R. White
- Genetics top 0.05%
- Genomic variations and chromosomal abnormalities 39
- Pathology and Forensic Medicine top 0.1%
- Genetic factors in colorectal cancer 22
- Neurology top 0.2%
- Neurofibromatosis and Schwannoma Cases 23
- Cancer Research top 0.5%
- Cancer Genomics and Diagnostics 14
- Oncology top 0.5%
-
- DNA and Nucleic Acid Chemistry 40
- DNA Repair Mechanisms 34
- CRISPR and Genetic Engineering 23
- Genomics and Chromatin Dynamics 18
- Co-authors
- Mark H. SkolnickDavid BotsteinRonald W. DavisP. O’ConnellYusuke NakamuraMark LeppertBert VogelsteinStanley R. Hamilton
- Partner nations
- United StatesFranceUnited Kingdom
In The Last Decade
R. White
222 papers receiving 22.4k citations
Hit Papers
Peers
Comparison fields: 5 of 178
- Genetics 8.1k
- Pathology and Forensic Medicine 3.5k
- Neurology 3.0k
- Cancer Research 2.7k
- Oncology 4.1k
Countries citing papers authored by R. White
This map shows the geographic impact of R. White'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 R. White with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R. White more than expected).
Fields of papers citing papers by R. White
This network shows the impact of papers produced by R. White. 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 R. White. The network helps show where R. White may publish in the future.
Co-authorship network
The 25 scholars most cited alongside R. White, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 3 | |
| 2 | System Management by Exception, Part Final. | 2007 | 1 |
| 3 | 1995 | 17 | |
| 4 | 1995 | 33 | |
| 5 | 1994 | 7 | |
| 6 | 1993 | 19 | |
| 7 | 1991 | 98 | |
| 8 | 1991 | 92 | |
| 9 | 1990 | 444 | |
| 10 | The neurofibromatosis type 1 gene encodes a protein related to GAPbreakdown → | 1990 | 907 |
| 11 | 1990 | 41 | |
| 12 | 1989 | 2 | |
| 13 | 1989 | 1 | |
| 14 | 1988 | 1 | |
| 15 | 1988 | 5 | |
| 16 | 1988 | 2 | |
| 17 | 1988 | 3 | |
| 18 | 1988 | 8 | |
| 19 | 1987 | 29 | |
| 20 | 1987 | 1 |
About R. White
R. White is a scholar working on Genetics, Neurology, Molecular Biology, Pathology and Forensic Medicine and Cancer Research, having authored 225 papers that have together received 23.7k indexed citations. Recurring topics across this work include DNA and Nucleic Acid Chemistry (40 papers), Genomic variations and chromosomal abnormalities (39 papers), DNA Repair Mechanisms (34 papers), CRISPR and Genetic Engineering (23 papers), Neurofibromatosis and Schwannoma Cases (23 papers), Genetic factors in colorectal cancer (22 papers), Genomics and Chromatin Dynamics (18 papers) and Cancer Genomics and Diagnostics (14 papers). The work is most often cited by research in Genetics (8.1k citations), Pathology and Forensic Medicine (3.5k citations), Neurology (3.0k citations), Cancer Research (2.7k citations) and Oncology (4.1k citations). R. White has collaborated with scholars based in United States, France and United Kingdom. Frequent co-authors include Mark H. Skolnick, David Botstein, Ronald W. Davis, P. O’Connell, Yusuke Nakamura, Mark Leppert, Bert Vogelstein, Stanley R. Hamilton, Melanie Culver and Eric R. Fearon. Their work appears in journals such as Nucleic Acids Research, Genomics, Science, Proceedings of the National Academy of Sciences and Human 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.