Priscilla Short

480 total citations
6 papers, 362 citations indexed

About

Priscilla Short is a scholar working on Physiology, Pathology and Forensic Medicine and Neurology. According to data from OpenAlex, Priscilla Short has authored 6 papers receiving a total of 362 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Physiology, 2 papers in Pathology and Forensic Medicine and 1 paper in Neurology. Recurrent topics in Priscilla Short's work include Tuberous Sclerosis Complex Research (4 papers), Vascular Tumors and Angiosarcomas (1 paper) and Sarcoma Diagnosis and Treatment (1 paper). Priscilla Short is often cited by papers focused on Tuberous Sclerosis Complex Research (4 papers), Vascular Tumors and Angiosarcomas (1 paper) and Sarcoma Diagnosis and Treatment (1 paper). Priscilla Short collaborates with scholars based in United States, United Kingdom and Netherlands. Priscilla Short's co-authors include Virginia V. Michels, Vincent M. Riccardi, Fei‐Yu Han, Nathalie Chrétien, Bertil Hall, Catherine M. Phelan, Guy A. Rouleau, Martin Ruttledge, Dilys M. Parry and Katsumasa Kitamura and has published in prestigious journals such as PEDIATRICS, Annals of the New York Academy of Sciences and Genomics.

In The Last Decade

Priscilla Short

6 papers receiving 346 citations

Peers

Countries citing papers authored by Priscilla Short

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Priscilla Short

This figure shows the co-authorship network connecting the top 25 collaborators of Priscilla Short. A scholar is included among the top collaborators of Priscilla Short based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Priscilla Short. Priscilla Short is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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6 of 6 papers shown

#	Work	Indexed citations
1	Exon scanning of the entireTSC2 gene for germline mutations in 40 unrelated patients with tuberous sclerosis 1998 ·Human Mutation ·Roberta L. Beauchamp, (unknown), Patrick McNamara, (unknown), (unknown), Hope Northrup, Priscilla Short, Katherine B. Sims, Laurie J. Ozelius, Vijaya Ramesh	46
2	Exon scanning of the entire TSC2 gene for germline mutations in 40 unrelated patients with tuberous sclerosis 1998 ·Human Mutation ·Roberta L. Beauchamp, (unknown), Patrick McNamara, (unknown), (unknown), Hope Northrup, Priscilla Short, Katherine B. Sims, Laurie J. Ozelius, Vijaya Ramesh	2
3	Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease. 1996 ·PubMed ·Martin Ruttledge, Anne Andermann, Catherine M. Phelan, Jaime O. Claudio, Fei‐Yu Han, Nathalie Chrétien, (unknown), Mia MacCollin, Priscilla Short, Dilys M. Parry, Virginia V. Michels, Vincent M. Riccardi, Rosanna Weksberg, Katsumasa Kitamura, (unknown), Bertil Hall, Peter Propping, Guy A. Rouleau	196
4	Alternative Splicing of the Tuberous Sclerosis 2 (TSC2) Gene in Human and Mouse Tissues 1995 ·Genomics ·Lin Xu, Christopher J. Sterner, Magitha M. Maheshwar, Peter J. Wilson, Mark Nellist, Priscilla Short, Jonathan L. Haines, Julian R. Sampson, Vijaya Ramesh	53
5	A Comparative Study on Genetic Heterogeneity in Tuberous Sclerosis: Evidence for One Gene on 9q34 and a Second Gene on 11q22–23^a 1991 ·Annals of the New York Academy of Sciences ·(unknown), Sue Povey, (unknown), L. A. Sandkuyl, Dick Lindhout, Pamela Flodman, M. Smith, Julian R. Sampson, (unknown), (unknown), P Fleury, Priscilla Short, J. Amos, D. J. J. Halley	22
6	Campylobacter jejuni-Associated Hemolytic-Uremic Syndrome in a Mother and Daughter 1983 ·PEDIATRICS ·(unknown), Alan I. Hartstein, (unknown), (unknown), Priscilla Short, Ronald M. Katon	43

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.

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