Richard Segraves
- Genetics top 0.2%
- Molecular Biology top 2%
- Plant Science top 1%
- Cancer Research top 1%
- Pediatrics, Perinatology and Child Health top 1%
- Co-authors
- Joe W. GrayColin C. CollinsDaniel PinkelDonna G. AlbertsonJames C. FuscoeD. PinkelWen-Lin KuoShanaz H. Dairkee
- Topics
- Genomic variations and chromosomal abnormalities (20 papers)Chromosomal and Genetic Variations (16 papers)Gene expression and cancer classification (7 papers)
- Partner nations
- United StatesDenmarkUnited Kingdom
In The Last Decade
Richard Segraves
28 papers receiving 5.6k citations
Hit Papers
Peers
Comparison fields: 5 of 127
- Genetics 3.5k
- Molecular Biology 3.3k
- Plant Science 1.8k
- Cancer Research 1.1k
- Pediatrics, Perinatology and Child Health 764
Countries citing papers authored by Richard Segraves
This map shows the geographic impact of Richard Segraves'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 Richard Segraves with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Richard Segraves more than expected).
Fields of papers citing papers by Richard Segraves
This network shows the impact of papers produced by Richard Segraves. 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 Richard Segraves. The network helps show where Richard Segraves may publish in the future.
Co-authorship network of co-authors of Richard Segraves
This figure shows the co-authorship network connecting the top 25 collaborators of Richard Segraves. A scholar is included among the top collaborators of Richard Segraves 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 Richard Segraves. Richard Segraves is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 206 | |
| 2 | 95 | |
| 3 | 50 | |
| 4 | 79 | |
| 5 | 27 | |
| 6 | 212 | |
| 7 | 105 | |
| 8 | 61 | |
| 9 | High-resolution array CGH A validation study for the detection of submicroscopic deletions in DiGeorge and velo-cardio-facial syndromes | 1 |
| 10 | 269 | |
| 11 | 463 | |
| 12 | High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarraysbreakdown → | 1617 |
| 13 | 0 | |
| 14 | Detection of aneuploid human sperm by fluorescence in situ hybridization: evidence for a donor difference in frequency of sperm disomic for chromosomes 1 and Y. | 132 |
| 15 | 187 | |
| 16 | 30 | |
| 17 | 76 | |
| 18 | Detection of aneuploidy involving chromosomes 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes. | 100 |
| 19 | 39 | |
| 20 | Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.breakdown → | 1089 |
About Richard Segraves
Richard Segraves is a scholar working on Genetics, Plant Science and Molecular Biology, having authored 30 papers that have together received 5.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (20 papers), Chromosomal and Genetic Variations (16 papers) and Gene expression and cancer classification (7 papers). The work is most often cited by research in Genetics (3.5k citations), Cancer Research (1.1k citations) and Molecular Biology (3.3k citations). Richard Segraves has collaborated with scholars based in United States, Denmark and United Kingdom. Frequent co-authors include Joe W. Gray, Colin C. Collins, Daniel Pinkel, Donna G. Albertson, James C. Fuscoe, D. Pinkel, Wen-Lin Kuo, Shanaz H. Dairkee, J. N. Lucas and David Kowbel. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Blood.
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.