Derek J. Nancarrow
Impact in
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
- Genetics top 5%
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Oncology 25
- Cutaneous Melanoma Detection and Management 9
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- Cancer Genomics and Diagnostics 13
- Co-authors
- Nicholas K. Hayward (33 shared papers)David C. Whiteman (11 shared papers)Marilyn K. Walters (16 shared papers)Marion A. Maw (2 shared papers)Jane M. Palmer (9 shared papers)Mitchell S. Stark (4 shared papers)Bryan J. Mowry (15 shared papers)Graeme J. Walker (7 shared papers)
- Journals
- PLoS ONE (5 papers)International Journal of Cancer (4 papers)Human Genetics (4 papers)Gastroenterology (3 papers)Nature Genetics (3 papers)
- Partner nations
- AustraliaUnited StatesIndia
In The Last Decade
Derek J. Nancarrow
80 papers receiving 3.2k citations
Peers
Comparison fields: 5 of 116
- Cancer Research 471
- Genetics 855
- Oncology 606
- Molecular Biology 1.5k
- Biological Psychiatry 49
Countries citing papers authored by Derek J. Nancarrow
This map shows the geographic impact of Derek J. Nancarrow'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 Derek J. Nancarrow with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Derek J. Nancarrow more than expected).
Fields of papers citing papers by Derek J. Nancarrow
This network shows the impact of papers produced by Derek J. Nancarrow. 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 Derek J. Nancarrow. The network helps show where Derek J. Nancarrow may publish in the future.
Co-authors
The 25 scholars most cited alongside Derek J. Nancarrow, 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 81 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 296 | |
| 2 | 2014 | 225 | |
| 3 | 1996 | 204 | |
| 4 | 2010 | 175 | |
| 5 | 1998 | 170 | |
| 6 | 1996 | 166 | |
| 7 | 2003 | 96 | |
| 8 | 1999 | 92 | |
| 9 | Confirmation of chromosome 9p linkage in familial melanoma. | 1993 | 82 |
| 10 | 2010 | 80 | |
| 11 | 2007 | 74 | |
| 12 | 2008 | 74 | |
| 13 | 2011 | 74 | |
| 14 | 2000 | 68 | |
| 15 | 1995 | 60 | |
| 16 | 1997 | 60 | |
| 17 | 2015 | 58 | |
| 18 | The contribution of the DFNB1 locus to neurosensory deafness in a Caucasian population. | 1995 | 57 |
| 19 | 2008 | 51 | |
| 20 | 2010 | 48 |
About Derek J. Nancarrow
Derek J. Nancarrow is a scholar working on Oncology, Cancer Research, Genetics, Molecular Biology and Surgery, having authored 81 papers that have together received 3.3k indexed citations. Recurring topics across this work include Esophageal Cancer Research and Treatment (16 papers), Cancer Genomics and Diagnostics (13 papers), Genomic variations and chromosomal abnormalities (11 papers), Genetic Associations and Epidemiology (10 papers), Cutaneous Melanoma Detection and Management (9 papers), Epigenetics and DNA Methylation (6 papers), Genetic factors in colorectal cancer (5 papers) and Cancer-related gene regulation (5 papers). The work is most often cited by research in Cancer Research (471 citations), Genetics (855 citations), Oncology (606 citations), Molecular Biology (1.5k citations) and Biological Psychiatry (49 citations). Derek J. Nancarrow has collaborated with scholars based in Australia, United States and India. Frequent co-authors include Nicholas K. Hayward, David C. Whiteman, Marilyn K. Walters, Marion A. Maw, Jane M. Palmer, Mitchell S. Stark, Bryan J. Mowry, Graeme J. Walker, David Ian Watson and Joseph Kurian Mukkadan. Their work appears in journals such as PLoS ONE, International Journal of Cancer, Human Genetics, Gastroenterology and Nature Genetics.
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.