Andrew Rowan
Impact in
- Pathology and Forensic Medicine top 0.2%
- Genetic factors in colorectal cancer
- Cancer Research top 1%
- Cancer Genomics and Diagnostics
Papers in
-
- Genetic factors in colorectal cancer 38
- Oncology 22
- Colorectal Cancer Treatments and Studies 10
- Colorectal Cancer Screening and Detection 7
- Co-authors
- Walter Fred Bodmer (25 shared papers)Ian P.M. Tomlinson (23 shared papers)Mohammad Ilyas (7 shared papers)D C Bicknell (8 shared papers)Nanda R. Rodrigues (1 shared paper)Mark E. Smith (1 shared paper)I. Ballini Kerr (1 shared paper)Julian Gannon (1 shared paper)
- Journals
- Proceedings of the National Academy of Sciences (10 papers)Nature Genetics (6 papers)Cancer Research (5 papers)Human Mutation (4 papers)British Journal of Cancer (4 papers)
- Partner nations
- United KingdomUnited StatesFinland
In The Last Decade
Andrew Rowan
65 papers receiving 8.9k citations
Andrew Rowan's Hit Papers
Peers
Comparison fields: 5 of 124
- Pathology and Forensic Medicine 2.9k
- Cancer Research 1.9k
- Oncology 2.7k
- Molecular Biology 4.2k
- Genetics 1.6k
Countries citing papers authored by Andrew Rowan
This map shows the geographic impact of Andrew Rowan'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 Andrew Rowan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrew Rowan more than expected).
Fields of papers citing papers by Andrew Rowan
This network shows the impact of papers produced by Andrew Rowan. 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 Andrew Rowan. The network helps show where Andrew Rowan may publish in the future.
Co-authors
The 25 scholars most cited alongside Andrew Rowan, 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 66 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer Hit paper breakdown → | 2002 | 1297 |
| 2 | p53 mutations in colorectal cancer. Hit paper breakdown → | 1990 | 920 |
| 3 | A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21 Hit paper breakdown → | 2007 | 696 |
| 4 | Replication stress links structural and numerical cancer chromosomal instability Hit paper breakdown → | 2013 | 681 |
| 5 | 2008 | 482 | |
| 6 | 1997 | 446 | |
| 7 | 2007 | 439 | |
| 8 | 2000 | 420 | |
| 9 | 1999 | 299 | |
| 10 | 2007 | 261 | |
| 11 | 2004 | 164 | |
| 12 | 2001 | 162 | |
| 13 | 1993 | 159 | |
| 14 | 2000 | 154 | |
| 15 | 2005 | 147 | |
| 16 | 1998 | 142 | |
| 17 | 1994 | 128 | |
| 18 | 2002 | 116 | |
| 19 | 2003 | 113 | |
| 20 | 2000 | 108 |
About Andrew Rowan
Andrew Rowan is a scholar working on Pathology and Forensic Medicine, Oncology, Cancer Research, Genetics and Molecular Biology, having authored 66 papers that have together received 9.2k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (38 papers), Cancer Genomics and Diagnostics (13 papers), Colorectal Cancer Treatments and Studies (10 papers), Wnt/β-catenin signaling in development and cancer (10 papers), Genomic variations and chromosomal abnormalities (7 papers), Colorectal Cancer Screening and Detection (7 papers), Cancer-related gene regulation (6 papers) and TGF-β signaling in diseases (4 papers). The work is most often cited by research in Pathology and Forensic Medicine (2.9k citations), Cancer Research (1.9k citations), Oncology (2.7k citations), Molecular Biology (4.2k citations) and Genetics (1.6k citations). Andrew Rowan has collaborated with scholars based in United Kingdom, United States and Finland. Frequent co-authors include Walter Fred Bodmer, Ian P.M. Tomlinson, Mohammad Ilyas, D C Bicknell, Nanda R. Rodrigues, Mark E. Smith, I. Ballini Kerr, Julian Gannon, David Philip Lane and Massimo N. Pignatelli. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics, Cancer Research, Human Mutation and British Journal of Cancer.
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.