Ryan E. Mills
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 2%
- Genomics and Phylogenetic Studies
- RNA and protein synthesis mechanisms
- RNA Research and Splicing
- RNA modifications and cancer
- CRISPR and Genetic Engineering
- Nuclear Structure and Function
Papers in
-
- Genomics and Phylogenetic Studies 17
- RNA and protein synthesis mechanisms 14
- CRISPR and Genetic Engineering 5
- Nuclear Structure and Function 3
- Gene expression and cancer classification 3
- Genetics 20
- Genomic variations and chromosomal abnormalities 11
- Genomics and Rare Diseases 4
- Co-authors
- Scott E. Devine (11 shared papers)W. Stephen Pittard (6 shared papers)Anita H. Corbett (3 shared papers)Allison Lange (3 shared papers)Rebecca C. Iskow (7 shared papers)Murray Stewart (1 shared paper)E. Andrew Bennett (3 shared papers)Alexander E. Urban (1 shared paper)
- Journals
- Genome Research (4 papers)Genome biology (4 papers)Proceedings of the National Academy of Sciences (4 papers)Nucleic Acids Research (3 papers)Journal of Virology (2 papers)
- Partner nations
- United StatesUnited KingdomSouth Korea
In The Last Decade
Ryan E. Mills
51 papers receiving 5.4k citations
Ryan E. Mills's Hit Papers
Peers
Comparison fields: 5 of 138
- Genetics 1.8k
- Molecular Biology 3.7k
- Plant Science 1.5k
- Cancer Research 350
- Aging 29
Countries citing papers authored by Ryan E. Mills
This map shows the geographic impact of Ryan E. Mills'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 E. Mills with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ryan E. Mills more than expected).
Fields of papers citing papers by Ryan E. Mills
This network shows the impact of papers produced by Ryan E. Mills. 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 E. Mills. The network helps show where Ryan E. Mills may publish in the future.
Co-authors
The 25 scholars most cited alongside Ryan E. Mills, 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 52 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Classical Nuclear Localization Signals: Definition, Function, and Interaction with Importin α Hit paper breakdown → | 2006 | 949 |
| 2 | 2006 | 481 | |
| 3 | 2010 | 438 | |
| 4 | 2013 | 374 | |
| 5 | 2007 | 363 | |
| 6 | Structural variation in the sequencing era Hit paper breakdown → | 2019 | 354 |
| 7 | 2010 | 242 | |
| 8 | 2017 | 219 | |
| 9 | 2008 | 201 | |
| 10 | 2011 | 184 | |
| 11 | 2016 | 136 | |
| 12 | 2014 | 135 | |
| 13 | 2004 | 125 | |
| 14 | 2006 | 120 | |
| 15 | 2011 | 97 | |
| 16 | 2009 | 97 | |
| 17 | 2003 | 87 | |
| 18 | 2003 | 86 | |
| 19 | 2019 | 56 | |
| 20 | 2013 | 55 |
About Ryan E. Mills
Ryan E. Mills is a scholar working on Molecular Biology, Genetics, Plant Science, Cancer Research and Cellular and Molecular Neuroscience, having authored 52 papers that have together received 5.5k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (17 papers), Chromosomal and Genetic Variations (15 papers), RNA and protein synthesis mechanisms (14 papers), Genomic variations and chromosomal abnormalities (11 papers), CRISPR and Genetic Engineering (5 papers), Genomics and Rare Diseases (4 papers), Nuclear Structure and Function (3 papers) and Gene expression and cancer classification (3 papers). The work is most often cited by research in Genetics (1.8k citations), Molecular Biology (3.7k citations), Plant Science (1.5k citations), Cancer Research (350 citations) and Aging (29 citations). Ryan E. Mills has collaborated with scholars based in United States, United Kingdom and South Korea. Frequent co-authors include Scott E. Devine, W. Stephen Pittard, Anita H. Corbett, Allison Lange, Rebecca C. Iskow, Murray Stewart, E. Andrew Bennett, Alexander E. Urban, Steve S. Ho and Circe Tsui. Their work appears in journals such as Genome Research, Genome biology, Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Virology.
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.