R. Williamson
- Genetics top 0.5%
- Hemoglobinopathies and Related Disorders 19
- Genomic variations and chromosomal abnormalities 14
- Reproductive Medicine top 1%
- Genetics top 0.5%
- Hemoglobinopathies and Related Disorders 19
- Genomic variations and chromosomal abnormalities 14
- Molecular Biology top 2%
- DNA and Nucleic Acid Chemistry 28
- RNA and protein synthesis mechanisms 21
- RNA modifications and cancer 18
- DNA Repair Mechanisms 14
- RNA Research and Splicing 13
- Hematology top 2%
-
- Cystic Fibrosis Research Advances 32
- Co-authors
- Kay E. DaviesSteve E. HumphriesPeter ScamblerP.F.R. LittleJeffrey MurrayDavinia WhiteLucille VoullaireL. Wilton
- Cited by
- GeneticsReproductive Medicine
- Journals
- Human Genetics (26 papers)Journal of Medical Genetics (13 papers)Nucleic Acids Research (11 papers)
- Partner nations
- United KingdomUnited StatesSouth Africa
In The Last Decade
R. Williamson
185 papers receiving 7.3k citations
Peers
Comparison fields: 5 of 160
- Genetics 1.1k
- Reproductive Medicine 639
- Genetics 2.0k
- Molecular Biology 3.8k
- Hematology 588
Countries citing papers authored by R. Williamson
This map shows the geographic impact of R. Williamson'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. Williamson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R. Williamson more than expected).
Fields of papers citing papers by R. Williamson
This network shows the impact of papers produced by R. Williamson. 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. Williamson. The network helps show where R. Williamson may publish in the future.
Co-authorship network
The 25 scholars most cited alongside R. Williamson, 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 | 2009 | 8 | |
| 2 | 2005 | 66 | |
| 3 | 2000 | 260 | |
| 4 | The new genetics. What are the everyday clinical applications? | 1999 | 2 |
| 5 | 1999 | 33 | |
| 6 | The views of general practitioners on community carrier screening for cystic fibrosis. | 1996 | 29 |
| 7 | 1995 | 19 | |
| 8 | 1993 | 18 | |
| 9 | Attitudes to carrier screening for cystic fibrosis: a survey of health care professionals, relatives of sufferers and other members of the public. | 1991 | 55 |
| 10 | 1991 | 2 | |
| 11 | 1990 | 17 | |
| 12 | 1989 | 61 | |
| 13 | 1989 | 38 | |
| 14 | 1988 | 5 | |
| 15 | 1988 | 12 | |
| 16 | 1987 | 115 | |
| 17 | 1986 | 7 | |
| 18 | Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids. | 1984 | 137 |
| 19 | 1983 | 2 | |
| 20 | 1983 | 44 |
About R. Williamson
R. Williamson is a scholar working on Genetics, Genetics and Molecular Biology, having authored 185 papers that have together received 7.9k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (32 papers), DNA and Nucleic Acid Chemistry (28 papers), RNA and protein synthesis mechanisms (21 papers), Hemoglobinopathies and Related Disorders (19 papers), RNA modifications and cancer (18 papers), DNA Repair Mechanisms (14 papers), Genomic variations and chromosomal abnormalities (14 papers) and RNA Research and Splicing (13 papers). The work is most often cited by research in Genetics (1.1k citations), Reproductive Medicine (639 citations) and Genetics (2.0k citations). R. Williamson has collaborated with scholars based in United Kingdom, United States and South Africa. Frequent co-authors include Kay E. Davies, Steve E. Humphries, Peter Scambler, P.F.R. Little, Jeffrey Murray, Davinia White, Lucille Voullaire, L. Wilton, Howard R. Slater and P. Pearson. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, Nucleic Acids Research, Cytogenetic and Genome Research and Nature.
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.