Rohan Taylor

3.7k total citations
13 papers, 887 citations indexed

About

Rohan Taylor is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Rohan Taylor has authored 13 papers receiving a total of 887 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Surgery. Recurrent topics in Rohan Taylor's work include Genetic Syndromes and Imprinting (2 papers), Genetic Associations and Epidemiology (2 papers) and BRCA gene mutations in cancer (2 papers). Rohan Taylor is often cited by papers focused on Genetic Syndromes and Imprinting (2 papers), Genetic Associations and Epidemiology (2 papers) and BRCA gene mutations in cancer (2 papers). Rohan Taylor collaborates with scholars based in United Kingdom, Australia and Brazil. Rohan Taylor's co-authors include R. Scott Poethig, Randall A. Kerstetter, Kirsten Bomblies, Ian Jacobs, Ranjit Manchanda, Chris Jacobs, Usha Menon, Matthew Burnell, Trevor W. Stone and L. Gail Darlington and has published in prestigious journals such as Nature, JNCI Journal of the National Cancer Institute and Journal of Neurochemistry.

In The Last Decade

Rohan Taylor

12 papers receiving 873 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rohan Taylor United Kingdom 10 575 485 234 80 63 13 887
Caroline Schluth‐Bolard France 15 434 0.8× 125 0.3× 375 1.6× 24 0.3× 43 0.7× 43 786
Yuan Wei China 14 229 0.4× 79 0.2× 169 0.7× 55 0.7× 31 0.5× 37 585
Nicola Vickaryous Australia 10 572 1.0× 56 0.1× 273 1.2× 69 0.9× 59 0.9× 16 769
Cathy M. Tuck‐Müller United States 17 515 0.9× 167 0.3× 428 1.8× 19 0.2× 49 0.8× 37 855
Neda Sharifi Ireland 8 693 1.2× 45 0.1× 76 0.3× 21 0.3× 66 1.0× 12 890
Ilia V. Soloviev Russia 14 356 0.6× 160 0.3× 579 2.5× 10 0.1× 68 1.1× 26 788
Gregoriy A. Dokshin United States 9 532 0.9× 55 0.1× 137 0.6× 32 0.4× 47 0.7× 10 726
Tomohiko Akiyama Japan 17 1.0k 1.7× 74 0.2× 126 0.5× 21 0.3× 34 0.5× 32 1.1k
P Goetz Czechia 13 382 0.7× 150 0.3× 251 1.1× 63 0.8× 77 1.2× 30 629
Turan Tufan United States 11 483 0.8× 34 0.1× 120 0.5× 63 0.8× 39 0.6× 17 611

Countries citing papers authored by Rohan Taylor

Since Specialization
Citations

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

Fields of papers citing papers by Rohan Taylor

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rohan Taylor

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

All Works

13 of 13 papers shown
1.
Manchanda, Ranjit, Oleg Blyuss, Faiza Gaba, et al.. (2018). Current detection rates and time-to-detection of all identifiable BRCA carriers in the Greater London population. Journal of Medical Genetics. 55(8). 538–545. 47 indexed citations
2.
Manchanda, Ranjit, K Loggenberg, Saskia C. Sanderson, et al.. (2014). Population Testing for Cancer Predisposing BRCA1/BRCA2 Mutations in the Ashkenazi-Jewish Community: A Randomized Controlled Trial. JNCI Journal of the National Cancer Institute. 107(1). 379–379. 139 indexed citations
3.
4.
Gordon, Kristiana, Fiona Connell, Glen Brice, et al.. (2012). FLT4/VEGFR3and Milroy Disease: Novel Mutations, a Review of Published Variants and Database Update. Human Mutation. 34(1). 23–31. 54 indexed citations
5.
Baple, Emma L., Sahar Mansour, I. Karen Temple, et al.. (2011). An atypical case of hypomethylation at multiple imprinted loci. European Journal of Human Genetics. 19(3). 360–362. 29 indexed citations
6.
Forrest, Caroline M., Gillian Mackay, Nicholas Stoy, et al.. (2009). Blood levels of kynurenines, interleukin‐23 and soluble human leucocyte antigen‐G at different stages of Huntington’s disease. Journal of Neurochemistry. 112(1). 112–122. 65 indexed citations
7.
Hearle, Nicholas, Ian Tomlinson, Wendy Lim, et al.. (2005). Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome. BMC Genomics. 6(1). 38–38. 11 indexed citations
8.
Kerstetter, Randall A., et al.. (2001). KANADI regulates organ polarity in Arabidopsis. Nature. 411(6838). 706–709. 493 indexed citations
9.
10.
Crosby, Andrew H., Steven Jeffery, Tessa Homfray, Rohan Taylor, & Michael A. Patton. (1999). Prenatal Diagnosis and the Subsequent Mutation Analysis in a Family with Carbohydrate-Deficient Glycoprotein Type I Syndrome: Growing Evidence to Support Founder Effects within CDG1 Populations. Genetic Testing. 3(3). 305–307. 3 indexed citations
11.
Taylor, Rohan, et al.. (1991). An unusual variant detected using a ?-globin probe for an individual with the sickle cell trait. Human Genetics. 87(5). 631–631. 1 indexed citations
12.
13.
Davison, John, et al.. (1987). Recombinant DNA technology and low-density lipoprotein receptor defects. Biochemical Society Transactions. 15(2). 202–203. 1 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Caroline Schluth‐Bolard Breakdown of academic impact, for papers by Yuan Wei Breakdown of academic impact, for papers by Nicola Vickaryous Breakdown of academic impact, for papers by Cathy M. Tuck‐Müller Breakdown of academic impact, for papers by Neda Sharifi Breakdown of academic impact, for papers by Ilia V. Soloviev Breakdown of academic impact, for papers by Gregoriy A. Dokshin Breakdown of academic impact, for papers by Tomohiko Akiyama Breakdown of academic impact, for papers by P Goetz Breakdown of academic impact, for papers by Turan Tufan
Rankless by CCL
2026