Amanda Springer
Impact in
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- Autophagy in Disease and Therapy
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- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
Papers in
- Genetics 5
- Genomics and Rare Diseases 5
- BRCA gene mutations in cancer 1
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- RNA modifications and cancer 3
- RNA Research and Splicing 2
- Co-authors
- James P. Lodolce (1 shared paper)Urszula Dougherty (1 shared paper)Wesley A. Grimm (1 shared paper)Sonia S. Kupfer (1 shared paper)Sarah Bartulis (1 shared paper)Marc Bissonnette (1 shared paper)Jeannette S. Messer (1 shared paper)Nathan A. Ellis (1 shared paper)
In The Last Decade
Amanda Springer
7 papers receiving 116 citations
Peers
Comparison fields: 5 of 42
- Epidemiology 49
- Cancer Research 17
- Genetics 30
- Molecular Biology 62
- Immunology 18
Countries citing papers authored by Amanda Springer
This map shows the geographic impact of Amanda Springer'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 Amanda Springer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amanda Springer more than expected).
Fields of papers citing papers by Amanda Springer
This network shows the impact of papers produced by Amanda Springer. 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 Amanda Springer. The network helps show where Amanda Springer may publish in the future.
Co-authors
The 25 scholars most cited alongside Amanda Springer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 71 | |
| 2 | 2019 | 23 | |
| 3 | 2020 | 8 | |
| 4 | 2022 | 6 | |
| 5 | 2022 | 4 | |
| 6 | 2024 | 2 | |
| 7 | 2020 | 2 |
About Amanda Springer
Amanda Springer is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Biochemistry, having authored 7 papers that have together received 116 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), RNA modifications and cancer (3 papers), RNA Research and Splicing (2 papers), interferon and immune responses (1 paper), Metabolism and Genetic Disorders (1 paper), Ethics and Legal Issues in Pediatric Healthcare (1 paper), BRCA gene mutations in cancer (1 paper) and Cancer-related molecular mechanisms research (1 paper). The work is most often cited by research in Epidemiology (49 citations), Cancer Research (17 citations), Genetics (30 citations), Molecular Biology (62 citations) and Immunology (18 citations). Amanda Springer has collaborated with scholars based in Australia, Italy and Ireland. Frequent co-authors include James P. Lodolce, Urszula Dougherty, Wesley A. Grimm, Sonia S. Kupfer, Sarah Bartulis, Marc Bissonnette, Jeannette S. Messer, Nathan A. Ellis, Dezheng Huo and David L. Boone. Their work appears in journals such as Human Mutation, Molecular Case Studies, Pathology, npj Genomic Medicine and Gut.
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.