Rachel Porter
- Topics
- Glycogen Storage Diseases and Myoclonus (2 papers)Genetics and Neurodevelopmental Disorders (1 paper)Genomic variations and chromosomal abnormalities (1 paper)
- Cited by
- RheumatologyCancer ResearchNeurology
- Journals
- Annals of NeurologyMutagenesisPubMed
- Partner nations
- United StatesUnited Kingdom
In The Last Decade
Rachel Porter
3 papers receiving 77 citations
Peers
Comparison fields: 5 of 32
- Rheumatology 48
- Molecular Biology 32
- Genetics 27
- Physiology 22
- Cancer Research 17
Countries citing papers authored by Rachel Porter
This map shows the geographic impact of Rachel Porter'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 Rachel Porter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rachel Porter more than expected).
Fields of papers citing papers by Rachel Porter
This network shows the impact of papers produced by Rachel Porter. 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 Rachel Porter. The network helps show where Rachel Porter may publish in the future.
Co-authorship network of co-authors of Rachel Porter
This figure shows the co-authorship network connecting the top 25 collaborators of Rachel Porter. A scholar is included among the top collaborators of Rachel Porter 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 Rachel Porter. Rachel Porter is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 29 | |
| 2 | 44 | |
| 3 | Lafora's disease; diagnosis by liver biopsy. | 11 |
About Rachel Porter
Rachel Porter is a scholar working on Clinical Biochemistry, Rheumatology and Genetics, having authored 3 papers that have together received 84 indexed citations. Recurring topics across this work include Glycogen Storage Diseases and Myoclonus (2 papers), Genetics and Neurodevelopmental Disorders (1 paper) and Genomic variations and chromosomal abnormalities (1 paper). The work is most often cited by research in Rheumatology (48 citations), Cancer Research (17 citations) and Neurology (16 citations). Rachel Porter has collaborated with scholars based in United States and United Kingdom. Frequent co-authors include Sian James, J. A. Barranger, Kamal G. Ishak and R. Nishimura. Their work appears in journals such as Annals of Neurology, Mutagenesis and PubMed.
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.