Ryan M. Layer
Impact in
- Cancer Research top 2%
- Cancer Genomics and Diagnostics
- Cancer-related molecular mechanisms research
- Genetics top 2%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 17
- Genomics and Rare Diseases 11
- Genomic variations and chromosomal abnormalities 6
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- Cancer Genomics and Diagnostics 4
- Co-authors
- Aaron R. Quinlan (14 shared papers)Ira M. Hall (5 shared papers)Colby Chiang (4 shared papers)Brent S. Pedersen (7 shared papers)Anindya Dutta (6 shared papers)Jeffrey Gagan (4 shared papers)Gábor Marth (3 shared papers)Bijan K. Dey (3 shared papers)
- Journals
- Nature Methods (4 papers)Genome biology (3 papers)PLoS ONE (2 papers)Frontiers in Genetics (2 papers)Nature Genetics (2 papers)
- Partner nations
- United StatesUnited KingdomNorway
In The Last Decade
Ryan M. Layer
39 papers receiving 3.8k citations
Ryan M. Layer's Hit Papers
Peers
Comparison fields: 5 of 138
- Cancer Research 895
- Genetics 1.5k
- Molecular Biology 2.0k
- Plant Science 483
- Pathology and Forensic Medicine 148
Countries citing papers authored by Ryan M. Layer
This map shows the geographic impact of Ryan M. Layer'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 M. Layer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ryan M. Layer more than expected).
Fields of papers citing papers by Ryan M. Layer
This network shows the impact of papers produced by Ryan M. Layer. 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 M. Layer. The network helps show where Ryan M. Layer may publish in the future.
Co-authors
The 25 scholars most cited alongside Ryan M. Layer, 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 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | LUMPY: a probabilistic framework for structural variant discovery Hit paper breakdown → | 2014 | 1077 |
| 2 | 2015 | 408 | |
| 3 | 2012 | 235 | |
| 4 | A complete reference genome improves analysis of human genetic variation Hit paper breakdown → | 2022 | 227 |
| 5 | 2018 | 188 | |
| 6 | 2020 | 187 | |
| 7 | 2018 | 157 | |
| 8 | 2011 | 145 | |
| 9 | 2018 | 133 | |
| 10 | 2016 | 132 | |
| 11 | 2017 | 121 | |
| 12 | 2014 | 120 | |
| 13 | 2013 | 87 | |
| 14 | 2021 | 81 | |
| 15 | 2020 | 77 | |
| 16 | 2012 | 76 | |
| 17 | 2018 | 65 | |
| 18 | 2012 | 47 | |
| 19 | 2015 | 45 | |
| 20 | 2019 | 43 |
About Ryan M. Layer
Ryan M. Layer is a scholar working on Genetics, Cancer Research, Molecular Biology, Computer Science Applications and Control and Systems Engineering, having authored 40 papers that have together received 3.8k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (15 papers), Genomics and Rare Diseases (11 papers), Genomic variations and chromosomal abnormalities (6 papers), Genomics and Chromatin Dynamics (6 papers), Gene expression and cancer classification (5 papers), Cancer Genomics and Diagnostics (4 papers), RNA Research and Splicing (4 papers) and RNA modifications and cancer (3 papers). The work is most often cited by research in Cancer Research (895 citations), Genetics (1.5k citations), Molecular Biology (2.0k citations), Plant Science (483 citations) and Pathology and Forensic Medicine (148 citations). Ryan M. Layer has collaborated with scholars based in United States, United Kingdom and Norway. Frequent co-authors include Aaron R. Quinlan, Ira M. Hall, Colby Chiang, Brent S. Pedersen, Anindya Dutta, Jeffrey Gagan, Gábor Marth, Bijan K. Dey, Erik P. Garrison and Michael R. Lindberg. Their work appears in journals such as Nature Methods, Genome biology, PLoS ONE, Frontiers in Genetics and Nature 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.