Ryan J. Taft
Impact in
- Cancer Research top 0.2%
- Cancer-related molecular mechanisms research
- MicroRNA in disease regulation
- Molecular Biology top 1%
- RNA modifications and cancer
- RNA Research and Splicing
- RNA and protein synthesis mechanisms
- Circular RNAs in diseases
- RNA regulation and disease
- Genomics and Phylogenetic Studies
Papers in
-
- RNA modifications and cancer 15
- RNA Research and Splicing 14
- RNA and protein synthesis mechanisms 12
- RNA regulation and disease 11
- Genetics 24
- Genomics and Rare Diseases 13
- Genomic variations and chromosomal abnormalities 11
- Co-authors
- John S. Mattick (27 shared papers)Marcel E. Dinger (7 shared papers)Tim R. Mercer (6 shared papers)Ken C. Pang (1 shared paper)Michael Pheasant (1 shared paper)Selene L. Fernández-Valverde (5 shared papers)Piero Carninci (3 shared papers)Yoshihide Hayashizaki (3 shared papers)
- Journals
- Neurology (4 papers)RNA (4 papers)npj Genomic Medicine (4 papers)Genetics in Medicine (3 papers)BMC Genomics (3 papers)
- Partner nations
- United StatesAustraliaUnited Kingdom
In The Last Decade
Ryan J. Taft
86 papers receiving 6.7k citations
Ryan J. Taft's Hit Papers
Peers
Comparison fields: 5 of 150
- Cancer Research 3.0k
- Molecular Biology 4.9k
- Developmental Neuroscience 146
- Genetics 867
- Neurology 164
Countries citing papers authored by Ryan J. Taft
This map shows the geographic impact of Ryan J. Taft'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 Ryan J. Taft with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ryan J. Taft more than expected).
Fields of papers citing papers by Ryan J. Taft
This network shows the impact of papers produced by Ryan J. Taft. 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 Ryan J. Taft. The network helps show where Ryan J. Taft may publish in the future.
Co-authors
The 25 scholars most cited alongside Ryan J. Taft, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 87 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Non‐coding RNAs: regulators of disease Hit paper breakdown → | 2009 | 865 |
| 2 | The relationship between non‐protein‐coding DNA and eukaryotic complexity Hit paper breakdown → | 2007 | 502 |
| 3 | 2009 | 373 | |
| 4 | 2011 | 351 | |
| 5 | 2013 | 332 | |
| 6 | 2009 | 202 | |
| 7 | 2009 | 193 | |
| 8 | 2018 | 187 | |
| 9 | 2011 | 181 | |
| 10 | 2010 | 177 | |
| 11 | 2015 | 169 | |
| 12 | 2010 | 137 | |
| 13 | 2015 | 136 | |
| 14 | 2014 | 133 | |
| 15 | 2013 | 123 | |
| 16 | 2014 | 122 | |
| 17 | 2008 | 116 | |
| 18 | 2010 | 110 | |
| 19 | 2012 | 110 | |
| 20 | 2020 | 100 |
About Ryan J. Taft
Ryan J. Taft is a scholar working on Molecular Biology, Genetics, Cancer Research, Pathology and Forensic Medicine and Physiology, having authored 87 papers that have together received 6.9k indexed citations. Recurring topics across this work include RNA modifications and cancer (15 papers), RNA Research and Splicing (14 papers), Genomics and Rare Diseases (13 papers), RNA and protein synthesis mechanisms (12 papers), RNA regulation and disease (11 papers), Genomic variations and chromosomal abnormalities (11 papers), Cancer-related molecular mechanisms research (9 papers) and MicroRNA in disease regulation (9 papers). The work is most often cited by research in Cancer Research (3.0k citations), Molecular Biology (4.9k citations), Developmental Neuroscience (146 citations), Genetics (867 citations) and Neurology (164 citations). Ryan J. Taft has collaborated with scholars based in United States, Australia and United Kingdom. Frequent co-authors include John S. Mattick, Marcel E. Dinger, Tim R. Mercer, Ken C. Pang, Michael Pheasant, Selene L. Fernández-Valverde, Piero Carninci, Yoshihide Hayashizaki, Michael B. Clark and Cas Simons. Their work appears in journals such as Neurology, RNA, npj Genomic Medicine, Genetics in Medicine and BMC Genomics.
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.