Amanda Prowse
Impact in
- Cancer Research top 2%
- Cancer, Hypoxia, and Metabolism
- Cancer Genomics and Diagnostics
- Reproductive Medicine top 5%
Papers in
-
- Epigenetics and DNA Methylation 3
- Renal and related cancers 2
- Retinoids in leukemia and cellular processes 2
- Genetics 6
- BRCA gene mutations in cancer 2
- Co-authors
- Nabeel A. Affara (4 shared papers)Eamonn R. Maher (4 shared papers)Paul A. Crossey (3 shared papers)Malcolm A. Ferguson-Smith (2 shared papers)Keith Foster (2 shared papers)Eamonn R. Maher (2 shared papers)Frances M. Richards (2 shared papers)Charles H.C.M. Buys (1 shared paper)
- Journals
- Human Molecular Genetics (3 papers)Genes Chromosomes and Cancer (2 papers)International Journal of Cancer (2 papers)Journal of Medical Genetics (2 papers)Modern Pathology (1 paper)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
Amanda Prowse
17 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 67
- Cancer Research 761
- Reproductive Medicine 140
- Molecular Biology 940
- Pulmonary and Respiratory Medicine 420
- Obstetrics and Gynecology 80
Countries citing papers authored by Amanda Prowse
This map shows the geographic impact of Amanda Prowse'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 Amanda Prowse with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amanda Prowse more than expected).
Fields of papers citing papers by Amanda Prowse
This network shows the impact of papers produced by Amanda Prowse. 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 Amanda Prowse. The network helps show where Amanda Prowse may publish in the future.
Co-authors
The 25 scholars most cited alongside Amanda Prowse, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1994 | 307 | |
| 2 | 1994 | 304 | |
| 3 | 1998 | 227 | |
| 4 | Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumors. | 1997 | 178 |
| 5 | 1995 | 127 | |
| 6 | 2006 | 119 | |
| 7 | Expression of OVCA1, a candidate tumor suppressor, is reduced in tumors and inhibits growth of ovarian cancer cells. | 1999 | 56 |
| 8 | 1994 | 37 | |
| 9 | 2001 | 34 | |
| 10 | 2002 | 22 | |
| 11 | 2002 | 22 | |
| 12 | 2003 | 20 | |
| 13 | 2005 | 20 | |
| 14 | 2002 | 17 | |
| 15 | 2016 | 9 | |
| 16 | 2020 | 8 | |
| 17 | 2024 | 3 |
About Amanda Prowse
Amanda Prowse is a scholar working on Molecular Biology, Genetics, Cancer Research, Oncology and Pulmonary and Respiratory Medicine, having authored 17 papers that have together received 1.5k indexed citations. Recurring topics across this work include Cancer, Hypoxia, and Metabolism (4 papers), Epigenetics and DNA Methylation (3 papers), Cancer-related Molecular Pathways (3 papers), Renal and related cancers (2 papers), Endometrial and Cervical Cancer Treatments (2 papers), BRCA gene mutations in cancer (2 papers), Ovarian cancer diagnosis and treatment (2 papers) and Retinoids in leukemia and cellular processes (2 papers). The work is most often cited by research in Cancer Research (761 citations), Reproductive Medicine (140 citations), Molecular Biology (940 citations), Pulmonary and Respiratory Medicine (420 citations) and Obstetrics and Gynecology (80 citations). Amanda Prowse has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Nabeel A. Affara, Eamonn R. Maher, Paul A. Crossey, Malcolm A. Ferguson-Smith, Keith Foster, Eamonn R. Maher, Frances M. Richards, Charles H.C.M. Buys, Steven C. Clifford and Andrew K. Godwin. Their work appears in journals such as Human Molecular Genetics, Genes Chromosomes and Cancer, International Journal of Cancer, Journal of Medical Genetics and Modern Pathology.
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.