Gordon S. Stephen
- Topics
- Genomic variations and chromosomal abnormalities (6 papers)Prenatal Screening and Diagnostics (5 papers)Congenital heart defects research (3 papers)
- Journals
- BJOG An International Journal of Obstetrics & GynaecologyJournal of Medical GeneticsClinical Genetics
- Partner nations
- United Kingdom
In The Last Decade
Gordon S. Stephen
14 papers receiving 211 citations
Peers
Comparison fields: 5 of 38
- Genetics 171
- Molecular Biology 100
- Pediatrics, Perinatology and Child Health 66
- Plant Science 62
- Surgery 24
Countries citing papers authored by Gordon S. Stephen
This map shows the geographic impact of Gordon S. Stephen'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 Gordon S. Stephen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gordon S. Stephen more than expected).
Fields of papers citing papers by Gordon S. Stephen
This network shows the impact of papers produced by Gordon S. Stephen. 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 Gordon S. Stephen. The network helps show where Gordon S. Stephen may publish in the future.
Co-authorship network of co-authors of Gordon S. Stephen
This figure shows the co-authorship network connecting the top 25 collaborators of Gordon S. Stephen. A scholar is included among the top collaborators of Gordon S. Stephen 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 Gordon S. Stephen. Gordon S. Stephen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 15 | |
| 3 | 1 | |
| 4 | 17 | |
| 5 | 3 | |
| 6 | 42 | |
| 7 | 7 | |
| 8 | 29 | |
| 9 | 3 | |
| 10 | 1 | |
| 11 | 24 | |
| 12 | 65 | |
| 13 | 14 | |
| 14 | 6 | |
| 15 | 12 |
About Gordon S. Stephen
Gordon S. Stephen is a scholar working on Developmental Biology, Hematology and Genetics, having authored 15 papers that have together received 239 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers) and Congenital heart defects research (3 papers). The work is most often cited by research in Genetics (171 citations), Pediatrics, Perinatology and Child Health (66 citations) and Reproductive Medicine (16 citations). Gordon S. Stephen has collaborated with scholars based in United Kingdom. Frequent co-authors include D A Couzin, J L Watt, Alan Johnston, John Dean, Ken Ward, E.L. McKay, Elizabeth Gray, R Rankin, Dongeun Yong and Sharon Simpson. Their work appears in journals such as BJOG An International Journal of Obstetrics & Gynaecology, Journal of Medical Genetics and Clinical 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.