E.R. Giblett
About
In The Last Decade
E.R. Giblett
53 papers receiving 2.0k citations
Hit Papers
Peers
Comparison fields: 5 of 131
- Hematology 980
- Genetics 522
- Molecular Biology 506
- Physiology 450
- Genetics 409
Countries citing papers authored by E.R. Giblett
This map shows the geographic impact of E.R. Giblett'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 E.R. Giblett with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E.R. Giblett more than expected).
Fields of papers citing papers by E.R. Giblett
This network shows the impact of papers produced by E.R. Giblett. 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 E.R. Giblett. The network helps show where E.R. Giblett may publish in the future.
Co-authorship network of co-authors of E.R. Giblett
This figure shows the co-authorship network connecting the top 25 collaborators of E.R. Giblett. A scholar is included among the top collaborators of E.R. Giblett 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 E.R. Giblett. E.R. Giblett is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | Segregation of marker loci in families with an inherited paracentric insertion of chromosome 9. | 21 |
| 2 | Human C4 haplotypes with duplicated C4A or C4B. | 60 |
| 3 | 5 | |
| 4 | 12 | |
| 5 | 1 | |
| 6 | 5 | |
| 7 | 12 | |
| 8 | 3 | |
| 9 | 51 | |
| 10 | 91 | |
| 11 | 9 | |
| 12 | 10 | |
| 13 | 9 | |
| 14 | Cytidine deaminase: a new genetic polymorphism demonstrated in human granulocytes. | 19 |
| 15 | 6 | |
| 16 | Uridine monophosphate kinase: A new genetic polymorphism with possible clinical implications. | 46 |
| 17 | Genetic variation of the soluble form of NADP-dependent isocitric dehydrogenase in man. | 33 |
| 18 | Population genetic studies in the Congo. 3. Blood groups (ABO, MNSs, Rh, Jsa). | 25 |
| 19 | 8 | |
| 20 | 7 |
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.