Robert Williamson
Impact in
- Physiology top 0.2%
- Alzheimer's disease research and treatments
- Genetics top 0.5%
- Hemoglobinopathies and Related Disorders
Papers in
-
- RNA and protein synthesis mechanisms 18
- DNA and Nucleic Acid Chemistry 17
- Genetics 34
- Hemoglobinopathies and Related Disorders 20
- Co-authors
- John Hardy (2 shared papers)Martin N. Rossor (2 shared papers)Andrew R. Haynes (1 shared paper)A.D. Roses (1 shared paper)Liana Fidani (1 shared paper)Penelope Roques (1 shared paper)Karen Rooke (1 shared paper)Chris J. Talbot (1 shared paper)
- Journals
- Human Genetics (11 papers)Human Molecular Genetics (11 papers)Nature (10 papers)Genomics (9 papers)Nucleic Acids Research (8 papers)
- Partner nations
- United KingdomAustraliaUnited States
In The Last Decade
Robert Williamson
214 papers receiving 12.7k citations
Robert Williamson's Hit Papers
Peers
Comparison fields: 5 of 192
- Physiology 3.2k
- Genetics 1.0k
- Cellular and Molecular Neuroscience 1.7k
- Genetics 2.5k
- Molecular Biology 6.0k
Countries citing papers authored by Robert Williamson
This map shows the geographic impact of Robert 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 Robert Williamson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert Williamson more than expected).
Fields of papers citing papers by Robert Williamson
This network shows the impact of papers produced by Robert 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 Robert Williamson. The network helps show where Robert Williamson may publish in the future.
Co-authors
The 25 scholars most cited alongside Robert 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
Showing the 20 most-cited of 216 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease Hit paper breakdown → | 1991 | 3446 |
| 2 | A Mutation in the Interferon-γ –Receptor Gene and Susceptibility to Mycobacterial Infection Hit paper breakdown → | 1996 | 914 |
| 3 | Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis Hit paper breakdown → | 1995 | 531 |
| 4 | Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy Hit paper breakdown → | 1992 | 516 |
| 5 | 1985 | 372 | |
| 6 | 1994 | 372 | |
| 7 | 1987 | 278 | |
| 8 | 1994 | 256 | |
| 9 | 1997 | 254 | |
| 10 | 1988 | 223 | |
| 11 | 1981 | 217 | |
| 12 | 1974 | 193 | |
| 13 | 1989 | 168 | |
| 14 | 1991 | 165 | |
| 15 | 1996 | 164 | |
| 16 | 1999 | 138 | |
| 17 | 1981 | 135 | |
| 18 | 1993 | 116 | |
| 19 | 2003 | 113 | |
| 20 | 1970 | 111 |
About Robert Williamson
Robert Williamson is a scholar working on Molecular Biology, Genetics, Genetics, Safety, Risk, Reliability and Quality and Cellular and Molecular Neuroscience, having authored 216 papers that have together received 13.4k indexed citations. Recurring topics across this work include Fire dynamics and safety research (25 papers), Genetic Neurodegenerative Diseases (22 papers), Hemoglobinopathies and Related Disorders (20 papers), Cystic Fibrosis Research Advances (19 papers), RNA and protein synthesis mechanisms (18 papers), DNA and Nucleic Acid Chemistry (17 papers), Prenatal Screening and Diagnostics (16 papers) and Fire effects on concrete materials (12 papers). The work is most often cited by research in Physiology (3.2k citations), Genetics (1.0k citations), Cellular and Molecular Neuroscience (1.7k citations), Genetics (2.5k citations) and Molecular Biology (6.0k citations). Robert Williamson has collaborated with scholars based in United Kingdom, Australia and United States. Frequent co-authors include John Hardy, Martin N. Rossor, Andrew R. Haynes, A.D. Roses, Liana Fidani, Penelope Roques, Karen Rooke, Chris J. Talbot, R. Mant and Alison Goate. Their work appears in journals such as Human Genetics, Human Molecular Genetics, Nature, Genomics and Nucleic Acids Research.
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.