Ryan E. Mills
Impact in
- Genetics top 0.05%
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 0.5%
- Genomics and Phylogenetic Studies
- RNA and protein synthesis mechanisms
- RNA modifications and cancer
Papers in
- Genetics 43
- Genomic variations and chromosomal abnormalities 26
- Genomics and Rare Diseases 21
- Genetic Associations and Epidemiology 10
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- Genomics and Phylogenetic Studies 24
- RNA and protein synthesis mechanisms 16
- CRISPR and Genetic Engineering 6
- Co-authors
- Scott E. Devine (7 shared papers)Allison Lange (3 shared papers)Anita H. Corbett (3 shared papers)Rebecca C. Iskow (7 shared papers)Murray Stewart (1 shared paper)W. Stephen Pittard (3 shared papers)Steve S. Ho (1 shared paper)Alexander Eckehart Urban (1 shared paper)
- Journals
- Nature (8 papers)Proceedings of the National Academy of Sciences (6 papers)Genome biology (5 papers)Nature Communications (4 papers)The American Journal of Human Genetics (3 papers)
- Partner nations
- United StatesUnited KingdomSouth Korea
In The Last Decade
Ryan E. Mills
82 papers receiving 24.6k citations
Ryan E. Mills's Hit Papers
Peers
Comparison fields: 5 of 199
- Genetics 11.2k
- Molecular Biology 11.4k
- Cancer Research 2.3k
- Plant Science 2.6k
- Aging 107
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 85 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A global reference for human genetic variation Hit paper breakdown → | 2015 | 12574 |
| 2 | An integrated map of structural variation in 2,504 human genomes Hit paper breakdown → | 2015 | 1624 |
| 3 | Classical Nuclear Localization Signals: Definition, Function, and Interaction with Importin α Hit paper breakdown → | 2006 | 955 |
| 4 | Mapping copy number variation by population-scale genome sequencing Hit paper breakdown → | 2011 | 854 |
| 5 | Multi-platform discovery of haplotype-resolved structural variation in human genomes Hit paper breakdown → | 2019 | 563 |
| 6 | High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios Hit paper breakdown → | 2022 | 516 |
| 7 | A global reference for human genetic variation Hit paper breakdown → | 2015 | 476 |
| 8 | Demographic history and rare allele sharing among human populations Hit paper breakdown → | 2011 | 475 |
| 9 | 2010 | 452 | |
| 10 | Haplotype-resolved diverse human genomes and integrated analysis of structural variation Hit paper breakdown → | 2021 | 429 |
| 11 | 2010 | 416 | |
| 12 | 2013 | 399 | |
| 13 | Structural variation in the sequencing era Hit paper breakdown → | 2019 | 378 |
| 14 | 2007 | 362 | |
| 15 | 2011 | 341 | |
| 16 | 2014 | 321 | |
| 17 | 2009 | 252 | |
| 18 | 2010 | 251 | |
| 19 | 2020 | 238 | |
| 20 | 2012 | 200 |
About Ryan E. Mills
Ryan E. Mills is a scholar working on Genetics, Molecular Biology, Plant Science, Cancer Research and Oncology, having authored 85 papers that have together received 25.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (26 papers), Genomics and Phylogenetic Studies (24 papers), Genomics and Rare Diseases (21 papers), Chromosomal and Genetic Variations (18 papers), RNA and protein synthesis mechanisms (16 papers), Genetic Associations and Epidemiology (10 papers), Cancer Genomics and Diagnostics (6 papers) and CRISPR and Genetic Engineering (6 papers). The work is most often cited by research in Genetics (11.2k citations), Molecular Biology (11.4k citations), Cancer Research (2.3k citations), Plant Science (2.6k citations) and Aging (107 citations). Ryan E. Mills has collaborated with scholars based in United States, United Kingdom and South Korea. Frequent co-authors include Scott E. Devine, Allison Lange, Anita H. Corbett, Rebecca C. Iskow, Murray Stewart, W. Stephen Pittard, Steve S. Ho, Alexander Eckehart Urban, E. Andrew Bennett and Julienne M. Mullaney. Their work appears in journals such as Nature, Proceedings of the National Academy of Sciences, Genome biology, Nature Communications and The American Journal of Human Genetics.
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.