Samantha E. Boyle

842 total citations
11 papers, 611 citations indexed

About

Samantha E. Boyle is a scholar working on Genetics, Cancer Research and Molecular Biology. According to data from OpenAlex, Samantha E. Boyle has authored 11 papers receiving a total of 611 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 7 papers in Cancer Research and 6 papers in Molecular Biology. Recurrent topics in Samantha E. Boyle's work include Cancer Genomics and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and RNA modifications and cancer (3 papers). Samantha E. Boyle is often cited by papers focused on Cancer Genomics and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and RNA modifications and cancer (3 papers). Samantha E. Boyle collaborates with scholars based in Australia, Switzerland and South Korea. Samantha E. Boyle's co-authors include Ian Campbell, Kylie L. Gorringe, Louise H. Williams, Manasa Ramakrishna, Anita Sridhar, Terence P. Speed, Richard W. Tothill, Jason Li, Mark Shackleton and David D.L. Bowtell and has published in prestigious journals such as Bioinformatics, PLoS ONE and Cancer Research.

In The Last Decade

Samantha E. Boyle

11 papers receiving 602 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Samantha E. Boyle Australia 11 406 224 156 143 84 11 611
Anita Sridhar Australia 6 420 1.0× 262 1.2× 218 1.4× 79 0.6× 42 0.5× 6 642
Jude M. Mulligan United Kingdom 9 346 0.9× 148 0.7× 200 1.3× 176 1.2× 72 0.9× 14 555
Carolina Sánchez‐Estévez Spain 10 361 0.9× 132 0.6× 202 1.3× 72 0.5× 125 1.5× 11 661
Rosanna Lacalamita Italy 15 358 0.9× 233 1.0× 223 1.4× 130 0.9× 78 0.9× 30 647
Guillaume Rieunier United Kingdom 9 459 1.1× 212 0.9× 374 2.4× 140 1.0× 50 0.6× 15 654
Azat Garipov United States 6 679 1.7× 204 0.9× 182 1.2× 42 0.3× 168 2.0× 6 837
Christine M. Maugard Canada 13 313 0.8× 102 0.5× 165 1.1× 138 1.0× 45 0.5× 20 544
Paula M. Gilmore United Kingdom 12 468 1.2× 166 0.7× 300 1.9× 215 1.5× 66 0.8× 15 835
Magdalena Ratajska Poland 16 379 0.9× 189 0.8× 206 1.3× 339 2.4× 105 1.3× 34 654
Zelda Lichtensztejn Canada 17 423 1.0× 109 0.5× 175 1.1× 58 0.4× 85 1.0× 23 579

Countries citing papers authored by Samantha E. Boyle

Since Specialization
Citations

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

Fields of papers citing papers by Samantha E. Boyle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Samantha E. Boyle. 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 Samantha E. Boyle. The network helps show where Samantha E. Boyle may publish in the future.

Co-authorship network of co-authors of Samantha E. Boyle

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

All Works

11 of 11 papers shown
1.
Boyle, Samantha E., Clare G. Fedele, Vincent Corbin, et al.. (2016). CD271 Expression on Patient Melanoma Cells Is Unstable and Unlinked to Tumorigenicity. Cancer Research. 76(13). 3965–3977. 24 indexed citations
2.
Ryland, Georgina L., Maria Doyle, David L. Goode, et al.. (2015). Loss of heterozygosity: what is it good for?. BMC Medical Genomics. 8(1). 45–45. 67 indexed citations
3.
4.
Jorissen, Robert N., Sheren Al-Obaidi, Teresa Ward, et al.. (2015). The transcription cofactor c-JUN mediates phenotype switching and BRAF inhibitor resistance in melanoma. Science Signaling. 8(390). ra82–ra82. 106 indexed citations
5.
Schröder, Jan, Arthur Hsu, Samantha E. Boyle, et al.. (2014). Socrates: identification of genomic rearrangements in tumour genomes by re-aligning soft clipped reads. Bioinformatics. 30(8). 1064–1072. 47 indexed citations
6.
Ryland, Georgina L., Maria Doyle, Samantha E. Boyle, et al.. (2012). MicroRNA Genes and Their Target 3′-Untranslated Regions Are Infrequently Somatically Mutated in Ovarian Cancers. PLoS ONE. 7(4). e35805–e35805. 25 indexed citations
7.
Thompson, Ella R., Samantha E. Boyle, Julie K. Johnson, et al.. (2011). Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients. Human Mutation. 33(1). 95–99. 53 indexed citations
8.
Gorringe, Kylie L., Ella R. Thompson, Ken Opeskin, et al.. (2011). Identification of copy number alterations associated with the progression of DCIS to invasive ductal carcinoma. Breast Cancer Research and Treatment. 133(3). 889–898. 51 indexed citations
9.
Gorringe, Kylie L., Joshy George, Michael S. Anglesio, et al.. (2010). Copy Number Analysis Identifies Novel Interactions Between Genomic Loci in Ovarian Cancer. PLoS ONE. 5(9). e11408–e11408. 71 indexed citations
10.
Ramakrishna, Manasa, Louise H. Williams, Samantha E. Boyle, et al.. (2010). Identification of Candidate Growth Promoting Genes in Ovarian Cancer through Integrated Copy Number and Expression Analysis. PLoS ONE. 5(4). e9983–e9983. 101 indexed citations
11.
Gorringe, Kylie L., Manasa Ramakrishna, Louise H. Williams, et al.. (2009). Are there any more ovarian tumor suppressor genes? A new perspective using ultra high‐resolution copy number and loss of heterozygosity analysis. Genes Chromosomes and Cancer. 48(10). 931–942. 53 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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