R Harris
Impact in
- Neurology top 0.5%
- Neurofibromatosis and Schwannoma Cases
- Vascular Malformations Diagnosis and Treatment
- Rheumatology top 0.5%
- Folate and B Vitamins Research
Papers in
- Genetics 53
- BRCA gene mutations in cancer 17
- Genomics and Rare Diseases 11
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- Sexual Differentiation and Disorders 8
- Co-authors
- Valerie Newton (9 shared papers)Andrew Read (26 shared papers)Caroline Benjamin (13 shared papers)Dian Donnai (10 shared papers)E. O. Ukaejiofo (2 shared papers)D. Gareth Evans (8 shared papers)M.A. Ferguson‐Smith (3 shared papers)John R.W. Yates (3 shared papers)
- Journals
- Journal of Medical Genetics (30 papers)The Lancet (15 papers)British Journal of Cancer (7 papers)BJOG An International Journal of Obstetrics & Gynaecology (7 papers)Nature (5 papers)
- Partner nations
- United KingdomSouth AfricaUnited States
In The Last Decade
R Harris
168 papers receiving 6.7k citations
R Harris's Hit Papers
Peers
Comparison fields: 5 of 152
- Neurology 1.2k
- Rheumatology 923
- Cancer Research 871
- Genetics 1.4k
- Transplantation 108
Countries citing papers authored by R Harris
This map shows the geographic impact of R Harris'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 Harris with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R Harris more than expected).
Fields of papers citing papers by R Harris
This network shows the impact of papers produced by R Harris. 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 Harris. The network helps show where R Harris may publish in the future.
Co-authors
The 25 scholars most cited alongside R Harris, 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 173 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Clinical Features and Natural History of von Hippel-Lindau Disease Hit paper breakdown → | 1990 | 679 |
| 2 | Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene Hit paper breakdown → | 1992 | 543 |
| 3 | A Clinical Study of Type 2 Neurofibromatosis Hit paper breakdown → | 1992 | 478 |
| 4 | 1991 | 415 | |
| 5 | FURTHER EXPERIENCE OF VITAMIN SUPPLEMENTATION FOR PREVENTION OF NEURAL TUBE DEFECT RECURRENCES Hit paper breakdown → | 1983 | 356 |
| 6 | 1992 | 337 | |
| 7 | 1981 | 248 | |
| 8 | 1969 | 176 | |
| 9 | 1993 | 168 | |
| 10 | 1999 | 147 | |
| 11 | 1970 | 128 | |
| 12 | 1992 | 123 | |
| 13 | 1979 | 123 | |
| 14 | 1997 | 116 | |
| 15 | 1989 | 94 | |
| 16 | Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse. | 1990 | 94 |
| 17 | 1987 | 88 | |
| 18 | 1981 | 82 | |
| 19 | 1983 | 75 | |
| 20 | 2010 | 75 |
About R Harris
R Harris is a scholar working on Genetics, Molecular Biology, Immunology, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 173 papers that have together received 7.1k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (17 papers), Immune Cell Function and Interaction (14 papers), T-cell and B-cell Immunology (13 papers), Monoclonal and Polyclonal Antibodies Research (11 papers), Genomics and Rare Diseases (11 papers), Prenatal Screening and Diagnostics (10 papers), Neurofibromatosis and Schwannoma Cases (9 papers) and Sexual Differentiation and Disorders (8 papers). The work is most often cited by research in Neurology (1.2k citations), Rheumatology (923 citations), Cancer Research (871 citations), Genetics (1.4k citations) and Transplantation (108 citations). R Harris has collaborated with scholars based in United Kingdom, South Africa and United States. Frequent co-authors include Valerie Newton, Andrew Read, Caroline Benjamin, Dian Donnai, E. O. Ukaejiofo, D. Gareth Evans, M.A. Ferguson‐Smith, John R.W. Yates, Eamonn R. Maher and W Neary. Their work appears in journals such as Journal of Medical Genetics, The Lancet, British Journal of Cancer, BJOG An International Journal of Obstetrics & Gynaecology 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.