Lettie E. Rawlins
- Co-authors
- Malcolm WoollardJulia WilliamsEmma L. BapleAndrew H. CrosbyGaurav V. HarlalkaBarry A. ChiozaHannah JonesJames Fasham
- Topics
- Genetics and Neurodevelopmental Disorders (4 papers)Genomics and Rare Diseases (3 papers)Hereditary Neurological Disorders (3 papers)
- Partner nations
- United KingdomUnited StatesPakistan
In The Last Decade
Lettie E. Rawlins
15 papers receiving 131 citations
Peers
Comparison fields: 5 of 42
- Molecular Biology 56
- Genetics 46
- Emergency Medicine 41
- Physiology 18
- Epidemiology 17
Countries citing papers authored by Lettie E. Rawlins
This map shows the geographic impact of Lettie E. Rawlins'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 Lettie E. Rawlins with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lettie E. Rawlins more than expected).
Fields of papers citing papers by Lettie E. Rawlins
This network shows the impact of papers produced by Lettie E. Rawlins. 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 Lettie E. Rawlins. The network helps show where Lettie E. Rawlins may publish in the future.
Co-authorship network of co-authors of Lettie E. Rawlins
This figure shows the co-authorship network connecting the top 25 collaborators of Lettie E. Rawlins. A scholar is included among the top collaborators of Lettie E. Rawlins 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 Lettie E. Rawlins. Lettie E. Rawlins is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 1 | |
| 3 | 2 | |
| 4 | 2 | |
| 5 | 1 | |
| 6 | 2 | |
| 7 | 0 | |
| 8 | 8 | |
| 9 | 6 | |
| 10 | 16 | |
| 11 | 23 | |
| 12 | 20 | |
| 13 | 6 | |
| 14 | 15 | |
| 15 | 1 | |
| 16 | 30 |
About Lettie E. Rawlins
Lettie E. Rawlins is a scholar working on Genetics, Neurology and Sensory Systems, having authored 16 papers that have together received 134 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Hereditary Neurological Disorders (3 papers). The work is most often cited by research in Emergency Medicine (41 citations), Genetics (46 citations) and Radiological and Ultrasound Technology (8 citations). Lettie E. Rawlins has collaborated with scholars based in United Kingdom, United States and Pakistan. Frequent co-authors include Malcolm Woollard, Julia Williams, Emma L. Baple, Andrew H. Crosby, Gaurav V. Harlalka, Barry A. Chioza, Hannah Jones, James Fasham, Peter O’Meara and Graham Munro. Their work appears in journals such as Cellular and Molecular Life Sciences, PLoS Genetics and European Journal of Human 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.