Edward Edkins

940 total citations
24 papers, 468 citations indexed

About

Edward Edkins is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Oncology. According to data from OpenAlex, Edward Edkins has authored 24 papers receiving a total of 468 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Pathology and Forensic Medicine, 7 papers in Molecular Biology and 6 papers in Oncology. Recurrent topics in Edward Edkins's work include Genetic factors in colorectal cancer (7 papers), Metabolism and Genetic Disorders (4 papers) and Colorectal Cancer Screening and Detection (4 papers). Edward Edkins is often cited by papers focused on Genetic factors in colorectal cancer (7 papers), Metabolism and Genetic Disorders (4 papers) and Colorectal Cancer Screening and Detection (4 papers). Edward Edkins collaborates with scholars based in Australia, United States and Hong Kong. Edward Edkins's co-authors include I.A. Hansen, Boxin Tang, Maija R.J. Kohonen‐Corish, Niels C. R. Räihä, Sue Forrest, Richard G.H. Cotton, Steven Nasioulas, P. Meera Khan, Finlay Macrae and Ian Faragher and has published in prestigious journals such as The Lancet, Gastroenterology and Journal of Lipid Research.

In The Last Decade

Edward Edkins

24 papers receiving 448 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Edward Edkins Australia	13	187	136	90	76	66	24	468
Herena Eixarch Spain	18	393 2.1×	132 1.0×	87 1.0×	33 0.4×	107 1.6×	31	781
Margaret Crisp United States	8	395 2.1×	56 0.4×	65 0.7×	51 0.7×	160 2.4×	14	633
Winston Thomas United States	10	350 1.9×	33 0.2×	153 1.7×	63 0.8×	143 2.2×	15	789
Reena Ray Canada	5	478 2.6×	39 0.3×	56 0.6×	151 2.0×	32 0.5×	7	638
Melissa S. McNulty United States	13	470 2.5×	73 0.5×	89 1.0×	68 0.9×	88 1.3×	19	702
Diego G. Ogando United States	15	245 1.3×	60 0.4×	18 0.2×	45 0.6×	48 0.7×	35	659
M J Keller United States	7	598 3.2×	36 0.3×	83 0.9×	58 0.8×	198 3.0×	7	826
R Roubin France	13	204 1.1×	21 0.2×	56 0.6×	15 0.2×	56 0.8×	21	560
Hidemasa Uchimura Japan	13	230 1.2×	26 0.2×	40 0.4×	71 0.9×	69 1.0×	38	658
Pablo García‐Miranda Spain	13	281 1.5×	23 0.2×	43 0.5×	41 0.5×	45 0.7×	33	486

Countries citing papers authored by Edward Edkins

Since Specialization

Citations

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

Fields of papers citing papers by Edward Edkins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edward Edkins

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

All Works

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20 of 20 papers shown

Balasubramaniam, Shanti, Lisa G. Riley, Anand Vasudevan, et al.. (2017). EPG5-Related Vici Syndrome: A Primary Defect of Autophagic Regulation with an Emerging Phenotype Overlapping with Mitochondrial Disorders. JIMD Reports. 42. 19–29. 11 indexed citations

Heron, Sarah E., Marta Hernández, Caitlin Edwards, et al.. (2009). Neonatal seizures and long QT Syndrome: A cardiocerebral channelopathy?. Epilepsia. 51(2). 293–296. 56 indexed citations

Woon, See‐Tarn, Rohan Ameratunga, M. C. Croxson, et al.. (2008). Follicular Lymphoma in a X‐linked Lymphoproliferative Syndrome Carrier Female. Scandinavian Journal of Immunology. 68(2). 153–158. 14 indexed citations

Sellner, Loryn N., Edward Edkins, & Nicholas M. Smith. (2006). Screening for RB1 Mutations in Tumor Tissue Using Denaturing High Performance Liquid Chromatography, Multiplex Ligation-Dependent Probe Amplification, and Loss of Heterozygosity Analysis. Pediatric and Developmental Pathology. 9(1). 31–37. 11 indexed citations

McPhillips, Mary, et al.. (2005). Deletion Mutations in an Australian Series of HNPCC Patients. Hereditary Cancer in Clinical Practice. 3(1). 43–7. 2 indexed citations

Weston, Susan A., et al.. (2004). Identification of WASP mutations in 10 Australian families with Wiskott–Aldrich syndrome and X-linked thrombocytopenia. Pathology. 36(3). 262–264. 4 indexed citations

Sellner, Loryn N., Edward Edkins, Lawrence Greed, & Barry Lewis. (2004). Detection of mutations in the glycine decarboxylase gene in patients with nonketotic hyperglycinaemia. Molecular Genetics and Metabolism. 84(2). 167–171. 10 indexed citations

Edkins, Edward, et al.. (2000). Identification of a novel deletion of the entire OCRL1 gene detected by FISH analysis in a family with Lowe syndrome. Clinical Genetics. 58(6). 479–482. 15 indexed citations

Baskaran, G., et al.. (2000). Predictive testing for familial adenomatous polyposis in a rural South Indian community. Clinical Genetics. 58(1). 57–60. 2 indexed citations

10.

Bateman, John F., Susanna Freddi, Peter H. Byers, et al.. (1999). Reliable and sensitive detection of premature termination mutations using a protein truncation test designed to overcome problems of nonsense-mediated mRNA instability. Human Mutation. 13(4). 311–317. 45 indexed citations

11.

Bateman, John F., Susanna Freddi, Shireen R. Lamandé, et al.. (1999). Reliable and sensitive detection of premature termination mutations using a protein truncation test designed to overcome problems of nonsense-mediated mRNA instability. Human Mutation. 13(4). 311–311. 2 indexed citations

12.

Cotton, Richard G.H., Edward Edkins, & Sue Forrest. (1998). Mutation detection : a practical approach. Oxford University Press eBooks. 31 indexed citations

13.

Edkins, Edward, et al.. (1997). The clinical correlates of a 3' truncating mutation (codons 1982-1983) in the adenomatous polyposis coli gene. Gastroenterology. 113(1). 326–331. 33 indexed citations

14.

Kohonen‐Corish, Maija R.J., W F Doe, Edward Edkins, et al.. (1996). RNA-based mutation screening in hereditary nonpolyposis colorectal cancer.. PubMed. 59(4). 818–24. 77 indexed citations

15.

Yeoh, George C., et al.. (1988). The development of phenylalanine hydroxylase in rat liver; in vivo, and in vitro studies utilizing fetal hepatocyte cultures. Differentiation. 38(1). 42–48. 16 indexed citations

16.

Yeoh, George C., et al.. (1979). Synthesis and secretion of albumin and transferrin by foetal RAT hepatocyte cultures. Biochimica et Biophysica Acta (BBA) - Nucleic Acids and Protein Synthesis. 565(2). 347–355. 16 indexed citations

17.

Räihä, Niels C. R. & Edward Edkins. (1977). Insulin Antagonism of Dexamethasone-Induced Increase of Argininosuccinate Synthetase and Argininosuccinate Lyase Activities in Cultured Fetal Rat Liver. Neonatology. 31(5-6). 266–270. 19 indexed citations

18.

Edkins, Edward & I.A. Hansen. (1972). Wax esters secreted by the uropygial glands of some Australian waterfowl, including the magpie goose. Comparative Biochemistry and Physiology Part B Comparative Biochemistry. 41(1). 105–112. 8 indexed citations

19.

Edkins, Edward. (1966). Estimation of xanthurenic acid. Clinica Chimica Acta. 14(2). 283–284. 2 indexed citations

20.

Dugdale, A. E. & Edward Edkins. (1964). URINARY UREA/CREATININE RATIO IN HEALTHY AND MALNOURISHED CHILDREN. The Lancet. 283(7342). 1062–1064. 14 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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