Amanda Heppell-Parton
- Co-authors
- Pamela RabbittsHelen ImpeyAndrew J.H. SmithMaria de SousaBernard Kwabi‐AddoP R TwentymanMargery A. BarrandNicholas J. Lowe
- Topics
- Chromosomal and Genetic Variations (6 papers)Genomic variations and chromosomal abnormalities (6 papers)Cancer Genomics and Diagnostics (3 papers)
- Cited by
- GeneticsMolecular BiologyOncology
- Partner nations
- United KingdomUnited StatesSweden
In The Last Decade
Amanda Heppell-Parton
17 papers receiving 717 citations
Peers
Comparison fields: 5 of 72
- Molecular Biology 525
- Genetics 271
- Oncology 167
- Plant Science 139
- Cancer Research 91
Countries citing papers authored by Amanda Heppell-Parton
This map shows the geographic impact of Amanda Heppell-Parton'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 Heppell-Parton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amanda Heppell-Parton more than expected).
Fields of papers citing papers by Amanda Heppell-Parton
This network shows the impact of papers produced by Amanda Heppell-Parton. 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 Heppell-Parton. The network helps show where Amanda Heppell-Parton may publish in the future.
Co-authorship network of co-authors of Amanda Heppell-Parton
This figure shows the co-authorship network connecting the top 25 collaborators of Amanda Heppell-Parton. A scholar is included among the top collaborators of Amanda Heppell-Parton based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Amanda Heppell-Parton. Amanda Heppell-Parton is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 2 | |
| 2 | 11 | |
| 3 | 97 | |
| 4 | Gene mapping by fluorescence in situ hybridization. | 6 |
| 5 | 25 | |
| 6 | 19 | |
| 7 | 212 | |
| 8 | 126 | |
| 9 | 20 | |
| 10 | 124 | |
| 11 | 13 | |
| 12 | 12 | |
| 13 | 1 | |
| 14 | 36 | |
| 15 | 10 | |
| 16 | 8 | |
| 17 | 7 |
About Amanda Heppell-Parton
Amanda Heppell-Parton is a scholar working on Genetics, Cancer Research and Oncology, having authored 17 papers that have together received 729 indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (6 papers), Genomic variations and chromosomal abnormalities (6 papers) and Cancer Genomics and Diagnostics (3 papers). The work is most often cited by research in Genetics (271 citations), Molecular Biology (525 citations) and Oncology (167 citations). Amanda Heppell-Parton has collaborated with scholars based in United Kingdom, United States and Sweden. Frequent co-authors include Pamela Rabbitts, Helen Impey, Andrew J.H. Smith, Maria de Sousa, Bernard Kwabi‐Addo, P R Twentyman, Margery A. Barrand, Nicholas J. Lowe, C. Tease and Malcolm Ferguson-Smith. Their work appears in journals such as Nature Genetics, JNCI Journal of the National Cancer Institute and Oncogene.
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.