Ryan J. Taft

13.7k citations
86 papers · 6.5k indexed · 1 hit paper · h-index 43
    • Cancer-related molecular mechanisms research 11
    • MicroRNA in disease regulation 10
    • RNA modifications and cancer 23
    • RNA Research and Splicing 19
    • RNA and protein synthesis mechanisms 14
    • RNA regulation and disease 13
  • Genetics top 2%
    • Genomics and Rare Diseases 14
    • Genomic variations and chromosomal abnormalities 11
  • Neurology top 5%

Ryan J. Taft

86 papers receiving 6.4k citations

Hit Papers

Non‐coding RNAs: regulators of disease8172009202620142020250500750

Peers

Ryan J. Taft
Comparison fields: 5 of 151
  • Cancer Research 3.1k
  • Molecular Biology 5.1k
  • Developmental Neuroscience 135
  • Genetics 869
  • Neurology 177
Replace Jiangwen Zhang with:
Jiangwen Zhang United States
Stefan Stamm United States
Bryce W. Carey United States
John C. Castle United States
Kornel E. Schuebel United States
Michael D. Wilson Canada
Paul Zumbo United States
Alistair R. R. Forrest Australia
Hedi Peterson Estonia
Janine Altmüller Germany
Ryan J. Taft relative to Jiangwen Zhang United States Jiangwen Zhang's profile →
Citations per field
00.5×1.5×2.1×
Jiangwen Zhang · 1×
Citations per year

Countries citing papers authored by Ryan J. Taft

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network

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.

Border = papers with Ryan J. Taft Line = papers co-authored together Ryan J. Taft links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 202154
2 20211
3 20214
4 202085
5 202079
6 202095
7 201977
8 201773
9 201739
10 2015132
11 201549
12 2014116
13 20149
14 2012104
15 2011174
16 201116
17 2010128
18 20049
19 200436
20
CULTURED HUMAN BRAIN TUMOR CELLS DO NOT RESPOND TO JOHREI TREATMENT
20034

About Ryan J. Taft

Ryan J. Taft is a scholar working on Cancer Research, Genetics, Molecular Biology, Developmental Neuroscience and Clinical Biochemistry, having authored 86 papers that have together received 6.5k indexed citations. Recurring topics across this work include RNA modifications and cancer (23 papers), RNA Research and Splicing (19 papers), Genomics and Rare Diseases (14 papers), RNA and protein synthesis mechanisms (14 papers), RNA regulation and disease (13 papers), Cancer-related molecular mechanisms research (11 papers), Genomic variations and chromosomal abnormalities (11 papers) and MicroRNA in disease regulation (10 papers). The work is most often cited by research in Cancer Research (3.1k citations), Molecular Biology (5.1k citations), Developmental Neuroscience (135 citations), Genetics (869 citations) and Neurology (177 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, npj Genomic Medicine, RNA, 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.

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