Ellie M. Wright
Impact in
- Neurology top 5%
- Neurofibromatosis and Schwannoma Cases
- Neuroblastoma Research and Treatments
- Vascular Malformations Diagnosis and Treatment
- Rheumatology top 10%
- Soft tissue tumor case studies
Papers in
- Genetics 6
- Virus-based gene therapy research 2
- Genomic variations and chromosomal abnormalities 2
-
- Neurofibromatosis and Schwannoma Cases 3
- Neuroblastoma Research and Treatments 2
- Co-authors
- Pamela R. Fain (5 shared papers)David Barker (3 shared papers)Peter O'Connell (2 shared papers)K. Nguyen (4 shared papers)Huntington F. Willard (4 shared papers)J. Kivlin (3 shared papers)John C. Carey (3 shared papers)Mark H. Skolnick (2 shared papers)
- Journals
- Genomics (2 papers)Mammalian Genome (1 paper)International Journal of Radiation Oncology*Biology*Physics (1 paper)Science (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Ellie M. Wright
15 papers receiving 837 citations
Ellie M. Wright's Hit Papers
Peers
Comparison fields: 5 of 60
- Neurology 454
- Rheumatology 130
- Genetics 185
- Ophthalmology 46
- Cancer Research 76
Countries citing papers authored by Ellie M. Wright
This map shows the geographic impact of Ellie M. Wright'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 Ellie M. Wright with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ellie M. Wright more than expected).
Fields of papers citing papers by Ellie M. Wright
This network shows the impact of papers produced by Ellie M. Wright. 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 Ellie M. Wright. The network helps show where Ellie M. Wright may publish in the future.
Co-authors
The 25 scholars most cited alongside Ellie M. Wright, 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 | Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17 Hit paper breakdown → | 1987 | 571 |
| 2 | 1988 | 131 | |
| 3 | 1987 | 53 | |
| 4 | Refined physical and genetic mapping of the NF1 region on chromosome 17. | 1989 | 32 |
| 5 | 1996 | 23 | |
| 6 | The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints. | 1989 | 23 |
| 7 | 1997 | 13 | |
| 8 | Complex Y chromosome aberrations are a recurrent secondary event in radiation-induced murine acute myeloid leukaemia. | 1995 | 11 |
| 9 | Hematopoietic stem cell- and marrow stromal cell-specific requirements for gamma irradiation leukemogenesis in vitro. | 1990 | 10 |
| 10 | 1989 | 9 | |
| 11 | 1987 | 8 | |
| 12 | 1989 | 2 | |
| 13 | 2024 | 2 | |
| 14 | 2024 | 1 | |
| 15 | Cellular aspects of radiation-induced leukaemia. | 1991 | 1 |
About Ellie M. Wright
Ellie M. Wright is a scholar working on Genetics, Neurology, Molecular Biology, Pulmonary and Respiratory Medicine and Radiology, Nuclear Medicine and Imaging, having authored 15 papers that have together received 890 indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (3 papers), Genomics and Chromatin Dynamics (3 papers), Chromosomal and Genetic Variations (2 papers), Virus-based gene therapy research (2 papers), Sarcoma Diagnosis and Treatment (2 papers), Neuroblastoma Research and Treatments (2 papers), Effects of Radiation Exposure (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Neurology (454 citations), Rheumatology (130 citations), Genetics (185 citations), Ophthalmology (46 citations) and Cancer Research (76 citations). Ellie M. Wright has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Pamela R. Fain, David Barker, Peter O'Connell, K. Nguyen, Huntington F. Willard, J. Kivlin, John C. Carey, Mark H. Skolnick, Leslie Anne Leinwand and Lisa A. Cannon. Their work appears in journals such as Genomics, Mammalian Genome, International Journal of Radiation Oncology*Biology*Physics, Science and Journal of Medical 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.