Dean Phelan

2.2k total citations
15 papers, 398 citations indexed

About

Dean Phelan is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Dean Phelan has authored 15 papers receiving a total of 398 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Dean Phelan's work include Genomics and Rare Diseases (4 papers), Cardiomyopathy and Myosin Studies (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Dean Phelan is often cited by papers focused on Genomics and Rare Diseases (4 papers), Cardiomyopathy and Myosin Studies (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Dean Phelan collaborates with scholars based in Australia, United States and Canada. Dean Phelan's co-authors include Mark Cummins, Roland A.H. van Oorschot, Paul A. James, Andrew M. Davis, Belinda Chong, Zornitza Stark, Sebastian Lunke, David J. Amor, Lucas Eastaugh and Susan M. White and has published in prestigious journals such as International Journal of Molecular Sciences, European Heart Journal and Human Mutation.

In The Last Decade

Dean Phelan

14 papers receiving 383 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dean Phelan Australia 11 188 180 79 51 42 15 398
Rose Veile United States 11 395 2.1× 103 0.6× 19 0.2× 96 1.9× 38 0.9× 13 572
Tiia Reimand Estonia 13 229 1.2× 291 1.6× 18 0.2× 23 0.5× 2 0.0× 41 488
Va Lip United States 12 474 2.5× 367 2.0× 77 1.0× 82 1.6× 2 0.0× 17 883
Matthew F. Hunter Australia 13 225 1.2× 273 1.5× 4 0.1× 51 1.0× 5 0.1× 35 478
Imen Chakchouk United States 13 203 1.1× 84 0.5× 24 0.3× 134 2.6× 12 0.3× 20 354
Polona Le Quesne Stabej United Kingdom 14 348 1.9× 167 0.9× 93 1.2× 123 2.4× 1 0.0× 18 535
Jiguang Peng China 10 181 1.0× 75 0.4× 11 0.1× 59 1.2× 6 0.1× 17 279
Rita Teek Estonia 9 126 0.7× 124 0.7× 5 0.1× 27 0.5× 6 0.1× 14 221
Mariem Ben Saïd Tunisia 11 174 0.9× 95 0.5× 5 0.1× 214 4.2× 10 0.2× 26 369
Janice C. Palumbos United States 8 245 1.3× 161 0.9× 16 0.2× 32 0.6× 13 391

Countries citing papers authored by Dean Phelan

Since Specialization
Citations

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

Fields of papers citing papers by Dean Phelan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dean Phelan

This figure shows the co-authorship network connecting the top 25 collaborators of Dean Phelan. A scholar is included among the top collaborators of Dean Phelan 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 Dean Phelan. Dean Phelan 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.
Horton, Ari, Meredith A. Allen, Stacy Goergen, et al.. (2022). Ethylmalonic encephalopathy masquerading as meningococcemia. Molecular Case Studies. 8(2). mcs.a006193–mcs.a006193. 4 indexed citations
2.
Ramchand, Jay, Mathew Wallis, Ivan Macciocca, et al.. (2020). Prospective Evaluation of the Utility of Whole Exome Sequencing in Dilated Cardiomyopathy. Journal of the American Heart Association. 9(2). e013346–e013346. 26 indexed citations
3.
Tan, Natalie B., Rachel Stapleton, Zornitza Stark, et al.. (2020). Evaluating systematic reanalysis of clinical genomic data in rare disease from single center experience and literature review. Molecular Genetics & Genomic Medicine. 8(11). e1508–e1508. 44 indexed citations
4.
5.
Tan, Tiong Yang, Sebastian Lunke, Belinda Chong, et al.. (2019). A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis. European Journal of Human Genetics. 27(12). 1791–1799. 35 indexed citations
6.
Downie, Lilian, Jane Halliday, Rachel Burt, et al.. (2019). Exome sequencing in infants with congenital hearing impairment: a population-based cohort study. European Journal of Human Genetics. 28(5). 587–596. 44 indexed citations
7.
Field, Michael, Tracy Dudding‐Byth, Marta Arpone, et al.. (2019). Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing. International Journal of Molecular Sciences. 20(16). 3907–3907. 13 indexed citations
8.
Abrams, Alexander J., Flavia Fontanesi, Natalie B. Tan, et al.. (2018). Insights into the genotype-phenotype correlation and molecular function of SLC25A46. Human Mutation. 39(12). 1995–2007. 24 indexed citations
9.
Woodcock, Ian, Manoj P. Menezes, Lee Coleman, et al.. (2017). Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome. Seminars in Pediatric Neurology. 26. 2–9. 25 indexed citations
10.
11.
Phelan, Dean, et al.. (2013). The genetics of cardiomyopathy, new technologies and the path to personalised medicine. 1(1). 1 indexed citations
12.
Eastaugh, Lucas, Paul A. James, Dean Phelan, & Andrew M. Davis. (2011). Brugada Syndrome Caused by a Large Deletion in SCN5A Only Detected by Multiplex Ligation-Dependent Probe Amplification. Journal of Cardiovascular Electrophysiology. 22(9). 1073–1076. 28 indexed citations
13.
Siemering, Kirby, Shehnaaz S.M. Manji, Wendy Hutchison, et al.. (2006). Detection of Mutations in Genes Associated with Hearing Loss Using a Microarray-Based Approach. Journal of Molecular Diagnostics. 8(4). 483–489. 18 indexed citations
14.
Oorschot, Roland A.H. van, et al.. (2003). Are you collecting all the available DNA from touched objects?. International Congress Series. 1239. 803–807. 95 indexed citations
15.
Porter, J., et al.. (1999). Anaphylaxis due to suxamethonium — Manifested at induction of anaesthesia by bradycardia and cardiac arrest. Irish Journal of Medical Science (1971 -). 168(2). 99–101. 2 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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