Diana Eccles
Impact in
- Genetics top 0.2%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Cancer Research top 0.5%
- Cancer Genomics and Diagnostics
- Breast Cancer Treatment Studies
Papers in
- Genetics 74
- BRCA gene mutations in cancer 63
- Genomic variations and chromosomal abnormalities 9
- Genetic Associations and Epidemiology 8
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- DNA Repair Mechanisms 15
- Co-authors
- D. Gareth Evans (51 shared papers)Douglas F. Easton (10 shared papers)Nazneen Rahman (10 shared papers)Sheila Seal (8 shared papers)Michael R. Stratton (8 shared papers)Rita Barfoot (6 shared papers)Anthony Renwick (6 shared papers)Hiran Jayatilake (5 shared papers)
- Journals
- British Journal of Cancer (14 papers)Journal of Medical Genetics (13 papers)Disease Markers (8 papers)Cancer Research (6 papers)Nature Genetics (4 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Diana Eccles
136 papers receiving 7.0k citations
Diana Eccles's Hit Papers
Peers
Comparison fields: 5 of 135
- Genetics 3.4k
- Cancer Research 1.6k
- Pathology and Forensic Medicine 1.6k
- Oncology 1.8k
- Reproductive Medicine 307
Countries citing papers authored by Diana Eccles
This map shows the geographic impact of Diana Eccles'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 Diana Eccles with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Diana Eccles more than expected).
Fields of papers citing papers by Diana Eccles
This network shows the impact of papers produced by Diana Eccles. 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 Diana Eccles. The network helps show where Diana Eccles may publish in the future.
Co-authors
The 25 scholars most cited alongside Diana Eccles, 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 141 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene Hit paper breakdown → | 2006 | 729 |
| 2 | Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles Hit paper breakdown → | 2006 | 545 |
| 3 | ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles Hit paper breakdown → | 2006 | 541 |
| 4 | 2003 | 332 | |
| 5 | 1993 | 219 | |
| 6 | 2013 | 184 | |
| 7 | 2004 | 173 | |
| 8 | 2004 | 170 | |
| 9 | 2011 | 167 | |
| 10 | Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene. | 1996 | 158 |
| 11 | p53 mutation is a common genetic event in ovarian carcinoma. | 1993 | 158 |
| 12 | 2013 | 153 | |
| 13 | 2006 | 149 | |
| 14 | 2008 | 148 | |
| 15 | 2011 | 109 | |
| 16 | 1998 | 106 | |
| 17 | 2009 | 103 | |
| 18 | 2006 | 99 | |
| 19 | 2003 | 98 | |
| 20 | 2002 | 95 |
About Diana Eccles
Diana Eccles is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Oncology and Cancer Research, having authored 141 papers that have together received 7.3k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (63 papers), Genetic factors in colorectal cancer (32 papers), Cancer Genomics and Diagnostics (17 papers), DNA Repair Mechanisms (15 papers), Genomic variations and chromosomal abnormalities (9 papers), Ovarian cancer diagnosis and treatment (8 papers), Genetic Associations and Epidemiology (8 papers) and Cancer-related Molecular Pathways (7 papers). The work is most often cited by research in Genetics (3.4k citations), Cancer Research (1.6k citations), Pathology and Forensic Medicine (1.6k citations), Oncology (1.8k citations) and Reproductive Medicine (307 citations). Diana Eccles has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include D. Gareth Evans, Douglas F. Easton, Nazneen Rahman, Sheila Seal, Michael R. Stratton, Rita Barfoot, Anthony Renwick, Hiran Jayatilake, Lesley McGuffog and Deborah J. Thompson. Their work appears in journals such as British Journal of Cancer, Journal of Medical Genetics, Disease Markers, Cancer Research 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.