N.K. Spurr
Impact in
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- Genetic factors in colorectal cancer
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
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- CRISPR and Genetic Engineering 4
- DNA Repair Mechanisms 4
- Glutathione Transferases and Polymorphisms 3
- RNA Research and Splicing 2
- Genetics 10
- Genomic variations and chromosomal abnormalities 4
- Co-authors
- E. Solomon (5 shared papers)Denise Sheer (3 shared papers)Walter F. Bodmer (7 shared papers)C. Roland Wolf (5 shared papers)H J R Bussey (1 shared paper)Patricia Gorman (1 shared paper)Sue Rider (1 shared paper)Frances C. Lucibello (1 shared paper)
- Journals
- Genomics (7 papers)Nucleic Acids Research (4 papers)Annals of Human Genetics (3 papers)Nature (3 papers)Cytogenetic and Genome Research (3 papers)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
N.K. Spurr
44 papers receiving 3.7k citations
N.K. Spurr's Hit Papers
Peers
Comparison fields: 5 of 130
- Pathology and Forensic Medicine 786
- Cancer Research 577
- Oncology 994
- Genetics 870
- Molecular Biology 2.0k
Countries citing papers authored by N.K. Spurr
This map shows the geographic impact of N.K. Spurr'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 N.K. Spurr with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites N.K. Spurr more than expected).
Fields of papers citing papers by N.K. Spurr
This network shows the impact of papers produced by N.K. Spurr. 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 N.K. Spurr. The network helps show where N.K. Spurr may publish in the future.
Co-authors
The 25 scholars most cited alongside N.K. Spurr, 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 45 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Localization of the gene for familial adenomatous polyposis on chromosome 5 Hit paper breakdown → | 1987 | 1014 |
| 2 | 1989 | 437 | |
| 3 | 1993 | 380 | |
| 4 | 1989 | 264 | |
| 5 | 1996 | 249 | |
| 6 | 1992 | 194 | |
| 7 | 1988 | 173 | |
| 8 | 1984 | 146 | |
| 9 | 1995 | 104 | |
| 10 | 1994 | 95 | |
| 11 | 1997 | 69 | |
| 12 | Human cytochrome P-450 PB-1: a multigene family involved in mephenytoin and steroid oxidations that maps to chromosome 10. | 1988 | 68 |
| 13 | 1995 | 67 | |
| 14 | 1985 | 61 | |
| 15 | 1993 | 51 | |
| 16 | 1992 | 46 | |
| 17 | 1993 | 44 | |
| 18 | 1997 | 40 | |
| 19 | 1994 | 38 | |
| 20 | 1995 | 36 |
About N.K. Spurr
N.K. Spurr is a scholar working on Molecular Biology, Genetics, Oncology, Cancer Research and Pathology and Forensic Medicine, having authored 45 papers that have together received 3.8k indexed citations. Recurring topics across this work include CRISPR and Genetic Engineering (4 papers), DNA Repair Mechanisms (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetic factors in colorectal cancer (3 papers), Glutathione Transferases and Polymorphisms (3 papers), Carcinogens and Genotoxicity Assessment (2 papers), RNA Research and Splicing (2 papers) and Cardiomyopathy and Myosin Studies (2 papers). The work is most often cited by research in Pathology and Forensic Medicine (786 citations), Cancer Research (577 citations), Oncology (994 citations), Genetics (870 citations) and Molecular Biology (2.0k citations). N.K. Spurr has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include E. Solomon, Denise Sheer, Walter F. Bodmer, C. Roland Wolf, H J R Bussey, Patricia Gorman, Sue Rider, Frances C. Lucibello, Anthony Ellis and Victoria A. Murday. Their work appears in journals such as Genomics, Nucleic Acids Research, Annals of Human Genetics, Nature and Cytogenetic and Genome 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.