Richard H. Scott
- Molecular Biology top 10%
- Genetics top 5%
- Pediatrics, Perinatology and Child Health top 5%
- Pulmonary and Respiratory Medicine
- Cancer Research
- Co-authors
- Zornitza StarkHelen BrittainNatalie TrumpEllen ThomasC. R. BoustredLyn S. ChittyJane A. HurstManju A. Kurian
- Topics
- Genomics and Rare Diseases (20 papers)Genomic variations and chromosomal abnormalities (8 papers)BRCA gene mutations in cancer (5 papers)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Richard H. Scott
40 papers receiving 1.5k citations
Hit Papers
Peers
Comparison fields: 5 of 113
- Molecular Biology 760
- Genetics 676
- Pediatrics, Perinatology and Child Health 363
- Pulmonary and Respiratory Medicine 159
- Cancer Research 155
Countries citing papers authored by Richard H. Scott
This map shows the geographic impact of Richard H. Scott'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 H. Scott with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Richard H. Scott more than expected).
Fields of papers citing papers by Richard H. Scott
This network shows the impact of papers produced by Richard H. Scott. 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 H. Scott. The network helps show where Richard H. Scott may publish in the future.
Co-authorship network of co-authors of Richard H. Scott
This figure shows the co-authorship network connecting the top 25 collaborators of Richard H. Scott. A scholar is included among the top collaborators of Richard H. Scott 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 H. Scott. Richard H. Scott is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 8 | |
| 2 | 16 | |
| 3 | Genomic newborn screening for rare diseasesbreakdown → | 88 |
| 4 | 0 | |
| 5 | 26 | |
| 6 | 45 | |
| 7 | 16 | |
| 8 | 43 | |
| 9 | 30 | |
| 10 | 19 | |
| 11 | 30 | |
| 12 | 16 | |
| 13 | 7 | |
| 14 | 34 | |
| 15 | 92 | |
| 16 | 147 | |
| 17 | 11 | |
| 18 | 48 | |
| 19 | 5 | |
| 20 | 87 |
About Richard H. Scott
Richard H. Scott is a scholar working on Genetics, Cancer Research and Molecular Biology, having authored 42 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (20 papers), Genomic variations and chromosomal abnormalities (8 papers) and BRCA gene mutations in cancer (5 papers). The work is most often cited by research in Genetics (676 citations), Pediatrics, Perinatology and Child Health (363 citations) and Clinical Biochemistry (108 citations). Richard H. Scott has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Zornitza Stark, Helen Brittain, Natalie Trump, Ellen Thomas, C. R. Boustred, Lyn S. Chitty, Jane A. Hurst, Manju A. Kurian, Suzanne Drury and Nicholas Lench. Their work appears in journals such as The Lancet, Nature Medicine and Nature 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.