Peter Beighton
About
In The Last Decade
Peter Beighton
361 papers receiving 11.7k citations
Hit Papers
Peers
Comparison fields: 5 of 166
- Genetics 5.8k
- Molecular Biology 4.3k
- Surgery 2.6k
- Rheumatology 2.2k
- Oncology 2.0k
Countries citing papers authored by Peter Beighton
This map shows the geographic impact of Peter Beighton'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 Peter Beighton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Beighton more than expected).
Fields of papers citing papers by Peter Beighton
This network shows the impact of papers produced by Peter Beighton. 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 Peter Beighton. The network helps show where Peter Beighton may publish in the future.
Co-authorship network of co-authors of Peter Beighton
This figure shows the co-authorship network connecting the top 25 collaborators of Peter Beighton. A scholar is included among the top collaborators of Peter Beighton 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 Peter Beighton. Peter Beighton is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 4 | |
| 2 | The University of Cape Town's contribution to medical genetics in Africa: from the past into the future | 4 |
| 3 | Familial Hyperdontia in the Deciduous Dentition | 1 |
| 4 | Marfan syndrome in South Africa: a molecular genetic approach to diagnosis. | 0 |
| 5 | Ehlers-Danlos syndromes: Revised nosology, Villefranche, 1997 breakdown → | 1192 |
| 6 | Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL) in three neonates. | 5 |
| 7 | 14 | |
| 8 | Duchenne muscular dystrophy in South Africa. Prevention by molecular techniques. | 2 |
| 9 | 20 | |
| 10 | Skeletal complications in osteogenesis imperfecta. A review of 153 South African patients. | 25 |
| 11 | Osteopetrosis in South Africa. The benign, lethal and intermediate forms. | 54 |
| 12 | Sclerosteosis in South Africa. | 28 |
| 13 | The aetiology of partial deafness in childhood. | 6 |
| 14 | 4 | |
| 15 | Bone and joint disorders on Tristan da Cunha. | 11 |
| 16 | 13 | |
| 17 | Alimentary bleeding in cutis laxa of late onset. | 5 |
| 18 | 91 | |
| 19 | 32 | |
| 20 | 55 |
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.