Anna Elliott
Impact in
- Genetics top 2%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
-
- DNA Repair Mechanisms 3
- Epigenetics and DNA Methylation 2
- Renal and related cancers 1
- Genetics 6
- BRCA gene mutations in cancer 3
- Genomic variations and chromosomal abnormalities 2
- Genetics and Neurodevelopmental Disorders 1
- Co-authors
- Nazneen Rahman (8 shared papers)Sheila Seal (7 shared papers)Anthony Renwick (6 shared papers)D. Gareth Evans (3 shared papers)Diana Eccles (3 shared papers)Michael R. Stratton (3 shared papers)Lesley McGuffog (2 shared papers)Rita Barfoot (2 shared papers)
- Journals
- Nature Genetics (2 papers)The American Journal of Human Genetics (1 paper)Scientific Reports (1 paper)Human Molecular Genetics (1 paper)Nature Communications (1 paper)
- Partner nations
- United KingdomUnited StatesSouth Africa
In The Last Decade
Anna Elliott
10 papers receiving 1.5k citations
Anna Elliott's Hit Papers
Peers
Comparison fields: 5 of 72
- Genetics 1.1k
- Cancer Research 391
- Pathology and Forensic Medicine 300
- Molecular Biology 965
- Oncology 259
Countries citing papers authored by Anna Elliott
This map shows the geographic impact of Anna Elliott'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 Anna Elliott with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna Elliott more than expected).
Fields of papers citing papers by Anna Elliott
This network shows the impact of papers produced by Anna Elliott. 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 Anna Elliott. The network helps show where Anna Elliott may publish in the future.
Co-authors
The 25 scholars most cited alongside Anna Elliott, 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 | PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene Hit paper breakdown → | 2006 | 689 |
| 2 | Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles Hit paper breakdown → | 2006 | 513 |
| 3 | 2017 | 128 | |
| 4 | 2014 | 64 | |
| 5 | 2015 | 62 | |
| 6 | 2010 | 14 | |
| 7 | 2016 | 13 | |
| 8 | 1992 | 9 | |
| 9 | 2016 | 4 | |
| 10 | The ICR1000 UK exome series: a resource of gene variation in an outbred population [version 1; referees: 2 approved] | 2015 | 2 |
About Anna Elliott
Anna Elliott is a scholar working on Molecular Biology, Genetics, Surgery, Paleontology and Pharmacology, having authored 10 papers that have together received 1.5k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (3 papers), BRCA gene mutations in cancer (3 papers), Epigenetics and DNA Methylation (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Pancreatic function and diabetes (1 paper), Cancer Genomics and Diagnostics (1 paper), Renal and related cancers (1 paper) and Genetics and Neurodevelopmental Disorders (1 paper). The work is most often cited by research in Genetics (1.1k citations), Cancer Research (391 citations), Pathology and Forensic Medicine (300 citations), Molecular Biology (965 citations) and Oncology (259 citations). Anna Elliott has collaborated with scholars based in United Kingdom, United States and South Africa. Frequent co-authors include Nazneen Rahman, Sheila Seal, Anthony Renwick, D. Gareth Evans, Diana Eccles, Michael R. Stratton, Lesley McGuffog, Rita Barfoot, Douglas F. Easton and Deborah J. Thompson. Their work appears in journals such as Nature Genetics, The American Journal of Human Genetics, Scientific Reports, Human Molecular Genetics and Nature Communications.
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.