Diana Eccles
Impact in
- Genetics top 0.02%
- BRCA gene mutations in cancer
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Cancer Research top 0.2%
- Breast Cancer Treatment Studies
Papers in
- Genetics 305
- BRCA gene mutations in cancer 273
- Genetic Associations and Epidemiology 75
- Genomics and Rare Diseases 12
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- Ovarian cancer diagnosis and treatment 51
- Co-authors
- D. Gareth Evans (62 shared papers)Douglas F. Easton (11 shared papers)Nazneen Rahman (11 shared papers)Sheila Seal (9 shared papers)Anthony Renwick (7 shared papers)Ian Campbell (14 shared papers)Michael R. Stratton (8 shared papers)Rita Barfoot (6 shared papers)
- Journals
- Journal of Medical Genetics (36 papers)British Journal of Cancer (29 papers)Breast Cancer Research (25 papers)Nature Genetics (23 papers)Cancer Epidemiology Biomarkers & Prevention (12 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Diana Eccles
436 papers receiving 40.5k citations
Diana Eccles's Hit Papers
Peers
Comparison fields: 5 of 200
- Genetics 22k
- Cancer Research 4k
- Reproductive Medicine 2.4k
- Oncology 4.7k
- Pathology and Forensic Medicine 3.4k
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 448 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies Hit paper breakdown → | 2003 | 2873 |
| 2 | Genome-wide association study identifies novel breast cancer susceptibility loci Hit paper breakdown → | 2007 | 1919 |
| 3 | Association analysis identifies 65 new breast cancer risk loci Hit paper breakdown → | 2017 | 1040 |
| 4 | Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations Hit paper breakdown → | 2002 | 902 |
| 5 | Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk Hit paper breakdown → | 2015 | 859 |
| 6 | PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene Hit paper breakdown → | 2006 | 800 |
| 7 | Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial Hit paper breakdown → | 2011 | 781 |
| 8 | Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes Hit paper breakdown → | 2018 | 775 |
| 9 | Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results Hit paper breakdown → | 2008 | 742 |
| 10 | Cancer Risks for BRCA1 and BRCA2 Mutation Carriers: Results From Prospective Analysis of EMBRACE Hit paper breakdown → | 2013 | 723 |
| 11 | Germline BRCA Mutations Are Associated With Higher Risk of Nodal Involvement, Distant Metastasis, and Poor Survival Outcomes in Prostate Cancer Hit paper breakdown → | 2013 | 676 |
| 12 | Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls Hit paper breakdown → | 2010 | 641 |
| 13 | ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles Hit paper breakdown → | 2006 | 600 |
| 14 | Genome-wide association study identifies five new breast cancer susceptibility loci Hit paper breakdown → | 2010 | 591 |
| 15 | Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles Hit paper breakdown → | 2006 | 583 |
| 16 | Associations of Breast Cancer Risk Factors With Tumor Subtypes: A Pooled Analysis From the Breast Cancer Association Consortium Studies Hit paper breakdown → | 2010 | 575 |
| 17 | Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1 / 2 (CIMBA) Hit paper breakdown → | 2012 | 538 |
| 18 | Inherited Mutations in 17 Breast Cancer Susceptibility Genes Among a Large Triple-Negative Breast Cancer Cohort Unselected for Family History of Breast Cancer Hit paper breakdown → | 2014 | 522 |
| 19 | Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer Hit paper breakdown → | 2013 | 468 |
| 20 | Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants Hit paper breakdown → | 2015 | 450 |
About Diana Eccles
Diana Eccles is a scholar working on Genetics, Reproductive Medicine, Pathology and Forensic Medicine, Cancer Research and Oncology, having authored 448 papers that have together received 41.7k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (273 papers), Genetic Associations and Epidemiology (75 papers), Ovarian cancer diagnosis and treatment (51 papers), Genetic factors in colorectal cancer (38 papers), Breast Cancer Treatment Studies (29 papers), Cancer Risks and Factors (13 papers), Genomics and Rare Diseases (12 papers) and Prostate Cancer Diagnosis and Treatment (10 papers). The work is most often cited by research in Genetics (22k citations), Cancer Research (4k citations), Reproductive Medicine (2.4k citations), Oncology (4.7k citations) and Pathology and Forensic Medicine (3.4k 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, Anthony Renwick, Ian Campbell, Michael R. Stratton, Rita Barfoot, Hiran Jayatilake and Lesley McGuffog. Their work appears in journals such as Journal of Medical Genetics, British Journal of Cancer, Breast Cancer Research, Nature Genetics and Cancer Epidemiology Biomarkers & Prevention.
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.