Jonathan E. LoTempio
Impact in
Papers in
-
- Cancer Genomics and Diagnostics 4
- Genetics 6
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 3
- Co-authors
- M. Camille Harris (1 shared paper)Scott A. Jackson (1 shared paper)David Marshall Porterfield (1 shared paper)Michael Mishkind (1 shared paper)Lita M. Proctor (1 shared paper)Kelly D. Goodwin (1 shared paper)Linda A. Chrisey (1 shared paper)Jay L. Garland (1 shared paper)
- Journals
- Nature Communications (3 papers)Nature Genetics (2 papers)Genetics in Medicine (2 papers)Nature (2 papers)Cell Genomics (1 paper)
- Partner nations
- United StatesUnited KingdomFrance
In The Last Decade
Jonathan E. LoTempio
19 papers receiving 448 citations
Peers
Comparison fields: 5 of 101
- Health Informatics 8
- Biological Psychiatry 10
- Molecular Biology 230
- Infectious Diseases 57
- Gastroenterology 14
Countries citing papers authored by Jonathan E. LoTempio
This map shows the geographic impact of Jonathan E. LoTempio'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 Jonathan E. LoTempio with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jonathan E. LoTempio more than expected).
Fields of papers citing papers by Jonathan E. LoTempio
This network shows the impact of papers produced by Jonathan E. LoTempio. 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 Jonathan E. LoTempio. The network helps show where Jonathan E. LoTempio may publish in the future.
Co-authors
The 25 scholars most cited alongside Jonathan E. LoTempio, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 170 | |
| 2 | 2016 | 91 | |
| 3 | 2023 | 72 | |
| 4 | 2021 | 44 | |
| 5 | 2021 | 21 | |
| 6 | 2021 | 13 | |
| 7 | 2023 | 12 | |
| 8 | 2025 | 7 | |
| 9 | 2023 | 7 | |
| 10 | 2023 | 4 | |
| 11 | 2025 | 3 | |
| 12 | 2025 | 3 | |
| 13 | 2025 | 2 | |
| 14 | 2025 | 2 | |
| 15 | 2025 | 1 | |
| 16 | 2025 | 1 | |
| 17 | 2025 | 1 | |
| 18 | 2026 | 1 | |
| 19 | 2026 | 1 | |
| 20 | 2026 | 0 |
About Jonathan E. LoTempio
Jonathan E. LoTempio is a scholar working on Cancer Research, Genetics, Molecular Biology, Health Informatics and Clinical Biochemistry, having authored 23 papers that have together received 456 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Cancer Genomics and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Chromosomal and Genetic Variations (2 papers), Gut microbiota and health (2 papers), CRISPR and Genetic Engineering (1 paper), RNA modifications and cancer (1 paper) and Vaccine Coverage and Hesitancy (1 paper). The work is most often cited by research in Health Informatics (8 citations), Biological Psychiatry (10 citations), Molecular Biology (230 citations), Infectious Diseases (57 citations) and Gastroenterology (14 citations). Jonathan E. LoTempio has collaborated with scholars based in United States, United Kingdom and France. Frequent co-authors include M. Camille Harris, Scott A. Jackson, David Marshall Porterfield, Michael Mishkind, Lita M. Proctor, Kelly D. Goodwin, Linda A. Chrisey, Jay L. Garland, Deborah R. Fravel and Angela R. Records. Their work appears in journals such as Nature Communications, Nature Genetics, Genetics in Medicine, Nature and Cell Genomics.
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.