Jason E. Miller
Impact in
- Genetics top 5%
- Genetic Associations and Epidemiology
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
Papers in
- Genetics 13
- Genetic Associations and Epidemiology 8
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- RNA Research and Splicing 9
- RNA modifications and cancer 7
- RNA and protein synthesis mechanisms 4
- Epigenetics and DNA Methylation 3
- Genomics and Phylogenetic Studies 2
- Biomedical Text Mining and Ontologies 2
- Co-authors
- Joseph C. Reese (2 shared papers)Dokyoon Kim (10 shared papers)Timothy Walston (1 shared paper)Manu Shivakumar (7 shared papers)M. J. Harris (4 shared papers)Seonggyun Han (5 shared papers)Younghee Lee (6 shared papers)Marylyn DeRiggi Ritchie (4 shared papers)
- Journals
- BMC Medical Genomics (4 papers)Scientific Reports (3 papers)The American Journal of Human Genetics (2 papers)Nature (2 papers)Nature Genetics (1 paper)
- Partner nations
- United StatesCanadaFinland
In The Last Decade
Jason E. Miller
35 papers receiving 1.6k citations
Jason E. Miller's Hit Papers
Peers
Comparison fields: 5 of 122
- Genetics 647
- Cancer Research 126
- Obstetrics and Gynecology 61
- Molecular Biology 576
- Pediatrics, Perinatology and Child Health 84
Countries citing papers authored by Jason E. Miller
This map shows the geographic impact of Jason E. Miller'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 Jason E. Miller with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jason E. Miller more than expected).
Fields of papers citing papers by Jason E. Miller
This network shows the impact of papers produced by Jason E. Miller. 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 Jason E. Miller. The network helps show where Jason E. Miller may publish in the future.
Co-authors
The 25 scholars most cited alongside Jason E. Miller, 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 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The power of genetic diversity in genome-wide association studies of lipids Hit paper breakdown → | 2021 | 583 |
| 2 | A saturated map of common genetic variants associated with human height Hit paper breakdown → | 2022 | 456 |
| 3 | 2012 | 140 | |
| 4 | Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy Hit paper breakdown → | 2023 | 80 |
| 5 | 2022 | 46 | |
| 6 | 2018 | 44 | |
| 7 | 2022 | 27 | |
| 8 | 2019 | 20 | |
| 9 | 2017 | 19 | |
| 10 | 2024 | 19 | |
| 11 | 2018 | 19 | |
| 12 | 2010 | 18 | |
| 13 | 2021 | 16 | |
| 14 | 2019 | 16 | |
| 15 | 2025 | 16 | |
| 16 | 2017 | 15 | |
| 17 | 1994 | 12 | |
| 18 | 2022 | 11 | |
| 19 | 2019 | 11 | |
| 20 | 1993 | 11 |
About Jason E. Miller
Jason E. Miller is a scholar working on Genetics, Molecular Biology, Nature and Landscape Conservation, Cancer Research and Ecology, having authored 37 papers that have together received 1.7k indexed citations. Recurring topics across this work include RNA Research and Splicing (9 papers), Genetic Associations and Epidemiology (8 papers), RNA modifications and cancer (7 papers), RNA and protein synthesis mechanisms (4 papers), Epigenetics and DNA Methylation (3 papers), Genomics and Phylogenetic Studies (2 papers), Biomedical Text Mining and Ontologies (2 papers) and Cancer-related molecular mechanisms research (2 papers). The work is most often cited by research in Genetics (647 citations), Cancer Research (126 citations), Obstetrics and Gynecology (61 citations), Molecular Biology (576 citations) and Pediatrics, Perinatology and Child Health (84 citations). Jason E. Miller has collaborated with scholars based in United States, Canada and Finland. Frequent co-authors include Joseph C. Reese, Dokyoon Kim, Timothy Walston, Manu Shivakumar, M. J. Harris, Seonggyun Han, Younghee Lee, Marylyn DeRiggi Ritchie, Teresa M. Gunn and D. M. Juriloff. Their work appears in journals such as BMC Medical Genomics, Scientific Reports, The American Journal of Human Genetics, Nature 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.