Devin Absher
Impact in
Papers in
-
- Epigenetics and DNA Methylation 34
- Genetics 37
- Genetic Associations and Epidemiology 15
- Genetic diversity and population structure 8
- Genetic Syndromes and Imprinting 7
- Genomics and Rare Diseases 6
- Genetic and phenotypic traits in livestock 5
- Co-authors
- R Myers (27 shared papers)Felicity C. Jones (8 shared papers)David M. Kingsley (8 shared papers)Themistocles L. Assimes (10 shared papers)Yingguang Frank Chan (5 shared papers)Marcus W. Feldman (3 shared papers)Donna K. Arnett (28 shared papers)Steve Horvath (6 shared papers)
- Journals
- PLoS ONE (8 papers)Human Molecular Genetics (5 papers)PLoS Genetics (5 papers)Frontiers in Genetics (4 papers)Genome Research (3 papers)
- Partner nations
- United StatesSpainBrazil
In The Last Decade
Devin Absher
96 papers receiving 7.6k citations
Devin Absher's Hit Papers
Peers
Comparison fields: 5 of 154
- Genetics 3.0k
- Aging 145
- Molecular Biology 3.7k
- Cancer Research 514
- Pediatrics, Perinatology and Child Health 486
Countries citing papers authored by Devin Absher
This map shows the geographic impact of Devin Absher'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 Devin Absher with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Devin Absher more than expected).
Fields of papers citing papers by Devin Absher
This network shows the impact of papers produced by Devin Absher. 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 Devin Absher. The network helps show where Devin Absher may publish in the future.
Co-authors
The 25 scholars most cited alongside Devin Absher, 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 97 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Adaptive Evolution of Pelvic Reduction in Sticklebacks by Recurrent Deletion of a Pitx1 Enhancer Hit paper breakdown → | 2009 | 778 |
| 2 | Dynamic DNA methylation across diverse human cell lines and tissues Hit paper breakdown → | 2013 | 536 |
| 3 | 2009 | 428 | |
| 4 | 2012 | 368 | |
| 5 | 2016 | 346 | |
| 6 | 2009 | 310 | |
| 7 | 2009 | 306 | |
| 8 | 2014 | 296 | |
| 9 | 2013 | 280 | |
| 10 | 2013 | 270 | |
| 11 | 2015 | 238 | |
| 12 | 2009 | 231 | |
| 13 | 2011 | 188 | |
| 14 | 1994 | 170 | |
| 15 | 2014 | 161 | |
| 16 | 2016 | 128 | |
| 17 | 2013 | 124 | |
| 18 | 2009 | 124 | |
| 19 | 2013 | 122 | |
| 20 | 2008 | 121 |
About Devin Absher
Devin Absher is a scholar working on Molecular Biology, Genetics, Immunology, Cancer Research and Pediatrics, Perinatology and Child Health, having authored 97 papers that have together received 7.8k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (34 papers), Genetic Associations and Epidemiology (15 papers), Genetic diversity and population structure (8 papers), Genetic Syndromes and Imprinting (7 papers), Immune Cell Function and Interaction (6 papers), Genomics and Rare Diseases (6 papers), Genetic and phenotypic traits in livestock (5 papers) and Cancer Genomics and Diagnostics (5 papers). The work is most often cited by research in Genetics (3.0k citations), Aging (145 citations), Molecular Biology (3.7k citations), Cancer Research (514 citations) and Pediatrics, Perinatology and Child Health (486 citations). Devin Absher has collaborated with scholars based in United States, Spain and Brazil. Frequent co-authors include R Myers, Felicity C. Jones, David M. Kingsley, Themistocles L. Assimes, Yingguang Frank Chan, Marcus W. Feldman, Donna K. Arnett, Steve Horvath, Jane Grimwood and Jeremy Schmutz. Their work appears in journals such as PLoS ONE, Human Molecular Genetics, PLoS Genetics, Frontiers in Genetics and Genome Research.
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.