D. Averill
Impact in
- Genetics top 5%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 5
- BRCA gene mutations in cancer 4
- Genomic variations and chromosomal abnormalities 2
- Nutrition, Genetics, and Disease 1
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- Ethics in Clinical Research 2
- Co-authors
- Douglas F. Easton (5 shared papers)Michael R. Stratton (3 shared papers)Richard Wooster (2 shared papers)Rosalind A. Eeles (5 shared papers)Deborah Ford (2 shared papers)W. Ormiston (3 shared papers)Simon A. Smith (2 shared papers)David E. Goldgar (1 shared paper)
- Journals
- Psycho-Oncology (2 papers)Nature Genetics (1 paper)The American Journal of Human Genetics (1 paper)PubMed (3 papers)
- Partner nations
- United KingdomIrelandUnited States
In The Last Decade
D. Averill
7 papers receiving 612 citations
Peers
Comparison fields: 5 of 46
- Genetics 418
- Cancer Research 123
- Pathology and Forensic Medicine 134
- Oncology 151
- Reproductive Medicine 46
Countries citing papers authored by D. Averill
This map shows the geographic impact of D. Averill'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 D. Averill with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D. Averill more than expected).
Fields of papers citing papers by D. Averill
This network shows the impact of papers produced by D. Averill. 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 D. Averill. The network helps show where D. Averill may publish in the future.
Co-authors
The 25 scholars most cited alongside D. Averill, 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 | 1997 | 295 | |
| 2 | 1992 | 196 | |
| 3 | Constitutional mutation in exon 8 of the p53 gene in a patient with multiple primary tumours: molecular and immunohistochemical findings. | 1993 | 48 |
| 4 | Genetic heterogeneity and localization of a familial breast-ovarian cancer gene on chromosome 17q12-q21. | 1993 | 41 |
| 5 | No evidence for germline mutations in exons 5-9 of the p53 gene in 25 breast cancer families. | 1992 | 40 |
| 6 | 1996 | 37 | |
| 7 | 1996 | 1 |
About D. Averill
D. Averill is a scholar working on Genetics, Public Health, Environmental and Occupational Health, Economics and Econometrics, Molecular Biology and Pathology and Forensic Medicine, having authored 7 papers that have together received 658 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (4 papers), Health Systems, Economic Evaluations, Quality of Life (2 papers), Ethics in Clinical Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Multiple and Secondary Primary Cancers (1 paper), Prostate Cancer Treatment and Research (1 paper), Cancer Genomics and Diagnostics (1 paper) and Nutrition, Genetics, and Disease (1 paper). The work is most often cited by research in Genetics (418 citations), Cancer Research (123 citations), Pathology and Forensic Medicine (134 citations), Oncology (151 citations) and Reproductive Medicine (46 citations). D. Averill has collaborated with scholars based in United Kingdom, Ireland and United States. Frequent co-authors include Douglas F. Easton, Michael R. Stratton, Richard Wooster, Rosalind A. Eeles, Deborah Ford, W. Ormiston, Simon A. Smith, David E. Goldgar, Linda Steele and Susan L. Neuhausen. Their work appears in journals such as Psycho-Oncology, Nature Genetics, The American Journal of Human Genetics and PubMed.
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.