Pleiotropic Effect Locus Associated with Metabolic and Renal Disorder Markers. PLoS Genetics. 11(10). e1005593–e1005593. 3 indexed citations
13.
Benton, Miles C., Shani Stuart, Claire Bellis, et al.. (2015). ‘Mutiny on the Bounty’: the genetic history of Norfolk Island reveals extreme gender-biased admixture. PubMed. 6(1). 11–11. 7 indexed citations
14.
Benton, Miles C., Rod A. Lea, Donia Macartney‐Coxson, et al.. (2015). Serum bilirubin concentration is modified by UGT1A1 Haplotypes and influences risk of Type-2 diabetes in the Norfolk Island genetic isolate. BMC Genetics. 16(1). 136–136. 10 indexed citations
15.
Reuter, Hanna, Martin März, Matthias Christian Vogg, et al.. (2014). β-Catenin-Dependent Control of Positional Information along the AP Body Axis in Planarians Involves a Teashirt Family Member. Cell Reports. 10(2). 253–265. 56 indexed citations
16.
Benton, Miles C., Rod A. Lea, Donia Macartney‐Coxson, et al.. (2013). Mapping eQTLs in the Norfolk Island Genetic Isolate Identifies Candidate Genes for CVD Risk Traits. The American Journal of Human Genetics. 93(6). 1087–1099. 23 indexed citations
17.
Roxburgh, Richard, Fern Ashton, Alice M. George, et al.. (2012). The p.Ala510Val mutation in the SPG7 (paraplegin) gene is the most common mutation causing adult onset neurogenetic disease in patients of British ancestry. Journal of Neurology. 260(5). 1286–1294. 30 indexed citations
18.
Eccles, David, Donia Macartney‐Coxson, Geoffrey K. Chambers, & Rod A. Lea. (2012). A unique demographic history exists for the MAO-A gene in Polynesians. Journal of Human Genetics. 57(5). 294–300. 4 indexed citations
19.
Benton, Michael J., Donia Macartney‐Coxson, David Eccles, et al.. (2012). Complete Mitochondrial Genome Sequencing Reveals Novel Haplotypes in a Polynesian Population. PLoS ONE. 7(4). e35026–e35026. 1 indexed citations
20.
Myles, Sean, Rod A. Lea, Jun Ohashi, et al.. (2011). Testing the thrifty gene hypothesis: the Gly482Ser variant in PPARGC1Ais associated with BMI in Tongans. BMC Medical Genetics. 12(1). 10–10. 45 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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