Priscilla Short
Impact in
- Neurology top 10%
- Neurofibromatosis and Schwannoma Cases
- Vascular Malformations Diagnosis and Treatment
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- Bone Tumor Diagnosis and Treatments
Papers in
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- Tuberous Sclerosis Complex Research 4
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- Soft tissue tumors and treatment 1
- Tumors and Oncological Cases 1
- Co-authors
- Bertil Hall (1 shared paper)Catherine M. Phelan (1 shared paper)Mia MacCollin (1 shared paper)Rosanna Weksberg (1 shared paper)Jaime O. Claudio (1 shared paper)Peter Propping (1 shared paper)Dilys M. Parry (1 shared paper)Vincent M. Riccardi (1 shared paper)
- Journals
- Human Mutation (2 papers)Annals of the New York Academy of Sciences (1 paper)PEDIATRICS (1 paper)Genomics (1 paper)PubMed (1 paper)
- Partner nations
- United StatesUnited KingdomNetherlands
In The Last Decade
Priscilla Short
6 papers receiving 346 citations
Peers
Comparison fields: 5 of 46
- Neurology 178
- Rheumatology 67
- Endocrinology 22
- Physiology 103
- Epidemiology 115
Countries citing papers authored by Priscilla Short
This map shows the geographic impact of Priscilla Short'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 Priscilla Short with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Priscilla Short more than expected).
Fields of papers citing papers by Priscilla Short
This network shows the impact of papers produced by Priscilla Short. 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 Priscilla Short. The network helps show where Priscilla Short may publish in the future.
Co-authors
The 25 scholars most cited alongside Priscilla Short, 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 | Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease. | 1996 | 196 |
| 2 | 1995 | 53 | |
| 3 | 1998 | 46 | |
| 4 | 1983 | 43 | |
| 5 | 1991 | 22 | |
| 6 | 1998 | 2 |
About Priscilla Short
Priscilla Short is a scholar working on Physiology, Pathology and Forensic Medicine, Neurology, Pulmonary and Respiratory Medicine and Oncology, having authored 6 papers that have together received 362 indexed citations. Recurring topics across this work include Tuberous Sclerosis Complex Research (4 papers), Soft tissue tumors and treatment (1 paper), Vascular Tumors and Angiosarcomas (1 paper), Escherichia coli research studies (1 paper), Complement system in diseases (1 paper), Neurofibromatosis and Schwannoma Cases (1 paper), Tumors and Oncological Cases (1 paper) and Burkholderia infections and melioidosis (1 paper). The work is most often cited by research in Neurology (178 citations), Rheumatology (67 citations), Endocrinology (22 citations), Physiology (103 citations) and Epidemiology (115 citations). Priscilla Short has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include Bertil Hall, Catherine M. Phelan, Mia MacCollin, Rosanna Weksberg, Jaime O. Claudio, Peter Propping, Dilys M. Parry, Vincent M. Riccardi, Martin Ruttledge and Fei‐Yu Han. Their work appears in journals such as Human Mutation, Annals of the New York Academy of Sciences, PEDIATRICS, Genomics 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.